Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 169

1.

Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3.

Hejna JA, Timmers CD, Reifsteck C, Bruun DA, Lucas LW, Jakobs PM, Toth-Fejel S, Unsworth N, Clemens SL, Garcia DK, Naylor SL, Thayer MJ, Olson SB, Grompe M, Moses RE.

Am J Hum Genet. 2000 May;66(5):1540-51. Epub 2000 Apr 12.

PMID:
10762542
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.

Waisfisz Q, Saar K, Morgan NV, Altay C, Leegwater PA, de Winter JP, Komatsu K, Evans GR, Wegner RD, Reis A, Joenje H, Arwert F, Mathew CG, Pronk JC, Digweed M.

Am J Hum Genet. 1999 May;64(5):1400-5.

PMID:
10205272
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p.

Whitney M, Thayer M, Reifsteck C, Olson S, Smith L, Jakobs PM, Leach R, Naylor S, Joenje H, Grompe M.

Nat Genet. 1995 Nov;11(3):341-3.

PMID:
7581463
[PubMed - indexed for MEDLINE]
4.

The Fanconi anaemia group G gene FANCG is identical with XRCC9.

de Winter JP, Waisfisz Q, Rooimans MA, van Berkel CG, Bosnoyan-Collins L, Alon N, Carreau M, Bender O, Demuth I, Schindler D, Pronk JC, Arwert F, Hoehn H, Digweed M, Buchwald M, Joenje H.

Nat Genet. 1998 Nov;20(3):281-3.

PMID:
9806548
[PubMed - indexed for MEDLINE]
5.

Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9.

Strathdee CA, Duncan AM, Buchwald M.

Nat Genet. 1992 Jun;1(3):196-8.

PMID:
1303234
[PubMed - indexed for MEDLINE]
6.

An integrated physical and gene map of the 3.5-Mb chromosome 3p21.3 (AP20) region implicated in major human epithelial malignancies.

Protopopov A, Kashuba V, Zabarovska VI, Muravenko OV, Lerman MI, Klein G, Zabarovsky ER.

Cancer Res. 2003 Jan 15;63(2):404-12.

PMID:
12543795
[PubMed - indexed for MEDLINE]
Free Article
7.

Evidence for at least eight Fanconi anemia genes.

Joenje H, Oostra AB, Wijker M, di Summa FM, van Berkel CG, Rooimans MA, Ebell W, van Weel M, Pronk JC, Buchwald M, Arwert F.

Am J Hum Genet. 1997 Oct;61(4):940-4.

PMID:
9382107
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.

Yamashita T, Nakahata T.

Int J Hematol. 2001 Jul;74(1):33-41. Review.

PMID:
11530803
[PubMed - indexed for MEDLINE]
9.

The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG.

de Winter JP, van der Weel L, de Groot J, Stone S, Waisfisz Q, Arwert F, Scheper RJ, Kruyt FA, Hoatlin ME, Joenje H.

Hum Mol Genet. 2000 Nov 1;9(18):2665-74.

PMID:
11063725
[PubMed - indexed for MEDLINE]
Free Article
10.

A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumors.

Yang Y, Kiss H, Kost-Alimova M, Kedra D, Fransson I, Seroussi E, Li J, Szeles A, Kholodnyuk I, Imreh MP, Fodor K, Hadlaczky G, Klein G, Dumanski JP, Imreh S.

Genomics. 1999 Dec 1;62(2):147-55.

PMID:
10610706
[PubMed - indexed for MEDLINE]
12.

Identification of candidate liver tumor suppressor genes from human 11p11.2-p12.

Ricketts SL, Garcia NF, Betz BL, Coleman WB.

Genes Chromosomes Cancer. 2002 Jan;33(1):47-59.

PMID:
11746987
[PubMed - indexed for MEDLINE]
13.

A common deletion at chromosomal region 17q21 in sporadic prostate tumors distal to BRCA1.

Dai Q, Deubler DA, Maxwell TM, Zhu XL, Cui J, Rohr LR, Stephenson RA, Brothman AR.

Genomics. 2001 Feb 1;71(3):324-9.

PMID:
11170749
[PubMed - indexed for MEDLINE]
14.

Defining a common region of deletion at 13q21 in human cancers.

Chen C, Brabham WW, Stultz BG, Frierson HF Jr, Barrett JC, Sawyers CL, Isaacs JT, Dong JT.

Genes Chromosomes Cancer. 2001 Aug;31(4):333-44.

PMID:
11433524
[PubMed - indexed for MEDLINE]
15.

Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.

Pronk JC, Gibson RA, Savoia A, Wijker M, Morgan NV, Melchionda S, Ford D, Temtamy S, Ortega JJ, Jansen S, et al.

Nat Genet. 1995 Nov;11(3):338-40.

PMID:
7581462
[PubMed - indexed for MEDLINE]
16.

Abnormal rearrangements associated with V(D)J recombination in Fanconi anemia.

Smith J, Andrau JC, Kallenbach S, Laquerbe A, Doyen N, Papadopoulo D.

J Mol Biol. 1998 Sep 4;281(5):815-25.

PMID:
9719637
[PubMed - indexed for MEDLINE]
17.

Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.

Hussain S, Witt E, Huber PA, Medhurst AL, Ashworth A, Mathew CG.

Hum Mol Genet. 2003 Oct 1;12(19):2503-10. Epub 2003 Aug 5.

PMID:
12915460
[PubMed - indexed for MEDLINE]
Free Article
18.

A 3p21.3 region is preferentially eliminated from human chromosome 3/mouse microcell hybrids during tumor growth in SCID mice.

Kholodnyuk I, Kost-Alimova M, Kashuba V, Gizatulin R, Szeles A, Stanbridge EJ, Zabarovsky ER, Klein G, Imreh S.

Genes Chromosomes Cancer. 1997 Mar;18(3):200-11.

PMID:
9071573
[PubMed - indexed for MEDLINE]
19.

Isolation of a cDNA representing the Fanconi anemia complementation group E gene.

de Winter JP, Léveillé F, van Berkel CG, Rooimans MA, van Der Weel L, Steltenpool J, Demuth I, Morgan NV, Alon N, Bosnoyan-Collins L, Lightfoot J, Leegwater PA, Waisfisz Q, Komatsu K, Arwert F, Pronk JC, Mathew CG, Digweed M, Buchwald M, Joenje H.

Am J Hum Genet. 2000 Nov;67(5):1306-8. Epub 2000 Sep 19.

PMID:
11001585
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG).

Bench AJ, Nacheva EP, Hood TL, Holden JL, French L, Swanton S, Champion KM, Li J, Whittaker P, Stavrides G, Hunt AR, Huntly BJ, Campbell LJ, Bentley DR, Deloukas P, Green AR.

Oncogene. 2000 Aug 10;19(34):3902-13.

PMID:
10952764
[PubMed - indexed for MEDLINE]
Free Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk