212 related articles for article (PubMed ID: 37031326)
21. From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia.
Krausz C; Riera-Escamilla A; Chianese C; Moreno-Mendoza D; Ars E; Rajmil O; Pujol R; Bogliolo M; Blanco I; Rodríguez I; Badell I; Ruiz-Castañé E; Surrallés J
Genet Med; 2019 Jan; 21(1):189-194. PubMed ID: 29904161
[TBL] [Abstract][Full Text] [Related]
22. Risk of cancer in heterozygous relatives of patients with Fanconi anemia.
McReynolds LJ; Giri N; Leathwood L; Risch MO; Carr AG; Alter BP
Genet Med; 2022 Jan; 24(1):245-250. PubMed ID: 34906449
[TBL] [Abstract][Full Text] [Related]
23. Fanconi anemia and breast cancer susceptibility meet again.
Levy-Lahad E
Nat Genet; 2010 May; 42(5):368-9. PubMed ID: 20428093
[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. Esophageal cancer as initial presentation of Fanconi anemia in patients with a hypomorphic
Lach FP; Singh S; Rickman KA; Ruiz PD; Noonan RJ; Hymes KB; DeLacure MD; Kennedy JA; Chandrasekharappa SC; Smogorzewska A
Cold Spring Harb Mol Case Stud; 2020 Dec; 6(6):. PubMed ID: 33172906
[TBL] [Abstract][Full Text] [Related]
26. Most Fanconi anemia heterozygotes are not at increased cancer risk: A genome-first DiscovEHR cohort population study.
Deng J; Altintas B; Haley JS; Kim J; Ramos M; Carey DJ; Stewart DR; McReynolds LJ
Genet Med; 2024 Mar; 26(3):101042. PubMed ID: 38063144
[TBL] [Abstract][Full Text] [Related]
27. Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility.
Ramanagoudr-Bhojappa R; Carrington B; Ramaswami M; Bishop K; Robbins GM; Jones M; Harper U; Frederickson SC; Kimble DC; Sood R; Chandrasekharappa SC
PLoS Genet; 2018 Dec; 14(12):e1007821. PubMed ID: 30540754
[TBL] [Abstract][Full Text] [Related]
28. 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. PubMed ID: 11530803
[TBL] [Abstract][Full Text] [Related]
29. Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex.
Noll M; Battaile KP; Bateman R; Lax TP; Rathbun K; Reifsteck C; Bagby G; Finegold M; Olson S; Grompe M
Exp Hematol; 2002 Jul; 30(7):679-88. PubMed ID: 12135664
[TBL] [Abstract][Full Text] [Related]
30. Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2).
McReynolds LJ; Biswas K; Giri N; Sharan SK; Alter BP
Cancer Genet; 2021 Nov; 258-259():101-109. PubMed ID: 34687993
[TBL] [Abstract][Full Text] [Related]
31. Molecular defects identified by whole exome sequencing in a child with Fanconi anemia.
Zheng Z; Geng J; Yao RE; Li C; Ying D; Shen Y; Ying L; Yu Y; Fu Q
Gene; 2013 Nov; 530(2):295-300. PubMed ID: 23973728
[TBL] [Abstract][Full Text] [Related]
32. Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.
Popp I; Punekar M; Telford N; Stivaros S; Chandler K; Minnis M; Castleton A; Higham C; Hopewell L; Gareth Evans D; Raams A; Theil AF; Meyer S; Schindler D
BMC Med Genet; 2018 Jan; 19(1):7. PubMed ID: 29325523
[TBL] [Abstract][Full Text] [Related]
33. Dysfunctional DNA repair pathway via defective FANCD2 gene engenders multifarious exomic and transcriptomic effects in Fanconi anemia.
Velmurugan KR; Michalak P; Kang L; Fonville NC; Garner HR
Mol Genet Genomic Med; 2018 Nov; 6(6):1199-1208. PubMed ID: 30450770
[TBL] [Abstract][Full Text] [Related]
34. Intermediate DNA repair activity associated with the 322delG allele of the fanconi anemia complementation group C gene.
Donahue SL; Lundberg R; Campbell C
J Mol Biol; 2004 Oct; 342(5):1443-55. PubMed ID: 15364573
[TBL] [Abstract][Full Text] [Related]
35. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Meindl A; Hellebrand H; Wiek C; Erven V; Wappenschmidt B; Niederacher D; Freund M; Lichtner P; Hartmann L; Schaal H; Ramser J; Honisch E; Kubisch C; Wichmann HE; Kast K; Deissler H; Engel C; Müller-Myhsok B; Neveling K; Kiechle M; Mathew CG; Schindler D; Schmutzler RK; Hanenberg H
Nat Genet; 2010 May; 42(5):410-4. PubMed ID: 20400964
[TBL] [Abstract][Full Text] [Related]
36. [The role of the Fanconi anemia pathway in DNA repair and maintenance of genome stability].
Koczorowska AM; Białkowska A; Kluzek K; Zdzienicka MZ
Postepy Hig Med Dosw (Online); 2014 May; 68():459-72. PubMed ID: 24864098
[TBL] [Abstract][Full Text] [Related]
37. Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset.
Domogala DD; Gambin T; Zemet R; Wu CW; Schulze KV; Yang Y; Wilson TA; Machol I; Liu P; Stankiewicz P
Hum Genomics; 2021 Dec; 15(1):72. PubMed ID: 34930489
[TBL] [Abstract][Full Text] [Related]
38. Emerging functions of Fanconi anemia genes in replication fork protection pathways.
Kolinjivadi AM; Crismani W; Ngeow J
Hum Mol Genet; 2020 Oct; 29(R2):R158-R164. PubMed ID: 32420592
[TBL] [Abstract][Full Text] [Related]
39. Identification of a robust DNA methylation signature for Fanconi anemia.
Pagliara D; Ciolfi A; Pedace L; Haghshenas S; Ferilli M; Levy MA; Miele E; Nardini C; Cappelletti C; Relator R; Pitisci A; De Vito R; Pizzi S; Kerkhof J; McConkey H; Nazio F; Kant SG; Di Donato M; Agolini E; Matraxia M; Pasini B; Pelle A; Galluccio T; Novelli A; Barakat TS; Andreani M; Rossi F; Mecucci C; Savoia A; Sadikovic B; Locatelli F; Tartaglia M
Am J Hum Genet; 2023 Nov; 110(11):1938-1949. PubMed ID: 37865086
[TBL] [Abstract][Full Text] [Related]
40. Foci on fanconi.
Hoatlin M; Reuter T
Trends Mol Med; 2001 Jun; 7(6):237-9. PubMed ID: 11378500
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]