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65 Possible Causes for Hox 1

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  • Hand-Foot-Genital Syndrome

    Am J Hum Genet. 2000 Jul;67(1):197-202. Epub 2000 Jun 5. Goodman FR, Scambler PJ. Human HOX gene mutations. Clin Genet. 2001 Jan;59(1):1-11. Review. Goodman FR.[ghr.nlm.nih.gov] A nonsense mutation in the homeobox of HOXA13 has been identified in one affected family, making HFGS the second human syndrome shown to be caused by a HOX gene mutation.[ncbi.nlm.nih.gov] Limb malformations and the human HOX genes. Am J Med Genet. 2002 Oct 15;112(3):256-65. Review.[ghr.nlm.nih.gov]

  • Postaxial Oligodactyly, Tetramelic

    COL2A1), homeotic genes (HOX), Notch and Wnt signaling pathways, among many others.[obgyn.mhmedical.com] Point mutations in either the HOX or PBX half-site of the PPE disrupt the formation of the HOX.PBX complex and dramatically decrease transcriptional activity of the Ren-1([proteinlounge.com] "The thyroid transcription factor-1 gene is a candidate target for regulation by Hox proteins" . The EMBO Journal . 13 (14): 3339–47. PMC 395231 . PMID 7913891 .[en.wikipedia.org]

  • Athabaskan Brainstem Dysgenesis Syndrome

    Product Name HOXA1, Peptide Also Known As HOXA1 Immunizing Peptide Product Synonym Names HOXA1; homeobox A1; BSAS; HOX1; HOX1F; MGC45232; HOX A1 homeodomain protein; Hox 1[mybiosource.com] . 6-like protein; homeo box A1; homeobox 1F; homeobox protein HOX-A1; lab-like protein Research Use Only For Research Use Only.[mybiosource.com]

  • Cherubism

    Hox-gene Msx-1).[ncbi.nlm.nih.gov]

  • T-cell Acute Lymphoblastic Leukemia

    […] homeobox gene (HOX) cluster D, which is expressed during the early stages of T-cell development.[ncbi.nlm.nih.gov] […] report a case of T-cell ALL in a 13-year-old boy with t(2;12)(q31;p13) involving ETV6, resulting in the relocation of the ETV6 from 12p13 to 2q31 locus that harbors the class 1[ncbi.nlm.nih.gov]

  • Peritoneal Metastasis

    We analyzed the expression levels of two lncRNAs-Metastasis-Associated Lung Adenocarcinoma Transcript 1 (MALAT1) and HOX-Antisense Intergenic RNA (HOTAIR)-by real-time reverse[ncbi.nlm.nih.gov]

  • Syndactyly Type 3

    – 343 Homeobox protein Hox-D13 Add BLAST 343 Proteomic databases PTM databases Expression i Gene expression databases Organism-specific databases Interaction i Protein-protein[uniprot.org] View Article : Google Scholar : PubMed/NCBI 9 Goodman FR and Scambler PJ: Human Hox gene mutations. Clin Genet. 59:1–11. 2001.[spandidos-publications.com] Brison N, Tylzanowski P, Debeer P (2012) Limb skeletal malformations - what the HOX is going on? Eur J Med Genet 55: 1–7. View Article Google Scholar 26.[journals.plos.org]

  • Brachydactyly Type E

    Molecular genetic studies failed to identify mutations in the GNAS 1 gene, in the PTH receptor gene and in the HOX D13 gene.[ncbi.nlm.nih.gov]

  • Facioauriculoradial Dysplasia

    COL2A1), homeotic genes (HOX), Notch and Wnt signaling pathways, among many others.[obgyn.mhmedical.com] […] growth factors (FGFs), Sonic hedgehog (SHH), cartilage-derived morphogenetic protein (CDMP), Indian hedgehog (IHH), mammalian SRY box 9 (SOX-9), procollagen type 2 alpha 1([obgyn.mhmedical.com]

  • Hypodontia - Dysplasia of Nails Syndrome

    Aliases for MSX1 Gene Msh Homeobox 1 2 3 5 Msh Homeobox 1-Like Protein 3 4 Homeobox Protein Hox-7 3 4 HOX7 3 4 Msh (Drosophila) Homeo Box Homolog 1 (Formerly Homeo Box 7)[genecards.org]

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