Cellular Resolution Maps of X Chromosome Inactivation: Implications for Neural Development, Function, and Disease

Neuron

Volumn 81, Issue 1, 2014, Pages 103-119

  Wu, Hao ^a   Luo, Junjie ^a   Yu, Huimin ^a   Rattner, Amir ^a   Mo, Alisa ^a   Wang, Yanshu ^a   Smallwood, PhilipM ^a   Erlanger, Bracha ^a   Wheelan, SarahJ ^a   Nathans, Jeremy ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; AUTOSOME MOSAICISM; BRAIN ASYMMETRY; BRAIN CORTEX; BRAIN DISEASE; CELL FUNCTION; CELL FUSION; CONTROLLED STUDY; CORTI ORGAN; EMBRYONIC STEM CELL; EPIGENETICS; FEMALE; GABAERGIC TRANSMISSION; GENE EXPRESSION; GENE LOCUS; GENETIC DISORDER; LOXP SITE; MOSAICISM; MOUSE; NERVE CELL DIFFERENTIATION; NONHUMAN; NORRIE DISEASE; PHOTORECEPTOR; PLACENTAL MAMMALS; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RETINA AMACRINE CELL; RETINA BLOOD VESSEL OCCLUSION; RETINA CONE; SOMITE; VASCULARIZATION; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKAGE; ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; BRAIN BLOOD VESSEL; BRAIN CELL; CELL NUCLEUS; CENTRAL NERVOUS SYSTEM FUNCTION; CHROMOSOMAL LOCALIZATION; CHROMOSOME ANALYSIS; CHROMOSOME MAP; CHROMOSOME STRUCTURE; CHROMOSOME VARIANT; DEVELOPMENTAL GENE; DISEASE CARRIER; EMBRYO; EMBRYO DEVELOPMENT; GENDER IDENTITY; GENE DELETION; GENE FREQUENCY; GENE TARGETING; GENETIC ENGINEERING; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HPRT GENE; MOLECULAR IMAGING; MOUSE MODEL; NERVOUS SYSTEM DEVELOPMENT; OPTICAL RESOLUTION; PROTEIN LOCALIZATION; QUANTITATIVE STUDY; REPORTER GENE; RETINA BLOOD VESSEL; RETINA BLOOD VESSEL DYSFUNCTION; RETINA DISEASE; SINGLE CELL RESOLUTION MAP; SINGLE NUCLEOTIDE POLYMORPHISM; SPATIAL ANALYSIS; STOCHASTIC MODEL; TRANSGENE;

CRE RECOMBINASE; GREEN FLUORESCENT PROTEIN;

ANIMALS; ANIMALS, NEWBORN; BRAIN; CHOLINE O-ACETYLTRANSFERASE; EMBRYO, MAMMALIAN; FEMALE; FUNCTIONAL LATERALITY; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GREEN FLUORESCENT PROTEINS; HUMANS; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; MICE; MICE, TRANSGENIC; MOSAICISM; NERVE TISSUE PROTEINS; NEURONS; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINA; X CHROMOSOME; X CHROMOSOME INACTIVATION;

EID: 84891818179     PISSN: 08966273     EISSN: 10974199     Source Type: Journal    
DOI: 10.1016/j.neuron.2013.10.051     Document Type: Article

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