Literature DB >> 9096118

Mouse homeobox-containing gene, Otx2, maps to mouse chromosome 14.

M Oyanagi1, I Matsuo, Y Wakabayashi, S Aizawa, R Kominami.   

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Year:  1997        PMID： 9096118     DOI： 10.1007/s003359900417

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  10 in total

1.  Developmental anomalies in mice resulting from action of the gene, disorganization, a semi-dominant lethal.

Authors:  K P HUMMEL
Journal:  Pediatrics       Date:  1959-01       Impact factor: 7.124

Review 2.  Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology.

Authors:  M M Cohen
Journal:  Teratology       Date:  1989-09

3.  Mouse Otx2 functions in the formation and patterning of rostral head.

Authors:  I Matsuo; S Kuratani; C Kimura; N Takeda; S Aizawa
Journal:  Genes Dev       Date:  1995-11-01       Impact factor: 11.361

4.  A case of proximal 14 trisomy with pathological findings.

Authors:  K Cottrall; I Magrath; J A Bootes; V Prouten; C Brooker; A Stewart; B W Richards
Journal:  J Ment Defic Res       Date:  1981-03

Review 5.  Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature.

Authors:  M Münke; B S Emanuel; E H Zackai
Journal:  Am J Med Genet       Date:  1988-08

6.  Genetic and developmental studies of a new mouse mutation that produces otocephaly.

Authors:  D M Juriloff; K K Sulik; T H Roderick; B K Hogan
Journal:  J Craniofac Genet Dev Biol       Date:  1985

7.  Novel mouse microsatellites: primer sequences and chromosomal location.

Authors:  T Suda; M Oyanagi; S Wakana; Y Takahashi; H Kanada; H Yonekawa; N Miyashita; T Shiroishi; K Moriwaki; R Kominami
Journal:  DNA Res       Date:  1994       Impact factor: 4.458

8.  Forebrain and midbrain regions are deleted in Otx2-/- mutants due to a defective anterior neuroectoderm specification during gastrulation.

Authors:  D Acampora; S Mazan; Y Lallemand; V Avantaggiato; M Maury; A Simeone; P Brûlet
Journal:  Development       Date:  1995-10       Impact factor: 6.868

9.  Chromosome locations of human EMX and OTX genes.

Authors:  K Kastury; T Druck; K Huebner; C Barletta; D Acampora; A Simeone; A Faiella; E Boncinelli
Journal:  Genomics       Date:  1994-07-01       Impact factor: 5.736

10.  A targeted mouse Otx2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain.

Authors:  S L Ang; O Jin; M Rhinn; N Daigle; L Stevenson; J Rossant
Journal:  Development       Date:  1996-01       Impact factor: 6.868
  10 in total

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