54 related articles for article (PubMed ID: 10205272)
1. Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing.
Gille JJ; Floor K; Kerkhoven L; Ameziane N; Joenje H; de Winter JP
Anemia; 2012; 2012():603253. PubMed ID: 22778927
[TBL] [Abstract][Full Text] [Related]
2. The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature.
Thompson AS; Saba N; McReynolds LJ; Munir S; Ahmed P; Sajjad S; Jones K; Yeager M; Donovan FX; Chandrasekharappa SC; Alter BP; Savage SA; Rehman S
Mol Genet Genomic Med; 2021 Jul; 9(7):e1693. PubMed ID: 33960719
[TBL] [Abstract][Full Text] [Related]
3. A never-ending story: the steadily growing family of the FA and FA-like genes.
Gueiderikh A; Rosselli F; Neto JBC
Genet Mol Biol; 2017; 40(2):398-407. PubMed ID: 28558075
[TBL] [Abstract][Full Text] [Related]
4. Dearth and Delayed Maturation of Testicular Germ Cells in Fanconi Anemia E Mutant Male Mice.
Fu C; Begum K; Jordan PW; He Y; Overbeek PA
PLoS One; 2016; 11(8):e0159800. PubMed ID: 27486799
[TBL] [Abstract][Full Text] [Related]
5. Mechanisms of interstrand DNA crosslink repair and human disorders.
Hashimoto S; Anai H; Hanada K
Genes Environ; 2016; 38():9. PubMed ID: 27350828
[TBL] [Abstract][Full Text] [Related]
6. Update of the human and mouse Fanconi anemia genes.
Dong H; Nebert DW; Bruford EA; Thompson DC; Joenje H; Vasiliou V
Hum Genomics; 2015 Nov; 9():32. PubMed ID: 26596371
[TBL] [Abstract][Full Text] [Related]
7. Coregulation of FANCA and BRCA1 in human cells.
Haitjema A; Mol BM; Kooi IE; Massink MP; Jørgensen JA; Rockx DA; Rooimans MA; de Winter JP; Meijers-Heijboer H; Joenje H; Dorsman JC
Springerplus; 2014; 3():381. PubMed ID: 25161863
[TBL] [Abstract][Full Text] [Related]
8. A protein prioritization approach tailored for the FA/BRCA pathway.
Haitjema A; Brandt BW; Ameziane N; May P; Heringa J; de Winter JP; Joenje H; Dorsman JC
PLoS One; 2013; 8(4):e62017. PubMed ID: 23620800
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 11001585
[TBL] [Abstract][Full Text] [Related]
10. Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.
Joenje H; Levitus M; Waisfisz Q; D'Andrea A; Garcia-Higuera I; Pearson T; van Berkel CG; Rooimans MA; Morgan N; Mathew CG; Arwert F
Am J Hum Genet; 2000 Sep; 67(3):759-62. PubMed ID: 10936108
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 10762542
[TBL] [Abstract][Full Text] [Related]
12. High frequency of large intragenic deletions in the Fanconi anemia group A gene.
Morgan NV; Tipping AJ; Joenje H; Mathew CG
Am J Hum Genet; 1999 Nov; 65(5):1330-41. PubMed ID: 10521298
[TBL] [Abstract][Full Text] [Related]
13. A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA.
Waisfisz Q; de Winter JP; Kruyt FA; de Groot J; van der Weel L; Dijkmans LM; Zhi Y; Arwert F; Scheper RJ; Youssoufian H; Hoatlin ME; Joenje H
Proc Natl Acad Sci U S A; 1999 Aug; 96(18):10320-5. PubMed ID: 10468606
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 10205272
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 9806548
[TBL] [Abstract][Full Text] [Related]
16. 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; 9(18):2665-74. PubMed ID: 11063725
[TBL] [Abstract][Full Text] [Related]
17. Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
Bouchlaka C; Abdelhak S; Amouri A; Ben Abid H; Hadiji S; Frikha M; Ben Othman T; Amri F; Ayadi H; Hachicha M; Rebaï A; Saad A; Dellagi K;
J Hum Genet; 2003; 48(7):352-61. PubMed ID: 12827451
[TBL] [Abstract][Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]