PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15115672-7	2004	RESULTS AND CONCLUSIONS: The F450L, P455L, P477L, P477*, and T446* (*=stop codon) mutations reduced HCII secretion 6.6- to 24-fold, while the F402L, A404T, and P407L mutations reduced AT secretion in COS-1 cells 1.7- to 5.2-fold.	carbonyl sulfide	200-203	serpin family D member 1	Homo sapiens	100-104	
11204559-2	2001	To investigate the molecular pathogenesis of our patient, we performed sequencing analysis and expressed recombinant human wild-type and mutant HC II molecules in COS-1 and CHO-K1 cells.	carbonyl sulfide	163-166	serpin family D member 1	Homo sapiens	144-149	
11204559-6	2001	Transient transfection, metabolic labeling and pulse-chase experiments followed by immunoprecipitation analysis showed that the recombinant mutant HC II molecules were secreted from COS-1 cells in reduced amounts compared with the wild-type, and that an enhanced intracellular association of the mutant molecules with a chaperone, GRP78/BiP, was observed in CHO-K1 cells.	carbonyl sulfide	182-185	serpin family D member 1	Homo sapiens	147-152	
11204559-8	2001	Immunohistochemical staining of the transfected cells revealed that COS-1 cells expressing the mutant HC II molecules were stained mainly in the perinuclear area.	carbonyl sulfide	68-71	serpin family D member 1	Homo sapiens	102-107