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26 Possible Causes for RBBP6, human, protein

Did you mean: RBBP6, human, proteus

  • Dengue Virus

    In the present study, we have demonstrated that primary human naive CD4 and CD8 T cells are permissive for DV infection.[ncbi.nlm.nih.gov] Silencing RBBP6 (Retinoblastoma Binding Protein 6) sensitises breast cancer cells MCF7 to staurosporine and camptothecin-induced cell death .[doi.org] The non-structural protein (NS) 4A is one of the least characterized DV proteins.[ncbi.nlm.nih.gov]

  • Entamoeba Histolytica

    Distance to human settlements explained the variation in E. histolytica infection seen in lemurs.[ncbi.nlm.nih.gov] RBBP6 isoforms regulate the human polyadenylation machinery and modulate expression of mRNAs with AU-rich 3' UTRs.[frontiersin.org] KEYWORDS: ALIX family proteins; EhADH; Entamoeba histolytica; cysteine proteases; molecular dynamics simulation; proteinprotein docking[ncbi.nlm.nih.gov]

  • Hypoinsulinemic Hypoglycemia and Body Hemihypertrophy

    Information by UniProt Functional Studies - Recombinant human AKT2 protein (ab60322) Sample Kinase Activity Plot.[abcam.com] Phosphorylates ATF4, CIR1, PTN, RAD26L, RBBP6, RPS7, RPS6KB1, TRIP4, STAT3 and histones H1 and H3. Phosphorylates KIF11 to promote mitotic spindle formation.[molsoft.com] PHLPP1 - PH domain leucine-rich repeat-containing protein phosphatase 1; Protein phosphatase involved in regulation of Akt and PKC signaling.[string-db.org]

  • Retinoblastoma

    Gelb , Robust identification of mosaic variants in congenital heart disease , Human Genetics , 10.1007/s00439-018-1871-6 , 137 , 2 , (183-193) , (2018) . A. Foster, L.[doi.org] Abstract The retinoblastoma binding protein 6 (RBBP6), a p53 negative regulator, is essential for embryonic development.[ncbi.nlm.nih.gov] A C-terminal LxCxE motif in ORFV119 enabled the protein to interact with the retinoblastoma protein (pRb) a multifunctional protein best known for its tumor suppressor activity[ncbi.nlm.nih.gov]

  • Myeloproliferative Disease

    Human myeloproliferative disorders form a range of clonal haematological malignant diseases, the main members of which are polycythaemia vera, essential thrombocythaemia,[ncbi.nlm.nih.gov] RBBP6 germline gain-of-function mutations mostly associated with primary myelofibrosis, observed in 5% of the familial and 0.6% of the sporadic MPN cases.[atlasgeneticsoncology.org] The protein encoded by NOG, noggin, acts as an antagonist to bone morphogenetic secreted protein 2 and 4 (BMP2 and BMP4).[ncbi.nlm.nih.gov]

  • Griscelli Syndrome, Type 2

    RAB27A cDNA ORF Clone, Human, C-OFPSpark tag: Alternative Names GS2 cDNA ORF Clone, Human; HsT18676 cDNA ORF Clone, Human; RAB27 cDNA ORF Clone, Human; RAM cDNA ORF Clone,[sinobiological.com] Overexpression of rbbp6, alone or combined with mutant tp53, is predictive of poor prognosis in colon cancer. PLoS One. 2013;8:e66524.[link.springer.com] The protein is membrane-bound and may be involved in protein transport and small GTPase mediated signal transduction.[genetex.com]

  • AICA-Ribosiduria

    […] line (HepG2), sarcoma osteogenic cells (Saos-2), human embryonic kidney cells (HEK293), human skin fibroblasts (SF) and primary human keratinocytes (KC) cultured in purine-depleted[ncbi.nlm.nih.gov] RBBP6 G:600938 . . RBBP7 G:300825 . . RBBP8 G:604124 . Jawad syndrome, 251255 (3) RBBP8 G:604124 . Pancreatic carcinoma, somatic (3) RBBP8 G:604124 .[usegalaxy.org] AICAR induction of TXNIP depended on MondoA, but was independent of AMPK (AMP-activated protein kinase) activation and calcium.[biochemj.org]

  • Autosomal Recessive Myeloproliferative Disease

    […] genetic diseases Drosophila Models of Human Diseases - a blog about Drosophila disease models Drosophila and Human Disease - a resource from Bloomington Drosophila Stock[sdbonline.org] RBBP6 germline gain-of-function mutations mostly associated with primary myelofibrosis, observed in 5% of the familial and 0.6% of the sporadic MPN cases.[atlasgeneticsoncology.org] W), which is predicted to change the structure of the protein. Figure 3.[academic.oup.com]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    Human genomes (the complete set of genes or genetic material present in a cell or organism) consist of 3 million DNA base pairs.[dna.universeofatoms.com] RBBP6 G:600938 . . RBBP7 G:300825 . . RBBP8 G:604124 . Jawad syndrome, 251255 (3) RBBP8 G:604124 . Pancreatic carcinoma, somatic (3) RBBP8 G:604124 .[usegalaxy.org] […] in InterPro IPR036236 Znf_C2H2_sf IPR013087 Znf_C2H2_type SMART i View protein in SMART SM00355 ZnF_C2H2, 13 hits SUPFAM i SSF57667 SSF57667, 7 hits PROSITE i View protein[uniprot.org]

  • Nestor-Guillermo Progeria Syndrome

    Less than 1% of human primary somatic cells can usually turn into iPSCs.[aimspress.com] RBBP6 G:600938 . . RBBP7 G:300825 . . RBBP8 G:604124 . Jawad syndrome, 251255 (3) RBBP8 G:604124 . Pancreatic carcinoma, somatic (3) RBBP8 G:604124 .[usegalaxy.org] Cell signaling mechanisms often transmit information via posttranslational protein modifications, most importantly reversible protein phosphorylation.[scienceopen.com]