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The Journal of Nutrition
|
November 1, 1990
Effects of cellular copper content on copper uptake and metallothionein and ceruloplasmin mRNA levels in mouse hepatocytes
H J McArdle, J F Mercer, A M Sargeson, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1980
Observations indicating the nature of the mutation in phenylketonuria
K H Choo, R G Cotton, I G Jennings, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome)
K Hayasaka, G K Brown, D M Danks, et al.
The American Journal of Physiology
|
June 1, 1990
Role of albumin's copper binding site in copper uptake by mouse hepatocytes
H J McArdle, S M Gross, D M Danks, et al.
Biochemical and Molecular Medicine
|
April 1, 1995
Normal metallothionein synthesis in fibroblasts obtained from children with Indian childhood cirrhosis or copper-associated childhood cirrhosis
S H Hahn, M S Tanner, D M Danks, et al.
Lancet (London, England)
|
April 14, 1990
Screening for cystic fibrosis: use of delta F508 mutation
F G Bowling, J J McGill, R W Shepherd, et al.
The Biochemical Journal
|
June 1, 1986
A study of the role of metallothionein in the inherited copper toxicosis of dogs
D M Hunt, S A Wake, J F Mercer, et al.
Australian Paediatric Journal
|
September 1, 1979
Hereditary hyperammonaemic syndromes--a six year experience
E A Haan, D M Danks, N J Hoogenraad, et al.
The Biochemical Journal
|
August 1, 1979
Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria
K H Choo, R G Cotton, D M Danks, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 1, 1987
Stability of protein and mRNA in human postmortem liver--analysis by two-dimensional gel electrophoresis
J M Finger, J F Mercer, R G Cotton, et al.
Page
of 26
Search research articles
Search
Showing results (171-180 of 255) with videos related to
Sort By:
Page
of 26
The Journal of Nutrition
|
November 1, 1990
Effects of cellular copper content on copper uptake and metallothionein and ceruloplasmin mRNA levels in mouse hepatocytes
H J McArdle, J F Mercer, A M Sargeson, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1980
Observations indicating the nature of the mutation in phenylketonuria
K H Choo, R G Cotton, I G Jennings, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome)
K Hayasaka, G K Brown, D M Danks, et al.
The American Journal of Physiology
|
June 1, 1990
Role of albumin's copper binding site in copper uptake by mouse hepatocytes
H J McArdle, S M Gross, D M Danks, et al.
Biochemical and Molecular Medicine
|
April 1, 1995
Normal metallothionein synthesis in fibroblasts obtained from children with Indian childhood cirrhosis or copper-associated childhood cirrhosis
S H Hahn, M S Tanner, D M Danks, et al.
Lancet (London, England)
|
April 14, 1990
Screening for cystic fibrosis: use of delta F508 mutation
F G Bowling, J J McGill, R W Shepherd, et al.
The Biochemical Journal
|
June 1, 1986
A study of the role of metallothionein in the inherited copper toxicosis of dogs
D M Hunt, S A Wake, J F Mercer, et al.
Australian Paediatric Journal
|
September 1, 1979
Hereditary hyperammonaemic syndromes--a six year experience
E A Haan, D M Danks, N J Hoogenraad, et al.
The Biochemical Journal
|
August 1, 1979
Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria
K H Choo, R G Cotton, D M Danks, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 1, 1987
Stability of protein and mRNA in human postmortem liver--analysis by two-dimensional gel electrophoresis
J M Finger, J F Mercer, R G Cotton, et al.
Page
of 26