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H A Simmonds

Showing results (121-130 of 250) with videos related to

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The Journal of Biological Chemistry|December 15, 1995
T-lymphocytes from AIDS patients are unable to synthesize ribonucleotides de novo in response to mitogenic stimulation. Impaired pyrimidine responses are already evident at early stages of HIV-1 infectionM Bofill, L D Fairbanks, K Ruckemann, et al.
Bioscience Reports|February 1, 1989
ATP formation from deoxyadenosine in human erythrocytes: evidence for a hitherto unidentified route involving adenine and S-adenosylhomocysteine hydrolaseH A Simmonds, L D Fairbanks, J A Duley, et al.
Birth Defects Original Article Series|January 1, 1983
Prenatal diagnosis for severe combined immunodeficiencyD C Linch, C H Rodeck, H A Simmonds, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Evaluation of adenine concentration in plasma of patients with renal failure using improved ultrafiltration techniqueM Marlewski, R T Smolenski, A Laurence, et al.
The Biochemical Journal|August 1, 1976
The identification of 2,8-dihydroxyadenine, a new component of urinary stonesH A Simmonds, K J Van Acker, J S Cameron, et al.
QJM : Monthly Journal of the Association of Physicians|January 30, 2004
Familial juvenile hyperuricaemic nephropathyL D Fairbanks, A M Marinaki, H A Simmonds, et al.
Transplantation|May 1, 1992
The importance of thiopurine methyltransferase activity for the use of azathioprine in transplant recipientsP R Chocair, J A Duley, H A Simmonds, et al.
Journal of Inherited Metabolic Disease|June 1, 1997
When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indicationsH A Simmonds, J A Duley, L D Fairbanks, et al.
Advances in Experimental Medicine and Biology|January 1, 1979
Purine and pyrimidine metabolism in hereditary oroticaciduria during a 15 year follow-up studyD 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 failureJ S Cameron, H A Simmonds, D R Webster, et al.
Pageof 25

Showing results (121-130 of 250) with videos related to

Sort By:
Pageof 25
The Journal of Biological Chemistry|December 15, 1995
T-lymphocytes from AIDS patients are unable to synthesize ribonucleotides de novo in response to mitogenic stimulation. Impaired pyrimidine responses are already evident at early stages of HIV-1 infectionM Bofill, L D Fairbanks, K Ruckemann, et al.
Bioscience Reports|February 1, 1989
ATP formation from deoxyadenosine in human erythrocytes: evidence for a hitherto unidentified route involving adenine and S-adenosylhomocysteine hydrolaseH A Simmonds, L D Fairbanks, J A Duley, et al.
Birth Defects Original Article Series|January 1, 1983
Prenatal diagnosis for severe combined immunodeficiencyD C Linch, C H Rodeck, H A Simmonds, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Evaluation of adenine concentration in plasma of patients with renal failure using improved ultrafiltration techniqueM Marlewski, R T Smolenski, A Laurence, et al.
The Biochemical Journal|August 1, 1976
The identification of 2,8-dihydroxyadenine, a new component of urinary stonesH A Simmonds, K J Van Acker, J S Cameron, et al.
QJM : Monthly Journal of the Association of Physicians|January 30, 2004
Familial juvenile hyperuricaemic nephropathyL D Fairbanks, A M Marinaki, H A Simmonds, et al.
Transplantation|May 1, 1992
The importance of thiopurine methyltransferase activity for the use of azathioprine in transplant recipientsP R Chocair, J A Duley, H A Simmonds, et al.
Journal of Inherited Metabolic Disease|June 1, 1997
When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indicationsH A Simmonds, J A Duley, L D Fairbanks, et al.
Advances in Experimental Medicine and Biology|January 1, 1979
Purine and pyrimidine metabolism in hereditary oroticaciduria during a 15 year follow-up studyD 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 failureJ S Cameron, H A Simmonds, D R Webster, et al.
Pageof 25