143 related articles for article (PubMed ID: 8004092)
1. Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex.
Roux AF; Rommens J; McDowell C; Anson-Cartwright L; Bell S; Schappert K; Fishman GA; Musarella M
Hum Mol Genet; 1994 Feb; 3(2):257-63. PubMed ID: 8004092
[TBL] [Abstract][Full Text] [Related]
2. Cloning of a human homologue of the mouse Tctex-5 gene within the MHC class I region.
Giffon T; Lepourcelet M; Pichon L; Jezequel P; Bouric P; Carn G; Pontarotti P; Gall JY; David V
Immunogenetics; 1996; 44(5):331-9. PubMed ID: 8781118
[TBL] [Abstract][Full Text] [Related]
3. Cloning, expression, and mapping of TCTEL1, a putative human homologue of murine Tcte1, to 6q.
Watanabe TK; Fujiwara T; Shimizu F; Okuno S; Suzuki M; Takahashi E; Nakamura Y; Hirai Y
Cytogenet Cell Genet; 1996; 73(1-2):153-6. PubMed ID: 8646886
[TBL] [Abstract][Full Text] [Related]
4. Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1.
Roepman R; van Duijnhoven G; Rosenberg T; Pinckers AJ; Bleeker-Wagemakers LM; Bergen AA; Post J; Beck A; Reinhardt R; Ropers HH; Cremers FP; Berger W
Hum Mol Genet; 1996 Jul; 5(7):1035-41. PubMed ID: 8817343
[TBL] [Abstract][Full Text] [Related]
5. Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3).
Dry KL; Aldred MA; Edgar AJ; Brown J; Manson FD; Ho MF; Prosser J; Hardwick LJ; Lennon AA; Thomson K
Hum Mol Genet; 1995 Dec; 4(12):2347-53. PubMed ID: 8634709
[TBL] [Abstract][Full Text] [Related]
6. A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus.
Guillonneau X; Piriev NI; Danciger M; Kozak CA; Cideciyan AV; Jacobson SG; Farber DB
Hum Mol Genet; 1999 Aug; 8(8):1541-6. PubMed ID: 10401003
[TBL] [Abstract][Full Text] [Related]
7. A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.
Fujita R; Bingham E; Forsythe P; McHenry C; Aita V; Navia BA; Dry K; Segal M; Devoto M; Bruns G; Wright AF; Ott J; Sieving PA; Swaroop A
Am J Hum Genet; 1996 Jul; 59(1):152-8. PubMed ID: 8659520
[TBL] [Abstract][Full Text] [Related]
8. Physical mapping at a potential X-linked retinitis pigmentosa locus (RP3) by pulsed-field gel electrophoresis.
Musarella MA; Anson-Cartwright CL; McDowell C; Burghes AH; Coulson SE; Worton RG; Rommens JM
Genomics; 1991 Oct; 11(2):263-72. PubMed ID: 1769646
[TBL] [Abstract][Full Text] [Related]
9. Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.
Brown J; Dry KL; Edgar AJ; Pryde FE; Hardwick LJ; Aldred MA; Lester DH; Boyle S; Kaplan J; Dufier JL; Ho MF; Monaco AM; Musarella MA; Wright AF
Genomics; 1996 Oct; 37(2):200-10. PubMed ID: 8921393
[TBL] [Abstract][Full Text] [Related]
10. A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3).
Meindl A; Dry K; Herrmann K; Manson F; Ciccodicola A; Edgar A; Carvalho MR; Achatz H; Hellebrand H; Lennon A; Migliaccio C; Porter K; Zrenner E; Bird A; Jay M; Lorenz B; Wittwer B; D'Urso M; Meitinger T; Wright A
Nat Genet; 1996 May; 13(1):35-42. PubMed ID: 8673101
[TBL] [Abstract][Full Text] [Related]
11. Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.
Fisher SE; Ciccodicola A; Tanaka K; Curci A; Desicato S; D'urso M; Craig IW
Genomics; 1997 Oct; 45(2):340-7. PubMed ID: 9344658
[TBL] [Abstract][Full Text] [Related]
12. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
Lee PL; Gelbart T; West C; Halloran C; Beutler E
Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
[TBL] [Abstract][Full Text] [Related]
13. DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements.
Kirschner R; Erturk D; Zeitz C; Sahin S; Ramser J; Cremers FP; Ropers HH; Berger W
Hum Genet; 2001 Sep; 109(3):271-8. PubMed ID: 11702207
[TBL] [Abstract][Full Text] [Related]
14. A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa.
Meindl A; Carvalho MR; Herrmann K; Lorenz B; Achatz H; Lorenz B; Apfelstedt-Sylla E; Wittwer B; Ross M; Meitinger T
Hum Mol Genet; 1995 Dec; 4(12):2339-46. PubMed ID: 8634708
[TBL] [Abstract][Full Text] [Related]
15. Positional cloning of the gene for X-linked retinitis pigmentosa 2.
Schwahn U; Lenzner S; Dong J; Feil S; Hinzmann B; van Duijnhoven G; Kirschner R; Hemberger M; Bergen AA; Rosenberg T; Pinckers AJ; Fundele R; Rosenthal A; Cremers FP; Ropers HH; Berger W
Nat Genet; 1998 Aug; 19(4):327-32. PubMed ID: 9697692
[TBL] [Abstract][Full Text] [Related]
16. Isolation of a new gene GS2 (DXS1283E) from a CpG island between STS and KAL1 on Xp22.3.
Lee WC; Salido E; Yen PH
Genomics; 1994 Jul; 22(2):372-6. PubMed ID: 7806223
[TBL] [Abstract][Full Text] [Related]
17. Structure and expression of the gene encoding mouse t-complex polypeptide (Tcp-1).
Kubota H; Willison K; Ashworth A; Nozaki M; Miyamoto H; Yamamoto H; Matsushiro A; Morita T
Gene; 1992 Oct; 120(2):207-15. PubMed ID: 1383093
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.
Sippel KC; DeStefano JD; Berson EL; Dryja TP
Invest Ophthalmol Vis Sci; 1998 Mar; 39(3):665-70. PubMed ID: 9501883
[TBL] [Abstract][Full Text] [Related]
19. Identification, genomic structure, and screening of the vacuolar proton-ATPase membrane sector-associated protein M8-9 gene within the COD1 critical region (Xp11.4).
Demirci FY; White NJ; Rigatti BW; Lewis KF; Gorin MB
Mol Vis; 2001 Oct; 7():234-9. PubMed ID: 11590366
[TBL] [Abstract][Full Text] [Related]
20. Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains.
Miano MG; Testa F; Filippini F; Trujillo M; Conte I; Lanzara C; Millán JM; De Bernardo C; Grammatico B; Mangino M; Torrente I; Carrozzo R; Simonelli F; Rinaldi E; Ventruto V; D'Urso M; Ayuso C; Ciccodicola A
Hum Mutat; 2001 Aug; 18(2):109-19. PubMed ID: 11462235
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
