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Human Mutation
|
December 29, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databases: II. Journey in progress
C R Scriver, P M Nowacki, H Lehväslaiho
Journal of Bacteriology
|
November 1, 1970
Isolation and properties of a beta-alanine transaminaseless mutant of Pseudomonas fluorescens
P Hechtman, C R Scriver, R B Middleton
Metabolism: Clinical and Experimental
|
March 1, 1974
Branched-chain alpha-keto acids isolated as oxime derivatives: relationship to the corresponding hydroxy acids and amino acids in maple syrup urine disease
G Lancaster, O A Mamer, C R Scriver
Biochimica Et Biophysica Acta
|
December 3, 1971
The ontogeny of amino acid transport in rat kidney. I. Effect on distribution ratios and intracellular metabolism of proline and glycine
K E Baerlocher, C R Scriver, F Mohyuddin
Biochemical Medicine
|
June 1, 1974
Pyruvate carboxylase in human liver. Apparent loss of a component of catalytic activity in a form of lactic acidosis with hypoglycemia
E Delvin, C R Scriver, J L Neal
Human Mutation
|
August 19, 2006
CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene
B C Murphy, C R Scriver, S M Singh
Annals of the New York Academy of Sciences
|
January 1, 1985
Cultured human fibroblasts and plasma membrane vesicles to investigate transport function and the effects of genetic mutation
J A Buchanan, D S Rosenblatt, C R Scriver
Nature
|
May 23, 2000
Science's neglected legacy
S M Maurer, R B Firestone, C R Scriver
Lancet (London, England)
|
April 18, 1970
Use of dithiothreitol to correct cystine storage in cultured cystinotic fibroblasts
H Goldman, C R Scriver, K Aaron, et al.
Medicine
|
May 1, 1991
X-linked hypophosphatemia: an appreciation of a classic paper and a survey of progress since 1958
C R Scriver, H S Tenenhouse, F H Glorieux
Page
of 32
Search research articles
Search
Showing results (151-160 of 317) with videos related to
Sort By:
Page
of 32
Human Mutation
|
December 29, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databases: II. Journey in progress
C R Scriver, P M Nowacki, H Lehväslaiho
Journal of Bacteriology
|
November 1, 1970
Isolation and properties of a beta-alanine transaminaseless mutant of Pseudomonas fluorescens
P Hechtman, C R Scriver, R B Middleton
Metabolism: Clinical and Experimental
|
March 1, 1974
Branched-chain alpha-keto acids isolated as oxime derivatives: relationship to the corresponding hydroxy acids and amino acids in maple syrup urine disease
G Lancaster, O A Mamer, C R Scriver
Biochimica Et Biophysica Acta
|
December 3, 1971
The ontogeny of amino acid transport in rat kidney. I. Effect on distribution ratios and intracellular metabolism of proline and glycine
K E Baerlocher, C R Scriver, F Mohyuddin
Biochemical Medicine
|
June 1, 1974
Pyruvate carboxylase in human liver. Apparent loss of a component of catalytic activity in a form of lactic acidosis with hypoglycemia
E Delvin, C R Scriver, J L Neal
Human Mutation
|
August 19, 2006
CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene
B C Murphy, C R Scriver, S M Singh
Annals of the New York Academy of Sciences
|
January 1, 1985
Cultured human fibroblasts and plasma membrane vesicles to investigate transport function and the effects of genetic mutation
J A Buchanan, D S Rosenblatt, C R Scriver
Nature
|
May 23, 2000
Science's neglected legacy
S M Maurer, R B Firestone, C R Scriver
Lancet (London, England)
|
April 18, 1970
Use of dithiothreitol to correct cystine storage in cultured cystinotic fibroblasts
H Goldman, C R Scriver, K Aaron, et al.
Medicine
|
May 1, 1991
X-linked hypophosphatemia: an appreciation of a classic paper and a survey of progress since 1958
C R Scriver, H S Tenenhouse, F H Glorieux
Page
of 32