Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 342 Records) |
Query Trace: SOD1[original query] |
---|
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, , |
Analysis of SOD1 and C9orf72 mutations in patients with amyotrophic lateral sclerosis in Antioquia, Colombia. Biomedica : revista del Instituto Nacional de Salud 2022 12 42 (4): 623-632. Jaramillo Jimena, Solano Juan M, Aristizábal Alejandra, Martínez Julia |
Predictors for progression in amyotrophic lateral sclerosis associated to SOD1 mutation: insight from two population-based registries. Journal of neurology 2023 9 . Ilaria Martinelli, Andrea Ghezzi, Elisabetta Zucchi, Giulia Gianferrari, Laura Ferri, Cristina Moglia, Umberto Manera, Luca Solero, Rosario Vasta, Antonio Canosa, Maurizio Grassano, Maura Brunetti, Letizia Mazzini, Fabiola De Marchi, Cecilia Simonini, Nicola Fini, Marco Vinceti, Marcello Pinti, Adriano Chiò, Andrea Calvo, Jessica Mandrio |
Another de novo mutation in the SOD1 gene: the first Turkish patient with SOD1-His47Arg, a case report. Frontiers in genetics 2023 9 14 1208673. Elif Bayraktar, Vildan Çiftçi, Hilmi Uysal, A Nazl? Ba? |
The Predisposition for Type 2 Diabetes Mellitus and Metabolic Syndrome. Balkan journal of medical genetics : BJMG 2023 8 26 (1): 21-26. C Zenoaga-Barb?ro?ie, L Berca, T Vassu-Dimov, M Toma, M I Nica, O A Alexiu-Toma, C Ciornei, A Albu, S Nica, C Nistor, R Ni |
Prevalence of SOD1 allele associated with degenerative myelopathy in canine population in Greece. Research in veterinary science 2023 7 162 104959. Antonis Kountourantzis, Styliani Minoudi, Nikoleta Karaiskou, Spiros Papakostas, Aristotelis Moulistanos, Rania D Baka, Valentina Tsartsianidou, Antonios Vlachavas, Michalis Aivaliotis, Zoe S Polizopoulou, Alexandros Triantafyllid |
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis. Brain communications 2023 5 5 (3): fcad152. Wolfgang P Ruf, Matej Boros, Axel Freischmidt, David Brenner, Veselin Grozdanov, Joao de Meirelles, Thomas Meyer, Torsten Grehl, Susanne Petri, Julian Grosskreutz, Ute Weyen, Rene Guenther, Martin Regensburger, Tim Hagenacker, Jan C Koch, Alexander Emmer, Annekathrin Roediger, Robert Steinbach, Joachim Wolf, Jochen H Weishaupt, Paul Lingor, Marcus Deschauer, Isabell Cordts, Thomas Klopstock, Peter Reilich, Florian Schoeberl, Berthold Schrank, Daniel Zeller, Andreas Hermann, Antje Knehr, Kornelia Günther, Johannes Dorst, Joachim Schuster, Reiner Siebert, Albert C Ludolph, Kathrin Müll |
Genetic variability of oxidative stress and DNA repair genes associated with pre-treatment cancer-related fatigue in women with breast cancer. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer 2023 5 31 (6): 345. Tara Davis, Theresa Koleck, Alex Conway, Catherine Bender, Yvette Conl |
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis. Neurology 2023 5 . Adriano Chio, Cristina Moglia, Antonio Canosa, Umberto Manera, Maurizio Grassano, Rosario Vasta, Francesca Palumbo, Salvatore Gallone, Maura Brunetti, Marco Barberis, Fabiola De Marchi, Clifton Dalgard, Ruth Chia, Gabriele Mora, Barbara Iazzolino, Laura Peotta, Bryan J Traynor, Lucia Corrado, Sandra Dalfonso, Letizia Mazzini, Andrea Cal |
Risk factors of amyotrophic lateral sclerosis: a global meta-summary. Frontiers in neuroscience 2023 5 17 1177431. Qing-Qing Duan, Zheng Jiang, Wei-Ming Su, Xiao-Jing Gu, Han Wang, Yang-Fan Cheng, Bei Cao, Xia Gao, Yi Wang, Yong-Ping Ch |
Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations. Brain communications 2023 4 5 (2): fcad087. Wiesenfarth Maximilian, Günther Kornelia, Müller Kathrin, Witzel Simon, Weiland Ulrike, Mayer Kristina, Herrmann Christine, Brenner David, Schuster Joachim, Freischmidt Axel, Lulé Dorothée, Meyer Thomas, Regensburger Martin, Grehl Torsten, Emmer Alexander, Petri Susanne, Großkreutz Julian, Rödiger Annekathrin, Steinbach Robert, Klopstock Thomas, Reilich Peter, Schöberl Florian, Wolf Joachim, Hagenacker Tim, Weyen Ute, Zeller Daniel, Ludolph Albert C, Dorst Johann |
Protein kinetics of superoxide dismutase-1 in familial and sporadic amyotrophic lateral sclerosis. Annals of clinical and translational neurology 2023 4 . Cindy V Ly, Margaret D Ireland, Wade K Self, James Bollinger, Jennifer Jockel-Balsarotti, Hillary Herzog, Peggy Allred, Leah Miller, Michael Doyle, Isabel Anez-Bruzual, Bhavesh Trikamji, Ted Hyman, Tyler Kung, Katherine Nicholson, Robert C Bucelli, Bruce W Patterson, Randall J Bateman, Timothy M Mill |
Molecular Surveillance of Canine Degenerative Myelopathy in Breeding Kennels from Romania. Animals : an open access journal from MDPI 2023 4 13 (8): . Vlad Cocostîrc, Anamaria Ioana Pa?tiu, Anca-Alexandra Dobo?i, Felix Daniel Lucaci, Maria-Carmen Turcu, Mihai Marian Borzan, Dana Liana Pus |
Association of functional superoxide gene polymorphism with chlamydia trachomatis-associated recurrent spontaneous abortion. Molecular biology reports 2023 4 . Ankita Ray, Tanu Bhati, Renu Arora, Suhel Parvez, Sangita Rasto |
SOD1 gene variants rs4817415, rs2070424, and rs1041740 and their association with breast cancer risk. European review for medical and pharmacological sciences 2023 4 27 (7): 3088-3095. M P Gallegos-Arreola, M G Márquez-Rosales, B C Gómez-Meda, G M Zúñiga-González, A M Puebla-Pérez, A L Zamora-Pérez, J I Delgado-Saucedo, L E Figue |
Genetic variability in sporadic amyotrophic lateral sclerosis. Brain : a journal of neurology 2023 4 . Van Daele Sien Hilde, Moisse Matthieu, van Vugt Joke J F A, Zwamborn Ramona A J, van der Spek Rick, van Rheenen Wouter, Van Eijk Kristel, Kenna Kevin, Corcia Philippe, Vourc'h Patrick, Couratier Philippe, Hardiman Orla, McLaughin Russell, Gotkine Marc, Drory Vivian, Ticozzi Nicola, Silani Vincenzo, Ratti Antonia, de Carvalho Mamede, Mora Pardina Jesús S, Povedano Monica, Andersen Peter M, Weber Markus, Ba?ak Nazli A, Shaw Chris, Shaw Pamela J, Morrison Karen E, Landers John E, Glass Jonathan D, van Es Michael, van den Berg Leonard H, Al-Chalabi Ammar, Veldink Jan, Van Damme Phil |
Lack of association of superoxide dismutase I/D variant with osteopenia/osteoporosis in Turkish postmenopausal women. Nucleosides, nucleotides & nucleic acids 2023 3 1-12. Nacar Mehmet Can, Yigit Serbule |
SOD1-Related Cerebellar Ataxia and Motor Neuron Disease: Cp Variant as Functional Modifier? Cerebellum (London, England) 2023 2 . Marsili Luca, Davis Jennie L, Espay Alberto J, Gilthorpe Jonathan, Williams Chloe, Kauffman Marcelo A, Porollo Aleks |
The evaluation of superoxide dismutase 1 gene insertion/deletion variant in athletes. Revista da Associacao Medica Brasileira (1992) 2023 12 69 (12): e20230575. Ay?e Feyda Nursal, ?aban Ünver, Serbülent Yi?it, Ömür Mevlüt Orhan, Tülin At |
Impact of a 50bp insertion/deletion polymorphism of the superoxide dismutase-1 on oxidative stress status and risk of keratoconus. Experimental eye research 2023 12 238 109742. Mohammad-Reza Sedaghat, Hamidreza Shiri, Jalil Tavakkol-Afshari, Mohammad-Erfan Norouzmahani, Faegheh Bahri, Saba Fooladi, Hamed Momeni-Moghaddam, Zeynab Danesh, Amin Reza Nikpoor, Mohammad Amin Momeni-Moghaddam, Mohammad Hadi Nematollahi, Javad Sadeg |
Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis. Journal of neurology 2023 11 . Teuta Domi, Paride Schito, Giacomo Sferruzza, Tommaso Russo, Laura Pozzi, Federica Agosta, Paola Carrera, Nilo Riva, Massimo Filippi, Angelo Quattrini, Yuri Matteo Falzo |
Variability of DNA Repair and Oxidative Stress Genes Associated with Worst Pain in Breast Cancer Survivors on Aromatase Inhibitors. Genes 2023 11 14 (11): . Monica A Wagner, Theresa A Koleck, Alex Conway, Catherine M Bender, Yvette P Conl |
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS. medRxiv : the preprint server for health sciences 2023 10 . Tess D Pottinger, Joshua E Motelow, Gundula Povysil, Cristiane A Martins Moreno, Zhong Ren, Hemali Phatnani, , Timothy J Aitman, Javier Santoyo-Lopez, , Hiroshi Mitsumoto, , , , David B Goldstein, Matthew B Har |
Disease survival and progression in TARDBP ALS patients from Sardinia, Italy. Journal of neurology 2023 10 . Giuseppe Borghero, Francesca Pili, Antonella Muroni, Tommaso Ercoli, Maria Ida Pateri, Silvy Pilotto, Alessandra Maccabeo, Giovanni Defaz |
Somatosensory pathway dysfunction in patients with amyotrophic lateral sclerosis in a completely locked-in state. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2023 10 . Toshio Shimizu, Yuki Nakayama, Kentaro Hayashi, Yoko Mochizuki, Chiharu Matsuda, Michiko Haraguchi, Kota Bokuda, Takashi Komori, Kazushi Takahas |
Genetic variations of antioxidant genes and their association with male infertility in Vietnamese men. Journal of clinical laboratory analysis 2023 1 37 (2): e24829. Bach Huy Anh, Vu Phuong Nhung, Ma Thi Huyen Thuong, Nguyen Hai Ha, Tran Duc Phan, Bui Minh Duc, Nong Van Hai, Nguyen Dang T |
Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 1 1-6. Yilmaz Rüstem, Grehl Torsten, Eckrich Lukas, Marschalkowski Ines, Weishaupt Kanchi, Valkadinov Ivan, Simic Melita, Brenner David, Andersen Peter M, Wolf Joachim, Weishaupt Jochen |
Association of SOD1 gene variants (50 bp Ins/Del, rs4817415, rs2070424, rs1041740, rs17880135) with plasma protein levels in vitiligo patients and their analysis in silico. European review for medical and pharmacological sciences 2024 4 28 (6): 2464-2482. B C Gómez-Meda, G M Zúñiga-González, L D Bañuelos-Díaz, M P Oceguera-Angel, A Galindo-Gómez, M G Sánchez-Parada, A F Garibaldi-Ríos, B M Torres-Mendoza, A L Zamora-Perez, J I Delgado-Saucedo, M G Márquez-Rosales, M P Gallegos-Arreo |
Superoxide Dismutase (rs2070424, rs4880, rs2536512) and Catalase (rs794316, rs1001179) SNPs and their Association with Breast Cancer Risk: Findings from a Hospital Based Case-Control Study. Asian Pacific journal of cancer prevention : APJCP 2024 1 25 (1): 175-184. Kailas D Datkhile, Rashmi A Gudur, Suresh J Bhosale, Anand Krishnarao Gudur, Pratik P Durgawale, Nilam J Jagdale, Ashwini L More, Satish R Pat |
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS. Research square 2024 1 . Tess D Pottinger, Joshua E Motelow, Gundula Povysil, Cristiane A Martins Moreno, Zhong Ren, Hemali Phatnani, , Timothy J Aitman, Javier Santoyo-Lopez, , Hiroshi Mitsumoto, , David B Goldstein, Matthew B Har |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: