SNPing away at sickle cell pathophysiology

Blood

Volumn 111, Issue 12, 2008, Pages 5420-5421

  Steinberg, Martin H ^a  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN; GLUCURONOSYLTRANSFERASE 1A1; HEMOGLOBIN S; HLA ANTIGEN; LOW DENSITY LIPOPROTEIN RECEPTOR; TRANSFORMING GROWTH FACTOR BETA; TUMOR NECROSIS FACTOR ALPHA; VASCULAR CELL ADHESION MOLECULE 1;

BACTEREMIA; BONE NECROSIS; CHOLELITHIASIS; GENETIC ASSOCIATION; HEMOLYTIC ANEMIA; HOMOZYGOSITY; HUMAN; KIDNEY FAILURE; LEG ULCER; NOTE; PATHOPHYSIOLOGY; PHENOTYPE; PRIAPISM; PRIORITY JOURNAL; PULMONARY HYPERTENSION; SICKLE CELL ANEMIA; SINGLE NUCLEOTIDE POLYMORPHISM; STROKE;

EID: 61849098181     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2008-01-135392     Document Type: Note

References (3)

1. Gladwin MT, Sachdev V, Jison ML, et al. Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med. 2004;3550:886-895.
2. Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH. Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nat Genet. 2005;37:435-440.
3. Saxena R, Voight BF, Lyssenko V, et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007;316:1331-1336.