Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Mukesh, Gautam"'
Autor:
Mukesh Gautam, Mohammad MansourLakouraj, Rakib Hossain, Narayan Bhusal, Mohammed Benidris, Hanif Livani
Publikováno v:
IEEE Access, Vol 12, Pp 5222-5236 (2024)
The integration of distributed energy resources (DERs) into the power grid has made it important for distribution systems to participate in frequency regulation. Regulatory authorities (e.g., Federal Electricity Regulatory Commission in the United St
Externí odkaz:
https://doaj.org/article/658a6e2002c54f4693341ee112c6b41e
Autor:
Mukesh Gautam
Publikováno v:
Electricity, Vol 4, Iss 4, Pp 336-380 (2023)
In recent years, deep reinforcement learning (DRL) has garnered substantial attention in the context of enhancing resilience in power and energy systems. Resilience, characterized by the ability to withstand, absorb, and quickly recover from natural
Externí odkaz:
https://doaj.org/article/0ef39ab15ca34e5ea9bc5858960823cb
Publikováno v:
IEEE Access, Vol 11, Pp 54822-54838 (2023)
The ever-increasing penetration of intermittent renewable resources in low-voltage power grids necessitates efficient operational strategies for voltage regulation as well as power scheduling of the available resources. In this paper, a risk-aware Vo
Externí odkaz:
https://doaj.org/article/f4036d1f30e8492d8ab501668f56ec01
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Mitochondrial defects result in dysregulation of metabolomics and energy homeostasis that are detected in upper motor neurons (UMNs) with TDP-43 pathology, a pathology that is predominantly present in both familial and sporadic cases of amyo
Externí odkaz:
https://doaj.org/article/f6559ee45b4545dcae417a9feab81be9
Autor:
Barış Genç, Mukesh Gautam, Benjamin R. Helmold, Nuran Koçak, Aksu Günay, Gashaw M. Goshu, Richard B. Silverman, P. Hande Ozdinler
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Even though amyotrophic lateral sclerosis (ALS) is a disease of the upper and lower motor neurons, to date none of the compounds in clinical trials have been tested for improving the health of diseased upper motor neurons (UMNs). There is an
Externí odkaz:
https://doaj.org/article/1615426b1cc142ffaf71653ae54dfb5a
Autor:
Mukesh Gautam, Barış Genç, Benjamin Helmold, Angela Ahrens, Janis Kuka, Marina Makrecka-Kuka, Aksu Günay, Nuran Koçak, Izaak R. Aguilar-Wickings, Dennis Keefe, Guozhu Zheng, Suchitra Swaminathan, Martin Redmon, Hatim A. Zariwala, P. Hande Özdinler
Publikováno v:
Neurobiology of Disease, Vol 178, Iss , Pp 106022- (2023)
Mitochondrial defects are one of the common underlying causes of neuronal vulnerability in neurodegenerative diseases, such as amyotrophic lateral sclerosis (ALS), and TDP-43 pathology is the most commonly observed proteinopathy. Disrupted inner mito
Externí odkaz:
https://doaj.org/article/500a9a36e006467bbaa75e89a1dedef4
Publikováno v:
IEEE Access, Vol 9, Pp 40402-40416 (2021)
Several wired and wireless advanced communication technologies have been used for coordinated voltage regulation schemes in distribution systems. These technologies have been employed to both receive voltage measurements from field sensors and transm
Externí odkaz:
https://doaj.org/article/b20cc2040c4e471a88e900e853ed9fd6
Autor:
Javier H. Jara, Mukesh Gautam, Nuran Kocak, Edward F. Xie, Qinwen Mao, Eileen H. Bigio, P. Hande Özdinler
Publikováno v:
Journal of Neuroinflammation, Vol 16, Iss 1, Pp 1-16 (2019)
Abstract Background The involvement of non-neuronal cells and the cells of innate immunity has been attributed to the initiation and progression of ALS. TDP-43 pathology is observed in a broad spectrum of ALS cases and is one of the most commonly sha
Externí odkaz:
https://doaj.org/article/4fb169a5f82540d09bc348b70cdffa81
Autor:
Barış Genç, Mukesh Gautam, Öge Gözütok, Ina Dervishi, Santana Sanchez, Gashaw M. Goshu, Nuran Koçak, Edward Xie, Richard B. Silverman, P. Hande Özdinler
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 2, Pp n/a-n/a (2021)
Abstract Background Upper motor neurons (UMNs) are a key component of motor neuron circuitry. Their degeneration is a hallmark for diseases, such as hereditary spastic paraplegia (HSP), primary lateral sclerosis (PLS), and amyotrophic lateral scleros
Externí odkaz:
https://doaj.org/article/5370d3704c9349de99b927f4e9b91ea3
Autor:
Mukesh Gautam, Renata Del Carratore, Benjamin Helmold, Alessandra Tessa, Oge Gozutok, Navdeep Chandel, Halil Idrisoglu, Paolo Bongioanni, Roberta Battini, P.Hande Ozdinler
Publikováno v:
Metabolites, Vol 12, Iss 2, p 174 (2022)
Pathogenic variants in ALS2 have been detected mostly in juvenile cases of amyotrophic lateral sclerosis (ALS), affecting mainly children and teenagers. Patients with ALS2 mutations demonstrate early onset cortical involvement in ALS. Currently, ther
Externí odkaz:
https://doaj.org/article/9dd60907849b4ab3b3bd9c5fb1d6b964