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Catherine J. Pallen

Catherine J. Pallen

University of British Columbia
Canada

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Enzyme
  • Amino acid

Catherine J. Pallen mostly deals with Protein tyrosine phosphatase, Biochemistry, Cell biology, Phosphorylation and Signal transduction. Her Protein tyrosine phosphatase research incorporates elements of Tyrosine kinase, Metastasis, Molecular biology and Tyrosine phosphorylation. She mostly deals with Phosphatase in her studies of Biochemistry.

Her Cell biology study combines topics from a wide range of disciplines, such as Genetics and Chinese hamster ovary cell. Her work on Proto-oncogene tyrosine-protein kinase Src is typically connected to Y box binding protein 1 as part of general Phosphorylation study, connecting several disciplines of science. Catherine J. Pallen has researched Proto-oncogene tyrosine-protein kinase Src in several fields, including Integrin and Focal adhesion.

Her most cited work include:

  • F3/contactin acts as a functional ligand for Notch during oligodendrocyte maturation. (302 citations)
  • PRL-3 and PRL-1 promote cell migration, invasion, and metastasis. (251 citations)
  • Akt phosphorylates the Y-box binding protein 1 at Ser102 located in the cold shock domain and affects the anchorage-independent growth of breast cancer cells (221 citations)

What are the main themes of her work throughout her whole career to date?

Her primary scientific interests are in Protein tyrosine phosphatase, Biochemistry, Cell biology, Phosphorylation and Phosphatase. Her Protein tyrosine phosphatase research is multidisciplinary, incorporating elements of Tyrosine kinase, FYN, Proto-oncogene tyrosine-protein kinase Src, Tyrosine phosphorylation and Molecular biology. Her work in the fields of Calmodulin, Enzyme, Tyrosine and Mutant overlaps with other areas such as Calcineurin.

Catherine J. Pallen interconnects Receptor and Cell membrane in the investigation of issues within Cell biology. Catherine J. Pallen integrates Phosphorylation and Autophosphorylation in her research. Catherine J. Pallen studied Phosphatase and Cell culture that intersect with Cell growth.

She most often published in these fields:

  • Protein tyrosine phosphatase (70.45%)
  • Biochemistry (43.18%)
  • Cell biology (44.32%)

What were the highlights of her more recent work (between 2006-2021)?

  • Protein tyrosine phosphatase (70.45%)
  • Cancer research (21.59%)
  • Cell biology (44.32%)

In recent papers she was focusing on the following fields of study:

Her primary areas of investigation include Protein tyrosine phosphatase, Cancer research, Cell biology, Phosphorylation and FYN. Her research in Protein tyrosine phosphatase intersects with topics in Tyrosine kinase and Tyrosine phosphorylation. Her research integrates issues of Mast cell, Matrigel and Neocortex in her study of Cell biology.

Her research investigates the link between Phosphorylation and topics such as Kinase that cross with problems in Syk and Molecular biology. The FYN study combines topics in areas such as GAB2 and Cdc42 GTP-Binding Protein, RAC1. Catherine J. Pallen has included themes like Cell and Phosphatase in her Signal transduction study.

Between 2006 and 2021, her most popular works were:

  • PRL PTPs: mediators and markers of cancer progression. (151 citations)
  • Ewing Sarcoma with Novel Translocation t(2;16) Producing an In-Frame Fusion of FUS and FEV (108 citations)
  • Distinct FAK-Src activation events promote α5β1 and α4β1 integrin-stimulated neuroblastoma cell motility (81 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Enzyme
  • Amino acid

Catherine J. Pallen mainly investigates Cell biology, Protein tyrosine phosphatase, Cancer research, Focal adhesion and Proto-oncogene tyrosine-protein kinase Src. Her Cell biology research is multidisciplinary, relying on both Cancer cell and Gene silencing. To a larger extent, Catherine J. Pallen studies Signal transduction with the aim of understanding Protein tyrosine phosphatase.

Her Cancer research study also includes

  • Kinase that intertwine with fields like Small interfering RNA, Molecular biology and Growth inhibition,
  • Sarcoma and related Neuroblastoma, Genetics, Gene rearrangement and Chromosomal translocation. Her Focal adhesion study incorporates themes from Integrin and Small hairpin RNA. The various areas that Catherine J. Pallen examines in her Proto-oncogene tyrosine-protein kinase Src study include Paxillin and Motility.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Cell transformation and activation of pp60c-src by overexpression of a protein tyrosine phosphatase.

Xin Min Zheng;Yue Wang;C. J. Pallen.
Nature (1992)

580 Citations

F3/contactin acts as a functional ligand for Notch during oligodendrocyte maturation.

Qi Dong Hu;Qi Dong Hu;Beng Ti Ang;Beng Ti Ang;Meliha Karsak;Wei Ping Hu.
Cell (2003)

425 Citations

PRL-3 and PRL-1 promote cell migration, invasion, and metastasis.

Qi Zeng;Jing-Ming Dong;Ke Guo;Jie Li.
Cancer Research (2003)

376 Citations

Akt phosphorylates the Y-box binding protein 1 at Ser102 located in the cold shock domain and affects the anchorage-independent growth of breast cancer cells

Brent W Sutherland;Jill Kucab;Joyce Wu;Cathy Lee.
Oncogene (2005)

326 Citations

Prenylation-dependent association of protein-tyrosine phosphatases PRL-1, -2, and -3 with the plasma membrane and the early endosome.

Qi Zeng;Xiaoning Si;Heinrich Horstmann;Yue Xu.
Journal of Biological Chemistry (2000)

289 Citations

Calmodulin-stimulated dephosphorylation of p-nitrophenyl phosphate and free phosphotyrosine by calcineurin.

C J Pallen;J H Wang.
Journal of Biological Chemistry (1983)

278 Citations

Targeted disruption of the tyrosine phosphatase PTPα leads to constitutive downregulation of the kinases Src and Fyn

Sathivel Ponniah;Dennis Z.M. Wang;Kah Leong Lim;Catherine J. Pallen.
Current Biology (1999)

257 Citations

PRL PTPs: mediators and markers of cancer progression.

Darrell C. Bessette;Dexin Qiu;Catherine J. Pallen.
Cancer and Metastasis Reviews (2008)

236 Citations

PTPα regulates integrin-stimulated FAK autophosphorylation and cytoskeletal rearrangement in cell spreading and migration

Li Zeng;Xiaoning Si;Xiaoning Si;Wei-Ping Yu;Hoa Thi Le;Hoa Thi Le.
Journal of Cell Biology (2003)

187 Citations

Ewing sarcoma with novel translocation t(2;16) producing an in-frame fusion of FUS and FEV.

Tony L. Ng;Maureen J. O'Sullivan;Catherine J. Pallen;Malcolm Hayes.
The Journal of Molecular Diagnostics (2007)

176 Citations

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