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Buscar por Autor Morín, M
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| Fecha de publicación | Título | Autor(es) | | jul-2011 | DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss | Hildebrand, MS; Morín, M; Meyer, NC; Mayo-Merino, F; Modamio-Høybjør, S; Mencía, A; Olavarrieta, L; Morales-Angulo, Carmelo; Nishimura, CJ; Workman, H; DeLuca, AP; del Castillo, I; Taylor, KR; Tompkins, B; Goodman, CW; Schrauwen, I; Van Wesemael, M; Lachlan, K; Shearer, AE; Braun, TA; Huygen, PLM; Kremer, H; Van Camp, G; Moreno, F; Casavant, TL; Smith, RJH; Moreno-Pelayo, MA |
| ago-2009 | In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment | Morín, M; Bryan, KE; Mayo-Merino, F; Goodyear, R; Mencía, A; Modamio-Høybjør, S; del Castillo, I; Cabalka, JM; Richardson, GP; Moreno, F; Rubenstein, PA; Moreno-Pelayo, MA |
| may-2009 | Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss | Mencía, A; Modamio-Høybjør, S; Redshaw, N; Morín, M; Mayo-Merino, F; Olavarrieta, L; Aguirre, LA; del Castillo, I; Steel, KP; Dalmay, T; Moreno, F; Moreno-Pelayo, MA |
| may-2014 | Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane | Legan, PK; Goodyear, RJ; Morín, M; Mencía, A; Pollard, H; Olavarrieta, L; Korchagina, J; Modamio-Høybjør, S; Mayo, F; Moreno, F; Moreno-Pelayo, MA; Richardson, GP |
Mostrando resultados 1 a 4 de 4
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