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Pharmacogenomics of statin response.

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Differential effects of ramipril on ambulatory blood pressure in African Americans and Caucasians.

  • Read more about Differential effects of ramipril on ambulatory blood pressure in African Americans and Caucasians.

Family history, environmental exposures in early life, and childhood asthma.

  • Read more about Family history, environmental exposures in early life, and childhood asthma.

Disruption of sphingolipid metabolism elicits apoptosis-associated reproductive defects in Drosophila.

  • Read more about Disruption of sphingolipid metabolism elicits apoptosis-associated reproductive defects in Drosophila.

Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.

  • Read more about Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.

Polymorphisms in IL13, total IgE, eosinophilia, and asthma exacerbations in childhood.

  • Read more about Polymorphisms in IL13, total IgE, eosinophilia, and asthma exacerbations in childhood.

Increased plasma concentrations of lipoprotein(a) during a low-fat, high-carbohydrate diet are associated with increased plasma concentrations of apolipoprotein C-III bound to apolipoprotein B-containing lipoproteins.

  • Read more about Increased plasma concentrations of lipoprotein(a) during a low-fat, high-carbohydrate diet are associated with increased plasma concentrations of apolipoprotein C-III bound to apolipoprotein B-containing lipoproteins.

NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.

  • Read more about NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.

CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.

  • Read more about CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.

Genetic nondiscrimination legislation: a critical prerequisite for pharmacogenomics data sharing.

  • Read more about Genetic nondiscrimination legislation: a critical prerequisite for pharmacogenomics data sharing.

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