203 related articles for article (PubMed ID: 32106311)
1. Association of clinical severity with FANCB variant type in Fanconi anemia.
Jung M; Ramanagoudr-Bhojappa R; van Twest S; Rosti RO; Murphy V; Tan W; Donovan FX; Lach FP; Kimble DC; Jiang CS; Vaughan R; Mehta PA; Pierri F; Dufour C; Auerbach AD; Deans AJ; Smogorzewska A; Chandrasekharappa SC
Blood; 2020 Apr; 135(18):1588-1602. PubMed ID: 32106311
[TBL] [Abstract][Full Text] [Related]
2. Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype.
Asur RS; Kimble DC; Lach FP; Jung M; Donovan FX; Kamat A; Noonan RJ; Thomas JW; Park M; Chines P; Vlachos A; Auerbach AD; Smogorzewska A; Chandrasekharappa SC
Mol Genet Genomic Med; 2018 Jan; 6(1):77-91. PubMed ID: 29193904
[TBL] [Abstract][Full Text] [Related]
3. The genetic and biochemical basis of FANCD2 monoubiquitination.
Rajendra E; Oestergaard VH; Langevin F; Wang M; Dornan GL; Patel KJ; Passmore LA
Mol Cell; 2014 Jun; 54(5):858-69. PubMed ID: 24905007
[TBL] [Abstract][Full Text] [Related]
4. Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway.
van Twest S; Murphy VJ; Hodson C; Tan W; Swuec P; O'Rourke JJ; Heierhorst J; Crismani W; Deans AJ
Mol Cell; 2017 Jan; 65(2):247-259. PubMed ID: 27986371
[TBL] [Abstract][Full Text] [Related]
5. Evidence for subcomplexes in the Fanconi anemia pathway.
Medhurst AL; Laghmani el H; Steltenpool J; Ferrer M; Fontaine C; de Groot J; Rooimans MA; Scheper RJ; Meetei AR; Wang W; Joenje H; de Winter JP
Blood; 2006 Sep; 108(6):2072-80. PubMed ID: 16720839
[TBL] [Abstract][Full Text] [Related]
6. Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
Ameziane N; Errami A; Léveillé F; Fontaine C; de Vries Y; van Spaendonk RM; de Winter JP; Pals G; Joenje H
Hum Mutat; 2008 Jan; 29(1):159-66. PubMed ID: 17924555
[TBL] [Abstract][Full Text] [Related]
7. Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50.
Chandrasekharappa SC; Chinn SB; Donovan FX; Chowdhury NI; Kamat A; Adeyemo AA; Thomas JW; Vemulapalli M; Hussey CS; Reid HH; Mullikin JC; Wei Q; Sturgis EM
Cancer; 2017 Oct; 123(20):3943-3954. PubMed ID: 28678401
[TBL] [Abstract][Full Text] [Related]
8. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
Chandrasekharappa SC; Lach FP; Kimble DC; Kamat A; Teer JK; Donovan FX; Flynn E; Sen SK; Thongthip S; Sanborn E; Smogorzewska A; Auerbach AD; Ostrander EA;
Blood; 2013 May; 121(22):e138-48. PubMed ID: 23613520
[TBL] [Abstract][Full Text] [Related]
9. The FANCD2-FANCI complex is recruited to DNA interstrand crosslinks before monoubiquitination of FANCD2.
Liang CC; Li Z; Lopez-Martinez D; Nicholson WV; Vénien-Bryan C; Cohn MA
Nat Commun; 2016 Jul; 7():12124. PubMed ID: 27405460
[TBL] [Abstract][Full Text] [Related]
10. A defined role for multiple Fanconi anemia gene products in DNA-damage-associated ubiquitination.
Tan W; Deans AJ
Exp Hematol; 2017 Jun; 50():27-32. PubMed ID: 28315701
[TBL] [Abstract][Full Text] [Related]
11. Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells.
Siddique MA; Nakanishi K; Taniguchi T; Grompe M; D'Andrea AD
Exp Hematol; 2001 Dec; 29(12):1448-55. PubMed ID: 11750104
[TBL] [Abstract][Full Text] [Related]
12. The phenotype of FancB-mutant mouse embryonic stem cells.
Kim TM; Ko JH; Choi YJ; Hu L; Hasty P
Mutat Res; 2011 Jul; 712(1-2):20-7. PubMed ID: 21458466
[TBL] [Abstract][Full Text] [Related]
13. A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
George M; Solanki A; Chavan N; Rajendran A; Raj R; Mohan S; Nemani S; Kanvinde S; Munirathnam D; Rao S; Radhakrishnan N; Lashkari HP; Ghildhiyal RG; Manglani M; Shanmukhaiah C; Bhat S; Ramesh S; Cherian A; Junagade P; Vundinti BR
Hum Mutat; 2021 Dec; 42(12):1648-1665. PubMed ID: 34585473
[TBL] [Abstract][Full Text] [Related]
14. Coordinate nuclear targeting of the FANCD2 and FANCI proteins via a FANCD2 nuclear localization signal.
Boisvert RA; Rego MA; Azzinaro PA; Mauro M; Howlett NG
PLoS One; 2013; 8(11):e81387. PubMed ID: 24278431
[TBL] [Abstract][Full Text] [Related]
15. Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
Rickman KA; Lach FP; Abhyankar A; Donovan FX; Sanborn EM; Kennedy JA; Sougnez C; Gabriel SB; Elemento O; Chandrasekharappa SC; Schindler D; Auerbach AD; Smogorzewska A
Cell Rep; 2015 Jul; 12(1):35-41. PubMed ID: 26119737
[TBL] [Abstract][Full Text] [Related]
16. AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.
Virts EL; Jankowska A; Mackay C; Glaas MF; Wiek C; Kelich SL; Lottmann N; Kennedy FM; Marchal C; Lehnert E; Scharf RE; Dufour C; Lanciotti M; Farruggia P; Santoro A; Savasan S; Scheckenbach K; Schipper J; Wagenmann M; Lewis T; Leffak M; Farlow JL; Foroud TM; Honisch E; Niederacher D; Chakraborty SC; Vance GH; Pruss D; Timms KM; Lanchbury JS; Alpi AF; Hanenberg H
Hum Mol Genet; 2015 Sep; 24(18):5093-108. PubMed ID: 26085575
[TBL] [Abstract][Full Text] [Related]
17. Cyclin-Dependent Kinase-Mediated Phosphorylation of FANCD2 Promotes Mitotic Fidelity.
Cantres-Velez JA; Blaize JL; Vierra DA; Boisvert RA; Garzon JL; Piraino B; Tan W; Deans AJ; Howlett NG
Mol Cell Biol; 2021 Jul; 41(8):e0023421. PubMed ID: 34096775
[TBL] [Abstract][Full Text] [Related]
18. The ubiquitination machinery of the Fanconi Anemia DNA repair pathway.
Tan W; Deans AJ
Prog Biophys Mol Biol; 2021 Aug; 163():5-13. PubMed ID: 33058944
[TBL] [Abstract][Full Text] [Related]
19. Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.
Adachi D; Oda T; Yagasaki H; Nakasato K; Taniguchi T; D'Andrea AD; Asano S; Yamashita T
Hum Mol Genet; 2002 Dec; 11(25):3125-34. PubMed ID: 12444097
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]