126 related articles for article (PubMed ID: 36721989)
21. Fanconi anemia: correlating central nervous system malformations and genetic complementation groups.
Johnson-Tesch BA; Gawande RS; Zhang L; MacMillan ML; Nascene DR
Pediatr Radiol; 2017 Jun; 47(7):868-876. PubMed ID: 28283722
[TBL] [Abstract][Full Text] [Related]
22. Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study.
Kastellan S; Kalb R; Sajjad B; McReynolds LJ; Giri N; Samuel D; Milde T; Elbracht M; Holzhauer S; Niewisch MR; Kratz CP
J Hematol Oncol; 2024 Apr; 17(1):26. PubMed ID: 38685107
[TBL] [Abstract][Full Text] [Related]
23. Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children.
Svojgr K; Sumerauer D; Puchmajerova A; Vicha A; Hrusak O; Michalova K; Malis J; Smisek P; Kyncl M; Novotna D; Machackova E; Jencik J; Pycha K; Vaculik M; Kodet R; Stary J
Eur J Med Genet; 2016 Mar; 59(3):152-7. PubMed ID: 26657402
[TBL] [Abstract][Full Text] [Related]
24. Breast cancer and Fanconi anemia: what are the connections?
Zdzienicka MZ; Arwert F
Trends Mol Med; 2002 Oct; 8(10):458-60. PubMed ID: 12383764
[TBL] [Abstract][Full Text] [Related]
25. [Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report].
Puchmajerová A; Švojgr K; Novotná D; Macháčková E; Sumerauer D; Smíšek P; Kodet R; Kynčl M; Křepelová A; Foretová L
Klin Onkol; 2016; 29 Suppl 1():S89-92. PubMed ID: 26691948
[TBL] [Abstract][Full Text] [Related]
26. Screening Fanconi anemia lymphoid cell lines of non-A, C, D2, E, F, G subtypes for defects in BRCA2/FANCD1.
Popp H; Kalb R; Fischer A; Lobitz S; Kokemohr I; Hanenberg H; Schindler D
Cytogenet Genome Res; 2003; 103(1-2):54-7. PubMed ID: 15004464
[TBL] [Abstract][Full Text] [Related]
27. Biallelic FANCD1/BRCA2 mutations predisposing to glioblastoma multiforme with multiple oncogenic amplifications.
Dodgshun AJ; Sexton-Oates A; Saffery R; Sullivan MJ
Cancer Genet; 2016; 209(1-2):53-6. PubMed ID: 26740091
[TBL] [Abstract][Full Text] [Related]
28. Fanconi anaemia and cancer: an intricate relationship.
Nalepa G; Clapp DW
Nat Rev Cancer; 2018 Mar; 18(3):168-185. PubMed ID: 29376519
[TBL] [Abstract][Full Text] [Related]
29. Fanconi Anaemia, Childhood Cancer and the
Woodward ER; Meyer S
Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680915
[TBL] [Abstract][Full Text] [Related]
30. Fanconi anemia-D1 due to homozygosity for the BRCA2 gene Cypriot founder mutation: A case report.
Loizidou MA; Hadjisavvas A; Tanteles GA; Spanou-Aristidou E; Kyriacou K; Christophidou-Anastasiadou V
Oncol Lett; 2016 Jan; 11(1):471-473. PubMed ID: 26834852
[TBL] [Abstract][Full Text] [Related]
31. A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.
Meyer S; Fergusson WD; Oostra AB; Medhurst AL; Waisfisz Q; de Winter JP; Chen F; Carr TF; Clayton-Smith J; Clancy T; Green M; Barber L; Eden OB; Will AM; Joenje H; Taylor GM
Genes Chromosomes Cancer; 2005 Apr; 42(4):404-15. PubMed ID: 15645491
[TBL] [Abstract][Full Text] [Related]
32. A Hypomorphic PALB2 Allele Gives Rise to an Unusual Form of FA-N Associated with Lymphoid Tumour Development.
Byrd PJ; Stewart GS; Smith A; Eaton C; Taylor AJ; Guy C; Eringyte I; Fooks P; Last JI; Horsley R; Oliver AW; Janic D; Dokmanovic L; Stankovic T; Taylor AM
PLoS Genet; 2016 Mar; 12(3):e1005945. PubMed ID: 26990772
[TBL] [Abstract][Full Text] [Related]
33. A distinct replication fork protection pathway connects Fanconi anemia tumor suppressors to RAD51-BRCA1/2.
Schlacher K; Wu H; Jasin M
Cancer Cell; 2012 Jul; 22(1):106-16. PubMed ID: 22789542
[TBL] [Abstract][Full Text] [Related]
34. Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia.
Wagner JE; Tolar J; Levran O; Scholl T; Deffenbaugh A; Satagopan J; Ben-Porat L; Mah K; Batish SD; Kutler DI; MacMillan ML; Hanenberg H; Auerbach AD
Blood; 2004 Apr; 103(8):3226-9. PubMed ID: 15070707
[TBL] [Abstract][Full Text] [Related]
35. Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia-like phenotype, and no chromosome fragility.
Keupp K; Hampp S; Hübbel A; Maringa M; Kostezka S; Rhiem K; Waha A; Wappenschmidt B; Pujol R; Surrallés J; Schmutzler RK; Wiesmüller L; Hahnen E
Mol Genet Genomic Med; 2019 Sep; 7(9):e863. PubMed ID: 31347298
[TBL] [Abstract][Full Text] [Related]
36. Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2.
Hussain S; Wilson JB; Blom E; Thompson LH; Sung P; Gordon SM; Kupfer GM; Joenje H; Mathew CG; Jones NJ
DNA Repair (Amst); 2006 May; 5(5):629-40. PubMed ID: 16621732
[TBL] [Abstract][Full Text] [Related]
37. Investigation of mutations in Fanconi anemia genes and malignancy predisposition in Brazilian patients.
Pillonetto DV; Piovezan BZ; Nichele S; Lima ACM; Pasquini R; Pereira NF; Bonfim C
Int J Lab Hematol; 2023 Feb; 45(1):82-89. PubMed ID: 36333938
[TBL] [Abstract][Full Text] [Related]
38. Functional interplay between BRCA2/FancD1 and FancC in DNA repair.
Kitao H; Yamamoto K; Matsushita N; Ohzeki M; Ishiai M; Takata M
J Biol Chem; 2006 Jul; 281(30):21312-21320. PubMed ID: 16687415
[TBL] [Abstract][Full Text] [Related]
39. Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.
Hirsch B; Shimamura A; Moreau L; Baldinger S; Hag-alshiekh M; Bostrom B; Sencer S; D'Andrea AD
Blood; 2004 Apr; 103(7):2554-9. PubMed ID: 14670928
[TBL] [Abstract][Full Text] [Related]
40. Cross-links between Fanconi anaemia and BRCA2.
West SC
DNA Repair (Amst); 2003 Feb; 2(2):231-4. PubMed ID: 12531392
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]