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Biochemical Pharmacology
|
October 9, 1991
Effects of adenosine analogues on ATP concentrations in human erythrocytes. Further evidence for a route independent of adenosine kinase
R T Smolenski, C Montero, J A Duley, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
NAD synthesis in human erythrocytes: determination of the activities of some enzymes
M Rocchigiani, S Sestini, V Micheli, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Urinary uracil concentrations are a useful guide to genetic disorders associated with neurological deficits and abnormal pyrimidine metabolism
P M Davies, L D Fairbanks, J A Duley, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
December 2, 2004
Nucleotide degradation products in cerebrospinal fluid (CSF) in inherited and acquired pathologies
L D Fairbanks, J C Harris, J A Duley, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1980
Tienilic acid in the treatment of gout and hypertension
T Gibson, C Potter, H A Simmonds, et al.
The New England Journal of Medicine
|
July 21, 1977
Complete deficiency of adenine phosphoribosyltransferase. Report of a family
K J Van Acker, H A Simmonds, C Potter, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
Thiopurine methyltransferase activity and efficacy of azathioprine immunosuppression in transplant recipients
P R Chocair, J A Duley, H A Simmonds, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
HPLC assay of uridine monophosphate synthase (UMPS) in chorionic villus samples (CVS) and erythrocytes (RBC)
L D Fairbanks, J A Duley, A J Shores, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 1, 1990
Inosine triphosphate pyrophosphohydrolase deficiency in a kindred with adenosine deaminase deficiency
J A Duley, H A Simmonds, D A Hopkinson, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Heterogeneity of symptomatology in two male siblings with thymine uraciluria
M J Henderson, S Jones, P Walker, et al.
Page
of 25
Search research articles
Search
Showing results (101-110 of 250) with videos related to
Sort By:
Page
of 25
Biochemical Pharmacology
|
October 9, 1991
Effects of adenosine analogues on ATP concentrations in human erythrocytes. Further evidence for a route independent of adenosine kinase
R T Smolenski, C Montero, J A Duley, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
NAD synthesis in human erythrocytes: determination of the activities of some enzymes
M Rocchigiani, S Sestini, V Micheli, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Urinary uracil concentrations are a useful guide to genetic disorders associated with neurological deficits and abnormal pyrimidine metabolism
P M Davies, L D Fairbanks, J A Duley, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
December 2, 2004
Nucleotide degradation products in cerebrospinal fluid (CSF) in inherited and acquired pathologies
L D Fairbanks, J C Harris, J A Duley, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1980
Tienilic acid in the treatment of gout and hypertension
T Gibson, C Potter, H A Simmonds, et al.
The New England Journal of Medicine
|
July 21, 1977
Complete deficiency of adenine phosphoribosyltransferase. Report of a family
K J Van Acker, H A Simmonds, C Potter, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
Thiopurine methyltransferase activity and efficacy of azathioprine immunosuppression in transplant recipients
P R Chocair, J A Duley, H A Simmonds, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
HPLC assay of uridine monophosphate synthase (UMPS) in chorionic villus samples (CVS) and erythrocytes (RBC)
L D Fairbanks, J A Duley, A J Shores, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 1, 1990
Inosine triphosphate pyrophosphohydrolase deficiency in a kindred with adenosine deaminase deficiency
J A Duley, H A Simmonds, D A Hopkinson, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Heterogeneity of symptomatology in two male siblings with thymine uraciluria
M J Henderson, S Jones, P Walker, et al.
Page
of 25