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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1999 | 1 |
2003 | 1 |
2004 | 1 |
2005 | 1 |
2006 | 2 |
2008 | 1 |
2024 | 0 |
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Page 1
Mapping of genetic modifiers of Eya1 ( bor/bor ) in CAST/EiJ and BALB/cJ that suppress cochlear aplasia and associated deafness.
Mamm Genome. 2008 Sep;19(9):634-9. doi: 10.1007/s00335-008-9145-6. Epub 2008 Oct 4.
Mamm Genome. 2008.
PMID: 18836772
Genetics of hearing loss: Allelism and modifier genes produce a phenotypic continuum.
McHugh RK, Friedman RA.
McHugh RK, et al.
Anat Rec A Discov Mol Cell Evol Biol. 2006 Apr;288(4):370-81. doi: 10.1002/ar.a.20297.
Anat Rec A Discov Mol Cell Evol Biol. 2006.
PMID: 16550584
Free article.
Review.
Item in Clipboard
Identification of two major loci that suppress hearing loss and cochlear dysmorphogenesis in Eya1bor/bor mice.
Niu H, Makmura L, Shen T, Sheth SS, Blair K, Friedman RA.
Niu H, et al.
Genomics. 2006 Sep;88(3):302-8. doi: 10.1016/j.ygeno.2006.01.005. Epub 2006 Feb 20.
Genomics. 2006.
PMID: 16488112
Free article.
Item in Clipboard
Eya1 acts upstream of Tbx1, Neurogenin 1, NeuroD and the neurotrophins BDNF and NT-3 during inner ear development.
Friedman RA, Makmura L, Biesiada E, Wang X, Keithley EM.
Friedman RA, et al.
Mech Dev. 2005 May;122(5):625-34. doi: 10.1016/j.mod.2004.12.011. Epub 2005 Jan 8.
Mech Dev. 2005.
PMID: 15817220
Free article.
Item in Clipboard
A comparative study of Eya1 and Eya4 protein function and its implication in branchio-oto-renal syndrome and DFNA10.
Zhang Y, Knosp BM, Maconochie M, Friedman RA, Smith RJ.
Zhang Y, et al.
J Assoc Res Otolaryngol. 2004 Sep;5(3):295-304. doi: 10.1007/s10162-004-4044-3. Epub 2004 Jun 24.
J Assoc Res Otolaryngol. 2004.
PMID: 15492887
Free PMC article.
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A natural allele of Nxf1 suppresses retrovirus insertional mutations.
Floyd JA, Gold DA, Concepcion D, Poon TH, Wang X, Keithley E, Chen D, Ward EJ, Chinn SB, Friedman RA, Yu HT, Moriwaki K, Shiroishi T, Hamilton BA.
Floyd JA, et al.
Nat Genet. 2003 Nov;35(3):221-8. doi: 10.1038/ng1247. Epub 2003 Sep 28.
Nat Genet. 2003.
PMID: 14517553
Free PMC article.
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Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome.
Johnson KR, Cook SA, Erway LC, Matthews AN, Sanford LP, Paradies NE, Friedman RA.
Johnson KR, et al.
Hum Mol Genet. 1999 Apr;8(4):645-53. doi: 10.1093/hmg/8.4.645.
Hum Mol Genet. 1999.
PMID: 10072433
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