Cellular models for the serpinopathies

Methods in Molecular Biology

Volumn 1826, Issue , 2018, Pages 109-121

  Fra, Annamaria ^a   D’Acunto, Emanuela ^b   Laffranchi, Mattia ^a   Miranda, Elena ^b,c  

^a UNIVERSITY OF BRESCIA   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

Antitrypsin; Cell culture; Cell lines; Cell transfection; Neuroserpin; Polyethylenimine (PEI); Serpin polymers

Indexed keywords

ALPHA 1 ANTITRYPSIN; COMPLEMENTARY DNA; NEUROSERPIN; PLASMID DNA; POLYMER; SERINE PROTEINASE INHIBITOR; NEUROPEPTIDE; SERPINA1 PROTEIN, HUMAN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; CELL CULTURE; CELL DIFFERENTIATION; CONTROLLED STUDY; DNA INTEGRATION; EXPRESSION VECTOR; FEMALE; GENE INDUCTION; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; MOUSE; NERVE CELL DIFFERENTIATION; NEURAL STEM CELL; NONHUMAN; PHYSICAL DISEASE BY ETIOLOGY AND PATHOGENESIS; PROMOTER REGION; PROTEIN CONFORMATION; PROTEIN EXPRESSION; PROTEIN SYNTHESIS; SERPINOPATHY; STABLE EXPRESSION; TRANSIENT EXPRESSION; TRANSIENT TRANSFECTION; ANIMAL; BIOLOGICAL MODEL; CHLOROCEBUS AETHIOPS; CV-1 CELL LINE; DEMYELINATING DISEASE; EMPHYSEMA; GENETICS; HEK293 CELL LINE; METABOLISM; MUTATION; MYOCLONUS EPILEPSY; PATHOLOGY; PC12 CELL LINE (PHEOCHROMOCYTOMA); RAT;

ALPHA 1-ANTITRYPSIN; ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; EMPHYSEMA; EPILEPSIES, MYOCLONIC; HEK293 CELLS; HEREDODEGENERATIVE DISORDERS, NERVOUS SYSTEM; HUMANS; MICE; MODELS, BIOLOGICAL; MUTATION; NEUROPEPTIDES; PC12 CELLS; RATS; SERPINS;

EID: 85053082215     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4939-8645-3_7     Document Type: Chapter

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