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Annals of the New York Academy of Sciences
|
December 18, 2003
Ethnic differences in the associations between the HLA-DRB1*04 subtypes and type 1 diabetes
Amanda Rewers, Sunanda Babu, Tian Bao Wang, et al.
Neurology
|
November 12, 2003
Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter
T M Burns, H R Jones, L H Phillips, et al.
Stroke
|
July 11, 2006
Polymorphisms of the phosphodiesterase 4D, cAMP-specific (PDE4D) gene and risk of ischemic stroke: a prospective, nested case-control evaluation
Robert Y L Zee, Victoria H Brophy, Suzanne Cheng, et al.
Clinical Chemistry and Laboratory Medicine
|
November 30, 2000
Familial studies on the genetics of cardiovascular diseases: the Stanislas cohort
S Visvikis, C Sass, C Pallaud, et al.
The New England Journal of Medicine
|
March 12, 1987
Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis
S H Embury, S J Scharf, R K Saiki, et al.
Nature
|
May 24, 1990
Limited heterogeneity of rearranged T-cell receptor V alpha transcripts in brains of multiple sclerosis patients
J R Oksenberg, S Stuart, A B Begovich, et al.
Cancer
|
April 15, 1991
Bladder cancer. Human leukocyte antigen II, interleukin-6, and interleukin-6 receptor expression determined by the polymerase chain reaction
F J Meyers, P H Gumerlock, E S Kawasaki, et al.
Stroke
|
October 27, 2007
Intercellular adhesion molecule 1 (ICAM1) Lys56Met and Gly241Arg gene variants, plasma-soluble ICAM1 concentrations, and risk of incident cardiovascular events in 23,014 initially healthy white women
Robert Y L Zee, Suzanne Cheng, Henry A Erlich, et al.
Diabetes
|
September 28, 2005
Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families
Patrick Concannon, Henry A Erlich, Cecile Julier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 21, 2000
Transient antiislet autoantibodies: infrequent occurrence and lack of association with "genetic" risk factors
J Yu, L Yu, T L Bugawan, et al.
Page
of 28
Search research articles
Search
Showing results (141-150 of 276) with videos related to
Sort By:
Page
of 28
Annals of the New York Academy of Sciences
|
December 18, 2003
Ethnic differences in the associations between the HLA-DRB1*04 subtypes and type 1 diabetes
Amanda Rewers, Sunanda Babu, Tian Bao Wang, et al.
Neurology
|
November 12, 2003
Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter
T M Burns, H R Jones, L H Phillips, et al.
Stroke
|
July 11, 2006
Polymorphisms of the phosphodiesterase 4D, cAMP-specific (PDE4D) gene and risk of ischemic stroke: a prospective, nested case-control evaluation
Robert Y L Zee, Victoria H Brophy, Suzanne Cheng, et al.
Clinical Chemistry and Laboratory Medicine
|
November 30, 2000
Familial studies on the genetics of cardiovascular diseases: the Stanislas cohort
S Visvikis, C Sass, C Pallaud, et al.
The New England Journal of Medicine
|
March 12, 1987
Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis
S H Embury, S J Scharf, R K Saiki, et al.
Nature
|
May 24, 1990
Limited heterogeneity of rearranged T-cell receptor V alpha transcripts in brains of multiple sclerosis patients
J R Oksenberg, S Stuart, A B Begovich, et al.
Cancer
|
April 15, 1991
Bladder cancer. Human leukocyte antigen II, interleukin-6, and interleukin-6 receptor expression determined by the polymerase chain reaction
F J Meyers, P H Gumerlock, E S Kawasaki, et al.
Stroke
|
October 27, 2007
Intercellular adhesion molecule 1 (ICAM1) Lys56Met and Gly241Arg gene variants, plasma-soluble ICAM1 concentrations, and risk of incident cardiovascular events in 23,014 initially healthy white women
Robert Y L Zee, Suzanne Cheng, Henry A Erlich, et al.
Diabetes
|
September 28, 2005
Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families
Patrick Concannon, Henry A Erlich, Cecile Julier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 21, 2000
Transient antiislet autoantibodies: infrequent occurrence and lack of association with "genetic" risk factors
J Yu, L Yu, T L Bugawan, et al.
Page
of 28