Resultados de procura - Chamberlain, Stormy

RNAs of the human chromsome 15q11-q13 imprinted region por Chamberlain, Stormy J.

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Prader-Willi, Angelman, and 15q11-q13 duplication syndromes por Kalsner, Louisa, Chamberlain, Stormy J.

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Angelman Syndrome, a Genomic Imprinting Disorder of the Brain por Chamberlain, Stormy J., Lalande, Marc

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A protein regulated by UBE3A PEGs a potential biomarker por Germain, Noelle D., Chamberlain, Stormy J.

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Polycomb Repressive Complex 2 is dispensable for maintenance of embryonic stem cell pluripotency por Chamberlain, Stormy J., Yee, Della, Magnuson, Terry

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IPSC Models of Chromosome 15Q Imprinting Disorders: From Disease Modeling to Therapeutic Strategies por Germain, Noelle D., Levine, Eric S., Chamberlain, Stormy J.

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Prader-Willi syndrome: reflections on seminal studies and future therapies por Chung, Michael S., Langouët, Maéva, Chamberlain, Stormy J., Carmichael, Gordon G.

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RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing por Chen, Pin-Fang, Hsiao, Jack S., Sirois, Carissa L., Chamberlain, Stormy J.

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Neuronal chromatin dynamics of imprinting in development and disease por Leung, Karen N., Chamberlain, Stormy J., Lalande, Marc, LaSalle, Janine M.

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Communication‐related assessments in an Angelman syndrome mouse model por Perrino, Peter A., Chamberlain, Stormy J., Eigsti, Inge‐Marie, Fitch, Roslyn Holly

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Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs por Cruvinel, Estela, Budinetz, Tara, Germain, Noelle, Chamberlain, Stormy, Lalande, Marc, Martins-Taylor, Kristen

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Transcription Is Required to Establish Maternal Imprinting at the Prader-Willi Syndrome and Angelman Syndrome Locus por Smith, Emily Y., Futtner, Christopher R., Chamberlain, Stormy J., Johnstone, Karen A., Resnick, James L.

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Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications por Kalsner, Louisa, Twachtman‐Bassett, Jennifer, Tokarski, Kristin, Stanley, Christine, Dumont‐Mathieu, Thyde, Cotney, Justin, Chamberlain, Stormy

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A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10 por Sanz, Lionel A, Chamberlain, Stormy, Sabourin, Jean-Charles, Henckel, Amandine, Magnuson, Terry, Hugnot, Jean-Philippe, Feil, Robert, Arnaud, Philippe

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Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes por Chamberlain, Stormy J., Chen, Pin-Fang, Ng, Khong Y., Bourgois-Rocha, Fany, Lemtiri-Chlieh, Fouad, Levine, Eric S., Lalande, Marc

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Abundance and localization of human UBE3A protein isoforms por Sirois, Carissa L, Bloom, Judy E, Fink, James J, Gorka, Dea, Keller, Steffen, Germain, Noelle D, Levine, Eric S, Chamberlain, Stormy J

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A bipartite boundary element restricts UBE3A imprinting to mature neurons por Hsiao, Jack S., Germain, Noelle D., Wilderman, Andrea, Stoddard, Christopher, Wojenski, Luke A., Villafano, Geno J., Core, Leighton, Cotney, Justin, Chamberlain, Stormy J.

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Angelman syndrome genotypes manifest varying degrees of clinical severity and developmental impairment por Keute, Marius, Miller, Meghan T., Krishnan, Michelle L., Sadhwani, Anjali, Chamberlain, Stormy, Thibert, Ronald L., Tan, Wen-Hann, Bird, Lynne M., Hipp, Joerg F.

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Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion por Martins-Taylor, Kristen, Hsiao, Jack S., Chen, Pin-Fang, Glatt-Deeley, Heather, De Smith, Adam J., Blakemore, Alexandra I.F., Lalande, Marc, Chamberlain, Stormy J.

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Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells por Fink, James J., Robinson, Tiwanna M., Germain, Noelle D., Sirois, Carissa L., Bolduc, Kaitlyn A., Ward, Amanda J., Rigo, Frank, Chamberlain, Stormy J., Levine, Eric S.

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