Analysis of circadian liver gene expression by ADDER, a highly sensitive method for the display of differentially expressed mRNAs

Nucleic Acids Research

Volumn 29, Issue 11, 2020, Pages

  Kornmann, Benoît ^a   Preitner, Nicolas ^a   Rifat, Danièle ^a   Fleury Olela, Fabienne ^a   Schibler, Ueli ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; PRESENILIN 2; COMPLEMENTARY DNA;

3' UNTRANSLATED REGION; ALZHEIMER DISEASE; AMPLIFICATION OF DOUBLE STRANDED CDNA END RESTRICTION FRAGMENT; ANALYTIC METHOD; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; DETOXIFICATION; FOOD PROCESSING; GENE AMPLIFICATION; GENE EXPRESSION; GENE EXPRESSION PROFILING; MOLECULAR CLONING; MOUSE; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA ISOLATION; RNA SEQUENCING; SENSITIVITY AND SPECIFICITY; SEQUENCE ANALYSIS; ANIMAL; C57BL MOUSE; CIRCADIAN RHYTHM; GENETICS; LIVER; METABOLISM; METHODOLOGY; MOUSE STRAIN; PHYSIOLOGY;

ANIMALS; CIRCADIAN RHYTHM; DNA, COMPLEMENTARY; GENE EXPRESSION PROFILING; LIVER; MICE; MICE, INBRED C57BL; MICE, INBRED STRAINS; POLYMERASE CHAIN REACTION; RNA, MESSENGER; SENSITIVITY AND SPECIFICITY;

MLCS; MLOWN;

EID: 0035377585     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/29.11.e51     Document Type: Article

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