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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 2 |
2003 | 1 |
2009 | 1 |
2010 | 1 |
2014 | 1 |
2022 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 259236
7 results
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Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness.
BMC Med Genomics. 2022 Jun 16;15(1):133. doi: 10.1186/s12920-022-01287-9.
BMC Med Genomics. 2022.
PMID: 35710363
Free PMC article.
Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE.
Ganapathy A, Pandey N, Srisailapathy CR, Jalvi R, Malhotra V, Venkatappa M, Chatterjee A, Sharma M, Santhanam R, Chadha S, Ramesh A, Agarwal AK, Rangasayee RR, Anand A.
Ganapathy A, et al.
PLoS One. 2014 Jan 8;9(1):e84773. doi: 10.1371/journal.pone.0084773. eCollection 2014.
PLoS One. 2014.
PMID: 24416283
Free PMC article.
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Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss.
Yang JJ, Su MC, Chien KH, Hsin CH, Li SY.
Yang JJ, et al.
Int J Pediatr Otorhinolaryngol. 2010 May;74(5):489-93. doi: 10.1016/j.ijporl.2010.02.001. Epub 2010 Mar 4.
Int J Pediatr Otorhinolaryngol. 2010.
PMID: 20206386
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A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia.
Sirmaci A, Oztürkmen-Akay H, Erbek S, Incesulu A, Duman D, Taşir-Yilmaz S, Ozdağ H, Tekin M.
Sirmaci A, et al.
Clin Genet. 2009 Jun;75(6):562-7. doi: 10.1111/j.1399-0004.2009.01183.x. Epub 2009 May 5.
Clin Genet. 2009.
PMID: 19438934
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Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
Cho KI, Lee JW, Kim KS, Lee EJ, Suh JG, Lee HJ, Kim HT, Hong SH, Chung WH, Chang KT, Hyun BH, Oh YS, Ryoo ZY.
Cho KI, et al.
Comp Med. 2003 Dec;53(6):642-8.
Comp Med. 2003.
PMID: 14727813
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Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailpathy S, Deshmukh D, Riazuddin S, Griffith AJ, Friedman TB, Smith RJ, Wilcox ER.
Naz S, et al.
Am J Hum Genet. 2002 Sep;71(3):632-6. doi: 10.1086/342193. Epub 2002 Jul 24.
Am J Hum Genet. 2002.
PMID: 12145746
Free PMC article.
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Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.
Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC.
Mitchem KL, et al.
Hum Mol Genet. 2002 Aug 1;11(16):1887-98. doi: 10.1093/hmg/11.16.1887.
Hum Mol Genet. 2002.
PMID: 12140191
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