110 related articles for article (PubMed ID: 9330635)
1. Chromosomal localization to 19q13.3, partial genomic structure and 5' cDNA sequence of the human symplekin gene.
Ueki K; Ramaswamy S; Billings SJ; Mohrenweiser HW; Louis DN
Somat Cell Mol Genet; 1997 May; 23(3):229-31. PubMed ID: 9330635
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Structure, 5'-flanking sequence, and chromosome location of the human N-formyl peptide receptor gene. A single-copy gene comprised of two exons on chromosome 19q.13.3 that yields two distinct transcripts by alternative polyadenylation.
Haviland DL; Borel AC; Fleischer DT; Haviland JC; Wetsel RA
Biochemistry; 1993 Apr; 32(16):4168-74. PubMed ID: 7682842
[TBL] [Abstract][Full Text] [Related]
4. Cloning of a highly conserved human protein serine-threonine phosphatase gene from the glioma candidate region on chromosome 19q13.3.
Yong WH; Ueki K; Chou D; Reeves SA; von Deimling A; Gusella JF; Mohrenweiser HW; Buckler AJ; Louis DN
Genomics; 1995 Sep; 29(2):533-6. PubMed ID: 8666404
[TBL] [Abstract][Full Text] [Related]
5. Cloning of the VASP (vasodilator-stimulated phosphoprotein) genes in human and mouse: structure, sequence, and chromosomal localization.
Zimmer M; Fink T; Fischer L; Hauser W; Scherer K; Lichter P; Walter U
Genomics; 1996 Sep; 36(2):227-33. PubMed ID: 8812448
[TBL] [Abstract][Full Text] [Related]
6. Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12.
Xie YG; Han FY; Peyrard M; Ruttledge MH; Fransson I; DeJong P; Collins J; Dunham I; Nordenskjöld M; Dumanski JP
Hum Mol Genet; 1993 Sep; 2(9):1361-8. PubMed ID: 8242058
[TBL] [Abstract][Full Text] [Related]
7. Structural organization and complete sequence of the human alpha-N-acetylgalactosaminidase gene: homology with the alpha-galactosidase A gene provides evidence for evolution from a common ancestral gene.
Wang AM; Desnick RJ
Genomics; 1991 May; 10(1):133-42. PubMed ID: 1646157
[TBL] [Abstract][Full Text] [Related]
8. 14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome region.
Chong SS; Tanigami A; Roschke AV; Ledbetter DH
Genome Res; 1996 Aug; 6(8):735-41. PubMed ID: 8858348
[TBL] [Abstract][Full Text] [Related]
9. cDNA isolation, genomic structure, regulation, and chromosomal localization of human lung Kruppel-like factor.
Wani MA; Conkright MD; Jeffries S; Hughes MJ; Lingrel JB
Genomics; 1999 Aug; 60(1):78-86. PubMed ID: 10458913
[TBL] [Abstract][Full Text] [Related]
10. Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.
Olsen AS; Georgescu A; Johnson S; Carrano AV
Genomics; 1996 Jun; 34(2):223-5. PubMed ID: 8661053
[TBL] [Abstract][Full Text] [Related]
11. Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.
Shutler G; Korneluk RG; Tsilfidis C; Mahadevan M; Bailly J; Smeets H; Jansen G; Wieringa B; Lohman F; Aslanidis C
Genomics; 1992 Jul; 13(3):518-25. PubMed ID: 1639380
[TBL] [Abstract][Full Text] [Related]
12. Molecular cloning, expression and chromosomal localization of a novel human REG family gene, REG III.
Nata K; Liu Y; Xu L; Ikeda T; Akiyama T; Noguchi N; Kawaguchi S; Yamauchi A; Takahashi I; Shervani NJ; Onogawa T; Takasawa S; Okamoto H
Gene; 2004 Sep; 340(1):161-70. PubMed ID: 15556304
[TBL] [Abstract][Full Text] [Related]
13. ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3.
Ueki K; Ramaswamy S; Billings SJ; Mohrenweiser HW; Louis DN
Neurogenetics; 1997 May; 1(1):31-6. PubMed ID: 10735272
[TBL] [Abstract][Full Text] [Related]
14. Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis.
Scott HS; Kyriakou DS; Peterson P; Heino M; Tähtinen M; Krohn K; Chen H; Rossier C; Lalioti MD; Antonarakis SE
Genomics; 1998 Jan; 47(1):64-70. PubMed ID: 9465297
[TBL] [Abstract][Full Text] [Related]
15. Molecular cloning and expression analysis of five novel genes in chromosome 1p36.
Onyango P; Lubyova B; Gardellin P; Kurzbauer R; Weith A
Genomics; 1998 Jun; 50(2):187-98. PubMed ID: 9653645
[TBL] [Abstract][Full Text] [Related]
16. A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.
Rouquier S; Giorgi D; Trask B; Bergmann A; Phillips MS; MacLennan DH; de Jong P
Genomics; 1993 Aug; 17(2):330-40. PubMed ID: 8406483
[TBL] [Abstract][Full Text] [Related]
17. Symplekin, a novel type of tight junction plaque protein.
Keon BH; Schäfer S; Kuhn C; Grund C; Franke WW
J Cell Biol; 1996 Aug; 134(4):1003-18. PubMed ID: 8769423
[TBL] [Abstract][Full Text] [Related]
18. Isolation and mapping of a novel human gene encoding a protein containing zinc-finger structures.
Saito H; Fujiwara T; Takahashi EI; Shin S; Okui K; Nakamura Y
Genomics; 1996 Feb; 31(3):376-9. PubMed ID: 8838321
[TBL] [Abstract][Full Text] [Related]
19. Molecular cloning and characterization of a human cDNA and gene encoding a novel acid ceramidase-like protein.
Hong SB; Li CM; Rhee HJ; Park JH; He X; Levy B; Yoo OJ; Schuchman EH
Genomics; 1999 Dec; 62(2):232-41. PubMed ID: 10610717
[TBL] [Abstract][Full Text] [Related]
20. Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites.
Sohocki MM; Sullivan LS; Harrison WR; Sodergren EJ; Elder FF; Weinstock G; Tanase S; Daiger SP
Genomics; 1997 Mar; 40(2):247-52. PubMed ID: 9119391
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]