(Q41735610)

English

Small molecule inhibitors of the platelet-derived growth factor receptor, the fibroblast growth factor receptor, and Src family tyrosine kinases

scientific article published on October 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

1 reference

Europe PubMed Central

Small molecule inhibitors of the platelet-derived growth factor receptor, the fibroblast growth factor receptor, and Src family tyrosine kinases (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

author name string

Showalter HD

1

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

Kraker AJ

2

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

publication date

1 October 1997

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

Pharmacology & Therapeutics

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

76

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

1-3

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

55-71

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

Sequence requirements for binding of Src family tyrosine kinases to activated growth factor receptors

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Effects of trapidil and suramin on growth factor-induced calcium response and tyrosine phosphorylation in human glioma cells.

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Intracellular Signaling in Arterial Smooth Muscle Migration versus Proliferation

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Radicicol, a protein tyrosine kinase inhibitor, suppresses the expression of mitogen-inducible cyclooxygenase in macrophages stimulated with lipopolysaccharide and in experimental glomerulonephritis

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Recombinant mitotoxin basic fibroblast growth factor-saporin reduces venous anastomotic intimal hyperplasia in the arteriovenous graft

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Exploration of the sequence specificity of pp60c-src tyrosine kinase. Minimal peptide sequence required for maximal activity

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Damnacanthal is a highly potent, selective inhibitor of p56lck tyrosine kinase activity

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Inhibition of T lymphocyte activation by a novel p56lck tyrosine kinase inhibitor

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Protein tyrosine kinase and protein kinase C inhibition by fungal anthraquinones related to emodin.

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Inhibitors of protein tyrosine kinases

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Angiogenesis as a target for tumor treatment

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Tyrphostins. 5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins

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Structure−Activity Relationships for a Novel Series of Pyrido[2,3-d]pyrimidine Tyrosine Kinase Inhibitors

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Discovery of a novel, potent, and Src family-selective tyrosine kinase inhibitor. Study of Lck- and FynT-dependent T cell activation

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Structure of angelmicin B, A novel src signal transduction inhibitor

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Pharmacology of smooth muscle cell replication

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Phosphorylation site-specific inhibition of platelet-derived growth factor beta-receptor autophosphorylation by the receptor blocking tyrphostin AG1296.

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Expression of basic fibroblast growth factor and its receptor by smooth muscle cells and endothelium in injured rat arteries. An en face study

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A subpopulation of smooth muscle cells in injured rat arteries expresses platelet-derived growth factor-B chain mRNA

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Identification of GIYWHHY as a novel peptide substrate for human p60c-src protein tyrosine kinase

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Local infusion of FGF-saporin reduces intimal hyperplasia

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Inhibition of the epidermal growth factor receptor tyrosine kinase activity by leflunomide

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In vivo pharmacology and anti-tumour evaluation of the tyrphostin tyrosine kinase inhibitor RG13022.

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Inhibition by 5'-methylthioadenosine of cell growth and tyrosine kinase activity stimulated by fibroblast growth factor receptor in human gliomas

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Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors

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Tight-binding inhibitory sequences against pp60(c-src) identified using a random 15-amino-acid peptide library

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Tyrosine kinase inhibitors. 4. Structure-activity relationships among N- and 3-substituted 2,2'-dithiobis(1H-indoles) for in vitro inhibition of receptor and nonreceptor protein tyrosine kinases.

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The biology of platelet-derived growth factor

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In vitro characterization of a novel series of platelet-derived growth factor receptor tyrosine kinase inhibitors

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Tyrosine kinase inhibitors inhibit multiple steps of the cell cycle of vascular smooth muscle cells

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Tyrosine kinase inhibitors. 6. Structure-activity relationships among N- and 3-substituted 2,2'-diselenobis(1H-indoles) for inhibition of protein tyrosine kinases and comparative in vitro and in vivo studies against selected sulfur congeners

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Crystal structure of the Src family tyrosine kinase Hck

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Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice

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Increase in activity and level of pp60c-src in progressive stages of human colorectal cancer

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Angelmicins, new inhibitors of oncogenic src signal transduction

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Sequence-independent inhibition of in vitro vascular smooth muscle cell proliferation, migration, and in vivo neointimal formation by phosphorothioate oligodeoxynucleotides

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Inhibitors of protein tyrosine phosphorylation reduce the proliferation of two human glioma cell lines

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Three-dimensional structure of the tyrosine kinase c-Src

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Angelmicin B, a new inhibitor of oncogenic signal transduction, inhibits growth and induces myelomonocytic differentiation of human myeloid leukemia HL-60 cells

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Platelet-Derived Growth Factor Stimlates Sodium-Dependent Pi Transport in Osteoblastic Cells via Phospholipase Cγ and Phosphatidylinositol 3′-Kinase

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RETRACTED: Selective inhibition of the platelet-derived growth factor signal transduction pathway by a protein-tyrosine kinase inhibitor of the 2-phenylaminopyrimidine class

1 reference

30 December 2023

https://opencitations.net/index/api/v1/citations/10.1073/PNAS.92.7.2558

Identifiers

10.1016/S0163-7258(97)00097-1

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

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