P C White|V Jenkins - JoVE Visualize

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Molecular Endocrinology (Baltimore, Md.)|May 1, 1997

Angiotensin II and potassium regulate human CYP11B2 transcription through common cis-elementsC D Clyne, Y Zhang, L Slutsker, et al.

Human Genetics|April 1, 1994

Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blotP W Speiser, P C White, J Dupont, et al.

Journal of Dental Research|October 8, 2015

Neutrophil Extracellular Traps in Periodontitis: A Web of IntrigueP C White, I J Chicca, P R Cooper, et al.

Journal of Internal Medicine|August 11, 1998

Associations between aldosterone synthase gene polymorphism and the adrenocortical function in malesA Hautanena, L Lankinen, M Kupari, et al.

Immunogenetics|January 1, 1992

Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7A Selvakumar, B K Mohanraj, R L Eddy, et al.

Journal of Cell Science|November 11, 2017

Effects of mutating α-tubulin lysine 40 on sensory dendrite developmentBrian V Jenkins, Harriet A J Saunders, Helena L Record, et al.

Theranostics|January 28, 2014

Gold nanocage-photosensitizer conjugates for dual-modal image-guided enhanced photodynamic therapyAvinash Srivatsan, Samir V Jenkins, Mansik Jeon, et al.

Clinical Science (London, England : 1979)|December 1, 1991

Metabolic balance studies of mineral supplementation in osteoporosisT Stamp, M Katakity, A J Goldstein, et al.

Clinical Science (London, England : 1979)|August 1, 1988

Fluoride therapy in osteoporosis: acute effects on parathyroid and mineral homoeostasisT C Stamp, M V Jenkins, N Loveridge, et al.

Human Molecular Genetics|December 1, 1996

Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigreesD J Day, P W Speiser, E Schulze, et al.

Pageof 29

Showing results (171-180 of 284) with videos related to

Sort By:

Pageof 29

Molecular Endocrinology (Baltimore, Md.)|May 1, 1997

Angiotensin II and potassium regulate human CYP11B2 transcription through common cis-elementsC D Clyne, Y Zhang, L Slutsker, et al.

Human Genetics|April 1, 1994

Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blotP W Speiser, P C White, J Dupont, et al.

Journal of Dental Research|October 8, 2015

Neutrophil Extracellular Traps in Periodontitis: A Web of IntrigueP C White, I J Chicca, P R Cooper, et al.

Journal of Internal Medicine|August 11, 1998

Associations between aldosterone synthase gene polymorphism and the adrenocortical function in malesA Hautanena, L Lankinen, M Kupari, et al.

Immunogenetics|January 1, 1992

Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7A Selvakumar, B K Mohanraj, R L Eddy, et al.

Journal of Cell Science|November 11, 2017

Effects of mutating α-tubulin lysine 40 on sensory dendrite developmentBrian V Jenkins, Harriet A J Saunders, Helena L Record, et al.

Theranostics|January 28, 2014

Gold nanocage-photosensitizer conjugates for dual-modal image-guided enhanced photodynamic therapyAvinash Srivatsan, Samir V Jenkins, Mansik Jeon, et al.

Clinical Science (London, England : 1979)|December 1, 1991

Metabolic balance studies of mineral supplementation in osteoporosisT Stamp, M Katakity, A J Goldstein, et al.

Clinical Science (London, England : 1979)|August 1, 1988

Fluoride therapy in osteoporosis: acute effects on parathyroid and mineral homoeostasisT C Stamp, M V Jenkins, N Loveridge, et al.

Human Molecular Genetics|December 1, 1996

Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigreesD J Day, P W Speiser, E Schulze, et al.

Pageof 29