Detalhe da pesquisa
1.
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis.
Nat Genet
; 3(2): 122-6, 1993 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-8499945
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2.
Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines.
Nat Genet
; 3(2): 118-21, 1993 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-8499944
3.
A translocation interrupts the COL5A1 gene in a patient with Ehlers-Danlos syndrome and hypomelanosis of Ito.
Nat Genet
; 13(3): 361-5, 1996 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-8673139
4.
Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice.
Nat Genet
; 6(4): 374-8, 1994 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-8054977
5.
CATCHing a break on 22.
Nat Genet
; 10(3): 257-8, 1995 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-7670460
6.
Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites.
Oncogene
; 25(32): 4381-8, 2006 Jul 27.
Artigo
Inglês
| MEDLINE | ID: mdl-16732333
7.
Genomic amplification of MET with boundaries within fragile site FRA7G and upregulation of MET pathways in esophageal adenocarcinoma.
Oncogene
; 25(3): 409-18, 2006 Jan 19.
Artigo
Inglês
| MEDLINE | ID: mdl-16186806
8.
Effects of harman and norharman on spontaneous and ultraviolet light-induced mutagenesis in cultured Chinese hamster cells.
Cancer Res
; 38(12): 4527-33, 1978 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-719638
9.
Distinct areas of allelic loss on chromosomal regions 10p and 10q in human prostate cancer.
Cancer Res
; 56(10): 2263-7, 1996 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-8625295
10.
A minimal critical region of the 8p22-23 amplicon in esophageal adenocarcinomas defined using sequence tagged site-amplification mapping and quantitative polymerase chain reaction includes the GATA-4 gene.
Cancer Res
; 60(5): 1341-7, 2000 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-10728696
11.
Identification and characterization of a 19q12 amplicon in esophageal adenocarcinomas reveals cyclin E as the best candidate gene for this amplicon.
Cancer Res
; 60(24): 7021-7, 2000 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-11156406
12.
Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors.
Cancer Res
; 56(19): 4347-50, 1996 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-8813121
13.
The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region.
Cancer Res
; 58(15): 3409-14, 1998 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-9699673
14.
Frequent deletions of FHIT and FRA3B in Barrett's metaplasia and esophageal adenocarcinomas.
Oncogene
; 15(14): 1653-9, 1997 Oct 02.
Artigo
Inglês
| MEDLINE | ID: mdl-9349498
15.
Association of a mature B cell leukemia with a 4p+ chromosomal abnormality: derivation and characterization of a cell line.
Leukemia
; 3(9): 643-7, 1989 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-2548046
16.
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.
J Med Genet
; 38(11): 761-6, 2001 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-11694548
Texto completo17.
A phosphoglycerate mutase brain isoform (PGAM 1) pseudogene is localized within the human Menkes disease gene (ATP7 A).
Gene
; 198(1-2): 37-41, 1997 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-9370262
18.
Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant.
Gene
; 254(1-2): 87-96, 2000 Aug 22.
Artigo
Inglês
| MEDLINE | ID: mdl-10974539
19.
Common fragile sites.
Cytogenet Genome Res
; 100(1-4): 92-100, 2003.
Artigo
Inglês
| MEDLINE | ID: mdl-14526169
20.
Severe anomalies associated with ring chromosome 7.
Am J Med Genet
; 40(4): 429-31, 1991 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-1746606
