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Cedric Shackleton

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The Journal of Steroid Biochemistry and Molecular Biology|March 2, 2010
Clinical steroid mass spectrometry: a 45-year history culminating in HPLC-MS/MS becoming an essential tool for patient diagnosisCedric Shackleton
Steroids|November 18, 2008
Steroid analysis and doping control 1960-1980: scientific developments and personal anecdotesCedric Shackleton
Steroids|November 20, 2003
Apparent pregnene hydroxylation deficiency (APHD): seeking the parentage of an orphan metabolomeCedric Shackleton, Ewa Malunowicz
Journal of the Endocrine Society|August 11, 2018
GC/MS in Recent Years Has Defined the Normal and Clinically Disordered Steroidome: Will It Soon Be Surpassed by LC/Tandem MS in This Role?Cedric Shackleton, Oscar J Pozo, Josep Marcos
Pediatrics International : Official Journal of the Japan Pediatric Society|October 20, 2004
Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylaseMasanori Adachi, Yumi Asakura, Katsuhiko Tachibana, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 10, 2010
Steroid profiling and analytics: going towards steromeUta Ceglarek, Cedric Shackleton, Frank Z Stanczyk, et al.
American Journal of Medical Genetics. Part A|August 19, 2004
Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotypeCedric Shackleton, Josep Marcos, Wiebke Arlt, et al.
The Journal of Steroid Biochemistry and Molecular Biology|September 1, 2010
Hair and skin sterols in normal mice and those with deficient dehydrosterol reductase (DHCR7), the enzyme associated with Smith-Lemli-Opitz syndromeMontserrat Serra, Xavier Matabosch, Lee Ying, et al.
Molecular Genetics and Metabolism Reports|September 9, 2015
Delivery of the 7-dehydrocholesterol reductase gene to the central nervous system using adeno-associated virus vector in a mouse model of Smith-Lemli-Opitz SyndromeSaloni Pasta, Omoye Akhile, Dorothy Tabron, et al.
Molecular Genetics and Metabolism Reports|July 16, 2014
Biochemical and Physiological Improvement in a Mouse Model of Smith-Lemli-Opitz Syndrome (SLOS) Following Gene Transfer with AAV VectorsLee Ying, Xavier Matabosch, Montserrat Serra, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
The Journal of Steroid Biochemistry and Molecular Biology|March 2, 2010
Clinical steroid mass spectrometry: a 45-year history culminating in HPLC-MS/MS becoming an essential tool for patient diagnosisCedric Shackleton
Steroids|November 18, 2008
Steroid analysis and doping control 1960-1980: scientific developments and personal anecdotesCedric Shackleton
Steroids|November 20, 2003
Apparent pregnene hydroxylation deficiency (APHD): seeking the parentage of an orphan metabolomeCedric Shackleton, Ewa Malunowicz
Journal of the Endocrine Society|August 11, 2018
GC/MS in Recent Years Has Defined the Normal and Clinically Disordered Steroidome: Will It Soon Be Surpassed by LC/Tandem MS in This Role?Cedric Shackleton, Oscar J Pozo, Josep Marcos
Pediatrics International : Official Journal of the Japan Pediatric Society|October 20, 2004
Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylaseMasanori Adachi, Yumi Asakura, Katsuhiko Tachibana, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 10, 2010
Steroid profiling and analytics: going towards steromeUta Ceglarek, Cedric Shackleton, Frank Z Stanczyk, et al.
American Journal of Medical Genetics. Part A|August 19, 2004
Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotypeCedric Shackleton, Josep Marcos, Wiebke Arlt, et al.
The Journal of Steroid Biochemistry and Molecular Biology|September 1, 2010
Hair and skin sterols in normal mice and those with deficient dehydrosterol reductase (DHCR7), the enzyme associated with Smith-Lemli-Opitz syndromeMontserrat Serra, Xavier Matabosch, Lee Ying, et al.
Molecular Genetics and Metabolism Reports|September 9, 2015
Delivery of the 7-dehydrocholesterol reductase gene to the central nervous system using adeno-associated virus vector in a mouse model of Smith-Lemli-Opitz SyndromeSaloni Pasta, Omoye Akhile, Dorothy Tabron, et al.
Molecular Genetics and Metabolism Reports|July 16, 2014
Biochemical and Physiological Improvement in a Mouse Model of Smith-Lemli-Opitz Syndrome (SLOS) Following Gene Transfer with AAV VectorsLee Ying, Xavier Matabosch, Montserrat Serra, et al.
Pageof 3