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The New England Journal of Medicine
|
September 1, 1988
Predictive testing for Huntington's disease using linked DNA markers
M R Hayden, M Bloch, M Fahy
Human Molecular Genetics
|
December 1, 1992
The genomic organization of a novel regulatory myosin light chain gene (MYL5) that maps to chromosome 4p16.3 and shows different patterns of expression between primates
C Collins, K Schappert, M R Hayden
Brain Pathology (Zurich, Switzerland)
|
October 1, 1992
New insights into the clinical features, pathogenesis and molecular genetics of Huntington disease
B Kremer, B Weber, M R Hayden
Biochemical Society Transactions
|
April 8, 2015
Post-translational myristoylation at the cross roads of cell death, autophagy and neurodegeneration
Dale D O Martin, Michael R Hayden
Advances in Neurology
|
January 1, 1995
Psychological effects of predictive testing for Huntington's disease
M R Hayden, M Bloch, S Wiggins
Seminars in Dialysis
|
July 20, 2010
Sodium thiosulfate: new hope for the treatment of calciphylaxis
Melvin R Hayden, David J A Goldsmith
Human Molecular Genetics
|
September 1, 1992
(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16
O Riess, B Weber, M R Hayden
Italian Journal of Neurological Sciences
|
June 1, 1996
Update on genetics of Huntington's disease: availability of direct and accurate predictive test
F Squitieri, G Campanella, M R Hayden
Annals of Emergency Medicine
|
February 25, 2023
The Knowledge Gap: Mentorship in Emergency Medicine Residency
Julia Sobel, Stephen R Hayden, Gabriel Wardi
Gene
|
March 14, 2024
Research progress of RP1L1 gene in disease
Jiali Liu, Melvin R Hayden, Ying Yang
Page
of 104
Search research articles
Search
Showing results (121-130 of 1,032) with videos related to
Sort By:
Page
of 104
The New England Journal of Medicine
|
September 1, 1988
Predictive testing for Huntington's disease using linked DNA markers
M R Hayden, M Bloch, M Fahy
Human Molecular Genetics
|
December 1, 1992
The genomic organization of a novel regulatory myosin light chain gene (MYL5) that maps to chromosome 4p16.3 and shows different patterns of expression between primates
C Collins, K Schappert, M R Hayden
Brain Pathology (Zurich, Switzerland)
|
October 1, 1992
New insights into the clinical features, pathogenesis and molecular genetics of Huntington disease
B Kremer, B Weber, M R Hayden
Biochemical Society Transactions
|
April 8, 2015
Post-translational myristoylation at the cross roads of cell death, autophagy and neurodegeneration
Dale D O Martin, Michael R Hayden
Advances in Neurology
|
January 1, 1995
Psychological effects of predictive testing for Huntington's disease
M R Hayden, M Bloch, S Wiggins
Seminars in Dialysis
|
July 20, 2010
Sodium thiosulfate: new hope for the treatment of calciphylaxis
Melvin R Hayden, David J A Goldsmith
Human Molecular Genetics
|
September 1, 1992
(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16
O Riess, B Weber, M R Hayden
Italian Journal of Neurological Sciences
|
June 1, 1996
Update on genetics of Huntington's disease: availability of direct and accurate predictive test
F Squitieri, G Campanella, M R Hayden
Annals of Emergency Medicine
|
February 25, 2023
The Knowledge Gap: Mentorship in Emergency Medicine Residency
Julia Sobel, Stephen R Hayden, Gabriel Wardi
Gene
|
March 14, 2024
Research progress of RP1L1 gene in disease
Jiali Liu, Melvin R Hayden, Ying Yang
Page
of 104