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133 Possible Causes for DLL4, mouse, protein

Did you mean: DLL4, morus, proteus

  • LIG4 Syndrome

    […] rickets DCX Lissencephaly, Subcortical laminal heterotopia DHCR7 Smith-Lemli-Opitz syndrome DHCR24 Desmosterolosis DIS3L2 Perlman syndrome DLL3 Spondylocostal dysostosis DLL4[] […] send to {{ username }} {{geneWatchAttr}} Analyze Gene Strain QTL List Functional Annotation unavailable Annotation Distribution unavailable Genomic Variants unavailble for Mouse[] Tandem BRCT domains of LigIV mediate a unique mode of protein-protein interaction.[]

  • Alexander Disease

    CCDC88A, CHMP2B, CLCN2, CLN6, CLP1, COL4A1, COL4A2, COX10, COX15, COX7B, CPLX1, CSF1R, CTBP1, CTC1, CTDP1, CYP27A1, CYP7B1, D2HGDH, DAG1, DARS, DARS2, DDHD2, DEAF1, DHFR, DHH, DLL4[] A transgenic mouse line (Tg73.7) over-expressing human GFAP produces astrocytic aggregates indistinguishable from those seen in the human disease, making them a model of this[] The topological analysis of human protein interaction network strategy to identify highly interconnected sub-network modules from which six proteins are found i.e.[]

  • T-cell Acute Lymphoblastic Leukemia

    […] vivo caused hedgehog pathway activation in both lymphoid and epithelial cells in the thymus and resulted in increased expression of important T-cell stimulatory ligands (Dll4[] Yet, retroviral insertional mutagenesis screens identify RUNX genes as collaborating oncogenes in MYC-driven leukemia mouse models.[] * Neoplasm Proteins/biosynthesis Neoplasm Proteins/genetics Nuclear Proteins/antagonists & inhibitors Precursor T-Cell Lymphoblastic Leukemia-Lymphoma/drug therapy* Protein[]

  • Hereditary Hypophosphatemic Rickets with Hypercalciuria

    DLX3, MMP13, SNX10, INPPL1, MAFB, MMP9, SLCO2A1, PCYT1A, NPR2, BMP2, FAM83H, WDR34, BHLHA9, IHH, XYLT1, LTBP3, DVL1, TBX6, ENAM, NOG, PAPSS2, ACAN, ADAMTS17, KIF22, TBX4, DLL4[] Models phenotype-based associations Disease phenotypes are compared with mouse phenotypes, with each mouse model contributing one point to the diagram.[] Pages: 1 NPT2C Polyclonal Antibody Gene Names: NPT2C ; SLC34A3; HHRH; NPTIIc Other Names: Sodium-dependent phosphate transport protein 2C; Sodium-phosphate transport protein[]

  • Adams-Oliver Syndrome 5

    In total, we identified nine families with mutations in DLL4 .[] Another proposed etiology of AOS includes abnormal pericyte recruitment, supported by a mouse model in which ALK1-deficient mice show poor migration, recruitment, and proliferation[] NOTCH1, UBR1, ARHGAP31, DOCK6, RBPJ, EOGT, KCTD1, DLL4 Specificity 13 % Genes 100 % Comprehensive Skeletal Dysplasias and Disorders Panel.[]

  • Adams-Oliver Syndrome

    A defect in DLL4 was also detected in two families via whole-exome or genome sequencing.[] In keeping with the prominent developmental role described for Notch1 in mouse vasculature, we observed cardiac and multiple vascular defects in four of the five families.[] Functional assays confirmed impaired DNA binding of mutated RBPJ, placing it among other notch-pathway proteins altered in human genetic syndromes.[]

  • Hermanski-Pudlak Syndrome

    […] syndrome, Rothmund-Thomson syndrome WRN Werner syndrome ZMPSTE24 Mandibuloacral dysplasia with B lipodystrophy, Restrictive dermopathy, lethal ARHGAP31 Adams-Oliver syndrome DLL4[] Here, we analyzed agonist-stimulated secretion from other storage granules in platelets from mouse HPS models that lack adaptor protein (AP)-3 or biogenesis of lysosome-related[] ( en ) 1999-03-10 1999-03-10 Isolation and characterization of Hermansky Pudlak Syndrome (HPS) protein complexes and HPS protein-interacting proteins PCT/US2000/006518 WO2000053733A2[]


    CCDC88A, CHMP2B, CLCN2, CLN6, CLP1, COL4A1, COL4A2, COX10, COX15, COX7B, CPLX1, CSF1R, CTBP1, CTC1, CTDP1, CYP27A1, CYP7B1, D2HGDH, DAG1, DARS, DARS2, DDHD2, DEAF1, DHFR, DHH, DLL4[] […] mRNAs Mouse ESTs Other mRNAs Expression and Regulation CpG Islands...[] The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...[]

  • Human Herpesvirus 8

    KSHV manipulates Notch signaling by DLL4 and JAG1 to alter cell cycle genes in lymphatic endothelia.[] The patient was treated with Rituximab, a chimeric (human-mouse) anti-CD20 monoclonal antibody. Thirteen months later, the patient continued in clinical remission.[] […] response signaling in addition to enhancing viral protein folding.[]

  • Xeroderma Pigmentosum Complementation Group B

    FGF10, SALL4, TBX5, FANCA, FANCG, FANCF, FANCE, SLX4, FANCM, FANCL, FANCI, FANCD2, XRCC2, ERCC4, RBM8A, ESCO2, WNT7A, SF3B4, ARHGAP31, DOCK6, RBPJ, GDF5, TBX3, EOGT, BHLHA9, DLL4[] The human and mouse ERCC3 proteins contain several sequence motifs suggesting that it is a nucleic acid or chromatin binding helicase.[] 4 DNA Repair Protein Complementing XP-C Cells 3 Xeroderma Pigmentosum Group C Protein 2 Mutant Xeroderma Pigmentosum Group C 3 RAD4 3 XP3 3 External Ids for XPC Gene Previous[]