Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Deepak Kamnasaran"'
Protective Role of Neuronal PAS Domain Protein 3 NPAS3 Gene in the Survival of Human Brain Stem Cell
Publikováno v:
Asian Journal of Applied Sciences. 11:76-82
Autor:
Deepak Kamnasaran, Martin Broome, Yvan Vial, Sébastien Jacquemont, Consolato Sergi, Eric Giannoni
Publikováno v:
Pediatrics and Neonatology, Vol 57, Iss 1, Pp 65-68 (2016)
Syngnathia is an extremely rare condition involving congenital fusion of the maxilla with the mandible. Clinical presentations vary from simple mucosal bands (synechiae) to complete bony fusion (synostosis). Most cases are unilateral incomplete fusio
Publikováno v:
Future Oncology. 9:1215-1229
Aim: The treatment of pediatric low-grade gliomas with current treatment modalities still remains ineffective among a subset of patients; hence, justifying the need to further investigate more effective therapies. Dipotassium bisperoxo (picolinato) o
Publikováno v:
Cancer Letters. 330:130-140
Medulloblastomas are highly aggressive tumors of the cerebellum with an embryonal origin. Despite current treatment modalities which include a combination of surgery, chemotherapy and/or radiation, challenges still exist to effectively treat some pat
Publikováno v:
Cancer Letters. 330:96-105
Pediatric low grade gliomas are the most common central nervous system tumors and are still incurable among a subset of patients despite current treatment modalities. Steroid biosynthesis occurs in a wide variety of organs including the brain, to med
Autor:
Lotta Mononen, Jacques Huot, Anne-Laure Pin, Norbert F. Ajeawung, Deepak Kamnasaran, Andrea Thorn, Harish C. Joshi
Publikováno v:
Journal of pediatric oncology
Background : Intervention aimed at disrupting or inhibiting newly formed vascular network is highly desired to attenuate the progression of angiogenesis-dependent diseases. In cancer, this is tightly associated with the generation of VEGF by hypoxia
Autor:
O Ozyuncu, Ş Yiğit, Gülen Eda Utine, T Sozen, T Çelik, PO Simsek, Koray Boduroğlu, Beril Talim, Deepak Kamnasaran
Publikováno v:
Clinical Genetics. 81:294-297
Autor:
Gerald Steiner, Stefan Rutkowski, David M. Loeb, Jochen Herms, Samuel D. Rabkin, G.J. Kaspers, Ling-Yuan Kong, Reiner Salzer, Tokomo Ozawa, Anneke C. Navis, Rob C. Hoeben, John J. Lannutti, Nalin Gupta, ZhaoBin Zhang, Alfredo Quinones-Hinojosa, Dolores Hambardzumyan, Jon D. Weingart, Mariano S. Viapiano, Michał Nowicki, Gregory J. Riggins, Celina Crisman, Chen Gang, Elena I. Fomchenko, Martine L.M. Lamfers, Yuan Rong, Carol Tucker-Burden, I Zondervan, P. Wesseling, Deepak Kamnasaran, Enio A. Chiocca, Jose Bergeron, Julia Sisti, Sanne K. van den Hengel, Anat Stemmer-Rachamimov, Nikolaus Schultz, Gabriele Schackert, Jun Wei, Jonathan P. Yun, Bob C. Hamans, Fabien G. Lafaille, Shengguo Li, Amparo Wolf, Paula A. Agudelo, Jochem K H Spoor, Rolf Bjerkvig, Abhijit Guha, Sameer Agnihotri, Preeti Shah, Andreas Lorenz, Gregory N. Fuller, Xiaoyan Zhu, Nesrin Sabha, Michael Lim, Stephen Yip, Frits Thorsen, Viviane Tabar, Allison Stelling, Judith W. M. Jeuken, William T. Curry, Arend Heerschap, Nduka Amankulor, Hiroaki Wakimoto, Lakshmi Katuri, Yasuyuki Aoki, Hadie Adams, Jenneke Kloezeman, Raelene Endersby, P. van der Valk, T. Wurdinger, Wesley Hsu, André Von Bueren, Antonio Aliaga, Suzanne J. Baker, Matthias Kirsch, David W. Ellison, Sander Idema, Yuhui Yang, Norbert Ajewung, Massimo Squatrito, C. Molthoff, D. H. Meijer, Gayatry Mohapatra, Pim J. French, Rutger K. Balvers, An Claes, M. Bugiani, Hans A. Kretzschmar, Michael Castelli, Pui K. Li, Thomas Kosztowski, Ganesh Rao, Zev A. Binder, W. Vos, M. Barazas, Eric C. Holland, Amanda M. Katz, Anne Kleijn, Chunxu Qu, Jeffrey N. Bruce, P.M. van der Stoop, Robert L. Martuza, Sidney Croul, Ahmed Mohyeldin, Shante Williams, Jed Johnson, Heike Immervoll, Aurelia Peraud, W.P. Vandertop, Sherri Rankin, Erwin Van Meir, Anne Lenferink, Adam Studebaker, Amy B. Heimberger, Lorenz Studer, Clemens M F Dirven, E. Hulleman, Sieger Leenstra, Ziya L. Gokaskan, Peter Canoll, Sagar R. Shah, Henry Brem, Pieter Wesseling, Ulrike S. Trojahn, Gary L. Gallia, Ryuichi Kanai, Vafi Salmasi, Mengqing Xiang, Julia Pöschl, D.J. Brat, Stephen D. Nimer, Craig Soderquist, Lionel M. Chow, T. Lagerweij, Tiffany Doucette, Jean-Paul Wolinsky, Elena Bazzoli, Jörg-Christian Tonn, Christoph Krafft, Maureen O'Connor-McCourt, Ulrich Schüller, Andreas von Deimling, Inderjit Daphu, Rintaro Hashizume, Alessandro Olivi, Adam Sonabend, William P.J. Leenders, Lisa M. DeAngelis, Liang Lei, C.D. James, D. Noske, Cameron Brennan, Sean E. Lawler, Junyuan Zhang, B. Hamans, Corey Raffel, Jinbo Wang, Barry J. Bedell, V. Caretti, Zachary R. Barnard
Publikováno v:
Neuro-Oncology. 12:iv130-iv136
Publikováno v:
Fetal and Pediatric Pathology. 29:207-211
Otocephaly is a severe and lethal malformation. We report a new case of a fetus with Agnathia-Otocephaly, presenting only the facial findings but with otherwise normal organs. The fetal karyotype was normal. We examined the fetal DNA for uniparental
Autor:
Tim-Rasmus Kiehl, Gelareh Zadeh, Abhijit Guha, Joydeep Mukherjee, Ivan Radovanovic, Anand Balasubramaniam, Deepak Kamnasaran
Publikováno v:
Cancer Research. 69:5099-5107
Schwannomas, although benign, can be fatal or give rise to significant morbidity due to an unpredictable growth rate. They can reoccur after surgery or radiation, current treatments each with significant inherent risks. These risks are further amplif