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93 Possible Causes for A9, Gene, Homeobox

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  • Leber Congenital Amaurosis

    BACKGROUND: The cone-rod homeobox (CRX) gene plays an important role in photoreceptor development.[ncbi.nlm.nih.gov] To date, 23 LCA genes have been identified. Gene replacement in the RPE65 form of LCA represents a major advance in treatment, although limitations have been recognized.[ncbi.nlm.nih.gov] T * p.Q120X c.258C T * p.Q120X Yes A73 c.2334C T p.T745M c.1313G A * p.C438Y Yes A77 c.2401A T p.K801X c.2401A T p.K801X Yes A78 c.25555T C p.1852T c.2334C T p.T745M Yes A9[iovs.arvojournals.org]

  • Cholangiocarcinoma

    In patients with CCA, potential novel biomarkers wre immunoglobulin heavy chain, translocated in liposarcoma (TLS), visual system homeobox 2 (VSX2) and an unnamed protein[ncbi.nlm.nih.gov] KEYWORDS: Ribonucleic acid sequencing; biliary tract cancers; gene expression networks; regulatory genes; systems biology[ncbi.nlm.nih.gov] Upregulation of six proteins in tumor interstitial fluid, including S100 calcium binding protein A6 (S100A6), S100 calcium binding protein A9, aldo-keto reductase family 1[ncbi.nlm.nih.gov]

  • Myeloproliferative Disease

    Abstract The p75 CCAAT-displacement protein/Cut homeobox (CDP/Cux) isoform was previously reported to be overexpressed in human breast cancers.[ncbi.nlm.nih.gov] We found that a bacterial artificial chromosome (BAC) encompassing the breakpoint on chromosome 17 long arm contained only one gene, NOG.[ncbi.nlm.nih.gov] HLA-typing disclosed the same haplotype (A2, A9, B5, B21, C5) in both patients.[ncbi.nlm.nih.gov]

  • Colorectal Carcinoma

    […] immunohistochemical results for the histological type of the deepest invasive portion of the tissue specimen were positive for thyroid transcription factor-1 but negative for Caudal-type homeobox[ncbi.nlm.nih.gov] BACKGROUND: The KRAS gene mutation is the most common somatic change in colorectal carcinoma (CRC) and is predictive of resistance to anti-epidermal growth factor receptor[ncbi.nlm.nih.gov] Furthermore, mechanistic investigation revealed that NAC1 increased drug resistance via inducing homeobox A9 (HOXA9) expression, and that knockdown of HOXA9 abrogated NAC1[ncbi.nlm.nih.gov]

  • Paclitaxel

    In the A2780 cell line, we also observed increased expression of the C4orf18 gene and decreased expression of the PCDH9 and SEMA3A genes after PAC treatment.[ncbi.nlm.nih.gov] Droghe per uso medico, Ovvero della famiglia del farmaco Taxol e della famiglia del farmaco Limus, ovvero derivati di Limus, siroliumus, rampicina, everolimus, biolimus A9[it.glosbe.com] We examined changes in the expression levels of miR-34a target genes JAG1 and Notch1 and their downstream genes via miR-34a transfection by quantitative reverse transcription[ncbi.nlm.nih.gov]

  • Mesoaxial Synostotic Syndactyly with Phalangeal Reduction

    Polyalanine tract expansion mutations in the homeobox containing gene HOXD13 have been described for SPD (Muragaki et al. 1996).[en.youscribe.com] In this thesis I report on the clinical and molecular data as well as gene localizations in three large Pakistani families with non-syndromic syndactylies. · I have categorized[archiv.ub.uni-marburg.de] We demonstrate that three neighboring missense mutations affecting the highly conserved DNA-binding region of the basic helix-loop-helix A9 transcription factor (BHLHA9) are[ncbi.nlm.nih.gov]

  • Aortic Valve Calcification

    Furthermore, gene expression of calcigenic markers, ALP, bone morphogenetic protein 2 (BMP2), and distal-less homeobox 5 (Dlx5) were significantly increased after 6 days of[jpet.aspetjournals.org] We used polymerase chain reaction to determine ACE gene polymorphism.[ncbi.nlm.nih.gov] Am J Cardiol 84: 1084-5. 1999 Nov 1 A9 10.1016/S0002-9149(99)00504-4 Google Scholar Fox CS, Vasan RS, Parise H, Levy D, O'Donnel CJ, D'Agostino RB, Benjamin EJ, Framingham[cardiovascularultrasound.biomedcentral.com]

  • Non-Syndromic Tibial Hemimelia

    Sexual Development 8(4): 156-159, 2015 Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation .[m.eurekamag.com] TUMOR PROTEIN p63; TP63 [omim:603273] SPLIT-HAND/FOOT MALFORMATION 4; SHFM4 [omim:605289] ACTIVE BCR-RELATED GENE; ABR [omim:600365] BASIC HELIX-LOOP-HELIX FAMILY, MEMBER A9[bio2rdf.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Squamous Cell Carcinoma of the Head and Neck

    Zinc finger E-box binding homeobox 1 promotes invasion and bone metastasis of small cell lung cancer in vitro and in vivo. Cancer science. 2012, 103:1420-1428. 11.[oapublishinglondon.com] BACKGROUND: Genomic imprinting is associated with many human diseases, including various types of cancers, however, no studies on gene imprinting are related to squamous cell[ncbi.nlm.nih.gov] These cytokines augmented expression of HLA-class I, HLA-class II, and intercellular adhesion molecule I, but not squamous cell carcinoma-associated antigens, E7 and A9, on[ncbi.nlm.nih.gov]

  • Leber Congenital Amaurosis 16

    De novo mutations in the CRX homeobox geneassociated with Leber congenital amaurosis. Nat Genet. 1998;18311- 312 PubMed Google Scholar Crossref 21.[jamanetwork.com] The results confirm that pupillometry is a useful objective measure for the assessment of therapeutic effect of gene therapy in patients with LCA.[wrap.warwick.ac.uk] T * p.Q120X c.258C T * p.Q120X Yes A73 c.2334C T p.T745M c.1313G A * p.C438Y Yes A77 c.2401A T p.K801X c.2401A T p.K801X Yes A78 c.25555T C p.1852T c.2334C T p.T745M Yes A9[iovs.arvojournals.org]