Zobrazeno 1 - 10
of 250
pro vyhledávání: '"Simon G, Gregory"'
Autor:
George D. Dalton, Stephen K. Siecinski, Viktoriya D. Nikolova, Gary P. Cofer, Kathryn J. Hornburg, Yi Qi, G. Allan Johnson, Yong-Hui Jiang, Sheryl S. Moy, Simon G. Gregory
Publikováno v:
Behavioral and Brain Functions, Vol 20, Iss 1, Pp 1-23 (2024)
Abstract Background Autism Spectrum Disorder (ASD) is a group of neurodevelopmental disorders with higher incidence in males and is characterized by atypical verbal/nonverbal communication, restricted interests that can be accompanied by repetitive b
Externí odkaz:
https://doaj.org/article/3a0dc3d8da37446598bf596a2a78dc61
Autor:
Joshua A. Regal, María E. Guerra García, Vaibhav Jain, Vidyalakshmi Chandramohan, David M. Ashley, Simon G. Gregory, Eric M. Thompson, Giselle Y. López, Zachary J. Reitman
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-3 (2024)
Externí odkaz:
https://doaj.org/article/01b4c740b36b4a8ca05ca73eba28ca23
Autor:
Andrew J. Graves, Joshua S. Danoff, Minah Kim, Samantha R. Brindley, Amalia M. Skyberg, Stephanie N. Giamberardino, Morgan E. Lynch, Brenda C. Straka, Travis S. Lillard, Simon G. Gregory, Jessica J. Connelly, James P. Morris
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-18 (2024)
Abstract While chronological age is a strong predictor for health-related risk factors, it is an incomplete metric that fails to fully characterize the unique aging process of individuals with different genetic makeup, neurodevelopment, and environme
Externí odkaz:
https://doaj.org/article/0a7474c6984a4e0cbc2d95f4ae620d46
Autor:
Mengyi Liu, Zhicheng Ji, Vaibhav Jain, Vanessa L. Smith, Emily Hocke, Anoop P. Patel, Roger E. McLendon, David M. Ashley, Simon G. Gregory, Giselle Y. López
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-12 (2024)
Abstract Glioblastoma (GBM) remains an untreatable malignant tumor with poor patient outcomes, characterized by palisading necrosis and microvascular proliferation. While single-cell technology made it possible to characterize different lineage of gl
Externí odkaz:
https://doaj.org/article/15939242c18842f1a4a601f94efff0d5
Autor:
Joshua A. Regal, María E. Guerra García, Vaibhav Jain, Vidyalakshmi Chandramohan, David M. Ashley, Simon G. Gregory, Eric M. Thompson, Giselle Y. López, Zachary J. Reitman
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-30 (2023)
Abstract Gangliogliomas are brain tumors composed of neuron-like and macroglia-like components that occur in children and young adults. Gangliogliomas are often characterized by a rare population of immature astrocyte-appearing cells expressing CD34,
Externí odkaz:
https://doaj.org/article/d9a27d880bbe4ad09edb99a558ed71db
Autor:
Minato Hirano, Gaddiel Galarza-Muñoz, Chloe Nagasawa, Geraldine Schott, Liuyang Wang, Alejandro L Antonia, Vaibhav Jain, Xiaoying Yu, Steven G Widen, Farren BS Briggs, Simon G Gregory, Dennis C Ko, William S Fagg, Shelton Bradrick, Mariano A Garcia-Blanco
Publikováno v:
eLife, Vol 12 (2023)
Genes associated with increased susceptibility to multiple sclerosis (MS) have been identified, but their functions are incompletely understood. One of these genes codes for the RNA helicase DExD/H-Box Polypeptide 39B (DDX39B), which shows genetic an
Externí odkaz:
https://doaj.org/article/c38f1aa37a0a4f6ba7bae9127557c87f
Autor:
Aaditya Khatri, Jamie L. Todd, Fran L. Kelly, Andrew Nagler, Zhicheng Ji, Vaibhav Jain, Simon G. Gregory, Kent J. Weinhold, Scott M. Palmer
Publikováno v:
JCI Insight, Vol 8, Iss 6 (2023)
Chronic lung allograft dysfunction (CLAD) is the leading cause of death in lung transplant recipients. CLAD is characterized clinically by a persistent decline in pulmonary function and histologically by the development of airway-centered fibrosis kn
Externí odkaz:
https://doaj.org/article/239550e2e86c4f2f94dc6c6368c0fde1
Autor:
Jennifer R. Dungan, Xue Qin, Simon G. Gregory, Rhonda Cooper-Dehoff, Julio D. Duarte, Huaizhen Qin, Martha Gulati, Jacquelyn Y. Taylor, Carl J. Pepine, Elizabeth R. Hauser, William E. Kraus
Publikováno v:
American Heart Journal Plus, Vol 17, Iss , Pp 100152- (2022)
Background: Ischemic coronary heart disease (IHD) is the leading cause of death worldwide. Genetic variation is presumed to be a major factor underlying sex differences for IHD events, including mortality. The purpose of this study was to identify se
Externí odkaz:
https://doaj.org/article/fa77f6ee4da64a489a866dcb5de07427
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Human red blood cells (RBCs), or erythrocytes, are the most abundant blood cells responsible for gas exchange. RBC diseases affect hundreds of millions of people and impose enormous financial and personal burdens. One well-recognized, but poorly unde
Externí odkaz:
https://doaj.org/article/2be376b95d61463c8adf09a31b146017
Autor:
Elliott D SoRelle, Joanne Dai, Emmanuela N Bonglack, Emma M Heckenberg, Jeffrey Y Zhou, Stephanie N Giamberardino, Jeffrey A Bailey, Simon G Gregory, Cliburn Chan, Micah A Luftig
Publikováno v:
eLife, Vol 10 (2021)
Externí odkaz:
https://doaj.org/article/21eb6e23050f439b98a23e68178db44c