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[PDF] Top 20 Wdr74 is required for blastocyst formation in the mouse.

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Wdr74 is required for blastocyst formation in the mouse.

Wdr74 is required for blastocyst formation in the mouse.

... to the blastocyst stage (data not ...to the morula stage. qRT- PCR confirmed expected knockdown in each group (Figure ...at the morula stage with obvious morphological signs of dying ... See full document

9

Prox1 Inhibits Proliferation and Is Required for Differentiation of the Oligodendrocyte Cell Lineage in the Mouse.

Prox1 Inhibits Proliferation and Is Required for Differentiation of the Oligodendrocyte Cell Lineage in the Mouse.

... cells in Prox1-CKO-/- homo- zygous mutants might suggest that the net observed reduction in BrdU+ cells could have been due to a requirement for Prox1 in the proliferation of ... See full document

19

Kruppel-like factor 2 is required for normal mouse cardiac development.

Kruppel-like factor 2 is required for normal mouse cardiac development.

... (KLF2) is expressed in endothelial cells in the developing heart, particularly in areas of high shear stress, such as the atrioventricular (AV) ...by mouse embryonic day ... See full document

13

Activation of GSK3β by Sirt2 is required for early lineage commitment of mouse embryonic stem cell.

Activation of GSK3β by Sirt2 is required for early lineage commitment of mouse embryonic stem cell.

... affect the self-renewal of mouse ESCs ...differentiation, the absence of Sirt2 inhibits the formation of ectoderm while promoting the differentiation of mesoderm and endoderm; ... See full document

8

HIPPO pathway members restrict SOX2 to the inner cell mass where it promotes ICM fates in the mouse blastocyst.

HIPPO pathway members restrict SOX2 to the inner cell mass where it promotes ICM fates in the mouse blastocyst.

... SOX2 is one of the earliest known unique markers of ICM progenitors is supported by the observation that SOX2 is also one of the first pluripotency genes to localize to ICM ... See full document

13

The Nanos3-3'UTR is required for germ cell specific NANOS3 expression in mouse embryos.

The Nanos3-3'UTR is required for germ cell specific NANOS3 expression in mouse embryos.

... that the expression of maternal mRNAs depends on the corresponding 39UTR in many animal ...species. The 39UTRs of nanos homologs play essential roles in the respective mRNA ... See full document

10

Maternal Setdb1 Is Required for Meiotic Progression and Preimplantation Development in Mouse.

Maternal Setdb1 Is Required for Meiotic Progression and Preimplantation Development in Mouse.

... KMT1E, is a lysine methyltransferase (KMT) specific for the repressive histone H3 lysine 9 di- and tri-methyl (H3K9me2/me3) marks ...It is associated with transcriptional repression of euchromatic ... See full document

26

Epidermal transglutaminase (TGase 3) is required for proper hair development, but not the formation of the epidermal barrier.

Epidermal transglutaminase (TGase 3) is required for proper hair development, but not the formation of the epidermal barrier.

... occur in mouse embryonic skin, starting abruptly at E16 and being complete by E17 ...delay in skin barrier development with isolated corneocytes being more easily fragmented by ...It is ... See full document

12

Model of knowledge representation about materials in the form of a relational database for CAPCAST system

Model of knowledge representation about materials in the form of a relational database for CAPCAST system

... diagram in Figure 1 shows the basic requirements for a material-related module in a CAPCAST ...system. The system user (manufacturer or his employees) introduces to the system ... See full document

6

HrpA, an RNA helicase involved in RNA processing, is required for mouse infectivity and tick transmission of the Lyme disease spirochete.

HrpA, an RNA helicase involved in RNA processing, is required for mouse infectivity and tick transmission of the Lyme disease spirochete.

... of the more highly regulated proteins or operons: downregulated bb0241 [glpK], bb0242, bb0603, and bba74; and upregulated bb0502, bbb19, bb0443, bbi39, and bba24 ...from the hrpA mutant and complement were ... See full document

16

Rev. Bras. Psiquiatr.  vol.26 número3 en a11v26n3

Rev. Bras. Psiquiatr. vol.26 número3 en a11v26n3

... amygdala is often spoken of in the context of learning fearful or other negative emotional responses, but it also participates in processing memories related to positive ...example, the ... See full document

4

Effect of hydrophobic mutations in the H2-H3 subdomain of prion protein on stability and conversion in vitro and in vivo.

Effect of hydrophobic mutations in the H2-H3 subdomain of prion protein on stability and conversion in vitro and in vivo.

... investigate the role of hydrophobic mutations in the H2–H3 subdomain of the globular domain of ...mutations in the globular domain are associated with human prion ...observed ... See full document

9

Phosphorylation by Cdk1 increases the binding of Eg5 to microtubules in vitro and in Xenopus egg extract spindles.

Phosphorylation by Cdk1 increases the binding of Eg5 to microtubules in vitro and in Xenopus egg extract spindles.

... Eg5 in buffer with its behavior in the presence of all its potential binding partners, using spindle reconstitutions in Xenopus egg ...there is a critical concentration of Eg5 in ... See full document

10

A transgenic model for conditional induction and rescue of portal hypertension reveals a role of VEGF-mediated regulation of sinusoidal fenestrations.

A transgenic model for conditional induction and rescue of portal hypertension reveals a role of VEGF-mediated regulation of sinusoidal fenestrations.

... VEGF is constitutively expressed in the adult liver and continuously transmitting VEGF-induced signals [13], we reasoned that VEGF might play a maintenance role in the hepatic ... See full document

8

Ppargamma2 is a key driver of longevity in the mouse.

Ppargamma2 is a key driver of longevity in the mouse.

... for the randomly selected sets as ...that the associated biological phenom- ena are deliberate such that other ‘unknown’ age-related genes and/or biological processes may be ...theory is reminiscent ... See full document

7

Use of ornamental rock residues for mould flux development

Use of ornamental rock residues for mould flux development

... productivity in continuous casting, a mould flux powder that allows obtaining the fastest casting speed as pos- sible while at the same time keeping an excellent quality of the solidified ... See full document

8

The NIP7 protein is required for accurate pre-rRNA processing in human cells

The NIP7 protein is required for accurate pre-rRNA processing in human cells

... protein is required for pre-rRNA processing and ribosome biosynthesis ...with the C-terminal region corresponding to the PUA domain (named after pseudouridine synthases and archaeosine-specific ... See full document

18

Drosophila Mcm10 is required for DNA replication and differentiation in the compound eye.

Drosophila Mcm10 is required for DNA replication and differentiation in the compound eye.

... defects in the S and M phases of the cell cycle could result in genomic DNA ...damage. In fact, our studies revealed that the depletion of dMcm10 in the eye discs ... See full document

15

The TollNF- κB signaling pathway is required for epidermal wound repair in Drosophila

The TollNF- κB signaling pathway is required for epidermal wound repair in Drosophila

... at the wound edge fails in Dif dl ...of the wound edge in wild-type and Dif dl embryos (boxed regions in A and ...E). In wild type, wound-edge membranes have low levels of ... See full document

10

Brahma is required for proper expression of the floral repressor FLC in Arabidopsis.

Brahma is required for proper expression of the floral repressor FLC in Arabidopsis.

... role in vegetative, embryonic and reproductive plant development ...of the genes were differentially expressed in brm ...when the same experiments were carried out with leaves from 14-day-old ... See full document

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