Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
4R37HL032987-17
Application #
6447204
Study Section
Special Emphasis Panel (NSS)
Program Officer
Qasba, Pankaj
Project Start
1985-05-01
Project End
2007-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
17
Fiscal Year
2002
Total Cost
$502,565
Indirect Cost
Name
Rockefeller University
Department
Genetics
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Ali, Abdullah Mahmood; Kirby, Michelle; Jansen, Michael et al. (2009) Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group. Hum Mutat 30:E761-70
Auerbach, Arleen D (2009) Fanconi anemia and its diagnosis. Mutat Res 668:4-10
Morales, Jose F; Song, Tingting; Auerbach, Arleen D et al. (2008) Phenotyping genetic diseases using an extension of mu-scores for multivariate data. Stat Appl Genet Mol Biol 7:Article 19
Sims, Ashley E; Spiteri, Elizabeth; Sims 3rd, Robert J et al. (2007) FANCI is a second monoubiquitinated member of the Fanconi anemia pathway. Nat Struct Mol Biol 14:564-7
Berwick, Marianne; Satagopan, Jaya M; Ben-Porat, Leah et al. (2007) Genetic heterogeneity among Fanconi anemia heterozygotes and risk of cancer. Cancer Res 67:9591-6
Reid, Sarah; Schindler, Detlev; Hanenberg, Helmut et al. (2007) Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet 39:162-4
Ling, Chen; Ishiai, Masamichi; Ali, Abdullah Mahmood et al. (2007) FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway. EMBO J 26:2104-14
Farzin, Azadeh; Davies, Stella M; Smith, Franklin O et al. (2007) Matched sibling donor haematopoietic stem cell transplantation in Fanconi anaemia: an update of the Cincinnati Children's experience. Br J Haematol 136:633-40
Kalb, Reinhard; Neveling, Kornelia; Hoehn, Holger et al. (2007) Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype. Am J Hum Genet 80:895-910
Wagner, John E; Eapen, Mary; MacMillan, Margaret L et al. (2007) Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia. Blood 109:2256-62

Showing the most recent 10 out of 63 publications