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Clinical Case Reports
|
January 14, 2014
Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome
Hagit N Baris, Wai-Man Chan, Caroline Andrews, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 1, 1996
CD1c restricts responses of mycobacteria-specific T cells. Evidence for antigen presentation by a second member of the human CD1 family
E M Beckman, A Melián, S M Behar, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 22, 2009
Vaccine-induced antibody isotypes are skewed by impaired CD4 T cell and invariant NKT cell effector responses in MyD88-deficient mice
Onyinye I Iweala, Donald W Smith, Kabir S Matharu, et al.
Human Mutation
|
July 17, 2008
A novel 154-bp deletion in the human mitochondrial DNA control region in healthy individuals
Doron M Behar, Jason Blue-Smith, David F Soria-Hernanz, et al.
Cardiology Research and Practice
|
September 28, 2019
Erratum to "Comparison of Echocardiographic and Electrocardiographic Mapping for Cardiac Resynchronisation Therapy Optimisation"
Helder Pereira, Tom A Jackson, Simon Claridge, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 8, 2003
Lysosomal localization of murine CD1d mediated by AP-3 is necessary for NK T cell development
Manuela Cernadas, Masahiko Sugita, Nicole van der Wel, et al.
Cardiology Research and Practice
|
March 29, 2019
Comparison of Echocardiographic and Electrocardiographic Mapping for Cardiac Resynchronisation Therapy Optimisation
Helder Pereira, Tom A Jackson, Simon Claridge, et al.
Human Molecular Genetics
|
February 11, 2010
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans
Doron M Behar, Saharon Rosset, Shay Tzur, et al.
Journal of Lipid Research
|
November 23, 2013
Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency
Doron M Behar, Lina Basel-Vanagaite, Fabian Glaser, et al.
BMC Evolutionary Biology
|
December 24, 2010
Population expansion in the North African late Pleistocene signalled by mitochondrial DNA haplogroup U6
Luísa Pereira, Nuno M Silva, Ricardo Franco-Duarte, et al.
Page
of 38
Search research articles
Search
Showing results (251-260 of 373) with videos related to
Sort By:
Page
of 38
Clinical Case Reports
|
January 14, 2014
Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome
Hagit N Baris, Wai-Man Chan, Caroline Andrews, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 1, 1996
CD1c restricts responses of mycobacteria-specific T cells. Evidence for antigen presentation by a second member of the human CD1 family
E M Beckman, A Melián, S M Behar, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 22, 2009
Vaccine-induced antibody isotypes are skewed by impaired CD4 T cell and invariant NKT cell effector responses in MyD88-deficient mice
Onyinye I Iweala, Donald W Smith, Kabir S Matharu, et al.
Human Mutation
|
July 17, 2008
A novel 154-bp deletion in the human mitochondrial DNA control region in healthy individuals
Doron M Behar, Jason Blue-Smith, David F Soria-Hernanz, et al.
Cardiology Research and Practice
|
September 28, 2019
Erratum to "Comparison of Echocardiographic and Electrocardiographic Mapping for Cardiac Resynchronisation Therapy Optimisation"
Helder Pereira, Tom A Jackson, Simon Claridge, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
October 8, 2003
Lysosomal localization of murine CD1d mediated by AP-3 is necessary for NK T cell development
Manuela Cernadas, Masahiko Sugita, Nicole van der Wel, et al.
Cardiology Research and Practice
|
March 29, 2019
Comparison of Echocardiographic and Electrocardiographic Mapping for Cardiac Resynchronisation Therapy Optimisation
Helder Pereira, Tom A Jackson, Simon Claridge, et al.
Human Molecular Genetics
|
February 11, 2010
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans
Doron M Behar, Saharon Rosset, Shay Tzur, et al.
Journal of Lipid Research
|
November 23, 2013
Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency
Doron M Behar, Lina Basel-Vanagaite, Fabian Glaser, et al.
BMC Evolutionary Biology
|
December 24, 2010
Population expansion in the North African late Pleistocene signalled by mitochondrial DNA haplogroup U6
Luísa Pereira, Nuno M Silva, Ricardo Franco-Duarte, et al.
Page
of 38