These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
173 related articles for article (PubMed ID: 9441737)
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; 46(3):345-54. PubMed ID: 9441737 [TBL] [Abstract][Full Text] [Related]
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; Miyamoto RT; Linthicum FH; Lubianca Neto JF; Hudspeth AJ; Seidman CE; Morton CC; Seidman JG Nat Genet; 1998 Nov; 20(3):299-303. PubMed ID: 9806553 [TBL] [Abstract][Full Text] [Related]
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; 23(1):42-50. PubMed ID: 7829101 [TBL] [Abstract][Full Text] [Related]
4. 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; 71(1):40-52. PubMed ID: 11161796 [TBL] [Abstract][Full Text] [Related]
5. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues. Pasteris NG; Gorski JL Genomics; 1999 Aug; 60(1):57-66. PubMed ID: 10458911 [TBL] [Abstract][Full Text] [Related]
6. [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. PubMed ID: 12812072 [TBL] [Abstract][Full Text] [Related]
7. 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; 66(3):242-8. PubMed ID: 10873378 [TBL] [Abstract][Full Text] [Related]
9. 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; 49(3):419-29. PubMed ID: 9615227 [TBL] [Abstract][Full Text] [Related]
10. 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; 54(1):19-30. PubMed ID: 9806826 [TBL] [Abstract][Full Text] [Related]
11. 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; 48(1):46-51. PubMed ID: 9503015 [TBL] [Abstract][Full Text] [Related]
12. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Liang Y; Wang A; Belyantseva IA; Anderson DW; Probst FJ; Barber TD; Miller W; Touchman JW; Jin L; Sullivan SL; Sellers JR; Camper SA; Lloyd RV; Kachar B; Friedman TB; Fridell RA Genomics; 1999 Nov; 61(3):243-58. PubMed ID: 10552926 [TBL] [Abstract][Full Text] [Related]
13. cDNA cloning and chromosomal mapping of the mouse type VII collagen gene (Col7a1): evidence for rapid evolutionary divergence of the gene. Li K; Christiano AM; Copeland NG; Gilbert DJ; Chu ML; Jenkins NA; Uitto J Genomics; 1993 Jun; 16(3):733-9. PubMed ID: 8325648 [TBL] [Abstract][Full Text] [Related]
14. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes]. Zhang DL; Ji L; Li YD Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601 [TBL] [Abstract][Full Text] [Related]
15. Cloning, expression patterns, and chromosome localization of three human and two mouse homologues of GABA(A) receptor-associated protein. Xin Y; Yu L; Chen Z; Zheng L; Fu Q; Jiang J; Zhang P; Gong R; Zhao S Genomics; 2001 Jun; 74(3):408-13. PubMed ID: 11414770 [TBL] [Abstract][Full Text] [Related]
16. Cloning and characterization of human DDX24 and mouse Ddx24, two novel putative DEAD-Box proteins, and mapping DDX24 to human chromosome 14q32. Zhao Y; Yu L; Fu Q; Chen W; Jiang J; Gao J; Zhao S Genomics; 2000 Aug; 67(3):351-5. PubMed ID: 10936056 [TBL] [Abstract][Full Text] [Related]
17. Aup1, a novel gene on mouse chromosome 6 and human chromosome 2p13. Jang W; Weber JS; Bashir R; Bushby K; Meisler MH Genomics; 1996 Sep; 36(2):366-8. PubMed ID: 8812468 [TBL] [Abstract][Full Text] [Related]
18. Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes. Pappano WN; Scott IC; Clark TG; Eddy RL; Shows TB; Greenspan DS Genomics; 1998 Sep; 52(2):236-9. PubMed ID: 9782094 [TBL] [Abstract][Full Text] [Related]
19. Structure of the human gene (COX6A2) for the heart/muscle isoform of cytochrome c oxidase subunit VIa and its chromosomal location in humans, mice, and cattle. Bachman NJ; Riggs PK; Siddiqui N; Makris GJ; Womack JE; Lomax MI Genomics; 1997 May; 42(1):146-51. PubMed ID: 9177785 [TBL] [Abstract][Full Text] [Related]
20. JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24. Morita R; Miyazaki E; Fong CY; Chen XN; Korenberg JR; Delgado-Escueta AV; Yamakawa K Biochem Biophys Res Commun; 1998 Jul; 248(2):307-14. PubMed ID: 9675132 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]