Epigenetics in critical illness: a new frontier. - Wikidata - awgldk - TriplyDB

Epigenetics in critical illness: a new frontier.

Epigenetics in critical illness: a new frontier.

http://www.wikidata.org/entity/Q37044569

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Soluble adhesion molecules as markers for sepsis and the potential pathophysiological discrepancy in neonates, children and adults.Methylation Profiling of Multiple Tumor Suppressor Genes in Hepatocellular Carcinoma and the Epigenetic Mechanism of 3OST2 Regulation

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Epigenetics in critical illness: a new frontier.

http://www.wikidata.org/entity/Q37044569

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 09 July 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Epigenetics in critical illness: a new frontier.

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Epigenetics in critical illness: a new frontier.

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type

label

Epigenetics in critical illness: a new frontier.

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Epigenetics in critical illness: a new frontier.

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prefLabel

Epigenetics in critical illness: a new frontier.

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Epigenetics in critical illness: a new frontier.

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Nursing Research and Practice

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Epigenetics in critical illness: a new frontier.

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Brian T Graves

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Cindy L Munro

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Epigenetic principles and mechanisms underlying nervous system functions in health and disease

Epigenetics: a landscape takes shape

Epigenetic reprogramming and imprinting in origins of disease

Renal kallikrein excretion and epigenetics in human acute kidney injury: expression, mechanisms and consequences.

APACHE-acute physiology and chronic health evaluation: a physiologically based classification system.

Integrating microRNAs into a system biology approach to acute lung injury

Epigenetic regulation of immune cell functions during post-septic immunosuppression.

The APACHE III prognostic system. Risk prediction of hospital mortality for critically ill hospitalized adults.

MicroRNA in central nervous system trauma and degenerative disorders.

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

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503686

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scholarly article

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10.1155/2013/503686

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2013

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2013-07-09T00:00:00Z

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255737706

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