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Keywords: growth factors
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Journal Articles
J Cell Sci (2007) 120 (20): 3688–3699.
Published: 15 October 2007
... Transactivation Growth factors The EGF receptor (EGFR, also known as erbB1 and HER1) tyrosine kinase system is vitally involved in normal physiological processes such as tissue morphogenesis and wound repair, because these events require the key cell responses of survival, proliferation and migration...
Includes: Supplementary data
Journal Articles
J Cell Sci (2006) 119 (1): 172–183.
Published: 1 January 2006
..., or with the growth factors, IGF-1 or BDNF, increases SIRPα phosphorylation and SHP-2 binding rapidly and transiently, via Src family kinase activation; phosphorylated SIRPα dissociates from the lipid microdomains. A cytoplasmic tail fragment of SIRPα (cSIRPα), when expressed in primary cortical neurons, also...
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J Cell Sci (2001) 114 (7): 1417–1425.
Published: 1 April 2001
...Laura A. Maile; Jane Badley-Clarke; David R. Clemmons ABSTRACT The disintegrin echistatin inhibits ligand occupancy of the αVβ3 integrin and reduces Insulin-like growth factor I (IGF-I) stimulated migration, DNA synthesis, and receptor autophosphorylation in smooth muscle cells. This suggests...
Journal Articles
In collection:
Metabolism
J Cell Sci (1994) 107 (1): 241–252.
Published: 1 January 1994
... mitogens growth factors immediate early genes delayed early genes cell cycle gene regulation cell metabolism DNA After exiting from mitosis, mammalian cells have the option to either start a new round of cell division or to leave the cell cycle and enter a resting state, usually referred...
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Journal Articles
J Cell Sci (1993) 104 (1): 69–76.
Published: 1 January 1993
... in the developing mouse and to study the regulation of tenascin expression by growth factors in vitro. At postnatal day 1 tenascin mRNAs are abundant in regions of bone and cartilage formation, as well as in the ependymal layer of the central nervous system. Previous studies have demonstrated that transforming...
Journal Articles
J Cell Sci (1992) 103 (2): 453–461.
Published: 1 October 1992
... and acid treatment. EC-FBS was inactivated by passage over a heparin-Agarose column. The column-bound activity could be eluted as a single peak at ∼1.0 M NaCl. Stimulation of pericyte growth was also achieved with platelet-derived growth factor (PDGF), acidic fibroblast growth factor (aFGF) and basic...
Journal Articles
J Cell Sci (1990) 97 (3): 463–471.
Published: 1 November 1990
... of Biologists 1990 human hair follicles organ maintenance growth factors The hair follicle is composed of epithelial components (the matrix and outer root sheath) and dermal components (the dermal papilla and connective tissue sheath). Hair growth, which is effected by the division of the hair...
Journal Articles
J Cell Sci (1990) 96 (2): 271–274.
Published: 1 June 1990
... released by entrapped platelets, such as platelet-derived growth factor. We suggest that the supernatant remaining after the fibrinogen-thrombin reaction could stimulate fibroblast replication, even in the absence of other blood components. To examine this hypothesis we expressed liquid from a fibrin clot...
Journal Articles
J Cell Sci (1990) 1990 (Supplement_13): 31–42.
Published: 1 January 1990
...William J. Larochelle; Neill Giese; Mary May-Siroff; Keith C. Robbins; Stuart A. Aaronson ABSTRACT Human platelet-derived growth factor (PDGF) is a connective tissue cell mitogen comprising two related chains encoded by distinct genes. The B chain is the homolog of the v-sis oncogene product...
Journal Articles
J Cell Sci (1990) 1990 (Supplement_13): 75–85.
Published: 1 January 1990
.... The expression of DIA/LIF in vitro is both developmentally programmed and controlled by the action of other growth factors, the most notable of which are members of the fibroblast growth factor family expressed by the stem cells themselves. This indicates that differentiation and proliferation in early...
Journal Articles
J Cell Sci (1989) 92 (3): 513–518.
Published: 1 March 1989
... are tedious to perform, or methods based on uptake of radiolabelled thymidine, which may be prone to errors caused by precursor pool artefacts. We describe here an assay for estimating the number of adherent cells present in a microculture and its application to the study of growth factors. The assay depends...
Journal Articles
J Cell Sci (1988) 91 (2): 239–247.
Published: 1 October 1988
...Clare M. Heyworth; Ian L. O. Ponting; T. Michael Dexter ABSTRACT Haemopoietic cell growth factors are normally assayed using unfractionated marrow cells (NBM). However, using this population it is difficult to distinguish between direct versus indirect effects, because of the low incidence...
Journal Articles
J Cell Sci (1988) 90 (4): 601–612.
Published: 1 August 1988
...Robert F. Brooks; Peter N. Riddle ABSTRACT When the proliferation rate of Swiss 3T3 cells is decreased by limiting the availability of growth factors, cell cycle variability increases, as predicted by the transition probability model. Nevertheless, the transition probabilities would appear to play...
Journal Articles
J Cell Sci (1988) 1988 (Supplement_10): 257–266.
Published: 1 February 1988
... and embryonic stem (ES) cells. EC cells have proved to be a useful source of embryonic growth factors. A potent mitogen, ECDGF has been isolated from EC cell conditioned medium. ECDGF appears to be a novel member of the heparin binding growth factor family. A remarkable feature of heparin binding growth factors...
Journal Articles
J Cell Sci (1988) 1988 (Supplement_10): 243–255.
Published: 1 February 1988
...William L. Farrar; Stuart W. Evans; Annick Harel-Bellan; Douglas K. Ferris ABSTRACT Haemopoietic growth factors stimulate a number of consensus biochemical and molecular events regardless of the specificity detailed by unique ligand and receptor structures. Analysis of three distinct colony...
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