Next generation transcriptomics and genomics elucidate biological complexity of microglia in health and disease

GLIA

Volumn 64, Issue 2, 2016, Pages 197-213

  Wes, Paul D ^a   Holtman, Inge R ^b   Boddeke, Erik W G M ^b   Möller, Thomas ^a   Eggen, Bart J L ^b  

^a LUNDBECK RESEARCH USA   (United States)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

Aging; Alzheimer's disease; Amyotrophic lateral sclerosisl epigenetics; Gene expression

Indexed keywords

COMPLEMENT; TRANSCRIPTOME;

AGING; ALZHEIMER DISEASE; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; BONE MARROW CELL; BRAIN CELL; BRAIN TISSUE; CELL FUNCTION; CELL POPULATION; CELL STRUCTURE; CENTRAL NERVOUS SYSTEM; DEGENERATIVE DISEASE; ENHANCER REGION; EPIGENETICS; GENE EXPRESSION; GENE EXPRESSION REGULATION; GENE FUNCTION; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENOMICS; GLIA CELL; HISTONE MODIFICATION; HUMAN; IMMUNE RESPONSE; MACROPHAGE; MICROGLIA; NERVOUS SYSTEM INFLAMMATION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; TRANSCRIPTOMICS; ANIMAL; GENE EXPRESSION PROFILING; GENETIC EPIGENESIS; METABOLISM; PROCEDURES;

ANIMALS; EPIGENESIS, GENETIC; GENE EXPRESSION PROFILING; GENOMICS; HUMANS; MACROPHAGES; MICROGLIA; NEURODEGENERATIVE DISEASES;

EID: 84953840062     PISSN: 08941491     EISSN: 10981136     Source Type: Journal    
DOI: 10.1002/glia.22866     Document Type: Article

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