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A Sahota

Showing results (41-50 of 90) with videos related to

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Human Mutation|January 1, 1994
Occurrence of a missense mutation in one allele and a seven basepair deletion in the other allele in a patient with adenine phosphoribosyltransferase deficiencyA Sahota, J Chen, S Bye, et al.
Experimental Hematology|July 31, 1999
Pattern of localization of primitive hematopoietic cells in vivo using a novel mouse modelR Bolante-Cervantes, S Li, A Sahota, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 4, 2021
Vertebroplasty for vertebral fragility fractures in the 'very elderly': experience from a regional UK spine unitA Sahota, T Ong, A Kumar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1983
Methylthioadenosine phosphorylase activity in human erythrocytesA Sahota, D R Webster, C F Potter, et al.
Clinical Chemistry|July 1, 1996
Improved procedure for eluting DNA from dried blood spotsM Yang, H C Hendrie, K S Hall, et al.
The Clinical Investigator|July 1, 1994
Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasisS Bye, R Mallmann, J Duley, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|November 18, 1997
The association between Apo E genotype and depressive symptoms in elderly African-American subjectsC A Class, F W Unverzagt, S Gao, et al.
Ciba Foundation Symposium|January 1, 1978
Purine metabolism in adenosine deaminase deficiencyH A Simmonds, A Sahota, C F Potter, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Neonatal screening for dihydropteridine reductase deficiencyA Sahota, J A Blair, P A Barford, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Adenosine and deoxyadenosine metabolism in the erythrocytes of a patient with adenosine deaminase deficiencyA Sahota, H A Simmonds, C F Potter, et al.
Pageof 9

Showing results (41-50 of 90) with videos related to

Sort By:
Pageof 9
Human Mutation|January 1, 1994
Occurrence of a missense mutation in one allele and a seven basepair deletion in the other allele in a patient with adenine phosphoribosyltransferase deficiencyA Sahota, J Chen, S Bye, et al.
Experimental Hematology|July 31, 1999
Pattern of localization of primitive hematopoietic cells in vivo using a novel mouse modelR Bolante-Cervantes, S Li, A Sahota, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 4, 2021
Vertebroplasty for vertebral fragility fractures in the 'very elderly': experience from a regional UK spine unitA Sahota, T Ong, A Kumar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1983
Methylthioadenosine phosphorylase activity in human erythrocytesA Sahota, D R Webster, C F Potter, et al.
Clinical Chemistry|July 1, 1996
Improved procedure for eluting DNA from dried blood spotsM Yang, H C Hendrie, K S Hall, et al.
The Clinical Investigator|July 1, 1994
Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasisS Bye, R Mallmann, J Duley, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|November 18, 1997
The association between Apo E genotype and depressive symptoms in elderly African-American subjectsC A Class, F W Unverzagt, S Gao, et al.
Ciba Foundation Symposium|January 1, 1978
Purine metabolism in adenosine deaminase deficiencyH A Simmonds, A Sahota, C F Potter, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Neonatal screening for dihydropteridine reductase deficiencyA Sahota, J A Blair, P A Barford, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Adenosine and deoxyadenosine metabolism in the erythrocytes of a patient with adenosine deaminase deficiencyA Sahota, H A Simmonds, C F Potter, et al.
Pageof 9