Fgf10

Summary

Gene Symbol: Fgf10
Description: fibroblast growth factor 10
Alias: AEY17, BB213776, Fgf-10, Gsfaey17, keratinocyte growth factor 2
Species: mouse

Top Publications

  1. ncbi An FGF signaling loop sustains the generation of differentiated progeny from stem cells in mouse incisors
    Ophir D Klein
    Department of Anatomy and Program in Developmental Biology, School of Medicine, University of California at San Francisco, San Francisco, CA 94143 2711, USA
    Development 135:377-85. 2008
  2. ncbi Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart
    Chen Leng Cai
    Institute of Molecular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA
    Dev Cell 5:877-89. 2003
  3. ncbi Fgf10 is an oncogene activated by MMTV insertional mutagenesis in mouse mammary tumors and overexpressed in a subset of human breast carcinomas
    Vassiliki Theodorou
    Division of Tumor Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands
    Oncogene 23:6047-55. 2004
  4. ncbi A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes
    M K Hajihosseini
    Imperial Cancer Research Fund, 44 Lincoln s Inn Fields, London WC2A 3PX, United Kingdom
    Proc Natl Acad Sci U S A 98:3855-60. 2001
  5. ncbi Lung hypoplasia and neonatal death in Fgf9-null mice identify this gene as an essential regulator of lung mesenchyme
    J S Colvin
    Department of Molecular Biology and Pharmacology, Washington University Medical School, Campus Box 8103, 660 S Euclid Avenue, St Louis, MO 63110, USA
    Development 128:2095-106. 2001
  6. ncbi Cloning and expression pattern of a mouse homologue of drosophila sprouty in the mouse embryo
    A A de Maximy
    Institut Curie UMR 144 CNRS, 26 Rue d Ulm, 75248, Paris Cedex 05, France
    Mech Dev 81:213-6. 1999
  7. ncbi The splanchnic mesodermal plate directs spleen and pancreatic laterality, and is regulated by Bapx1/Nkx3.2
    Jacob Hecksher-Sørensen
    Comparative and Developmental Genetics Section, MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK
    Development 131:4665-75. 2004
  8. ncbi Apoptosis, proliferation and gene expression patterns in mouse developing tongue
    Xuguang Nie
    Section of Anatomy and Cell Biology, Department of Biomedicine, University of Bergen, Jonas Lies V91, 5009, Bergen, Norway
    Anat Embryol (Berl) 210:125-32. 2005
  9. ncbi Bmp4 is essential for the formation of the vestibular apparatus that detects angular head movements
    Weise Chang
    National Institute on Deafness and Other Communication Disorders, NIH, Rockville, Maryland, United States of America
    PLoS Genet 4:e1000050. 2008
  10. ncbi TBX1 is required for inner ear morphogenesis
    Francesca Vitelli
    Department of Pediatrics Cardiology, Baylor College of Medicine, Houston, TX 77030, USA
    Hum Mol Genet 12:2041-8. 2003

Scientific Experts

Detail Information

Publications127 found, 100 shown here

  1. ncbi An FGF signaling loop sustains the generation of differentiated progeny from stem cells in mouse incisors
    Ophir D Klein
    Department of Anatomy and Program in Developmental Biology, School of Medicine, University of California at San Francisco, San Francisco, CA 94143 2711, USA
    Development 135:377-85. 2008
    ..These data reveal that the generation of differentiated progeny from a particular stem cell population can be differently regulated in the embryo and adult...
  2. ncbi Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart
    Chen Leng Cai
    Institute of Molecular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA
    Dev Cell 5:877-89. 2003
    ..Our results have implications for the development of specific cardiac lineages, left-right asymmetry, cardiac evolution, and isolation of cardiac progenitor cells...
  3. ncbi Fgf10 is an oncogene activated by MMTV insertional mutagenesis in mouse mammary tumors and overexpressed in a subset of human breast carcinomas
    Vassiliki Theodorou
    Division of Tumor Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands
    Oncogene 23:6047-55. 2004
    ..in mammary tumors from BALB/c mice infected with C3H-MMTV, we have found a common MMTV insertion site in the Fgf10 locus...
  4. ncbi A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes
    M K Hajihosseini
    Imperial Cancer Research Fund, 44 Lincoln s Inn Fields, London WC2A 3PX, United Kingdom
    Proc Natl Acad Sci U S A 98:3855-60. 2001
    ..This phenotype has strong parallels to some Apert's and Pfeiffer's syndrome patients...
  5. ncbi Lung hypoplasia and neonatal death in Fgf9-null mice identify this gene as an essential regulator of lung mesenchyme
    J S Colvin
    Department of Molecular Biology and Pharmacology, Washington University Medical School, Campus Box 8103, 660 S Euclid Avenue, St Louis, MO 63110, USA
    Development 128:2095-106. 2001
    ..Fibroblast growth factors (FGFs) often mediate epithelial-mesenchymal interactions and mesenchymal Fgf10 is essential for epithelial branching in the developing lung...
  6. ncbi Cloning and expression pattern of a mouse homologue of drosophila sprouty in the mouse embryo
    A A de Maximy
    Institut Curie UMR 144 CNRS, 26 Rue d Ulm, 75248, Paris Cedex 05, France
    Mech Dev 81:213-6. 1999
    ..Sprouty4 expression is also detected in the lateral region of the somites. In the developing lung, Sprouty4 is expressed broadly in the distal mesenchyme...
  7. ncbi The splanchnic mesodermal plate directs spleen and pancreatic laterality, and is regulated by Bapx1/Nkx3.2
    Jacob Hecksher-Sørensen
    Comparative and Developmental Genetics Section, MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK
    Development 131:4665-75. 2004
    ..In the absence of Fgf10 expression, the spleno-pancreatic mesenchyme and surrounding SMP grow laterally but contain no endodermal ..
  8. ncbi Apoptosis, proliferation and gene expression patterns in mouse developing tongue
    Xuguang Nie
    Section of Anatomy and Cell Biology, Department of Biomedicine, University of Bergen, Jonas Lies V91, 5009, Bergen, Norway
    Anat Embryol (Berl) 210:125-32. 2005
    ..High expression of Fgf7 and Fgf10 was also detected in the mesenchyme at the early embryonic stage of tongue development, corresponding to the Fgfr ..
  9. ncbi Bmp4 is essential for the formation of the vestibular apparatus that detects angular head movements
    Weise Chang
    National Institute on Deafness and Other Communication Disorders, NIH, Rockville, Maryland, United States of America
    PLoS Genet 4:e1000050. 2008
    ..regulating genes required for prosensory development in the inner ear such as Serrate1 (Jagged1 in mouse), Fgf10, and Sox2...
  10. ncbi TBX1 is required for inner ear morphogenesis
    Francesca Vitelli
    Department of Pediatrics Cardiology, Baylor College of Medicine, Houston, TX 77030, USA
    Hum Mol Genet 12:2041-8. 2003
    ..Our data suggest that Tbx1 deletion in del22q11 patients may cause not only external and middle ear defects but also sensorineural and vestibular phenotypes observed in these patients...
  11. ncbi Fgf9 signaling regulates inner ear morphogenesis through epithelial-mesenchymal interactions
    Ulla Pirvola
    Institute of Biotechnology, University of Helsinki, 00014 Helsinki, Finland
    Dev Biol 273:350-60. 2004
    ..Together, these data show that Fgf9 signaling is required for inner ear morphogenesis...
  12. ncbi Specification of the mammalian cochlea is dependent on Sonic hedgehog
    Martin M Riccomagno
    Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA
    Genes Dev 16:2365-78. 2002
    ..Taken together, our data support a model whereby auditory cell fates in the otic vesicle are established by the direct action of Shh...
  13. ncbi Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract
    Huansheng Xu
    Program in Cardiovascular Sciences, Baylor College of Medicine, Houston, TX 77030, USA
    Development 131:3217-27. 2004
    ..This process might be regulated in part by Fgf10, which we show for the first time to be a direct target of Tbx1 in vitro...
  14. ncbi Gene expression profiles of mouse submandibular gland development: FGFR1 regulates branching morphogenesis in vitro through BMP- and FGF-dependent mechanisms
    Matthew P Hoffman
    Craniofacial Developmental Biology and Regeneration Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, 30 Convent Drive, MSC 4370, Bethesda, MD 20892 4370, USA
    Development 129:5767-78. 2002
    ..FGFR1 signaling regulates Fgfr1, Fgf1, Fgf3 and Bmp7 expression and indirectly regulates Fgf7, Fgf10 and Bmp4. Exogenous FGFs and BMPs added to glands in culture reveal distinct effects on gland morphology...
  15. ncbi FGF8 dose-dependent regulation of embryonic submandibular salivary gland morphogenesis
    Tina Jaskoll
    Laboratory for Developmental Genetics, University of Southern California, Los Angeles, CA 90089 0641, USA
    Dev Biol 268:457-69. 2004
    ..Furthermore, since FGF10 and Shh expression is modulated by Fgf8 levels, we postulated that exogenous FGF10, Shh, or FGF10 + Shh peptide ..
  16. ncbi Pitx1 and Pitx2 are required for development of hindlimb buds
    Alexandre Marcil
    Laboratoire de Genetique Moleculaire, Institut de Recherches Cliniques de Montreal, 110 avenue des Pins Ouest, Montreal, QC H2W 1R7, Canada
    Development 130:45-55. 2003
    ..Thus, Pitx1 and Pitx2 genes are required for sustained hindlimb bud growth and formation of hindlimbs...
  17. ncbi beta-Catenin is required for specification of proximal/distal cell fate during lung morphogenesis
    Michael L Mucenski
    Division of Pulmonary Biology, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
    J Biol Chem 278:40231-8. 2003
    ..These observations establish, for the first time, both the sites and timing of specification of the proximal and peripheral airways in the developing lung, and that beta-catenin is one of the essential components of this specification...
  18. ncbi FGF10 signaling maintains the pancreatic progenitor cell state revealing a novel role of Notch in organ development
    Gitte Anker Norgaard
    Barbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, Denver, CO 80262, USA
    Dev Biol 264:323-38. 2003
    b>FGF10 plays an important role in the morphogenesis of several tissues by control of mesenchymal-to-epithelial signaling...
  19. ncbi Fgf10 maintains notch activation, stimulates proliferation, and blocks differentiation of pancreatic epithelial cells
    Alan Hart
    Umeå Center for Molecular Medicine, University of Umea, Umea, Sweden
    Dev Dyn 228:185-93. 2003
    ..The fibroblast growth factor receptor (FGFR) 2b high-affinity ligand FGF10 has been linked to pancreatic epithelial cell proliferation, and we have shown previously that Notch signalling ..
  20. ncbi Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice
    Victoria Randall
    Molecular Medicine Unit, Institute of Child Health, London, United Kingdom
    J Clin Invest 119:3301-10. 2009
    ..We could not rescue PAA morphogenesis by restoring neural crest Chd7 expression. Rather, biallelic expression of Chd7 and Tbx1 in the pharyngeal ectoderm was required for normal PAA development...
  21. ncbi Tbx2 is essential for patterning the atrioventricular canal and for morphogenesis of the outflow tract during heart development
    Zachary Harrelson
    Department of Genetics and Development, College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA
    Development 131:5041-52. 2004
    ....
  22. ncbi Hes1 is expressed in the second heart field and is required for outflow tract development
    Francesca Rochais
    Developmental Biology Institute of Marseilles Luminy, UMR 6216 CNRS Université de la Méditerranée, Campus de Luminy, Marseille, France
    PLoS ONE 4:e6267. 2009
    ..In order to provide further insight into second heart field development we characterized the insertion site of a transgene expressed in the second heart field and outflow tract as the result of an integration site position effect...
  23. ncbi Enhanced paracrine FGF10 expression promotes formation of multifocal prostate adenocarcinoma and an increase in epithelial androgen receptor
    Sanaz Memarzadeh
    Department of Obstetrics and Gynecology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA
    Cancer Cell 12:572-85. 2007
    Enhanced mesenchymal expression of FGF10 led to the formation of multifocal PIN or prostate cancer. Inhibition of epithelial FGFR1 signaling using DN FGFR1 led to reversal of the cancer phenotype...
  24. ncbi In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea
    Huansheng Xu
    Institute of Biosciences and Technology, Texas A and M Health Science Center, Houston, TX 77030, USA
    Dev Biol 310:329-40. 2007
    ..This model provides a striking demonstration of the essential role played by the periotic mesenchyme in the organogenesis of the cochlea...
  25. ncbi Fgf10 dosage is critical for the amplification of epithelial cell progenitors and for the formation of multiple mesenchymal lineages during lung development
    Suresh K Ramasamy
    Developmental Biology Program, Saban Research Institute of Childrens Hospital Los Angeles, Los Angeles, CA 90027, USA
    Dev Biol 307:237-47. 2007
    The key role played by Fgf10 during early lung development is clearly illustrated in Fgf10 knockout mice, which exhibit lung agenesis...
  26. ncbi Multiple dose-dependent roles for Sox2 in the patterning and differentiation of anterior foregut endoderm
    Jianwen Que
    Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA
    Development 134:2521-31. 2007
    ..These findings suggest that Sox2 plays a second role in establishing the boundary between the keratinized, squamous esophagus/forestomach and glandular hindstomach...
  27. ncbi Levels of mesenchymal FGFR2 signaling modulate smooth muscle progenitor cell commitment in the lung
    Stijn P De Langhe
    Developmental Biology Program, Department of Surgery, Saban Research Institute of Childrens Hospital Los Angeles, CA 90027, USA
    Dev Biol 299:52-62. 2006
    ..Using a set of in vivo and in vitro studies, we show that an autocrine FGF10-FGFR2b signaling loop is established in the mutant lung mesenchyme, which has several consequences...
  28. ncbi Dlx5 and Dlx6 homeobox genes are required for specification of the mammalian vestibular apparatus
    Raymond F Robledo
    The Jackson Laboratory, Bar Harbor, Maine
    Genesis 44:425-37. 2006
    ..Given their proximity to the disease locus and the observed phenotype in Dlx5/6 null mice, Dlx5/6 are likely candidates to mediate the inner ear defects observed in patients with split hand/split foot malformation...
  29. ncbi Sprouty genes control diastema tooth development via bidirectional antagonism of epithelial-mesenchymal FGF signaling
    Ophir D Klein
    Department of Anatomy and Program in Developmental Biology, School of Medicine, University of California, San Francisco, San Francisco, California 94143, USA
    Dev Cell 11:181-90. 2006
    ....
  30. ncbi Gata3 is required for early morphogenesis and Fgf10 expression during otic development
    Kersti Lilleväli
    Institute of Biotechnology, University of Helsinki, Viikinkaari 9, 00710 Helsinki, Finland
    Mech Dev 123:415-29. 2006
    ..Inactivation of Gata3 leads also to a loss of Fgf10 expression in otic epithelium and auditory ganglion demonstrating that Gata3 is an important regulator of Fgf-..
  31. ncbi Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice
    Anita Marguerie
    Cancer Research UK, London Research Institute, 61 Lincoln s Inn Fields, London WC2A 3PX, UK
    Cardiovasc Res 71:50-60. 2006
    Myocardial progenitor cells expressing Fgf10 give rise to the outflow tract and right ventricle of the mammalian heart...
  32. ncbi Stomach development is dependent on fibroblast growth factor 10/fibroblast growth factor receptor 2b-mediated signaling
    Bradley Spencer-Dene
    Experimental Pathology Laboratory, Cancer Research UK, London Research Institute, London, England
    Gastroenterology 130:1233-44. 2006
    ..unknown; however, the developmental expression profile of the IIIb isoform of Fgfr2 (Fgfr2b) and its main ligand, Fgf10, suggest that they may be strong candidates...
  33. ncbi Differential role of FGF9 on epithelium and mesenchyme in mouse embryonic lung
    Pierre Marie del Moral
    Developmental Biology Program, Saban Research Institute of Children s Hospital Los Angeles, Los Angeles, CA 90027, USA
    Dev Biol 293:77-89. 2006
    ..At the molecular level, FGF9 up-regulates Fgf10 expression in the mesenchyme likely via increased expression of Tbx4 and 5 and controls the transcription of ..
  34. ncbi VEGF-A signaling through Flk-1 is a critical facilitator of early embryonic lung epithelial to endothelial crosstalk and branching morphogenesis
    Pierre Marie del Moral
    Developmental Biology Program, Saban Research Institute, Children s Hospital Los Angeles, Department of Pediatric Surgery, USC Keck School of Medicine, 4650 Sunset Blvd, Los Angeles, CA 90027, USA
    Dev Biol 290:177-88. 2006
    ..These results demonstrate that the VEGF pathway is involved in driving epithelial to endothelial crosstalk in embryonic mouse lung morphogenesis...
  35. ncbi Fgf10 expression identifies parabronchial smooth muscle cell progenitors and is required for their entry into the smooth muscle cell lineage
    Arnaud A Mailleux
    UMR144 CNRS Institut Curie, 75248 Paris Cedex 05, France
    Development 132:2157-66. 2005
    ..Using a transgenic mouse line expressing LacZ under the control of Fgf10 regulatory sequences, we show that the pool of Fgf10-positive cells in the distal lung mesenchyme contains ..
  36. ncbi An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome
    Deborah U Frank
    Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT 84112, USA
    Development 129:4591-603. 2002
    ..and heart due, at least in part, to failure to form the fourth pharyngeal arch arteries, altered expression of Fgf10 in the pharyngeal mesenchyme, and abnormal apoptosis in pharyngeal and cardiac neural crest...
  37. ncbi FGF10 maintains stem cell compartment in developing mouse incisors
    Hidemitsu Harada
    Second Department of Oral Anatomy and Cell Biology, Kyushu Dental College, 2 6 1, Manazuru, Kokurakita ku, Kitakyushu, 803 8580, Japan
    Development 129:1533-41. 2002
    ..To further illustrate the role of FGF10 in the formation of the stem cell compartment during tooth organogenesis, we have analyzed incisor development in ..
  38. ncbi Fibroblast growth factor receptor 2-IIIb acts upstream of Shh and Fgf4 and is required for limb bud maintenance but not for the induction of Fgf8, Fgf10, Msx1, or Bmp4
    J M Revest
    Imperial Cancer Research Fund, Lincoln s Inn Fields, London, WC2A 3PX, United Kingdom
    Dev Biol 231:47-62. 2001
    ..Its absence did not prevent expression of Fgf8, Fgf10, Bmp4, and Msx1, but did prevent induction of Shh and Fgf4, indicating that they are downstream targets of FgfR2-..
  39. ncbi FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development
    H Ohuchi
    Department of Genetic Biochemistry, Kyoto University Graduate School of Pharmaceutical Sciences, 46 29 Yoshida shimo adachi cho, Sakyo ku, Kyoto City, Kyoto, 606 8501, Japan
    Biochem Biophys Res Commun 277:643-9. 2000
    ..One of the candidate ligands is FGF10, because FGF10 binds to FGFR2b with high affinity and the formation of the limb and lung is arrested in FGF10 null ..
  40. ncbi Fibroblast growth factor 10 (FGF10) and branching morphogenesis in the embryonic mouse lung
    S Bellusci
    Department of Cell Biology, Vanderbilt University Medical Center, Nashville, Tennessee 37232 2175, USA
    Development 124:4867-78. 1997
    ..We report here that fibroblast growth factor 10 (Fgf10) is expressed dynamically in the mesenchyme adjacent to the distal buds from the earliest stages of lung ..
  41. ncbi Fgf10 is essential for maintaining the proliferative capacity of epithelial progenitor cells during early pancreatic organogenesis
    A Bhushan
    INSERM 457, Hospital Robert Debre, 75019 Paris, France
    Development 128:5109-17. 2001
    ..We demonstrate here that Fgf10, a member of the fibroblast growth factor family (FGFs), plays an essential role in this process...
  42. ncbi Endogenous and ectopic gland induction by FGF-10
    V Govindarajan
    Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, 77030, USA
    Dev Biol 225:188-200. 2000
    ..In addition, lacrimal and Harderian glands were not seen in FGF-10 null fetuses. Based on these results we propose that FGF-10 is an inductive signal that initiates ocular gland morphogenesis...
  43. ncbi Mouse fibroblast growth factor 10: cDNA cloning, protein characterization, and regulation of mRNA expression
    H D Beer
    Human Genome Sciences, Inc, Rockville, Maryland 20850, USA
    Oncogene 15:2211-8. 1997
    ..These results demonstrate a differential regulation of mFGF-10 and FGF-7 expression in vitro and during the wound healing process...
  44. ncbi Fibroblast growth factor interactions in the developing lung
    D Lebeche
    Pulmonary Center, Boston University School of Medicine, 80 East Concord Street R 304, Boston, MA 02118, USA
    Mech Dev 86:125-36. 1999
    ..Our data support a model in which Shh, TGFbeta-1 and BMP-4 counteract the bud promoting effects of FGF-10, and where FGF levels are maintained throughout lung development by other FGFs and Shh...
  45. ncbi FGF-10 is a chemotactic factor for distal epithelial buds during lung development
    W Y Park
    Pulmonary Center, Boston University School of Medicine, Boston, Massachusetts 02118, USA
    Dev Biol 201:125-34. 1998
    ....
  46. ncbi Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development
    S Vainio
    Department of Pedodontics and Orthodontics, University of Helsinki, Finland
    Cell 75:45-58. 1993
    ..In addition, BMP-4 induced its own mesenchymal expression. These findings support the hypothesis that BMP-4 mediates epithelial-mesenchymal interactions during early tooth development...
  47. ncbi Embryonic submandibular gland morphogenesis: stage-specific protein localization of FGFs, BMPs, Pax6 and Pax9 in normal mice and abnormal SMG phenotypes in FgfR2-IIIc(+/Delta), BMP7(-/-) and Pax6(-/-) mice
    Tina Jaskoll
    Laboratory for Developmental Genetics, University of Southern California, Los Angeles, CA 90089 0641, USA
    Cells Tissues Organs 170:83-98. 2002
    ..Finally, our observations of abnormal SMGs in BMP7(-/-) and Pax6(-/-) indicate that both BMP7 and Pax6 play important roles during embryonic SMG branching morphogenesis...
  48. ncbi Evidence that SPROUTY2 functions as an inhibitor of mouse embryonic lung growth and morphogenesis
    A A Mailleux
    UMR144 CNRS Institut Curie, 26 Rue d Ulm, 75248 Cedex 05, Paris, France
    Mech Dev 102:81-94. 2001
    ..We and others have shown that Fibroblast Growth Factor 10 (FGF10) is a key positive regulator of lung branching morphogenesis...
  49. ncbi Wnt5a participates in distal lung morphogenesis
    Changgong Li
    Department of Pediatrics, Women s and Children s Hospital, Los Angeles, CA 90033, USA
    Dev Biol 248:68-81. 2002
    ..Absence of WNT5a activity in the mutant lungs leads to increased expression of Fgf-10, Bmp4, Shh, and its receptor Ptc, raising the possibility that WNT5a, FGF-10, BMP4, and SHH signaling pathways are functionally interactive...
  50. ncbi Role of FGF10/FGFR2b signaling during mammary gland development in the mouse embryo
    Arnaud André Mailleux
    UMR144 CNRS Institut Curie, 26 rue d Ulm 75248 Paris Cedex 05, France
    Development 129:53-60. 2002
    ..placode development using Lef1 as a marker for the epithelial component of the placode, and mice deficient for Fgf10 or Fgfr2b, both of which fail to develop normal mammary glands...
  51. ncbi FGF-10 disrupts lung morphogenesis and causes pulmonary adenomas in vivo
    J C Clark
    Division of Pulmonary Biology, Children s Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH 45229 3039, USA
    Am J Physiol Lung Cell Mol Physiol 280:L705-15. 2001
    ..FGF-10 disrupted lung morphogenesis and induced multifocal pulmonary tumors in vivo and caused reversible type II cell differentiation of the respiratory epithelium...
  52. ncbi Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to Drosophila branchless
    H Min
    Department of Molecular Genetics, Amgen, Inc, Thousand Oaks, California 91320 1789 USA
    Genes Dev 12:3156-61. 1998
    ..The pulmonary phenotype of Fgf-10(-/-) mice is strikingly similar to that of the Drosophila mutant branchless, an Fgf homolog...
  53. ncbi Hes1 is required for pituitary growth and melanotrope specification
    Lori T Raetzman
    University of Michigan, Ann Arbor 48109 0618, USA
    Dev Biol 304:455-66. 2007
    ..These results demonstrate that Notch signaling plays multiple roles in pituitary development, influencing precursor number, organ size, cell differentiation and ultimately cell fate...
  54. ncbi Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands
    Miriam Entesarian
    Department of Genetics and Pathology, Uppsala University, The Rudbeck Laboratory, SE 751 85 Uppsala, Sweden
    Nat Genet 37:125-7. 2005
    ..We mapped ALSG to 5p13.2-5q13.1, which coincides with the gene fibroblast growth factor 10 (FGF10). In two extended pedigrees, we identified heterozygous mutations in FGF10 in all individuals with ALSG...
  55. ncbi Wnt5a regulates Shh and Fgf10 signaling during lung development
    Changgong Li
    Department of Pediatrics, Women s and Children s Hospital, USC Keck School of Medicine, Los Angeles, CA 90033, USA
    Dev Biol 287:86-97. 2005
    ..During early lung development, over-expression of Wnt5a in the epithelium resulted in increased Fgf10 in the mesenchyme and decreased Shh in the epithelium...
  56. ncbi FGF9 and SHH signaling coordinate lung growth and development through regulation of distinct mesenchymal domains
    Andrew C White
    Department of Molecular Biology and Pharmacology, Washington University Medical School, St Louis, MO 63110, USA
    Development 133:1507-17. 2006
    ....
  57. ncbi Fgf10 is essential for limb and lung formation
    K Sekine
    Institute of Molecular and Cellular Biosciences, The University of Tokyo, Japan
    Nat Genet 21:138-41. 1999
    ..In particular, Fgf10 is predicted to function as a regulator of brain, lung and limb development on the basis of its spatiotemporal ..
  58. ncbi The arterial pole of the mouse heart forms from Fgf10-expressing cells in pharyngeal mesoderm
    R G Kelly
    Departement de Biologie Moleculaire, Institut Pasteur, Paris, France
    Dev Cell 1:435-40. 2001
    ..The nlacZ transgene has integrated upstream of the fibroblast growth factor 10 (Fgf10) gene and comparison with the expression pattern of Fgf10 in pharyngeal mesoderm indicates transgene control by ..
  59. ncbi Noggin regulates Bmp4 activity during pituitary induction
    Shannon W Davis
    Department of Human Genetics, University of Michigan Medical School, 4909 Buhl Building, 1241 E Catherine St, Ann Arbor, MI 48109 0618, USA
    Dev Biol 305:145-60. 2007
    ..This work demonstrates the importance of attenuating the activity of Bmp signaling during pituitary induction in order to maintain the proper balance of signaling factors necessary for pituitary organogenesis...
  60. ncbi BMP signals control limb bud interdigital programmed cell death by regulating FGF signaling
    Sangeeta Pajni-Underwood
    Laboratory of Cancer and Developmental Biology National Institutes of Health, Frederick, MD 21702, USA
    Development 134:2359-68. 2007
    ..We conclude that during normal embryogenesis, BMP signaling to the AER indirectly regulates interdigit PCD by regulating AER-FGFs, which act as survival factors for the interdigit mesenchyme...
  61. ncbi 2,3,7,8-Tetrachlorodibenzo-p-dioxin inhibits fibroblast growth factor 10-induced prostatic bud formation in mouse urogenital sinus
    Chad M Vezina
    Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin, Madison, Wisconsin 53705 2222, USA
    Toxicol Sci 113:198-206. 2010
    ..The purpose of this study was to determine whether inhibition of fibroblast growth factor 10 (FGF10) signaling is mechanistically linked to mouse prostatic budding impairment by TCDD...
  62. ncbi The Cdk4-E2f1 pathway regulates early pancreas development by targeting Pdx1+ progenitors and Ngn3+ endocrine precursors
    So Yoon Kim
    Regenerative Biology Section, Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA
    Development 138:1903-12. 2011
    ....
  63. ncbi Sonic hedgehog signaling regulates reciprocal epithelial-mesenchymal interactions controlling palatal outgrowth
    Yu Lan
    Center for Oral Biology and Department of Biomedical Genetics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
    Development 136:1387-96. 2009
    ..Furthermore, we show that Shh signaling regulates Bmp2, Bmp4 and Fgf10 expression in the developing palatal mesenchyme and that specific inactivation of Smo in the palatal mesenchyme ..
  64. ncbi Regulation of FGF10 by POU transcription factor Brn3a in the developing trigeminal ganglion
    Eric Cox
    Department of Psychiatry, University of California, San Diego and VA San Diego Healthcare System, La Jolla, California 92093, USA
    J Neurobiol 66:1075-83. 2006
    ..Here we show that expression of the developmental regulator FGF10 is approximately 35-fold increased in the developing trigeminal ganglia of Brn3a-null mice...
  65. ncbi Essential mesenchymal role of small GTPase Rac1 in interdigital programmed cell death during limb development
    Dai Suzuki
    Department of Biochemistry, Showa University, Hatanodai, Shinagawa, Tokyo, Japan
    Dev Biol 335:396-406. 2009
    ..Our findings from Rac1 conditional mutants indicate crucial roles for Rac1 in limb bud morphogenesis, especially interdigital programmed cell death...
  66. ncbi Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF
    J Pispa
    Institute of Biotechnology, Viikki Biocenter, University of Helsinki, Finland
    Dev Biol 216:521-34. 1999
    ..Instead FGF-10 partially restored morphogenesis and stimulated the development of additional tooth cusps in cultured Tabby molars...
  67. ncbi Stabilization of beta-catenin impacts pancreas growth
    Patrick W Heiser
    Diabetes Center, Department of Medicine, University of California, San Francisco, CA 94143, USA
    Development 133:2023-32. 2006
    ..Robust stabilization of beta-catenin during early organogenesis drives changes in hedgehog and Fgf10 signaling and induces a loss of Pdx1 expression in early pancreatic progenitor cells...
  68. ncbi Distinct roles for retinoic acid receptors alpha and beta in early lung morphogenesis
    Tushar J Desai
    Pulmonary Center, Boston University School of Medicine, 80 East Concord Street R 304, Boston, MA 02118, USA
    Dev Biol 291:12-24. 2006
    ..We show that activation of RAR beta, but not alpha, induces expression of the fibroblast growth factor Fgf10 and bud morphogenesis in the lung field...
  69. ncbi TGF-beta mediated FGF10 signaling in cranial neural crest cells controls development of myogenic progenitor cells through tissue-tissue interactions during tongue morphogenesis
    Ryoichi Hosokawa
    Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA
    Dev Biol 341:186-95. 2010
    ..Loss of Tgfbr2 in CNC cells (Wnt1-Cre;Tgfbr2(flox/flox)) results in microglossia with reduced Scleraxis and Fgf10 expression as well as decreased myogenic cell proliferation, reduced cell number and disorganized tongue muscles...
  70. ncbi Characterization and in vivo pharmacological rescue of a Wnt2-Gata6 pathway required for cardiac inflow tract development
    Ying Tian
    Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA
    Dev Cell 18:275-87. 2010
    ..These data reveal a molecular pathway regulating the posterior cardiac mesoderm and demonstrate that cardiovascular defects caused by loss of Wnt signaling can be rescued pharmacologically in vivo...
  71. ncbi FGF signaling regulates otic placode induction and refinement by controlling both ectodermal target genes and hindbrain Wnt8a
    Lisa D Urness
    Department of Human Genetics, University of Utah, 15 N 2030 E, RM 2100, Salt Lake City, UT 84112 5330, USA
    Dev Biol 340:595-604. 2010
    ..Mouse embryos lacking both Fgf3 and Fgf10 fail to initiate inner ear development because appropriate patterns of gene expression fail to be specified within ..
  72. ncbi Mouse R-spondin2 is required for apical ectodermal ridge maintenance in the hindlimb
    Ju Suk Nam
    Center for Molecular Medicine, Maine Medical Center Research Institute, 81 Research Drive, Scarborough, ME 04074, USA
    Dev Biol 311:124-35. 2007
    ..Our findings strongly suggest that Rspo2 expression in the AER is required for AER maintenance likely by regulating Wnt/beta-catenin signaling...
  73. ncbi Keratinocyte growth factor receptor ligands target the receptor to different intracellular pathways
    Francesca Belleudi
    Dipartimento di Medicina Sperimentale, Universita di Roma La Sapienza, Viale Regina Elena 324, 00161 Roma, Italy
    Traffic 8:1854-72. 2007
    ..interaction with two different ligands, keratinocyte growth factor (KGF)/fibroblast growth factor (FGF)7 and FGF10/KGF2, which are characterized by an opposite requirement of heparan sulfate proteoglycans and heparin for binding ..
  74. ncbi Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse
    M A Crackower
    Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada
    Dev Biol 201:78-89. 1998
    ..Moreover, the data suggest that the role of the AER maintenance factor is to promote cell proliferation in the ridge. Based on our findings, we propose a model for AER maintenance in the vertebrate limb...
  75. ncbi The loss of ventral ectoderm identity correlates with the inability to form an AER in the legless hindlimb bud
    S M Bell
    Division of Developmental Biology Children s Hospital Research Foundation, 3333 Burnet Avenue, Cincinnati, OH 45229, USA
    Mech Dev 74:41-50. 1998
    ..These data suggest that establishment of a dorso-ventral ectodermal interface is not sufficient for AER formation and that restriction of lmx-1b to the dorsal mesenchyme is coordinately linked to AER formation...
  76. ncbi Mesenchymal cells are required for functional development of thymic epithelial cells
    Manami Itoi
    Department of Immunology and Microbiology, Meiji University of Oriental Medicine, Hiyoshi cho, Nantan, Kyoto 629 0392, Japan
    Int Immunol 19:953-64. 2007
    ..In addition, our data suggest that mesenchymal cells are required to create the thymic microenvironment and to maintain epithelial architecture and function...
  77. ncbi Formation and differentiation of multiple mesenchymal lineages during lung development is regulated by beta-catenin signaling
    Stijn P De Langhe
    Developmental Biology Program, Department of Surgery, Saban Research Institute of Childrens Hospital Los Angeles, Los Angeles, California, USA
    PLoS ONE 3:e1516. 2008
    ..The role of ss-catenin signaling in mesodermal lineage formation and differentiation has been elusive...
  78. ncbi The migrating gubernaculum grows like a "limb bud"
    Sophie S Nightingale
    Department of General Surgery, Royal Children s Hospital, Melbourne 3052, Australia
    J Pediatr Surg 43:387-90. 2008
    ..Recent studies show active proliferation in the tip. We hypothesized that the gubernacular tip may grow like a limb bud...
  79. ncbi Sprouty-2 regulates oncogenic K-ras in lung development and tumorigenesis
    Alice T Shaw
    Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, and Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston 02114, USA
    Genes Dev 21:694-707. 2007
    ..These findings indicate that in the lung, Sprouty-2 plays a critical role in the regulation of oncogenic K-ras, and implicate counter-regulatory mechanisms in the pathogenesis of Ras-based disease...
  80. ncbi Terminal end bud maintenance in mammary gland is dependent upon FGFR2b signaling
    Sara Parsa
    Developmental Biology Program, Saban Research Institute of Childrens Hospital Los Angeles, Los Angeles, CA 90027, USA
    Dev Biol 317:121-31. 2008
    We previously demonstrated that Fibroblast Growth Factor 10 (FGF10) and its receptor FGFR2b play a key role in controlling the very early stages of mammary gland development during embryogenesis [Mailleux, A.A., Spencer-Dene, B...
  81. ncbi Tbx3 is required for outflow tract development
    Karim Mesbah
    Developmental Biology Institute of Marseilles Luminy, France
    Circ Res 103:743-50. 2008
    ....
  82. ncbi FGF alters epithelial competence for EGF at the initiation of branching morphogenesis of mouse submandibular gland
    Mari Nitta
    Department of Biology, Graduate School of Science, Chiba University, Chiba, Japan
    Dev Dyn 238:315-23. 2009
    ..branching occurred under the same culture conditions; however, both E12 and E13 epithelia elongated in response to FGF10. Reverse transcriptase-polymerase chain reaction studies showed that the expression of ErbB1 among four EGF ..
  83. ncbi Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart
    Kazuko Koshiba-Takeuchi
    Programs in Cardiovascular Research, The Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada
    Nat Genet 38:175-83. 2006
    ..Thus, a positive and negative feed-forward circuit between Tbx5 and Sall4 ensures precise patterning of embryonic limb and heart and provides a unifying mechanism for heart/hand syndromes...
  84. ncbi Molecular analysis of external genitalia formation: the role of fibroblast growth factor (Fgf) genes during genital tubercle formation
    R Haraguchi
    Center for Animal Resources and Development CARD, Kumamoto University, Honjo 2 2 1, Kumamoto 860 0811, Japan
    Development 127:2471-9. 2000
    ..in the distal urethral plate epithelium of the genital tubercle (GT) together with other markers such as the Msx1, Fgf10, Hoxd13 and Bmp4 expressed in the mesenchyme...
  85. ncbi Temporal effects of Sprouty on lung morphogenesis
    Anne Karina T Perl
    Division of Pulmonary Biology, Cincinnati Children s Hospital Medical Center, Cincinnati, OH 45229 3039, USA
    Dev Biol 258:154-68. 2003
    ..These findings demonstrate that the embryonic-pseudoglandular stage is a critical time period during which Spry-sensitive pathways are required for branching morphogenesis, lobulation, and formation of the peripheral lung parenchyma...
  86. ncbi The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis
    Robert G Kelly
    Department of Genetics and Development, Columbia University, New York, NY 10032, USA
    Hum Mol Genet 13:2829-40. 2004
    ..Tbx1 is also required for normal expression of Tlx1 and Fgf10 in pharyngeal mesoderm, in addition to correct neural crest cell patterning in the mandibular arch...
  87. ncbi Associations of FGF-3 and FGF-10 with signaling networks regulating tooth morphogenesis
    P Kettunen
    Developmental Biology Programme, Institute of Biotechnology, Viikki Biocenter, University of Helsinki, Finland
    Dev Dyn 219:322-32. 2000
    ..The dynamic expression patterns of different Fgfs in dental epithelium and mesenchyme and their interactions suggest existence of regulatory signaling cascades between epithelial and mesenchymal FGFs during tooth development...
  88. ncbi The roles of Fgf4 and Fgf8 in limb bud initiation and outgrowth
    Anne M Boulet
    Department of Human Genetics, Howard Hughes Medical Institute, University of Utah School of Medicine, Salt Lake City, UT 84112, USA
    Dev Biol 273:361-72. 2004
    ..mesoderm (IM) has been proposed to play a critical role in the initiation of limb bud outgrowth via restriction of Fgf10 expression to the appropriate region of the lateral plate mesoderm...
  89. ncbi FGF22 and its close relatives are presynaptic organizing molecules in the mammalian brain
    Hisashi Umemori
    Department of Anatomy and Neurobiology, Washington University Medical School, St Louis, MO 63110, USA
    Cell 118:257-70. 2004
    ..FGF7 and FGF10, the closest relatives of FGF22, share this activity; other FGFs have distinct effects...
  90. ncbi Heparan sulfates expressed in the distal lung are required for Fgf10 binding to the epithelium and for airway branching
    Konstantin I Izvolsky
    Pulmonary Ctr, Boston Univ School of Medicine, 80 E Concord St R 304, Boston, MA 02118, USA
    Am J Physiol Lung Cell Mol Physiol 285:L838-46. 2003
    Fibroblast growth factor (Fgf) 10 is a critical regulator of bud formation during lung morphogenesis. fgf10 is expressed in distal lung mesenchyme at sites of prospective budding from the earliest developmental stages and signals through ..
  91. ncbi Fibroblast growth factor receptor-3 is expressed in undifferentiated intestinal epithelial cells during murine crypt morphogenesis
    Alda Vidrich
    Digestive Health Center of Excellence, University of Virginia, Charlottesville, Virginia 22908, USA
    Dev Dyn 230:114-23. 2004
    ..These data suggest that signaling through FGFR-3 plays a role in regulating morphogenic events involved in formation of intestinal crypts and/or the fate of epithelial stem cells...
  92. ncbi The mapping of the gene of susceptibility to catalepsy in mice using polymorphic microsatellite markers
    A V Kulikov
    Institute of Cytology and Genetics, Siberian Division, Russian Academy of Sciences, pr. Akademika Lavrent'eva 10, Novosibirsk, 630090 Russia
    Dokl Biol Sci 393:531-4. 2003
  93. ncbi Transgenic expression of FGF8 and FGF10 induces transdifferentiation of pancreatic islet cells into hepatocytes and exocrine cells
    Takashi Yamaoka
    Division of Genetic Information, Institute for Genome Research, University of Tokushima, Tokushima 770 8503, Japan
    Biochem Biophys Res Commun 292:138-43. 2002
    ..To examine the effects of overexpressed FGF8 and FGF10 on pancreatic development, we generated FGF8- and FGF10-transgenic mice (Tg mice) under the control of the ..
  94. ncbi Cellular and molecular mechanisms of development of the external genitalia
    Gen Yamada
    Center for Animal Resources and Development CARD and Graduate School of Medical and Pharmaceutical Sciences, Kumamoto University, Honjo, Kumamoto 860 0811, Japan
    Differentiation 71:445-60. 2003
    ....
  95. ncbi Tumor chemopreventive activity of 3-O-acylated (--)-epigallocatechins
    Ayako Kumagai
    Department of Biotechnology, Faculty of Engineering, Kansai University, Suita, Osaka 564 8680, Japan
    Bioorg Med Chem 11:5143-8. 2003
    ..As a result, these derivatives inhibited a papilloma formation 1.3-1.6-fold more strongly than (--)-epigallocatechin gallate well established as anti-tumor promoter...
  96. ncbi Defective terminal differentiation and hypoplasia of the epidermis in mice lacking the Fgf10 gene
    K Suzuki
    Center for Animal Resources and Development, Kumamoto University, Japan
    FEBS Lett 481:53-6. 2000
    Here, we characterized the skin and hair phenotype of mice lacking the fibroblast growth factor 10 gene (Fgf10), a newly identified member of the fibroblast growth factor family...
  97. ncbi Expression and function of FGF10 in mammalian inner ear development
    Sarah Pauley
    Creighton University, Department of Biomedical Sciences, Omaha, Nebraska 68178, USA
    Dev Dyn 227:203-15. 2003
    We have investigated the expression of FGF10 during ear development and the effect of an FGF10 null mutation on ear development...
  98. ncbi Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse model
    Mohammad K Hajihosseini
    School of Biological Sciences, University of East Anglia, Norwich, United Kingdom
    Dev Dyn 238:376-85. 2009
    ..We have generated mice that harbour an AS mutation but are deficient in or heterozygous for Fgf10. The genetic knockdown of Fgf10 can rescue the skeletal as well as some of the visceral defects observed in this ..
  99. ncbi FGFR1 is required for the development of the auditory sensory epithelium
    Ulla Pirvola
    Institute of Biotechnology, 00014 University of Helsinki, Helsinki, Finland
    Neuron 35:671-80. 2002
    ..Our data also suggest that FGFR1 might have a distinct later role in intercellular signaling within the differentiating auditory sensory epithelium...
  100. ncbi Reciprocal epithelial-mesenchymal FGF signaling is required for cecal development
    Xiuqin Zhang
    Department of Molecular Biology and Pharmacology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA
    Development 133:173-80. 2006
    ..In the gastrointestinal (GI) tract, FGF10 is expressed in the cecal mesenchyme and signals to an epithelial splice form of FGF receptor (FGFR) 2 to regulate ..
  101. ncbi The role of neural crest during cardiac development in a mouse model of DiGeorge syndrome
    Lazaros Kochilas
    Cardiovascular Division, University of Pennsylvania, Philadelphia 19104, USA
    Dev Biol 251:157-66. 2002
    ..Based on our studies, we propose that Lgdel genes are required for the expression of soluble signals that regulate neural crest cell differentiation...

Research Grants25

  1. Notch signaling regulates pituitary gland organogenesis
    Lori Raetzman; Fiscal Year: 2009
    ..They may also reveal genetic causes of congenital pituitary hormone deficiency and pituitary tumorigenesis and offer novel insight into the function of Notch signaling in endocrine cell differentiation. ..
  2. Fetal Lung Development:Role of Wnt5a Signaling
    Changgong Li; Fiscal Year: 2007
    ..This information will be of utility in understanding the molecular mechanisms of congenital and induced lung disease. ..
  3. Eda/Edar Regulation of Embryonic SMG Development
    Tina Jaskoll; Fiscal Year: 2007
    ....
  4. Role of microRNAs in mammalian ear development and neurosensory specification
    Garrett A Soukup; Fiscal Year: 2010
    ..Understanding how these small RNAs influence such processes is expected to impact molecular therapeutic strategies designed to regenerate sensory cells and restoring hearing. ..
  5. Role of homeobox proteins in muscle development
    Helen P Makarenkova; Fiscal Year: 2010
    ..Defining the roles of Barx2 in muscle development, function and repair should help to build a more complete understanding of the muscle regulatory network that may aid in diagnosing or treating muscle disease. ..
  6. Notch Sigaling in Morphogenesis of Mouse Prostate
    Irina Grishina; Fiscal Year: 2007
    ..In perspective, those results may aid towards novel therapies to overcome genetic or injury inflicted pathologies in branched glands. ..
  7. The function of Foxi3 in craniofacial development
    Takahiro Ohyama; Fiscal Year: 2007
    ..This project has significant potential for the future study of craniofacial and sensory organ development that will shed light on the genetic mechanisms of craniofacial birth defects. ..
  8. COBRE: CREIGHTON UNIVERISTY: P1:ROLE OF MICRORNAS IN DEVELOPMENT OF THE EAR
    Garrett A Soukup; Fiscal Year: 2009
    ..Specific Aim 3. To identify downstream effector genes through which EGFR regulates the development of the PNS. ..