PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 7508936-7 1994 MA-alpha 2M also blocks NGF-promoted incorporation of 32P from [32P]ATP into trk receptors in vitro. Phosphorus-32 54-57 nerve growth factor Rattus norvegicus 24-27 7508936-7 1994 MA-alpha 2M also blocks NGF-promoted incorporation of 32P from [32P]ATP into trk receptors in vitro. Phosphorus-32 64-67 nerve growth factor Rattus norvegicus 24-27 1861152-2 1991 We found that NGF and TPA, alone or in combination, increased (a) the incorporation of [32P]Pi into NF-M and (b) the rate of conversion of NF-M from a poorly phosphorylated to a more highly phosphorylated form. Phosphorus-32 88-91 nerve growth factor Rattus norvegicus 14-17 1319464-5 1992 Incorporation of 32P into ERK1 and ERK2 occurred primarily on tyrosine and threonine residues and was associated with a single tryptic peptide, which is identical to one whose phosphorylation is increased by treatment of intact PC12 cells with NGF. Phosphorus-32 17-20 nerve growth factor Rattus norvegicus 244-247 3106121-11 1987 By immunoprecipitation of vinculin from 32P-labeled cells, vinculin phosphorylation was found to be increased within 1 hr of NGF treatment. Phosphorus-32 40-43 nerve growth factor Rattus norvegicus 125-128 2720800-1 1989 It has been shown that in PC12 and its subclone PC12h treatment of the cells with nerve growth factor (NGF) induces a selective decrease in the incorporation of radioactive phosphate into a 100,000-dalton protein, designated in an earlier study as Nsp100, in the subsequent phosphorylation of soluble extracts from cells with (gamma-32P)ATP. Phosphorus-32 333-336 nerve growth factor Rattus norvegicus 82-101 2720800-1 1989 It has been shown that in PC12 and its subclone PC12h treatment of the cells with nerve growth factor (NGF) induces a selective decrease in the incorporation of radioactive phosphate into a 100,000-dalton protein, designated in an earlier study as Nsp100, in the subsequent phosphorylation of soluble extracts from cells with (gamma-32P)ATP. Phosphorus-32 333-336 nerve growth factor Rattus norvegicus 103-106 2538812-5 1989 NGF stimulates [3H]myristate- or [32P]phosphate-labeled phosphatidic acid production over the same time course. Phosphorus-32 34-38 nerve growth factor Rattus norvegicus 0-3 3372590-6 1988 As measured by incorporation of [32P]phosphate, NGF had a dual effect on MAP1.2. Phosphorus-32 33-36 nerve growth factor Rattus norvegicus 48-51 3804999-7 1987 NGF also increased the stability of the modified form of M. All three subunits were 32P-labeled, and NGF increased the incorporation of 32P into M and H. Neurofilament subunits were also immunoprecipitated from a soluble fraction of [35S]methionine-labeled PC12 cells. Phosphorus-32 84-87 nerve growth factor Rattus norvegicus 0-3 3804999-7 1987 NGF also increased the stability of the modified form of M. All three subunits were 32P-labeled, and NGF increased the incorporation of 32P into M and H. Neurofilament subunits were also immunoprecipitated from a soluble fraction of [35S]methionine-labeled PC12 cells. Phosphorus-32 136-139 nerve growth factor Rattus norvegicus 0-3 3804999-7 1987 NGF also increased the stability of the modified form of M. All three subunits were 32P-labeled, and NGF increased the incorporation of 32P into M and H. Neurofilament subunits were also immunoprecipitated from a soluble fraction of [35S]methionine-labeled PC12 cells. Phosphorus-32 136-139 nerve growth factor Rattus norvegicus 101-104 3772374-3 1986 Half-maximal incorporation of 32P from [32P]ATP into S6 occurred after 4-7 min of NGF treatment. Phosphorus-32 30-33 nerve growth factor Rattus norvegicus 82-85 3772374-3 1986 Half-maximal incorporation of 32P from [32P]ATP into S6 occurred after 4-7 min of NGF treatment. Phosphorus-32 40-43 nerve growth factor Rattus norvegicus 82-85 3948029-2 1986 Here we show, using dot hybridization of mRNA with a 32P-labelled cDNA probe for beta-nerve growth factor (beta NGF), that mRNA sequences homologous to beta NGF appear in muscle in parallel with increased motoneurone survival activity. Phosphorus-32 53-56 nerve growth factor Rattus norvegicus 81-105 3948029-2 1986 Here we show, using dot hybridization of mRNA with a 32P-labelled cDNA probe for beta-nerve growth factor (beta NGF), that mRNA sequences homologous to beta NGF appear in muscle in parallel with increased motoneurone survival activity. Phosphorus-32 53-56 nerve growth factor Rattus norvegicus 107-115 3948029-2 1986 Here we show, using dot hybridization of mRNA with a 32P-labelled cDNA probe for beta-nerve growth factor (beta NGF), that mRNA sequences homologous to beta NGF appear in muscle in parallel with increased motoneurone survival activity. Phosphorus-32 53-56 nerve growth factor Rattus norvegicus 152-160 15372494-6 2004 In response to ATP, NGF, or NGF + ATP, MAPK activity (measured by 32P incorporation) was maximal within 2 hr and remained statistically elevated over control levels throughout the 24 hr monitored. Phosphorus-32 66-69 nerve growth factor Rattus norvegicus 20-23 15372494-6 2004 In response to ATP, NGF, or NGF + ATP, MAPK activity (measured by 32P incorporation) was maximal within 2 hr and remained statistically elevated over control levels throughout the 24 hr monitored. Phosphorus-32 66-69 nerve growth factor Rattus norvegicus 28-31 15372494-7 2004 At maximal 32P incorporation, MAPK activity in response to ATP, NGF, and NGF + ATP was two-, four-, and sixfold higher, respectively, than control values; the observed increase was qualitatively confirmed using Western blots. Phosphorus-32 11-14 nerve growth factor Rattus norvegicus 64-67 15372494-7 2004 At maximal 32P incorporation, MAPK activity in response to ATP, NGF, and NGF + ATP was two-, four-, and sixfold higher, respectively, than control values; the observed increase was qualitatively confirmed using Western blots. Phosphorus-32 11-14 nerve growth factor Rattus norvegicus 73-76