Results 101 to 110 of about 1,393 (149)

CRISPR screens in sister chromatid cohesion defective cells reveal PAXIP1-PAGR1 as regulator of chromatin association of cohesin. [PDF]

open access: yesNucleic Acids Res, 2023
van Schie JJM   +14 more
europepmc   +1 more source

The Roberts syndrome: a case report of an infant with valvular aortic stenosis and mutation in ESCO2.

open access: yesJPMA. The Journal of the Pakistan Medical Association, 2014
Roberts syndrome, which is inherited as an autosomal recessive group of disorders, is a rare syndrome characterized with symmetrical extremity defects, craniofacial abnormalities, and prenatal and postnatal growth retardation. Here, we present a case of Roberts Syndrome brought to the clinic with diarrhoea and multiple abnormalities, that had tetra ...
Dogan, M.   +7 more
openaire   +2 more sources

Symmetric control of sister chromatid cohesion establishment. [PDF]

open access: yesNucleic Acids Res, 2023
Zhang J   +14 more
europepmc   +1 more source

The cohesin modifier ESCO2 is stable during DNA replication. [PDF]

open access: yesChromosome Res, 2023
Jevitt AM, Rankin BD, Chen J, Rankin S.
europepmc   +1 more source

Clonal expansion of alveolar fibroblast progeny drives pulmonary fibrosis in mouse models. [PDF]

open access: yesJ Clin Invest
Molina C   +7 more
europepmc   +1 more source

Cohesin: an emerging master regulator at the heart of cardiac development. [PDF]

open access: yesMol Biol Cell, 2023
Mfarej MG   +5 more
europepmc   +1 more source

The non-redundant function of cohesin acetyltransferase Esco2

open access: yes, 2021
Whelan, Gabriela   +3 more
openaire   +1 more source

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