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Results: 5

1.

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.

Ahmed ZM, Masmoudi S, Kalay E, Belyantseva IA, Mosrati MA, Collin RW, Riazuddin S, Hmani-Aifa M, Venselaar H, Kawar MN, Tlili A, van der Zwaag B, Khan SY, Ayadi L, Riazuddin SA, Morell RJ, Griffith AJ, Charfedine I, Caylan R, Oostrik J, Karaguzel A, Ghorbel A, Riazuddin S, Friedman TB, Ayadi H, Kremer H.

Nat Genet. 2008 Nov;40(11):1335-40. doi: 10.1038/ng.245. Epub 2008 Oct 26.

PMID:
18953341
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Deafness genes.

Kitamura K, Takahashi K, Tamagawa Y, Noguchi Y, Kuroishikawa Y, Ishikawa K, Hagiwara H.

J Med Dent Sci. 2000 Mar;47(1):1-11. Review.

PMID:
12162522
[PubMed - indexed for MEDLINE]
3.

Unconventional myosins and the genetics of hearing loss.

Friedman TB, Sellers JR, Avraham KB.

Am J Med Genet. 1999 Sep 24;89(3):147-57. Review.

PMID:
10704189
[PubMed - indexed for MEDLINE]
4.

MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness.

Friedman LM, Avraham KB.

Mamm Genome. 2009 Sep-Oct;20(9-10):581-603. doi: 10.1007/s00335-009-9230-5. Epub 2009 Oct 30. Review.

PMID:
19876605
[PubMed - indexed for MEDLINE]
5.

Mouse models to study inner ear development and hereditary hearing loss.

Friedman LM, Dror AA, Avraham KB.

Int J Dev Biol. 2007;51(6-7):609-31. Review.

PMID:
17891721
[PubMed - indexed for MEDLINE]
Free Article

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