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Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders
Tian, Yun, Wang, Jun-Ling, Huang, Wen, Zeng, Sheng, Jiao, Bin, Liu, Zhen, Chen, Zhao, Li, Yujing, Wang, Ying, Min, Hao-Xuan, Wang, Xue-Jing, You, Yong, Zhang, Ru-Xu, Chen, Xiao-Yu, Yi, Fang, Zhou, Ya-Fang, Long, Hong-Yu, Zhou, Chao-Jun, Hou, Xuan, Wang, Jun-Pu, Xie, Bin, Liang, Fan, Yang, Zhuan-Yi, Sun, Qi-Ying, Allen, Emily G., Shafik, Andrew Mark, Kong, Ha Eun, Guo, Ji-Feng, Yan, Xin-Xiang, Hu, Zheng-Mao, Xia, Kun, Jiang, Hong, Xu, Hong-Wei, Duan, Ran-Hui, Jin, Peng, Tang, Bei-Sha, Shen, Lu
Published in American journal of human genetics (03.07.2019)
Published in American journal of human genetics (03.07.2019)
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AIBP-mediated cholesterol efflux instructs hematopoietic stem and progenitor cell fate
Gu, Qilin, Yang, Xiaojie, Lv, Jie, Zhang, Jiaxiong, Xia, Bo, Kim, Jun-dae, Wang, Ruoyu, Xiong, Feng, Meng, Shu, Clements, Thomas P., Tandon, Bhavna, Wagner, Daniel S., Diaz, Miguel F., Wenzel, Pamela L., Miller, Yury I., Traver, David, Cooke, John P., Li, Wenbo, Zon, Leonard I., Chen, Kaifu, Bai, Yongping, Fang, Longhou
Published in Science (American Association for the Advancement of Science) (08.03.2019)
Published in Science (American Association for the Advancement of Science) (08.03.2019)
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Unraveling the features of somatic transposition in the Drosophila intestine
Siudeja, Katarzyna, van den Beek, Marius, Riddiford, Nick, Boumard, Benjamin, Wurmser, Annabelle, Stefanutti, Marine, Lameiras, Sonia, Bardin, Allison J
Published in The EMBO journal (03.05.2021)
Published in The EMBO journal (03.05.2021)
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Determination of Blood NOTCH3 Extracellular Domain and Jagged-1 Levels in Healthy Subjects
Kim, Hyesung, Jang, Bogun, Kim, Yang-Ji, Choi, Jay Chol
Published in International journal of molecular sciences (11.09.2022)
Published in International journal of molecular sciences (11.09.2022)
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Interpretation of NOTCH3 mutations in the diagnosis of CADASIL
Rutten, Julie W, Haan, Joost, Terwindt, Gisela M, van Duinen, Sjoerd G, Boon, Elles MJ, Lesnik Oberstein, Saskia AJ
Published in Expert review of molecular diagnostics (01.06.2014)
Published in Expert review of molecular diagnostics (01.06.2014)
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Incident lacunes preferentially localize to the edge of white matter hyperintensities: insights into the pathophysiology of cerebral small vessel disease
Duering, M., Csanadi, E., Gesierich, B., Jouvent, E., Herve, D., Seiler, S., Belaroussi, B., Ropele, S., Schmidt, R., Chabriat, H., Dichgans, M.
Published in Brain (London, England : 1878) (01.09.2013)
Published in Brain (London, England : 1878) (01.09.2013)
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Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation
Viswanathan, Ranjith, Necakov, Aleksandar, Trylinski, Mateusz, Harish, Rohit Krishnan, Krueger, Daniel, Esposito, Emilia, Schweisguth, Francois, Neveu, Pierre, De Renzis, Stefano
Published in EMBO reports (05.12.2019)
Published in EMBO reports (05.12.2019)
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Bone morphogenetic protein and Notch signalling crosstalk in poor‐prognosis, mesenchymal‐subtype colorectal cancer
Irshad, Shazia, Bansal, Mukesh, Guarnieri, Paolo, Davis, Hayley, Al Haj Zen, Ayman, Baran, Brygida, Pinna, Claudia Maria Assunta, Rahman, Haseeb, Biswas, Sujata, Bardella, Chiara, Jeffery, Rosemary, Wang, Lai Mun, East, James Edward, Tomlinson, Ian, Lewis, Annabelle, Leedham, Simon John
Published in The Journal of pathology (01.06.2017)
Published in The Journal of pathology (01.06.2017)
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Importance of hedgehog interacting protein and other lung function genes in asthma
Li, Xingnan, Howard, Timothy D., Moore, Wendy C., Ampleford, Elizabeth J., Li, Huashi, Busse, William W., Calhoun, William J., Castro, Mario, Chung, Kian Fan, Erzurum, Serpil C., Fitzpatrick, Anne M., Gaston, Benjamin, Israel, Elliot, Jarjour, Nizar N., Teague, W. Gerald, Wenzel, Sally E., Peters, Stephen P., Hawkins, Gregory A., Bleecker, Eugene R., Meyers, Deborah A.
Published in Journal of allergy and clinical immunology (01.06.2011)
Published in Journal of allergy and clinical immunology (01.06.2011)
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CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients
Bianchi, Silvia, Zicari, Enza, Carluccio, Alessandra, Di Donato, Ilaria, Pescini, Francesca, Nannucci, Serena, Valenti, Raffaella, Ragno, Michele, Inzitari, Domenico, Pantoni, Leonardo, Federico, Antonio, Dotti, Maria Teresa
Published in Journal of neurology (01.01.2015)
Published in Journal of neurology (01.01.2015)
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Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
Jakobsdottir, Johanna, van der Lee, Sven J., Bis, Joshua C., Chouraki, Vincent, Li-Kroeger, David, Yamamoto, Shinya, Grove, Megan L., Naj, Adam, Vronskaya, Maria, Salazar, Jose L., DeStefano, Anita L., Brody, Jennifer A., Smith, Albert V., Amin, Najaf, Sims, Rebecca, Ibrahim-Verbaas, Carla A., Choi, Seung-Hoan, Satizabal, Claudia L., Lopez, Oscar L., Beiser, Alexa, Ikram, M. Arfan, Garcia, Melissa E., Hayward, Caroline, Varga, Tibor V., Ripatti, Samuli, Franks, Paul W., Hallmans, Göran, Rolandsson, Olov, Jansson, Jan-Håkon, Porteous, David J., Salomaa, Veikko, Eiriksdottir, Gudny, Rice, Kenneth M., Bellen, Hugo J., Levy, Daniel, Uitterlinden, Andre G., Emilsson, Valur, Rotter, Jerome I., Aspelund, Thor, O’Donnell, Christopher J., Fitzpatrick, Annette L., Launer, Lenore J., Hofman, Albert, Wang, Li-San, Williams, Julie, Schellenberg, Gerard D., Boerwinkle, Eric, Psaty, Bruce M., Seshadri, Sudha, Shulman, Joshua M., Gudnason, Vilmundur, van Duijn, Cornelia M.
Published in PLoS genetics (01.10.2016)
Published in PLoS genetics (01.10.2016)
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Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease
Schmidt, Helena, Zeginigg, Marion, Wiltgen, Marco, Freudenberger, Paul, Petrovic, Katja, Cavalieri, Margherita, Gider, Pierre, Enzinger, Christian, Fornage, Myriam, Debette, Stephanie, Rotter, Jerome I., Ikram, Mohammad A., Launer, Lenore J., Schmidt, Reinhold
Published in Brain (London, England : 1878) (01.11.2011)
Published in Brain (London, England : 1878) (01.11.2011)
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MicroRNA-199b-5p is involved in the Notch signaling pathway in osteosarcoma
Won, Kyu Yeoun, Kim, Youn Wha, Kim, Hyun-Sook, Lee, Seung Kwan, Jung, Woon-Won, Park, Yong-Koo
Published in Human pathology (01.08.2013)
Published in Human pathology (01.08.2013)
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Modeling Transposition of the Great Arteries with Patient-Specific Induced Pluripotent Stem Cells
Ontoria-Oviedo, Imelda, Földes, Gabor, Tejedor, Sandra, Panadero, Joaquín, Kitani, Tomoya, Vázquez, Alejandro, Wu, Joseph C., Harding, Sian E., Sepúlveda, Pilar
Published in International journal of molecular sciences (09.12.2021)
Published in International journal of molecular sciences (09.12.2021)
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Hypomorphic NOTCH3 Alleles Do Not Cause CADASIL in Humans
Rutten, Julie W., Boon, Elles M.J., Liem, Michael K., Dauwerse, Johannes G., Pont, Margot J., Vollebregt, Ellen, Maat-Kievit, Anneke J., Ginjaar, Hendrika B., Lakeman, Phillis, van Duinen, Sjoerd G., Terwindt, Gisela M., Lesnik Oberstein, Saskia A.J.
Published in Human mutation (01.11.2013)
Published in Human mutation (01.11.2013)
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Down-regulation of the Notch Pathway in Human Airway Epithelium in Association with Smoking and Chronic Obstructive Pulmonary Disease
Tilley, Ann E, Harvey, Ben-Gary, Heguy, Adriana, Hackett, Neil R, Wang, Rui, O'Connor, Timothy P, Crystal, Ronald G
Published in American journal of respiratory and critical care medicine (15.03.2009)
Published in American journal of respiratory and critical care medicine (15.03.2009)
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Hypomorphic NOTCH3 mutation in an Italian family with CADASIL features
Moccia, Marcello, Mosca, Lorena, Erro, Roberto, Cervasio, Mariarosaria, Allocca, Roberto, Vitale, Carmine, Leonardi, Antonio, Caranci, Ferdinando, Del Basso-De Caro, Maria Laura, Barone, Paolo, Penco, Silvana
Published in Neurobiology of aging (01.01.2015)
Published in Neurobiology of aging (01.01.2015)
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