Literature DB >> 15173240

Haplotype analysis of human AMPD1 gene: origin of common mutant allele.

K Toyama, H Morisaki, Y Kitamura, M Gross, T Tamura, Y Nakahori, J M Vance, M Speer, N Kamatani, T Morisaki.   

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Year:  2004        PMID： 15173240      PMCID： PMC1735804          DOI： 10.1136/jmg.2003.013151

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

1.  AMP deaminase deficiency in skeletal muscle is unlikely to be of clinical relevance.

Authors:  Frank Hanisch; Pushpa Joshi; Stephan Zierz
Journal:  J Neurol       Date:  2008-03-14       Impact factor: 4.849

2.  AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases.

Authors:  Krzysztof Safranow; Janina Suchy; Katarzyna Jakubowska; Maria Olszewska; Agnieszka Bińczak-Kuleta; Grzegorz Kurzawski; Ryszard Rzeuski; Edyta Czyżycka; Beata Łoniewska; Zdzisława Kornacewicz-Jach; Andrzej Ciechanowicz; Dariusz Chlubek
Journal:  J Appl Genet       Date:  2010-11-25       Impact factor: 3.240

3.  Effects of AMPD1 common mutation on the metabolic-chronotropic relationship: Insights from patients with myoadenylate deaminase deficiency.

Authors:  Fabrice Rannou; Virginie Scotet; Pascale Marcorelles; Roxane Monnoyer; Cédric Le Maréchal
Journal:  PLoS One       Date:  2017-11-02       Impact factor: 3.240

Review 4.  AMP deaminase 1 gene polymorphism and heart disease-a genetic association that highlights new treatment.

Authors:  Ryszard T Smolenski; Iwona Rybakowska; Jacek Turyn; Paweł Romaszko; Magdalena Zabielska; Anne Taegtmeyer; Ewa M Słomińska; Krystian K Kaletha; Paul J R Barton
Journal:  Cardiovasc Drugs Ther       Date:  2014-04       Impact factor: 3.727
  4 in total

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