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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 2 |
2005 | 2 |
2006 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 342839
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Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.
Am J Hum Genet. 2006 Jan;78(1):144-52. doi: 10.1086/499495. Epub 2005 Nov 21.
Am J Hum Genet. 2006.
PMID: 16385458
Free PMC article.
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
Riazuddin S, Khan SN, Ahmed ZM, Ghosh M, Caution K, Nazli S, Kabra M, Zafar AU, Chen K, Naz S, Antonellis A, Pavan WJ, Green ED, Wilcox ER, Friedman PL, Morell RJ, Riazuddin S, Friedman TB.
Riazuddin S, et al.
Am J Hum Genet. 2006 Jan;78(1):137-43. doi: 10.1086/499164. Epub 2005 Nov 21.
Am J Hum Genet. 2006.
PMID: 16385457
Free PMC article.
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Identification of novel transcribed sequences on human chromosome 22 by expressed sequence tag mapping.
Hirosawa M, Nagase T, Murahashi Y, Kikuno R, Ohara O.
Hirosawa M, et al.
DNA Res. 2001 Feb 28;8(1):1-9. doi: 10.1093/dnares/8.1.1.
DNA Res. 2001.
PMID: 11258795
Free article.
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Tara, a novel F-actin binding protein, associates with the Trio guanine nucleotide exchange factor and regulates actin cytoskeletal organization.
Seipel K, O'Brien SP, Iannotti E, Medley QG, Streuli M.
Seipel K, et al.
J Cell Sci. 2001 Jan;114(Pt 2):389-99. doi: 10.1242/jcs.114.2.389.
J Cell Sci. 2001.
PMID: 11148140
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