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Huntingtin-interacting protein 1 (Hip1) functions in Notch (zeige NOTCH1 ELISA Kits)-mediated neurogenesis and provides a functional link between Notch (zeige NOTCH1 ELISA Kits) signaling and proteins related to Huntington disease (zeige HTT ELISA Kits).
HIP1 deletion is not involved in Williams-Beuren syndrome.
Huntingtin-interacting protein-1 (HIP1) is known to play a role in tumorigenesis. metastasis. Read More: http://www.atsjournals.org/doi/full/10.1164/rccm.201412-2226OC#.V8DF69LrtNs
SHON is a novel human oncogene (zeige RAB1A ELISA Kits) with predictive utility in ER(+) breast cancer, perhaps offering a simple biomarker to predict the therapeutic efficacy of antiestrogen therapy in patients with breast cancer.
SHON plays an important role in EMT (zeige ITK ELISA Kits) and contributes to breast cancer progression.
HIP1-ALK (zeige ALK ELISA Kits), a novel fusion protein is associated with lung adenocarcinoma.
HIP1-ALK (zeige ALK ELISA Kits)-rearranged tumor is sensitive to treatment with crizotinib, implicating HIP1-ALKas an oncogenic driver of lung tumorigenesis
Identified a four-tyrosine "HIP1 phosphorylation motif" in (zeige EGFR ELISA Kits) the N-terminal region of HIP1 that is required for phosphorylation mediated by both EGFR and PDGFbetaR but not by the oncoproteins HIP1/PDGFbetaR (H/P), and TEL/PDGFbetaR (T/P).
Three neuronal proteins (Huntingtin interacting protein 1, neurofascin (zeige NFASC ELISA Kits), and olfactomedin-like 2a) are novel components of podocyte major processes and their expression in glomerular crescents supports their role in crescent (zeige SFRP5 ELISA Kits) formation.
flexibility of the HIP1 coiled-coil domain is important for normal function and may lead to new insights into Huntington's disease
Huntingtin-interacting protein 1 is a Merkel cell carcinoma marker that interacts with c-Kit (zeige KIT ELISA Kits)
we show that M. tuberculosis impairs dendritic cell cytokine secretion, maturation, and antigen presentation through the cell envelope-associated serine hydrolase, Hip1.
HIP1 association with and phosphorylation mediated by EGFR (zeige EGFR ELISA Kits) and EGFRvIII.
Results show that pro-apoptotic Hippi (zeige IFT57 ELISA Kits)-Hip-1 heterodimers can recruit procaspase-8 into a complex of Hippi (zeige IFT57 ELISA Kits), Hip-1 and procaspase-8, and launch apoptosis through components of the 'extrinsic' cell-death pathw
HIP1 is the first endocytic protein to be directly implicated in tumor formation
disuprtion results in neurological deficits and decreased AMPA (zeige GRIA3 ELISA Kits) receptor trafficking
mice deficient in both HIP1 and HIP1r have accelerated development of abnormalities seen in Hip1 -deficient mice, including kypholordosis and growth defects
The various abnormalities corroborate reduced fertility levels in HIP1(-/-) mice and suggest a role for HIP1 in stabilizing actin and microtubules, enabling normal spermatid and Sertoli cell morphology and function.
we have shown that HIP1 influences important NMDAR (zeige GRIN1 ELISA Kits) functions and that both HIP1 and htt (zeige HTT ELISA Kits) participate in NMDA-induced cell death.
Degenerative phenotypes seen in knockout mice are due mainly to HIP1 and HIP1r protein deficiency rather than altered expression of neighboring genes or disrupted intronic elements.
The product of this gene is a membrane-associated protein that colocalizes with huntingtin. This protein has similarities to cytoskeleton proteins and its interaction with huntingtin is thought to play a functional role in the cell filament network. Loss of normal huntingtin-HIP1 interaction in Huntington disease may contribute to a defect in membrane-cytoskeletal integrity in the brain. This gene could help in the understanding of the normal function of huntingtin and also the pathogenesis of Huntington disease. It also has been implicated in the pathogenesis of hematopoietic malignancies. Two transcript variants encoding different isoforms have been found for this gene.
, huntingtin interacting protein 1
, huntingtin-interacting protein 1
, huntingtin-interacting protein I