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G Rumsby

Showing results (101-110 of 111) with videos related to

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Clinical Endocrinology|May 14, 1998
Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acneL S Ostlere, G Rumsby, P Holownia, et al.
Developmental Biology|September 24, 2004
Specific PKC isoforms regulate blastocoel formation during mouse preimplantation developmentJudith J Eckert, Amanda McCallum, Andrew Mears, et al.
Developmental Biology|November 8, 2005
Relative contribution of cell contact pattern, specific PKC isoforms and gap junctional communication in tight junction assembly in the mouse early embryoJudith J Eckert, Amanda McCallum, Andrew Mears, et al.
Human Genetics|July 1, 1994
Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase geneC J Danpure, G M Birdsey, G Rumsby, et al.
British Journal of Cancer|November 2, 2019
Phospholipase D2 in prostate cancer: protein expression changes with Gleason scoreAmanda R Noble, Karen Hogg, Rakesh Suman, et al.
The Biochemical Journal|January 15, 1994
A role for protein kinase C subtypes alpha and epsilon in phorbol-ester-enhanced K(+)- and carbachol-evoked noradrenaline release from the human neuroblastoma SH-SY5YN A Turner, M G Rumsby, J H Walker, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 1, 1997
A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: lack of relationship between genotype, enzymic phenotype, and disease severityB Hoppe, C J Danpure, G Rumsby, et al.
Clinical Endocrinology|April 1, 1980
Familial male pseudohermaphroditism due to deficiency of 5 alpha-reductaseM O Savage, M A Preece, S L Jeffcoate, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2006
A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiencyA M Brooke, N F Taylor, J H Shepherd, et al.
Journal of Medical Genetics|January 14, 2000
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?W Reardon, A Smith, J W Honour, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
Clinical Endocrinology|May 14, 1998
Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acneL S Ostlere, G Rumsby, P Holownia, et al.
Developmental Biology|September 24, 2004
Specific PKC isoforms regulate blastocoel formation during mouse preimplantation developmentJudith J Eckert, Amanda McCallum, Andrew Mears, et al.
Developmental Biology|November 8, 2005
Relative contribution of cell contact pattern, specific PKC isoforms and gap junctional communication in tight junction assembly in the mouse early embryoJudith J Eckert, Amanda McCallum, Andrew Mears, et al.
Human Genetics|July 1, 1994
Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase geneC J Danpure, G M Birdsey, G Rumsby, et al.
British Journal of Cancer|November 2, 2019
Phospholipase D2 in prostate cancer: protein expression changes with Gleason scoreAmanda R Noble, Karen Hogg, Rakesh Suman, et al.
The Biochemical Journal|January 15, 1994
A role for protein kinase C subtypes alpha and epsilon in phorbol-ester-enhanced K(+)- and carbachol-evoked noradrenaline release from the human neuroblastoma SH-SY5YN A Turner, M G Rumsby, J H Walker, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 1, 1997
A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: lack of relationship between genotype, enzymic phenotype, and disease severityB Hoppe, C J Danpure, G Rumsby, et al.
Clinical Endocrinology|April 1, 1980
Familial male pseudohermaphroditism due to deficiency of 5 alpha-reductaseM O Savage, M A Preece, S L Jeffcoate, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2006
A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiencyA M Brooke, N F Taylor, J H Shepherd, et al.
Journal of Medical Genetics|January 14, 2000
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?W Reardon, A Smith, J W Honour, et al.
Pageof 12