Mouse Oocytes
Cell cycle dependent behavior of microtubules in hybrids of mouse oocytes and blastomeres
... 1nt Y De\' BioI 35; 421 427 (1991) 421 Origil/a/ Arlir/I' Cell cycle dependent behavior of microtubules in hybrids of mouse oocytes and blastomeres' JACEK Z KUBIAK Department of Embryology, Institute[.] ...
7
The Influence of Meiotic Spindle Configuration by Cysteamine during in vitro Maturation of Mouse Oocytes
... Various thiol compounds especially cysteine and cysteamine are commonly added to IVM media to support GSH synthesis, and to improve the developmental competence of oocytes. Low molecular weight compounds such as ...
6
Zfp207 is a Bub3 binding protein regulating meiotic chromosome alignment in mouse oocytes
... Zinc finger proteins are among the most abundant proteins in eukaryotic genomes and participate in diverse biological eventsas interaction modules that bind DNA, RNA, proteins, or other small molecules [26, 27]. Recent ...
11
Control of microtubule nucleating activity in the cytoplasm of maturing mouse oocytes
... Int ,I DH BioI J6 143 150 (1992) 143 Control of microtubule nucleating activity in the cytoplasm of maturing mouse oocytes ANNE VAN CAUWENBERGE" and HENRI ALEXANDRE',' ILaboratory of Molecular Cytolog[.] ...
8
Activation of in vitro matured mouse oocytes arrested at first or second meiotic metaphase
... Int J De\' BioI 39 1015 1020 (1995) 10]5 O,iginal Article Activation of in vitro matured mouse oocytes arrested at first or second meiotic metaphase ZBIGNIEW POLANSKI* Department of Genetics and Evolu[.] ...
6
Cyclin B2 is required for progression through meiosis in mouse oocytes
... from oocytes arrested in prophase with cilostamide (time 0) or collected 2, 4, 6 and 8 h after meiotic ...I. Oocytes were injected with a 1:1 mix of oligo-adenylated YFP-(Ccnb2-short, Ccnb2-long, ...
12
HDAC3 promotes meiotic apparatus assembly in mouse oocytes by modulating tubulin acetylation
... grown oocytes were microinjected with specifically designed HDAC3 siRNAs, with a negative siRNA injected as ...the oocytes were arrested at GV stage for 20 h with milrinone to degrade ...in mouse ...
9
SMC5/6 is required for the formation of segregation competent bivalent chromosomes during meiosis I in mouse oocytes
... in mouse oocytes, an oocyte-specific conditional knockout (cKO) mouse was created, deleting a floxed Smc5 allele using the Zp3-Cre transgene, which is expressed in growing oocytes before ...
13
Early changes in embryonic nuclei fused to chemically enucleated mouse oocytes
... Int I De, BinI 37; 433 439 (19931 433 Original Articlr Early changes in embryonic nuclei fused to chemically enucleated mouse oocytes JOSEF FULKA, Jr ', ELENA NOTARIANNI, LORENA PASSONI and ROBERT M M[.] ...
7
Spindle assembly checkpoint signalling is uncoupled from chromosomal position in mouse oocytes
... mammalian oocytes, meiosis I (MI) is notoriously error prone and polar-displaced chromosomes do not prevent anaphase ...wild-type mouse oocytes, in which polar chromosomes are rare, or of ...
6
Symmetry breaking in mouse oocytes requires transient F actin meshwork destabilization
... in oocytes are often devoid of canonical centrosomes and astral microtubules (Szöllösi et ...I mouse oocytes have a central nucleus and show no sign of polarization (FitzHarris et ...
6
The methyltransferase Setdb1 is essential for meiosis and mitosis in mouse oocytes and early embryos
... Fig. 5. Setdb1 controls expression of repeats. (A) Volcano plot showing false discovery rates and relative expression changes of differentially expressed repClass groups upon Setdb1 depletion in GV oocytes ...
13
Supplementation of L-carnitine during in vitro maturation of mouse oocytes affects expression of genes involved in oocyte and embryo competence: An experimental study
... BCB+ oocytes with LC during IVM improved fertilization rate and BDR, but it had no significant effect on the number of ICM and TE in the ...bovine oocytes with LC ...of oocytes and embryos; however, ...
8
Expression of simian virus 40 early and late genes in mouse oocytes and embryos.
... The synthesis of T-Ag and V-Ag was also measured in virus-infected CV-1 cells African green monkey cells permissive for SV40 replication and 3T6 cells nonpermissive mouse fibroblasts to [r] ...
9
Cell volume regulation is initiated in mouse oocytes after ovulation
... Fertilized mouse eggs regulate their size principally by accumulating glycine as an intracellular osmolyte using the GLYT1 (SLC6A9) transporter, a mechanism of cell volume homeostasis apparently unique to early ...
8
CDC42 controls the activation of primordial follicles by regulating PI3K signaling in mouse oocytes
... Fig. 2 Manipulating the expression of Cdc42 controls the activation of primordial follicles. a, b Validating the efficiency of Cdc42 knockdown in cultured ovaries. Ovaries at 1 dpp were injected with Cdc42 esiRNA or ...
16
Effect of genistein alone and in combination with okadaic acid on the cell cycle resumption of mouse oocytes
... treated oocytes, and to compare the cytological effects of genistein to those induced by the few other pharmacological agents display- ing the same cytostatic effect (Alexandre and Mulnard, 1988; Alexandre et ...
12
The role of inositol 1,4,5-triphosphate receptors in mammalian oocytes and preimplantation embryos
... mature mouse oocytes express high levels of type I InsP^R I next investigated how the pattern of expression of the three subtypes changes during preimplantation ...ME oocytes alongside late 2-cell ...
212
La spermatide ronde partenaire de l’ovocyte: autopsie d’un échec
... : Fertilization and in vitro development of porcine ooeytes following intracytoplasmic injection of round spermatid or round spermatid nuclei.. : Mouse oocytes injected wi[r] ...
8
KL/KIT co expression in mouse fetal oocytes
... during mouse oogenesis, mRNA encoding Kit and protein has been found in mitotic primordial germ cells but not in oocytes undergoing the first stages of meiosis during fetal life (Manova and Bachvarova, ...
7