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Human Heredity
|
January 1, 1978
Oculocutaneous albinism and mental disorder. A report of two autistic boys
M A Rogawski, S J Funderburk, S D Cederbaum
Pediatric Research
|
December 1, 1983
Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients
E B Spector, S C Rice, S D Cederbaum
Clinical Chemistry
|
October 1, 1979
Adsorption of organic acids from amniotic fluid and urine onto silica gel before analysis by gas chromatography and combined gas chromatography/mass spectrometry
V P Williams, D K Ching, S D Cederbaum
Isozymes
|
January 1, 1987
Human arginase isozymes
W W Grody, G J Dizikes, S D Cederbaum
Lancet (London, England)
|
June 5, 1976
Letter: Biochemical abnormalities in Leigh's disease
J P Blass, S D Cederbaum, H G Dunn
The New England Journal of Medicine
|
August 23, 1979
Hypertrophic cardiomyopathy
S E Hodge, M A Spence, S D Cederbaum
Comparative Biochemistry and Physiology. Part B, Biochemistry & Molecular Biology
|
May 1, 1996
Comparative properties of arginases
C P Jenkinson, W W Grody, S D Cederbaum
Somatic Cell and Molecular Genetics
|
July 1, 1986
Cloning of rat liver arginase cDNA and elucidation of regulation of arginase gene expression in H4 rat hepatoma cells
G J Dizikes, E B Spector, S D Cederbaum
Biochemical Genetics
|
October 1, 1980
Properties of arginase from liver of Macaca fascicularis; comparison of normals with red blood cell arginase deficient monkeys
K Terasaki, E B Spector, R Hendrickson, et al.
American Journal of Human Genetics
|
January 1, 1980
Properties of fetal and adult red blood cell arginase: a possible prenatal diagnostic test for arginase deficiency
E B Spector, M Kiernan, B Bernard, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 93) with videos related to
Sort By:
Page
of 10
Human Heredity
|
January 1, 1978
Oculocutaneous albinism and mental disorder. A report of two autistic boys
M A Rogawski, S J Funderburk, S D Cederbaum
Pediatric Research
|
December 1, 1983
Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients
E B Spector, S C Rice, S D Cederbaum
Clinical Chemistry
|
October 1, 1979
Adsorption of organic acids from amniotic fluid and urine onto silica gel before analysis by gas chromatography and combined gas chromatography/mass spectrometry
V P Williams, D K Ching, S D Cederbaum
Isozymes
|
January 1, 1987
Human arginase isozymes
W W Grody, G J Dizikes, S D Cederbaum
Lancet (London, England)
|
June 5, 1976
Letter: Biochemical abnormalities in Leigh's disease
J P Blass, S D Cederbaum, H G Dunn
The New England Journal of Medicine
|
August 23, 1979
Hypertrophic cardiomyopathy
S E Hodge, M A Spence, S D Cederbaum
Comparative Biochemistry and Physiology. Part B, Biochemistry & Molecular Biology
|
May 1, 1996
Comparative properties of arginases
C P Jenkinson, W W Grody, S D Cederbaum
Somatic Cell and Molecular Genetics
|
July 1, 1986
Cloning of rat liver arginase cDNA and elucidation of regulation of arginase gene expression in H4 rat hepatoma cells
G J Dizikes, E B Spector, S D Cederbaum
Biochemical Genetics
|
October 1, 1980
Properties of arginase from liver of Macaca fascicularis; comparison of normals with red blood cell arginase deficient monkeys
K Terasaki, E B Spector, R Hendrickson, et al.
American Journal of Human Genetics
|
January 1, 1980
Properties of fetal and adult red blood cell arginase: a possible prenatal diagnostic test for arginase deficiency
E B Spector, M Kiernan, B Bernard, et al.
Page
of 10