Spelling suggestions: "subject:"erowth 5factors"" "subject:"erowth allactors""
151 |
Functions of Rx in early vertebrate ocular developmentZamora, Brian G. January 2009 (has links)
Thesis (Ph. D.)--West Virginia University, 2009. / Title from document title page. Document formatted into pages; contains x, 148 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 136-148).
|
152 |
Studies on the growth inhibition and differentiation of serum-free mouse embryo (SFME) cellsVarga Weisz, Patrick D. 05 June 1992 (has links)
Serum-free mouse embryo (SFME) cells are derived
in medium in which serum is replaced with growth
factors and other supplements. They display unusual
properties. They do not lose proliferative potential
or show gross chromosomal aberration upon extended
culture, they depend on epidermal growth factor (EGF)
for survival, and are reversibly growth inhibited by
plasma and serum. In the presence of transforming
growth factor beta (TGF-β) SFME cells express the
astrocyte marker, glial fibrillary acidic protein
(GFAP).
The growth inhibitory activity of human plasma
on serum-free mouse embryo cells was investigated.
Human plasma did not inhibit SFME cells transformed
with the human Ha-ras oncogene. The activity was
present in delipidated plasma and was not dialyzable
against 1 M acetic acid. The activity could be
precipitated by methanol, bound to concanavalin Aagarose
and was retarded by Sephadex G-50 in 200 mM
acetic acid. A fifty to hundred fold purification was
achieved, although the differential inhibition of
untransformed versus transformed cells was lost in the
course of the purification.
Using the technique of differential
screening of a cDNA library a calf serum- and TGF -β-regulated
mRNA species was identified in SFME cells.
This mRNA was approximately 8.5 kilobases in size and
brain-specific. Picomolar quantities of TGF-β caused
an increase of this message in SFME cells within four
hours. This increase was reversed when TGF-β was
removed from the culture medium. / Graduation date: 1993
|
153 |
The proteoglycan perlecan regulates long bone growth through interactions with developmental proteins in the growth plateSmith, Simone Marsha-Lee. January 2007 (has links)
Dissertation (Ph.D.)--University of South Florida, 2007. / Title from PDF of title page. Document formatted into pages; contains 168 pages. Includes vita. Includes bibliographical references.
|
154 |
Exercise and angiogenic growth factors in human skeletal muscle /Gustafsson, Thomas, January 2005 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2005. / Härtill 5 uppsatser.
|
155 |
Studies of VEGF-B and novel PDGFs in tumorigenesis and angiogenesis /Li, Hong, January 2004 (has links)
Diss. (sammanfattning) Stockholm : Karol inst., 2004. / Härtill 4 uppsatser.
|
156 |
Lymphangiogenesis and lymphatic metastasis /Björndahl, Meit A., January 2005 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2005. / Härtill 4 uppsatser.
|
157 |
The proteoglycan perlecan regulates long bone growth through interactions with developmental proteins in the growth plate /Smith, Simone Marsha-Lee. January 2007 (has links)
Dissertation (Ph.D.)--University of South Florida, 2007. / Includes vita. Includes bibliographical references. Also available online.
|
158 |
Transforming growth factor-[beta] and Smad4 regulation of invasive and metastatic behavior in cancer cellsShiou, Sheng-Ru. January 2006 (has links)
Thesis (Ph. D. in Cell Biology)--Vanderbilt University, May 2006. / Title from title screen. Includes bibliographical references.
|
159 |
The characterization of novel fibroblast growth factor response genes in Xenopus laevis /Winsor, Wendy, Unknown Date (has links)
Thesis (M.Sc.)--Memorial University of Newfoundland, Faculty of Medicine, 1999. / Typescript. Bibliography: leaves 145-163.
|
160 |
Design, synthesis, structure, and dynamics of a polypeptide with supersecondary structure a helix-loop-helix dimer /Olofsson, Susanne. January 1994 (has links)
Thesis (Ph. D.)--University of Göteborg, 1994. / Published dissertation.
|
Page generated in 0.1652 seconds