-
1
-
-
14544268189
-
DNA repair defects in stem cell function and aging
-
DOI 10.1146/annurev.med.56.082103.104546
-
Park Y, Gerson SL: DNA repair defects in stem cell function and aging. Annu Rev Med 2005;56:495-508. (Pubitemid 40299795)
-
(2005)
Annual Review of Medicine
, vol.56
, pp. 495-508
-
-
Park, Y.1
Gerson, S.L.2
-
2
-
-
24944546620
-
Genetic instability in cancer: Theory and experiment
-
DOI 10.1016/j.semcancer.2005.06.007, PII S1044579X05000428, Somatic Evolution of Cancer Cells
-
Beckman RA, Loeb LA: Genetic instability in cancer: theory and experiment. Semin Cancer Biol 2005;15:423-435. (Pubitemid 41318043)
-
(2005)
Seminars in Cancer Biology
, vol.15
, Issue.6
, pp. 423-435
-
-
Beckman, R.A.1
Loeb, L.A.2
-
3
-
-
13444250245
-
How Fanconi anemia proteins promote the four Rs: Replication, recombination, repair, and recovery
-
Thompson LH, Hinz JM, Yamada NA, Jones NJ: How Fanconi anemia proteins promote the four Rs: replication, recombination, repair, and recovery. Environ Mol Mutagen 2005;45:128-142.
-
(2005)
Environ Mol Mutagen
, vol.45
, pp. 128-142
-
-
Thompson, L.H.1
Hinz, J.M.2
Yamada, N.A.3
Jones, N.J.4
-
4
-
-
0037439356
-
Cancer in Fanconi anemia, 1927-2001
-
DOI 10.1002/cncr.11046
-
Alter BP: Cancer in Fanconi anemia, 1927-2001. Cancer 2003;97:425-440. (Pubitemid 36133810)
-
(2003)
Cancer
, vol.97
, Issue.2
, pp. 425-440
-
-
Alter, B.P.1
-
5
-
-
13944271408
-
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe fanconi anemia and biallelic FANCD1/BRCA2 mutations
-
DOI 10.1002/gcc.20153
-
Meyer S, Fergusson WD, Oostra AB, Medhurst AL, Waisfisz Q, et al: A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations. Genes Chromosomes Cancer 2005;42:404-415. (Pubitemid 40271283)
-
(2005)
Genes Chromosomes and Cancer
, vol.42
, Issue.4
, pp. 404-415
-
-
Meyer, S.1
Fergusson, W.D.2
Oostra, A.B.3
Medhurst, A.L.4
Waisfisz, Q.5
De Winter, J.P.6
Chen, F.7
Carr, T.F.8
Clayton-Smith, J.9
Clancy, T.10
Green, M.11
Barber, L.12
Eden, O.B.13
Will, A.M.14
Joenje, H.15
Taylor, G.M.16
-
6
-
-
13444274594
-
Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour
-
DOI 10.1136/jmg.2004.022673
-
Reid S, Renwick A, Seal S, Baskcomb L, Barfoot R, et al: Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour. J Med Genet 2005;42:147-151. (Pubitemid 40204369)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.2
, pp. 147-151
-
-
Reid, S.1
Renwick, A.2
Seal, S.3
Baskcomb, L.4
Barfoot, R.5
Jayatilake, H.6
Pritchard-Jones, K.7
Stratton, M.R.8
Ridolfi-Luthy, A.9
Rahman, N.10
-
7
-
-
0037441757
-
A 20-year perspective on the International Fanconi Anemia Registry (IFAR)
-
DOI 10.1182/blood-2002-07-2170
-
Kutler DI, Singh B, Satagopan J, Batish SD, Berwick M, et al: A 20-year perspective on the International Fanconi Anemia Registry (IFAR). Blood 2003;101:1249-1256. (Pubitemid 36182492)
-
(2003)
Blood
, vol.101
, Issue.4
, pp. 1249-1256
-
-
Kutler, D.I.1
Singh, B.2
Satagopan, J.3
Batish, S.D.4
Berwick, M.5
Giampietro, P.F.6
Hanenberg, H.7
Auerbach, A.D.8
-
8
-
-
0033995109
-
Fanconi anemia: Myelodysplasia as a predictor of outcome
-
DOI 10.1016/S0165-4608(99)00159-4, PII S0165460899001594
-
Alter BP, Caruso JP, Drachtman RA, Uchida T, Velagaleti GV, Elghetany MT: Fanconi anemia: myelodysplasia as a predictor of outcome. Cancer Genet Cytogenet 2000;117:125-131. (Pubitemid 30125811)
-
(2000)
Cancer Genetics and Cytogenetics
, vol.117
, Issue.2
, pp. 125-131
-
-
Alter, B.P.1
Caruso, J.P.2
Drachtman, R.A.3
Uchida, T.4
Velagaleti, G.V.N.5
Elghetany, M.T.6
-
9
-
-
0020083491
-
Acute myeloid leukemia as the first hematologic manifestation of fanconi anemia
-
DOI 10.1002/ajh.2830120312
-
Auerbach AD, Weiner MA, Warburton D, Yeboa K, Lu L, Broxmeyer HE: Acute myeloid leukemia as the first hematologic manifestation of Fanconi anemia. Am J Hematol 1982;12:289-300. (Pubitemid 12122270)
-
(1982)
American Journal of Hematology
, vol.12
, Issue.3
, pp. 289-300
-
-
Auerbach, A.D.1
Weiner, M.A.2
Warburton, D.3
-
10
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, et al: Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 1982;51:189-199. (Pubitemid 12073508)
-
(1982)
British Journal of Haematology
, vol.51
, Issue.2
, pp. 189-199
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
-
11
-
-
0028198465
-
Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints
-
DOI 10.1111/j.1601-5223.1994.00047.x
-
Fundia A, Gorla N, Larripa I: Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints. Hereditas 1994;120:47-50. (Pubitemid 24118576)
-
(1994)
Hereditas
, vol.120
, Issue.1
, pp. 47-50
-
-
Fundia, A.1
Gorla, N.2
Larripa, I.3
-
13
-
-
0036844159
-
Two different karyotypes with 1q abnormalities in a patient with Fanconi anemia
-
DOI 10.1016/S0145-2126(02)00038-3, PII S0145212602000383
-
Oliveira NI, Ribeiro EM, Raimondi SC, Bittencourt MA, Pasquini R, Cavalli IJ: Two different karyotypes with 1q abnormalities in a patient with Fanconi anemia. Leuk Res 2002;26:1047-1049. (Pubitemid 35287217)
-
(2002)
Leukemia Research
, vol.26
, Issue.11
, pp. 1047-1049
-
-
Oliveira, N.I.S.S.1
Ribeiro, E.M.S.F.2
Raimondi, S.C.3
Bittencourt, M.A.4
Pasquini, R.5
Cavalli, I.J.6
-
14
-
-
0038603848
-
Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: Gains of the chromosomal segment 3q26q29 as an adverse risk factor
-
DOI 10.1182/blood-2002-10-3243
-
Tonnies H, Huber S, Kuhl JS, Gerlach A, Ebell W, Neitzel H: Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor. Blood 2003;101:3872-3874. (Pubitemid 36857860)
-
(2003)
Blood
, vol.101
, Issue.10
, pp. 3872-3874
-
-
Tonnies, H.1
Huber, S.2
Kuhl, J.-S.3
Gerlach, A.4
Ebell, W.5
Neitzel, H.6
-
15
-
-
23044466578
-
Fanconi anemia: Adult head and neck cancer and hematopoietic mosaicism
-
DOI 10.1001/archotol.131.7.635
-
Alter BP, Joenje H, Oostra AB, Pals G: Fanconi anemia: adult head and neck cancer and hematopoietic mosaicism. Arch Otolaryngol Head Neck Surg 2005;131:635-639. (Pubitemid 41058056)
-
(2005)
Archives of Otolaryngology - Head and Neck Surgery
, vol.131
, Issue.7
, pp. 635-639
-
-
Alter, B.P.1
Joenje, H.2
Oostra, A.B.3
Pals, G.4
-
16
-
-
33645091213
-
Delayed diagnosis and complications of Fanconi anaemia at advanced age - A paradigm
-
Huck K, Hanenberg H, Gudowius S, Fenk R, Kalb R, et al: Delayed diagnosis and complications of Fanconi anaemia at advanced age - a paradigm. Br J Haematol 2006;133:188-197.
-
(2006)
Br J Haematol
, vol.133
, pp. 188-197
-
-
Huck, K.1
Hanenberg, H.2
Gudowius, S.3
Fenk, R.4
Kalb, R.5
-
17
-
-
0037228326
-
High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia
-
Kutler DI, Auerbach AD, Satagopan J, Giampietro PF, Batish SD, et al: High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia. Arch Otolaryngol Head Neck Surg 2003;129:106-112. (Pubitemid 36070885)
-
(2003)
Archives of Otolaryngology - Head and Neck Surgery
, vol.129
, Issue.1
, pp. 106-112
-
-
Kutler, D.I.1
Auerbach, A.D.2
Satagopan, J.3
Giampietro, P.F.4
Batish, S.D.5
Huvos, A.G.6
Goberdhan, A.7
Shah, J.P.8
Singh, B.9
-
18
-
-
2342595266
-
A causal role for human papillomavirus in head and neck cancer
-
Gillison ML, Lowy DR: A causal role for human papillomavirus in head and neck cancer. Lancet 2004;363:1488-1489.
-
(2004)
Lancet
, vol.363
, pp. 1488-1489
-
-
Gillison, M.L.1
Lowy, D.R.2
-
19
-
-
0345720836
-
Human papillomavirus DNA and p53 polymorphisms in squamous cell carcinomas from Fanconi anemia patients
-
Kutler DI, Wreesmann VB, Goberdhan A, Ben-Porat L, Satagopan J, et al: Human papillomavirus DNA and p53 polymorphisms in squamous cell carcinomas from Fanconi anemia patients. J Natl Cancer Inst 2003;95:1718-1721. (Pubitemid 37509080)
-
(2003)
Journal of the National Cancer Institute
, vol.95
, Issue.22
, pp. 1718-1721
-
-
Kutler, D.I.1
Wreesmann, V.B.2
Goberdhan, A.3
Ben-Porat, L.4
Satagopan, J.5
Ngai, I.6
Huvos, A.G.7
Giampietro, P.8
Levran, O.9
Pujara, K.10
Diotti, R.11
Carlson, D.12
Huryn, L.A.13
Auerbach, A.D.14
Singh, B.15
-
20
-
-
13944254363
-
Generation and molecular characterization of head and neck squamous cell lines of Fanconi anemia patients
-
DOI 10.1158/0008-5472.CAN-04-3665
-
Van Zeeburg HJ, Snijders PJ, Pals G, Hermsen MA, Rooimans MA, et al: Generation and molecular characterization of head and neck squamous cell lines of Fanconi anemia patients. Cancer Res 2005;65:1271-1276. (Pubitemid 40270153)
-
(2005)
Cancer Research
, vol.65
, Issue.4
, pp. 1271-1276
-
-
Van Zeeburg, H.J.T.1
Snijders, P.J.F.2
Pals, G.3
Hermsen, M.A.J.A.4
Rooimans, M.A.5
Bagby, G.6
Soulier, J.7
Gluckman, E.8
Wennerberg, J.9
Leemans, C.R.10
Joenje, H.11
Brakenhoff, R.H.12
-
21
-
-
0035761326
-
Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemia
-
Hermsen MA, Xie Y, Rooimans MA, Meijer GA, Baak JP, et al: Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemia. Fam Cancer 2001;1:39-43.
-
(2001)
Fam Cancer
, vol.1
, pp. 39-43
-
-
Hermsen, M.A.1
Xie, Y.2
Rooimans, M.A.3
Meijer, G.A.4
Baak, J.P.5
-
22
-
-
7244234131
-
Androgens and liver tumors: Fanconi's anemia and non-Fanconi's conditions
-
DOI 10.1002/ajh.20183
-
Velazquez I, Alter BP: Androgens and liver tumors: Fanconi's anemia and non-Fanconi's conditions. Am J Hematol 2004;77:257-267. (Pubitemid 39430704)
-
(2004)
American Journal of Hematology
, vol.77
, Issue.3
, pp. 257-267
-
-
Velazquez, I.1
Alter, B.P.2
-
23
-
-
12444257433
-
Fanconi anaemia proteins: Major roles in cell protection against oxidative damage
-
DOI 10.1002/bies.10283
-
Pagano G, Youssoufian H: Fanconi anaemia proteins: major roles in cell protection against oxidative damage. Bioessays 2003;25:589-595. (Pubitemid 36705510)
-
(2003)
BioEssays
, vol.25
, Issue.6
, pp. 589-595
-
-
Pagano, G.1
Youssoufian, H.2
Anak, S.S.3
Brunk, U.T.4
Calzone, R.5
Clarke, A.A.6
Degan, P.7
D'Ischia, M.8
Dunster, C.9
Giudice, A.10
Iaccarino, M.11
Hirsch-Kauffmann, M.12
Kelly, F.J.13
Lloret, A.14
Malorni, W.15
Manini, P.16
Masella, R.17
Nobili, B.18
Pallardo, F.V.19
Schweiger, M.20
Vuttariello, E.21
Youssoufian, G.22
Zatterale, A.23
more..
-
24
-
-
22444431937
-
Oxidative stress as a multiple effector in Fanconi anaemia clinical phenotype
-
DOI 10.1111/j.1600-0609.2005.00507.x
-
Pagano G, Degan P, D'Ischia M, Kelly FJ, Nobili B, et al: Oxidative stress as a multiple effector in Fanconi anaemia clinical phenotype. Eur J Haematol 2005;75:93-100. (Pubitemid 41008278)
-
(2005)
European Journal of Haematology
, vol.75
, Issue.2
, pp. 93-100
-
-
Pagano, G.1
Degan, P.2
D'Ischia, M.3
Kelly, F.J.4
Nobili, B.5
Pallardo, F.V.6
Youssoufian, H.7
Zatterale, A.8
-
25
-
-
0019444973
-
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia
-
DOI 10.1038/290142a0
-
Joenje H, Arwert F, Eriksson AW, De Koning H, Oostra AB: Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia. Nature 1981;290:142-143. (Pubitemid 11149688)
-
(1981)
Nature
, vol.290
, Issue.5802
, pp. 142-143
-
-
Joenje, H.1
Arwert, F.2
Eriksson, A.W.3
-
26
-
-
0023685747
-
Fanconi anemia mutation causes cellular susceptibility to ambient oxygen
-
Schindler D, Hoehn H: Fanconi anemia mutation causes cellular susceptibility to ambient oxygen. Am J Hum Genet 1988;43:429-435.
-
(1988)
Am J Hum Genet
, vol.43
, pp. 429-435
-
-
Schindler, D.1
Hoehn, H.2
-
27
-
-
33744481750
-
Molecular pathogenesis of Fanconi anemia: Recent progress
-
DOI 10.1182/blood-2005-10-4240
-
Taniguchi T, D'Andrea AD: The molecular pathogenesis of Fanconi anemia: recent progress. Blood 2006;107:4223-4233. (Pubitemid 43801344)
-
(2006)
Blood
, vol.107
, Issue.11
, pp. 4223-4233
-
-
Taniguchi, T.1
D'Andrea, A.D.2
-
28
-
-
30144439816
-
Disruption of the Fanconi anemia/BRCA pathway in sporadic cancer
-
DOI 10.1016/j.canlet.2005.07.038, PII S0304383505008256
-
Lyakhovich A, Surralles J: Disruption of the Fanconi anemia/BRCA pathway in sporadic cancer. Cancer Lett 2006;232:99-106. (Pubitemid 43053937)
-
(2006)
Cancer Letters
, vol.232
, Issue.1
, pp. 99-106
-
-
Lyakhovich, A.1
Surralles, J.2
-
29
-
-
0037968656
-
Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia
-
DOI 10.1182/blood-2002-09-2781
-
Lensch MW, Tischkowitz M, Christianson TA, Reifsteck CA, Speckhart SA, et al: Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia. Blood 2003;102:7-16. (Pubitemid 36759629)
-
(2003)
Blood
, vol.102
, Issue.1
, pp. 7-16
-
-
Lensch, M.W.1
Tischkowitz, M.2
Christianson, T.A.3
Reifsteck, C.A.4
Speckhart, S.A.5
Jakobs, P.M.6
O'Dwyer, M.E.7
Olson, S.B.8
Le Beau, M.M.9
Hodgson, S.V.10
Mathew, C.G.11
Larson, R.A.12
Bagby Jr., G.C.13
-
30
-
-
1542713417
-
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia
-
DOI 10.1038/sj.leu.2403280
-
Tischkowitz MD, Morgan NV, Grimwade D, Eddy C, Ball S, et al: Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia. Leukemia 2004;18:420-425. (Pubitemid 38425854)
-
(2004)
Leukemia
, vol.18
, Issue.3
, pp. 420-425
-
-
Tischkowitz, M.D.1
Morgan, N.V.2
Grimwade, D.3
Eddy, C.4
Ball, S.5
Vorechovsky, I.6
Langabeer, S.7
Stoger, R.8
Hodgson, S.V.9
Mathew, C.G.10
-
31
-
-
0033836935
-
A heterozygous frameshift mutation in the Fanconi Anemia C gene in familiary T-aLL and secondary malignancy
-
DOI 10.1055/s-2000-9673
-
Rischewski JR, Clausen H, Leber V, Niemeyer C, Ritter J, et al: A heterozygous frameshift mutation in the Fanconi anemia C gene in familial T-ALL and secondary malignancy. Klin Padiatr 2000;212:174-176. (Pubitemid 30654812)
-
(2000)
Klinische Padiatrie
, vol.212
, Issue.4
, pp. 174-176
-
-
Rischewski, J.R.1
Clausen, H.2
Leber, V.3
Niemeyer, C.4
Ritter, J.5
Schindler, D.6
Schneppenheim, R.7
-
32
-
-
0037393869
-
Constitutional sequence variation in the Fanconi anaemia group C (FANCC) gene in childhood acute myeloid leukaemia
-
DOI 10.1046/j.1365-2141.2003.04234.x
-
Barber LM, McGrath HE, Meyer S, Will AM, Birch JM, et al: Constitutional sequence variation in the Fanconi anaemia group C (FANCC) gene in childhood acute myeloid leukaemia. Br J Haematol 2003;121:57-62. (Pubitemid 36461268)
-
(2003)
British Journal of Haematology
, vol.121
, Issue.1
, pp. 57-62
-
-
Barber, L.M.1
McGrath, H.E.N.2
Meyer, S.3
Will, A.M.4
Birch, J.M.5
Eden, O.B.6
Taylor, G.M.7
-
33
-
-
27244442927
-
Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia [3]
-
DOI 10.1111/j.1365-2141.2005.05677.x
-
Barber LM, Barlow RA, Meyer S, White DJ, Will AM, et al: Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia. Br J Haematol 2005;130:796-797. (Pubitemid 43906656)
-
(2005)
British Journal of Haematology
, vol.130
, Issue.5
, pp. 796-797
-
-
Barber, L.M.1
Barlow, R.A.2
Meyer, S.3
White, D.J.4
Will, A.M.5
Eden, T.O.B.6
Taylor, G.M.7
-
34
-
-
33645453358
-
Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia
-
Meyer S, Barber LM, White DJ, Will AM, Birch JM, et al: Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia. Br J Haematol 2006;133:284-292.
-
(2006)
Br J Haematol
, vol.133
, pp. 284-292
-
-
Meyer, S.1
Barber, L.M.2
White, D.J.3
Will, A.M.4
Birch, J.M.5
-
35
-
-
0037505830
-
Fanconi anemia gene mutations in young-onset pancreatic cancer
-
Van der Heijden MS, Yeo CJ, Hruban RH, Kern SE: Fanconi anemia gene mutations in youngonset pancreatic cancer. Cancer Res 2003;63:2585-2588. (Pubitemid 36605199)
-
(2003)
Cancer Research
, vol.63
, Issue.10
, pp. 2585-2588
-
-
Van Der Heijden, M.S.1
Yeo, C.J.2
Hruban, R.H.3
Kern, S.E.4
-
36
-
-
12544255089
-
Germ line Fanconi anemia complementation group C mutations and pancreatic cancer
-
Couch FJ, Johnson MR, Rabe K, Boardman L, McWilliams R, et al: Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Cancer Res 2005;65:383-386.
-
(2005)
Cancer Res
, vol.65
, pp. 383-386
-
-
Couch, F.J.1
Johnson, M.R.2
Rabe, K.3
Boardman, L.4
McWilliams, R.5
-
37
-
-
3042581455
-
The genetics of FANCC and FANCG in familial pancreatic cancer
-
Rogers CD, Van der Heijden MS, Brune K, Yeo CJ, Hruban RH, et al: The genetics of FANCC and FANCG in familial pancreatic cancer. Cancer Biol Ther 2004;3:167-169. (Pubitemid 41350898)
-
(2004)
Cancer Biology and Therapy
, vol.3
, Issue.2
, pp. 167-169
-
-
Rogers, C.D.1
Van Der Heijden, M.S.2
Brune, K.3
Yeo, C.J.4
Hruban, R.H.5
Kern, S.E.6
Goggins, M.7
-
38
-
-
28744457912
-
Genetics of the FANCA gene in familial pancreatic cancer
-
Rogers CD, Couch FJ, Brune K, Martin ST, Philips J, et al: Genetics of the FANCA gene in familial pancreatic cancer. J Med Genet 2004;41:e126.
-
(2004)
J Med Genet
, vol.41
-
-
Rogers, C.D.1
Couch, F.J.2
Brune, K.3
Martin, S.T.4
Philips, J.5
-
39
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster R, Neuhausen SL, Mangion J, Quirk Y, Ford D, et al: Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 1994;265:2088-2090. (Pubitemid 24325690)
-
(1994)
Science
, vol.265
, Issue.5181
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Ormiston, W.21
McManus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
Stratton, M.R.31
more..
-
40
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
DOI 10.1038/378789a0
-
Wooster R, Bignell G, Lancaster J, Swift S, Seal S, et al: Identification of the breast cancer susceptibility gene BRCA2. Nature 1995;378:789-792. (Pubitemid 26004412)
-
(1995)
Nature
, vol.378
, Issue.6559
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Mangion, J.6
Collins, N.7
Gregory, S.8
Gumbs, C.9
Micklem, G.10
Barfoot, R.11
Hamoudl, R.12
Patel, S.13
Rice, C.14
Biggs, P.15
Hashim, Y.16
Smith, A.17
Connor, F.18
Arason, A.19
Gudmundsson, J.20
Ficenec, D.21
Kelsell, D.22
Ford, D.23
Tonin, P.24
Bishop, D.T.25
Spurr, N.K.26
Ponder, B.A.J.27
Eeles, R.28
Peto, J.29
Devilee, P.30
Cornelisse, C.31
Lynch, H.32
Narod, S.33
Lenoir, G.34
Egilsson, V.35
Barkadottir, R.B.36
Easton, D.F.37
Bentley, D.R.38
Futreal, P.A.39
Ashworth, A.40
Stratton, M.R.41
more..
-
41
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
DOI 10.1126/science.1073834
-
Howlett NG, Taniguchi T, Olson S, Cox B, Waisfisz Q, et al: Biallelic inactivation of BRCA2 in Fanconi anemia. Science 2002;297:606-609. (Pubitemid 34815345)
-
(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
Persky, N.7
Grompe, M.8
Joenje, H.9
Pals, G.10
Ikeda, H.11
Fox, E.A.12
D'Andrea, A.D.13
-
42
-
-
0142054687
-
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia
-
Offit K, Levran O, Mullaney B, Mah K, Nafa K, et al: Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia. J Natl Cancer Inst 2003;95:1548-1551. (Pubitemid 37322099)
-
(2003)
Journal of the National Cancer Institute
, vol.95
, Issue.20
, pp. 1548-1551
-
-
Offit, K.1
Levran, O.2
Mullaney, B.3
Mah, K.4
Nafa, K.5
Batish, S.D.6
Diotti, R.7
Scheider, H.8
Deffenbaugh, A.9
Scholl, T.10
Proud, V.K.11
Robson, M.12
Norton, L.13
Ellis, N.14
Hanenberg, H.15
Auerbach, A.D.16
-
43
-
-
11144353924
-
Germline mutations in BRCA2: Shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia
-
DOI 10.1182/blood-2003-09-3138
-
Wagner JE, Tolar J, Levran O, Scholl T, Deffenbaugh A, et al: Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia. Blood 2004;103:3226-3229. (Pubitemid 38451703)
-
(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
Ben-Porat, L.7
Mah, K.8
Batish, S.D.9
Kutler, D.I.10
MacMillan, M.L.11
Hanenberg, H.12
Auerbach, A.D.13
-
45
-
-
9044225148
-
BRCA2 mutations in primary breast and ovarian cancers
-
DOI 10.1038/ng0696-238
-
Lancaster JM, Wooster R, Mangion J, Phelan CM, Cochran C, et al: BRCA2 mutations in primary breast and ovarian cancers. Nat Genet 1996;13:238-240. (Pubitemid 26000445)
-
(1996)
Nature Genetics
, vol.13
, Issue.2
, pp. 238-240
-
-
Lancaster, J.M.1
Wooster, R.2
Mangion, J.3
Phelan, C.M.4
Cochran, C.5
Gumbs, C.6
Seal, S.7
Barfoot, R.8
Collins, N.9
Bignell, G.10
Patel, S.11
Hamoudi, R.12
Larsson, C.13
Wiseman, R.W.14
Berchuck, A.15
Iglehart, J.D.16
Marks, J.R.17
Ashworth, A.18
Stratton, M.R.19
Futreal, P.A.20
more..
-
46
-
-
0030058209
-
Mutation analysis in the BRCA2 gene in primary breast cancers
-
DOI 10.1038/ng0696-245
-
Miki Y, Katagiri T, Kasumi F, Yoshimoto T, Nakamura Y: Mutation analysis in the BRCA2 gene in primary breast cancers. Nat Genet 1996;13:245-247. (Pubitemid 26000446)
-
(1996)
Nature Genetics
, vol.13
, Issue.2
, pp. 245-247
-
-
Miki, Y.1
Katagiri, T.2
Kasumi, F.3
Yoshimoto, T.4
Nakamura, Y.5
-
47
-
-
9344251625
-
Low incidence of BRCA2 mutations in breast carcinoma and other cancers
-
DOI 10.1038/ng0696-241
-
Teng DH, Bogden R, Mitchell J, Baumgard M, Bell R, et al: Low incidence of BRCA2 mutations in breast carcinoma and other cancers. Nat Genet 1996;13:241-244. (Pubitemid 26166161)
-
(1996)
Nature Genetics
, vol.13
, Issue.2
, pp. 241-244
-
-
Teng, D.H.-F.1
Bogden, R.2
Mitchell, J.3
Baumgard, M.4
Bell, R.5
Berry, S.6
Davis, T.7
Ha, P.C.8
Kehrer, R.9
Jammulapati, S.10
Chen, Q.11
Offit, K.12
Skolnick, M.H.13
Tavtigian, S.V.14
Jhanwar, S.15
Swedlund, B.16
Wong, A.K.C.17
Kamb, A.18
-
48
-
-
0029820321
-
A somatic truncating mutation in BRCA2 in a sporadic breast tumor [2]
-
Weber BH, Brohm M, Stec I, Backe J, Caffier H: A somatic truncating mutation in BRCA2 in a sporadic breast tumor. Am J Hum Genet 1996;59:962-964. (Pubitemid 26328096)
-
(1996)
American Journal of Human Genetics
, vol.59
, Issue.4
, pp. 962-964
-
-
Weber, B.H.F.1
Brohm, M.2
Stec, I.3
Backe, J.4
Caffier, H.5
-
49
-
-
0037140117
-
Somatic mutations in the BRCA2 gene and high frequency of allelic loss of BRCA2 in sporadic male breast cancer
-
DOI 10.1002/ijc.10289
-
Kwiatkowska E, Teresiak M, Breborowicz D, Mackiewicz A: Somatic mutations in the BRCA2 gene and high frequency of allelic loss of BRCA2 in sporadic male breast cancer. Int J Cancer 2002;98:943-945. (Pubitemid 34286695)
-
(2002)
International Journal of Cancer
, vol.98
, Issue.6
, pp. 943-945
-
-
Kwiatkowska, E.1
Teresiak, M.2
Breborowicz, D.3
Mackiewicz, A.4
-
50
-
-
0037130885
-
Inactivation of BRCA1 and BRCA2 in ovarian cancer
-
Hilton JL, Geisler JP, Rathe JA, Hattermann-Zogg MA, De Young B, Buller RE: Inactivation of BRCA1 and BRCA2 in ovarian cancer. J Natl Cancer Inst 2002;94:1396-1406. (Pubitemid 35154144)
-
(2002)
Journal of the National Cancer Institute
, vol.94
, Issue.18
, pp. 1396-1406
-
-
Hilton, J.L.1
Geisler, J.P.2
Rathe, J.A.3
Hattermann-Zogg, M.A.4
Deyoung, B.5
Buller, R.E.6
-
51
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
DOI 10.1038/ng1624, PII NG1624
-
Levran O, Attwooll C, Henry RT, Milton KL, Neveling K, et al: The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nat Genet 2005;37:931-933. (Pubitemid 43086147)
-
(2005)
Nature Genetics
, vol.37
, Issue.9
, pp. 931-933
-
-
Levran, O.1
Attwooll, C.2
Henry, R.T.3
Milton, K.L.4
Neveling, K.5
Rio, P.6
Batish, S.D.7
Kalb, R.8
Velleuer, E.9
Barral, S.10
Ott, J.11
Petrini, J.12
Schindler, D.13
Hanenberg, H.14
Auerbach, A.D.15
-
52
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
-
DOI 10.1038/ng1625, PII NG1625
-
Levitus M, Waisfisz Q, Godthelp BC, De Vries Y, Hussain S, et al: The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nat Genet 2005;37:934-935. (Pubitemid 43086148)
-
(2005)
Nature Genetics
, vol.37
, Issue.9
, pp. 934-935
-
-
Levitus, M.1
Waisfisz, Q.2
Godthelp, B.C.3
De Vries, Y.4
Hussain, S.5
Wiegant, W.W.6
Elghalbzouri-Maghrani, E.7
Steltenpool, J.8
Rooimans, M.A.9
Pals, G.10
Arwert, F.11
Mathew, C.G.12
Zdzienicka, M.Z.13
Hiom, K.14
De Winter, J.P.15
Joenje, H.16
-
53
-
-
20644461718
-
BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function
-
DOI 10.1016/S0092-8674(01)00304-X
-
Cantor SB, Bell DW, Ganesan S, Kass EM, Drapkin R, et al: BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell 2001;105:149-160. (Pubitemid 32323924)
-
(2001)
Cell
, vol.105
, Issue.1
, pp. 149-160
-
-
Cantor, S.B.1
Bell, D.W.2
Ganesan, S.3
Kass, E.M.4
Drapkin, R.5
Grossman, S.6
Wahrer, D.C.R.7
Sgroi, D.C.8
Lane, W.S.9
Haber, D.A.10
Livingston, D.M.11
-
54
-
-
3042829470
-
Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes
-
Sigurdson AJ, Hauptmann M, Chatterjee N, Alexander BH, Doody MM, et al: Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes. BMC Cancer 2004;4:9.
-
(2004)
BMC Cancer
, vol.4
, pp. 9
-
-
Sigurdson, A.J.1
Hauptmann, M.2
Chatterjee, N.3
Alexander, B.H.4
Doody, M.M.5
-
55
-
-
0036533574
-
No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22 [1]
-
DOI 10.1002/ijc.10214
-
Luo L, Lei H, Du Q, Von Wachenfeldt A, Kockum I, et al: No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22. Int J Cancer 2002;98:638-639. (Pubitemid 34208569)
-
(2002)
International Journal of Cancer
, vol.98
, Issue.4
, pp. 638-639
-
-
Luo, L.1
Lei, H.2
Du, Q.3
Von Wachenfeldt, A.4
Kockum, I.5
Luthman, H.6
Vorechovsky, I.7
Lindblom, A.8
-
56
-
-
34447619477
-
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
-
Lewis AG, Flanagan J, Marsh A, Pupo GM, Mann G, et al: Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer. Breast Cancer Res 2005;7:R1005-R1016.
-
(2005)
Breast Cancer Res
, vol.7
-
-
Lewis, A.G.1
Flanagan, J.2
Marsh, A.3
Pupo, G.M.4
Mann, G.5
-
57
-
-
33144489382
-
BACH1 Ser919Pro variant and breast cancer risk
-
Vahteristo P, Yliannala K, Tamminen A, Eerola H, Blomqvist C, Nevanlinna H: BACH1 Ser919Pro variant and breast cancer risk. BMC Cancer 2006;6:19.
-
(2006)
BMC Cancer
, vol.6
, pp. 19
-
-
Vahteristo, P.1
Yliannala, K.2
Tamminen, A.3
Eerola, H.4
Blomqvist, C.5
Nevanlinna, H.6
-
58
-
-
9144268932
-
Evaluation of Fanconi Anemia Genes in Familial Breast Cancer Predisposition
-
Seal S, Barfoot R, Jayatilake H, Smith P, Renwick A, et al: Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Cancer Res 2003;63:8596-8599. (Pubitemid 38064032)
-
(2003)
Cancer Research
, vol.63
, Issue.24
, pp. 8596-8599
-
-
Seal, S.1
Barfoot, R.2
Jayatilake, H.3
Smith, P.4
Renwick, A.5
Bascombe, L.6
McGuffog, L.7
Evans, D.G.8
Eccles, D.9
Easton, D.F.10
Stratton, M.R.11
Rahman, N.12
-
59
-
-
26844460665
-
A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer
-
Thompson E, Dragovic RL, Stephenson SA, Eccles DM, Campbell IG, Dobrovic A: A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer. BMC Cancer 2005;5:43.
-
(2005)
BMC Cancer
, vol.5
, pp. 43
-
-
Thompson, E.1
Dragovic, R.L.2
Stephenson, S.A.3
Eccles, D.M.4
Campbell, I.G.5
Dobrovic, A.6
-
60
-
-
33748172915
-
FANCD2 associated with sporadic breast cancer risk
-
DOI 10.1093/carcin/bgl062
-
Barroso E, Milne RL, Fernandez LP, Zamora P, Arias JI, et al: FANCD2 associated with sporadic breast cancer risk. Carcinogenesis 2006;27:1930-1937. (Pubitemid 44307832)
-
(2006)
Carcinogenesis
, vol.27
, Issue.9
, pp. 1930-1937
-
-
Barroso, E.1
Milne, R.L.2
Fernandez, L.P.3
Zamora, P.4
Arias, J.I.5
Benitez, J.6
Ribas, G.7
-
61
-
-
0036554733
-
Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma
-
Hu N, Li G, Li WJ, Wang C, Goldstein AM, et al: Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma. Clin Cancer Res 2002;8:1121-1126. (Pubitemid 35177365)
-
(2002)
Clinical Cancer Research
, vol.8
, Issue.4
, pp. 1121-1126
-
-
Hu, N.1
Li, G.2
Li, W.-J.3
Wang, C.4
Goldstein, A.M.5
Tang, Z.-Z.6
Roth, M.J.7
Dawsey, S.M.8
Huang, J.9
Wang, Q.-H.10
Ding, T.11
Giffen, C.12
Taylor, P.R.13
Emmert-Buck, M.R.14
-
62
-
-
33745225604
-
Genome-wide profiling of oral squamous cell carcinoma by array-based comparative genomic hybridization
-
DOI 10.1097/01.mlg.0000205141.54471.7f, PII 0000553720060500000010
-
Sparano A, Quesnelle KM, Kumar MS, Wang Y, Sylvester AJ, et al: Genome-wide profiling of oral squamous cell carcinoma by array-based comparative genomic hybridization. Laryngoscope 2006;116:735-741. (Pubitemid 44318029)
-
(2006)
Laryngoscope
, vol.116
, Issue.5
, pp. 735-741
-
-
Sparano, A.1
Quesnelle, K.M.2
Kumar, M.S.3
Wang, Y.4
Sylvester, A.J.5
Feldman, M.6
Sewell, D.A.7
Weinstein, G.S.8
Brose, M.S.9
-
63
-
-
0033989248
-
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM
-
DOI 10.1038/71626
-
De Winter JP, Rooimans MA, Van der Weel L, Van Berkel CG, Alon N, et al: The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM. Nat Genet 2000;24:15-16. (Pubitemid 30041412)
-
(2000)
Nature Genetics
, vol.24
, Issue.1
, pp. 15-16
-
-
De Winter, J.P.1
Rooimans, M.A.2
Van Der Weel, L.3
Van Berkel, C.G.M.4
Alon, N.5
Bosnoyan-Collins, L.6
De Groot, J.7
Zhi, Y.8
Waisfisz, Q.9
Pronk, J.C.10
Arwert, F.11
Mathew, C.G.12
Scheper, R.J.13
Hoatlin, M.E.14
Buchwald, M.15
Joenje, H.16
-
64
-
-
4544355937
-
The Fanconi anemia gene product FANCF is a flexible adaptor protein
-
DOI 10.1074/jbc.M407034200
-
Leveille F, Blom E, Medhurst AL, Bier P, Laghmani El H, et al: The Fanconi anemia gene product FANCF is a flexible adaptor protein. J Biol Chem 2004;279:39421-39430. (Pubitemid 39258207)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.38
, pp. 39421-39430
-
-
Leveille, F.1
Blom, E.2
Medhurst, A.L.3
Bier, P.4
Laghmani, E.H.5
Johnson, M.6
Rooimans, M.A.7
Sobeck, A.8
Waisfisz, Q.9
Arwert, F.10
Patel, K.J.11
Hoatlin, M.E.12
Joenje, H.13
De Winter, J.P.14
-
65
-
-
0038075462
-
Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors
-
DOI 10.1038/nm852
-
Taniguchi T, Tischkowitz M, Ameziane N, Hodgson SV, Mathew CG, et al: Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors. Nat Med 2003;9:568-574. (Pubitemid 36597103)
-
(2003)
Nature Medicine
, vol.9
, Issue.5
, pp. 568-574
-
-
Taniguchi, T.1
Tischkowitz, M.2
Ameziane, N.3
Hodgson, S.V.4
Mathew, C.G.5
Joenje, H.6
Mok, S.C.7
D'Andrea, A.D.8
-
66
-
-
33745056414
-
Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer
-
DOI 10.1073/pnas.0600645103
-
Agrelo R, Cheng WH, Setien F, Ropero S, Espada J, et al: Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer. Proc Natl Acad Sci USA 2006;103:8822-8827. (Pubitemid 43878103)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.23
, pp. 8822-8827
-
-
Agrelo, R.1
Cheng, W.-H.2
Setien, F.3
Ropero, S.4
Espada, J.5
Fraga, M.F.6
Herranz, M.7
Paz, M.F.8
Sanchez-Cespedes, M.9
Artiga, M.J.10
Guerrero, D.11
Castells, A.12
Von Kobbe, C.13
Bohr, V.A.14
Esteller, M.15
-
67
-
-
0013568733
-
The short arm of chromosome 11 is a 'hot spot' for hypermethylation in human neoplasia
-
De Bustros A, Nelkin BD, Silverman A, Ehrlich G, Poiesz B, Baylin SB: The short arm of chromosome 11 is a 'hot spot' for hypermethylation in human neoplasia. Proc Natl Acad Sci USA 1988;85:5693-5697.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 5693-5697
-
-
De Bustros, A.1
Nelkin, B.D.2
Silverman, A.3
Ehrlich, G.4
Poiesz, B.5
Baylin, S.B.6
-
68
-
-
14044278146
-
Multiple mechanisms downregulate CDKN1C in human bladder cancer
-
DOI 10.1002/ijc.20749
-
Hoffmann MJ, Florl AR, Seifert HH, Schulz WA: Multiple mechanisms downregulate CDKN1C in human bladder cancer. Int J Cancer 2005;114:406-413. (Pubitemid 40279961)
-
(2005)
International Journal of Cancer
, vol.114
, Issue.3
, pp. 406-413
-
-
Hoffmann, M.J.1
Florl, A.R.2
Seifert, H.-H.3
Schulz, W.A.4
-
69
-
-
3242658933
-
Fanconi anaemia and leukaemia - Clinical and molecular aspects
-
DOI 10.1111/j.1365-2141.2004.05023.x
-
Tischkowitz M, Dokal I: Fanconi anaemia and leukaemia - clinical and molecular aspects. Br J Haematol 2004;126:176-191. (Pubitemid 38961936)
-
(2004)
British Journal of Haematology
, vol.126
, Issue.2
, pp. 176-191
-
-
Tischkowitz, M.1
Dokal, I.2
-
70
-
-
33644601309
-
Does tumorigenesis select for or against mutations of the DNA repair-associated genes BRCA2 and MRE11?: Considerations from somatic mutations in microsatellite unstable (MSI) gastrointestinal cancers
-
Van der Heijden MS, Brody JR, Elghalbzouri-Maghrani E, Zdzienicka MZ, Kern SE: Does tumorigenesis select for or against mutations of the DNA repair-associated genes BRCA2 and MRE11?: considerations from somatic mutations in microsatellite unstable (MSI) gastrointestinal cancers. BMC Genet 2006;7:3.
-
(2006)
BMC Genet
, vol.7
, pp. 3
-
-
Van Der Heijden, M.S.1
Brody, J.R.2
Elghalbzouri-Maghrani, E.3
Zdzienicka, M.Z.4
Kern, S.E.5
-
71
-
-
0242298162
-
Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia
-
DOI 10.1046/j.1365-2141.2003.04640.x
-
Tischkowitz M, Ameziane N, Waisfisz Q, De Winter JP, Harris R, et al: Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia. Br J Haematol 2003;123:469-471. (Pubitemid 37363488)
-
(2003)
British Journal of Haematology
, vol.123
, Issue.3
, pp. 469-471
-
-
Tischkowitz, M.1
Ameziane, N.2
Waisfisz, Q.3
De Winter, J.P.4
Harris, R.5
Taniguchi, T.6
D'Andrea, A.7
Hodgson, S.V.8
Mathew, C.G.9
Joenje, H.10
-
72
-
-
21644441072
-
Functional screen of the fanconi anemia pathway in cancer cells by Fancd2 immunoblot
-
Van der Heijden MS, Brody JR, Kern SE: Functional screen of the Fanconi anemia pathway in cancer cells by Fancd2 immunoblot. Cancer Biol Ther 2004;3:534-537. (Pubitemid 41351123)
-
(2004)
Cancer Biology and Therapy
, vol.3
, Issue.6
, pp. 534-537
-
-
Van Der Heijden, M.S.1
Brody, J.R.2
Kern, S.E.3
-
73
-
-
33744791826
-
No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia
-
DOI 10.1111/j.1365-2141.2006.06107.x
-
Meyer S, White DJ, Will AM, Eden T, Sim A, et al: No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia. Br J Haematol 2006;134:61-63. (Pubitemid 43830029)
-
(2006)
British Journal of Haematology
, vol.134
, Issue.1
, pp. 61-63
-
-
Meyer, S.1
White, D.J.2
Will, A.M.3
Eden, T.4
Sim, A.5
Brown, R.6
Strathdee, G.7
-
74
-
-
1342301467
-
Inactivation of the Fanconi anemia/BRCA pathway in lung and oral cancers: Implications for treatment and survival
-
DOI 10.1038/sj.onc.1207256
-
Marsit CJ, Liu M, Nelson HH, Posner M, Suzuki M, Kelsey KT: Inactivation of the Fanconi anemia/BRCA pathway in lung and oral cancers: implications for treatment and survival. Oncogene 2004;23:1000-1004. (Pubitemid 38250946)
-
(2004)
Oncogene
, vol.23
, Issue.4
, pp. 1000-1004
-
-
Marsit, C.J.1
Liu, M.2
Nelson, H.H.3
Posner, M.4
Suzuki, M.5
Kelsey, K.T.6
-
75
-
-
1542509662
-
FANCF methylation contributes to chemoselectivity in ovarian cancer
-
DOI 10.1016/S1535-6108(03)00111-9, PII S1535610803001119
-
Olopade OI, Wei M: FANCF methylation contributes to chemoselectivity in ovarian cancer. Cancer Cell 2003;3:417-420. (Pubitemid 38340287)
-
(2003)
Cancer Cell
, vol.3
, Issue.5
, pp. 417-420
-
-
Olopade, O.I.1
Wei, M.2
-
76
-
-
2342633174
-
Promoter Hypermethylation of FANCF: Disruption of Fanconi Anemia-BRCA Pathway in Cervical Cancer
-
DOI 10.1158/0008-5472.CAN-04-0245
-
Narayan G, Arias-Pulido H, Nandula SV, Basso K, Sugirtharaj DD, et al: Promoter hypermethylation of FANCF: disruption of Fanconi Anemia-BRCA pathway in cervical cancer. Cancer Res 2004;64:2994-2997. (Pubitemid 38581394)
-
(2004)
Cancer Research
, vol.64
, Issue.9
, pp. 2994-2997
-
-
Narayan, G.1
Arias-Pulido, H.2
Nandula, S.V.3
Basso, K.4
Sugirtharaj, D.D.5
Vargas, H.6
Mansukhani, M.7
Villella, J.8
Meyer, L.9
Schneider, A.10
Gissmann, L.11
Durst, M.12
Pothuri, B.13
Murty, V.V.V.S.14
-
77
-
-
33845652128
-
Variation in cisplatinum sensitivity is not associated with Fanconi Anemia/BRCA pathway inactivation in head and neck squamous cell carcinoma cell lines
-
Snyder ER, Ricker JL, Chen Z, Waes CV: Variation in cisplatinum sensitivity is not associated with Fanconi Anemia/BRCA pathway inactivation in head and neck squamous cell carcinoma cell lines. Cancer Lett 2006;245:75-80.
-
(2006)
Cancer Lett
, vol.245
, pp. 75-80
-
-
Snyder, E.R.1
Ricker, J.L.2
Chen, Z.3
Waes, C.V.4
-
78
-
-
13644254920
-
CpG methylation of the FHIT, FANCF, cyclin-D2, BRCA2 and RUNX3 genes in granulosa cell tumors (GCTs) of ovarian origin
-
Dhillon VS, Shahid M, Husain SA: CpG methylation of the FHIT, FANCF, cyclin-D2, BRCA2 and RUNX3 genes in granulosa cell tumors (GCTs) of ovarian origin. Mol Cancer 2004;3:33.
-
(2004)
Mol Cancer
, vol.3
, pp. 33
-
-
Dhillon, V.S.1
Shahid, M.2
Husain, S.A.3
-
79
-
-
25444485414
-
CpG island methylation of DNA damage response genes in advanced ovarian cancer
-
DOI 10.1158/0008-5472.CAN-05-1187
-
Teodoridis JM, Hall J, Marsh S, Kannall HD, Smyth C, et al: CpG island methylation of DNA damage response genes in advanced ovarian cancer. Cancer Res 2005;65:8961-8967. (Pubitemid 41377387)
-
(2005)
Cancer Research
, vol.65
, Issue.19
, pp. 8961-8967
-
-
Teodoridis, J.M.1
Hall, J.2
Marsh, S.3
Kannall, H.D.4
Smyth, C.5
Curto, J.6
Siddiqui, N.7
Gabra, H.8
McLeod, H.L.9
Strathdee, G.10
Brown, R.11
-
80
-
-
33646415108
-
Promoter hypermethylation of FANCF plays an important role in the occurrence of ovarian cancer through disrupting Fanconi Anemia-BRCA pathway
-
Wang Z, Li M, Lu S, Zhang Y, Wang H: Promoter hypermethylation of FANCF plays an important role in the occurrence of ovarian cancer through disrupting Fanconi Anemia-BRCA pathway. Cancer Biol Ther 2006;5:256-260.
-
(2006)
Cancer Biol Ther
, vol.5
, pp. 256-260
-
-
Wang, Z.1
Li, M.2
Lu, S.3
Zhang, Y.4
Wang, H.5
-
81
-
-
2942617040
-
Role of promoter hypermethylation in cisplatin treatment response of male germ cell tumors
-
Koul S, McKiernan JM, Narayan G, Houldsworth J, Bacik J, et al: Role of promoter hypermethylation in cisplatin treatment response of male germ cell tumors. Mol Cancer 2004;3:16.
-
(2004)
Mol Cancer
, vol.3
, pp. 16
-
-
Koul, S.1
McKiernan, J.M.2
Narayan, G.3
Houldsworth, J.4
Bacik, J.5
-
82
-
-
9144236362
-
Acute graft-versus-host disease in patients with Fanconi anemia or acquired aplastic anemia undergoing bone marrow transplantation from HLA-identical sibling donors: Risk factors and influence on outcome
-
DOI 10.1182/blood-2003-06-2146
-
Guardiola P, Socié G, Li X, Ribaus P, Devergie A, et al: Acute graft-versus-host disease in patients with Fanconi anemia or aquired aplastic anemia undergoing bone marrow transplantation from HLA-identical sibling donors: risk factors and influence on outcome. Blood 2004;103:73-77. (Pubitemid 38029920)
-
(2004)
Blood
, vol.103
, Issue.1
, pp. 73-77
-
-
Guardiola, P.1
Socie, G.2
Li, X.3
Ribaud, P.4
Devergie, A.5
Esperou, H.6
Richard, P.7
Traineau, R.8
Janin, A.9
Gluckman, E.10
-
83
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
DOI 10.1038/ng1902, PII NG1902
-
Seal S, Thompson D, Renwick D, Elliott A, Kelly P, et al: Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet 2006;38:1239-1241. (Pubitemid 44646283)
-
(2006)
Nature Genetics
, vol.38
, Issue.11
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
North, B.11
McGuffog, L.12
Evans, D.G.13
Eccles, D.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
-
84
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
DOI 10.1038/ng1959, PII NG1959
-
Rahman N, Seil S, Thompson D, Kelly P, Renwick A, et al: PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet 2007;39:165-167. (Pubitemid 46184346)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
Kelly, P.4
Renwick, A.5
Elliott, A.6
Reid, S.7
Spanova, K.8
Barfoot, R.9
Chagtai, T.10
Jayatilake, H.11
McGuffog, L.12
Hanks, S.13
Evans, D.G.14
Eccles, D.15
Easton, D.F.16
Stratton, M.R.17
-
85
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
DOI 10.1038/nature05609, PII NATURE05609
-
Erkko H, Xia B, Nikkila J, Schleutker J, Syrjakoski K, et al: A recurrent mutation in PALB2 in Finnish cancer families. Nature 2007;446:316-319. (Pubitemid 46426155)
-
(2007)
Nature
, vol.446
, Issue.7133
, pp. 316-319
-
-
Erkko, H.1
Xia, B.2
Nikkila, J.3
Schleutker, J.4
Syrjakoski, K.5
Mannermaa, A.6
Kallioniemi, A.7
Pylkas, K.8
Karppinen, S.-M.9
Rapakko, K.10
Miron, A.11
Sheng, Q.12
Li, G.13
Mattila, H.14
Bell, D.W.15
Haber, D.A.16
Grip, M.17
Reiman, M.18
Jukkola-Vuorinen, A.19
Mustonen, A.20
Kere, J.21
Aaltonen, L.A.22
Kosma, V.-M.23
Kataja, V.24
Soini, Y.25
Drapkin, R.I.26
Livingston, D.M.27
Winqvist, R.28
more..
-
86
-
-
36248949158
-
Disruption of the FA/BRCA pathway in bladder cancer
-
in press
-
Neveling K, Kalb R, Florl AR, Herterich S, Friedl R, et al: Disruption of the FA/BRCA pathway in bladder cancer. Cytogenet Genome Res 2007, in press.
-
(2007)
Cytogenet Genome Res
-
-
Neveling, K.1
Kalb, R.2
Florl, A.R.3
Herterich, S.4
Friedl, R.5
-
87
-
-
36549083551
-
Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer
-
Epub ahead of print
-
Van der Groep P, Hoelzel M, Buerger H, Joenje H, De Winter JP, et al: Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer. Breast Cancer Res Treat 2007; Epub ahead of print.
-
(2007)
Breast Cancer Res Treat
-
-
Van Der Groep, P.1
Hoelzel, M.2
Buerger, H.3
Joenje, H.4
De Winter, J.P.5
|