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Results: 1 to 20 of 165

1.

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.

Robertson NG, Skvorak AB, Yin Y, Weremowicz S, Johnson KR, Kovatch KA, Battey JF, Bieber FR, Morton CC.

Genomics. 1997 Dec 15;46(3):345-54.

PMID:
9441737
[PubMed - indexed for MEDLINE]
2.

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.

Robertson NG, Lu L, Heller S, Merchant SN, Eavey RD, McKenna M, Nadol JB Jr, Miyamoto RT, Linthicum FH Jr, Lubianca Neto JF, Hudspeth AJ, Seidman CE, Morton CC, Seidman JG.

Nat Genet. 1998 Nov;20(3):299-303.

PMID:
9806553
[PubMed - indexed for MEDLINE]
3.

Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening.

Robertson NG, Khetarpal U, Gutiérrez-Espeleta GA, Bieber FR, Morton CC.

Genomics. 1994 Sep 1;23(1):42-50.

PMID:
7829101
[PubMed - indexed for MEDLINE]
4.

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.

de Kok YJ, Bom SJ, Brunt TM, Kemperman MH, van Beusekom E, van der Velde-Visser SD, Robertson NG, Morton CC, Huygen PL, Verhagen WI, Brunner HG, Cremers CW, Cremers FP.

Hum Mol Genet. 1999 Feb;8(2):361-6.

PMID:
9931344
[PubMed - indexed for MEDLINE]
Free Article
5.

Identification and characterization of an inner ear-expressed human melanoma inhibitory activity (MIA)-like gene (MIAL) with a frequent polymorphism that abolishes translation.

Rendtorff ND, Frödin M, Attié-Bitach T, Vekemans M, Tommerup N.

Genomics. 2001 Jan 1;71(1):40-52.

PMID:
11161796
[PubMed - indexed for MEDLINE]
6.

Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9.

Robertson NG, Resendes BL, Lin JS, Lee C, Aster JC, Adams JC, Morton CC.

Hum Mol Genet. 2001 Oct 15;10(22):2493-500.

PMID:
11709536
[PubMed - indexed for MEDLINE]
Free Article
7.

Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.

Robertson NG, Cremers CW, Huygen PL, Ikezono T, Krastins B, Kremer H, Kuo SF, Liberman MC, Merchant SN, Miller CE, Nadol JB Jr, Sarracino DA, Verhagen WI, Morton CC.

Hum Mol Genet. 2006 Apr 1;15(7):1071-85. Epub 2006 Feb 15.

PMID:
16481359
[PubMed - indexed for MEDLINE]
Free Article
8.

Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue.

Pasteris NG, Nagata K, Hall A, Gorski JL.

Gene. 2000 Jan 25;242(1-2):237-47.

PMID:
10721717
[PubMed - indexed for MEDLINE]
9.
10.

Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.

Scott DA, Greinwald JH Jr, Marietta JR, Drury S, Swiderski RE, Viñas A, DeAngelis MM, Carmi R, Ramesh A, Kraft ML, Elbedour K, Skworak AB, Friedman RA, Srikumari Srisailapathy CR, Verhoeven K, Van Gamp G, Lovett M, Deininger PL, Batzer MA, Morton CC, Keats BJ, Smith RJ, Sheffield VC.

Gene. 1998 Jul 30;215(2):461-9.

PMID:
9758550
[PubMed - indexed for MEDLINE]
11.

Molecular cloning and characterization of the mouse and human TUSP gene, a novel member of the tubby superfamily.

Li QZ, Wang CY, Shi JD, Ruan QG, Eckenrode S, Davoodi-Semiromi A, Kukar T, Gu Y, Lian W, Wu D, She JX.

Gene. 2001 Aug 8;273(2):275-84.

PMID:
11595174
[PubMed - indexed for MEDLINE]
12.

[Molecular cloning for testis spermatogenesis cell apoptosis related gene TSARG1 and Mtsarg1 and expression analysis for Mtsarg1 gene].

Fu JJ, Lu GX, Li LY, Liu G, Xing XW, Liu SF.

Yi Chuan Xue Bao. 2003 Jan;30(1):25-9. Chinese.

PMID:
12812072
[PubMed - indexed for MEDLINE]
13.

A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mapping.

Robertson NG, Heller S, Lin JS, Resendes BL, Weremowicz S, Denis CS, Bell AM, Hudspeth AJ, Morton CC.

Genomics. 2000 Jun 15;66(3):242-8.

PMID:
10873378
[PubMed - indexed for MEDLINE]
14.

cDNA sequencing and analysis of POV1 (PB39): a novel gene up-regulated in prostate cancer.

Cole KA, Chuaqui RF, Katz K, Pack S, Zhuang Z, Cole CE, Lyne JC, Linehan WM, Liotta LA, Emmert-Buck MR.

Genomics. 1998 Jul 15;51(2):282-7.

PMID:
9722952
[PubMed - indexed for MEDLINE]
15.

Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin.

Grabski R, Szul T, Sasaki T, Timpl R, Mayne R, Hicks B, Sztul E.

Hum Genet. 2003 Oct;113(5):406-16. Epub 2003 Aug 20.

PMID:
12928864
[PubMed - indexed for MEDLINE]
16.

Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.

Cooper PR, Nowak NJ, Higgins MJ, Church DM, Shows TB.

Genomics. 1998 May 1;49(3):419-29.

PMID:
9615227
[PubMed - indexed for MEDLINE]
17.

The LCCL module.

Trexler M, Bányai L, Patthy L.

Eur J Biochem. 2000 Sep;267(18):5751-7.

PMID:
10971586
[PubMed - indexed for MEDLINE]
Free Article
18.

Identification and structural analysis of human RBM8A and RBM8B: two highly conserved RNA-binding motif proteins that interact with OVCA1, a candidate tumor suppressor.

Salicioni AM, Xi M, Vanderveer LA, Balsara B, Testa JR, Dunbrack RL Jr, Godwin AK.

Genomics. 2000 Oct 1;69(1):54-62.

PMID:
11013075
[PubMed - indexed for MEDLINE]
19.

Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.

Mohlke KL, Purkayastha AA, Westrick RJ, Ginsburg D.

Genomics. 1998 Nov 15;54(1):19-30.

PMID:
9806826
[PubMed - indexed for MEDLINE]
20.

Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness.

Hughes DC, Legan PK, Steel KP, Richardson GP.

Genomics. 1998 Feb 15;48(1):46-51.

PMID:
9503015
[PubMed - indexed for MEDLINE]

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