Syndecan-4 and focal adhesion function.

Research output: Contribution to journal › Journal article › Research › peer-review

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Syndecan-4 and focal adhesion function. / Woods, A; Couchman, J R.

In: Current Opinion in Cell Biology, Vol. 13, No. 5, 2001, p. 578-83.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Woods, A & Couchman, JR 2001, 'Syndecan-4 and focal adhesion function.', Current Opinion in Cell Biology, vol. 13, no. 5, pp. 578-83.

APA

Woods, A., & Couchman, J. R. (2001). Syndecan-4 and focal adhesion function. Current Opinion in Cell Biology, 13(5), 578-83.

Vancouver

Woods A, Couchman JR. Syndecan-4 and focal adhesion function. Current Opinion in Cell Biology. 2001;13(5):578-83.

Author

Woods, A ; Couchman, J R. / Syndecan-4 and focal adhesion function. In: Current Opinion in Cell Biology. 2001 ; Vol. 13, No. 5. pp. 578-83.

Bibtex

@article{e1e3a4d0596e11dd8d9f000ea68e967b,
title = "Syndecan-4 and focal adhesion function.",
abstract = "Two groups have now reported the viability of mice that lack syndecan-4. These mice have wound healing/angiogenesis problems, and fibroblasts from these animals differ in adhesion and migration from normal. This is consistent with recent in vitro data indicating a need for signaling via syndecan-4 for focal adhesion formation, and reports that overexpression of proteins that bind syndecan-4 can modify cell adhesion and migration.",
author = "A Woods and Couchman, {J R}",
note = "Keywords: Animals; Focal Adhesions; Integrins; Membrane Glycoproteins; Mice; Mice, Knockout; Models, Biological; Neovascularization, Pathologic; Protein Structure, Tertiary; Proteoglycans; Signal Transduction; Syndecan-4; Wound Healing",
year = "2001",
language = "English",
volume = "13",
pages = "578--83",
journal = "Current Opinion in Cell Biology",
issn = "0955-0674",
publisher = "Elsevier Ltd. * Current Opinion Journals",
number = "5",

}

RIS

TY - JOUR

T1 - Syndecan-4 and focal adhesion function.

AU - Woods, A

AU - Couchman, J R

N1 - Keywords: Animals; Focal Adhesions; Integrins; Membrane Glycoproteins; Mice; Mice, Knockout; Models, Biological; Neovascularization, Pathologic; Protein Structure, Tertiary; Proteoglycans; Signal Transduction; Syndecan-4; Wound Healing

PY - 2001

Y1 - 2001

N2 - Two groups have now reported the viability of mice that lack syndecan-4. These mice have wound healing/angiogenesis problems, and fibroblasts from these animals differ in adhesion and migration from normal. This is consistent with recent in vitro data indicating a need for signaling via syndecan-4 for focal adhesion formation, and reports that overexpression of proteins that bind syndecan-4 can modify cell adhesion and migration.

AB - Two groups have now reported the viability of mice that lack syndecan-4. These mice have wound healing/angiogenesis problems, and fibroblasts from these animals differ in adhesion and migration from normal. This is consistent with recent in vitro data indicating a need for signaling via syndecan-4 for focal adhesion formation, and reports that overexpression of proteins that bind syndecan-4 can modify cell adhesion and migration.

M3 - Journal article

C2 - 11544026

VL - 13

SP - 578

EP - 583

JO - Current Opinion in Cell Biology

JF - Current Opinion in Cell Biology

SN - 0955-0674

IS - 5

ER -

ID: 5162938