Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and HNRNPA2B1[original query] |
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| hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. Neurobiology of aging 2014 Apr 35 (4): 934.e5-6. Le Ber Isabelle, Van Bortel Inge, Nicolas Gael, Bouya-Ahmed Kawtar, Camuzat Agnès, Wallon David, De Septenville Anne, Latouche Morwena, Lattante Serena, Kabashi Edor, Jornea Ludmila, Hannequin Didier, Brice Alexis, |
| Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis. Neuro-degenerative diseases 2017 11 17 (6): 304-312. Fifita Jennifer A, Zhang Katharine Y, Galper Jasmin, Williams Kelly L, McCann Emily P, Hogan Alison L, Saunders Neil, Bauer Denis, Tarr Ingrid S, Pamphlett Roger, Nicholson Garth A, Rowe Dominic, Yang Shu, Blair Ian |
| Clinical Characteristics and Pathogenic Gene Identification in Chinese Patients With Paget's Disease of Bone. Frontiers in endocrinology 2022 3 13 850462. Tao Xiaohui, Liu Li, Yang Xingguang, Wei Zhe, Chen Zhongzhong, Zhang Ge, Zhang Zhenlin, Yue H |
| A Broad m6A Modification Landscape in Inflammatory Bowel Disease. Frontiers in cell and developmental biology 2022 2 9 782636. Nie Kai, Yi Jun, Yang Yuanyuan, Deng Minzi, Yang Yan, Wang Tianyu, Chen Xuejie, Zhang Zhaoyu, Wang Xiaoy |
| Genotype-phenotype characterisation of long survivors with motor neuron disease in Scotland. Journal of neurology 2022 12 . Leighton Danielle J, Ansari Morad, Newton Judith, Parry David, Cleary Elaine, Colville Shuna, Stephenson Laura, Larraz Juan, Johnson Micheala, Beswick Emily, Wong Michael, Gregory Jenna, Carod Artal Javier, Davenport Richard, Duncan Callum, Morrison Ian, Smith Colin, Swingler Robert, Deary Ian J, Porteous Mary, Aitman Timothy J, Chandran Siddharthan, Gorrie George H, Pal Suvankar, , |
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