PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
6486424-6	1984	The [32P]vitellogenin labeled in situ was incorporated by oocytes at a rate similar to [32P]vitellogenin labeled in vivo, was translocated to the yolk platelets, and was correctly processed into the yolk proteins.	Phosphorus-32	5-8	a1-a	Xenopus laevis	9-21	
2345348-5	1990	Vitellogenic as well as maturational-stage oocytes were found to sequester X. laevis [32P]VTG from the medium, and incorporation was found to be linear with time for at least up to 12 hr.	Phosphorus-32	86-89	a1-a	Xenopus laevis	90-93	
2345348-6	1990	Once incorporated into the oocyte, [32P]VTG did not appear to undergo turnover.	Phosphorus-32	36-39	a1-a	Xenopus laevis	40-43	
2345348-7	1990	The effect of different [32P]VTG concentrations on incorporation indicated that the uptake mechanism was saturable.	Phosphorus-32	25-28	a1-a	Xenopus laevis	29-32	
2345348-8	1990	Unlabeled F. heteroclitus VTG and X. laevis VTG were also found to compete effectively with X. laevis [32P]VTG, whereas bovine serum albumin did not.	Phosphorus-32	103-106	a1-a	Xenopus laevis	26-29	
2345348-8	1990	Unlabeled F. heteroclitus VTG and X. laevis VTG were also found to compete effectively with X. laevis [32P]VTG, whereas bovine serum albumin did not.	Phosphorus-32	103-106	a1-a	Xenopus laevis	44-47	
7217071-7	1981	This is further supported by the analysis of newly synthesized and assembled [3H,32P]vitellogenin on sodium dodecyl sulfate-polyacrylamide gels and measurements of protein kinase activity in microsomal subfractions.	Phosphorus-32	81-84	a1-a	Xenopus laevis	85-97	
4724585-12	1973	The incorporation of [(32)P]P(i) into vitellogenin followed a pattern identical with that found for [(3)H]leucine in the pulse-labelling experiments and this indicates that synthesis of the polypeptide chain and incorporation of P(i) are closely linked processes.	Phosphorus-32	21-27	a1-a	Xenopus laevis	38-50