Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Sevda, Lule"'
Autor:
Shilpa Prabhakar, Roberta L. Beauchamp, Pike See Cheah, Akiko Yoshinaga, Edwina Abou Haidar, Sevda Lule, Gayathri Mani, Katia Maalouf, Anat Stemmer-Rachamimov, David H. Jung, D. Bradley Welling, Marco Giovannini, Scott R. Plotkin, Casey A. Maguire, Vijaya Ramesh, Xandra O. Breakefield
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 2, Pp 101262- (2024)
Externí odkaz:
https://doaj.org/article/3e5ab6a0da2740adbac015462c8c83b4
Autor:
Shilpa Prabhakar, Roberta L. Beauchamp, Pike See Cheah, Akiko Yoshinaga, Edwina Abou Haidar, Sevda Lule, Gayathri Mani, Katia Maalouf, Anat Stemmer-Rachamimov, David H. Jung, D. Bradley Welling, Marco Giovannini, Scott R. Plotkin, Casey A. Maguire, Vijaya Ramesh, Xandra O. Breakefield
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 26, Iss , Pp 169-180 (2022)
Loss of function of the neurofibromatosis type 2 (NF2) tumor suppressor gene leads to the formation of schwannomas, meningiomas, and ependymomas, comprising ∼50% of all sporadic cases of primary nervous system tumors. NF2 syndrome is an autosomal d
Externí odkaz:
https://doaj.org/article/7beaec1f53b24b3a8b2e347e32d796ca
Autor:
Tong Zi, Sriram Sathyanarayanan, Katherine Kirwin, Su Chul Jang, Kyriakos Economides, John Lin, Kelvin Zhang, Shil Patel, Xudong Feng, Sevda Lule, Paloma Sanchez-Jauregui, Samuel Kasera, Silvia Siso, Wendy Broom
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss Suppl 2 (2021)
Externí odkaz:
https://doaj.org/article/b9ed0903da974154918e2734159b209f
Autor:
Ayse Ilksen Colpak, Banu Balci-Peynircioglu, Alp Can, Yasemin Gursoy-Ozdemir, Sevda Lule, Umut Kalyoncu, Turgay Dalkara
Publikováno v:
Data in Brief, Vol 15, Iss , Pp 170-173 (2017)
The data presented in this article are related to the research article entitled âBehcet Disease serum is immunoreactive to neurofilament medium which share common epitopes to bacterial HSP-65, a putative triggerâ (Lule et a. 2017) [1]. The immunore
Externí odkaz:
https://doaj.org/article/ae47d3ed25504879a64923e83ed8b55b
Autor:
Edwina Abou Haidar, Shilpa Prabhakar, Pike See Cheah, Sevda Lule, Roberta L. Beauchamp, Akiko Yoshinaga, Alexandra L. Geffrey, Anat Stemmer-Rachamimov, Vijaya Ramesh, Casey A. Maguire, Xandra O. Breakefield
Publikováno v:
Monday, April 24.
Autor:
Saef Izzy, Qiong Liu, Zhou Fang, Sevda Lule, Limin Wu, Joon Yong Chung, Aliyah Sarro-Schwartz, Alexander Brown-Whalen, Caroline Perner, Suzanne E. Hickman, David L. Kaplan, Nikolaos A. Patsopoulos, Joseph El Khoury, Michael J. Whalen
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
The neuroinflammatory response to traumatic brain injury (TBI) is critical to both neurotoxicity and neuroprotection, and has been proposed as a potentially modifiable driver of secondary injury in animal and human studies. Attempts to broadly target
Externí odkaz:
https://doaj.org/article/4d51f33285324077b52c79c485bef401
Autor:
Saef Izzy, Alexander Brown-Whalen, Taha Yahya, Aliyah Sarro-Schwartz, Gina Jin, Joon Yong Chung, Sevda Lule, Liza M. Morsett, Ali Alquraini, Limin Wu, Suzanne E. Hickman, Michael J. Whalen, Joseph El Khoury
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 2, p 907 (2021)
Repetitive closed head injury (rCHI) is commonly encountered in young athletes engaged in contact and collision sports. Traumatic brain injury (TBI) including rCHI has been reported to be an important risk factor for several tauopathies in studies of
Externí odkaz:
https://doaj.org/article/148e1c1d215c40d6bf2dfd9fae98c369
Autor:
Sepideh, Afshar, Sevda, Lule, Gengyang, Yuan, Xiying, Qu, Chuzhi, Pan, Michael, Whalen, Anna-Liisa, Brownell, Maria, Mody
Publikováno v:
Translational Neuroscience. 13:80-92
Fragile X syndrome (FXS) is a monogenic disorder characterized by intellectual disability and behavioral challenges. It is caused by aberrant methylation of the fragile X mental retardation 1 (FMR1) gene. Given the failure of clinical trials in FXS a
Publikováno v:
Turkish Neurosurgery
AIM: To investigate the suppression of aquaporin-4 (AQP4) synthesis through intracerebroventricular (i.c.v.) injection of antisense oligonucleotide after focal cortical contusion injury in mice. MATERIAL and METHODS: This study used 12-week-old femal
Autor:
Joon Yong Chung, Tanya Songtachalert, Alexei Degterev, David L. Kaplan, Gina Jin, Aliyah Sarro-Schwartz, Neil D. Fernandes, Michael J. Whalen, William J Edmiston, Saef Izzy, Siddharth Balachandran, So Hee Ahn, Sevda Lule, Eng H. Lo, Limin Wu
Publikováno v:
J Cereb Blood Flow Metab
Receptor-interacting protein kinase-1 (RIPK1) is a master regulator of cell death and inflammation, and mediates programmed necrosis (necroptosis) via mixed-lineage kinase like (MLKL) protein. Prior studies in experimental intracerebral hemorrhage (I