Literature DB >> 9216040

Forebrain overgrowth (fog): a new mutation in the mouse affecting neural tube development.

B S Harris1, T Franz, S Ullrich, S Cook, R T Bronson, M T Davisson.   

Abstract

Forebrain overgrowth, fog, is a spontaneous autosomal recessive mutation in the mouse producing forebrain, lumbo-sacral, and facial defects. The defects appear to result from excessive growth or cellular proliferation leading to abnormalities in neural tube closure. Three unique features of the mutant are: (1) the growth of telencephalon cells into the surrounding mesenchyme, (2) presence of an encephalocele through the midline cleft in some mutants, and (3) dissociation of the tail defect from the caudal neural tube defect. We used an intersubspecific intercross between mice carrying the fog mutation and mice from an inbred Mus musculus castaneus strain (CAST/Ei) to map the fog mutation to mouse Chromosome 10 near D10Mit262 and D10Mit230 in a region with several potential candidate genes.

Entities:  

Mesh:

Year:  1997        PMID: 9216040     DOI: 10.1002/(SICI)1096-9926(199704)55:4<231::AID-TERA3>3.0.CO;2-3

Source DB:  PubMed          Journal:  Teratology        ISSN: 0040-3709


  8 in total

1.  Discovery Genetics - The History and Future of Spontaneous Mutation Research.

Authors:  Muriel T Davisson; David E Bergstrom; Laura G Reinholdt; Leah Rae Donahue
Journal:  Curr Protoc Mouse Biol       Date:  2012-06-01

2.  Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders.

Authors:  Marie Beaumont; Linda Akloul; Wilfrid Carré; Chloé Quélin; Hubert Journel; Laurent Pasquier; Mélanie Fradin; Sylvie Odent; Houda Hamdi-Rozé; Erwan Watrin; Valérie Dupé; Christèle Dubourg; Véronique David
Journal:  Hum Genet       Date:  2019-03-05       Impact factor: 4.132

3.  Craniofacial features resembling frontonasal dysplasia with a tubulonodular interhemispheric lipoma in the adult 3H1 tuft mouse.

Authors:  Keith S K Fong; Tiffiny Baring Cooper; Wallace C Drumhiller; S Jack Somponpun; Shiming Yang; Thomas Ernst; Linda Chang; Scott Lozanoff
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2012-01-13

4.  Apaf-1 deficiency and neural tube closure defects are found in fog mice.

Authors:  N Honarpour; S L Gilbert; B T Lahn; X Wang; J Herz
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-14       Impact factor: 11.205

Review 5.  Neurulation in the cranial region--normal and abnormal.

Authors:  Andrew J Copp
Journal:  J Anat       Date:  2005-11       Impact factor: 2.610

6.  HIV protease inhibitors provide neuroprotection through inhibition of mitochondrial apoptosis in mice.

Authors:  Toshio Hisatomi; Toru Nakazawa; Kousuke Noda; Lama Almulki; Shinsuke Miyahara; Shintaro Nakao; Yasuhiro Ito; Haicheng She; Riichiro Kohno; Norman Michaud; Tatsuro Ishibashi; Ali Hafezi-Moghadam; Andrew D Badley; Guido Kroemer; Joan W Miller
Journal:  J Clin Invest       Date:  2008-06       Impact factor: 14.808

7.  Apaf1 apoptotic function critically limits Sonic hedgehog signaling during craniofacial development.

Authors:  A B Long; W J Kaiser; E S Mocarski; T Caspary
Journal:  Cell Death Differ       Date:  2013-07-26       Impact factor: 15.828

Review 8.  Genetics and development of neural tube defects.

Authors:  Andrew J Copp; Nicholas D E Greene
Journal:  J Pathol       Date:  2010-01       Impact factor: 7.996

  8 in total

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