Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Wählen Sie die Spezies und Applikation aus
Sie gelangen zu unserer vorgefilterten Suche.
The expression of AtMutSgamma (MSH7 and MSH2) in Saccharomyces cerevisiae suggest that AtMutSgamma affects yeast genomic stability by recognizing specific mismatches.
The contribution of MutSalpha (MSH2-MSH6) to ultraviolet-induced DNA lesion repair and cell cycle regulation was investigated.
reported that AtMSH2 has a broad range of anti-recombination effects: it suppresses recombination between divergent direct repeats in somatic cells or between homologues from different ecotypes during meiosis
Deletion of the MSH2 C-terminus severely affected the stability of the MSH2/MSH6 (zeige MSH6 Antikörper) heterodimer and consequently strongly attenuated DNA mismatch repair. The C-terminal truncation MSH2 mutant predisposed mice to tumor formation.Mutations deleting the MSH2 C-terminus can therefore unambiguously be considered as pathogenic and a cause of Lynch syndrome.
Normal Msh2-deficient organoids showed increased inheritable transient cyst-like growth, which became independent of R-spondin. intestinal stem cell (ISC) proceeded faster in vitro than in vivo independent of the underlying genotype but more under Mutations in mismatch repair deficiency.
Study shows that MSH2-/- mice develop spontaneous thymic lymphomas.
Data show that in mutS homolog 2 protein Msh2(+/-) mice, azathioprine (Aza) induced a high incidence of microsatellite instability (MSI (zeige EBP Antikörper)) lymphomas in a dose-dependent manner.
In Msh2-/- mice, red meat enhanced survival compared to control (p<0.01) and lowered total tumour burden compared to resistant starch (p<0.167).
Angptl2 (zeige ANGPTL2 Antikörper)-induced inflammation increases susceptibility to microenvironmental changes, allowing increased oxidative stress and decreased Msh2 expression.
Gut (zeige GUSB Antikörper) microbes did not induce colorectal cancer in APC (zeige APC Antikörper)(Min/+)MSH2(-/-) mice through an inflammatory response or the production of DNA mutagens but rather by providing carbohydrate-derived metabolites such as butyrate that fuel hyperproliferation of MSH2(-/-) colon epithelial cells.
MSH2-MSH3 (zeige MSH3 Antikörper) suppresses chromosomal instability and modulates the tumor spectrum in p53 (zeige TP53 Antikörper)-deficient tumorigenesis.
Results suggest that MSH2 is rate limiting for expansion in fragile X (zeige FMR1 Antikörper) premutation mouse model and that MSH2 levels may be a key factor that accounts for tissue-specific differences in expansion risk.
Toxicity, induced by tert (zeige TERT Antikörper)-butyl-hydroperoxide and potassium bromate, differs in base excision repair proficient (Mpg (zeige MPG Antikörper) (+/+), Nth1 (+/+)) and deficient (Mpg (zeige MPG Antikörper) (-/-), Nth1 (-/-)) mouse embryonic fibroblasts following Msh2 knockdown, was examined.
Identification and characterization of novel knockout mutants of the three major MMR (zeige MRC1 Antikörper) genes, mlh1 (zeige MLH1 Antikörper), msh2, and msh6 (zeige MSH6 Antikörper), in zebrafish that develop tumors at low frequencies.
study to estimate frequency of point mutations and chromosomal rearrangements in 3 mismatch repair (MMR (zeige MRC1 Antikörper)) genes MLH1 (zeige MLH1 Antikörper), MSH2, and MSH6 (zeige MSH6 Antikörper) among unselected patients with ovarian cancer; estimate that approximately 0.6% of unselected ovarian cancer patients have mutations in the MMR (zeige MRC1 Antikörper) genes
MSH2 rs2303425 Polymorphism is Associated with Early-Onset Breast Cancer.
Five out of twelve patients with defects in either of MSH2, RAD50 (zeige RAD50 Antikörper) and NBN (zeige NBN Antikörper) genes suffered from rare life-threatening AE, more frequently than in control group (p = 0.0005). When all detected variants were taken into account, the majority of patients (8 out of 15) suffered from life-threatening toxicity during chemotherapy.
MSH2 inversion of exons 1-7 was found in four probands previously suspected to have Lynch syndrome based on family history and tumor testing
Loss of MSH2 expression is associated with colorectal carcinoma.
Findings indicate that carriers of the MSH5 (zeige MSH5 Antikörper) rs707939 T allele, the MSH2 rs6544991 C allele, the MSH3 (zeige MSH3 Antikörper) rs6151627 and rs6151670 G alleles, and the MSH3 (zeige MSH3 Antikörper) rs7709909 T allele have poor toxicity tolerance to platinum-based chemotherapy in non-small cell lung cancer patients.
Overexpression of MutL homolog 1 and MutS homolog 2 proteins have reversed prognostic implications for stage I-II colon cancer
MSH2 mutations contribute to colorectal cancer susceptibility in Algerian families with suspected Lynch syndrome.
The data suggest that EZH2 (zeige EZH2 Antikörper)-H3K27me3 regulatory mechanism dynamically changes the expression levels of DNA mismatch repair gene MutS homolog 2, through epigenetic mark H3K27me3.
Genetic changes between MLH1 (zeige MLH1 Antikörper) and MSH2 were significantly positively correlated (p = 0.032). We also noted a positive correlation between genetic changes of MSH2 and DVL3 (zeige DVL3 Antikörper) genes (p = 0.034).
Overexpression of Tinman and Pannier resulted in 20% of embryos with ectopic Hand and Sur (zeige ABCC8 Antikörper) expression. By adding MEF2 (zeige MYEF2 Antikörper) alongside Tinman and Pannier, an expansion in expression of Hand and Sur (zeige ABCC8 Antikörper) was observed.
Findings provide mechanistic insight into the brake on myogenesis that occurs during mesoderm specification: twist and tin expression at early stages in turn activate the myogenic inhibitor Him; yet, once Twist or Tin levels decline at mid-embryogenesis, Him is no longer expressed in the mesoderm, and MEF2 (zeige MYEF2 Antikörper)-dependent muscle differentiation can proceed.
Plasticity in Hox/PBC (zeige DLAT Antikörper) interaction modes is a common molecular strategy for shaping Hox transcriptional activities.
The enhancers active in the heart progenitor cells and the heart generally are dependent on tinman gene activity, whereas those active in non-cardiac mesoderm are often bound neutrally by Tinman
Genetic interaction analysis shows that spir functionally interacts with Dorsocross, tin, and pannier to properly specify the cardiac fate.
Tin is a direct regulator of midline in fly heart development.
wg and dpp (zeige TGFb Antikörper) contribute progressively to the elaboration of the expression pattern of the mesoderm-specific homeobox (zeige PRRX1 Antikörper)-containing gene tinman (tin), and the overlap of wg and dpp (zeige TGFb Antikörper) in the presence of tin-expressing cells directs cardiac-specific differentiation
We show that salivary gland posterior migration requires the activities of genes that position the visceral mesoderm precursors, such as heartless, thickveins, and tinman, but does not require a differentiated visceral mesoderm.
one of the major functions of mid and H15 during cardioblast development is the re-activation of tin expression at a stage when the induction of tin by Dpp (zeige TGFb Antikörper) in the dorsal mesoderm has ceased
dSUR is regulated by tinman and plays a protective role against hypoxic stress and pacing-induced heart failure
This locus is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Two transcript variants encoding different isoforms have been found for this gene.
mismatch repair protein
, DNA mismatch repair protein Msh2
, mutS protein homolog 2
, mismatch repair protein Msh2
, mutS-like protein 2
, MutS-like protein 2