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Aharon Razin

Showing results (11-20 of 22) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 10, 2009
Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domainYotam Kaufman, Maya Heled, Jonathan Perk, et al.
Human Molecular Genetics|March 11, 2005
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expressionKirill Makedonski, Liron Abuhatzira, Yotam Kaufman, et al.
Human Molecular Genetics|February 14, 2004
Control elements within the PWS/AS imprinting box and their function in the imprinting processBoris Kantor, Kirill Makedonski, Yael Green-Finberg, et al.
Autonomic Neuroscience : Basic & Clinical|November 26, 2013
Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patientsDavid Cheishvili, Efrat Laiba, David Rekhtman, et al.
The EMBO Journal|November 2, 2002
The imprinting mechanism of the Prader-Willi/Angelman regional control centerJonathan Perk, Kirill Makedonski, Laura Lande, et al.
Journal of Molecular Neuroscience : MN|May 1, 2016
Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot StudyDavid Cheishvili, Channa Maayan, Naama Holzer, et al.
Plos One|April 25, 2014
IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formationDavid Cheishvili, Paula Dietrich, Channa Maayan, et al.
Human Molecular Genetics|January 29, 2011
IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomiaDavid Cheishvili, Channa Maayan, Rachel Cohen-Kupiec, et al.
Human Genetics|September 1, 2005
Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosisLiron Abuhatzira, Kirill Makedonski, Yael Petel Galil, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2017
Islet cells share promoter hypomethylation independently of expression, but exhibit cell-type-specific methylation in enhancersDaniel Neiman, Joshua Moss, Merav Hecht, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2009
Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domainYotam Kaufman, Maya Heled, Jonathan Perk, et al.
Human Molecular Genetics|March 11, 2005
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expressionKirill Makedonski, Liron Abuhatzira, Yotam Kaufman, et al.
Human Molecular Genetics|February 14, 2004
Control elements within the PWS/AS imprinting box and their function in the imprinting processBoris Kantor, Kirill Makedonski, Yael Green-Finberg, et al.
Autonomic Neuroscience : Basic & Clinical|November 26, 2013
Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patientsDavid Cheishvili, Efrat Laiba, David Rekhtman, et al.
The EMBO Journal|November 2, 2002
The imprinting mechanism of the Prader-Willi/Angelman regional control centerJonathan Perk, Kirill Makedonski, Laura Lande, et al.
Journal of Molecular Neuroscience : MN|May 1, 2016
Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot StudyDavid Cheishvili, Channa Maayan, Naama Holzer, et al.
Plos One|April 25, 2014
IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formationDavid Cheishvili, Paula Dietrich, Channa Maayan, et al.
Human Molecular Genetics|January 29, 2011
IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomiaDavid Cheishvili, Channa Maayan, Rachel Cohen-Kupiec, et al.
Human Genetics|September 1, 2005
Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosisLiron Abuhatzira, Kirill Makedonski, Yael Petel Galil, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2017
Islet cells share promoter hypomethylation independently of expression, but exhibit cell-type-specific methylation in enhancersDaniel Neiman, Joshua Moss, Merav Hecht, et al.
Pageof 3