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W Scherer

Showing results (331-340 of 915) with videos related to

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Langmuir : the ACS Journal of Surfaces and Colloids|April 8, 2009
Transport of water in small poresShuangyan Xu, Gregory C Simmons, T S Mahadevan, et al.
Human Molecular Genetics|September 25, 1997
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
The Journal of Physical Chemistry. A|August 26, 2011
Experimental and theoretical charge density studies at subatomic resolutionA Fischer, D Tiana, W Scherer, et al.
Genomics|March 1, 1993
Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybridsS W Scherer, E J Neufeld, P M Lievens, et al.
Genomics|January 8, 1999
Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12S Egan, J A Herbrick, L C Tsui, et al.
Genome|June 26, 1999
Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymusM Y Hwang, Y J Kang, Y H Kim, et al.
The Journal of Biological Chemistry|August 14, 1999
Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damageA Jilani, D Ramotar, C Slack, et al.
American Journal of Human Genetics|July 13, 2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individualJ B Vincent, J A Herbrick, H M Gurling, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 19, 2020
Refining critical regions in 15q24 microdeletion syndrome pertaining to autismYi Liu, Yanqing Zhang, Mehdi Zarrei, et al.
American Journal of Medical Genetics. Part A|December 31, 2013
Clinical characteristics in patients with interstitial deletions of chromosome region 12q21-q22 and identification of a critical region associated with keratosis pilarisAlmundher Al-Maawali, Christian R Marshall, Stephen W Scherer, et al.
Pageof 92

Showing results (331-340 of 915) with videos related to

Sort By:
Pageof 92
Langmuir : the ACS Journal of Surfaces and Colloids|April 8, 2009
Transport of water in small poresShuangyan Xu, Gregory C Simmons, T S Mahadevan, et al.
Human Molecular Genetics|September 25, 1997
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
The Journal of Physical Chemistry. A|August 26, 2011
Experimental and theoretical charge density studies at subatomic resolutionA Fischer, D Tiana, W Scherer, et al.
Genomics|March 1, 1993
Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybridsS W Scherer, E J Neufeld, P M Lievens, et al.
Genomics|January 8, 1999
Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12S Egan, J A Herbrick, L C Tsui, et al.
Genome|June 26, 1999
Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymusM Y Hwang, Y J Kang, Y H Kim, et al.
The Journal of Biological Chemistry|August 14, 1999
Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damageA Jilani, D Ramotar, C Slack, et al.
American Journal of Human Genetics|July 13, 2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individualJ B Vincent, J A Herbrick, H M Gurling, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 19, 2020
Refining critical regions in 15q24 microdeletion syndrome pertaining to autismYi Liu, Yanqing Zhang, Mehdi Zarrei, et al.
American Journal of Medical Genetics. Part A|December 31, 2013
Clinical characteristics in patients with interstitial deletions of chromosome region 12q21-q22 and identification of a critical region associated with keratosis pilarisAlmundher Al-Maawali, Christian R Marshall, Stephen W Scherer, et al.
Pageof 92