Search Results - Rahimov, Fedik

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

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

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

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

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

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

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Genetic Variants in IRF6 and the Risk of Facial Clefts: Single-Marker and Haplotype-Based Analyses in a Population-Based Case-Control Study of Facial Clefts in Norway by Jugessur, Astanand, Rahimov, Fedik, Lie, Rolv T., Wilcox, Allen J., Gjessing, Håkon K., Nilsen, Roy M., Nguyen, Truc Trung, Murray, Jeffrey C.

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CD82 is a marker for prospective isolation of human muscle satellite cells and is linked to muscular dystrophies by Alexander, Matthew S., Rozkalne, Anete, Colletta, Alessandro, Spinazzola, Janelle M., Johnson, Samuel, Rahimov, Fedik, Meng, Hui, Lawlor, Michael W., Estrella, Elicia, Kunkel, Louis M., Gussoni, Emanuela

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Telomere Position Effect (TPE) Regulates DUX4 in Human Facioscapulohumeral Muscular Dystrophy (FSHD) by Stadler, Guido, Rahimov, Fedik, King, Oliver D., Chen, Jennifer C. J., Robin, Jerome D., Wagner, Kathryn R., Shay, Jerry W., Emerson, Charles P., Wright, Woodring E.

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

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Comparative RNA Editing in Autistic and Neurotypical Cerebella by Eran, Alal, Li, Jin Billy, Vatalaro, Kayla, McCarthy, Jillian, Rahimov, Fedik, Collins, Christin, Markianos, Kyriacos, Margulies, David M., Brown, Emery N., Calvo, Sarah E., Kohane, Isaac S., Kunkel, Louis M.

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

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Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis by Pakula, Anna, Lek, Angela, Widrick, Jeffrey, Mitsuhashi, Hiroaki, Bugda Gwilt, Katlynn M, Gupta, Vandana A, Rahimov, Fedik, Criscione, June, Zhang, Yuanfan, Gibbs, Devin, Murphy, Quinn, Manglik, Anusha, Mead, Lillian, Kunkel, Louis

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Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2 by Mitsuhashi, Satomi, Boyden, Steven E, Estrella, Elicia A, Jones, Takako I, Rahimov, Fedik, Yu, Timothy W, Darras, Basil T, Amato, Anthony A, Folkerth, Rebecca D, Jones, Peter L, Kunkel, Louis M, Kang, Peter B

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

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

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

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An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects by Fakhouri, Walid D., Rahimov, Fedik, Attanasio, Catia, Kouwenhoven, Evelyn N., Ferreira De Lima, Renata L., Felix, Temis Maria, Nitschke, Larissa, Huver, David, Barrons, Julie, Kousa, Youssef A., Leslie, Elizabeth, Pennacchio, Len A., Van Bokhoven, Hans, Visel, Axel, Zhou, Huiqing, Murray, Jeffrey C., Schutte, Brian C.

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

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Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency by Heeney, Matthew M., Guo, Dongjing, De Falco, Luigia, Campagna, Dean R., Olbina, Gordana, Kao, Paige P.-C., Schmitz-Abe, Klaus, Rahimov, Fedik, Gutschow, Patrick, Westerman, Keith, Ostland, Vaughn, Jackson, Tracy, Klaassen, Robert E., Markianos, Kyriacos, Finberg, Karin E., Iolascon, Achille, Westerman, Mark, London, Wendy B., Fleming, Mark D.

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