hRED2

Summary

Gene Symbol: hRED2
Description: adenosine deaminase, RNA-specific, B2
Alias: ADAR3, RED2, RED2 homolog, RNA-dependent adenosine deaminase 3, RNA-editing deaminase 2, RNA-editing enzyme 2, adenosine deaminase, RNA-specific, B2 (RED1 homolog rat), adenosine deaminase, RNA-specific, B2 (RED2 homolog rat), double-stranded RNA-specific editase B2, dsRNA adenosine deaminase B2, homolog of rat BLUE
Species: human

Top Publications

  1. ncbi Adenosine deaminase binding to human CD26 is inhibited by HIV-1 envelope glycoprotein gp120 and viral particles
    A Valenzuela
    Department of Biochemistry and Molecular Biology, Faculty of Chemistry, University of Barcelona, Catalonia, Spain
    J Immunol 158:3721-9. 1997
  2. ncbi Novel exon of mammalian ADAR2 extends open reading frame
    Stefan Maas
    Department of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania, United States of America
    PLoS ONE 4:e4225. 2009
  3. ncbi RED2, a brain-specific member of the RNA-specific adenosine deaminase family
    T Melcher
    Laboratory for Neurobiology, Max Planck Institute for Medical Research, Jahnstrasse 12, 69120 Heidelberg, Germany
    J Biol Chem 271:31795-8. 1996
  4. ncbi Two sub-states of the red2 state of methyl-coenzyme M reductase revealed by high-field EPR spectroscopy
    Denise I Kern
    Laboratorium fur Physikalische Chemie, ETH Zurich, Wolfgang Pauli Strasse 10, Zurich, Switzerland
    J Biol Inorg Chem 12:1097-105. 2007
  5. ncbi Altered adenosine-to-inosine RNA editing in human cancer
    Nurit Paz
    Cancer Research Center, Chaim Sheba Medical Center, Tel Hashomer 52621, Israel
    Genome Res 17:1586-95. 2007
  6. ncbi Down-regulation of RNA editing in pediatric astrocytomas: ADAR2 editing activity inhibits cell migration and proliferation
    Caterina Cenci
    RNA editing Laboratory, Ospedale Pediatrico Bambino Gesu Research Institute, Piazza S Onofrio 4, 00165 Rome, Italy
    J Biol Chem 283:7251-60. 2008
  7. ncbi A nickel hydride complex in the active site of methyl-coenzyme m reductase: implications for the catalytic cycle
    Jeffrey Harmer
    Centre for Advanced Electron Spin Resonance, Department of Chemistry, University of Oxford, South Parks Road, OX1 3QR, Oxford, United Kingdom
    J Am Chem Soc 130:10907-20. 2008
  8. ncbi Expression of E-SOD, GPX5 mRNAs and immunoexpression of Cu/ZnSOD in epididymal epithelial cells of finasteride-treated rats
    A Kolasa
    Department of Histology and Embryology, Pomeranian Medical University, Szczecin, Poland
    Andrologia 40:303-11. 2008
  9. ncbi Origins and evolution of ADAR-mediated RNA editing
    Yongfeng Jin
    Institute of Biochemistry, College of Life Sciences, Zhejiang University Zijingang Campus, Hangzhou, Zhejiang, People s Republic of China
    IUBMB Life 61:572-8. 2009
  10. ncbi Identification of a selective nuclear import signal in adenosine deaminases acting on RNA
    Stefan Maas
    Department of Biological Sciences, Lehigh University, Bethlehem, PA, USA
    Nucleic Acids Res 37:5822-9. 2009

Research Grants

  1. MECHANISM OF INTERFERON ACTION
    CHARLES SAMUEL; Fiscal Year: 1980
  2. MECHANISM OF INTERFERON ACTION
    CHARLES SAMUEL; Fiscal Year: 2004
  3. STRUCTURE AND FUNCTION OF DSRNA ADENOSINE DEAMINASE
    Kazuko Nishikura; Fiscal Year: 2009
  4. Interaction between RNA interference and RNA editing pathways
    Kazuko Nishikura; Fiscal Year: 2011
  5. Interaction between RNA interference and RNA editing pathways
    Kazuko Nishikura; Fiscal Year: 2010
  6. STRUCTURE AND FUNCTION OF DSRNA ADENOSINE DEAMINASE
    Kazuko Nishikura; Fiscal Year: 2007
  7. STRUCTURE AND FUNCTION OF DSRNA ADENOSINE DEAMINASE
    Kazuko Nishikura; Fiscal Year: 2003
  8. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 2003
  9. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 2001
  10. 2/3-Brain Chemistry and Genetics in Pediatric Obsessive-Compulsive Disorder
    Gregory L Hanna; Fiscal Year: 2010

Scientific Experts

  • O A Sergeeva
  • Patricia Amara
  • J Harmer
  • Stefan Maas
  • P H Seeburg
  • CHARLES SAMUEL
  • G Kohr
  • J Blanco
  • Jochen Meier
  • Yongfeng Jin
  • Paola Sebastiani
  • Xiangyang Kong
  • GREGORY HANNA
  • Kazuko Nishikura
  • Weidong Yang
  • Jinghui Zhang
  • Dan Sung C Cho
  • Lin Fang Li
  • Sieglinde Ebner
  • Yoshiki Danbara
  • Nifang Niu
  • Natalia Vasilenko
  • Rudolf K Thauer
  • Bernhard Jaun
  • Meike Goenrich
  • Caterina Cenci
  • A Kolasa
  • Nurit Paz
  • S Goding
  • Denise I Kern
  • G Roversi
  • David J Wolyn
  • Joshua T Lee
  • Dan-Sung C Cho
  • A Valenzuela
  • John M Murray
  • Yukio Kawahara
  • R Franco
  • C Lluis
  • C Herrera
  • Stephen P Hunger
  • Michael Edmonson
  • James R Downing
  • Cheryl L Willman
  • Richard C Harvey
  • William L Carroll
  • W Paul Bowman
  • Gregory H Reaman
  • Mary V Relling
  • Charles G Mullighan
  • I Ming Chen
  • Daniela S Gerhard
  • Xiang Chen
  • Mignon L Loh
  • Bruce M Camitta
  • Malcolm A Smith
  • Meenakshi Devidas
  • Gang Wu
  • Kenneth H Buetow
  • Jing Han Wang
  • Qi Jun Qian
  • Anthony Batzler
  • Gregory D Jenkins
  • Jia Liu
  • Alexander Zakhartchouk
  • Chen Liu
  • C X Chen
  • Hua jun Jin
  • Brooke L Fridley
  • Meng Chao Wu
  • Igor Moshynskyy
  • Krishna R Kalari
  • Junmei Hou
  • Chang Qing Su
  • Xiao Qing Jiang
  • Huan Zhang Hu
  • Yuxin Qin
  • D Slavov
  • Tomoaki Sakamoto
  • Outa Uryu
  • Kenji Tomioka
  • Tse Yu Wu
  • Minjia Zhu
  • Hong Ping Wu
  • Jian Zhong Gu
  • Liewei Wang
  • MARY A O'CONNELL
  • Federica Galeano
  • M P de Zulueta
  • Angela Gallo

Detail Information

Publications38

  1. ncbi Adenosine deaminase binding to human CD26 is inhibited by HIV-1 envelope glycoprotein gp120 and viral particles
    A Valenzuela
    Department of Biochemistry and Molecular Biology, Faculty of Chemistry, University of Barcelona, Catalonia, Spain
    J Immunol 158:3721-9. 1997
    ..Because ADA deficiency leads to severe combined immunodefiency syndrome, it remains possible that HIV particle-mediated blockade of ADA-CD26 interaction may have significant consequences in the pathogenesis of AIDS...
  2. ncbi Novel exon of mammalian ADAR2 extends open reading frame
    Stefan Maas
    Department of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania, United States of America
    PLoS ONE 4:e4225. 2009
    ..Therefore, the characterization of ADAR expression and identification of alternative ADAR variants is an important prerequisite for understanding the mechanisms for regulation of RNA editing and the causes for deregulation in disease...
  3. ncbi RED2, a brain-specific member of the RNA-specific adenosine deaminase family
    T Melcher
    Laboratory for Neurobiology, Max Planck Institute for Medical Research, Jahnstrasse 12, 69120 Heidelberg, Germany
    J Biol Chem 271:31795-8. 1996
    ..We now report the molecular cloning of cDNA for RED2 (alias ADARB2), a third member of the RNA-specific adenosine deaminase family in the rodent...
  4. ncbi Two sub-states of the red2 state of methyl-coenzyme M reductase revealed by high-field EPR spectroscopy
    Denise I Kern
    Laboratorium fur Physikalische Chemie, ETH Zurich, Wolfgang Pauli Strasse 10, Zurich, Switzerland
    J Biol Inorg Chem 12:1097-105. 2007
    ..Addition of coenzyme B to the MCR-red1 state can partially and reversibly convert it into the MCR-red2 form, which shows a rhombic Ni(I)-based EPR signal (at X-band microwave frequencies of approximately 9.4 GHz)...
  5. ncbi Altered adenosine-to-inosine RNA editing in human cancer
    Nurit Paz
    Cancer Research Center, Chaim Sheba Medical Center, Tel Hashomer 52621, Israel
    Genome Res 17:1586-95. 2007
    ..Altered epigenetic control was recently shown to play a central role in oncogenesis. We suggest that A-to-I RNA editing may serve as an additional epigenetic mechanism relevant to cancer development and progression...
  6. ncbi Down-regulation of RNA editing in pediatric astrocytomas: ADAR2 editing activity inhibits cell migration and proliferation
    Caterina Cenci
    RNA editing Laboratory, Ospedale Pediatrico Bambino Gesu Research Institute, Piazza S Onofrio 4, 00165 Rome, Italy
    J Biol Chem 283:7251-60. 2008
    ..However, high expression levels of ADAR1 and ADAR3 were found in tumors when compared with normal tissues dissected in the same area of the brain...
  7. ncbi A nickel hydride complex in the active site of methyl-coenzyme m reductase: implications for the catalytic cycle
    Jeffrey Harmer
    Centre for Advanced Electron Spin Resonance, Department of Chemistry, University of Oxford, South Parks Road, OX1 3QR, Oxford, United Kingdom
    J Am Chem Soc 130:10907-20. 2008
    ..We report here on the coordinated ligands of the two paramagnetic MCR red2 states, induced when HS-CoM (a reversible competitive inhibitor) and the second substrate HS-CoB or its analogue ..
  8. ncbi Expression of E-SOD, GPX5 mRNAs and immunoexpression of Cu/ZnSOD in epididymal epithelial cells of finasteride-treated rats
    A Kolasa
    Department of Histology and Embryology, Pomeranian Medical University, Szczecin, Poland
    Andrologia 40:303-11. 2008
    ..The 5alpha-reductase is known to exist in two isoforms. Both 5alpha-red1 and 5alpha-red2 catalyse the irreversible conversion of T into DHT...
  9. ncbi Origins and evolution of ADAR-mediated RNA editing
    Yongfeng Jin
    Institute of Biochemistry, College of Life Sciences, Zhejiang University Zijingang Campus, Hangzhou, Zhejiang, People s Republic of China
    IUBMB Life 61:572-8. 2009
    ..ADAR1 and ADAR2 arose by gene duplications in early metazoan evolution, approximately 700 million years ago, while ADAR3 and TENR might originate after Urochordata-Vertebrata divergence...
  10. ncbi Identification of a selective nuclear import signal in adenosine deaminases acting on RNA
    Stefan Maas
    Department of Biological Sciences, Lehigh University, Bethlehem, PA, USA
    Nucleic Acids Res 37:5822-9. 2009
    ..We identify an in vivo ADAR3 interaction partner, importin alpha 1 (KPNA2) that specifically recognizes an arginine-rich ADAR3 sequence motif ..
  11. ncbi RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans
    Paola Sebastiani
    Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, United States of America
    PLoS ONE 4:e8210. 2009
    ..The majority of genes found thus far to be associated with longevity primarily function in lipoprotein metabolism and insulin/IGF-1 signaling. There are likely many more genetic modifiers of human longevity that remain to be discovered...
  12. ncbi Binding of coenzyme B induces a major conformational change in the active site of methyl-coenzyme M reductase
    Sieglinde Ebner
    Laboratory of Organic Chemistry, ETH Zurich, 8093 Zurich, Switzerland
    J Am Chem Soc 132:567-75. 2010
    ..Here we show that the two MCR(red2) signals can also be induced by the S-methyl- and the S-trifluoromethyl analogs of coenzyme B...
  13. ncbi SARS coronavirus protein 7a interacts with human Ap4A-hydrolase
    Natalia Vasilenko
    Vaccine and Infectious Disease Organization VIDO, University of Saskatchewan, 120 Veterinary Road, Saskatoon, SK S7N5E3, Canada
    Virol J 7:31. 2010
    ..Human tissue culture cells transiently expressing 7a and Ap4A-hydrolase tagged with EGFP and Ds-Red2 respectively show these proteins co-localize in the cytoplasm.
  14. ncbi [Establishment and characterization of a human gallbladder carcinoma cell line EH-GB1 originated from a metastatic tumor]
    Lin Fang Li
    Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China
    Zhonghua Zhong Liu Za Zhi 32:84-7. 2010
    ..To establish a human gallbladder carcinoma cell line derived from a metastatic gallbladder carcinoma and identify its biological characteristics...
  15. ncbi RNA interference of timeless gene does not disrupt circadian locomotor rhythms in the cricket Gryllus bimaculatus
    Yoshiki Danbara
    Graduate School of Natural Science and Technology, Okayama University, Okayama 700 8530, Japan
    J Insect Physiol 56:1738-45. 2010
    ..b>red2 (dsred2) dsrna...
  16. ncbi Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema
    Xiangyang Kong
    Research and Development, GlaxoSmithKline, 709 Swedeland Road, UW2230, King of Prussia, PA 19406, USA
    Am J Respir Crit Care Med 183:43-9. 2011
    ..Pulmonary emphysema is a major but variable component of COPD; familial data suggest that different components of COPD, such as emphysema, may be influenced by specific genetic factors...
  17. ncbi Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines
    Nifang Niu
    Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota 55905, USA
    Genome Res 20:1482-92. 2010
    ..Studies performed with LCLs can help to identify novel biomarkers that might contribute to variation in response to radiation therapy and enhance our understanding of mechanisms underlying that variation...
  18. ncbi Adenosine deaminases acting on RNA (ADARs) are both antiviral and proviral
    Charles E Samuel
    Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, CA 93106, USA
    Virology 411:180-93. 2011
    ..b>ADAR3, by contrast, has not yet been shown to be an active enzyme...
  19. ncbi Carbon monoxide dehydrogenase reaction mechanism: a likely case of abnormal CO2 insertion to a Ni-H(-) bond
    Patricia Amara
    Laboratoire de Cristallographie et de Cristallogenèse des Protéines, Institut de Biologie Structurale J P Ebel CEA, CNRS, Université Joseph Fourier 41, rue Jules Horowitz, 38027 Grenoble, France
    Inorg Chem 50:1868-78. 2011
    ..the spectroscopically well-characterized catalytic intermediates, C(red1) and the two-electron more-reduced C(red2)...
  20. ncbi Editing of AMPA and serotonin 2C receptors in individual central neurons, controlling wakefulness
    Olga A Sergeeva
    Department of Neurophysiology, Heinrich Heine Universitat, POB 101007, 40001 Dusseldorf, Germany
    Cell Mol Neurobiol 27:669-80. 2007
    ..maximal editing was found in neurons expressing both ADAR2 splice variants of the deaminase domain and lacking ADAR3. (4) Editing of the 5-HT2cR did not correlate with ADAR expression...
  21. ncbi Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder
    Gregory L Hanna
    Department of Psychiatry, University of Michigan, Ann Arbor, Michigan 48105, USA
    Biol Psychiatry 62:856-62. 2007
    ..The goal of this study was to identify chromosomal regions likely to contain susceptibility loci for obsessive-compulsive disorder (OCD)...
  22. ncbi Localization of a novel human RNA-editing deaminase (hRED2 or ADARB2) to chromosome 10p15
    L Mittaz
    Department of Genetics and Microbiology, University of Geneva Medical School, Switzerland
    Hum Genet 100:398-400. 1997
    ..Here we report the mapping of the human RED2 (hRED2; ADARB2) gene...
  23. ncbi HIV-1 envelope gp120 and viral particles block adenosine deaminase binding to human CD26
    A Valenzuela
    Departament de Bioquimica i Biologia Molecular, Facultad de Quimica, Universidad de Barcelona, Spain
    Adv Exp Med Biol 421:185-92. 1997
    ..Since the interaction ecto-ADA/CD26 is required for the activation of T cells, it remains possible that HIV particle-mediated blockade of ecto-ADA/CD26 interaction may have significant consequences in the pathogenesis of AIDS disease...
  24. ncbi Candidate editases for GluR channels in single neurons of rat hippocampus and cerebellum
    G Kohr
    Max Planck Institute for Medical Research, Molecular Neurobiology, Heidelberg, Germany
    Neuropharmacology 37:1411-7. 1998
    ..The recently cloned RNA dependent adenosine deaminases ADAR1, ADAR2 and ADAR3 form a small family of sequence-related candidate editases which are expressed in brain and other tissues at ..
  25. ncbi Reduced editing of low-affinity kainate receptor subunits in optic nerve glial cells
    M P de Zulueta
    Departamento de Neurociencias, Facultad de Medicina y Odontologia, Universidad del Pais Vasco, Leioa 48940, Biscay, Spain
    Brain Res Mol Brain Res 73:104-9. 1999
    ..In addition, we found that the adenosine deaminases, DRADA, RED1 and RED2, which edit ionotropic glutamate receptors in the brain, are expressed in the adult optic nerve and in ..
  26. ncbi Evidence for a proposed intermediate redox state in the CO/CO(2) active site of acetyl-CoA synthase (Carbon monoxide dehydrogenase) from Clostridium thermoaceticum
    D M Fraser
    Departments of Chemistry and of Biochemistry and Biophysics, Texas A and M University, College Station, Texas 77842, USA
    Biochemistry 38:15706-11. 1999
    ..Subsequent treatment with CO or dithionite yielded C(red2). The EPR-silent state formed within 1 min of adding Ti(3+) citrate, while C(red2) formed after 60 min...
  27. ncbi A third member of the RNA-specific adenosine deaminase gene family, ADAR3, contains both single- and double-stranded RNA binding domains
    C X Chen
    The Wistar Institute, Philadelphia, Pennsylvania 19104, USA
    RNA 6:755-67. 2000
    ..As originally reported for rat ADAR3 or RED2, purified ADAR3 proteins could not edit GluR-B RNA at the "Q/R" site, the "R/G" site, ..
  28. ncbi Comparative analysis of the RED1 and RED2 A-to-I RNA editing genes from mammals, pufferfish and zebrafish
    D Slavov
    Eleanor Roosevelt Institute, Denver, CO 80206 1210, USA
    Gene 250:41-51. 2000
    ..In mammals, two such A-to-I RNA editases are RED1, which edits some serotonin and glutamate receptors, and RED2, with unidentified substrates...
  29. ncbi The HIV-1 gp120 inhibits the binding of adenosine deaminase to CD26 by a mechanism modulated by CD4 and CXCR4 expression
    J Blanco
    Unité de Virologie et dImmunologie Cellulaire, ERS 572 CNRS, Institut Pasteur, 28 rue Dr Roux, 75724 Paris Cedex 15, France
    FEBS Lett 477:123-8. 2000
    ..These data suggest that the interaction of gp120 with CD4 or CXCR4 is required for efficient inhibition of ADA binding to CD26, although in the presence of CXCR4 the interaction of gp120 with CD4 may be dispensable...
  30. ncbi Comodulation of CXCR4 and CD26 in human lymphocytes
    C Herrera
    Department of Biochemistry and Molecular Biology, Faculty of Chemistry, University of Barcelona, Marti i Franques 1, 08028 Barcelona, Catalonia, Spain
    J Biol Chem 276:19532-9. 2001
    ..The physical association of CXCR4 and CD26, direct or part of a supramolecular structure, suggests a role on the function of the immune system and the pathophysiology of HIV infection...
  31. ncbi Requirement of dimerization for RNA editing activity of adenosine deaminases acting on RNA
    Dan Sung C Cho
    Wistar Institute, Philadelphia, Pennsylvania 19104, USA
    J Biol Chem 278:17093-102. 2003
    ..Three vertebrate ADAR gene family members, ADAR1, ADAR2, and ADAR3, have been identified...
  32. ncbi Low editing efficiency of GluR2 mRNA is associated with a low relative abundance of ADAR2 mRNA in white matter of normal human brain
    Yukio Kawahara
    Department of Neurology, Graduate School of Medicine, University of Tokyo, 7 3 1 Hongo, Bunkyo ku, Tokyo 113 8655, Japan
    Eur J Neurosci 18:23-33. 2003
    ..the first quantitative measurements of both mRNAs of the GluR subunits and mRNAs of the RNA editing enzymes ADAR1-ADAR3 in a comparison of the efficiency of editing at the Q/R site with the expression levels of ADAR mRNA in human ..
  33. ncbi Preferential accumulation of GABAA receptor gamma 2L, not gamma 2S, cytoplasmic loops at rat spinal cord inhibitory synapses
    Jochen Meier
    Developmental Physiology, Johannes Müller Institute, Humboldt University Medical School Charité, Tucholskystrasse 2, D 10117 Berlin, Germany
    J Physiol 559:355-65. 2004
    ..Furthermore, upon PKC activation Discosoma Red2-tagged GABAAR gamma2L (DsRed 2::gamma2L) colocalized with gephyrin in transfected COS-7 cells...
  34. ncbi Light-response quantitative trait loci identified with composite interval and eXtreme array mapping in Arabidopsis thaliana
    David J Wolyn
    Department of Plant Agriculture, University of Guelph, Ontario N1G 2W1, Canada
    Genetics 167:907-17. 2004
    ..The RED2 and RED5 QTL were verified in segregating lines...
  35. ncbi ADAR1 RNA deaminase limits short interfering RNA efficacy in mammalian cells
    Weidong Yang
    The Wistar Institute, Philadelphia, Pennsylvania 19104, USA
    J Biol Chem 280:3946-53. 2005
    ..Here we show that ADAR1 and ADAR2, but not ADAR3, avidly bind short interfering RNA (siRNA) without RNA editing...
  36. ncbi Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines
    G Roversi
    Department of Biology and Genetics, University of Milan, Milan, Italy
    Oncogene 25:1571-83. 2006
    ....
  37. ncbi Targeting of products of genes to tumor sites using adoptively transferred A-NK and T-LAK cells
    S Goding
    Department of Immunology, University of Pittsburgh, Pittsburgh, PA, USA
    Cancer Gene Ther 14:441-50. 2007
    ..consistently resulted in high (>60%) transduction rates and substantial expression of transgenes such as GFP, Red2, luciferase, beta-galactosidase and mIL-12 for at least 4 days...
  38. ncbi Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group
    Jinghui Zhang
    St Jude Children s Research Hospital, Memphis, TN, USA
    Blood 118:3080-7. 2011
    ..These data extend the range of genes that are recurrently mutated in high-risk childhood B-precursor acute lymphoblastic leukemia and highlight important new therapeutic targets for selected patient subsets...

Research Grants62

  1. MECHANISM OF INTERFERON ACTION
    CHARLES SAMUEL; Fiscal Year: 1980
    ....
  2. MECHANISM OF INTERFERON ACTION
    CHARLES SAMUEL; Fiscal Year: 2004
    ..Furthermore, the elucidation of the actions of interferon at the molecular level is of immediate importance in view of the potential applications of IFN in the clinic. ..
  3. STRUCTURE AND FUNCTION OF DSRNA ADENOSINE DEAMINASE
    Kazuko Nishikura; Fiscal Year: 2009
    ..first identified member of the ADAR gene family; this in turn led to the identification and cloning of ADAR2 and ADAR3. During the current grant support period, we created an ADAR1 null mutation in mice that causes widespread ..
  4. Interaction between RNA interference and RNA editing pathways
    Kazuko Nishikura; Fiscal Year: 2011
    ..This in turn has led to the identification and cloning of ADAR2 and ADAR3. Furthermore, we have created an ADAR1-/- mutation in mice that causes widespread apoptosis and consequent ..
  5. Interaction between RNA interference and RNA editing pathways
    Kazuko Nishikura; Fiscal Year: 2010
    ..This in turn has led to the identification and cloning of ADAR2 and ADAR3. Furthermore, we have created an ADAR1-/- mutation in mice that causes widespread apoptosis and consequent ..
  6. STRUCTURE AND FUNCTION OF DSRNA ADENOSINE DEAMINASE
    Kazuko Nishikura; Fiscal Year: 2007
    ..first identified member of the ADAR gene family; this in turn led to the identification and cloning of ADAR2 and ADAR3. During the current grant support period, we created an ADAR1 null mutation in mice that causes widespread ..
  7. STRUCTURE AND FUNCTION OF DSRNA ADENOSINE DEAMINASE
    Kazuko Nishikura; Fiscal Year: 2003
    ..dsRNA adenosine gene family, which led to identification and cloning of the second and third members, ADAR2 and ADAR3. We and others have demonstrated that these recombinantly expressed deaminases can indeed execute or modulate the ..
  8. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 2003
    ..Elucidation of the actions of IFN at the molecular level is of immediate importance in view of the use of IFN in the clinic. ..
  9. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 2001
    ..Furthermore, the elucidation of the actions of IFN at the molecular level is of immediate importance in view of the potential applications of IFN in the clinic. ..
  10. 2/3-Brain Chemistry and Genetics in Pediatric Obsessive-Compulsive Disorder
    Gregory L Hanna; Fiscal Year: 2010
    ..By combining brain imaging and genetics, as we do in this proposal, we can better understand the biology of pediatric OCD and, in turn, develop more effective treatments for this severe form of childhood psychopathology. ..
  11. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    Charles E Samuel; Fiscal Year: 2010
    ..Elucidation of the actions of interferon at the molecular level is of immediate importance in view of the use of interferon in the clinic. ..
  12. MECHANISM OF INTERFERON ACTION
    CHARLES SAMUEL; Fiscal Year: 2009
    ..Furthermore, elucidation of the actions of IFN at the molecular level is of importance in view of potential applications of interferon in the clinic. ..
  13. MECHANISM OF INTERFERON ACTION
    CHARLES SAMUEL; Fiscal Year: 2007
    ..Furthermore, elucidation of the actions of IFN at the molecular level is of importance in view of potential applications of interferon in the clinic. ..
  14. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 2006
    ..Elucidation of the actions of IFN at the molecular level is of immediate importance in view of the use of IFN in the clinic. ..
  15. Genetic Dissection of Sickle Cell Anemia Phenotypes
    Paola Sebastiani; Fiscal Year: 2006
    ..abstract_text> ..
  16. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 1993
    ....
  17. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 1991
    ..The effect of IFN type (Alpha, Gamma) and cell type (epithelial, fibroblast) will be examined. Two dimensional electrophoresis and immunoblot procedures will be used to quantitate P1 and eIF-2Alpha phosphorylation...
  18. INTERFERON ACTION AND PROTEIN PHOSPHORYLATION
    CHARLES SAMUEL; Fiscal Year: 2007
    ..Elucidation of the actions of IFN at the molecular level is of immediate importance in view of the use of IFN in the clinic. ..
  19. MOLECULAR GENETICS OF OBSESSIVE COMPULSIVE DISORDER
    GREGORY HANNA; Fiscal Year: 2001
    ..Parametric and nonparametric linkage analyses will be performed. Once evidence for linkage between early-onset OCD and a genetic marker is found, more precise gene localization will be pursued. ..