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288 Possible Causes for Tp63, protein,, zebrafish

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  • Rapp-Hodgkin Syndrome

    […] to TP63 mutations.[ncbi.nlm.nih.gov] The frameshift results in changes to the tail of p63 with the addition of 68 missense amino acids downstream and a delayed termination codon that extends the protein length[ncbi.nlm.nih.gov] Expression and phylogenetic analyses of three zebrafish FoxI class genes. Dev Dyn 2003; 228: 301–7.[link.springer.com]

  • Hereditary Hypophosphatemic Rickets with Hypercalciuria

    POLR1D, WDR35, CANT1, PTH1R, EBP, NSDHL, RAB23, MSX2, TWIST1, COMP, SOX9, PCNT, ADAMTSL2, DYM, TGFBR1, TGFBR2, SKI, FBN2, FKBP14, TNXB, CHST14, ZNF469, ACVR1, NFIX, GLI3, TP63[mendelian.co] Pages: 1 NPT2C Polyclonal Antibody Gene Names: NPT2C ; SLC34A3; HHRH; NPTIIc Other Names: Sodium-dependent phosphate transport protein 2C; Sodium-phosphate transport protein[mybiosource.com] Instead, zebrafish, having the most complete fish genome sequence, has four NaP i cotransporter genes, two each belonging to the type IIa family and the more divergent type[ncbi.nlm.nih.gov]

  • Werner Syndrome

    TP63 -Related Disorders V Reid Sutton and Hans van Bokhoven. Initial Posting: June 8, 2010; Last Update: August 6, 2015.[ncbi.nlm.nih.gov] Here we report that the WS protein does indeed catalyze DNA unwinding.[ncbi.nlm.nih.gov] I. ( 2005 ) A zebrafish bmyb mutation causes genome instability and increased cancer susceptibility. Proc. Natl. Acad. Sci. U. S.[doi.org]

  • Ectrodactyly-Cleft Palate Syndrome

    -gen TP63- and ADULT syndrome - see ADULT (A cro-Dermato-ungual-Lacrimal-Tooth) syndrome ... -gen TP63-.[ivami.com] Ortholog OMIM Term OMIM Phenotype ID TP63 tp63 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 604292 ZEBRAFISH MODELS No data available PHENOTYPE No[zfin.org] […] adult syndrome , and has symptoms including photophobia An important gene associated with Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 3 is TP63 (Tumor Protein[malacards.org]

  • Neuronal Ceroid Lipofuscinosis

    TNC TNFRSF10B TNFRSF11A TNFRSF11B TNFRSF13B TNFRSF13C TNFRSF1A TNFSF11 TNFSF12 TNFSF15 TNFSF4 TNK2 TNNC1 TNNI2 TNNI3 TNNT1 TNNT2 TNNT3 TNPO3 TNXB TOP2A TOPORS TOR1A TP53 TP63[csbg.cnb.csic.es] To gain insight into the function of CLN8 protein, we employed the split-ubiquitin membrane-based yeast two-hybrid (MYTH) system, which detects protein-protein interactions[ncbi.nlm.nih.gov] In zebrafish, there are two GRN homologues, Granulin A (Grna) and Granulin B (Grnb).[ncbi.nlm.nih.gov]

  • Bloom Syndrome

    TP63 -Related Disorders V Reid Sutton and Hans van Bokhoven. Initial Posting: June 8, 2010; Last Update: August 6, 2015.[ncbi.nlm.nih.gov] PRKAR1A and other protein kinase A (PKA) subunits were expressed in Bloom syndrome cells and their level of expression differed by subunit and cell type.[ncbi.nlm.nih.gov] . , 2008 Heritable targeted gene disruption in zebrafish using designed zinc-finger nucleases. Nat. Biotechnol. 26 : 702 –708. E ngels , W. R., D. M.[genetics.org]

  • Abetalipoproteinemia

    Dyskeratosis Congenita TINF2, TERC, TERT Dystonie TOR1A, ATP1A3, GCH1, SGCE, THAP1, TH, GNAL Ectodermal dysplasia 2, Clouston type GJB6 Ectrodactyly,Split hand/foot malformation TP63[meduniwien.ac.at] Abstract The microsomal triglyceride transfer protein (MTP) is a dimeric lipid transfer protein consisting of protein disulfide isomerase and a unique 97-kDa subunit.[ncbi.nlm.nih.gov] View Article Google Scholar Marza E, Barthe C, Andre M, Villeneuve L, Helou C, Babin PJ: Developmental expression and nutritional regulation of a zebrafish gene homologous[doi.org]

  • Oculocerebrorenal Syndrome

    ABCD-Syndrom 600501 ( A lbinism, B lack lock, C ell migration disorder of the neurocytes of the gut, and D eafness; EDNRB 131244 ) AEC-Syndrom, Hay-Wells-Syndrom 106260 ( TP63[medizinische-genetik-dresden.de] References "The Lowe's oculocerebrorenal syndrome gene encodes a protein highlyhomologous to inositol polyphosphate-5-phosphatase."[genscript.com] This is further supported by the defective cilia formation in zebrafish Kupffer's vesicles and in cilia-dependent melanosome transport assays in inpp5b morphants.[ncbi.nlm.nih.gov]

  • Amelogenesis Imperfecta Type 1G with Nephrocalcinosis

    SOX3, NSDHL, POR, MSX2, TWIST1, COMP, SOX9, RASA2, RRAS, CEP152, GLI2, PCNT, ATR, ADAMTSL2, DYM, TGFB2, SMAD3, TGFBR1, TGFBR2, SKI, FBN2, CHST14, ACVR1, NFIX, EZH2, GLI3, TP63[mendelian.co] (PMID: 15676076) Nalbant D … Williams SC (BMC genomics 2005) 3 4 22 58 A secretory kinase complex regulates extracellular protein phosphorylation.[genecards.org] Ortholog OMIM Term OMIM Phenotype ID FAM20A fam20a Amelogenesis imperfecta, type IG (enamel-renal syndrome) 204690 ZEBRAFISH MODELS No data available PHENOTYPE No data available[zfin.org]

  • Inflammation

    SOX2 and TP63 proteins clearly delineated tumour cells in invasive squamous cervical cancer [ 55 ].[doi.org] The rate of protein synthesis in vivo was measured by the incorporation of [3H]phenylalanine into liver proteins in a chronic (5 day) intra-abdominal abscess model.[doi.org] Spaink , Comparative studies of Toll-like receptor signalling using zebrafish , Developmental & Comparative Immunology , 46 , 1 , (35) , (2014) . Bruno A.[doi.org]