Search details
1.
Genetic determinants of micronucleus formation in vivo.
Nature
; 627(8002): 130-136, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38355793
2.
Tailoring heated intraperitoneal mitomycin C for peritoneal metastases originating from colorectal carcinoma: a translational approach to improve survival.
Br J Cancer
; 112(5): 851-6, 2015 Mar 03.
Article
in English
| MEDLINE | ID: mdl-25668003
3.
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
Nat Genet
; 20(3): 281-3, 1998 Nov.
Article
in English
| MEDLINE | ID: mdl-9806548
4.
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
Nat Genet
; 14(3): 320-3, 1996 Nov.
Article
in English
| MEDLINE | ID: mdl-8896563
5.
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
Nat Genet
; 14(4): 488, 1996 Dec.
Article
in English
| MEDLINE | ID: mdl-8944034
6.
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM.
Nat Genet
; 24(1): 15-6, 2000 Jan.
Article
in English
| MEDLINE | ID: mdl-10615118
7.
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.
Eur J Hum Genet
; 5(3): 137-48, 1997.
Article
in English
| MEDLINE | ID: mdl-9272737
8.
Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemia.
Fam Cancer
; 1(1): 39-43, 2001.
Article
in English
| MEDLINE | ID: mdl-14574014
9.
Clonally related but phenotypically divergent human cancer cell lines derived from a single follicular thyroid cancer recurrence (TT2609).
Thyroid
; 11(10): 909-17, 2001 Oct.
Article
in English
| MEDLINE | ID: mdl-11716037
10.
Apparent absence of BRCA2 protein in a proportion of acute myeloid leukemia cell lines.
Leukemia
; 18(11): 1918-20, 2004 Nov.
Article
in English
| MEDLINE | ID: mdl-15356654
11.
The Chinese hamster cell mutant V-H4 is homologous to Fanconi anemia (complementation group A).
Cytogenet Cell Genet
; 56(1): 23-6, 1991.
Article
in English
| MEDLINE | ID: mdl-1900747
12.
Genetic diversity of mitomycin C-hypersensitive Chinese hamster cell mutants: a new complementation group with chromosomal instability.
Somat Cell Mol Genet
; 19(5): 431-7, 1993 Sep.
Article
in English
| MEDLINE | ID: mdl-8291021
13.
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.
Am J Hum Genet
; 67(3): 759-62, 2000 Sep.
Article
in English
| MEDLINE | ID: mdl-10936108
14.
Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype.
Blood
; 86(6): 2156-60, 1995 Sep 15.
Article
in English
| MEDLINE | ID: mdl-7662964
15.
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21.
Hum Mol Genet
; 5(1): 151-4, 1996 Jan.
Article
in English
| MEDLINE | ID: mdl-8789453
16.
Cloning and characterization of murine fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary.
Mamm Genome
; 11(4): 326-31, 2000 Apr.
Article
in English
| MEDLINE | ID: mdl-10754110
17.
Evidence for at least eight Fanconi anemia genes.
Am J Hum Genet
; 61(4): 940-4, 1997 Oct.
Article
in English
| MEDLINE | ID: mdl-9382107
18.
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
Am J Hum Genet
; 67(5): 1306-8, 2000 Nov.
Article
in English
| MEDLINE | ID: mdl-11001585
19.
Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia C gene, FAC.
Hum Mutat
; 7(3): 264-5, 1996.
Article
in English
| MEDLINE | ID: mdl-8829660
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