Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. Zusätzlich bieten wir Ihnen SIM1 Antikörper (41) und viele weitere Produktgruppen zu diesem Protein an.
Showing 3 out of 3 products:
identified a novel SIM1 variant, p.D134N, in 4 obese individuals from a single pedigree which is also associated with lower preference for certain foods
no gene harboring deletions were identified in the SIM1 and MRAP2 regions in the Prader Willi like (PWL) cohort; further functional analysis of p.P352S found in SIM1 and p.A40S found in MRAP2 is useful; this would provide further support for possible role of SIM1 and MRAP2 in the pathogenesis of the PWL phenotype in a limited number of patients
Genotype-phenotype correlations confirmed the major role for SIM1 haploinsufficiency in obesity and the Prader-Willi-like phenotype
Aberrant DNA methylation (zeige HELLS Proteine) of the DLX4 (zeige DLX4 Proteine) and SIM1 genes may be a novel progression marker for uterine cervical low-grade squamous intraepithelial lesions.
Severe loss-of-function SIM1 mutations can be associated with a spectrum of developmental delay phenotypes and obesity.
functional in vitro analysis of SIM1 variants may help in distinguishing benign variants of no pathogenic significance from variants which contribute to the obesity phenotype.
Study found a statistically significant association between the SIM1 SNP rs3734354 (Pro352Thr) and scores for language impairment (p = .0004), but due to low statistical power this should be interpreted cautiously
two brain enhancers in the SIM1 locus are characterized with a set of obesity-specific SNPs within one of them, which may predispose individuals to obesity.
Data suggest selected SIM1 variants exhibit poor dimerization with ARNT2 (aryl-hydrocarbon receptor nuclear translocator 2 (zeige ARNT2 Proteine)) and anomalous intracellular localization; data were used to predict spot in SIM1/SIM2 (zeige SIM2 Proteine) (residues 290-326) critical in function.
Hence, we suggest that detailed endocrine evaluation and longitudinal endocrine follow up be performed in individuals with proximal interstitial 6q deletion involving SIM1
Results demonstrate that Sim1 is essential for proper migration and the guidance of commissural axons of the spinal V3 interneurons
These findings reveal Sim1 as a critical yet previously unrecognized modulator of skeletal homeostasis that functions through a central relay.
CB1 (zeige CNR1 Proteine) receptors on Sim1-positive neurons do not impact food intake but hinder energy expenditure during dietary environmental challenges that promote body weight gain.
Results show that Sim1 acts physiologically as well as developmentally to regulate body weight.
Paraventricular nucleus Sim1 neuron ablation mediated obesity is resistant to high fat diet.
Sim1 neurons in adult mice regulate both food intake and energy expenditure
Sim1 is a regulator of dorsal raphe nucleus specification acting upstream of Pet1 (zeige FEV Proteine) and Tph2 (zeige TPH2 Proteine).
Sim1 haploinsufficiency is thus associated with a decrease of several paraventricular nucleus and supraoptic nucleus of the hypothalamus cell types, which has the potential of affecting distinct homeostatic processes.
Differential activities of murine single minded 1 (SIM1) and SIM2 (zeige SIM2 Proteine) on a hypoxic response element
interaction between SIM1 and arylhydrocarbon receptor involved in the control of food intake
three SIM1 genotypes (CC, CT, TT) were found and their frequencies between domestic and foreign breeds were different
SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.
class E basic helix-loop-helix protein 14
, single-minded homolog 1
, single-minded 1
, single-minded-like 1