Found: 12
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The genetic bases for non-syndromic hearing loss among Chinese.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 3, p. 131, doi. 10.1038/jhg.2009.4
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- Article
Refinement of the DFNA41 locus and candidate genes analysis.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 516, doi. 10.1007/s10038-005-0286-0
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- Article
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31.
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- Human Genetics, 2009, v. 125, n. 1, p. 53, doi. 10.1007/s00439-008-0602-9
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- Article
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
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- Human Genetics, 2005, v. 116, n. 4, p. 292, doi. 10.1007/s00439-004-1227-2
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- Article
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians.
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- Human Genetics, 2003, v. 114, n. 1, p. 44, doi. 10.1007/s00439-003-1018-1
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- Article
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
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- Human Genetics, 2002, v. 111, n. 1, p. 26, doi. 10.1007/s00439-002-0736-0
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- Article
Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice.
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- International Journal of Experimental Pathology, 2011, v. 92, n. 1, p. 66, doi. 10.1111/j.1365-2613.2010.00751.x
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- Article
Mindin serves as a tumour suppressor gene during colon cancer progression through MAPK/ERK signalling pathway in mice.
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- Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 15, p. 8391, doi. 10.1111/jcmm.15332
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- Article
The pattern‐recognition molecule mindin binds integrin Mac‐1 to promote macrophage phagocytosis via Syk activation and NF‐κB p65 translocation.
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- Journal of Cellular & Molecular Medicine, 2019, v. 23, n. 5, p. 3402, doi. 10.1111/jcmm.14236
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- Article
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.
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- Human Molecular Genetics, 2005, v. 14, n. 1, p. 103, doi. 10.1093/hmg/ddi010
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- Article
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.
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- Human Molecular Genetics, 2003, v. 12, n. 10, p. 1155, doi. 10.1093/hmg/ddg127
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- Article
Mutations in GJA1(connexin43) are associated with non-syndromic autosomal recessive deafness.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 25, p. 2945, doi. 10.1093/hmg/10.25.2945
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- Article