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Microtubule-associated protein that mediates aggregation of mitochondria resulting in cell death and genomic destruction (MAGD).
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Results suggested that microtubule associated protein 1S (MAP1S) were up-regulated among Crohn's disease (CD) patients and MAP1S-related autophagy inhibits apoptosis of intestinal epithelial cells (IECs) through Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) signaling pathway which might play a vital role in the protection of intestinal mucosal barrier and inhibition the progression of CD.
Autophagy defects in the degradation of lipid droplets triggered by the MAP1S deficiency may enhance the initiation and development of ccRCC and reduce the survival of ccRCC patients.
HDAC4 (show HDAC4 Proteins) destabilizes MAP1S, suppresses autophagy flux and promotes the accumulation of mHTT aggregates.
Ddata underline the key role of MAP1S as a global regulator of microbutule stability and demonstrate a new primary function of MAP1S to regulate MT dynamics at the onset of cytokinesis.
results support a role for MAP1 (show MASP1 Proteins) proteins in promoting efficient retrograde trafficking of HIV-1 by stimulating the formation of stable microtubules and mediating the association of HIV-1 cores with microtubules.
The PU.1-regulated MAP1S gene is implicated in neutrophil differentiation and autophagy control.
clarify roles of MAP1S in bridging microtubules and mitochondria with autophagic and mitophagic initiation, maturation, trafficking, and lysosomal clearance.
The amino acid sequence of VCY2IP-1 shows 59.3% and 41.9% homology to two human microtubule-associated proteins (MAPs), MAP1B (show MAP1B Proteins) and MAP1A (show MAP1A Proteins), respectively. VCY2IP-1 has an extensive homology to the N-terminus and C-terminus regions of MAP1B (show MAP1B Proteins) and MAP1A (show MAP1A Proteins)
Deletion mutagenesis indicated that C19ORF5 selectively binds double stranded DNA through its microtubule binding domain.
These results suggest that the interaction of SOCS3 (show SOCS3 Proteins) with MAP1S and the integrity of the microtubule cytoskeleton play an important role in the negative regulation of SOCS3 (show SOCS3 Proteins) on IL-6 (show IL6 Proteins) signaling.
Depletion of MAP1S in mice leads to an accumulation of fibrosis-related proteins and the development of renal fibrosis in aged mice.
MAP1S-mediated autophagy plays an important role in maintaining mouse lifespan especially in the presence of extra amount of fibronectin (show FN1 Proteins).
Data (including data from studies in knockout mice) suggest that Map1s interacts directly with MyD88 (myeloid differentiation primary response gene 88 (show MYD88 Proteins)), a key adaptor of Toll (show TLR4 Proteins)-like receptors, as phagocytosis of bacteria is initiated in macrophages.
Data establish a link between MAP1S-enhanced autophagy and suppression of genomic instability and tumorigenesis.
MAP8 is a novel microtubule associated protein (show SPAG5 Proteins) containing two microtubule binding domains.
Axonal transport impairment may be a deleterious consequence of accumulated, toxic MAP8 protein.
Microtubule-associated protein that mediates aggregation of mitochondria resulting in cell death and genomic destruction (MAGD). Plays a role in anchoring the microtubule-organizing center to the centrosomes. Binds to DNA. Plays a role in apoptosis. Involved in the formation of microtubule bundles (By similarity).
microtubule-associated protein 1S
, BPY2 interacting protein 1
, BPY2-interacting protein 1
, VCY2 interacting protein 1
, VCY2-interacting protein 1
, microtubule-associated protein 8
, variable charge Y chromosome 2-interacting protein 1