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Thomas Haaf

Showing results (91-100 of 190) with videos related to

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Epigenetics|January 28, 2015
Epigenetic heterogeneity of developmentally important genes in human sperm: implications for assisted reproduction outcomeJuliane Kuhtz, Eberhard Schneider, Nady El Hajj, et al.
Ear and Hearing|February 6, 2016
Confirmation of PDZD7 as a Nonsyndromic Hearing Loss GeneBarbara Vona, Stanislav Lechno, Michaela A H Hofrichter, et al.
Aging|November 29, 2023
Effects of paternal and chronological age on <i>BEGAIN</i> methylation and its possible role in autismRamya Potabattula, Andreas Prell, Marcus Dittrich, et al.
Diabetes|December 5, 2012
Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitusNady El Hajj, Galyna Pliushch, Eberhard Schneider, et al.
European Journal of Medical Genetics|July 18, 2019
Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing lossMichaela A H Hofrichter, Julia Doll, Haleh Habibi, et al.
Cells|June 28, 2023
Genetic Characterization of Rat Hepatic Stellate Cell Line PAV-1Kiara Gäberlein, Sarah K Schröder, Indrajit Nanda, et al.
The American Journal of Pathology|January 23, 2010
Extreme methylation values of imprinted genes in human abortions and stillbirthsGalyna Pliushch, Eberhard Schneider, Daniela Weise, et al.
Epigenetics|March 8, 2016
CAF-like state in primary skin fibroblasts with constitutional BRCA1 epimutation sheds new light on tumor suppressor deficiency-related changes in healthy tissueAnna Etzold, Danuta Galetzka, Eva Weis, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2018
Phenotypic Characterization of DFNB16-associated Hearing LossDaniela Back, Wafaa Shehata-Dieler, Barbara Vona, et al.
Molecular Human Reproduction|December 17, 2009
Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conceptionUlrich Zechner, Galyna Pliushch, Eberhard Schneider, et al.
Pageof 19

Showing results (91-100 of 190) with videos related to

Sort By:
Pageof 19
Epigenetics|January 28, 2015
Epigenetic heterogeneity of developmentally important genes in human sperm: implications for assisted reproduction outcomeJuliane Kuhtz, Eberhard Schneider, Nady El Hajj, et al.
Ear and Hearing|February 6, 2016
Confirmation of PDZD7 as a Nonsyndromic Hearing Loss GeneBarbara Vona, Stanislav Lechno, Michaela A H Hofrichter, et al.
Aging|November 29, 2023
Effects of paternal and chronological age on <i>BEGAIN</i> methylation and its possible role in autismRamya Potabattula, Andreas Prell, Marcus Dittrich, et al.
Diabetes|December 5, 2012
Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitusNady El Hajj, Galyna Pliushch, Eberhard Schneider, et al.
European Journal of Medical Genetics|July 18, 2019
Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing lossMichaela A H Hofrichter, Julia Doll, Haleh Habibi, et al.
Cells|June 28, 2023
Genetic Characterization of Rat Hepatic Stellate Cell Line PAV-1Kiara Gäberlein, Sarah K Schröder, Indrajit Nanda, et al.
The American Journal of Pathology|January 23, 2010
Extreme methylation values of imprinted genes in human abortions and stillbirthsGalyna Pliushch, Eberhard Schneider, Daniela Weise, et al.
Epigenetics|March 8, 2016
CAF-like state in primary skin fibroblasts with constitutional BRCA1 epimutation sheds new light on tumor suppressor deficiency-related changes in healthy tissueAnna Etzold, Danuta Galetzka, Eva Weis, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2018
Phenotypic Characterization of DFNB16-associated Hearing LossDaniela Back, Wafaa Shehata-Dieler, Barbara Vona, et al.
Molecular Human Reproduction|December 17, 2009
Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conceptionUlrich Zechner, Galyna Pliushch, Eberhard Schneider, et al.
Pageof 19