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C H Shackleton

Showing results (91-100 of 175) with videos related to

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Rapid Communications in Mass Spectrometry : RCM|October 1, 1993
Taxoid side-chain structure determination by electrospray ionization tandem mass spectrometryF Bitsch, C H Shackleton, W Ma, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Long-lived testosterone esters in the ratW Borg, C H Shackleton, S L Pahuja, et al.
Journal of Steroid Biochemistry|June 1, 1978
Urinary steroid excretion in 17 alpha-hydroxylase deficiencyJ W Honour, J Tourniaire, E G Biglieri, et al.
Journal of Steroid Biochemistry|August 1, 1979
Reduction of aldosterone by anaerobic bacteria: origin of urinary 21-deoxy metabolites in manV D Bokkenheuser, J Winter, J W Honour, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1979
Metabolism of radiolabeled corticosterone in an adult with the 17 alpha-hydroxylase deficiency syndromeC H Shackleton, E G Biglieri, E Roitman, et al.
Hormone Research|January 11, 2001
Apparent cortisone reductase deficiency: a rare cause of hyperandrogenemia and hypercortisolismA Biason-Lauber, S L Suter, C H Shackleton, et al.
Steroids|July 1, 1996
Intact noncovalent dimer of estrogen receptor ligand-binding domain can be detected by electrospray ionization mass spectrometryH E Witkowska, B N Green, M Carlquist, et al.
Endocrinology|December 1, 1991
Androgen metabolism by porcine granulosa cells during the process of luteinization in vitro: identification of 19-oic-androstenedione as a major metabolite and possible precursor for the formation of C18 neutral steroidsW M Garrett, D J Hoover, C H Shackleton, et al.
Lancet (London, England)|February 24, 1990
5 alpha-reductase activity in polycystic ovary syndromeP M Stewart, C H Shackleton, G H Beastall, et al.
Clinical Endocrinology|May 1, 1981
Familial congenital Cushing's syndrome due to bilateral nodular adrenal hyperplasiaM D Donaldson, D B Grant, M J O'Hare, et al.
Pageof 18

Showing results (91-100 of 175) with videos related to

Sort By:
Pageof 18
Rapid Communications in Mass Spectrometry : RCM|October 1, 1993
Taxoid side-chain structure determination by electrospray ionization tandem mass spectrometryF Bitsch, C H Shackleton, W Ma, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Long-lived testosterone esters in the ratW Borg, C H Shackleton, S L Pahuja, et al.
Journal of Steroid Biochemistry|June 1, 1978
Urinary steroid excretion in 17 alpha-hydroxylase deficiencyJ W Honour, J Tourniaire, E G Biglieri, et al.
Journal of Steroid Biochemistry|August 1, 1979
Reduction of aldosterone by anaerobic bacteria: origin of urinary 21-deoxy metabolites in manV D Bokkenheuser, J Winter, J W Honour, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1979
Metabolism of radiolabeled corticosterone in an adult with the 17 alpha-hydroxylase deficiency syndromeC H Shackleton, E G Biglieri, E Roitman, et al.
Hormone Research|January 11, 2001
Apparent cortisone reductase deficiency: a rare cause of hyperandrogenemia and hypercortisolismA Biason-Lauber, S L Suter, C H Shackleton, et al.
Steroids|July 1, 1996
Intact noncovalent dimer of estrogen receptor ligand-binding domain can be detected by electrospray ionization mass spectrometryH E Witkowska, B N Green, M Carlquist, et al.
Endocrinology|December 1, 1991
Androgen metabolism by porcine granulosa cells during the process of luteinization in vitro: identification of 19-oic-androstenedione as a major metabolite and possible precursor for the formation of C18 neutral steroidsW M Garrett, D J Hoover, C H Shackleton, et al.
Lancet (London, England)|February 24, 1990
5 alpha-reductase activity in polycystic ovary syndromeP M Stewart, C H Shackleton, G H Beastall, et al.
Clinical Endocrinology|May 1, 1981
Familial congenital Cushing's syndrome due to bilateral nodular adrenal hyperplasiaM D Donaldson, D B Grant, M J O'Hare, et al.
Pageof 18