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Hans T Bjornsson

Showing results (1-10 of 46) with videos related to

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Developmental Medicine and Child Neurology|November 22, 2019
Clinical epigenetics: a primer for the practitionerDeniz Aygun, Hans T Bjornsson
Human Molecular Genetics|January 29, 2020
Corrigendum to: Mendelian disorders of the epigenetic machinery: postnatal malleability and therapeutic prospectsJill A Fahrner, Hans T Bjornsson
Human Molecular Genetics|October 10, 2019
Mendelian disorders of the epigenetic machinery: postnatal malleability and therapeutic prospectsJill A Fahrner, Hans T Bjornsson
Annual Review of Genomics and Human Genetics|September 4, 2014
Mendelian disorders of the epigenetic machinery: tipping the balance of chromatin statesJill A Fahrner, Hans T Bjornsson
Seminars in Neurology|September 6, 2014
Abnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunctionJacqueline Weissman, Sakkubai Naidu, Hans T Bjornsson
American Journal of Human Genetics|August 18, 2020
Promoter CpG Density Predicts Downstream Gene Loss-of-Function IntoleranceLeandros Boukas, Hans T Bjornsson, Kasper D Hansen
Trends in Genetics : TIG|July 21, 2004
An integrated epigenetic and genetic approach to common human diseaseHans T Bjornsson, M Daniele Fallin, Andrew P Feinberg
Gene|February 1, 2006
Transposon-derived repeats in the human genome and 5-methylcytosine-associated mutations in adjacent genesHans T Bjornsson, Lotta M Ellingsen, Jon J Jonsson
Plos One|April 14, 2017
Embryonic loss of human females with partial trisomy 19 identifies region critical for the single active XBarbara R Migeon, Michael A Beer, Hans T Bjornsson
Gene|November 19, 2011
Distribution of a marker of germline methylation differs between major families of transposon-derived repeats in the human genomeMartin I Sigurdsson, Albert V Smith, Hans T Bjornsson, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Developmental Medicine and Child Neurology|November 22, 2019
Clinical epigenetics: a primer for the practitionerDeniz Aygun, Hans T Bjornsson
Human Molecular Genetics|January 29, 2020
Corrigendum to: Mendelian disorders of the epigenetic machinery: postnatal malleability and therapeutic prospectsJill A Fahrner, Hans T Bjornsson
Human Molecular Genetics|October 10, 2019
Mendelian disorders of the epigenetic machinery: postnatal malleability and therapeutic prospectsJill A Fahrner, Hans T Bjornsson
Annual Review of Genomics and Human Genetics|September 4, 2014
Mendelian disorders of the epigenetic machinery: tipping the balance of chromatin statesJill A Fahrner, Hans T Bjornsson
Seminars in Neurology|September 6, 2014
Abnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunctionJacqueline Weissman, Sakkubai Naidu, Hans T Bjornsson
American Journal of Human Genetics|August 18, 2020
Promoter CpG Density Predicts Downstream Gene Loss-of-Function IntoleranceLeandros Boukas, Hans T Bjornsson, Kasper D Hansen
Trends in Genetics : TIG|July 21, 2004
An integrated epigenetic and genetic approach to common human diseaseHans T Bjornsson, M Daniele Fallin, Andrew P Feinberg
Gene|February 1, 2006
Transposon-derived repeats in the human genome and 5-methylcytosine-associated mutations in adjacent genesHans T Bjornsson, Lotta M Ellingsen, Jon J Jonsson
Plos One|April 14, 2017
Embryonic loss of human females with partial trisomy 19 identifies region critical for the single active XBarbara R Migeon, Michael A Beer, Hans T Bjornsson
Gene|November 19, 2011
Distribution of a marker of germline methylation differs between major families of transposon-derived repeats in the human genomeMartin I Sigurdsson, Albert V Smith, Hans T Bjornsson, et al.
Pageof 5