about
Evidence for a genomic mechanism of action for progesterone receptor membrane component-1Progesterone inhibits apoptosis in part by PGRMC1-regulated gene expression.Expression of progesterone receptor membrane component-1 in bovine reproductive system during estrous cycle.Plasminogen activator inhibitor 1 RNA-binding protein interacts with progesterone receptor membrane component 1 to regulate progesterone's ability to maintain the viability of spontaneously immortalized granulosa cells and rat granulosa cellsOocytes isolated from dairy cows with reduced ovarian reserve have a high frequency of aneuploidy and alterations in the localization of progesterone receptor membrane component 1 and aurora kinase B.Progesterone regulation of progesterone receptor membrane component 1 (PGRMC1) sumoylation and transcriptional activity in spontaneously immortalized granulosa cells.Effect of oral administration of low-dose follicle stimulating hormone on hyperandrogenized mice as a model of polycystic ovary syndrome.Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes.PGRMC1 participates in late events of bovine granulosa cells mitosis and oocyte meiosisRole of gap junction-mediated communications in regulating large-scale chromatin configuration remodeling and embryonic developmental competence acquisition in fully grown bovine oocyteChanges in large-scale chromatin structure and function during oogenesis: a journey in company with follicular cells.Chromatin remodelling and histone m RNA accumulation in bovine germinal vesicle oocytes.Accumulation of Chromatin Remodelling Enzyme and Histone Transcripts in Bovine Oocytes.Differences in cumulus cell gene expression indicate the benefit of a pre-maturation step to improve in-vitro bovine embryo production.Cryopreservation of immature bovine oocytes to reconstruct artificial gametes by germinal vesicle transplantation.Cytoplasmic changes and developmental competence of bovine oocytes cryopreserved without cumulus cells.Large-scale chromatin remodeling in germinal vesicle bovine oocytes: interplay with gap junction functionality and developmental competence.Progesterone receptor membrane component 1 expression and putative function in bovine oocyte maturation, fertilization, and early embryonic development.Transferability and inter-laboratory variability assessment of the in vitro bovine oocyte maturation (IVM) test within ReProTect.The effect of cilostamide on gap junction communication dynamics, chromatin remodeling, and competence acquisition in pig oocytes following parthenogenetic activation and nuclear transfer.Developmental capability of denuded bovine oocyte in a co-culture system with intact cumulus-oocyte complexes: role of cumulus cells, cyclic adenosine 3',5'-monophosphate, and glutathione.In vitro maturation affects chromosome segregation, spindle morphology and acetylation of lysine 16 on histone H4 in horse oocytes.Natriuretic peptide precursor C delays meiotic resumption and sustains gap junction-mediated communication in bovine cumulus-enclosed oocytes.Effect of gonadotropins during in vitro maturation of feline oocytes on oocyte-cumulus cells functional coupling and intracellular concentration of glutathione.Relationship between growth hormone concentrations in bovine oocytes and follicular fluid and oocyte developmental competence.PGRMC1 localization and putative function in the nucleolus of bovine granulosa cells and oocytes.Oviductal microvesicles and their effect on in vitro maturation of canine oocytes.Steroid hormones interact with natriuretic peptide C to delay nuclear maturation, to maintain oocyte-cumulus communication and to improve the quality of in vitro-produced embryos in cattle.Transferability and inter-laboratory variability assessment of the in vitro bovine oocyte fertilization test.Reductions in the number of mid-sized antral follicles are associated with markers of premature ovarian senescence in dairy cows.Changes in histone H4 acetylation during in vivo versus in vitro maturation of equine oocytes.Gap junction-mediated communications regulate chromatin remodeling during bovine oocyte growth and differentiation through cAMP-dependent mechanism(s).The endothelial nitric oxide synthase/nitric oxide system is involved in the defective quality of bovine oocytes from low mid-antral follicle count ovaries.Involvement of E-cadherin in early in vitro development of adult and juvenile sheep embryos.Developmental competence of gametes reconstructed by germinal vesicle transplantation from fresh and cryopreserved bovine oocytes.Oocyte morphology and transcriptional silencing in relation to chromatin remodeling during the final phases of bovine oocyte growth.Localization of DNA methyltransferase-1 during oocyte differentiation, in vitro maturation and early embryonic development in cowCharacterization and control of oocyte large-scale chromatin configuration in different cattle breeds
P50
Q27000111-4C1507E0-5DE7-4211-B6A6-E596D2A8CC8CQ33749200-23F5BC37-B2C7-4770-B62C-DC40F7E1CAA2Q35466966-23FA6A9B-F454-4D50-AC7B-E72AEEC7ACC7Q35617134-0C880C90-4D35-49E9-9C18-8638EDFA9D33Q35617549-D28AB881-8C9D-42F1-880E-F12031C0E744Q36113935-14A57967-5B03-4BD2-BD51-3C3F18166172Q36125610-5ED2CABF-3290-41AA-813E-DB85828EBD01Q36375024-3E911496-5A51-4553-98B9-1C7D3DF9D095Q37143188-DBA30B3C-3777-4A40-881C-91F04C9D8C7CQ37239551-0754778E-FA13-4B1E-A5ED-FBF83825C20EQ38229966-2A7275E2-A293-47EF-9F89-ECC7AB5679CAQ38299265-A99C0595-5273-41ED-87BE-B1548465B721Q38639548-6A97DB4B-D86A-4E3E-BCA1-2288B002F2E4Q39455473-C57DC0BB-6152-48F4-91CB-8099F3E0EF14Q41610888-711E42C0-45C7-4B3E-93D2-BBD382A480A9Q41614677-17B5D496-AEBD-4AB1-B00D-C4C4222ED96AQ42602203-E88020DC-98FC-4C2E-B3A3-62976520FED4Q42925833-96B26EDA-5F8B-4C80-87B8-E45105DEA296Q43161577-8BF11239-7DF0-4BDF-A1BB-C38C3BA9A37EQ43720364-F399DC59-81E8-495D-B220-F12C2DF5DF42Q46415792-2473F8DD-6DF4-44DC-8EAB-63F0C6849E14Q46626181-B905FCDC-A807-41B2-ABD2-0C1F9BBA8087Q46858788-15117D77-AC96-4997-BFB3-EA64D9722C9CQ46874302-294DCF42-BA33-4E5D-AC14-1DE3CF9ABFD6Q46962422-A199C7A7-F289-49D3-997B-EE03C81E3A2CQ47728982-DAEDA9AB-8C55-4E1B-99AA-D14D360F923CQ48518371-7363D750-8B90-46FF-99EF-48ABA5B4883BQ48525321-90AEA1B7-C7EA-4FA3-81B8-C89E31395317Q48586431-8593D132-29A4-4A3B-8F50-13D6E2E67FBBQ48632026-108EA7AA-53BC-4A16-A790-FDDD867F8FABQ48659470-A5F77C99-0048-4297-96E9-ED6AD229D05DQ48667250-CDBEFEC6-D053-491E-B960-411D1E7E6CB3Q48679052-710C72F5-32CA-4F89-B979-8CAB82F6F630Q48707648-9B1B5A68-3423-43D3-86C8-8808717C9470Q48736214-44F78887-81F1-4BD0-8B07-F77D6D9B3F7AQ48775239-83C27F78-CE01-453B-A990-C8C766512B2EQ60716312-85485ED7-8DD4-4230-B7EF-A585F9EC7670Q90200003-95C4C913-72FB-4E3D-8C6F-B777AF180351
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Valentina Lodde
@ast
Valentina Lodde
@en
Valentina Lodde
@es
Valentina Lodde
@nl
Valentina Lodde
@sl
type
label
Valentina Lodde
@ast
Valentina Lodde
@en
Valentina Lodde
@es
Valentina Lodde
@nl
Valentina Lodde
@sl
prefLabel
Valentina Lodde
@ast
Valentina Lodde
@en
Valentina Lodde
@es
Valentina Lodde
@nl
Valentina Lodde
@sl
P1053
G-3585-2015
P106
P21
P31
P3829
P496
0000-0002-9768-2292