The Sgp3 locus derived from the 129 strain is responsible for enhanced endogenous retroviral expression in macroH2A1-deficient mice

Journal of Autoimmunity

Volumn 35, Issue 4, 2010, Pages 398-403

  Baudino, Lucie ^a   Changolkar, Lakshmi N ^b   Pehrson, John R ^b   Izui, Shozo ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Endogenous retrovirus; Genetics; MacroH2A histone; Systemic lupus erythematosus

Indexed keywords

HISTONE H2A; MACROHISTONE H2A1; PROTEIN P70; RNA; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; GENE; GENE LOCATION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; LIVER CELL; LUPUS ERYTHEMATOSUS NEPHRITIS; MACROH2A1 GENE; MOUSE; MOUSE STRAIN; MUTANT; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETROVIRUS; SGP3 GENE; TRANSCRIPTION REGULATION; UPREGULATION; WILD TYPE;

ANIMALS; DISEASE MODELS, ANIMAL; ENDOGENOUS RETROVIRUSES; GENE EXPRESSION REGULATION; GLYCOPROTEINS; HEPATOCYTES; HISTONES; HUMANS; LUPUS ERYTHEMATOSUS, SYSTEMIC; LUPUS NEPHRITIS; MICE; MICE, 129 STRAIN; MICE, INBRED C57BL; MICE, INBRED NZB; MOLECULAR CHAPERONES; VIRAL ENVELOPE PROTEINS;

EID: 77958152650     PISSN: 08968411     EISSN: 10959157     Source Type: Journal    
DOI: 10.1016/j.jaut.2010.08.003     Document Type: Article

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