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anti-Mouse (Murine) HELLS Antikörper:
anti-Rat (Rattus) HELLS Antikörper:
anti-Human HELLS Antikörper:
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Lsh Is Essential for Maintaining Global DNA Methylation Levels in Amphibia and Fish and Interacts Directly with Dnmt1 (zeige DNMT1 Antikörper).
These results suggest that Lsh exerts epigenetic regulation at key regulators of neural stem cell fate ensuring adequate neural stem/progenitor cells self-renewal and maintenance during development.
fibroblasts derived from chromatin remodeling ATPase (zeige DNAH8 Antikörper) LSH (HELLS)-null mouse embryos, which lack DNA methylation from centromeric repeats, transposons and a number of gene promoters, are capable of reestablishing DNA methylation and silencing of misregulated genes upon re-expression of LSH.
Data suggest that HELLS controls cytosine methylation in a nuclear compartment that is in part defined by lamin B1 (zeige LMNB1 Antikörper) attachment regions.
histone H3 (zeige HIST3H3 Antikörper) lysine 4 methylation modification was assessed in murine embryonic fibroblasts (MEFs) derived from the DNA methylation mutant Lsh(-/-) mice.
These results indicate that in the absence of HELLS, proliferation of spermatogonia is reduced and germ cell differentiation arrested at the midpachytene stage, implicating an essential role for HELLS during male meiosis.
LSH is essential for developmentally programmed de novo DNA methylation at the promoters of protein coding genes and recruitment of G9a (zeige EHMT2 Antikörper)/GLP (zeige GOLGA6A Antikörper) complex to a subset of genomic loci.
Data show that hypomethylation in Lsh-/- cells is associated with efficient transcriptional elongation and splicing.
model in which Lsh is recruited by intact heterochromatin structure and then assists in maintaining heterochromatin organization by establishing CpG methylation patterns
PASG mutant mice display signs of growth retardation and premature aging, including low birth weight, failure to thrive, graying and loss of hair, reduced skin fat deposition, osteoporosis, kyphosis, cachexia, and premature death.
Lsh has a critical and previously unidentified role in epigenetic gene silencing and maintenance of genomic stability during female meiosis.
HELLS and CDCA7 (zeige CDCA7 Antikörper) comprise a bipartite nucleosome remodeling complex; immunodeficiency-centromeric instability-facial anomalies syndrome has a defective HELLS and CDCA7 (zeige CDCA7 Antikörper) bipartite nucleosome remodeling complex
This study elucidates the molecular basis of the c-Myc (zeige MYC Antikörper)/EGLN1 (zeige EGLN1 Antikörper)-mediated induction of LSH expression that inhibits ferroptosis
LSH is likely one of the mechanisms of genome instability underlying 5-hydroxymethylcytosine loss in cancer.
High mRNA levels of HELLS is independent predictor of poor outcome in Renal Cell Carcinoma (zeige MOK Antikörper) patients.
LSH promoted cancer progression in part by regulating expression of fumarate hydratase (FH (zeige FH Antikörper)).
Mutations in HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome type 4.
Mutations of HELLS gene is associated with stomach and colorectal cancers.
Upregulation of HELLS and UHRF1 (zeige UHRF1 Antikörper) is essential for the tumor phenotype. Also, these epigenetic regulators are important for the regulation of SYK (zeige SYK Antikörper).
just as E2F3, HELLS is overexpressed in human tumours including prostate cancer, indicating that either factor may contribute to the malignant progression of tumours
E2F1 (zeige E2F1 Antikörper) plays a crucial role in transcriptional control of the human Lsh gene and the decrease of Lsh expression in senescent cells is related to the repression of E2F1 (zeige E2F1 Antikörper)
This gene encodes a lymphoid-specific helicase. Other helicases function in processes involving DNA strand separation, including replication, repair, recombination, and transcription. This protein is thought to be involved with cellular proliferation and may play a role in leukemogenesis. Alternatively spliced transcript variants have been described, but their biological validity has not been determined.
, helicase, lymphoid specific
, lymphoid-specific helicase-like
, lymphocyte-specific helicase
, proliferation-associated SNF2-like protein
, TBC1D12: TBC1 domain family, member 12
, SWI/SNF2-related matrix-associated actin-dependent regulator of chromatin subfamily A member 6
, SWI/SNF2-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 6
, lymphoid-specific helicase