about
Nuclear reprogramming: kinetics of cell cycle and metabolic progression as determinants of successMitochondrial physiology and gene expression analyses reveal metabolic and translational dysregulation in oocyte-induced somatic nuclear reprogrammingInitiation of trophectoderm lineage specification in mouse embryos is independent of Cdx2.A signalling role for 4-hydroxy-2-nonenal in regulation of mitochondrial uncoupling.The reactions catalysed by the mitochondrial uncoupling proteins UCP2 and UCP3.Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3.Somatic cell nuclear reprogramming of mouse oocytes endures beyond reproductive decline.Reprogramming of two somatic nuclei in the same ooplasm leads to pluripotent embryonic stem cells.Carvedilol inhibits the mitochondrial permeability transition by an antioxidant mechanism.ART culture conditions change the probability of mouse embryo gestation through defined cellular and molecular responses.Calcium-dependent mitochondrial permeability transition is augmented in the kidney of Goto-Kakizaki diabetic ratGoverning cell lineage formation in cloned mouse embryos
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description
researcher, ORCID id # 0000-0002-8642-4722
@en
wetenschapper
@nl
name
Telma C Esteves
@ast
Telma C Esteves
@en
Telma C Esteves
@es
Telma C Esteves
@nl
type
label
Telma C Esteves
@ast
Telma C Esteves
@en
Telma C Esteves
@es
Telma C Esteves
@nl
prefLabel
Telma C Esteves
@ast
Telma C Esteves
@en
Telma C Esteves
@es
Telma C Esteves
@nl
P106
P1153
57027669500
P21
P31
P496
0000-0002-8642-4722