Zobrazeno 1 - 10
of 174
pro vyhledávání: '"Aishwarya .G"'
Autor:
Eliska Zlamalova, Catherine Rodger, Francesca Greco, Samuel R. Cheers, Julia Kleniuk, Aishwarya G. Nadadhur, Zuzana Kadlecova, Evan Reid
Publikováno v:
Neurobiology of Disease, Vol 199, Iss , Pp 106556- (2024)
Mutation of the ATL1 gene is one of the most common causes of hereditary spastic paraplegia (HSP), a group of genetic neurodegenerative conditions characterised by distal axonal degeneration of the corticospinal tract axons. Atlastin-1, the protein e
Externí odkaz:
https://doaj.org/article/f7c19cd2e45d43a18c6c19940487e4d8
Autor:
Zlamalova, Eliska, Rodger, Catherine, Greco, Francesca, Cheers, Samuel R., Kleniuk, Julia, Nadadhur, Aishwarya G., Kadlecova, Zuzana, Reid, Evan
Publikováno v:
In Neurobiology of Disease September 2024 199
Autor:
Nangia, Sapna, Burela, Nagarjuna, Sawant, Mayur, Aishwarya, G., Joshua, Patrick, Thiyagarajan, Vijay, Gaikwad, Utpal, Sharma, Dayananda S.
Publikováno v:
In Technical Innovations & Patient Support in Radiation Oncology June 2024 30
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Thoracic aortic disease (TAD) is often silent until a life-threatening complication occurs. However, genetic information can inform both identification and treatment at an early stage. Indeed, a diagnosis is important for personalised surveillance an
Externí odkaz:
https://doaj.org/article/3387252f1a2a4c048fe696975b735189
Akademický článek
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Autor:
Justin, Alexander W., Cammarata, Federico, Guy, Andrew A., Estevez, Silas R., Burgess, Sebastian, Davaapil, Hongorzul, Stavropoulou-Tatla, Agavi, Ong, John, Jacob, Aishwarya G., Saeb-Parsy, Kourosh, Sinha, Sanjay, Markaki, Athina E.
Publikováno v:
In Biomaterials Advances February 2023 145
Akademický článek
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Autor:
Paul, Jaison1 jaisonpaulth@gmail.com, Aishwarya G.1, Yadav P., Balarama Swamy2, K., Pradip Kumar1, A. B., Rema Shree1
Publikováno v:
Journal of Applied & Natural Science. 2023, Vol. 15 Issue 1, p235-241. 7p.
Autor:
Aishwarya G. Nadadhur, Mouhamed Alsaqati, Lisa Gasparotto, Paulien Cornelissen-Steijger, Eline van Hugte, Stephanie Dooves, Adrian J. Harwood, Vivi M. Heine
Publikováno v:
Stem Cell Reports, Vol 12, Iss 1, Pp 42-56 (2019)
Summary: Tuberous sclerosis complex (TSC) is a rare neurodevelopmental disorder resulting from autosomal dominant mutations in the TSC1 or TSC2 genes, leading to a hyperactivated mammalian target of rapamycin (mTOR) pathway, and gray and white matter
Externí odkaz:
https://doaj.org/article/03f59f6c7715412aa20eb66b5c45b209
Publikováno v:
Journal of Applied and Natural Science. 15:235-241
Small cardamom (Elettaria cardamomum (L.) Maton.), often referred to as the 'queen of spices' is believed to have originated in the moist evergreen forests of the Western Ghats of South India. The present study was conducted at the Indian Cardamom Re