Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Bilal Khalil"'
Publikováno v:
Molecular Neurodegeneration, Vol 19, Iss 1, Pp 1-29 (2024)
Abstract Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are fatal neurodegenerative disorders on a disease spectrum that are characterized by the cytoplasmic mislocalization and aberrant phase transitions of prion-like RNA-bind
Externí odkaz:
https://doaj.org/article/edeaa6bc37d04402bb9cd96766c0fcb5
Autor:
Bilal Khalil, Deepak Chhangani, Melissa C. Wren, Courtney L. Smith, Jannifer H. Lee, Xingli Li, Christian Puttinger, Chih-Wei Tsai, Gael Fortin, Dmytro Morderer, Junli Gao, Feilin Liu, Chun Kim Lim, Jingjiao Chen, Ching-Chieh Chou, Cara L. Croft, Amanda M. Gleixner, Christopher J. Donnelly, Todd E. Golde, Leonard Petrucelli, Björn Oskarsson, Dennis W. Dickson, Ke Zhang, James Shorter, Shige H. Yoshimura, Sami J. Barmada, Diego E. Rincon-Limas, Wilfried Rossoll
Publikováno v:
Molecular Neurodegeneration, Vol 17, Iss 1, Pp 1-27 (2022)
Abstract Background Cytoplasmic mislocalization and aggregation of TAR DNA-binding protein-43 (TDP-43) is a hallmark of the amyotrophic lateral sclerosis and frontotemporal dementia (ALS/FTD) disease spectrum, causing both nuclear loss-of-function an
Externí odkaz:
https://doaj.org/article/bbd064334e3c44abbee70cb5d84f3100
Autor:
Pin-Tse Lee, Jean-Charles Liévens, Shao-Ming Wang, Jian-Ying Chuang, Bilal Khalil, Hsiang-en Wu, Wen-Chang Chang, Tangui Maurice, Tsung-Ping Su
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
The (G4C2)-RNA hexanucleotide repeat expansion upstream of the start codon of the C9orf72 gene plays a critical role in familial ALS. The authors show that Sig1R, a ligand-regulated molecular chaperone, counteracts the aberrant nucleocytoplasmic dist
Externí odkaz:
https://doaj.org/article/3e69e0a8edd7453b8b1babe7a2048d98
Publikováno v:
Neurobiology of Disease, Vol 140, Iss , Pp 104835- (2020)
Amyotrophic lateral sclerosis (ALS) is a fatal late-onset neurodegenerative disease that specifically affects the function and survival of spinal and cortical motor neurons. ALS shares many genetic, clinical, and pathological characteristics with fro
Externí odkaz:
https://doaj.org/article/579d7fa6d8064331b9276baf57ce95c2
Autor:
Bilal Khalil, Jean-Charles Liévens
Publikováno v:
Neural Regeneration Research, Vol 12, Iss 7, Pp 1052-1061 (2017)
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder characterized by loss of upper and lower motor neurons. Different mechanisms contribute to the disease initiation and progression, including mitochondrial dysfunction whi
Externí odkaz:
https://doaj.org/article/ed6e9c695128436a91b0db07b4a9604f
Autor:
Muhammad Tariq Rasheed, null Imran Bodlah, null Muhammad Qurban, null Muhammad Bilal Khalil, null Muhammad Usama Khalil, null Junaid Ali Siddiqui, null Ammara Gull E Fareen, null Muhammad Adnan Bodlah
Publikováno v:
Proceedings of the Pakistan Academy of Sciences: B. Life and Environmental Sciences. 59:93-97
Urentius hystricellus is well known phytophagous and invasive true bug of family Tingidae. From Pakistan, this family is poorly studied despite having significant economic importance. Present species was identified with the help of most relevant and
Autor:
Ahmad Bilal Khalil
Publikováno v:
India Quarterly: A Journal of International Affairs. 78:558-584
The emergence of the Afghan Arabs phenomena is the by-product of the Afghan ‘jihad’. The Arabs that mostly came to Afghanistan sought to fulfil a ‘religious’ duty in the form of jihad. This migration process from the Arab countries to the Af-
Autor:
Jannifer H Lee, Dmytro Morderer, Bilal Khalil, Feilin Liu, Chih‐Wei Tsai, Cara L Croft, Yari Carlomagno, Michael DeTure, Michelle Salemi, Casey Cook, Brett Phinney, Dennis W. Dickson, Todd E Golde, Leonard Petrucelli, Wilfried Rossoll
Publikováno v:
Alzheimer's & Dementia. 18
Autor:
Jean-Charles Liévens, Pin Tse Lee, Hsiang En Wu, Shao Ming Wang, Jian Ying Chuang, Tsung-Ping Su, Bilal Khalil, Tangui Maurice, Wen Chang Chang
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2020, 11 (1), ⟨10.1038/s41467-020-19396-3⟩
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Nature Communications, Nature Publishing Group, 2020, 11 (1), ⟨10.1038/s41467-020-19396-3⟩
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
In a subgroup of patients with amyotrophic lateral sclerosis (ALS)/Frontotemporal dementia (FTD), the (G4C2)-RNA repeat expansion from C9orf72 chromosome binds to the Ran-activating protein (RanGAP) at the nuclear pore, resulting in nucleocytoplasmic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcf9b5bac8e99e96d2965aca54f357a3
https://lirias.kuleuven.be/handle/20.500.12942/716341
https://lirias.kuleuven.be/handle/20.500.12942/716341
Autor:
Tangui Maurice, Julien Roussel, Jean-Charles Liévens, Véronique Viguier, Simon Couly, Bilal Khalil
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (4), pp.529-540. ⟨10.1093/hmg/ddz267⟩
Human Molecular Genetics, 2020, 29 (4), pp.529-540. ⟨10.1093/hmg/ddz267⟩
Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (4), pp.529-540. ⟨10.1093/hmg/ddz267⟩
Human Molecular Genetics, 2020, 29 (4), pp.529-540. ⟨10.1093/hmg/ddz267⟩
Sigma-1 receptor (S1R) is an endoplasmic reticulum (ER) chaperone that regulates mitochondrial respiration but also controls cellular defense against ER and oxidative stress. This makes S1R a potential therapeutic target in amyotrophic lateral sclero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d069210fd87dbc3aeaf607586da50e62
https://hal.archives-ouvertes.fr/hal-02360092/file/ADW10A0.pdf
https://hal.archives-ouvertes.fr/hal-02360092/file/ADW10A0.pdf