检索结果 - Fedik Rahimov

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  1. 1
    Cellular and molecular mechanisms underlying muscular dystrophy

    Cellular and molecular mechanisms underlying muscular dystrophy 由 Fedik Rahimov, Louis M. Kunkel

    出版 2013
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  2. 2
    Genetics of Nonsyndromic Orofacial Clefts

    Genetics of Nonsyndromic Orofacial Clefts 由 Fedik Rahimov, Astanand Jugessur, Jeffrey C. Murray

    出版 2011
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  3. 3
    Emerging preclinical animal models for FSHD

    Emerging preclinical animal models for FSHD 由 Angela Lek, Fedik Rahimov, Peter L. Jones, Louis M. Kunkel

    出版 2015
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  4. 4
    Variation in the HLA-G Promoter Region Influences Miscarriage Rates

    Variation in the HLA-G Promoter Region Influences Miscarriage Rates 由 Carole Ober, Carrie Aldrich, Inna Chervoneva, Christine Billstrand, Fedik Rahimov, Heather Gray, Terry Hyslop

    出版 2003
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  5. 5
    Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers

    Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers 由 Fedik Rahimov, Oliver D. King, Doris G. Leung, Genila Bibat, Charles P. Emerson, Louis M. Kunkel, Kathryn R. Wagner

    出版 2012
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  6. 6
    Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor

    Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor 由 Fedik Rahimov, Oliver D. King, Leigh C. Warsing, Rachel E. Powell, Charles P. Emerson, Louis M. Kunkel, Kathryn R. Wagner

    出版 2011
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  7. 7
    Genetic variants in <i>IRF6</i> and the risk of facial clefts: single‐marker and haplotype‐based analyses in a population‐based case‐control study of facial clefts in Norway

    Genetic variants in <i>IRF6</i> and the risk of facial clefts: single‐marker and haplotype‐based analyses in a population‐based case‐control study of facial clefts in Norway... 由 Astanand Jugessur, Fedik Rahimov, Rolv T. Lie, Allen J. Wilcox, Håkon K. Gjessing, Roy M. Nilsen, Truc Trung Nguyen, Jeffrey C. Murray

    出版 2008
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  8. 8
    CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies

    CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies 由 Matthew S. Alexander, Anete Rozkalne, Alessandro Colletta, Janelle M. Spinazzola, Samuel Johnson, Fedik Rahimov, Hui Meng, Michael W. Lawlor, Elicia Estrella, Louis M. Kunkel, Emanuela Gussoni

    出版 2016
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  9. 9
    Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy

    Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy 由 Guido Stadler, Fedik Rahimov, Oliver D. King, Jennifer C. J. Chen, Jérôme D. Robin, Kathryn R. Wagner, Jerry W. Shay, Charles P. Emerson, Woodring E. Wright

    出版 2013
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  10. 10
    A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function

    A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function 由 Sachiko Homma, Jennifer C. J. Chen, Fedik Rahimov, Mary Lou Beermann, Kendal Hanger, Genila Bibat, Kathryn R. Wagner, Louis M. Kunkel, Charles P. Emerson, Jeffrey B. Miller

    出版 2011
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  11. 11
    Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences

    Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences 由 Justin E. Ideozu, Mengzhen Liu, Bridget Riley‐Gillis, Sri Paladugu, Fedik Rahimov, Preethi Krishnan, Rakesh Tripathi, Patrick Dorr, Hara Levy, Ashvani K. Singh, Jeffrey F. Waring, Aparna Vasanthakumar

    出版 2024
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  12. 12
    Comparative RNA editing in autistic and neurotypical cerebella

    Comparative RNA editing in autistic and neurotypical cerebella 由 Alal Eran, Jin Billy Li, Kayla Vatalaro, Jillian McCarthy, Fedik Rahimov, Christin Collins, Kyriacos Markianos, David Margulies, Emery N. Brown, Sarah E. Calvo, Isaac S. Kohane, Louis M. Kunkel

    出版 2012
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  13. 13
    Human skeletal muscle xenograft as a new preclinical model for muscle disorders

    Human skeletal muscle xenograft as a new preclinical model for muscle disorders 由 Tracy Zhang, Oliver D. King, Fedik Rahimov, Takako I. Jones, Christopher W. Ward, Jaclyn P. Kerr, Nan Liu, Charles P. Emerson, Louis M. Kunkel, Terence A. Partridge, Kathryn R. Wagner

    出版 2014
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  14. 14
    Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

    Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis 由 Takako I. Jones, Jennifer C. J. Chen, Fedik Rahimov, Sachiko Homma, Patrícia Arashiro, Mary Lou Beermann, Oliver D. King, Jeffrey B. Miller, Louis M. Kunkel, Charles P. Emerson, Kathryn R. Wagner, Peter L. Jones

    出版 2012
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  15. 15
    Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease

    Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease 由 Nathan Palmer, Jocelyn A. Silvester, Jessica J. Lee, Andrew L. Beam, Inbar Fried, Vladimir I. Valtchinov, Fedik Rahimov, Sek Won Kong, Saum Ghodoussipour, H Hood, Athos Bousvaros, Richard J. Grand, Louis M. Kunkel, Isaac S. Kohane

    出版 2019
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  16. 16
    MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms

    MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms 由 Matthew S. Alexander, Juan Carlos Casar, Norio Motohashi, Natássia M. Vieira, Iris Eisenberg, Jamie L. Marshall, Molly Gasperini, Angela Lek, Jennifer A. Myers, Elicia Estrella, Peter B. Kang, Frederic Shapiro, Fedik Rahimov, Genri Kawahara, Jeffrey J. Widrick, Louis M. Kunkel

    出版 2014
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  17. 17
    An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects

    An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects 由 Walid D. Fakhouri, Fedik Rahimov, Catia Attanasio, Evelyn N. Kouwenhoven, Renata Lacerda Lima, Têmis Maria Félix, Larissa Nitschke, D. Huver, J. Barrons, Youssef A. Kousa, Erin Leslie, L Pennacchio, Hans van Bokhoven, Axel Visel, Huiqing Zhou, Jeffrey C. Murray, Brian C. Schutte

    出版 2014
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  18. 18
    Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate

    Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate 由 Alexandre R. Vieira, Joseph R. Avila, Sandra Daack‐Hirsch, Ecaterina Dragan, Têmis Maria Félix, Fedik Rahimov, Jill Harrington, Rebecca R. Schultz, Yoriko Watanabe, Marla Johnson, Jennifer S. Fang, Sarah O’Brien, Iêda M. Orioli, Eduardo E. Castilla, David Fitzpatrick, Rulang Jiang, Mary L. Marazita, Jeffrey C. Murray

    出版 2005
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  19. 19
    Direct Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate

    Direct Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate 由 Alexandre R. Vieira, Joseph R. Avila, Sandra Daack‐Hirsch, Ecaterina Dragan, Têmis Maria Félix, Fedik Rahimov, Jill Harrington, Rebecca R. Schultz, Yoriko Watanabe, Marla Johnson, Jennifer S. Fang, Sarah O’Brien, Iêda M. Orioli, Eduardo E. Castilla, David Fitzpatrick, Rulang Jiang, Mary L. Marazita, Jeffrey C. Murray

    出版 2005
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  20. 20
    Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip

    Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip 由 Fedik Rahimov, Mary L. Marazita, Axel Visel, Margaret E. Cooper, Michael J. Hitchler, Michele Rubini, Frederick E. Domann, Manika Govil, Kaare Christensen, Camille Bille, Mads Melbye, Astanand Jugessur, Rolv T. Lie, Allen J. Wilcox, David Fitzpatrick, Eric D. Green, Peter Mossey, Julian Little, Régine P.M. Steegers‐Theunissen, L Pennacchio, Brian C. Schutte, Jeffrey C. Murray

    出版 2008
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