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Showing results (121-130 of 129) with videos related to

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Nucleic Acids Research|September 13, 2023
CRISPR screens in sister chromatid cohesion defective cells reveal PAXIP1-PAGR1 as regulator of chromatin association of cohesinJanne J M van Schie, Klaas de Lint, Thom M Molenaar, et al.
Epigenetics & Chromatin|December 31, 2016
The detailed 3D multi-loop aggregate/rosette chromatin architecture and functional dynamic organization of the human and mouse genomesTobias A Knoch, Malte Wachsmuth, Nick Kepper, et al.
Micropublication Biology|October 6, 2025
Cells stably expressing shRNA against MYO10 display altered cell motilityJoanna A Mas, Chase E Cristella, Vu Hao M N Phan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2013
Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cellsJessica Zuin, Jesse R Dixon, Michael I J A van der Reijden, et al.
Cell Reports|May 21, 2020
MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange SyndromeIlaria Parenti, Farah Diab, Sara Ruiz Gil, et al.
Clinical Genetics|December 17, 2015
Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk predictionI Parenti, C Gervasini, J Pozojevic, et al.
Brain : a Journal of Neurology|July 24, 2019
Cohesin complex-associated holoprosencephalyPaul Kruszka, Seth I Berger, Valentina Casa, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Pathogenic variants in the cohesin loader subunit MAU2 lead to a new Cornelia de Lange Syndrome subtypeIlaria Parenti, Alina Hesters, Marta Gil-Salvador, et al.
Nature Communications|March 30, 2026
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtypeIlaria Parenti, Alina Hesters, Marta Gil-Salvador, et al.
Pageof 13

Showing results (121-130 of 129) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 129 results.
Nucleic Acids Research|September 13, 2023
CRISPR screens in sister chromatid cohesion defective cells reveal PAXIP1-PAGR1 as regulator of chromatin association of cohesinJanne J M van Schie, Klaas de Lint, Thom M Molenaar, et al.
Epigenetics & Chromatin|December 31, 2016
The detailed 3D multi-loop aggregate/rosette chromatin architecture and functional dynamic organization of the human and mouse genomesTobias A Knoch, Malte Wachsmuth, Nick Kepper, et al.
Micropublication Biology|October 6, 2025
Cells stably expressing shRNA against MYO10 display altered cell motilityJoanna A Mas, Chase E Cristella, Vu Hao M N Phan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2013
Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cellsJessica Zuin, Jesse R Dixon, Michael I J A van der Reijden, et al.
Cell Reports|May 21, 2020
MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange SyndromeIlaria Parenti, Farah Diab, Sara Ruiz Gil, et al.
Clinical Genetics|December 17, 2015
Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk predictionI Parenti, C Gervasini, J Pozojevic, et al.
Brain : a Journal of Neurology|July 24, 2019
Cohesin complex-associated holoprosencephalyPaul Kruszka, Seth I Berger, Valentina Casa, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Pathogenic variants in the cohesin loader subunit MAU2 lead to a new Cornelia de Lange Syndrome subtypeIlaria Parenti, Alina Hesters, Marta Gil-Salvador, et al.
Nature Communications|March 30, 2026
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtypeIlaria Parenti, Alina Hesters, Marta Gil-Salvador, et al.
Pageof 13