Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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Age-specific changes in genome-wide methylation enrich for Foxa2 and estrogen receptor alpha binding sites Hydrogen sulfide improves postischemic neoangiogenesis in the hind limb of cystathionine-β-synthase mutant mice via PPAR-γ/VEGF axis

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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2016 nî lūn-bûn

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2016年論文

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy

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Avisek Majumder

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Jyotirmaya Behera

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Suresh C Tyagi

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P2860

Human DNA methylomes at base resolution show widespread epigenomic differences

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Homocysteine and reactive oxygen species in metabolic syndrome, type 2 diabetes mellitus, and atheroscleropathy: the pleiotropic effects of folate supplementation

Multidisciplinary approach and anesthetic management of a surgical cancer patient with methylene tetrahydrofolate reductase deficiency: a case report and review of the literature

Nutrient intake values for folate during pregnancy and lactation vary widely around the world

Epigenetic modifications: basic mechanisms and role in cardiovascular disease.

Chromatin modifications and their function

Cystathionine beta-synthase mutations in homocystinuria

The diverse functions of histone lysine methylation

Crosstalk of homocysteinylation, methylation and acetylation on histone H3.

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scholarly article

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10.1002/JCB.25841

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118

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2017-04-21T00:00:00Z

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Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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P2860

P2860

Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

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