Exosomes mediate the acquisition of the disease phenotypes by cells with normal genome in tuberous sclerosis complex

Oncogene

Volumn 35, Issue 23, 2016, Pages 3027-3036

  Patel, B ^a   Patel, J ^a   Cho, J H ^a   Manne, S ^a   Bonala, S ^a   Henske, E ^b   Roegiers, F ^c   Markiewski, M ^a   Karbowniczek, M ^a  

^a TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c FOX CHASE CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GAMMA SECRETASE; GLIAL FIBRILLARY ACIDIC PROTEIN; HAMARTIN; MAMMALIAN TARGET OF RAPAMYCIN; NESTIN; NOTCH1 RECEPTOR; PERIPHERIN; PROTEIN; PROTEIN S6; RHEB PROTEIN; SHORT HAIRPIN RNA; TSC1 PROTEIN; TUBERIN; UNCLASSIFIED DRUG;

ADULT; ANGIOMYOLIPOMA; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL COMMUNICATION; CELL DIFFERENTIATION; CELL FATE; CELL LYSATE; CONTROLLED STUDY; DIFFERENTIATION; ECTOPIC EXPRESSION; EMBRYO; EXOSOME; FLUORESCENCE ACTIVATED CELL SORTING; GENOME; IN VIVO STUDY; MOUSE; NERVE CELL DIFFERENTIATION; NERVE ENDING; NERVOUS SYSTEM DEVELOPMENT; NEURAL TUBE; NONHUMAN; NULL CELL; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DEPLETION; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; STOP CODON; TUBEROUS SCLEROSIS; TUBEROUS SCLEROSIS COMPLEX; WESTERN BLOTTING; ANIMAL; CELL PROLIFERATION; GENETICS; HUMAN; METABOLISM; PATHOLOGY; PHYSIOLOGY;

ANIMALS; CELL PROLIFERATION; EXOSOMES; GENOME; HUMANS; MICE; PHENOTYPE; TUBEROUS SCLEROSIS;

EID: 84973922940     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/onc.2015.358     Document Type: Article

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