181 related articles for article (PubMed ID: 9299232)
1. Identification and characterization of the human homologue of SH3BP2, an SH3 binding domain protein within a common region of deletion at 4p16.3 involved in bladder cancer.
Bell SM; Shaw M; Jou YS; Myers RM; Knowles MA
Genomics; 1997 Sep; 44(2):163-70. PubMed ID: 9299232
[TBL] [Abstract][Full Text] [Related]
2. A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1.
Hildebrandt F; Otto E; Rensing C; Nothwang HG; Vollmer M; Adolphs J; Hanusch H; Brandis M
Nat Genet; 1997 Oct; 17(2):149-53. PubMed ID: 9326933
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer.
Bednarek AK; Laflin KJ; Daniel RL; Liao Q; Hawkins KA; Aldaz CM
Cancer Res; 2000 Apr; 60(8):2140-5. PubMed ID: 10786676
[TBL] [Abstract][Full Text] [Related]
5. Molecular cloning and characterization of LCRG1 a novel gene localized to the tumor suppressor locus D17S800-D17S930.
Li Y; Chen Z
Cancer Lett; 2004 Jun; 209(1):75-85. PubMed ID: 15145523
[TBL] [Abstract][Full Text] [Related]
6. Two isoforms of a human intersectin (ITSN) protein are produced by brain-specific alternative splicing in a stop codon.
Guipponi M; Scott HS; Chen H; Schebesta A; Rossier C; Antonarakis SE
Genomics; 1998 Nov; 53(3):369-76. PubMed ID: 9799604
[TBL] [Abstract][Full Text] [Related]
7. Mutation spectrum of the 9q34 tuberous sclerosis gene TSC1 in transitional cell carcinoma of the bladder.
Knowles MA; Habuchi T; Kennedy W; Cuthbert-Heavens D
Cancer Res; 2003 Nov; 63(22):7652-6. PubMed ID: 14633685
[TBL] [Abstract][Full Text] [Related]
8. Cloning, mapping, and characterization of the human sorbin and SH3 domain containing 1 (SORBS1) gene: a protein associated with c-Abl during insulin signaling in the hepatoma cell line Hep3B.
Lin WH; Huang CJ; Liu MW; Chang HM; Chen YJ; Tai TY; Chuang LM
Genomics; 2001 May; 74(1):12-20. PubMed ID: 11374898
[TBL] [Abstract][Full Text] [Related]
9. Mutation of the 9q34 gene TSC1 in sporadic bladder cancer.
Hornigold N; Devlin J; Davies AM; Aveyard JS; Habuchi T; Knowles MA
Oncogene; 1999 Apr; 18(16):2657-61. PubMed ID: 10353610
[TBL] [Abstract][Full Text] [Related]
10. Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3.
Savino M; d'Apolito M; Centra M; van Beerendonk HM; Cleton-Jansen AM; Whitmore SA; Crawford J; Callen DF; Zelante L; Savoia A
Genomics; 1999 Oct; 61(2):219-26. PubMed ID: 10534407
[TBL] [Abstract][Full Text] [Related]
11. ARHGAP8 is a novel member of the RHOGAP family related to ARHGAP1/CDC42GAP/p50RHOGAP: mutation and expression analyses in colorectal and breast cancers.
Johnstone CN; Castellví-Bel S; Chang LM; Bessa X; Nakagawa H; Harada H; Sung RK; Piqué JM; Castells A; Rustgi AK
Gene; 2004 Jul; 336(1):59-71. PubMed ID: 15225876
[TBL] [Abstract][Full Text] [Related]
12. Cloning, chromosomal localization, and characterization of cDNA from a novel gene, SH3BP4, expressed by human corneal fibroblasts.
Dunlevy JR; Berryhill BL; Vergnes JP; SundarRaj N; Hassell JR
Genomics; 1999 Dec; 62(3):519-24. PubMed ID: 10644451
[TBL] [Abstract][Full Text] [Related]
13. Fluorescence in situ hybridization deletion mapping at 4p16.3 in bladder cancer cell lines refines the localisation of the critical interval to 30 kb.
Bell SM; Zuo J; Myers RM; Knowles MA
Genes Chromosomes Cancer; 1996 Oct; 17(2):108-17. PubMed ID: 8913728
[TBL] [Abstract][Full Text] [Related]
14. Characterization of RUSC1 and RUSC2 genes in silico.
Katoh M; Katoh M
Oncol Rep; 2004 Oct; 12(4):933-8. PubMed ID: 15375525
[TBL] [Abstract][Full Text] [Related]
15. The human mammary-derived growth inhibitor (MDGI) gene: genomic structure and mutation analysis in human breast tumors.
Phelan CM; Larsson C; Baird S; Futreal PA; Ruttledge MH; Morgan K; Tonin P; Hung H; Korneluk RG; Pollak MN; Narod SA
Genomics; 1996 May; 34(1):63-8. PubMed ID: 8661024
[TBL] [Abstract][Full Text] [Related]
16. The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium.
Lerman MI; Minna JD
Cancer Res; 2000 Nov; 60(21):6116-33. PubMed ID: 11085536
[TBL] [Abstract][Full Text] [Related]
17. Identification of a 428-kb homozygously deleted region disrupting the SEZ6L gene at 22q12.1 in a lung cancer cell line.
Nishioka M; Kohno T; Takahashi M; Niki T; Yamada T; Sone S; Yokota J
Oncogene; 2000 Dec; 19(54):6251-60. PubMed ID: 11175339
[TBL] [Abstract][Full Text] [Related]
18. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.
Cooper PR; Smilinich NJ; Day CD; Nowak NJ; Reid LH; Pearsall RS; Reece M; Prawitt D; Landers J; Housman DE; Winterpacht A; Zabel BU; Pelletier J; Weissman BE; Shows TB; Higgins MJ
Genomics; 1998 Apr; 49(1):38-51. PubMed ID: 9570947
[TBL] [Abstract][Full Text] [Related]
19. Isolation and characterization of e3B1, an eps8 binding protein that regulates cell growth.
Biesova Z; Piccoli C; Wong WT
Oncogene; 1997 Jan; 14(2):233-41. PubMed ID: 9010225
[TBL] [Abstract][Full Text] [Related]
20. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
Berti L; Mittler G; Przemeck GK; Stelzer G; Günzler B; Amati F; Conti E; Dallapiccola B; Hrabé de Angelis M; Novelli G; Meisterernst M
Genomics; 2001 Jun; 74(3):320-32. PubMed ID: 11414760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
