about
ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomesCEP63 deficiency promotes p53-dependent microcephaly and reveals a role for the centrosome in meiotic recombinationMouse TRIP13/PCH2 is required for recombination and normal higher-order chromosome structure during meiosisMeiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1.Meiotic recombination provokes functional activation of the p53 regulatory network.Female-specific features of recombinational double-stranded DNA repair in relation to synapsis and telomere dynamics in human oocytes.Cytogenetic analyses of human oocytes provide new data on non-disjunction mechanisms and the origin of trisomy 16.p53 and TAp63 participate in the recombination-dependent pachytene arrest in mouse spermatocytes.Expression of arf tumor suppressor in spermatogonia facilitates meiotic progression in male germ cells.Gene expression is altered after bisphenol A exposure in human fetal oocytes in vitro.The E3 ubiquitin ligase Cullin 4A regulates meiotic progression in mouse spermatogenesis.Presence of an extra chromosome alters meiotic double-stranded break repair dynamics and MLH1 foci distribution in human oocytes.Strong artificial selection in domestic mammals did not result in an increased recombination rate.The ATM signaling cascade promotes recombination-dependent pachytene arrest in mouse spermatocytes.Homeostatic control of recombination is implemented progressively in mouse meiosis.The use of foetal ovarian stromal cell culture for cytogenetic diagnosis. Stromal ovarian culture cytogenetic diagnosis.The ATM signaling network in development and disease.Maternal origin of the human aneuploidies. Are homolog synapsis and recombination to blame? Notes (learned) from the underbelly.Cytological techniques to study human female meiotic prophase.Meiosis in a bottle: new approaches to overcome Mammalian meiocyte study limitations.Dynamics of cohesin proteins REC8, STAG3, SMC1 beta and SMC3 are consistent with a role in sister chromatid cohesion during meiosis in human oocytes.Human meiotic progression and recombination are affected by Bisphenol A exposure during in vitro human oocyte development.A new culture technique that allows in vitro meiotic prophase development of fetal human oocytes.Pairing and synapsis in oocytes from female fetuses with euploid and aneuploid chromosome complements.H2AFX and MDC1 promote maintenance of genomic integrity in male germ cells.Human fetal ovarian culture permits meiotic progression and chromosome pairing process.Evolution of the meiotic prophase and of the chromosome pairing process during human fetal ovarian development.Chromosome 18 pairing behavior in human trisomic oocytes. Presence of an extra chromosome extends bouquet stage.Probing meiotic recombination decisions.ATR is required to complete meiotic recombination in mice.ATR is a multifunctional regulator of male mouse meiosis.Shu complex SWS1-SWSAP1 promotes early steps in mouse meiotic recombinationThe PSMA8 subunit of the spermatoproteasome is essential for proper meiotic exit and mouse fertilityATR function is indispensable to allow proper mammalian follicle development
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Ignasi Roig
@ast
Ignasi Roig
@en
Ignasi Roig
@es
Ignasi Roig
@fr
Ignasi Roig
@nl
Ignasi Roig
@sl
type
label
Ignasi Roig
@ast
Ignasi Roig
@en
Ignasi Roig
@es
Ignasi Roig
@fr
Ignasi Roig
@nl
Ignasi Roig
@sl
prefLabel
Ignasi Roig
@ast
Ignasi Roig
@en
Ignasi Roig
@es
Ignasi Roig
@fr
Ignasi Roig
@nl
Ignasi Roig
@sl
P214
P1053
A-9697-2012
P106
P1153
24345435300
P21
P214
P31
P3829
P496
0000-0003-0313-3581
P734
P7859
viaf-316752726