Dclk1+ small intestinal epithelial tuft cells display the hallmarks of quiescence and self-renewal

Oncotarget

Volumn 6, Issue 31, 2015, Pages 30876-30886

  Chandrakesan, Parthasarathy ^a,b   May, Randal ^a,c   Qu, Dongfeng ^a,c   Weygant, Nathaniel ^a   Taylor, Vivian E ^a   Li, James D ^a   Ali, Naushad ^a,b   Sureban, Sripathi M ^a   Qante, Michael ^d   Wang, Timothy C ^e   Bronze, Michael S ^a   Houchen, Courtney W ^a,b,c,f  

^a UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF OKLAHOMA   (United States)

^c Affairs Medical Center   (United States)

^d TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^e Howard Hughes Medical Institute   (United States)

^f NONE   (United States)

Author keywords

Dclk1; Pluripotency; Quiescence; Self renewal

Indexed keywords

MESSENGER RNA; YELLOW FLUORESCENT PROTEIN; DCAMKL1 PROTEIN, MOUSE; PROTEIN SERINE THREONINE KINASE;

ADULT; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL FUNCTION; CELL ISOLATION; CELL POPULATION; CELL SURVIVAL; CONTROLLED STUDY; DCLK1 CELL; FLUORESCENCE ACTIVATED CELL SORTING; GENE EXPRESSION; IN VITRO STUDY; INTESTINE EPITHELIUM CELL; LONGEVITY; MOUSE; NONHUMAN; ANIMAL; APOPTOSIS; CELL CULTURE; CELL PROLIFERATION; CYTOLOGY; ENZYME IMMUNOASSAY; EPITHELIUM CELL; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; PHYSIOLOGY; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SMALL INTESTINE; TRANSGENIC MOUSE;

ANIMALS; APOPTOSIS; CELL DIFFERENTIATION; CELL PROLIFERATION; CELLS, CULTURED; EPITHELIAL CELLS; HUMANS; IMMUNOENZYME TECHNIQUES; IN SITU HYBRIDIZATION, FLUORESCENCE; INTESTINE, SMALL; LONGEVITY; MICE; MICE, TRANSGENIC; PROTEIN-SERINE-THREONINE KINASES; REAL-TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 84945563254     PISSN: None     EISSN: 19492553     Source Type: Journal    
DOI: 10.18632/oncotarget.5129     Document Type: Article

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