Resultados de procura - Rahimov, Fedik

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

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

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

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