|Prediction of the coding sequences of unidentified human genes. IV. The coding sequences of 40 new genes (KIAA0121-KIAA0160) deduced by analysis of cDNA clones from human cell line KG-1.
|Human scribble (Vartul) is targeted for ubiquitin-mediated degradation by the high-risk papillomavirus E6 proteins and the E6AP ubiquitin-protein ligase.
|Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones.
|Robust phosphoproteomic profiling of tyrosine phosphorylation sites from human T cells using immobilized metal affinity chromatography and tandem mass spectrometry.
|Mammalian Scribble forms a tight complex with the betaPIX exchange factor.
|The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
|The tumor suppressor Scrib interacts with the zyxin-related protein LPP, which shuttles between cell adhesion sites and the nucleus.
|Thyrotropin receptor trafficking relies on the hScrib-betaPIX-GIT1-ARF6 pathway.
|Junctional recruitment of mammalian Scribble relies on E-cadherin engagement.
|hScrib interacts with ZO-2 at the cell-cell junctions of epithelial cells.
|The tumor suppressor Scrib selectively interacts with specific members of the zyxin family of proteins.
|The mammalian Scribble polarity protein regulates epithelial cell adhesion and migration through E-cadherin.
|DNA sequence and analysis of human chromosome 8.
|Human scribble, a novel tumor suppressor identified as a target of high-risk HPV E6 for ubiquitin-mediated degradation, interacts with adenomatous polyposis coli.
|Human homolog of Drosophila tumor suppressor Scribble negatively regulates cell-cycle progression from G1 to S phase by localizing at the basolateral membrane in epithelial cells.
|Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.
|Tick-borne encephalitis virus NS5 associates with membrane protein scribble and impairs interferon-stimulated JAK-STAT signalling.
|Combining protein-based IMAC, peptide-based IMAC, and MudPIT for efficient phosphoproteomic analysis.
|Loss of human Scribble cooperates with H-Ras to promote cell invasion through deregulation of MAPK signalling.
|A quantitative atlas of mitotic phosphorylation.
|Scrib regulates PAK activity during the cell migration process.
|Deregulation of scribble promotes mammary tumorigenesis and reveals a role for cell polarity in carcinoma.
|Large-scale proteomics analysis of the human kinome.
|Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.
|MCC, a new interacting protein for Scrib, is required for cell migration in epithelial cells.
|Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
|Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.
|Initial characterization of the human central proteome.
|System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.
|Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.
|The PDZ-binding motif of MCC is phosphorylated at position -1 and controls lamellipodia formation in colon epithelial cells.
|Toward a comprehensive characterization of a human cancer cell phosphoproteome.
|An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
|Loss of DLG5 promotes breast cancer malignancy by inhibiting the Hippo signaling pathway.