Zobrazeno 1 - 10
of 188
pro vyhledávání: '"Ephrin A5"'
Autor:
Yoji Kishi, Yoshinori Ino, Mari Shimasaki, Toshimitsu Iwasaki, Kazuaki Shimada, Kosei Nakajima, Nobuyoshi Hiraoka, Minoru Esaki, Utako Ishimoto, Satoshi Nara, Noriteru Doi, Chie Naito
Publikováno v:
Br J Cancer
BACKGROUND: The treatment of pancreatic cancer (PDAC) remains clinically challenging, and neoadjuvant therapy (NAT) offers down staging and improved surgical resectability. Abundant fibrous stroma is involved in malignant characteristic of PDAC. We a
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2020 (2020)
BioMed Research International, Vol 2020 (2020)
Retinal neovascularization (RNV) is an important pathological feature of vitreoretinopathy that can lead to severe vision loss. The purpose of this study was to identify the role of ephrin-A5 (Efna5) in RNV and to explore its mechanism. The expressio
Publikováno v:
European Journal of Pharmacology. 917:174588
Gliomas, tumors of glial cells, are the most common malignant tumors of the brain. Ephrins are protein ligands that act through tyrosine kinases receptor family, Eph receptors. In glioma, an inverse relationship has been identified between ephrin A1
Autor:
Lu Xu, Alan D. Flechtner, L. James Lee, Qiwen Shen, Paolo Fadda, Lianbo Yu, Jessica M. Marbourg, Rumana Yasmeen, Phillip G. Popovich, Ouliana Ziouzenkova
Publikováno v:
Translational Research. 192:1-14
Innervation is a fundamental basis for function and survival of tissues. In the peripheral tissues, degenerative diseases create a neurotoxic metabolic milieu that either causes neurodegeneration or fails to sustain regenerative growth and reinnervat
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-17 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-17 (2019)
Axonal growth cones are guided by molecular cues in the extracellular environment. The mechanisms of combinatorial integration of guidance signals at the growth cone cell membrane are still being unravelled. Limb-innervating axons of vertebrate spina
Autor:
Albert C. Ludolph, Jochen H. Weishaupt, Philip Van Damme, Annette Lenaerts, Wim Robberecht, Jasmijn van der Vos, Silke Smolders, Laura Rué, Patrick Oeckl, Ludo Van Den Bosch, Antina de Boer, Lindsay Poppe, Mieke Timmers, Robin Lemmens, Markus Otto
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-15 (2019)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that affects motor neurons in the brainstem, spinal cord and motor cortex. ALS is characterized by genetic and clinical heterogeneity, suggesting the existence of genetic factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3999b4f7642b8bc4a85ad649a1c41343
https://lirias.kuleuven.be/handle/123456789/644713
https://lirias.kuleuven.be/handle/123456789/644713
Autor:
Yuhan Hu, Annika G. Samuelson, Alexandra Magee, Laura Anne Lowery, Garrett M. Cammarata, Paula G. Slater
Publikováno v:
J Cell Sci
It has long been established that neuronal growth cone navigation depends on changes in microtubule (MT) and F-actin architecture downstream of guidance cues. However, the mechanisms by which MTs and F-actin are dually coordinated remain a fundamenta
Publikováno v:
Genes, Brain and Behavior. 16:271-284
During development of the nervous system, molecular signals mediating cell-cell interactions play critical roles in the guidance of axonal growth and establishment of synaptic functions. The Eph family of tyrosine kinase receptors and their ephrin li
Publikováno v:
Oncotarget
// Sara Ferluga 1 , Carla Maria Lema Tome 2 , Denise Mazess Herpai 1 , Ralph D’Agostino 3 , Waldemar Debinski 1 1 Department of Cancer Biology, Radiation Oncology and Neurosurgery, Brain Tumor Center of Excellence, Comprehensive Cancer Center of Wa
Autor:
Derek C. Adams, Klas Kullander, Leif Oxburgh, Rüdiger Klein, Christiane Peuckert, Pavlo Holenya, Smitha Sreedharan, Bejan Aresh, Annika Porthin, Louise Andersson, Stefan Wölfl, H. Pettersson
Publikováno v:
Kidney International. 90:373-388
A substantial portion of the human population is affected by urogenital birth defects resulting from a failure in ureter development. Although recent research suggests roles for several genes in facilitating the ureter/bladder connection, the underly