Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Waqas Tahir"'
Autor:
Sheng Chun Chang, Maria Immaculata Arifin, Waqas Tahir, Keegan John McDonald, Doris Zeng, Hermann M Schatzl, Samia Hannaoui, Sabine Gilch
Publikováno v:
PLoS Pathogens, Vol 20, Iss 7, p e1012370 (2024)
Prions can exist as different strains that consist of conformational variants of the misfolded, pathogenic prion protein isoform PrPSc. Defined by stably transmissible biological and biochemical properties, strains have been identified in a spectrum
Externí odkaz:
https://doaj.org/article/de325275fe614029ae575f10a16732fc
Publikováno v:
BJGP Open, Vol 8, Iss 1 (2024)
Background: Type two diabetes (T2D) is a leading cause of both chronic kidney disease (CKD) and onward progression to end-stage renal disease. Timely diagnosis coding of CKD in patients with T2D could lead to improvements in quality of care and patie
Externí odkaz:
https://doaj.org/article/0a8c7359a7244ed8b6695200bbe1b704
Publikováno v:
Neural Regeneration Research, Vol 17, Iss 8, Pp 1659-1665 (2022)
Prion diseases are infectious protein misfolding disorders of the central nervous system that result from misfolding of the cellular prion protein (PrPC) into the pathologic isoform PrPSc. Pathologic hallmarks of prion disease are depositions of path
Externí odkaz:
https://doaj.org/article/5429ecbd3f394a9a84bb326f19929c05
Autor:
Tahir Ali, Samia Hannaoui, Satish Nemani, Waqas Tahir, Irina Zemlyankina, Pearl Cherry, Su Yeon Shim, Valerie Sim, Hermann M. Schaetzl, Sabine Gilch
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-14 (2021)
Abstract Prion diseases are fatal, infectious, and incurable neurodegenerative disorders caused by misfolding of the cellular prion protein (PrPC) into the infectious isoform (PrPSc). In humans, there are sporadic, genetic and infectious etiologies,
Externí odkaz:
https://doaj.org/article/df386e613c3148bea1070a9c620720db
Autor:
Simrika Thapa, Cristobal Marrero Winkens, Waqas Tahir, Maria I. Arifin, Sabine Gilch, Hermann M. Schatzl
Publikováno v:
Viruses, Vol 14, Iss 3, p 609 (2022)
Prion diseases are fatal infectious neurodegenerative disorders affecting both humans and animals. They are caused by the misfolded isoform of the cellular prion protein (PrPC), PrPSc, and currently no options exist to prevent or cure prion diseases.
Externí odkaz:
https://doaj.org/article/bc31b748f7c2455983a79d7be93b3302
Autor:
Franc Llorens, Katrin Thüne, Waqas Tahir, Eirini Kanata, Daniela Diaz-Lucena, Konstantinos Xanthopoulos, Eleni Kovatsi, Catharina Pleschka, Paula Garcia-Esparcia, Matthias Schmitz, Duru Ozbay, Susana Correia, Ângela Correia, Ira Milosevic, Olivier Andréoletti, Natalia Fernández-Borges, Ina M. Vorberg, Markus Glatzel, Theodoros Sklaviadis, Juan Maria Torres, Susanne Krasemann, Raquel Sánchez-Valle, Isidro Ferrer, Inga Zerr
Publikováno v:
Molecular Neurodegeneration, Vol 12, Iss 1, Pp 1-21 (2017)
Abstract Background YKL-40 (also known as Chitinase 3-like 1) is a glycoprotein produced by inflammatory, cancer and stem cells. Its physiological role is not completely understood but YKL-40 is elevated in the brain and cerebrospinal fluid (CSF) in
Externí odkaz:
https://doaj.org/article/ecd452e7a5af49e1a47d32c0f9339fd5
Autor:
Franc Llorens, Katrin Thüne, Beata Sikorska, Matthias Schmitz, Waqas Tahir, Natalia Fernández-Borges, Maria Cramm, Nadine Gotzmann, Margarita Carmona, Nathalie Streichenberger, Uwe Michel, Saima Zafar, Anna-Lena Schuetz, Ashish Rajput, Olivier Andréoletti, Stefan Bonn, Andre Fischer, Pawel P. Liberski, Juan Maria Torres, Isidre Ferrer, Inga Zerr
Publikováno v:
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-20 (2017)
Abstract Sporadic Creutzfeldt-Jakob disease (sCJD) is the most prevalent form of human prion disease and it is characterized by the presence of neuronal loss, spongiform degeneration, chronic inflammation and the accumulation of misfolded and pathoge
Externí odkaz:
https://doaj.org/article/2e50321168ab46359a8ddcd179c4d0d2
Autor:
Khan, Imran, Ali, Amjad, Waqas, Tahir, Ullah, Sami, Ullah, Safi, Shah, Ashfaq Ahmad, Imran, Sajid
Publikováno v:
In International Journal of Disaster Risk Reduction 1 June 2022 75
1.AbstractBackgroundType 2 diabetes (T2D) is a leading cause of both chronic kidney disease (CKD) and onward progression to end stage renal disease. Timely diagnosis coding of CKD in patients with T2D could lead to improvements in quality of care and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::437ad3ac50343ff036e0183d2c87d284
https://doi.org/10.1101/2023.05.11.23289836
https://doi.org/10.1101/2023.05.11.23289836
Autor:
Ritambhara, Pandey, Devesh, Rai, Muhammad Waqas, Tahir, Abdul, Wahab, Dhrubajyoti, Bandyopadhyay, Emil, Lesho, Maryrose, Laguio-Vila, Emilio, Fentanes, Raseen, Tariq, Srihari S, Naidu, Wilbert S, Aronow
Publikováno v:
Archives of Medical Science – Atherosclerotic Diseases. 7:5-23
IntroductionWe performed a systematic review of comorbidities and symptoms of adult patients with coronavirus disease 2019 (COVID-19) to evaluate comorbidities, symptoms, and severity.Material and methodsWe searched databases and extracted comorbidit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b36f22e4262caaf96b0b53199d9dd39b
https://doi.org/10.5114/amsad.2022.115008
https://doi.org/10.5114/amsad.2022.115008