Psoriatic T cells reduce epidermal turnover time and affect cell proliferation contributed from differential gene expression

Journal of Dermatology

Volumn 42, Issue 9, 2015, Pages 874-880

  Li, Junqin ^a   Li, Xinhua ^a   Hou, Ruixia ^a   Liu, Ruifeng ^a   Zhao, Xincheng ^a   Dong, Feng ^b   Wang, Chunfang ^c   Yin, Guohua ^a   Zhang, Kaiming ^a  

^a Taiyuan Center Hospital   (China)

^b Changzhi City Second People's Hospital   (China)

^c SHANXI MEDICAL UNIVERSITY   (China)

Author keywords

differentially expressed genes; epidermal turnover time; keratinocyte; psoriasis; T cells

Indexed keywords

KI 67 ANTIGEN; MESSENGER RNA; MYC PROTEIN; PROTEIN BCL 2; PROTEIN P53; BACTERIAL ANTIGEN; BIOLOGICAL MARKER; MYC PROTEIN, HUMAN; STREPTOCOCCAL SUPERANTIGEN SSA;

AHNAK GENE; ANTIGEN EXPRESSION; ARTICLE; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; CELL CULTURE; CELL DIFFERENTIATION; CELL PROLIFERATION; CHCHD4 GENE; CLINICAL ARTICLE; COCULTURE; CONTROLLED STUDY; EPIDERMIS; FABP5 GENE; GENE; GENE EXPRESSION; GENE EXPRESSION PROFILING; GENE SEQUENCE; HSPH1 GENE; HUMAN; HUMAN CELL; IMMUNOHISTOCHEMISTRY; IN VITRO STUDY; KERATINOCYTE; MONOZYGOTIC TWINS; NOC2L GENE; NUP54 GENE; PLEKHG3 GENE; PPIL1 GENE; PROTEIN EXPRESSION; PSORIASIS; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ISOLATION; SENP3 GENE; SKIN CULTURE; SLC9A9 GENE; T LYMPHOCYTE; TSR1 GENE; TURNOVER TIME; CASE CONTROL STUDY; IMMUNOLOGY; METABOLISM; PATHOPHYSIOLOGY; PHYSIOLOGY; TWINS;

ANTIGENS, BACTERIAL; BIOMARKERS; CASE-CONTROL STUDIES; CELL PROLIFERATION; EPIDERMIS; GENE EXPRESSION PROFILING; HUMANS; KERATINOCYTES; KI-67 ANTIGEN; PROTO-ONCOGENE PROTEINS C-BCL-2; PROTO-ONCOGENE PROTEINS C-MYC; PSORIASIS; T-LYMPHOCYTES; TUMOR SUPPRESSOR PROTEIN P53;

EID: 84940959027     PISSN: 03852407     EISSN: 13468138     Source Type: Journal    
DOI: 10.1111/1346-8138.12961     Document Type: Article

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