Chen A - Search Results

1

A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.

O'Neill ME, Marietta J, Nishimura D, Wayne S, Van Camp G, Van Laer L, Negrini C, Wilcox ER, Chen A, Fukushima K, Ni L, Sheffield VC, Smith RJ. O'Neill ME, et al. Among authors: chen a. Hum Mol Genet. 1996 Jun;5(6):853-6. doi: 10.1093/hmg/5.6.853. Hum Mol Genet. 1996. PMID: 8776603

2

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.

Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Chen A, O'Neill M, Van Camp G, Coucke P, Smith SD, Kenyon JB, et al. Fukushima K, et al. Among authors: chen a. Hum Mol Genet. 1995 Sep;4(9):1643-8. doi: 10.1093/hmg/4.9.1643. Hum Mol Genet. 1995. PMID: 8541854

3

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.

Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Van Hauwe P, Zbar RI, Ashley J, Lovett M, Van Camp G, Smith RJ. Chen A, et al. Am J Med Genet. 1997 Sep 5;71(4):467-71. Am J Med Genet. 1997. PMID: 9286457

4

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4.

Bearer EL, Chen AF, Chen AH, Li Z, Mark HF, Smith RJ, Jackson CL. Bearer EL, et al. Among authors: chen af, chen ah. Ann Hum Genet. 2000 May;64(Pt 3):189-96. doi: 10.1046/j.1469-1809.2000.6430189.x. Ann Hum Genet. 2000. PMID: 11409409 Free PMC article.

5

MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.

Chen AH, Stephan DA, Hasson T, Fukushima K, Nelissen CM, Chen AF, Jun AI, Ramesh A, Van Camp G, Smith RJ. Chen AH, et al. Among authors: chen af. Arch Otolaryngol Head Neck Surg. 2001 Aug;127(8):921-5. doi: 10.1001/archotol.127.8.921. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11493199

6

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G. Verhoeven K, et al. Among authors: chen a. Nat Genet. 1998 May;19(1):60-2. doi: 10.1038/ng0598-60. Nat Genet. 1998. PMID: 9590290

7

Phenotypic manifestations of branchio-oto-renal syndrome.

Chen A, Francis M, Ni L, Cremers CW, Kimberling WJ, Sato Y, Phelps PD, Bellman SC, Wagner MJ, Pembrey M, et al. Chen A, et al. Am J Med Genet. 1995 Sep 25;58(4):365-70. doi: 10.1002/ajmg.1320580413. Am J Med Genet. 1995. PMID: 8533848

8

A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.

Jain PK, Lalwani AK, Li XC, Singleton TL, Smith TN, Chen A, Deshmukh D, Verma IC, Smith RJ, Wilcox ER. Jain PK, et al. Among authors: chen a. Genomics. 1998 Jun 1;50(2):290-2. doi: 10.1006/geno.1998.5320. Genomics. 1998. PMID: 9653658

9

Genomic structure, cochlear expression, and mutation screening of KCNK6, a candidate gene for DFNA4.

Mhatre AN, Li J, Chen AF, Yost CS, Smith RJ, Kindler CH, Lalwani AK. Mhatre AN, et al. J Neurosci Res. 2004 Jan 1;75(1):25-31. doi: 10.1002/jnr.10839. J Neurosci Res. 2004. PMID: 14689445

10

The restriction-modification genes of Escherichia coli K-12 may not be selfish: they do not resist loss and are readily replaced by alleles conferring different specificities.

O'Neill M, Chen A, Murray NE. O'Neill M, et al. Among authors: chen a. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14596-601. doi: 10.1073/pnas.94.26.14596. Proc Natl Acad Sci U S A. 1997. PMID: 9405658 Free PMC article.

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