Biallelic mutations in FANCD1/BRCA2 are associated with extraordinary risks of cancer.

被引：0

作者：

Alter, Blanche P.

Rosenberg, Philip S.

Brody, Lawrence C.

机构：

[1] Natl Canc Inst, Div Canc Epidemiol & Genet, Clin Genet Branch, Bethesda, MD USA

[2] Natl Canc Inst, Div Canc Epidemiol & Genet, Biostat Branch, Bethesda, MD USA

[3] Natl Inst Hlth, NHGRI, Genome Technol Branch, Bethesda, MD USA

来源：

BLOOD | 2006年 / 108卷 / 11期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

4326

引用

页码：160B / 160B

页数：1

共 50 条

[21] Treatment With Azacitidine in the Context of Palliative Care for a Patient With Acute Myeloid Leukemia Complicating Fanconi Anemia With Biallelic FANCD1/BRCA 2 Mutations
Berot, Aurelie
Pluchart, Claire
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2018, 40 (03) : 247 - 248
[22] Increased chromosome breakage in lymphocytes exposed to ionizing radiation can be used to distinguish FANCD1 caused by biallelic BRCA2 mutations from more common forms of Fanconi anaemia
Holden, Simon
Stewart, G.
Byrd, P.
Turnbull, C.
Kesterton, I.
McDonald, F.
Fulton, P.
Ridout, C.
Davidson, A.
Bye, H.
Mathew, C. G.
Taylor, A. M.
JOURNAL OF MEDICAL GENETICS, 2011, 48 : S18 - S18
[23] Family History of Cancer and Cancer Risks in Women with BRCA1 or BRCA2 Mutations
Metcalfe, Kelly
Lubinski, Jan
Lynch, Henry T.
Ghadirian, Parviz
Foulkes, William D.
Kim-Sing, Charmaine
Neuhausen, Susan
Tung, Nadine
Rosen, Barry
Gronwald, Jacek
Ainsworth, Peter
Sweet, Kevin
Eisen, Andrea
Sun, Ping
Narod, Steven A.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2010, 102 (24): : 1874 - 1878
[24] FANCD1/BRCA2 Plays Predominant Role in the Repair of DNA Damage Induced by ACNU or TMZ
Kondo, Natsuko
Takahashi, Akihisa
Mori, Eiichiro
Noda, Taichi
Zdzienicka, Malgorzata Z.
Thompson, Larry H.
Helleday, Thomas
Suzuki, Minoru
Kinashi, Yuko
Masunaga, Shinichiro
Ono, Koji
Hasegawa, Masatoshi
Ohnishi, Takeo
PLOS ONE, 2011, 6 (05):
[25] The prevalence of BRCA1 and BRCA2 mutations in Chinese women with breast cancer.
Hu, Z.
Li, W-F
Song, C-G
Shen, Z-Z
Huang, W.
Shao, Z-M
BREAST CANCER RESEARCH AND TREATMENT, 2006, 100 : S250 - S250
[26] Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants
Li, Shuai
Silvestri, Valentina
Leslie, Goska
Rebbeck, Timothy R.
Neuhausen, Susan L.
Hopper, John L.
Nielsen, Henriette Roed
Lee, Andrew
Yang, Xin
McGuffog, Lesley
Parsons, Michael T.
Andrulis, Irene L.
Arnold, Norbert
Belotti, Muriel
Borg, Ake
Buecher, Bruno
Buys, Saundra S.
Caputo, Sandrine M.
Chung, Wendy K.
Colas, Chrystelle
Colonna, Sarah, V
Cook, Jackie
Daly, Mary B.
de la Hoya, Miguel
de Pauw, Antoine
Delhomelle, Helene
Eason, Jacqueline
Engel, Christoph
Evans, D. Gareth
Faust, Ulrike
Fehm, Tanja N.
Fostira, Florentia
Fountzilas, George
Frone, Megan
Garcia-Barberan, Vanesa
Garre, Pilar
Gauthier-Villars, Marion
Gehrig, Andrea
Glendon, Gord
Goldgar, David E.
Golmard, Lisa
Greene, Mark H.
Hahnen, Eric
Hamann, Ute
Hanson, Helen
Hassan, Tiara
Hentschel, Julia
Horvath, Judit
Izatt, Louise
Janavicius, Ramunas
JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (14) : 1529 - +
[27] BRCA1 and BRCA2 cancer risks
Antoniou, Antonis C.
Pharoah, Paul D. P.
Easton, Douglas F.
Evans, D. Gareth
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (20) : 3312 - 3313
[28] Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia
Barber, LM
Barlow, RA
Meyer, S
White, DJ
Will, AM
Eden, TOB
Taylor, GM
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 130 (05) : 796 - 797
[29] Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
King, MC
Marks, JH
Mandell, JB
SCIENCE, 2003, 302 (5645) : 643 - 646
[30] Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2)
McReynolds, Lisa J.
Biswas, Kajal
Giri, Neelam
Sharan, Shyam K.
Alter, Blanche P.
CANCER GENETICS, 2021, 258 : 101 - 109

← 1 2 3 4 5 →