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Point mutation in FGF receptor eliminates phosphatidylinositol hydrolysis without affecting mitogenesis

Nature (London), 1992-08, Vol.358 (6388), p.681-684

1992

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Fibroblast growth factor receptor tyrosine kinases: molecular analysis and signal transduction

Biochimica et biophysica acta, 1992-06, Vol.1135 (2), p.185-199

1992

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Cloning and expression of two distinct high‐affinity receptors cross‐reacting with acidic and basic fibroblast growth factors

The EMBO journal, 1990-09, Vol.9 (9), p.2685-2692

1990

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Neurotrophins and Trk receptors in human pancreatic ductal adenocarcinoma: Expression patterns and effects on In vitro invasive behavior

International journal of cancer, 1999-05, Vol.81 (3), p.417-427

1999

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Sustained in vivo regression of Dunning H rat prostate cancers treated with combinations of androgen ablation and Trk tyrosine kinase inhibitors, CEP-751 (KT-6587) or CEP-701 (KT-5555)

Cancer research (Chicago, Ill.), 1999-05, Vol.59 (10), p.2395-2401

1999

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Cell cycle-independent death of prostate adenocarcinoma is induced by the trk tyrosine kinase inhibitor CEP-751 (KT6587)

Clinical cancer research, 1998-08, Vol.4 (8), p.1887-1898

1998

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Neurotrophic 3,9-Bis[(alkylthio)methyl]- and -Bis(alkoxymethyl)-K-252a Derivatives

Journal of medicinal chemistry, 1997-06, Vol.40 (12), p.1863-1869

1997

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Ligand‐induced transphosphorylation between different FGF receptors

The EMBO journal, 1991-10, Vol.10 (10), p.2849-2854

1991

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The Trk tyrosine kinase inhibitor CEP-701 (KT-5555) exhibits significant antitumor efficacy in preclinical xenograft models of human pancreatic ductal adenocarcinoma

Clinical cancer research, 1999-08, Vol.5 (8), p.2205-2212

1999

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A tyrosine-phosphorylated carboxy-terminal peptide of the fibroblast growth factor receptor (Flg) is a binding site for the SH2 domain of phospholipase C-gamma 1

Molecular and Cellular Biology, 1991-10, Vol.11 (10), p.5068-5078

1991

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Antitumor Activity of CEP-751 (KT-6587) on Human Neuroblastoma and Medulloblastoma Xenografts

Clinical cancer research, 1999-11, Vol.5 (11), p.3594-3602

1999

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Characterization and cDNA cloning of phospholipase C-gamma, a major substrate for heparin-binding growth factor 1 (acidic fibroblast growth factor)-activated tyrosine kinase

Molecular and Cellular Biology, 1990-09, Vol.10 (9), p.4770-4777

1990

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A Cytomegalovirus-Encoded Mitochondria-Localized Inhibitor of Apoptosis Structurally Unrelated to Bcl-2

Proceedings of the National Academy of Sciences - PNAS, 1999-10, Vol.96 (22), p.12536-12541

1999

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BEK and FLG, two receptors to members of the FGF family, are amplified in subsets of human breast cancers

Oncogene, 1991-04, Vol.6 (4), p.659-663

1991

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p53 status affects the rate of the onset but not the overall extent of doxorubicin-induced cell death in Rat-1 fibroblasts constitutively expressing c-Myc

Cancer research (Chicago, Ill.), 1997, Vol.57 (1), p.176-182

1997

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Acidic Fibroblast Growth Factor and Heart Development: Role in Myocyte Proliferation and Capillary Angiogenesis

Circulation research, 1993-01, Vol.72 (1), p.7-19

1993

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Motoneuron Apoptosis Is Blocked by CEP-1347 (KT 7515), a Novel Inhibitor of the JNK Signaling Pathway

The Journal of neuroscience, 1998-01, Vol.18 (1), p.104-111

1998

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Activation of fibroblast growth factor (FGF) receptors by recombinant human FGF-5

Oncogene, 1993-05, Vol.8 (5), p.1311-1316

1993

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Pan-trk Inhibition Decreases Metastasis and Enhances Host Survival in Experimental Models as a Result of Its Selective Induction of Apoptosis of Prostate Cancer Cells

Clinical cancer research, 2001-08, Vol.7 (8), p.2237-2245

2001

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K‐252a Induces Tyrosine Phosphorylation of the Focal Adhesion Kinase and Neurite Outgrowth in Human Neuroblastoma SH‐SY5Y Cells

Journal of neurochemistry, 1995-02, Vol.64 (2), p.540-549

1995

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A Tyrosine-Phosphorylated Carboxy-Terminal Peptide of the Fibroblast Growth Factor Receptor (Flg) Is a Binding Site for the SH2 Domain of Phospholipase C-γ1

Molecular and cellular biology, 1991-10, Vol.11 (10), p.5068-5078

1991

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High-affinity binding and activation of a truncated FGF receptor by both aFGF and bFGF

Oncogene, 1991-12, Vol.6 (12), p.2255-2262

1991

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Measuring Space

Design Theory, Language and Architectural Space in Lewis Carroll, 2024, p.21-44

Dionne, Caroline

1, 2024

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Navigating the Unknowable

Design Theory, Language and Architectural Space in Lewis Carroll, 2024, p.109-131

Dionne, Caroline

1, 2024

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Naming Things

Design Theory, Language and Architectural Space in Lewis Carroll, 2024, p.45-66

Dionne, Caroline

1, 2024

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Point mutation in FGF receptor eliminates phosphatidylinositol hydrolysis without affecting mitogenesis

Fibroblast growth factor receptor tyrosine kinases: molecular analysis and signal transduction

Cloning and expression of two distinct high‐affinity receptors cross‐reacting with acidic and basic fibroblast growth factors

Neurotrophins and Trk receptors in human pancreatic ductal adenocarcinoma: Expression patterns and effects on In vitro invasive behavior

Sustained in vivo regression of Dunning H rat prostate cancers treated with combinations of androgen ablation and Trk tyrosine kinase inhibitors, CEP-751 (KT-6587) or CEP-701 (KT-5555)

Cell cycle-independent death of prostate adenocarcinoma is induced by the trk tyrosine kinase inhibitor CEP-751 (KT6587)

Neurotrophic 3,9-Bis[(alkylthio)methyl]- and -Bis(alkoxymethyl)-K-252a Derivatives

Ligand‐induced transphosphorylation between different FGF receptors

The Trk tyrosine kinase inhibitor CEP-701 (KT-5555) exhibits significant antitumor efficacy in preclinical xenograft models of human pancreatic ductal adenocarcinoma

A tyrosine-phosphorylated carboxy-terminal peptide of the fibroblast growth factor receptor (Flg) is a binding site for the SH2 domain of phospholipase C-gamma 1

Antitumor Activity of CEP-751 (KT-6587) on Human Neuroblastoma and Medulloblastoma Xenografts

Characterization and cDNA cloning of phospholipase C-gamma, a major substrate for heparin-binding growth factor 1 (acidic fibroblast growth factor)-activated tyrosine kinase

A Cytomegalovirus-Encoded Mitochondria-Localized Inhibitor of Apoptosis Structurally Unrelated to Bcl-2

BEK and FLG, two receptors to members of the FGF family, are amplified in subsets of human breast cancers

p53 status affects the rate of the onset but not the overall extent of doxorubicin-induced cell death in Rat-1 fibroblasts constitutively expressing c-Myc

Acidic Fibroblast Growth Factor and Heart Development: Role in Myocyte Proliferation and Capillary Angiogenesis

Motoneuron Apoptosis Is Blocked by CEP-1347 (KT 7515), a Novel Inhibitor of the JNK Signaling Pathway

Activation of fibroblast growth factor (FGF) receptors by recombinant human FGF-5

Pan-trk Inhibition Decreases Metastasis and Enhances Host Survival in Experimental Models as a Result of Its Selective Induction of Apoptosis of Prostate Cancer Cells

K‐252a Induces Tyrosine Phosphorylation of the Focal Adhesion Kinase and Neurite Outgrowth in Human Neuroblastoma SH‐SY5Y Cells

A Tyrosine-Phosphorylated Carboxy-Terminal Peptide of the Fibroblast Growth Factor Receptor (Flg) Is a Binding Site for the SH2 Domain of Phospholipase C-γ1

High-affinity binding and activation of a truncated FGF receptor by both aFGF and bFGF

Measuring Space

Navigating the Unknowable

Naming Things

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