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70 Possible Causes for Hox 2

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  • Campomelic Dysplasia

    Review of the genetic map of the inverted region identified potential "structural" genes including the Hox-2-homeobox gene and the collagen gene, COLIA1, which may be involved[ncbi.nlm.nih.gov]

  • Short Rib-Polydactyly Syndrome Type Beemer-Langer

    It was speculated that disruption of 2 structural genes, Hox-2 and COLlAl, which have been mapped to 17q21-q22 and 17q21.3- 922, respectively [Rabin et al., 1985; Retiefet[documents.tips] Alternatively, disruption of 2 structural genes, Hox-2 and COLlAl, mapped to 17q21-q22 and 17q21.3-q22, respectively, may lead to variable phenotypes which in- clude lethal[documents.tips]

  • Cestoda

    The results suggest that Taenia Hox genes may have undergone independent gene duplication in two Hox paralogs.[ncbi.nlm.nih.gov] The failure to detect Post1/2 orthologs in T. asiatica may suggest that sequence divergence or the secondary loss of the posterior genes has occurred in the lineage leading[ncbi.nlm.nih.gov]

  • Isotretinoin

    Retinoic acid alters hindbrain Hox code and induces transformation of rhombomeres 2/3 into a 4/5 identity. Nature 360, 737-741. ‎[books.google.ro]

  • Abnormal Auricles

    Retinoic acid alters hindbrain Hox code and induces transformation of rhombomeres 2/3 into a 4/5 identity. Nature 360, 737-741. ‎[books.google.de]

  • Angelman Syndrome

    Chromosome 12: HOX genes of development, Matt Ridley Matt Ridley talks about chromosome 12, HOX genes of development. SOURCE: DNAi 15397.[dnalc.org] Chromosome 2: fusion of 2 small chromosomes, Matt Ridley Matt Ridley talks about chromosome 2, fusion of 2 small chromosomes. SOURCE: DNAi 881.[dnalc.org]

  • Bronchopulmonary Sequestration

    Aberrant cell adhesion molecule and Hox protein regulation are likely part of the mechanism involved in the development of BPS and CCAM.[ncbi.nlm.nih.gov] We conclude that in BPS and CCAM, altered alpha(2)-integrin cytoplasmic signaling contributes to abnormal cellular behavior in these lung lesions.[ncbi.nlm.nih.gov] We previously showed that the Hox protein HoxB5 is abnormally increased in bronchopulmonary sequestration (BPS) and congenital cystic adenomatoid malformation (CCAM), congenital[ncbi.nlm.nih.gov]

  • Holt Oram Syndrome

    Expression of homeobox genes Msx-1 (Hox-7) and Msx-2 (Hox-8) during cardiac development in the chick. J Cell Biochem Suppl 1993 ;17: 209 - 209 abstract.[nejm.org]

  • Pure Hair and Nail Ectodermal Dysplasia

    Aliases for HOXC13 Gene Homeobox C13 2 3 5 Homeobox Protein Hox-3G 3 4 HOX3G 3 4 Homeobox Protein Hox-C13 3 Homeo Box C13 2 Homeo Box 3G 3 NUP98/HOXC13 3 ECTD9 3 HOX3 3 External[genecards.org]

  • Ectodermal Dysplasia Type 5 Hair Nail

    Aliases for HOXC13 Gene Homeobox C13 2 3 5 Homeobox Protein Hox-3G 3 4 HOX3G 3 4 Homeobox Protein Hox-C13 3 Homeo Box C13 2 Homeo Box 3G 3 NUP98/HOXC13 3 ECTD9 3 HOX3 3 External[genecards.org]

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