-
1
-
-
33749023325
-
Fanconi anaemia genes and susceptibility to cancer
-
Mathew CG. Fanconi anaemia genes and susceptibility to cancer. Oncogene. 2006;25(43):5875–84.
-
(2006)
Oncogene
, vol.25
, Issue.43
, pp. 5875-5884
-
-
Mathew, C.G.1
-
2
-
-
23844444950
-
Skin disorders in ashkenazi jews: A review
-
Barankin B, Metelitsa AI, Schloss EH, Wasel NR. Skin disorders in Ashkenazi Jews: a review. Int J Dermatol. 2005;44(8):630–5.
-
(2005)
Int J Dermatol
, vol.44
, Issue.8
, pp. 630-635
-
-
Barankin, B.1
Metelitsa, A.I.2
Schloss, E.H.3
Wasel, N.R.4
-
3
-
-
14344284734
-
Molecular and genealogical evidence for a founder effect in fanconi anemia families of the Afrikaner population of South Africa
-
Tipping AJ, Pearson T, Morgan NV, Gibson RA, Kuyt LP, Havenga C, et al. Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa. Proc Natl Acad Sci U S A. 2001;98(10):5734–9.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, Issue.10
, pp. 5734-5739
-
-
Tipping, A.J.1
Pearson, T.2
Morgan, N.V.3
Gibson, R.A.4
Kuyt, L.P.5
Havenga, C.6
-
4
-
-
0028292273
-
The ashkenazi jewish fanconi anemia mutation: Incidence among patients and carrier frequency in the at-risk population
-
Whitney MA, Jakobs P, Kaback M, Moses RE, Grompe M. The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population. Hum Mutat. 1994;3(4):339–41.
-
(1994)
Hum Mutat
, vol.3
, Issue.4
, pp. 339-341
-
-
Whitney, M.A.1
Jakobs, P.2
Kaback, M.3
Moses, R.E.4
Grompe, M.5
-
5
-
-
84887566445
-
Fanconi anemia
-
2015 Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. Internet. Seattle (WA): University of Washington, Seattle. Access date February 7, 2013
-
Alter BP, and Kupfer G (1993–2015) Fanconi Anemia. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle. Available From http://www.ncbi.nlm.nih.gov/books/NBK1401/ Access date February 7, 2013.
-
(1993)
GeneReviews®
-
-
Alter, B.P.1
Kupfer, G.2
-
6
-
-
77956775152
-
The fanconi anemia pathway and ICL repair: Implications for cancer therapy
-
Wang LC, Gautier J. The Fanconi anemia pathway and ICL repair: implications for cancer therapy. Crit Rev Biochem Mol Biol. 2010;45(5):424–39.
-
(2010)
Crit Rev Biochem Mol Biol
, vol.45
, Issue.5
, pp. 424-439
-
-
Wang, L.C.1
Gautier, J.2
-
7
-
-
10944239213
-
X-linked inheritance of fanconi anemia complementation group b
-
Meetei AR, Levitus M, Xue Y, Medhurst AL, Zwaan M, Ling C, et al. X-linked inheritance of Fanconi anemia complementation group B. Nat Genet. 2004;36(11):1219–24.
-
(2004)
Nat Genet
, vol.36
, Issue.11
, pp. 1219-1224
-
-
Meetei, A.R.1
Levitus, M.2
Xue, Y.3
Medhurst, A.L.4
Zwaan, M.5
Ling, C.6
-
8
-
-
84876566569
-
Brief report: Human pluripotent stem cell models of fanconi anemia deficiency reveal an important role for fanconi anemia proteins in cellular reprogramming and survival of hematopoietic progenitors
-
Yung SK, Tilgner K, Ledran MH, Habibollah S, Neganova I, Singhapol C, et al. Brief report: human pluripotent stem cell models of Fanconi anemia deficiency reveal an important role for Fanconi anemia proteins in cellular reprogramming and survival of hematopoietic progenitors. Stem Cells. 2013;31(5):1022–9.
-
(2013)
Stem Cells
, vol.31
, Issue.5
, pp. 1022-1029
-
-
Yung, S.K.1
Tilgner, K.2
Ledran, M.H.3
Habibollah, S.4
Neganova, I.5
Singhapol, C.6
-
9
-
-
84923922333
-
Fanconi anemia and the development of leukemia
-
Alter BP. Fanconi anemia and the development of leukemia. Best Pract Res Clin Haematol. 2014;27(3–4):214–21.
-
(2014)
Best Pract Res Clin Haematol
, vol.27
, Issue.3-4
, pp. 214-221
-
-
Alter, B.P.1
-
10
-
-
33750315873
-
Guido fanconi (1892–1979): A jack of all trades
-
Lobitz S, Velleuer E. Guido Fanconi (1892–1979): a jack of all trades. Nat Rev Cancer. 2006;6(11):893–8.
-
(2006)
Nat Rev Cancer
, vol.6
, Issue.11
, pp. 893-898
-
-
Lobitz, S.1
Velleuer, E.2
-
11
-
-
84986563414
-
Global and disease-associated genetic variation in the human fanconi anemia gene family
-
Rogers KJ, Fu W, Akey JM, Monnat Jr RJ. Global and disease-associated genetic variation in the human Fanconi anemia gene family. Hum Mol Genet. 2014;23(25):6815–25.
-
(2014)
Hum Mol Genet
, vol.23
, Issue.25
, pp. 6815-6825
-
-
Rogers, K.J.1
Fu, W.2
Akey, J.M.3
Monnat, R.J.4
-
12
-
-
0026521238
-
Cloning of cDNAs for fanconi’s anaemia by functional complementation
-
Strathdee CA, Gavish H, Shannon WR, Buchwald M. Cloning of cDNAs for Fanconi’s anaemia by functional complementation. Nature. 1992;356(6372): 763–7.
-
(1992)
Nature
, vol.356
, Issue.6372
, pp. 763-767
-
-
Strathdee, C.A.1
Gavish, H.2
Shannon, W.R.3
Buchwald, M.4
-
13
-
-
1842337370
-
Expression cloning of a cDNA for the major fanconi anaemia gene, FAA
-
Lo Ten Foe JR, Rooimans MA, Bosnoyan-Collins L, Alon N, Wijker M, Parker L, et al. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA. Nat Genet. 1996;14(3):320–3.
-
(1996)
Nat Genet
, vol.14
, Issue.3
, pp. 320-323
-
-
Lo Ten Foe, J.R.1
Rooimans, M.A.2
Bosnoyan-Collins, L.3
Alon, N.4
Wijker, M.5
Parker, L.6
-
14
-
-
17344363009
-
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, et al. The Fanconi anaemia group G gene FANCG is identical with XRCC9. Nat Genet. 1998;20(3):281–3.
-
(1998)
Nat Genet
, vol.20
, Issue.3
, pp. 281-283
-
-
De Winter, J.P.1
Waisfisz, Q.2
Rooimans, M.A.3
Van Berkel, C.G.4
Bosnoyan-Collins, L.5
Alon, N.6
-
15
-
-
0033989248
-
The fanconi anaemia gene FANCF encodes a novel protein with homology to ROM
-
de Winter JP, Rooimans MA, van Der WL, van Berkel CG, Alon N, Bosnoyan-Collins L, et al. The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM. Nat Genet. 2000;24(1):15–6.
-
(2000)
Nat Genet
, vol.24
, Issue.1
, pp. 15-16
-
-
De Winter, J.P.1
Rooimans, M.A.2
Van Der, W.L.3
Van Berkel, C.G.4
Alon, N.5
Bosnoyan-Collins, L.6
-
16
-
-
0033759693
-
Isolation of a cDNA representing the fanconi anemia complementation group e gene
-
de Winter JP, Leveille F, van Berkel CG, Rooimans MA, van Der WL, Steltenpool J, et al. Isolation of a cDNA representing the Fanconi anemia complementation group E gene. Am J Hum Genet. 2000;67(5):1306–8.
-
(2000)
Am J Hum Genet
, vol.67
, Issue.5
, pp. 1306-1308
-
-
De Winter, J.P.1
Leveille, F.2
Van Berkel, C.G.3
Rooimans, M.A.4
Van Der, W.L.5
Steltenpool, J.6
-
17
-
-
84930389246
-
Fanconi anaemia: Genetics, molecular biology, and cancer––implications for clinical management in children and adults
-
Schneider M, Chandler K, Tischkowitz M, Meyer S. Fanconi anaemia: genetics, molecular biology, and cancer––implications for clinical management in children and adults. Clin Genet. 2014;88(1):13–24.
-
(2014)
Clin Genet
, vol.88
, Issue.1
, pp. 13-24
-
-
Schneider, M.1
Chandler, K.2
Tischkowitz, M.3
Meyer, S.4
-
18
-
-
84930673524
-
A case report and literature review of fanconi anemia (FA) diagnosed by genetic testing
-
Solomon PJ, Margaret P, Rajendran R, Ramalingam R, Menezes GA, Shirley AS, et al. A case report and literature review of Fanconi Anemia (FA) diagnosed by genetic testing. Ital J Pediatr. 2015;41:38.
-
(2015)
Ital J Pediatr
, vol.41
, pp. 38
-
-
Solomon, P.J.1
Margaret, P.2
Rajendran, R.3
Ramalingam, R.4
Menezes, G.A.5
Shirley, A.S.6
-
19
-
-
0035469852
-
The fanconi anemia complementation group c gene product: Structural evidence of multifunctionality
-
Pang Q, Christianson TA, Keeble W, Diaz J, Faulkner GR, Reifsteck C, et al. The Fanconi anemia complementation group C gene product: structural evidence of multifunctionality. Blood. 2001;98(5):1392–401.
-
(2001)
Blood
, vol.98
, Issue.5
, pp. 1392-1401
-
-
Pang, Q.1
Christianson, T.A.2
Keeble, W.3
Diaz, J.4
Faulkner, G.R.5
Reifsteck, C.6
-
20
-
-
8544271687
-
Fanconi anemia in ashkenazi jews
-
Kutler DI, Auerbach AD. Fanconi anemia in Ashkenazi Jews. Fam Cancer. 2004;3(3–4):241–8.
-
(2004)
Fam Cancer
, vol.3
, Issue.3-4
, pp. 241-248
-
-
Kutler, D.I.1
Auerbach, A.D.2
-
21
-
-
18844479804
-
Two common founder mutations of the fanconi anemia group g gene FANCG/ XRCC9 in the Japanese population
-
Yagasaki H, Oda T, Adachi D, Nakajima T, Nakahata T, Asano S, et al. Two common founder mutations of the Fanconi anemia group G gene FANCG/ XRCC9 in the Japanese population. Hum Mutat. 2003;21(5):555.
-
(2003)
Hum Mutat
, vol.21
, Issue.5
, pp. 555
-
-
Yagasaki, H.1
Oda, T.2
Adachi, D.3
Nakajima, T.4
Nakahata, T.5
Asano, S.6
-
22
-
-
84881616139
-
FANCA and FANCG are the major fanconi anemia genes in the Korean population
-
Park J, Chung NG, Chae H, Kim M, Lee S, Kim Y, et al. FANCA and FANCG are the major Fanconi anemia genes in the Korean population. Clin Genet. 2013;84(3):271–5.
-
(2013)
Clin Genet
, vol.84
, Issue.3
, pp. 271-275
-
-
Park, J.1
Chung, N.G.2
Chae, H.3
Kim, M.4
Lee, S.5
Kim, Y.6
-
23
-
-
72149119542
-
How the fanconi anemia pathway guards the genome
-
Moldovan GL, D’Andrea AD. How the Fanconi anemia pathway guards the genome. Annu Rev Genet. 2009;43:223–49.
-
(2009)
Annu Rev Genet
, vol.43
, pp. 223-249
-
-
Moldovan, G.L.1
D’Andrea, A.D.2
-
24
-
-
18444362122
-
Biallelic inactivation of BRCA2 in fanconi anemia
-
Howlett NG, Taniguchi T, Olson S, Cox B, Waisfisz Q, De Die-Smulders C, et al. Biallelic inactivation of BRCA2 in Fanconi anemia. Science. 2002;297(5581):606–9.
-
(2002)
Science
, vol.297
, Issue.5581
, pp. 606-609
-
-
Howlett, N.G.1
Taniguchi, T.2
Olson, S.3
Cox, B.4
Waisfisz, Q.5
De Die-Smulders, C.6
-
25
-
-
77952541315
-
Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2
-
Petrucelli N, Daly MB, Feldman GL. Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2. Genet Med. 2010;12(5):245–59.
-
(2010)
Genet Med
, vol.12
, Issue.5
, pp. 245-259
-
-
Petrucelli, N.1
Daly, M.B.2
Feldman, G.L.3
-
26
-
-
84870475682
-
Heterozygote FANCD2 mutations associated with childhood t cell ALL and testicular seminoma
-
Smetsers S, Muter J, Bristow C, Patel L, Chandler K, Bonney D, et al. Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma. Fam Cancer. 2012;11(4):661–5.
-
(2012)
Fam Cancer
, vol.11
, Issue.4
, pp. 661-665
-
-
Smetsers, S.1
Muter, J.2
Bristow, C.3
Patel, L.4
Chandler, K.5
Bonney, D.6
-
27
-
-
84917733605
-
Comprehensive analysis of pathogenic deletion variants in fanconi anemia genes
-
Flynn EK, Kamat A, Lach FP, Donovan FX, Kimble DC, Narisu N, et al. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes. Hum Mutat. 2014;35(11):1342–53.
-
(2014)
Hum Mutat
, vol.35
, Issue.11
, pp. 1342-1353
-
-
Flynn, E.K.1
Kamat, A.2
Lach, F.P.3
Donovan, F.X.4
Kimble, D.C.5
Narisu, N.6
-
28
-
-
0343312341
-
The fanconi anemia group e gene, FANCE, maps to chromosome 6p
-
Waisfisz Q, Saar K, Morgan NV, Altay C, Leegwater PA, de Winter JP, et al. The Fanconi anemia group E gene, FANCE, maps to chromosome 6p. Am J Hum Genet. 1999;64(5):1400–5.
-
(1999)
Am J Hum Genet
, vol.64
, Issue.5
, pp. 1400-1405
-
-
Waisfisz, Q.1
Saar, K.2
Morgan, N.V.3
Altay, C.4
Leegwater, P.A.5
De Winter, J.P.6
-
29
-
-
84873857548
-
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. Diagnosis of Fanconi anemia: mutation analysis by multiplex ligation-dependent probe amplification and PCR-based Sanger sequencing. Anemia. 2012;2012: 603253.
-
(2012)
Anemia
, vol.2012
, pp. 603253
-
-
Gille, J.J.1
Floor, K.2
Kerkhoven, L.3
Ameziane, N.4
Joenje, H.5
De Winter, J.P.6
-
30
-
-
34249281152
-
FANCI is a second monoubiquitinated member of the fanconi anemia pathway
-
Sims AE, Spiteri E, Sims III RJ, Arita AG, Lach FP, Landers T, et al. FANCI is a second monoubiquitinated member of the Fanconi anemia pathway. Nat Struct Mol Biol. 2007;14(6):564–7.
-
(2007)
Nat Struct Mol Biol
, vol.14
, Issue.6
, pp. 564-567
-
-
Sims, A.E.1
Spiteri, E.2
Sims, R.J.3
Arita, A.G.4
Lach, F.P.5
Landers, T.6
-
31
-
-
79951833152
-
Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair
-
Colnaghi L, Jones MJ, Cotto-Rios XM, Schindler D, Hanenberg H, Huang TT. Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair. Blood. 2011;117(7): 2247–56.
-
(2011)
Blood
, vol.117
, Issue.7
, pp. 2247-2256
-
-
Colnaghi, L.1
Jones, M.J.2
Cotto-Rios, X.M.3
Schindler, D.4
Hanenberg, H.5
Huang, T.T.6
-
32
-
-
77958512174
-
Fanconi anemia group j mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes
-
Wu Y, Sommers JA, Suhasini AN, Leonard T, Deakyne JS, Mazin AV, et al. Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes. Blood. 2010;116(19):3780–91.
-
(2010)
Blood
, vol.116
, Issue.19
, pp. 3780-3791
-
-
Wu, Y.1
Sommers, J.A.2
Suhasini, A.N.3
Leonard, T.4
Deakyne, J.S.5
Mazin, A.V.6
-
33
-
-
84898627366
-
Insight into the roles of helicase motif ia by characterizing fanconi anemia group j protein (FANCJ) patient mutations
-
Guo M, Vidhyasagar V, Ding H, Wu Y. Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutations. J Biol Chem. 2014;289(15):10551–65.
-
(2014)
J Biol Chem
, vol.289
, Issue.15
, pp. 10551-10565
-
-
Guo, M.1
Vidhyasagar, V.2
Ding, H.3
Wu, Y.4
-
34
-
-
84871404073
-
Diagnosis of fanconi anemia: Mutation analysis by next-generation sequencing
-
Ameziane N, Sie D, Dentro S, Ariyurek Y, Kerkhoven L, Joenje H, et al. Diagnosis of Fanconi anemia: mutation analysis by next-generation sequencing. Anemia. 2012;2012:132856.
-
(2012)
Anemia
, vol.2012
, pp. 132856
-
-
Ameziane, N.1
Sie, D.2
Dentro, S.3
Ariyurek, Y.4
Kerkhoven, L.5
Joenje, H.6
-
35
-
-
70849132066
-
Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known fanconi anemia genes, only FANCD1/ BRCA2 plays a major role in high-risk breast cancer predisposition
-
Garcia MJ, Fernandez V, Osorio A, Barroso A, Fernandez F, Urioste M, et al. Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi anemia genes, only FANCD1/ BRCA2 plays a major role in high-risk breast cancer predisposition. Carcinogenesis. 2009;30(11):1898–902.
-
(2009)
Carcinogenesis
, vol.30
, Issue.11
, pp. 1898-1902
-
-
Garcia, M.J.1
Fernandez, V.2
Osorio, A.3
Barroso, A.4
Fernandez, F.5
Urioste, M.6
-
36
-
-
33846569450
-
Biallelic mutations in PALB2 cause fanconi anemia subtype FA-N and predispose to childhood cancer
-
Reid S, Schindler D, Hanenberg H, Barker K, Hanks S, Kalb R, et al. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet. 2007;39(2):162–4.
-
(2007)
Nat Genet
, vol.39
, Issue.2
, pp. 162-164
-
-
Reid, S.1
Schindler, D.2
Hanenberg, H.3
Barker, K.4
Hanks, S.5
Kalb, R.6
-
37
-
-
84905460411
-
Distribution and medical impact of loss-of-function variants in the finnish founder population
-
Lim ET, Wurtz P, Havulinna AS, Palta P, Tukiainen T, Rehnstrom K, et al. Distribution and medical impact of loss-of-function variants in the Finnish founder population. PLoS Genet. 2014;10(7):e1004494.
-
(2014)
PLoS Genet
, vol.10
, Issue.7
, pp. e1004494
-
-
Lim, E.T.1
Wurtz, P.2
Havulinna, A.S.3
Palta, P.4
Tukiainen, T.5
Rehnstrom, K.6
-
38
-
-
77951720395
-
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, et al. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat Genet. 2010;42(5):410–4.
-
(2010)
Nat Genet
, vol.42
, Issue.5
, pp. 410-414
-
-
Meindl, A.1
Hellebrand, H.2
Wiek, C.3
Erven, V.4
Wappenschmidt, B.5
Niederacher, D.6
-
39
-
-
79251611165
-
Mutations of the SLX4 gene in fanconi anemia
-
Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A. Mutations of the SLX4 gene in Fanconi anemia. Nat Genet. 2011;43(2):142–6.
-
(2011)
Nat Genet
, vol.43
, Issue.2
, pp. 142-146
-
-
Kim, Y.1
Lach, F.P.2
Desetty, R.3
Hanenberg, H.4
Auerbach, A.D.5
Smogorzewska, A.6
-
40
-
-
84880916888
-
Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families
-
de Garibay GR, Diaz A, Gavina B, Romero A, Garre P, Vega A, et al. Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families. Eur J Hum Genet. 2013;21(8):883–6.
-
(2013)
Eur J Hum Genet
, vol.21
, Issue.8
, pp. 883-886
-
-
De Garibay, G.R.1
Diaz, A.2
Gavina, B.3
Romero, A.4
Garre, P.5
Vega, A.6
-
41
-
-
84877584276
-
Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause fanconi anemia
-
Bogliolo M, Schuster B, Stoepker C, Derkunt B, Su Y, Raams A, et al. Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia. Am J Hum Genet. 2013;92(5):800–6.
-
(2013)
Am J Hum Genet
, vol.92
, Issue.5
, pp. 800-806
-
-
Bogliolo, M.1
Schuster, B.2
Stoepker, C.3
Derkunt, B.4
Su, Y.5
Raams, A.6
-
42
-
-
84926505383
-
Biallelic mutations in BRCA1 cause a new fanconi anemia subtype
-
Sawyer SL, Tian L, Kahkonen M, Schwartzentruber J, Kircher M, Majewski J, et al. Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype. Cancer Discov. 2015;5(2):135–42.
-
(2015)
Cancer Discov
, vol.5
, Issue.2
, pp. 135-142
-
-
Sawyer, S.L.1
Tian, L.2
Kahkonen, M.3
Schwartzentruber, J.4
Kircher, M.5
Majewski, J.6
-
43
-
-
84865720442
-
Identifying and exploiting defects in the fanconi anemia/BRCA pathway in oncology
-
Stecklein SR, Jensen RA. Identifying and exploiting defects in the Fanconi anemia/BRCA pathway in oncology. Transl Res. 2012;160(3):178–97.
-
(2012)
Transl Res
, vol.160
, Issue.3
, pp. 178-197
-
-
Stecklein, S.R.1
Jensen, R.A.2
-
44
-
-
84876424557
-
Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancer
-
Domchek SM, Tang J, Stopfer J, Lilli DR, Hamel N, Tischkowitz M, et al. Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancer. Cancer Discov. 2013;3(4):399–405.
-
(2013)
Cancer Discov
, vol.3
, Issue.4
, pp. 399-405
-
-
Domchek, S.M.1
Tang, J.2
Stopfer, J.3
Lilli, D.R.4
Hamel, N.5
Tischkowitz, M.6
-
45
-
-
84870766296
-
Repair of strand breaks by homologous recombination
-
Jasin M, Rothstein R. Repair of strand breaks by homologous recombination. Cold Spring Harb Perspect Biol. 2013;5(11):a012740.
-
(2013)
Cold Spring Harb Perspect Biol
, vol.5
, Issue.11
, pp. a012740
-
-
Jasin, M.1
Rothstein, R.2
-
46
-
-
84938579589
-
A dominant mutation in human RAD51 reveals its function in DNA interstrand crosslink repair independent of homologous recombination
-
Wang AT, Kim T, Wagner JE, Conti BA, Lach FP, Huang AL, et al. A dominant mutation in human RAD51 reveals its function in DNA interstrand crosslink repair independent of homologous recombination. Mol Cell. 2015;59(3):478–90.
-
(2015)
Mol Cell
, vol.59
, Issue.3
, pp. 478-490
-
-
Wang, A.T.1
Kim, T.2
Wagner, J.E.3
Conti, B.A.4
Lach, F.P.5
Huang, A.L.6
-
47
-
-
33746957852
-
UBE2T is the E2 in the fanconi anemia pathway and undergoes negative autoregulation
-
Machida YJ, Machida Y, Chen Y, Gurtan AM, Kupfer GM, D’Andrea AD, et al. UBE2T is the E2 in the Fanconi anemia pathway and undergoes negative autoregulation. Mol Cell. 2006;23(4):589–96.
-
(2006)
Mol Cell
, vol.23
, Issue.4
, pp. 589-596
-
-
Machida, Y.J.1
Machida, Y.2
Chen, Y.3
Gurtan, A.M.4
Kupfer, G.M.5
D’Andrea, A.D.6
-
48
-
-
84938667462
-
Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause fanconi anemia
-
Hira A, Yoshida K, Sato K, Okuno Y, Shiraishi Y, Chiba K, et al. Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia. Am J Hum Genet. 2015;96(6):1001–7.
-
(2015)
Am J Hum Genet
, vol.96
, Issue.6
, pp. 1001-1007
-
-
Hira, A.1
Yoshida, K.2
Sato, K.3
Okuno, Y.4
Shiraishi, Y.5
Chiba, K.6
-
49
-
-
33645787286
-
The fanconi anemia gene network is conserved from zebrafish to human
-
Titus TA, Selvig DR, Qin B, Wilson C, Starks AM, Roe BA, et al. The Fanconi anemia gene network is conserved from zebrafish to human. Gene. 2006;371(2):211–23.
-
(2006)
Gene
, vol.371
, Issue.2
, pp. 211-223
-
-
Titus, T.A.1
Selvig, D.R.2
Qin, B.3
Wilson, C.4
Starks, A.M.5
Roe, B.A.6
-
50
-
-
33749989371
-
Drosophila homologs of FANCD2 and FANCL function in DNA repair
-
Marek LR, Bale AE. Drosophila homologs of FANCD2 and FANCL function in DNA repair. DNA Repair (Amst). 2006;5(11):1317–26.
-
(2006)
DNA Repair (Amst)
, vol.5
, Issue.11
, pp. 1317-1326
-
-
Marek, L.R.1
Bale, A.E.2
-
51
-
-
25144449181
-
A human ortholog of archaeal DNA repair protein hef is defective in fanconi anemia complementation group m
-
Meetei AR, Medhurst AL, Ling C, Xue Y, Singh TR, Bier P, et al. A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nat Genet. 2005;37(9):958–63.
-
(2005)
Nat Genet
, vol.37
, Issue.9
, pp. 958-963
-
-
Meetei, A.R.1
Medhurst, A.L.2
Ling, C.3
Xue, Y.4
Singh, T.R.5
Bier, P.6
-
52
-
-
0041378027
-
Sequence fingerprints in BRCA2 and RAD51: Implications for DNA repair and cancer
-
Lo T, Pellegrini L, Venkitaraman AR, Blundell TL. Sequence fingerprints in BRCA2 and RAD51: implications for DNA repair and cancer. DNA Repair (Amst). 2003;2(9):1015–28.
-
(2003)
DNA Repair (Amst)
, vol.2
, Issue.9
, pp. 1015-1028
-
-
Lo, T.1
Pellegrini, L.2
Venkitaraman, A.R.3
Blundell, T.L.4
-
53
-
-
33746189731
-
CeBRC-2 stimulates D-loop formation by RAD-51 and promotes DNA single-strand annealing
-
Petalcorin MI, Sandall J, Wigley DB, Boulton SJ. CeBRC-2 stimulates D-loop formation by RAD-51 and promotes DNA single-strand annealing. J Mol Biol. 2006;361(2):231–42.
-
(2006)
J Mol Biol
, vol.361
, Issue.2
, pp. 231-242
-
-
Petalcorin, M.I.1
Sandall, J.2
Wigley, D.B.3
Boulton, S.J.4
-
54
-
-
33750020933
-
C. Elegans FANCD2 responds to replication stress and functions in interstrand cross-link repair
-
Collis SJ, Barber LJ, Ward JD, Martin JS, Boulton SJ. C. elegans FANCD2 responds to replication stress and functions in interstrand cross-link repair. DNA Repair (Amst). 2006;5(11):1398–406.
-
(2006)
DNA Repair (Amst)
, vol.5
, Issue.11
, pp. 1398-1406
-
-
Collis, S.J.1
Barber, L.J.2
Ward, J.D.3
Martin, J.S.4
Boulton, S.J.5
-
55
-
-
40749095337
-
DOG-1 is the caenorhabditis elegans BRIP1/FANCJ homologue and functions in interstrand cross-link repair
-
Youds JL, Barber LJ, Ward JD, Collis SJ, O’Neil NJ, Boulton SJ, et al. DOG-1 is the Caenorhabditis elegans BRIP1/FANCJ homologue and functions in interstrand cross-link repair. Mol Cell Biol. 2008;28(5):1470–9.
-
(2008)
Mol Cell Biol
, vol.28
, Issue.5
, pp. 1470-1479
-
-
Youds, J.L.1
Barber, L.J.2
Ward, J.D.3
Collis, S.J.4
O’Neil, N.J.5
Boulton, S.J.6
-
56
-
-
84871196850
-
Fanconi-like crosslink repair in yeast
-
Daee DL, Myung K. Fanconi-like crosslink repair in yeast. Genome Integr. 2012;3(1):7.
-
(2012)
Genome Integr
, vol.3
, Issue.1
, pp. 7
-
-
Daee, D.L.1
Myung, K.2
-
57
-
-
84866156212
-
Components of a fanconi-like pathway control Pso2-independent DNA interstrand crosslink repair in yeast
-
Ward TA, Dudasova Z, Sarkar S, Bhide MR, Vlasakova D, Chovanec M, et al. Components of a Fanconi-like pathway control Pso2-independent DNA interstrand crosslink repair in yeast. PLoS Genet. 2012;8(8):e1002884.
-
(2012)
PLoS Genet
, vol.8
, Issue.8
, pp. e1002884
-
-
Ward, T.A.1
Dudasova, Z.2
Sarkar, S.3
Bhide, M.R.4
Vlasakova, D.5
Chovanec, M.6
-
58
-
-
84861675090
-
The fanconi anemia ortholog FANCM ensures ordered homologous recombination in both somatic and meiotic cells in arabidopsis
-
Knoll A, Higgins JD, Seeliger K, Reha SJ, Dangel NJ, Bauknecht M, et al. The Fanconi anemia ortholog FANCM ensures ordered homologous recombination in both somatic and meiotic cells in Arabidopsis. Plant Cell. 2012;24(4):1448–64.
-
(2012)
Plant Cell
, vol.24
, Issue.4
, pp. 1448-1464
-
-
Knoll, A.1
Higgins, J.D.2
Seeliger, K.3
Reha, S.J.4
Dangel, N.J.5
Bauknecht, M.6
-
59
-
-
70349667196
-
Xpf and not the fanconi anaemia proteins or Rev3 accounts for the extreme resistance to cisplatin in dictyostelium discoideum
-
Zhang XY, Langenick J, Traynor D, Babu MM, Kay RR, Patel KJ. Xpf and not the Fanconi anaemia proteins or Rev3 accounts for the extreme resistance to cisplatin in Dictyostelium discoideum. PLoS Genet. 2009;5(9):e1000645.
-
(2009)
PLoS Genet
, vol.5
, Issue.9
, pp. e1000645
-
-
Zhang, X.Y.1
Langenick, J.2
Traynor, D.3
Babu, M.M.4
Kay, R.R.5
Patel, K.J.6
-
60
-
-
0042519602
-
Epithelial cancer in fanconi anemia complementation group D2 (Fancd2) knockout mice
-
Houghtaling S, Timmers C, Noll M, Finegold MJ, Jones SN, Meyn MS, et al. Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice. Genes Dev. 2003;17(16):2021–35.
-
(2003)
Genes Dev
, vol.17
, Issue.16
, pp. 2021-2035
-
-
Houghtaling, S.1
Timmers, C.2
Noll, M.3
Finegold, M.J.4
Jones, S.N.5
Meyn, M.S.6
-
61
-
-
8944258558
-
Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the fanconi anemia c gene
-
Whitney MA, Royle G, Low MJ, Kelly MA, Axthelm MK, Reifsteck C, et al. Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene. Blood. 1996;88(1):49–58.
-
(1996)
Blood
, vol.88
, Issue.1
, pp. 49-58
-
-
Whitney, M.A.1
Royle, G.2
Low, M.J.3
Kelly, M.A.4
Axthelm, M.K.5
Reifsteck, C.6
-
63
-
-
0033852602
-
Mice with a targeted disruption of the fanconi anemia homolog fanca
-
Cheng NC, van de Vrugt HJ, van der Valk MA, Oostra AB, Krimpenfort P, de VY, et al. Mice with a targeted disruption of the Fanconi anemia homolog Fanca. Hum Mol Genet. 2000;9:1805–11.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1805-1811
-
-
Cheng, N.C.1
Van De Vrugt, H.J.2
Van Der Valk, M.A.3
Oostra, A.B.4
Krimpenfort, P.5
De, V.Y.6
-
64
-
-
0035760285
-
Targeted disruption of the murine fanconi anemia gene, fancg/Xrcc9
-
Yang Y, Kuang Y, De Montes OR, Hays T, Moreau L, Lu N, et al. Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9. Blood. 2001;98(12):3435–40.
-
(2001)
Blood
, vol.98
, Issue.12
, pp. 3435-3440
-
-
Yang, Y.1
Kuang, Y.2
De Montes, O.R.3
Hays, T.4
Moreau, L.5
Lu, N.6
-
65
-
-
0042921156
-
Targeted disruption of exons 1 to 6 of the fanconi anemia group a gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia
-
Wong JC, Alon N, Mckerlie C, Huang JR, Meyn MS, Buchwald M. Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia. Hum Mol Genet. 2003;12(16):2063–76.
-
(2003)
Hum Mol Genet
, vol.12
, Issue.16
, pp. 2063-2076
-
-
Wong, J.C.1
Alon, N.2
Mckerlie, C.3
Huang, J.R.4
Meyn, M.S.5
Buchwald, M.6
-
66
-
-
69449102249
-
Fancm-deficient mice reveal unique features of fanconi anemia complementation group m
-
Bakker ST, van de Vrugt HJ, Rooimans MA, Oostra AB, Steltenpool J, Delzenne-Goette E, et al. Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M. Hum Mol Genet. 2009;18(18): 3484–95.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.18
, pp. 3484-3495
-
-
Bakker, S.T.1
Van De Vrugt, H.J.2
Rooimans, M.A.3
Oostra, A.B.4
Steltenpool, J.5
Delzenne-Goette, E.6
-
67
-
-
79953801997
-
Loss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppression
-
Bouwman P, Drost R, Klijn C, Pieterse M, van der Gulden H, Song JY, et al. Loss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppression. J Pathol. 2011;224(1):10–21.
-
(2011)
J Pathol
, vol.224
, Issue.1
, pp. 10-21
-
-
Bouwman, P.1
Drost, R.2
Klijn, C.3
Pieterse, M.4
Van Der Gulden, H.5
Song, J.Y.6
-
68
-
-
82755194916
-
Fancf-deficient mice are prone to develop ovarian tumours
-
Bakker ST, van de Vrugt HJ, Visser JA, Delzenne-Goette E, van der Wal A, Berns MA, et al. Fancf-deficient mice are prone to develop ovarian tumours. J Pathol. 2012;226(1):28–39.
-
(2012)
J Pathol
, vol.226
, Issue.1
, pp. 28-39
-
-
Bakker, S.T.1
Van De Vrugt, H.J.2
Visser, J.A.3
Delzenne-Goette, E.4
Van Der Wal, A.5
Berns, M.A.6
-
69
-
-
0036786873
-
The fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC
-
Taniguchi T, D’Andrea AD. The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC. Blood. 2002;100(7):2457–62.
-
(2002)
Blood
, vol.100
, Issue.7
, pp. 2457-2462
-
-
Taniguchi, T.1
D’Andrea, A.D.2
-
70
-
-
84896786442
-
The carboxyl terminus of FANCE recruits FANCD2 to the fanconi anemia (FA) E3 ligase complex to promote the FA DNA repair pathway
-
Polito D, Cukras S, Wang X, Spence P, Moreau L, D’Andrea AD, et al. The carboxyl terminus of FANCE recruits FANCD2 to the Fanconi Anemia (FA) E3 ligase complex to promote the FA DNA repair pathway. J Biol Chem. 2014;289(10):7003–10.
-
(2014)
J Biol Chem
, vol.289
, Issue.10
, pp. 7003-7010
-
-
Polito, D.1
Cukras, S.2
Wang, X.3
Spence, P.4
Moreau, L.5
D’Andrea, A.D.6
-
71
-
-
33744958660
-
The WD40 repeats of FANCL are required for fanconi anemia core complex assembly
-
Gurtan AM, Stuckert P, D’Andrea AD. The WD40 repeats of FANCL are required for Fanconi anemia core complex assembly. J Biol Chem. 2006; 281(16):10896–905.
-
(2006)
J Biol Chem
, vol.281
, Issue.16
, pp. 10896-10905
-
-
Gurtan, A.M.1
Stuckert, P.2
D’Andrea, A.D.3
-
72
-
-
84870354208
-
Dysfunctional telomeres in primary cells from fanconi anemia FANCD2 patients
-
Joksic I, Vujic D, Guc-Scekic M, Leskovac A, Petrovic S, Ojani M, et al. Dysfunctional telomeres in primary cells from Fanconi anemia FANCD2 patients. Genome Integr. 2012;3(1):6.
-
(2012)
Genome Integr
, vol.3
, Issue.1
, pp. 6
-
-
Joksic, I.1
Vujic, D.2
Guc-Scekic, M.3
Leskovac, A.4
Petrovic, S.5
Ojani, M.6
-
73
-
-
84894412116
-
Why does the bone marrow fail in fanconi anemia?
-
Garaycoechea JI, Patel KJ. Why does the bone marrow fail in Fanconi anemia? Blood. 2014;123(1):26–34.
-
(2014)
Blood
, vol.123
, Issue.1
, pp. 26-34
-
-
Garaycoechea, J.I.1
Patel, K.J.2
-
74
-
-
84924352840
-
DNA damage response factors from diverse pathways, including DNA crosslink repair, mediate alternative end joining
-
Howard SM, Yanez DA, Stark JM. DNA damage response factors from diverse pathways, including DNA crosslink repair, mediate alternative end joining. PLoS Genet. 2015;11(1):e1004943.
-
(2015)
PLoS Genet
, vol.11
, Issue.1
, pp. e1004943
-
-
Howard, S.M.1
Yanez, D.A.2
Stark, J.M.3
-
75
-
-
0035510108
-
Fanconi anemia protein, FANCA, associates with BRG1, a component of the human SWI/SNF complex
-
Otsuki T, Furukawa Y, Ikeda K, Endo H, Yamashita T, Shinohara A, et al. Fanconi anemia protein, FANCA, associates with BRG1, a component of the human SWI/SNF complex. Hum Mol Genet. 2001;10(23):2651–60.
-
(2001)
Hum Mol Genet
, vol.10
, Issue.23
, pp. 2651-2660
-
-
Otsuki, T.1
Furukawa, Y.2
Ikeda, K.3
Endo, H.4
Yamashita, T.5
Shinohara, A.6
-
76
-
-
0037350437
-
Nonerythroid alpha II spectrin is required for recruitment of FANCA and XPF to nuclear foci induced by DNA interstrand cross-links
-
Sridharan D, Brown M, Lambert WC, McMahon LW, Lambert MW. Nonerythroid alpha II spectrin is required for recruitment of FANCA and XPF to nuclear foci induced by DNA interstrand cross-links. J Cell Sci. 2003;116(Pt 5):823–35.
-
(2003)
J Cell Sci
, vol.116
, pp. 823-835
-
-
Sridharan, D.1
Brown, M.2
Lambert, W.C.3
McMahon, L.W.4
Lambert, M.W.5
-
77
-
-
84883229635
-
Mitochondrial respiratory chain complex i defects in fanconi anemia complementation group a
-
Ravera S, Vaccaro D, Cuccarolo P, Columbaro M, Capanni C, Bartolucci M, et al. Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A. Biochimie. 2013;95(10):1828–37.
-
(2013)
Biochimie
, vol.95
, Issue.10
, pp. 1828-1837
-
-
Ravera, S.1
Vaccaro, D.2
Cuccarolo, P.3
Columbaro, M.4
Capanni, C.5
Bartolucci, M.6
-
78
-
-
84885124851
-
Fanconi anemia complementation group a (FANCA) localizes to centrosomes and functions in the maintenance of centrosome integrity
-
Kim S, Hwang SK, Lee M, Kwak H, Son K, Yang J, et al. Fanconi anemia complementation group A (FANCA) localizes to centrosomes and functions in the maintenance of centrosome integrity. Int J Biochem Cell Biol. 2013;45(9):1953–61.
-
(2013)
Int J Biochem Cell Biol
, vol.45
, Issue.9
, pp. 1953-1961
-
-
Kim, S.1
Hwang, S.K.2
Lee, M.3
Kwak, H.4
Son, K.5
Yang, J.6
-
79
-
-
12344282013
-
DNA interstrand crosslinks: Natural and drug-induced DNA adducts that induce unique cellular responses
-
Scharer OD. DNA interstrand crosslinks: natural and drug-induced DNA adducts that induce unique cellular responses. Chembiochem. 2005;6(1):27–32.
-
(2005)
Chembiochem
, vol.6
, Issue.1
, pp. 27-32
-
-
Scharer, O.D.1
-
80
-
-
79955096891
-
Coordinated action of the fanconi anemia and ataxia telangiectasia pathways in response to oxidative damage
-
Castillo P, Bogliolo M, Surralles J. Coordinated action of the Fanconi anemia and ataxia telangiectasia pathways in response to oxidative damage. DNA Repair (Amst). 2011;10(5):518–25.
-
(2011)
DNA Repair (Amst)
, vol.10
, Issue.5
, pp. 518-525
-
-
Castillo, P.1
Bogliolo, M.2
Surralles, J.3
-
81
-
-
0037123768
-
Convergence of theFanconi anemia and ataxia telangiectasia signaling pathways
-
Taniguchi T, Garcia-Higuera I, Xu B, Andreassen PR, Gregory RC, Kim ST, et al. Convergence of theFanconi anemia and ataxia telangiectasia signaling pathways. Cell. 2002;109(4):459–72.
-
(2002)
Cell
, vol.109
, Issue.4
, pp. 459-472
-
-
Taniguchi, T.1
Garcia-Higuera, I.2
Xu, B.3
Andreassen, P.R.4
Gregory, R.C.5
Kim, S.T.6
-
82
-
-
4544280871
-
Interaction of FANCD2 and NBS1 in the DNA damage response
-
Nakanishi K, Taniguchi T, Ranganathan V, New HV, Moreau LA, Stotsky M, et al. Interaction of FANCD2 and NBS1 in the DNA damage response. Nat Cell Biol. 2002;4(12):913–20.
-
(2002)
Nat Cell Biol
, vol.4
, Issue.12
, pp. 913-920
-
-
Nakanishi, K.1
Taniguchi, T.2
Ranganathan, V.3
New, H.V.4
Moreau, L.A.5
Stotsky, M.6
-
83
-
-
72149090671
-
FANCM connects the genome instability disorders bloom’s syndrome and fanconi anemia
-
Deans AJ, West SC. FANCM connects the genome instability disorders Bloom’s syndrome and Fanconi anemia. Mol Cell. 2009;36(6):943–53.
-
(2009)
Mol Cell
, vol.36
, Issue.6
, pp. 943-953
-
-
Deans, A.J.1
West, S.C.2
-
84
-
-
0037439356
-
Cancer in fanconi anemia, 1927–2001
-
Alter BP. Cancer in Fanconi anemia, 1927–2001. Cancer. 2003;97(2):425–40.
-
(2003)
Cancer
, vol.97
, Issue.2
, pp. 425-440
-
-
Alter, B.P.1
-
85
-
-
0030960336
-
Phenotypic consequences of mutations in the fanconi anemia FANCC gene: An international fanconi anemia registry study
-
Gillio AP, Verlander PC, Batish SD, Giampietro PF, Auerbach AD. Phenotypic consequences of mutations in the Fanconi anemia FANCC gene: an International Fanconi Anemia Registry study. Blood. 1997;90(1):105–10.
-
(1997)
Blood
, vol.90
, Issue.1
, pp. 105-110
-
-
Gillio, A.P.1
Verlander, P.C.2
Batish, S.D.3
Giampietro, P.F.4
Auerbach, A.D.5
-
86
-
-
0034651233
-
The IVS4 + 4 a to t mutation of the fanconi anemia gene FANCC is not associated with a severe phenotype in Japanese patients
-
Futaki M, Yamashita T, Yagasaki H, Toda T, Yabe M, Kato S, et al. The IVS4 + 4 A to T mutation of the Fanconi anemia gene FANCC is not associated with a severe phenotype in Japanese patients. Blood. 2000;95(4):1493–8.
-
(2000)
Blood
, vol.95
, Issue.4
, pp. 1493-1498
-
-
Futaki, M.1
Yamashita, T.2
Yagasaki, H.3
Toda, T.4
Yabe, M.5
Kato, S.6
-
87
-
-
11144353924
-
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, et al. Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia. Blood. 2004;103(8):3226–9.
-
(2004)
Blood
, vol.103
, Issue.8
, pp. 3226-3229
-
-
Wagner, J.E.1
Tolar, J.2
Levran, O.3
Scholl, T.4
Deffenbaugh, A.5
Satagopan, J.6
-
88
-
-
79955567163
-
Mutations in fanconi anemia genes and the risk of esophageal cancer
-
Akbari MR, Malekzadeh R, Lepage P, Roquis D, Sadjadi AR, Aghcheli K, et al. Mutations in Fanconi anemia genes and the risk of esophageal cancer. Hum Genet. 2011;129(5):573–82.
-
(2011)
Hum Genet
, vol.129
, Issue.5
, pp. 573-582
-
-
Akbari, M.R.1
Malekzadeh, R.2
Lepage, P.3
Roquis, D.4
Sadjadi, A.R.5
Aghcheli, K.6
-
89
-
-
12544255089
-
Germ line fanconi anemia complementation group c mutations and pancreatic cancer
-
Couch FJ, Johnson MR, Rabe K, Boardman L, McWilliams R, de AM, et al. Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Cancer Res. 2005;65(2):383–6.
-
(2005)
Cancer Res
, vol.65
, Issue.2
, pp. 383-386
-
-
Couch, F.J.1
Johnson, M.R.2
Rabe, K.3
Boardman, L.4
McWilliams, R.5
De, A.M.6
-
90
-
-
80054973810
-
Mutations in BRIP1 confer high risk of ovarian cancer
-
Rafnar T, Gudbjartsson DF, Sulem P, Jonasdottir A, Sigurdsson A, Jonasdottir A, et al. Mutations in BRIP1 confer high risk of ovarian cancer. Nat Genet. 2011;43(11):1104–7.
-
(2011)
Nat Genet
, vol.43
, Issue.11
, pp. 1104-1107
-
-
Rafnar, T.1
Gudbjartsson, D.F.2
Sulem, P.3
Jonasdottir, A.4
Sigurdsson, A.5
Jonasdottir, A.6
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