L
Lingtao You
Researcher at Heidelberg University
Publications - 6
Citations - 579
Lingtao You is an academic researcher from Heidelberg University. The author has contributed to research in topics: Phosphorylation & Gene expression. The author has an hindex of 6, co-authored 6 publications receiving 548 citations.
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Journal ArticleDOI
Cryopreserved human amniotic membrane for ocular surface reconstruction.
Friedrich E. Kruse,Antonia M. Joussen,Klaus Rohrschneider,Lingtao You,B. Sinn,J. Baumann,H. E. Völcker +6 more
TL;DR: The technique for preservation which is most widely used for ophthalmological amniotic membrane transplantation significantly impairs viability and proliferative capacity and seems to function primarily as matrix and not by virtue of transplanted functional cells.
Journal Article
Neurotrophic factors in the human cornea.
TL;DR: The differential expression of NT-4 and GDNF suggests a regulatory function within the cytokine network of the cornea, and Neurotrophic factors and tyrosine kinase receptors are transcribed in the human cornea.
Journal Article
Glial cell-derived neurotrophic factor (GDNF)-induced migration and signal transduction in corneal epithelial cells.
TL;DR: Corneal epithelial cells express receptors specific for GDNF that are used by GDNF to induce intracellular signaling and FAK and MAPK pathways seem to be activated byGDNF to modulate gene transcription and cell migration.
Journal Article
Bone morphogenetic proteins and growth and differentiation factors in the human cornea.
TL;DR: The results suggest that its members may be components of the corneal cytokine network and may participate in the regulation of cellular proliferation and differentiation.
Journal Article
Differential effect of activin A and BMP-7 on myofibroblast differentiation and the role of the Smad signaling pathway.
Lingtao You,Friedrich E. Kruse +1 more
TL;DR: Activin A and TGF-beta1, but not BMP-7, are regulators of corneal keratocyte differentiation and may play a role during myofibroblast transdifferentiation and further investigation of Smad signaling may help to better understand the function of T GF-beta family members in the cornea.