Výsledky vyhledávání - Rahimov, Fedik

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

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

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

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Variation in the HLA-G Promoter Region Influences Miscarriage Rates Autor 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 Autor 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 Autor 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 Autor 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 Autor 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) Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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