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Horsthemke

Showing results (311-320 of 368) with videos related to

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Journal of Medical Genetics|October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndromeB Horsthemke, A Maat-Kievit, E Sleegers, et al.
American Journal of Human Genetics|August 1, 1990
Microdissection of the fragile X regionR N MacKinnon, M C Hirst, M V Bell, et al.
Plos One|December 5, 2012
Parental diabetes: the Akita mouse as a model of the effects of maternal and paternal hyperglycemia in wildtype offspringCorinna Grasemann, Maureen J Devlin, Paulina A Rzeczkowska, et al.
Nature Genetics|January 13, 1998
Association of a human G-protein beta3 subunit variant with hypertensionW Siffert, D Rosskopf, G Siffert, et al.
Genomics|December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN geneA Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Cytogenetic and Genome Research|October 29, 2019
Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris SyndromeAlexander Kalmbach, Christopher Schröder, Ludger Klein-Hitpass, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15M Runte, C Färber, C Lich, et al.
Scientific Reports|October 17, 2022
No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorderElisabeth Hummel, Magdeldin Elgizouli, Maurizio Sicorello, et al.
The Journal of Biological Chemistry|March 15, 2017
Multiple roles of filopodial dynamics in particle capture and phagocytosis and phenotypes of Cdc42 and Myo10 deletionMarkus Horsthemke, Anne C Bachg, Katharina Groll, et al.
Nature|January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinismE M Rinchik, S J Bultman, B Horsthemke, et al.
Pageof 37

Showing results (311-320 of 368) with videos related to

Sort By:
Pageof 37
Journal of Medical Genetics|October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndromeB Horsthemke, A Maat-Kievit, E Sleegers, et al.
American Journal of Human Genetics|August 1, 1990
Microdissection of the fragile X regionR N MacKinnon, M C Hirst, M V Bell, et al.
Plos One|December 5, 2012
Parental diabetes: the Akita mouse as a model of the effects of maternal and paternal hyperglycemia in wildtype offspringCorinna Grasemann, Maureen J Devlin, Paulina A Rzeczkowska, et al.
Nature Genetics|January 13, 1998
Association of a human G-protein beta3 subunit variant with hypertensionW Siffert, D Rosskopf, G Siffert, et al.
Genomics|December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN geneA Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Cytogenetic and Genome Research|October 29, 2019
Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris SyndromeAlexander Kalmbach, Christopher Schröder, Ludger Klein-Hitpass, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15M Runte, C Färber, C Lich, et al.
Scientific Reports|October 17, 2022
No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorderElisabeth Hummel, Magdeldin Elgizouli, Maurizio Sicorello, et al.
The Journal of Biological Chemistry|March 15, 2017
Multiple roles of filopodial dynamics in particle capture and phagocytosis and phenotypes of Cdc42 and Myo10 deletionMarkus Horsthemke, Anne C Bachg, Katharina Groll, et al.
Nature|January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinismE M Rinchik, S J Bultman, B Horsthemke, et al.
Pageof 37