HuGE Literature Finder
Records
1
-
30
| Assessment of ANG variants in Parkinson's disease. Neurobiology of aging 2021 Mar . Grenn Francis P, Moore Anni, Bandres-Ciga Sara, Krohn Lynne, Blauwendraat Cornelis, |
| Angiogenin mutations in Hungarian patients with amyotrophic lateral sclerosis: Clinical, genetic, computational, and functional analyses. Brain and behavior 2019 Apr e01293. Tripolszki Kornélia, Danis Judit, Padhi Aditya K, Gomes James, Bozó Renáta, Nagy Zsófia F, Nagy Dóra, Klivényi Péter, Engelhardt József I, Széll Már |
| Targeted next-generation sequencing reveals novel and rare variants in Indian patients with amyotrophic lateral sclerosis. Neurobiology of aging 2018 May . Narain Priyam, Pandey Ashutosh, Gupta Shruti, Gomes James, Bhatia Rohit, Vivekanandan Perum |
| Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis. Neurobiology of aging 2017 05 53 194.e1-194.e8. Nishiyama Ayumi, Niihori Tetsuya, Warita Hitoshi, Izumi Rumiko, Akiyama Tetsuya, Kato Masaaki, Suzuki Naoki, Aoki Yoko, Aoki Masas |
| Lack of association between the Angiogenin (ANG) rs11701 polymorphism and amyotrophic lateral sclerosis risk: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 Jan . Pan Li-Shou, Deng Xin-Bo, Wang Zheng, Leng Hui-Lin, Zhu Xue-Peng, Ding D |
| Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers. Neurobiology of aging 2015 Dec . Dekker Annelot M, Seelen Meinie, van Doormaal Perry T C, van Rheenen Wouter, Bothof Reinoud J P, van Riessen Tim, Brands William J, van der Kooi Anneke J, de Visser Marianne, Voermans Nicol C, Pasterkamp R Jeroen, Veldink Jan H, van den Berg Leonard H, van Es Michael |
| Genetic studies of Russian patients with amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration 2015 Nov 1-7. Lysogorskaia Elena V, Abramycheva Nataliya Yu, Zakharova Mariya N, Stepanova Mariya S, Moroz Anna A, Rossokhin Alexey V, Illarioshkin Sergey |
| Association between the Angiogenin (ANG) K17I variant and amyotrophic lateral sclerosis risk in Caucasian: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Aug . Pan Lishou, Deng Xinbo, Ding Dan, Leng Huilin, Zhu Xuepeng, Wang Zhe |
| [The association between angiogenin gene variations and familial amyotrophic lateral sclerosis in Chinese Han patients]. Zhonghua nei ke za zhi 2015 Feb 54 (2): 122-4. Zhang Huagang, Zhang Yingshuang, Tang Lu, Zhang Nan, Fan Dongshe |
| Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system. Neurobiology of aging 2014 Dec 35 (12): 2881.e11-5. Liu Zhi-Jun, Li Hong-Fu, Tan Guo-He, Tao Qing-Qing, Ni Wang, Cheng Xue-Wen, Xiong Zhi-Qi, Wu Zhi-Yi |
| Mutational analysis of angiogenin gene in Parkinson's disease. PloS one 2014 9 (11): e112661. Chen Meng-Ling, Wu Ruey-Meei, Tai Chun-Hwei, Lin Chin-Hsi |
| Lack of unique neuropathology in amyotrophic lateral sclerosis associated with p.K54E angiogenin (ANG) mutation. Neuropathology and applied neurobiology 2013 Aug 39 (5): 562-71. Kirby J, Highley J R, Cox L, Goodall E F, Hewitt C, Hartley J A, Hollinger H C, Fox M, Ince P G, McDermott C J, Shaw P |
| Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations. Journal of neurology 2013 Jan 260 (1): 85-92. Ticozzi Nicola, Tiloca Cinzia, Mencacci Niccolò E, Morelli Claudia, Doretti Alberto, Rusconi Daniela, Colombrita Claudia, Sangalli Davide, Verde Federico, Finelli Palma, Messina Stefano, Ratti Antonia, Silani Vincen |
| Extensive genetics of ALS: a population-based study in Italy. Neurology 2012 Nov 79 (19): 1983-9. Chiò Adriano, Calvo Andrea, Mazzini Letizia, Cantello Roberto, Mora Gabriele, Moglia Cristina, Corrado Lucia, D'Alfonso Sandra, Majounie Elisa, Renton Alan, Pisano Fabrizio, Ossola Irene, Brunetti Maura, Traynor Bryan J, Restagno Gabriella, |
| Genetic overlap between apparently sporadic motor neuron diseases. PloS one 2012 7 (11): 11. van Blitterswijk M, Vlam L, van Es MA, van der Pol WL, Hennekam EA, Dooijes D, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH |
| Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease. Neurology 2012 Jul 79 (1): 66-72. Lattante Serena, Conte Amelia, Zollino Marcella, Luigetti Marco, Del Grande Alessandra, Marangi Giuseppe, Romano Angela, Marcaccio Alessandro, Meleo Emiliana, Bisogni Giulia, Rossini Paolo Maria, Sabatelli Mar |
| Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin. European journal of neurology : the official journal of the European Federation of Neurological Societies 2012 Jul 19 (7): 977-83. Zou Z-Y, Peng Y, Feng X-H, Wang X-N, Sun Q, Liu M-S, Li X-G, Cui L |
| Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 May 13 (3): 270-5. Zou Zhang-Yu, Wang Xin-Ning, Liu Ming-Sheng, Sun Qin, Li Xiao-Guang, Cui Li-Ying, Kong Jimi |
| Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS. Neurobiology of aging 2012 May 33 (5): 1017.e17-23. Kwon Min-Jung, Baek Wonki, Ki Chang-Seok, Kim Hyun Young, Koh Seong-Ho, Kim Jong-Won, Kim Seung Hy |
| SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 Feb 13 (2): 217-22. Brown Jeffrey A, Min Jionghong, Staropoli John F, Collin Elisa, Bi Stephen, Feng Xin, Barone Rosemary, Cao Yi, O'Malley Lei, Xin Winnie, Mullen Thomas E, Sims Katherine |
| Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Annals of neurology 2011 Dec 70 (6): 6. van Es MA, Schelhaas HJ, van Vught PW, Ticozzi N, Andersen PM, Groen EJ, Schulte C, Blauw HM, Koppers M, Diekstra FP, Fumoto K, Leclerc AL, Keagle P, Bloem BR, Scheffer H, van Nuenen BF, van Blitterswijk M, van Rheenen W, Wills AM, Lowe PP, Hu GF, Yu W, Kishikawa H, Wu D, Folkerth RD, Mariani C, Goldwurm S, Pezzoli G, Van Damme P, Lemmens R, Dahlberg C, Birve A, Fernández-Santiago R, Waibel S, Klein C, Weber M, van der Kooi AJ, de Visser M, Verbaan D, van Hilten JJ, Heutink P, Hennekam EA, Cuppen E, Berg D, Brown RH, Silani V, Gasser T, Ludolph AC, Robberecht W, Ophoff RA, Veldink JH, Pasterkamp RJ, de Bakker PI, Landers JE, van de Warrenburg BP, van den Berg LH |
| Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis. Journal of neurology, neurosurgery, and psychiatry 2011 Nov 82 (11): 1239-43. Del Bo R, Tiloca C, Pensato V, Corrado L, Ratti A, Ticozzi N, Corti S, Castellotti B, Mazzini L, Sorarù G, Cereda C, D'Alfonso S, Gellera C, Comi G P, Silani V, |
| FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS. Neurobiology of aging 2011 Mar 32 (3): 553.e13-21. Tsai Ching-Paio, Soong Bing-Wen, Lin Kon-Ping, Tu Pang-Hsien, Lin Jer-Li, Lee Yi-Chu |
| SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. Journal of medical genetics 2010 Aug 47 (8): 554-60. Millecamps Stéphanie, Salachas François, Cazeneuve Cécile, Gordon Paul, Bricka Bernard, Camuzat Agnès, Guillot-Noël Léna, Russaouen Odile, Bruneteau Gaëlle, Pradat Pierre-François, Le Forestier Nadine, Vandenberghe Nadia, Danel-Brunaud Véronique, Guy Nathalie, Thauvin-Robinet Christel, Lacomblez Lucette, Couratier Philippe, Hannequin Didier, Seilhean Danielle, Le Ber Isabelle, Corcia Philippe, Camu William, Brice Alexis, Rouleau Guy, LeGuern Eric, Meininger Vince |
| Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosis. PloS one 2010 5 (11): e15402. McLaughlin Russell Lewis, Phukan Julie, McCormack William, Lynch David S, Greenway Matthew, Cronin Simon, Saunders Jean, Slowik Agnieska, Tomik Barbara, Andersen Peter M, Bradley Daniel G, Jakeman Phil, Hardiman Or |
| Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis. Journal of neurology 2009 Aug 256 (8): 1337-42. Fernández-Santiago Rubén, Hoenig Sabine, Lichtner Peter, Sperfeld Anne-Dorte, Sharma Manu, Berg Daniela, Weichenrieder Oliver, Illig Thomas, Eger Katharina, Meyer Thomas, Anneser Johanna, Münch Christoph, Zierz Stephan, Gasser Thomas, Ludolph Albe |
| Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis. Archives of neurology 2008 Oct 65 (10): 1333-6. Paubel Agathe, Violette Jeremy, Amy Maïté, Praline Julien, Meininger Vincent, Camu William, Corcia Philippe, Andres Christian R, Vourc'h Patrick, |
| Screening of hypoxia-inducible genes in sporadic ALS. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2008 Oct 9 (5): 299-305. Cronin Simon, Greenway Matthew J, Andersen Peter M, Hardiman Or |
| Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis. Neurogenetics 2008 Feb 9 (1): 33-40. Gellera Cinzia, Colombrita Claudia, Ticozzi Nicola, Castellotti Barbara, Bragato Cinzia, Ratti Antonia, Taroni Franco, Silani Vincen |
| Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population. Journal of the neurological sciences 2007 Jul 258 (1-2): 123-7. Corrado Lucia, Battistini Stefania, Penco Silvana, Bergamaschi Laura, Testa Lucia, Ricci Claudia, Giannini Fabio, Greco Giuseppe, Patrosso Maria Cristina, Pileggi Simona, Causarano Renzo, Mazzini Letizia, Momigliano-Richiardi Patricia, D'Alfonso Sand |
- Page last reviewed:Feb 1, 2023
- Page last updated:Feb 03, 2023
- Content source: