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14-3-3ε Is required for germ cell migration in Drosophila.
... pole cell number was achieved with the high expressing transgene under Tub-Gal4, it completely failed under Act-Gal4 ...differences in their spatial ...differences in phenotypic ...demonstrated ... See full document
11
Tre1, a G protein-coupled receptor, directs transepithelial migration of Drosophila germ cells.
... serotonin. In mammals, two receptors for melatonin, Mel1a and Mel1b, have been identified, and nonmammalian vertebrate species have, in addition, a third melatonin receptor, Mel1c (Figure 2A) (Dubocovich ... See full document
13
In vitro germ cell differentiation from cynomolgus monkey embryonic stem cells.
... into germ cells in vitro, we produced EBs and examined the expression of germ cell markers using RT-PCR (Figure ...significantly in EBs by day 14, thus indicating that the ... See full document
10
A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.
... expression in animal species has been achieved in many biological model organisms from mouse to Drosophila using inducible expression vectors ...demonstrated in vitro and in transgenic ... See full document
9
14-3-3ε overexpression contributes to epithelial-mesenchymal transition of hepatocellular carcinoma.
... that 14-3-3e expression is in- creased in primary and metastatic ...Elevated 14-3-3e expression is correlated with higher risk of extrahepatic metastasis and lower ... See full document
12
The mechanism for primordial germ-cell migration is conserved between Japanese eel and zebrafish.
... it is possible to transplant a single visualized PGC into other embryos and produce germ-line chimera [14], ...during migration, the host fish PGCs were labeled with RFP by injecting RFP-nos1 ... See full document
8
Dicer is required for haploid male germ cell differentiation in mice.
... reported in male germ line that can function in post- transcriptional control of a wide variety of protein encoding mRNAs ...it is likely that at least some of the defects in Dicer1 ... See full document
12
The Nanos3-3'UTR is required for germ cell specific NANOS3 expression in mouse embryos.
... 39UTR in many animal ...roles in the respective mRNA localization, translation and degradation in ...elegans, Drosophila, and Zebrafish [1,9,36]. We have found in our present ... See full document
10
p120 catenin is required for the stress response in Drosophila.
... (p120ctn) is the prototypic member of the p120ctn family in mammals and, together with Armadillo Repeat gene deleted in Velco-Cardio-Facial syndrome (ARCVF), p0071 and delta-catenin, it binds the ... See full document
10
Liquid facets-related (lqfR) is required for egg chamber morphogenesis during Drosophila oogenesis.
... present in all cell types and tissues. Data from the Berkeley Drosophila Genome Project in situ hybridization database [25] suggest that Drosophila LqfR is expressed primarily ... See full document
10
Drosophila melanogaster Hox transcription factors access the RNA polymerase II machinery through direct homeodomain binding to a conserved motif of mediator subunit Med19.
... cloned in place of the equivalent fragment of ...mediated germ line transforma- tion or by site-specific integration using the WC-31 ...described in [32]. For BiFC in imaginal discs, late ... See full document
16
Involvement of LPA Receptor 3 in LPA-induced BGC- 803 Cell Migration
... LPA is shown to stimulate proliferation and motility via LPA receptors, LPAR1 and LPAR3 in several cancer cell lines, but the role of LPA receptors in gastric cancer cells is still ... See full document
6
The origin and migration of primordial germ cells in sturgeons.
... gene is a well-conserved gene in animals, although the function of the gene and protein as regards germplasm formation has not been well-studied except in zebrafish ...[42,53]. In zebrafish, ... See full document
10
Eyes absent tyrosine phosphatase activity is not required for Drosophila development or survival.
... (Eya) is an evolutionarily conserved transcriptional coactivator and protein phosphatase that regulates multiple developmental processes throughout the ...metazoans. Drosophila eya is necessary for ... See full document
8
E-cadherin is required for centrosome and spindle orientation in Drosophila male germline stem cells.
... abolished in the cnn mutant, the apc1 mutant appeared to retain some level of checkpoint ...molecules in centrosome orientation and the centrosome orientation checkpoint implies that the mechanism by which ... See full document
7
ESCRT-0 is not required for ectopic Notch activation and tumor suppression in Drosophila.
... as is the case of single Hrs or Stam mutant alleles, suggesting that the l(2)gl lesion in the original double mutant allele was responsible for the loss of tumor suppression ...to cell death, as we ... See full document
11
Anopheles albitarsis Embryogenesis: Morphological Identification of Major Events
... spheres in the interior of the egg plus smaller ones primarily concentrated at the periphery (Raminani & Cupp ...embedded in a sparse reticu- lum were observed in ...1967). In C. pipiens ... See full document
8
Nubp1 is required for lung branching morphogenesis and distal progenitor cell survival in mice.
... kept in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of ...mutation in Nubp1 was identified in a screen for ... See full document
11
It's all in your mind: determining germ cell fate by neuronal IRE-1 in C. elegans.
... misregulation in the ASI neurons does not indirectly abrogate the communication between the neurons and the gonad, how might it dictate germ cell survival or death? IRE-1 is a dual- activity ... See full document
14
Casimiro, Andreia Palos
... RNA is the most instable of nucleic ...between 3-7 days after eclosion, which gives the equivalent of a maximum of 50 mg of ...homogenized in 500 µl TRI Reagent® and centrifuged at 12000 g for 1 min, ... See full document
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