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The New England Journal of Medicine
|
May 29, 1986
Screening for biotinidase deficiency
I C Lyon, E A Mitchell, E K Atherton, et al.
Journal of Paediatrics and Child Health
|
October 8, 2004
Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsy
J R Skinner, B Chong, M Fawkner, et al.
The New England Journal of Medicine
|
May 17, 1984
Absence of immune deficiency in hereditary orotic aciduria
D M Becroft, L I Phillips, D R Webster, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
June 1, 1986
Relationship of metabolism of 2'-, 3'- and 5'-adenine nucleotides to presynaptic inhibition of transmitter release in rat vas deferens
D R Webster, G D Boston, N H Holford, et al.
Cell Death and Differentiation
|
January 30, 2010
Cyclin-C-dependent cell-cycle entry is required for activation of non-homologous end joining DNA repair in postmitotic neurons
A Tomashevski, D R Webster, P Grammas, et al.
The Journal of Cell Biology
|
July 1, 1987
Assembly and turnover of detyrosinated tubulin in vivo
D R Webster, G G Gundersen, J C Bulinski, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1979
Purine and pyrimidine metabolism in hereditary oroticaciduria during a 15 year follow-up study
D R Webster, H A Simmonds, C F Potter, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
Problems of diagnosis in an adolescent with hypoxanthine-guanine phosphoribosyltransferase deficiency and acute renal failure
J S Cameron, H A Simmonds, D R Webster, et al.
Bioscience Reports
|
May 1, 1982
Formation and degradation of deoxyadenosine nucleotides in inherited adenosine deaminase deficiency
H A Simmonds, D R Webster, D Perrett, et al.
Biochemical Pharmacology
|
March 15, 1982
GTP depletion and other erythrocyte abnormalities in inherited PNP deficiency
H A Simmonds, A R Watson, D R Webster, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 76) with videos related to
Sort By:
Page
of 8
The New England Journal of Medicine
|
May 29, 1986
Screening for biotinidase deficiency
I C Lyon, E A Mitchell, E K Atherton, et al.
Journal of Paediatrics and Child Health
|
October 8, 2004
Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsy
J R Skinner, B Chong, M Fawkner, et al.
The New England Journal of Medicine
|
May 17, 1984
Absence of immune deficiency in hereditary orotic aciduria
D M Becroft, L I Phillips, D R Webster, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
June 1, 1986
Relationship of metabolism of 2'-, 3'- and 5'-adenine nucleotides to presynaptic inhibition of transmitter release in rat vas deferens
D R Webster, G D Boston, N H Holford, et al.
Cell Death and Differentiation
|
January 30, 2010
Cyclin-C-dependent cell-cycle entry is required for activation of non-homologous end joining DNA repair in postmitotic neurons
A Tomashevski, D R Webster, P Grammas, et al.
The Journal of Cell Biology
|
July 1, 1987
Assembly and turnover of detyrosinated tubulin in vivo
D R Webster, G G Gundersen, J C Bulinski, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1979
Purine and pyrimidine metabolism in hereditary oroticaciduria during a 15 year follow-up study
D R Webster, H A Simmonds, C F Potter, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
Problems of diagnosis in an adolescent with hypoxanthine-guanine phosphoribosyltransferase deficiency and acute renal failure
J S Cameron, H A Simmonds, D R Webster, et al.
Bioscience Reports
|
May 1, 1982
Formation and degradation of deoxyadenosine nucleotides in inherited adenosine deaminase deficiency
H A Simmonds, D R Webster, D Perrett, et al.
Biochemical Pharmacology
|
March 15, 1982
GTP depletion and other erythrocyte abnormalities in inherited PNP deficiency
H A Simmonds, A R Watson, D R Webster, et al.
Page
of 8