Literature DB >> 9686356

Mottled gene expression and copper distribution in the macular mouse, an animal model for Menkes disease.

Y Murata1, H Kodama, Y Mori, M Kobayashi, T Abe.   

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Year:  1998        PMID： 9686356     DOI： 10.1023/a:1005383114315

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  8 in total

1.  Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.

Authors:  J Chelly; Z Tümer; T Tønnesen; A Petterson; Y Ishikawa-Brush; N Tommerup; N Horn; A P Monaco
Journal:  Nat Genet       Date:  1993-01       Impact factor: 38.330

2.  Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease.

Authors:  Y Murata; H Kodama; T Abe; N Ishida; M Nishimura; B Levinson; J Gitschier; S Packman
Journal:  Pediatr Res       Date:  1997-10       Impact factor: 3.756

3.  Histochemical localization of copper in various organs of brindled mice after copper therapy.

Authors:  N Yoshimura; K Kida; S Usutani; M Nishimura
Journal:  Pathol Int       Date:  1995-01       Impact factor: 2.534

4.  Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase.

Authors:  C Vulpe; B Levinson; S Whitney; S Packman; J Gitschier
Journal:  Nat Genet       Date:  1993-01       Impact factor: 38.330

5.  Isolation of a partial candidate gene for Menkes disease by positional cloning.

Authors:  J F Mercer; J Livingston; B Hall; J A Paynter; C Begy; S Chandrasekharappa; P Lockhart; A Grimes; M Bhave; D Siemieniak
Journal:  Nat Genet       Date:  1993-01       Impact factor: 38.330

6.  The mottled gene is the mouse homologue of the Menkes disease gene.

Authors:  B Levinson; C Vulpe; B Elder; C Martin; F Verley; S Packman; J Gitschier
Journal:  Nat Genet       Date:  1994-04       Impact factor: 38.330

7.  Genetic expression of Menkes disease in cultured astrocytes of the macular mouse.

Authors:  H Kodama; Y Meguro; T Abe; M H Rayner; K T Suzuki; S Kobayashi; M Nishimura
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

8.  Histochemical localization of copper in the intestine and kidney of macular mice: light and electron microscopic study.

Authors:  H Kodama; T Abe; M Takama; I Takahashi; M Kodama; M Nishimura
Journal:  J Histochem Cytochem       Date:  1993-10       Impact factor: 2.479
  8 in total
  4 in total

1.  Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein.

Authors:  Byung-Eun Kim; Michael J Petris
Journal:  J Med Genet       Date:  2007-05-04       Impact factor: 6.318

2.  Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease.

Authors:  Mark J Niciu; Xin-Ming Ma; Rajaâ El Meskini; Joel S Pachter; Richard E Mains; Betty A Eipper
Journal:  Neurobiol Dis       Date:  2007-05-23       Impact factor: 5.996

3.  Effect of copper and diethyldithiocarbamate combination therapy on the macular mouse, an animal model of Menkes disease.

Authors:  H Kodama; E Sato; Y-H Gu; K Shiga; C Fujisawa; T Kozuma
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.750

Review 4.  Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

Authors:  Hiroko Kodama; Chie Fujisawa; Wattanaporn Bhadhprasit
Journal:  Curr Drug Metab       Date:  2012-03       Impact factor: 3.731
  4 in total

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