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Pediatric Research
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May 1, 1990
Hepatic copper metabolism in a mouse model for Menkes' kinky hair syndrome
R O Castillo, M M Thaler, C O'Toole, et al.
Nature: New Biology
|
February 7, 1973
In vitro synthesis of DNA complementary to mRNA derived from a light chain-producing myeloma tumour
H Aviv, S Packman, D Swan, et al.
Clinical Pediatrics
|
September 1, 1994
Prenatal counseling in heterozygotes for ornithine transcarbamylase deficiency
M H Fries, J A Kuller, E Jurecki, et al.
Journal of Inorganic Biochemistry
|
November 1, 1983
Cadmium, zinc, and copper metabolism in the mottled mouse, an animal model for Menkes' kinky hair syndrome
S Packman, C O'Toole, D C Price, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1974
Organization of immunoglobulin genes: reiteration frequency of the mouse kappa chain constant region gene
T Honjo, S Packman, D Swan, et al.
Nature Genetics
|
January 1, 1993
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase
C Vulpe, B Levinson, S Whitney, et al.
The Journal of Clinical Investigation
|
September 1, 1986
Deficiency of the pyruvate dehydrogenase component in pyruvate dehydrogenase complex-deficient human fibroblasts. Immunological identification
L Ho, C W Hu, S Packman, et al.
The Journal of Pediatrics
|
May 1, 1978
Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency
S Packman, M J Mahoney, K Tanaka, et al.
Bibliotheca Haematologica
|
January 1, 1975
Induction of globin mRNA in Friend leukemia virus-infected cells and its presence in viral 60S RNA
J Ross, Y Ikawa, J Gielen, et al.
The Journal of Pediatrics
|
September 1, 1981
Biotin-responsive multiple carboxylase deficiency of infantile onset
S Packman, L Sweetman, M Yoshino, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 98) with videos related to
Sort By:
Page
of 10
Pediatric Research
|
May 1, 1990
Hepatic copper metabolism in a mouse model for Menkes' kinky hair syndrome
R O Castillo, M M Thaler, C O'Toole, et al.
Nature: New Biology
|
February 7, 1973
In vitro synthesis of DNA complementary to mRNA derived from a light chain-producing myeloma tumour
H Aviv, S Packman, D Swan, et al.
Clinical Pediatrics
|
September 1, 1994
Prenatal counseling in heterozygotes for ornithine transcarbamylase deficiency
M H Fries, J A Kuller, E Jurecki, et al.
Journal of Inorganic Biochemistry
|
November 1, 1983
Cadmium, zinc, and copper metabolism in the mottled mouse, an animal model for Menkes' kinky hair syndrome
S Packman, C O'Toole, D C Price, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1974
Organization of immunoglobulin genes: reiteration frequency of the mouse kappa chain constant region gene
T Honjo, S Packman, D Swan, et al.
Nature Genetics
|
January 1, 1993
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase
C Vulpe, B Levinson, S Whitney, et al.
The Journal of Clinical Investigation
|
September 1, 1986
Deficiency of the pyruvate dehydrogenase component in pyruvate dehydrogenase complex-deficient human fibroblasts. Immunological identification
L Ho, C W Hu, S Packman, et al.
The Journal of Pediatrics
|
May 1, 1978
Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency
S Packman, M J Mahoney, K Tanaka, et al.
Bibliotheca Haematologica
|
January 1, 1975
Induction of globin mRNA in Friend leukemia virus-infected cells and its presence in viral 60S RNA
J Ross, Y Ikawa, J Gielen, et al.
The Journal of Pediatrics
|
September 1, 1981
Biotin-responsive multiple carboxylase deficiency of infantile onset
S Packman, L Sweetman, M Yoshino, et al.
Page
of 10