Notch3 deletion regulates HIV-1 gene expression and systemic inflammation to ameliorate chronic kidney disease by Mackenzie Thornton, Nicole Sommer, Mercedes McGonigle, Anil Kumar Ram, Sireesha Yerrathota, Henrietta Ehirim, Aakriti Chaturvedi, Johnny Dinh Phan, Anubhav Chakraborty, V. Praveen Chakravarthi, Sumedha Gunewardena, Mudit Tyagi, Jaya Talreja, Tao Wang, Pravin Singhal, Pamela V. Tran, Timothy A. Fields, Patricio E. Ray, Navneet K. Dhillon, Madhulika Sharma

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Analysis of the pathogenicity and pathological characteristics of NOTCH3 gene-sparing cysteine mutations in vitro and in vivo models by Zhenping Gong, Wan Wang, Ying Zhao, Yadan Wang, Ruihua Sun, Ruihua Sun, Haohan Zhang, Haohan Zhang, Fengyu Wang, Yaru Lu, Jiewen Zhang, Jiewen Zhang, Jiewen Zhang, Jiewen Zhang

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Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early‐onset arteriopathy and cavitating leukoencephalopathy by Tommaso Pippucci, Alessandra Maresca, Pamela Magini, Giovanna Cenacchi, Vincenzo Donadio, Flavia Palombo, Valentina Papa, Alex Incensi, Giuseppe Gasparre, Maria Lucia Valentino, Carmela Preziuso, Annalinda Pisano, Michele Ragno, Rocco Liguori, Carla Giordano, Caterina Tonon, Raffaele Lodi, Antonia Parmeggiani, Valerio Carelli, Marco Seri

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Synergistic effects of mutation and glycosylation on disease progression by Shodai Suzuki, Motoyuki Itoh, Motoyuki Itoh, Motoyuki Itoh

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Analyses of NOTCH3 variants in Chinese patients with clinically diagnosed Alzheimer's disease and frontotemporal dementia by Haitian Nan, Min Chu, Ailing Yue, Qianqian He, Jieying Li, Yanchen Liu, Lijun Chi, Xiaoyan Liu, Guoping Peng, Liyong Wu

Subjects: “…NOTCH3…”
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Clinical and epidemiological profiles from a case series of 26 Brazilian CADASIL patients by Renata Nogueira, Christian Marques Couto, Pérola de Oliveira, Bernardo José Alves Ferreira Martins, Vinícius Viana Abreu Montanaro

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Active immunotherapy reduces NOTCH3 deposition in brain capillaries in a CADASIL mouse model by Daniel V Oliveira, Kirsten G Coupland, Wenchao Shao, Shaobo Jin, Francesca Del Gaudio, Sailan Wang, Rhys Fox, Julie W Rutten, Johan Sandin, Henrik Zetterberg, Johan Lundkvist, Saskia AJ Lesnik Oberstein, Urban Lendahl, Helena Karlström

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Contributions of Germline and Somatic Mosaic Genetics to Thoracic Aortic Aneurysms in Nonsyndromic Individuals by Ming Hui Chen, Ellen S. Deng, Jessica M. Yamada, Sangita Choudhury, Julia Scotellaro, Lily Kelley, Eric Isselbacher, Mark E. Lindsay, Christopher A. Walsh, Ryan N. Doan

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Association of Rare NOTCH3 Variants With Prevalent and Incident Stroke and Dementia in the General Population by Pei Wang, Ming Yao, Jing Yuan, Fei Han, Fei‐Fei Zhai, Ding‐Ding Zhang, Li‐Xin Zhou, Jun Ni, Shu‐Yang Zhang, Li‐Ying Cui, Yi‐Cheng Zhu

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Exome sequencing of a Portuguese cohort of early-onset Alzheimer’s disease implicates the X-linked lysosomal gene GLA by Miguel Tábuas-Pereira, José Brás, Ricardo Taipa, Kelly Del Tredici, Kimberly Paquette, Sophia Chaudhry, Kaitlyn DenHaan, João Durães, Marisa Lima, Catarina Bernardes, Susana Carmona, Inês Baldeiras, Rosário Almeida, Isabel Santana, Rita Guerreiro

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Androgen receptor inhibitor ameliorates pulmonary arterial hypertension by enhancing the apoptosis level through suppressing the Notch3/Hes5 pathway by Jiayan Sun, Jiayan Sun, Jiayan Sun, Jiancheng Lin, Jiancheng Lin, Jiancheng Lin, Di Yin, Di Yin, Di Yin, Zetao Pan, Zetao Pan, Zetao Pan, Yuheng Ye, Yuheng Ye, Yuheng Ye, Yi Wang, Yi Wang, Yi Wang, Xiaowan Wang, Xiaowan Wang, Xiaowan Wang, Qiang Guo, Qiang Guo, Qiang Guo, Qiang Guo

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Signaling pathways and molecular mechanisms involved in the onset and progression of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CAD... by Parasta Heidari, Motahareh Taghizadeh, Omid Vakili

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A clinical case of CADASIL syndrome in a patient after a new coronavirus infection COVID-19 by Z. Sh. Dzhalilova, E. A. Gavrilova, A. A. Yakovlev, A. G. Smochilin

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Case Report: Inflammatory CADASIL phenotype associated with a rare cysteine-sparing NOTCH3 variant by Abraham Madjidov, Mary-Alice Abbott, Katherine M. Mullen, Richard Hicks, Gottfried Schlaug

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Research progress on cerebral small vessel disease in 2024 by YI Haotong, MEN Xuejiao, QIN Bing, WEI Lei, CAI Wei, LU Zhengqi

Subjects: “…hereditary cerebral small vessel disease|cerebral amyloid angiopathy|notch3 gene|neuroimaging…”
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Mechanistic advances in factors influencing phenotypic variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a review by Ying Zhao, YaRu Lu, FengYu Wang, YaDan Wang, YaQiong Li, RuiHua Sun, JunKui Shang, Chao Jiang, Jiewen Zhang

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CADASIL: A NOTCH3-associated cerebral small vessel disease by Lamei Yuan, Xiangyu Chen, Joseph Jankovic, Hao Deng

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Notch3 enhances the synergistic effect of all-trans retinoic acid and calcipotriol in pancreatic stellate cell activation by Zheng Lian, Wei-hong Du, Paizi-guli Tusup-han, Yu-xiang Zhang

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SNORA74A Drives Self‐Renewal of Liver Cancer Stem Cells and Hepatocarcinogenesis Through Activation of Notch3 Signaling by Ziheng Zhou, Yang Gu, Zhibin Yi, Jianyi Wang, Zhen Xiong, Hui Guo, Ying Du, Xiaoxiao Zhu, Lei He, Weizheng Ren, Yong Tian, Yanying Wang, Zusen Fan

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Bruceine H Mediates EGFR-TKI Drug Persistence in NSCLC by Notch3-Dependent β-Catenin Activating FOXO3a Signaling by Jiahui Wu, Xiao He, Ziwei Xiong, Lingyu Shi, Daofeng Chen, Yulin Feng, Quan Wen

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