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A group of 195 patients manifesting non-obstructive azoospermia or oligozoospermia were tested for mutations of the NANOS1 gene.
Single nucleotide polymorphisms in CYP26B1, NANOS1 and STRA8 genes support involvement of meiotic program initiation in modifying azoospermia and oligozoospermia risk in a Han-Chinese population
NANOS1-PUMILIO2 complex, together with GEMIN3 (show DDX20 Proteins) and small noncoding RNAs, possibly regulate mRNA translation within the chromatoid body of the human germ cells.
Findings describe a new function for hNanos1 as a downstream effector of E-cadherin (show CDH1 Proteins) loss contributing to tumor progression.
The E-cadherin (show CDH1 Proteins)-repressed hNanos1 gene induces tumor cell invasion by upregulating MT1-MMP (show MMP14 Proteins) expression.
Data demonstrated that SNAPIN (show SNAPIN Proteins) interacts additionally with NANOS1 protein. This is the first report demonstrating that the N-terminal region of NANOS1 is necessary for protein binding.
Data indicate that nanos3 (show NANOS3 Proteins) function is required for the maintenance of germline stem cell (GSC (show GSC Proteins)), but not for their specification, and suggest that nanos2 (show NANOS2 Proteins) and nanos3 (show NANOS3 Proteins) are partially redundant in this role.
Both Nanos1 and Smaug2 function as a bimodal translational repression switch to control neurogenesis.
translation of nanos1 after fertilization requires Dead-end (show DND1 Proteins) 1 (show VPS11 Proteins) (Dnd1 (show DND1 Proteins)), a vertebrate-specific germline RNA-binding protein and binding the eIF3 (show NCL Proteins) complex
Nanos1 functions to translationally repress RNAs that normally specify endoderm and promote apoptosis, thus preserving the germline
Xenopus Nanos1 is a translational repressor and association with the RNA is required for this repression.
Xenopus germline nanos1 is translationally repressed by a novel structure-based mechanism.
This study demonstrated for the first time a strong expression of NGF, TrkA, CGRP, nNOS and neuronal specific enolase in the majority of esophageal enteric nervous system components.
Our results suggest that the presence of low mycotoxin doses in feed slows down the mRNA expression of nitric oxide synthase-1 and nitric oxide synthase-2 genes which probably lowers the concentrations of nitric oxide, a common precursor of inflammation.
nNOS (show NOS1 Proteins) is an important regulator of renal hemodynamics in the newborn kidney, but not in the adult.
Data suggest that pig sperm contain bNOS (show NOS1 Proteins), iNOS (show NOS2 Proteins), and eNOS (show NOS3 Proteins); up-regulation of NOS by leptin (show LEP Proteins) during acrosome reaction and inhibition of acrosome reaction by inhibitors of nitric oxide synthases suggests these enzymes are involved in acrosome reaction.
Periodic acceleration (pGz) acutely increases endothelial and neuronal nitric oxide synthase (show NOS1 Proteins) expression in endomyocardium of normal swine.
Regional difference in blood flow has no effect on nNOS (show NOS1 Proteins) protein content in different sized conduit arteries.
study concludes that in the cerebral cortex of newborn piglets, the mechanism of hypoxia-induced increased tyrosine phosphorylation of nNOS (show NOS1 Proteins) is mediated by nNOS (show NOS1 Proteins)-derived nitric oxide.
Data suggest that angiotensin II regulates nNOS and eNOS expression and NOS activity in afferent arterioles of the developing kidney via angiotensin 1 and 2 receptors.
enzyme that catalyzes the production of nitric oxide
, nanos homolog 1
, NOS type I
, constitutive NOS
, neuronal NOS
, nitric oxidase synthase
, nitric oxide synthase, brain
, peptidyl-cysteine S-nitrosylase NOS1
, nanos 1
, Nanos homolog 1
, LOW QUALITY PROTEIN: nanos homolog 1
, nanos C2HC-type zinc finger 1