Ding Wen Wu

Dr. Ding Wen Wu


Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 1991 in The Quarterly Review of Biology
Verified
Journal Article
Closed access
JDJohn G. Duman
John G. Duman
DWDing Wen Wu
Ding Wen Wu
LXLei Xu
Lei Xu
DTDonald Tursman
Donald Tursman
TOT. Mark Olsen
T. Mark Olsen

7 April 1998 in Journal of Comparative Physiology B
Verified
Journal Article
Closed access
PDF file
JDJ. G. Duman
J. G. Duman
NLN. Li
N. Li
DVD. Verleye
D. Verleye
FGF. W. Goetz
F. W. Goetz
DWDing Wen Wu
Ding Wen Wu
DPD. C. Parmelee
D. C. Parmelee

1 January 1991
Verified
Book Chapter
Closed access
PDF file
JDJohn G. Duman
John G. Duman
LXLei Xu
Lei Xu
LNLisa G. Neven
Lisa G. Neven
DTDonald Tursman
Donald Tursman
DWDing Wen Wu
Ding Wen Wu

1 February 1991 in Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology
Verified
Journal Article
Closed access
DWDing Wen Wu
Ding Wen Wu
JDJohn G. Duman
John G. Duman
LXLei Xu
Lei Xu

3 April 2001 in BMC Developmental Biology
Verified
Journal Article
Open access
TJTina Jaskoll
Tina Jaskoll
HCHaiming Chen
Haiming Chen
YZYan Min Zhou
Yan Min Zhou
DWDing Wen Wu
Ding Wen Wu
MMMichael Melnick
Michael Melnick
The regulation of programmed cell death is critical to developmental homeostasis and normal morphogenesis of embryonic tissues. Survivin, a member of the inhibitors of apoptosis protein (IAP) family primarily expressed in embryonic cells, is both an anti-apoptosis and a pro-survival factor. Since our previous studies have demonstrated the importance of apoptosis during embryonic submandibular salivary gland (SMG) development, we postulated that survivin is a likely mediator of SMG epithelial cell survival. We investigated the developmental expression of survivin in Pseudoglandular (approximately E14), Canalicular (approximately E15) and Terminal Bud (approximately E17) Stage SMGs. We report a significant 26% increase in transcript levels between the Canalicular and Terminal Bud Stages. Immunohistochemical studies demonstrate nuclear-localized survivin protein in epithelial cells bounding forming lumina in Canalicular and Terminal Bud Stage SMGs. Survivin is known to be a pro-survival and anti-apoptotic factor. Given that survivin translocation into the nucleus is required for the induction of entry into the cell cycle and the inhibition of apoptosis, our demonstration of nuclear-localized survivin protein in presumptive ductal and proacinar lumen-bounding cells suggests that survivin may be a key mediator of embryonic SMG epithelial cell survival.

1 July 1991 in Journal of Comparative Physiology B
Verified
Journal Article
Closed access
PDF file
DWDing Wen Wu
Ding Wen Wu
JDJohn G. Duman
John G. Duman