SH2-B, a membrane-associated adapter, is phosphorylated on multiple serines/threonines in response to nerve growth factor by kinases within the MEK/ERK cascade (Q78208143)

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scientific article published on 01 September 1999

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English	SH2-B, a membrane-associated adapter, is phosphorylated on multiple serines/threonines in response to nerve growth factor by kinases within the MEK/ERK cascade	scientific article published on 01 September 1999

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12 December 2019

SH2-B, a membrane-associated adapter, is phosphorylated on multiple serines/threonines in response to nerve growth factor by kinases within the MEK/ERK cascade (English)

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12 December 2019

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L Rui

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12 December 2019

J Herrington

2

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12 December 2019

C Carter-Su

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1 September 1999

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12 December 2019

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8

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Journal of Biological Chemistry

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12 December 2019

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12 December 2019

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12 December 2019

26485-26492

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12 December 2019

Dorsal root ganglion neurons are destroyed by exposure in utero to maternal antibody to nerve growth factor

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Mice lacking nerve growth factor display perinatal loss of sensory and sympathetic neurons yet develop basal forebrain cholinergic neurons

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The trk proto-oncogene encodes a receptor for nerve growth factor

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The trk proto-oncogene rescues NGF responsiveness in mutant NGF-nonresponsive PC12 cell lines

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High-affinity NGF binding requires coexpression of the trk proto-oncogene and the low-affinity NGF receptor

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The trk Proto-Oncogene Product: a Signal Transducing Receptor for Nerve Growth Factor

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Nerve growth factor mediates signal transduction through trk homodimer receptors

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Trk receptors use redundant signal transduction pathways involving SHC and PLC-gamma 1 to mediate NGF responses

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Shc Binding to Nerve Growth Factor Receptor Is Mediated by the Phosphotyrosine Interaction Domain

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Identification and characterization of novel substrates of Trk receptors in developing neurons

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SH2-B is required for nerve growth factor-induced neuronal differentiation

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Specificity of receptor tyrosine kinase signaling: transient versus sustained extracellular signal-regulated kinase activation

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Inhibition of growth factor-induced differentiation of PC12 cells by microinjection of antibody to ras p21

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Effect of a dominant inhibitory Ha-ras mutation on neuronal differentiation of PC12 cells

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Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells

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Association of the Shc and Grb2/Sem5 SH2-containing proteins is implicated in activation of the Ras pathway by tyrosine kinases

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Microinjection of the ras oncogene protein into PC12 cells induces morphological differentiation

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The cytoplasmic raf oncogene induces a neuronal phenotype in PC12 cells: a potential role for cellular raf kinases in neuronal growth factor signal transduction

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Identification of SH2-Bbeta as a substrate of the tyrosine kinase JAK2 involved in growth hormone signaling

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Platelet-derived growth factor (PDGF) stimulates the association of SH2-Bbeta with PDGF receptor and phosphorylation of SH2-Bbeta

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Inhibition of MAP Kinase Kinase Blocks the Differentiation of PC-12 Cells Induced by Nerve Growth Factor

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Characterization and differential expression of protein kinase C isoforms in PC12 cells. Differentiation parallels an increase in PKC beta II

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Transport of protein kinase C isoforms to the nucleus of PC12 cells by nerve growth factor: association of atypical zeta-PKC with the nuclear matrix.

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Nerve growth factor-induced differentiation of PC12 cells employs the PMA-insensitive protein kinase C-zeta isoform

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Nerve growth factor activates calcium-insensitive protein kinase C-epsilon in PC-12 rat pheochromocytoma cells

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Regulation of protein kinase C.

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Leukotriene D4 activates mitogen-activated protein kinase through a protein kinase Calpha-Raf-1-dependent pathway in human monocytic leukemia THP-1 cells

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Identifiers

10.1074/JBC.274.37.26485

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10473609%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10473609%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

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