Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 200 Records) |
Query Trace: PRNP[original query] |
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Clinical and Molecular Findings of Intermediate Allele Carriers in the HTT Gene from the Mexican Mestizo Population. Neuro-degenerative diseases 2022 Aug . Ramírez-García Miguel Ángel, Dávila-Ortiz de Montellano David José, Martínez-Ruano Leticia, Ochoa-Morales Adriana, Romero-Hidalgo Sandra, Zenteno Juan Carlos, Yescas-Gómez Pet |
Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease. Brain communications 2022 8 4 (4): fcac201. Nihat Ak?n, Ranson Janice M, Harris Dominique, McNiven Kirsty, Mok TzeHow, Rudge Peter, Collinge John, Llewellyn David J, Mead Sim |
Genetic Polymorphism at 15 Codons of the Prion Protein Gene in 156 Goats from Romania. Genes 2022 7 13 (8): . Gurau Maria Rodica, Negru Elena, Ionescu Teodor, Udriste Anca Amalia, Cornea C?lina Petru?a, Baraitareanu Steli |
PRNP gene polymorphism frequencies for comparing possible vulnerability to BSE in Chinese bovine population. Animal biotechnology 2022 7 1-8. He Xiaoming, Memon Sameeullah, Yue Dan, Zhu Junhong, Lu Ying, Liu Xingneng, Xiong Heli, Li Guozhi, Deng Weidong, Xi Dongm |
Genetic prion diseases presenting as frontotemporal dementia: clinical features and diagnostic challenge. Alzheimer's research & therapy 2022 6 14 (1): 90. Chen Zhongyun, Chu Min, Liu Li, Zhang Jing, Kong Yu, Xie Kexin, Cui Yue, Ye Hong, Li Junjie, Wang Lin, Wu Liyo |
Genetic landscape of early-onset dementia in Hungary. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Jun . Csaban Dora, Illes Anett, Renata Toth-Bencsik, Balicza Peter, Pentelenyi Klara, Molnar Viktor, Gezsi Andras, Grosz Zoltan, Gal Aniko, Kovacs Tibor, Klivenyi Peter, Molnar Maria Jud |
Alterations of Striatal Subregions in a Prion Protein Gene V180I Mutation Carrier Presented as Frontotemporal Dementia With Parkinsonism. Frontiers in aging neuroscience 2022 5 14 830602. Chen Zhongyun, Ma Jinghong, Liu Li, Liu Shuying, Zhang Jing, Chu Min, Wang Zhen, Chan Piu, Wu Liyo |
Genotype by environment interactions for chronic wasting disease in farmed US white-tailed deer. G3 (Bethesda, Md.) 2022 5 12 (7): . Seabury Christopher M, Lockwood Mitchell A, Nichols Tracy |
Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases. Journal of neurology, neurosurgery, and psychiatry 2022 4 93 (7): 779-784. Kosami Koki, Ae Ryusuke, Hamaguchi Tsuyoshi, Sanjo Nobuo, Tsukamoto Tadashi, Kitamoto Tetsuyuki, Yamada Masahito, Mizusawa Hidehiro, Nakamura Yosika |
Identification and analysis of a prognostic ferroptosis and iron-metabolism signature for esophageal squamous cell carcinoma. Journal of Cancer 2022 4 13 (5): 1611-1622. Zhao Mengnan, Li Ming, Zheng Yuansheng, Hu Zhengyang, Liang Jiaqi, Bi Guoshu, Bian Yunyi, Sui Qihai, Zhan Cheng, Lin Miao, Wang Q |
Low frequency of protective variants at regulatory region of PRNP gene indicating the genetically high risk of BSE in Ethiopian Bos indicus and Bos taurus africanus. Animal biotechnology 2022 4 1-6. Teferedegn Eden Yitna, Can Hüseyin, Erkunt Alak Sedef, Ün Cem |
First report of a strong association between genetic polymorphisms of the prion protein gene (PRNP) and susceptibility to chronic wasting disease in sika deer (Cervus nippon). Transboundary and emerging diseases 2022 3 69 (5): e2073-e2083. Roh In-Soon, Kim Yong-Chan, Won Sae-Young, Jeong Min-Ju, Park Kyung-Je, Park Hoo-Chang, Lee Yu-Ran, Kang Hae-Eun, Sohn Hyun-Joo, Jeong Byung-Ho |
Scrapie-associated polymorphisms of the prion protein gene (PRNP) in Nigerian native goats. Gene 2022 12 855 147121. Adeola Adeniyi C, Bello Semiu F, Abdussamad Abdussamad M, Mark Akanbi I, Sanke Oscar J, Onoja Anyebe B, Nneji Lotanna M, Abdullahi Nasiru, Olaogun Sunday C, Rogo Lawal D, Mangbon Godwin F, Pedro Shamsudeen L, Hiinan Manasseh P, Mukhtar Muhammad M, Ibrahim Jebi, Saidu Hayatu, Dawuda Philip M, Bala Rukayya K, Abdullahi Hadiza L, Salako Adebowale E, Kdidi Samia, Yahyaoui Mohamed Habib, Yin Ting-Ti |
Genetic Screening in Korean Patients with Frontotemporal Dementia Syndrome. Journal of Alzheimer's disease reports 2022 11 6 (1): 651-662. Kim Eun-Joo, Na Duk L, Kim Hee-Jin, Park Kyung Won, Lee Jae-Hong, Roh Jee Hoon, Kwon Jay C, Yoon Soo Jin, Jung Na-Yeon, Jeong Jee Hyang, Jang Jae-Won, Kim Hee-Jin, Park Kee Hyung, Choi Seong Hye, Kim SangYun, Park Young Ho, Kim Byeong C, Youn Young Chul, Ki Chang-Seok, Kim Seung Hyun, Seo Sang Won, Kim Young-E |
No association of prion protein gene (PRNP) polymorphisms with susceptibility to the pandemic 2009 swine flu. Molecular & cellular toxicology 2022 11 1-5. Kim Yong-Chan, Won Sae-Young, Jeong Byung-Ho |
[Prion diseases in The Netherlands: twenty-nine years of surveillance]. Nederlands tijdschrift voor geneeskunde 2022 10 166 . Karamuji?-?omi? Hata, Rozemuller Annemieke J M, Verbeek Marcel M, Lemstra Afina W, Ikram M Arfan, van Duijn Cornelia |
Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP). Journal of neurology 2023 9 . Astrid Van den Broecke, Alexander Decruyenaere, Nika Schuermans, Hannah Verdin, Jody Ghijsels, Anne Sieben, Bart Dermaut, Dimitri Hemelso |
Genetic Variants Associated with the Age of Onset Identified by Whole-Exome Sequencing in Fatal Familial Insomnia. Cells 2023 8 12 (16): . Katrin Thüne, Matthias Schmitz, John Wiedenhöft, Orr Shomroni, Stefan Göbel, Timothy Bunck, Neelam Younas, Saima Zafar, Peter Hermann, Inga Ze |
Risk of variant Creutzfeldt-Jakob disease in a simulated cohort of Canadian blood donors. Vox sanguinis 2023 7 . Alexis Pozzo di Borgo, Marc Germain, Sheila F O'Brien, Gilles Delage, Christian Renaud, Antoine Lew |
Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders. Journal of the neurological sciences 2023 6 451 120707. Martin Paucar, José Laffita-Mesa, Valter Niemelä, Helena Malmgren, Inger Nennesmo, Kristina Lagerstedt-Robinson, Magnus Nordenskjöld, Per Svenningss |
Identification of a novel risk factor for chronic wasting disease (CWD) in elk: S100G single nucleotide polymorphism (SNP) of the prion protein gene (PRNP). Veterinary research 2023 6 54 (1): 48. Yu-Ran Lee, Yong-Chan Kim, Sae-Young Won, Min-Ju Jeong, Kyung-Je Park, Hoo-Chang Park, In-Soon Roh, Hae-Eun Kang, Hyun-Joo Sohn, Byung-Hoon Jeo |
Octapeptide repeat alteration mutations of the prion protein gene in clinically diagnosed Alzheimer's disease and frontotemporal dementia. Clinical genetics 2023 5 . Haitian Nan, Li Liu, Zhongyun Chen, Min Chu, Jieying Li, Donglai Jing, Yihao Wang, Liyong |
Two Chinese patients of sporadic Creutzfeldt-Jacob disease with a S97N mutation in PRNP gene. Prion 2023 11 17 (1): 141-144. Dong-Lin Liang, Qi Shi, Kang Xiao, Ruhan A, Wei Zhou, Xiao-Ping Do |
NGS study in a sicilian case series with a genetic diagnosis for Gerstmann-Sträussler-Scheinker syndrome (PRNP, p.P102L). Molecular biology reports 2023 10 . Michele Salemi, Luana G M Mandarà, Maria Grazia Salluzzo, Francesca A Schillaci, Roberto Castiglione, Angela Cordella, Roberta Iorio, Concetta Simona Perrotta, Raffaele Ferri, Corrado Roma |
Prion Mutations in Republic of Republic of Korea, China, and Japan. International journal of molecular sciences 2023 1 24 (1): . Kim Dan Yeong, Shim Kyu Hwan, Bagyinszky Eva, An Seong Soo |
High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob Disease. Neurology. Genetics 2023 1 9 (1): e200054. Murley Alexander G, Nie Yu, Golder Zoe, Keogh Michael John, Smith Colin, Ironside James W, Chinnery Patrick |
Accumulation Area of a Japanese PRNP P102L Variant: The Ariake PRNP P102L Variant. Journal of clinical neurology (Seoul, Korea) 2024 1 . Kohei Suzuyama, Makoto Eriguchi, Hiromu Minagawa, Hiroyuki Honda, Keita Kai, Tetsuyuki Kitamoto, Hideo Ha |
National Prevalence of Caprine Prion Protein Genetic Variability at Codons 146, 211, and 222 in Goat Herds in the United States. Veterinary sciences 2024 1 11 (1): . Mohamed Zeineldin, Heather Cox-Struble, Patrick Camp, David Farrell, Randy Pritchard, Tyler C Thacker, Kimberly Lehm |
Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases. Acta neuropathologica 2024 1 147 (1): 17. Weiguanliu Zhang, Christina D Orrú, Aaron Foutz, Mingxuan Ding, Jue Yuan, Syed Zahid Ali Shah, Jing Zhang, Keisi Kotobelli, Maria Gerasimenko, Tricia Gilliland, Wei Chen, Michelle Tang, Mark Cohen, Jiri Safar, Bin Xu, Dao-Jun Hong, Li Cui, Andrew G Hughson, Lawrence B Schonberger, Curtis Tatsuoka, Shu G Chen, Justin J Greenlee, Zerui Wang, Brian S Appleby, Byron Caughey, Wen-Quan Z |
Biomarker changes preceding symptom onset in genetic prion disease. medRxiv : the preprint server for health sciences 2024 1 . Sonia M Vallabh, Meredith A Mortberg, Shona W Allen, Ashley C Kupferschmid, Pia Kivisäkk, Bruno L Hammerschlag, Anna Bolling, Bianca A Trombetta, Kelli Devitte-McKee, Abaigeal M Ford, Lauren Sather, Griffin Duffy, Ashley Rivera, Jessica Gerber, Alison J McManus, Eric Vallabh Minikel, Steven E Arno |
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- Page last updated:Apr 22, 2024
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