PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8820970-5	1996	The shift in sedimentation values of the separated AChE and BuChE species in sucrose gradients made with and without detergents revealed the occurrence of hydrophilic (H) and amphiphilic (A) variants of cholinesterases in the extracts.	Sucrose	77-84	acetylcholinesterase	Mus musculus	51-55	
7512968-4	1994	About 22% of the cell-associated AChE was membrane-linked as dimers and tetramers, required Triton X-100 for extraction, and bound to Triton X-100 as assessed by sucrose gradients.	Sucrose	162-169	acetylcholinesterase	Mus musculus	33-37	
8408164-7	1993	AChE activity was measured by differential extraction and velocity sedimentation on sucrose gradients.	Sucrose	84-91	acetylcholinesterase	Mus musculus	0-4	
1760105-3	1991	AChE activity at 3 weeks postburn was measured by differential extraction and velocity sedimentation on sucrose gradients.	Sucrose	104-111	acetylcholinesterase	Mus musculus	0-4	
19651088-4	1988	Among the several molecular forms of AChE, PIPLC specifically releases in a dose dependent manner one molecular form which migrates on linear sucrose gradients as a single peak of sedimentation coefficient 6.3 s. In other subcellular membrane fractions, including motor endplate enriched fraction, PIPLC fails to solubilize AChE.	Sucrose	142-149	acetylcholinesterase	Mus musculus	37-41	
3694264-4	1987	In normal mouse biceps the distribution of AChE forms, as shown by sucrose-gradient analysis, change substantially after birth; the most dramatic alteration is an increase in G4 AChE from 15 to 45% of total AChE during the third postnatal week.	Sucrose	67-74	acetylcholinesterase	Mus musculus	43-47	
3449398-1	1987	The pattern of acetylcholinesterase (AChE) molecular forms, obtained by sucrose gradient sedimentation, was studied at different in vitro developmental stages of myogenic cells isolated from adult mouse skeletal muscle.	Sucrose	72-79	acetylcholinesterase	Mus musculus	37-41	
3748455-4	1986	Sucrose density sedimentation analysis of muscle homogenates revealed an increase, by 2-3 times, in the proportion of the asymmetric (16S) molecular form of AChE in active muscle of both genotypes.	Sucrose	0-7	acetylcholinesterase	Mus musculus	157-161	
6237698-1	1984	Acetylcholinesterase (AChE) is composed of several distinct molecular forms, which are identified and partly resolved by velocity sedimentation analysis on sucrose gradients.	Sucrose	156-163	acetylcholinesterase	Mus musculus	0-20	
6237698-1	1984	Acetylcholinesterase (AChE) is composed of several distinct molecular forms, which are identified and partly resolved by velocity sedimentation analysis on sucrose gradients.	Sucrose	156-163	acetylcholinesterase	Mus musculus	22-26	
6237698-2	1984	We made the assumption that each AChE form sediments as a peak of activity with a gaussian shape in the continuous sucrose gradient.	Sucrose	115-122	acetylcholinesterase	Mus musculus	33-37	
6656838-1	1983	Acetylcholinesterase (AChE) was extracted from normal and dystrophic C57BL/6J mouse hindlimb muscles and its molecular forms fractionated by sucrose density gradient ultracentrifugation.	Sucrose	141-148	acetylcholinesterase	Mus musculus	0-20	
6656838-1	1983	Acetylcholinesterase (AChE) was extracted from normal and dystrophic C57BL/6J mouse hindlimb muscles and its molecular forms fractionated by sucrose density gradient ultracentrifugation.	Sucrose	141-148	acetylcholinesterase	Mus musculus	22-26	
6617773-4	1983	Three forms of AChE, distinguished by their sedimentation on sucrose gradients, were synthesized: 4-6S, 10S, and 16S.	Sucrose	61-68	acetylcholinesterase	Mus musculus	15-19	
6128176-9	1982	The acetylcholinesterase activities released by proteolytic enzymes were characterized by sucrose density gradient centrifugation.	Sucrose	90-97	acetylcholinesterase	Mus musculus	4-24	
750918-4	1978	The patterns of AChE activity, as separated by sucrose density gradient centrifugation, were distinctly different in extracts of dystrophic and normal muscle.	Sucrose	47-54	acetylcholinesterase	Mus musculus	16-20	
33322722-0	2020	Impact of Sucrose as Osmolyte on Molecular Dynamics of Mouse Acetylcholinesterase.	Sucrose	10-17	acetylcholinesterase	Mus musculus	61-81	
33322722-1	2020	The enzyme model, mouse acetylcholinesterase, which exhibits its active site at the bottom of a narrow gorge, was investigated in the presence of different concentrations of sucrose to shed light on the protein and water dynamics in cholinesterases.	Sucrose	174-181	acetylcholinesterase	Mus musculus	24-44	
29862455-7	2018	We demonstrate that high sucrose consumption and DSP4 treatment promote an early-stage AD-related phenotype after only 3-4 months, as evidenced by elevated fecal corticosterone, increased despair, spatial memory deficits, increased AChE activity, elevated NO production, decreased pGSK3beta and increased pTau.	Sucrose	25-32	acetylcholinesterase	Mus musculus	232-236