Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 14
Results: 10
Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD).
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2276, doi. 10.1093/hmg/ddl152
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- Article
Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice.
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2266, doi. 10.1093/hmg/ddl151
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- Article
Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease.
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2250, doi. 10.1093/hmg/ddl150
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- Article
Nucleolar localization of aprataxin is dependent on interaction with nucleolin and on active ribosomal DNA transcription.
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2239, doi. 10.1093/hmg/ddl149
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- Article
Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy.
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2225, doi. 10.1093/hmg/ddl148
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- Article
Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes.
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2216, doi. 10.1093/hmg/ddl147
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- Article
Ube3a expression is not altered in Mecp2 mutant mice.
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2210, doi. 10.1093/hmg/ddl146
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- Article
Calcium-sensing receptor dimerizes in the endoplasmic reticulum: biochemical and biophysical characterization of CASR mutants retained intracellularly.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2200, doi. 10.1093/hmg/ddl145
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- Article
Intronic variants in the dopa decarboxylase (DDC) gene are associated with smoking behavior in European-Americans and African-Americans.
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- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2192, doi. 10.1093/hmg/ddl144
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- Article
Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2185, doi. 10.1093/hmg/ddl143
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- Article