Research Topics
Genomes and Genes | Fernando SegadeSummaryAffiliation: University of Pennsylvania Country: USA Publications
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Detail Information
Publications
Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connectionFernando Segade
Department of Anatomy and Cell Biology, University of Pennsylvania, School of Dental Medicine, Philadelphia, PA 19104, USA
FEBS Lett 584:2990-4. 2010..In ATS, loss of GLUT10 results in defective collagen and/or elastin. TGFbeta activation represents a secondary response to a defective extracellular matrix...
Functional evolution of the microfibril-associated glycoproteinsFernando Segade
Department of Anatomy and Cell Biology, School of Dental Medicine, University of Pennsylvania, 240 S 40th St, Philadelphia, PA 19104, USA
Gene 439:43-54. 2009..Correlated evolution between MAGP1 and the developmental regulator, Notch1, may explain some of the selective forces acting on MAGP2...
The intracellular form of human MAGP1 elicits a complex and specific transcriptional responseFernando Segade
Center for Human Genomics, Wake Forest University School of Medicine, Winston Salem, NC 27157, USA
Int J Biochem Cell Biol 39:2303-13. 2007..These studies suggest a dual role for MAGP1, with extracellular MAGP1A involved in ECM function, and intracellular MAGP1B modulating the expression of genes that function in cell adhesion, migration and control of ECM deposition...
Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family StudyFernando Segade
Department of Internal Medicine, Wake Forest University School of Medicine, Winston Salem, NC 27157, USA
Arch Otolaryngol Head Neck Surg 132:729-33. 2006..We have evaluated single nucleotide polymorphisms (SNPs) in the FBXO11 gene for association with chronic otitis media with effusion/recurrent otitis media (COME/ROM)...
Regulatory elements of microfibril-associated glycoprotein-1 gene expression in muscle cellsFernando Segade
Department of Internal Medicine, Wake Forest University School of Medicine, Winston Salem, NC 27157, USA
Biochim Biophys Acta 1731:215-24. 2005..A sequence element spanning position -150 may represent the binding motif of an uncharacterized transcription factor. The basal transcriptional regulation of Mfap2 in muscle cells is discussed...
Molecular evolution of the fibulins: implications on the functionality of the elastic fibulinsFernando Segade
Department of Anatomy and Cell Biology, University of Pennsylvania School of Dental Medicine, Philadelphia, PA 19104, USA
Gene 464:17-31. 2010..Differentiation in gene expression further split Fibulin-5 from the other elastic fibulins, likely contributing to its nonredundant role in elastic fiber assembly...
Differential expression of facilitative glucose transporters in normal and tumour kidney tissuesNobuyasu Suganuma
Department of Biochemistry, Wake Forest University School of Medicine, Winston Salem, NC 27157, USA
BJU Int 99:1143-9. 2007....
Genetic analysis of the GLUT10 glucose transporter (SLC2A10) polymorphisms in Caucasian American type 2 diabetesJennifer L Bento
Department of Biochemistry, Wake Forest University School of Medicine, Winston Salem, North Carolina, 27157, USA
BMC Med Genet 6:42. 2005..GLUT10 (gene symbol SLC2A10) is a facilitative glucose transporter within the type 2 diabetes (T2DM)-linked region on chromosome 20q12-13.1. Therefore, we evaluated GLUT10 as a positional candidate gene for T2DM in Caucasian Americans...
Functional characterization of the promoter of the human glucose transporter 10 geneFernando Segade
Department of Internal Medicine, Wake Forest University School of Medicine, Winston Salem, NC 27157, USA
Biochim Biophys Acta 1730:147-58. 2005..In addition, a silencer region is present upstream of -696 which down-regulates SLC2A10 promoter activity independently of its distance to the transcript start site...
Identification of a major microfibril-associated glycoprotein-1-binding domain in fibrillin-2Claudio C Werneck
Department of Cell Biology, Washington University School of Medicine, St Louis, Missouri 63110, USA
J Biol Chem 279:23045-51. 2004..It is possible that these mutations alter the ability of fibrillin to bind MAGP-1, which may contribute to the severity of the disease...
Identification of a matrix-binding domain in MAGP1 and MAGP2 and intracellular localization of alternative splice formsFernando Segade
Department of Cell Biology and Physiology and the Division of Pulmonary and Critical Care Medicine, Barnes Jewish Hospital and Washington University School of Medicine, St Louis, Missouri 63110, USA
J Biol Chem 277:11050-7. 2002..This suggests a second action site for MAGP1...
Deficiency in microfibril-associated glycoprotein-1 leads to complex phenotypes in multiple organ systemsJustin S Weinbaum
Department of Cell Biology and Physiology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA
J Biol Chem 283:25533-43. 2008..Increased body size and fat deposition in MAGP-1-mutant animals are particularly intriguing given the localization of obesity traits in humans to the region on chromosome 1 containing the MAGP-1 gene...
