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Year | Number of Results |
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2001 | 1 |
2007 | 1 |
2008 | 1 |
2010 | 1 |
2024 | 0 |
PubMed (cited) for id: 602083
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Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F.
Hum Mol Genet. 2010 Apr 15;19(8):1515-27. doi: 10.1093/hmg/ddq025. Epub 2010 Jan 22.
Hum Mol Genet. 2010.
PMID: 20097680
Free PMC article.
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
Ahmed ZM, Riazuddin S, Aye S, Ali RA, Venselaar H, Anwar S, Belyantseva PP, Qasim M, Riazuddin S, Friedman TB.
Ahmed ZM, et al.
Hum Genet. 2008 Oct;124(3):215-23. doi: 10.1007/s00439-008-0543-3. Epub 2008 Aug 22.
Hum Genet. 2008.
PMID: 18719945
Free PMC article.
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In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndrome.
Rebibo-Sabbah A, Nudelman I, Ahmed ZM, Baasov T, Ben-Yosef T.
Rebibo-Sabbah A, et al.
Hum Genet. 2007 Nov;122(3-4):373-81. doi: 10.1007/s00439-007-0410-7. Epub 2007 Jul 25.
Hum Genet. 2007.
PMID: 17653769
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Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Ahmed ZM, Riazuddin S, Bernstein SL, Ahmed Z, Khan S, Griffith AJ, Morell RJ, Friedman TB, Riazuddin S, Wilcox ER.
Ahmed ZM, et al.
Am J Hum Genet. 2001 Jul;69(1):25-34. doi: 10.1086/321277. Epub 2001 Jun 7.
Am J Hum Genet. 2001.
PMID: 11398101
Free PMC article.
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