127 related articles for article (PubMed ID: 8162598)
1. One-megabase yeast artificial chromosome and 400-kilobase cosmid-phage contigs containing the von Hippel-Lindau tumor suppressor and Ca(2+)-transporting adenosine triphosphatase isoform 2 genes.
Kuzmin I; Stackhouse T; Latif F; Duh FM; Geil L; Gnarra J; Yao M; Orcutt ML; Li H; Tory K
Cancer Res; 1994 May; 54(9):2486-91. PubMed ID: 8162598
[TBL] [Abstract][Full Text] [Related]
2. von Hippel-Lindau syndrome: cloning and identification of the plasma membrane Ca(++)-transporting ATPase isoform 2 gene that resides in the von Hippel-Lindau gene region.
Latif F; Duh FM; Gnarra J; Tory K; Kuzmin I; Yao M; Stackhouse T; Modi W; Geil L; Schmidt L
Cancer Res; 1993 Feb; 53(4):861-7. PubMed ID: 8428366
[TBL] [Abstract][Full Text] [Related]
3. The isolation of a yeast artificial chromosome (YAC) contig extending for 2 megabases in the vicinity of the von Hippel Lindau disease gene.
Liu W; Piechocki M; Shridhar V; Lyles G; Song Z; Nakamura Y; Drabkin H; Vance J; Smith DI
Hum Mol Genet; 1993 Aug; 2(8):1177-82. PubMed ID: 8104627
[TBL] [Abstract][Full Text] [Related]
4. A complete YAC contig and cosmid interval map covering the entirety of human Xq21.33 to Xq22.3 from DXS3 to DXS287.
Kendall E; Evans W; Jin H; Holland J; Vetrie D
Genomics; 1997 Jul; 43(2):171-82. PubMed ID: 9244434
[TBL] [Abstract][Full Text] [Related]
5. Construction of a 600-kilobase cosmid clone contig and generation of a transcriptional map surrounding the lung cancer tumor suppressor gene (TSG) locus on human chromosome 3p21.3: progress toward the isolation of a lung cancer TSG.
Wei MH; Latif F; Bader S; Kashuba V; Chen JY; Duh FM; Sekido Y; Lee CC; Geil L; Kuzmin I; Zabarovsky E; Klein G; Zbar B; Minna JD; Lerman MI
Cancer Res; 1996 Apr; 56(7):1487-92. PubMed ID: 8603390
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.
Haas M; Aburatani H; Stanton VP; Bhatt M; Housman D; Ward DC
Genomics; 1993 Apr; 16(1):90-6. PubMed ID: 8486389
[TBL] [Abstract][Full Text] [Related]
8. Frequent allelic loss at chromosome arm 3p is distinct from genetic alterations of the Von-Hippel Lindau tumor suppressor gene in head and neck cancer.
Waber PG; Lee NK; Nisen PD
Oncogene; 1996 Jan; 12(2):365-9. PubMed ID: 8570213
[TBL] [Abstract][Full Text] [Related]
9. Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis.
Richards FM; Phipps ME; Latif F; Yao M; Crossey PA; Foster K; Linehan WM; Affara NA; Lerman MI; Zbar B
Hum Mol Genet; 1993 Jul; 2(7):879-82. PubMed ID: 8364570
[TBL] [Abstract][Full Text] [Related]
10. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.
Wilgenbus KK; Seranski P; Brown A; Leuchs B; Mincheva A; Lichter P; Poustka A
Genomics; 1997 May; 42(1):1-10. PubMed ID: 9177769
[TBL] [Abstract][Full Text] [Related]
11. Cloning and characterization of a mouse gene with homology to the human von Hippel-Lindau disease tumor suppressor gene: implications for the potential organization of the human von Hippel-Lindau disease gene.
Gao J; Naglich JG; Laidlaw J; Whaley JM; Seizinger BR; Kley N
Cancer Res; 1995 Feb; 55(4):743-7. PubMed ID: 7850784
[TBL] [Abstract][Full Text] [Related]
12. [Von Hippel-Lindau disease and molecular genetic diagnosis].
Jensen AM; Bisgaard ML
Ugeskr Laeger; 1999 Feb; 161(7):959-61. PubMed ID: 10051806
[TBL] [Abstract][Full Text] [Related]
13. An integrated high-resolution physical map of the DPC/BRCA2 region at chromosome 13q12.
Schutte M; Rozenblum E; Moskaluk CA; Guan X; Hoque AT; Hahn SA; da Costa LT; de Jong PJ; Kern SE
Cancer Res; 1995 Oct; 55(20):4570-4. PubMed ID: 7553631
[TBL] [Abstract][Full Text] [Related]
14. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Yu CE; Oshima J; Hisama FM; Matthews S; Trask BJ; Schellenberg GD
Genomics; 1996 Aug; 35(3):431-40. PubMed ID: 8812476
[TBL] [Abstract][Full Text] [Related]
15. Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3.
Lapenta V; Sossi V; Gosset P; Vayssettes C; Vitali T; Rabatel N; Tassone F; Blouin JL; Scott HS; Antonarakis SE; Créau N; Brahe C
Genomics; 1998 Apr; 49(1):1-13. PubMed ID: 9570943
[TBL] [Abstract][Full Text] [Related]
16. A second-generation YAC contig map of human chromosome 3.
Gemmill RM; Chumakov I; Scott P; Waggoner B; Rigault P; Cypser J; Chen Q; Weissenbach J; Gardiner K; Wang H
Nature; 1995 Sep; 377(6547 Suppl):299-319. PubMed ID: 7566097
[TBL] [Abstract][Full Text] [Related]
17. The detailed characterisation of a 400 kb cosmid walk in the BRCA1 region: identification and localisation of 10 genes including a dual-specificity phosphatase.
Jones KA; Black DM; Brown MA; Griffiths BL; Nicolai HM; Chambers JA; Bonjardim M; Xu CF; Boyd M; McFarlane R
Hum Mol Genet; 1994 Nov; 3(11):1927-34. PubMed ID: 7874108
[TBL] [Abstract][Full Text] [Related]
18. A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3.
Arai Y; Hosoda F; Nakayama K; Ohki M
Genomics; 1996 Jul; 35(1):196-206. PubMed ID: 8661121
[TBL] [Abstract][Full Text] [Related]
19. An integrated YAC-overlap and 'cosmid-pocket' map of the human chromosome 21.
Nizetić D; Gellen L; Hamvas RM; Mott R; Grigoriev A; Vatcheva R; Zehetner G; Yaspo ML; Dutriaux A; Lopes C
Hum Mol Genet; 1994 May; 3(5):759-70. PubMed ID: 8081363
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]