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Horsthemke

Showing results (331-340 of 368) with videos related to

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Scientific Reports|July 25, 2022
Evidence for correlations between BMI-associated SNPs and circRNAsLuisa Sophie Rajcsanyi, Inga Diebels, Lydia Pastoors, et al.
Cancer Research|April 20, 2001
Partial deletions of the long and short arm of chromosome 3 point to two tumor suppressor genes in uveal melanomaF Tschentscher, G Prescher, D E Horsman, et al.
Nature Genetics|June 25, 2013
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3Marcel Martin, Lars Maßhöfer, Petra Temming, et al.
European Journal of Human Genetics : EJHG|July 14, 2016
Novel microdeletions on chromosome 14q32.2 suggest a potential role for non-coding RNAs in Kagami-Ogata syndromeIlse M van der Werf, Karin Buiting, Christina Czeschik, et al.
Aging Cell|September 20, 2020
A germ cell-specific ageing pattern in otherwise healthy menSandra Laurentino, Jann-Frederik Cremers, Bernhard Horsthemke, et al.
Epigenetics & Chromatin|July 28, 2017
Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential functionChristopher Schröder, Elsa Leitão, Stefan Wallner, et al.
American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Scientific Reports|January 26, 2019
Phenotypic analysis of Myo10 knockout (Myo10<sup>tm2/tm2</sup>) mice lacking full-length (motorized) but not brain-specific headless myosin XAnne C Bachg, Markus Horsthemke, Boris V Skryabin, et al.
Orphanet Journal of Rare Diseases|October 20, 2020
The adult phenotype of Schaaf-Yang syndromeFelix Marbach, Magdeldin Elgizouli, Megan Rech, et al.
Pageof 37

Showing results (331-340 of 368) with videos related to

Sort By:
Pageof 37
Scientific Reports|July 25, 2022
Evidence for correlations between BMI-associated SNPs and circRNAsLuisa Sophie Rajcsanyi, Inga Diebels, Lydia Pastoors, et al.
Cancer Research|April 20, 2001
Partial deletions of the long and short arm of chromosome 3 point to two tumor suppressor genes in uveal melanomaF Tschentscher, G Prescher, D E Horsman, et al.
Nature Genetics|June 25, 2013
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3Marcel Martin, Lars Maßhöfer, Petra Temming, et al.
European Journal of Human Genetics : EJHG|July 14, 2016
Novel microdeletions on chromosome 14q32.2 suggest a potential role for non-coding RNAs in Kagami-Ogata syndromeIlse M van der Werf, Karin Buiting, Christina Czeschik, et al.
Aging Cell|September 20, 2020
A germ cell-specific ageing pattern in otherwise healthy menSandra Laurentino, Jann-Frederik Cremers, Bernhard Horsthemke, et al.
Epigenetics & Chromatin|July 28, 2017
Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential functionChristopher Schröder, Elsa Leitão, Stefan Wallner, et al.
American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Scientific Reports|January 26, 2019
Phenotypic analysis of Myo10 knockout (Myo10<sup>tm2/tm2</sup>) mice lacking full-length (motorized) but not brain-specific headless myosin XAnne C Bachg, Markus Horsthemke, Boris V Skryabin, et al.
Orphanet Journal of Rare Diseases|October 20, 2020
The adult phenotype of Schaaf-Yang syndromeFelix Marbach, Magdeldin Elgizouli, Megan Rech, et al.
Pageof 37