Literature DB >> 6494904

Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus.

V Lindgren, B de Martinville, A L Horwich, L E Rosenberg, U Francke.   

Abstract

The gene for the mitochondrial enzyme ornithine transcarbamylase was mapped to the short arm of the X chromosome by in situ hybridization experiments, with DNA complementary to the human ornithine transcarbamylase gene used as a probe. A series of cell lines with X chromosome abnormalities was used to localize the gene to band Xp21.1. Because the gene maps near the Duchenne muscular dystrophy locus, the ornithine transcarbamylase probe may be useful in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy as well as of ornithine transcarbamylase deficiency.

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Year:  1984        PMID: 6494904     DOI: 10.1126/science.6494904

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  49 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site.

Authors:  E M Petty; R Carstens; A E Bale
Journal:  Nucleic Acids Res       Date:  1991-02-11       Impact factor: 16.971

3.  Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

Authors:  T L Yang-Feng; L J DeGennaro; U Francke
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

4.  Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Authors:  K A Ellison; C P Fill; J Terwilliger; L J DeGennaro; A Martin-Gallardo; M Anvret; A K Percy; J Ott; H Zoghbi
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

Review 5.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

6.  Determination of mutation patterns in human ornithine transcarbamylase precursor.

Authors:  Shaomin Yan; Guang Wu
Journal:  J Clin Monit Comput       Date:  2009-02-10       Impact factor: 2.502

7.  Assignment of the gene for human DNA polymerase alpha to the X chromosome.

Authors:  T S Wang; B E Pearson; H A Suomalainen; T Mohandas; L J Shapiro; J Schröder; D Korn
Journal:  Proc Natl Acad Sci U S A       Date:  1985-08       Impact factor: 11.205

8.  Two novel mutations of ornithine transcarbamylase gene identified from three Chinese neonates with ornithine transcarbamylase deficiency.

Authors:  Jing Liu; Lei Dong; Yan Wang; Mei Zhang
Journal:  Int J Clin Exp Med       Date:  2015-02-15

9.  Fatal hyperammonemia resulting from a C-to-T mutation at a MspI site of the ornithine transcarbamylase gene.

Authors:  D Hentzen; A Pelet; D Feldman; D Rabier; J Berthelot; A Munnich
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

10.  Site specific screening for point mutations in ornithine transcarbamylase deficiency.

Authors:  D Feldmann; J M Rozet; A Pelet; D Hentzen; P Briand; P Hubert; C Largilliere; D Rabier; J P Farriaux; A Munnich
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

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