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W Scherer

Showing results (361-370 of 915) with videos related to

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Cytogenetics and Cell Genetics|March 7, 2000
Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24M A Crackower, D S Sinasac, J R Lee, et al.
Scientific Reports|December 8, 2017
Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjectsIván de Jesús Ascencio-Montiel, Dalila Pinto, Esteban J Parra, et al.
G3 (Bethesda, Md.)|February 14, 2018
Genomic Context Analysis of <i>de Novo STXBP1</i> Mutations Identifies Evidence of Splice Site DNA-Motif Associated HotspotsMohammed Uddin, Marc Woodbury-Smith, Ada J S Chan, et al.
Atherosclerosis|August 12, 1998
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta HutteritesA P Boright, P W Connelly, J H Brunt, et al.
Pest Management Science|November 13, 2024
Efficacy and utility of isocycloseram a novel isoxazoline insecticide against urban pests and public health disease vectorsRaj Kumar Saran, Mark Hoppé, Sarah Mayor, et al.
Genes, Chromosomes & Cancer|August 19, 1999
Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridizationS Tosi, G Giudici, A Rambaldi, et al.
Cancer Letters|December 13, 2003
Chromosome 7q31 allelic imbalance and somatic mutations of RAY1/ST7 gene in colorectal cancerRiad Haddad, John B Vincent, Robert Gryfe, et al.
Canadian Psychiatric Association Journal|February 1, 1973
Instrumental control of autonomic responses with the use of a cognitive strategy. A case reportJ A Corson, C Bouchard, M W Scherer, et al.
Neurology|August 12, 2004
Progressive myoclonus epilepsy with polyglucosans (Lafora disease): evidence for a third locusE M Chan, S Omer, M Ahmed, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 27, 2004
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probandsJohn B Vincent, Debbie Kolozsvari, Wendy S Roberts, et al.
Pageof 92

Showing results (361-370 of 915) with videos related to

Sort By:
Pageof 92
Cytogenetics and Cell Genetics|March 7, 2000
Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24M A Crackower, D S Sinasac, J R Lee, et al.
Scientific Reports|December 8, 2017
Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjectsIván de Jesús Ascencio-Montiel, Dalila Pinto, Esteban J Parra, et al.
G3 (Bethesda, Md.)|February 14, 2018
Genomic Context Analysis of <i>de Novo STXBP1</i> Mutations Identifies Evidence of Splice Site DNA-Motif Associated HotspotsMohammed Uddin, Marc Woodbury-Smith, Ada J S Chan, et al.
Atherosclerosis|August 12, 1998
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta HutteritesA P Boright, P W Connelly, J H Brunt, et al.
Pest Management Science|November 13, 2024
Efficacy and utility of isocycloseram a novel isoxazoline insecticide against urban pests and public health disease vectorsRaj Kumar Saran, Mark Hoppé, Sarah Mayor, et al.
Genes, Chromosomes & Cancer|August 19, 1999
Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridizationS Tosi, G Giudici, A Rambaldi, et al.
Cancer Letters|December 13, 2003
Chromosome 7q31 allelic imbalance and somatic mutations of RAY1/ST7 gene in colorectal cancerRiad Haddad, John B Vincent, Robert Gryfe, et al.
Canadian Psychiatric Association Journal|February 1, 1973
Instrumental control of autonomic responses with the use of a cognitive strategy. A case reportJ A Corson, C Bouchard, M W Scherer, et al.
Neurology|August 12, 2004
Progressive myoclonus epilepsy with polyglucosans (Lafora disease): evidence for a third locusE M Chan, S Omer, M Ahmed, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 27, 2004
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probandsJohn B Vincent, Debbie Kolozsvari, Wendy S Roberts, et al.
Pageof 92