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M Rennert

Showing results (191-200 of 250) with videos related to

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Journal of Pediatric Surgery|September 1, 1989
Familial congenital diaphragmatic hernia is an autosomal recessive variantD C Hitch, J A Carson, E I Smith, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Severe skeletal complications in Japanese patients with type 1 Gaucher diseaseH Ida, O M Rennert, S Kato, et al.
European Journal of Endocrinology|August 14, 1998
Testicular seminoma in a patient with a constitutively activating mutation of the luteinizing hormone/chorionic gonadotropin receptorM M Martin, S M Wu, A L Martin, et al.
Biochemical and Biophysical Research Communications|March 16, 1983
Androgen receptors in the brain of neonatal normal male and androgen insensitive ratsK W Chung, W Y Chan, J B Dressler, et al.
Pharmacology, Biochemistry, and Behavior|July 1, 1987
Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCMT W Seale, K A Abla, T H Roderick, et al.
The Biochemical Journal|October 15, 1981
On the formation of amino acids deriving from spermidine and spermineN Seiler, B Knödgen, M W Gittos, et al.
Fertility and Sterility|August 20, 2010
Methylation patterns of Brahma during spermatogenesis and oogenesis: potential implicationsSohan R Nagrani, Eric D Levens, Vanessa Baxendale, et al.
Journal of Molecular Neuroscience : MN|September 25, 2015
Shared Pathways Among Autism Candidate Genes Determined by Co-expression Network Analysis of the Developing Human Brain TranscriptomeAhmed Mahfouz, Mark N Ziats, Owen M Rennert, et al.
Differentiation; Research in Biological Diversity|December 1, 2005
A novel function of differentiation revealed by cDNA microarray profiling of p75NTR-regulated gene expressionAngèle Nalbandian, Alan L Y Pang, Owen M Rennert, et al.
Clinical Genetics|November 1, 1984
A supernumerary microchromosome in amniotic cell cultures and talipes equinovarus in a live born femaleR S Muneer, J R Himes, R M Payne-Howell, et al.
Pageof 25

Showing results (191-200 of 250) with videos related to

Sort By:
Pageof 25
Journal of Pediatric Surgery|September 1, 1989
Familial congenital diaphragmatic hernia is an autosomal recessive variantD C Hitch, J A Carson, E I Smith, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Severe skeletal complications in Japanese patients with type 1 Gaucher diseaseH Ida, O M Rennert, S Kato, et al.
European Journal of Endocrinology|August 14, 1998
Testicular seminoma in a patient with a constitutively activating mutation of the luteinizing hormone/chorionic gonadotropin receptorM M Martin, S M Wu, A L Martin, et al.
Biochemical and Biophysical Research Communications|March 16, 1983
Androgen receptors in the brain of neonatal normal male and androgen insensitive ratsK W Chung, W Y Chan, J B Dressler, et al.
Pharmacology, Biochemistry, and Behavior|July 1, 1987
Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCMT W Seale, K A Abla, T H Roderick, et al.
The Biochemical Journal|October 15, 1981
On the formation of amino acids deriving from spermidine and spermineN Seiler, B Knödgen, M W Gittos, et al.
Fertility and Sterility|August 20, 2010
Methylation patterns of Brahma during spermatogenesis and oogenesis: potential implicationsSohan R Nagrani, Eric D Levens, Vanessa Baxendale, et al.
Journal of Molecular Neuroscience : MN|September 25, 2015
Shared Pathways Among Autism Candidate Genes Determined by Co-expression Network Analysis of the Developing Human Brain TranscriptomeAhmed Mahfouz, Mark N Ziats, Owen M Rennert, et al.
Differentiation; Research in Biological Diversity|December 1, 2005
A novel function of differentiation revealed by cDNA microarray profiling of p75NTR-regulated gene expressionAngèle Nalbandian, Alan L Y Pang, Owen M Rennert, et al.
Clinical Genetics|November 1, 1984
A supernumerary microchromosome in amniotic cell cultures and talipes equinovarus in a live born femaleR S Muneer, J R Himes, R M Payne-Howell, et al.
Pageof 25