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S Seneca

Showing results (1-10 of 60) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
DNA diagnosis of X-linked adrenoleukodystrophyS Seneca, W Lissens
Journal of Inherited Metabolic Disease|July 1, 1997
Molecular analysis in 23 Hunter disease familiesW Lissens, S Seneca, I Liebaers
Current Genetics|February 1, 1988
Arginine repression of the Saccharomyces cerevisiae ARG1 gene. Comparison of the ARG1 and ARG3 control regionsM Crabeel, S Seneca, K Devos, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Pyruvate dehydrogenase E1 alpha deficiency in a family: different clinical presentation in two siblingsL De Meirleir, N Specola, S Seneca, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Importance of sequence analysis in NARP syndromeS Seneca, L De Meirleir, I Liebaers, et al.
Andrology|April 11, 2017
Are AZFb deletions always incompatible with sperm production?K Stouffs, V Vloeberghs, A Gheldof, et al.
Journal of Medical Genetics|July 21, 2010
Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the diseaseC Spits, S Seneca, P Hilven, et al.
Oncogene|March 1, 1991
Ets1, when fused to the GAL4 DNA binding domain, efficiently enhances galactose promotor dependent gene expression in yeastS Seneca, B Punyammalee, M Bailly, et al.
Pediatric Neurology|October 1, 1995
Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 geneL De Meirleir, S Seneca, W Lissens, et al.
The Netherlands Journal of Medicine|July 26, 2017
A new mutation in the calcium-sensing receptor gene causing hypocalcaemia: case report of a father and two sonsM K Schoutteten, B Bravenboer, S Seneca, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1995
DNA diagnosis of X-linked adrenoleukodystrophyS Seneca, W Lissens
Journal of Inherited Metabolic Disease|July 1, 1997
Molecular analysis in 23 Hunter disease familiesW Lissens, S Seneca, I Liebaers
Current Genetics|February 1, 1988
Arginine repression of the Saccharomyces cerevisiae ARG1 gene. Comparison of the ARG1 and ARG3 control regionsM Crabeel, S Seneca, K Devos, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Pyruvate dehydrogenase E1 alpha deficiency in a family: different clinical presentation in two siblingsL De Meirleir, N Specola, S Seneca, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Importance of sequence analysis in NARP syndromeS Seneca, L De Meirleir, I Liebaers, et al.
Andrology|April 11, 2017
Are AZFb deletions always incompatible with sperm production?K Stouffs, V Vloeberghs, A Gheldof, et al.
Journal of Medical Genetics|July 21, 2010
Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the diseaseC Spits, S Seneca, P Hilven, et al.
Oncogene|March 1, 1991
Ets1, when fused to the GAL4 DNA binding domain, efficiently enhances galactose promotor dependent gene expression in yeastS Seneca, B Punyammalee, M Bailly, et al.
Pediatric Neurology|October 1, 1995
Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 geneL De Meirleir, S Seneca, W Lissens, et al.
The Netherlands Journal of Medicine|July 26, 2017
A new mutation in the calcium-sensing receptor gene causing hypocalcaemia: case report of a father and two sonsM K Schoutteten, B Bravenboer, S Seneca, et al.
Pageof 6