Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 42 Records) |
Query Trace: GLO1[original query] |
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[Molecular pathophysiology of schizophrenia and preventive strategy in pubertal period]. Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica 2011 113 (7): 672-8. Itokawa Masanari, Arai Makoto, Ichikawa Tomoe, Miyashita Mitsuhiro, Yoshikawa Takeo, Okazaki Yuji, Miyata Tosh |
Association of two glyoxalase I gene polymorphisms with nephropathy and retinopathy in Type 2 diabetes. Journal of endocrinological investigation 2011 Nov 34 (10): e343-8. Wu J C, Li X H, Peng Y D, Wang J B, Tang J F, Wang Y |
Identification of glyoxalase 1 polymorphisms associated with enzyme activity. Gene 2012 Nov . Peculis R, Konrade I, Skapare E, Fridmanis D, Nikitina-Zake L, Lejnieks A, Pirags V, Dambrova M, Klovins J |
C332C genotype of glyoxalase 1 and its association with late diabetic complications. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2013 Jul 121 (7): 436-9. Groener J B, Reismann P, Fleming T, Kalscheuer H, Lehnhoff D, Hamann A, Roser P, Bierhaus A, Nawroth P P, Rudofsky |
Glyoxalase 1 enzyme activity in erythrocytes and Ala111Glu polymorphism in type 1-diabetes patients. Scandinavian journal of clinical and laboratory investigation 2013 Jan . Sakhi AK, Berg JP, Berg TJ |
The GLO1 C332 (Ala111) allele confers autism vulnerability: family-based genetic association and functional correlates. Journal of psychiatric research 2014 Dec 59 108-16. Gabriele Stefano, Lombardi Federica, Sacco Roberto, Napolioni Valerio, Altieri Laura, Tirindelli Maria Cristina, Gregorj Chiara, Bravaccio Carmela, Rousseau Francis, Persico Antonio |
Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease. PLoS genetics 2014 Jul 10 (7): e1004502. Mäkinen Ville-Petteri, Civelek Mete, Meng Qingying, Zhang Bin, Zhu Jun, Levian Candace, Huan Tianxiao, Segrè Ayellet V, Ghosh Sujoy, Vivar Juan, Nikpay Majid, Stewart Alexandre F R, Nelson Christopher P, Willenborg Christina, Erdmann Jeanette, Blakenberg Stefan, O'Donnell Christopher J, März Winfried, Laaksonen Reijo, Epstein Stephen E, Kathiresan Sekar, Shah Svati H, Hazen Stanley L, Reilly Muredach P, , Lusis Aldons J, Samani Nilesh J, Schunkert Heribert, Quertermous Thomas, McPherson Ruth, Yang Xia, Assimes Themistocles |
Fructosamine 3-kinase and glyoxalase I polymorphisms and their association with soluble RAGE and adhesion molecules in diabetes. Physiological research / Academia Scientiarum Bohemoslovaca 2014 63 Suppl 2 S283-91. Škrha J, Muravská A, Fleka? M, Horová E, Novák J, Novotný A, Prázný M, Škrha J, Kvasni?ka J, Landová L, Jáchymová M, Zima T, Kalousová |
Weak association of glyoxalase 1 (GLO1) variants with autism spectrum disorder. European child & adolescent psychiatry 2015 Jan 24 (1): 75-82. Kova? Jernej, Podkrajšek Katarina Trebušak, Lukši? Marta Macedoni, Battelino Tad |
Polymorphisms of the receptor for advanced glycation end-products and glyoxalase I in patients with renal cancer. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Mar 36 (3): 2121-6. Chocholatý Matúš, Jáchymová Marie, Schmidt Marek, Havlová Klára, K?epelová Anna, Zima Tomáš, Babjuk Marko, Kalousová Mar |
Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome. Sleep medicine 2015 Sep 16 (9): 1151-5. Gan-Or Ziv, Zhou Sirui, Ambalavanan Amirthagowri, Leblond Claire S, Xie Pingxing, Johnson Amelie, Spiegelman Dan, Allen Richard P, Earley Christopher J, Desautels Alex, Montplaisir Jacques Y, Dion Patrick A, Xiong Lan, Rouleau Guy |
GLYOXALASE I A111E, PARAOXONASE 1 Q192R AND L55M POLYMORPHISMS IN ITALIAN PATIENTS WITH SPORADIC CEREBRAL CAVERNOUS MALFORMATIONS: A PILOT STUDY. Journal of biological regulators and homeostatic agents 0 29 (2): 493-500. Rinaldi C, Bramanti P, Famà A, Scimone C, Donato L, Antognelli C, Alafaci C, Tomasello F, D'Angelo R, Sidoti |
Genetic analysis of the glyoxalase system in schizophrenia. Progress in neuro-psychopharmacology & biological psychiatry 2015 Jun 59 105-10. Bangel Fabian N, Yamada Kazuo, Arai Makoto, Iwayama Yoshimi, Balan Shabeesh, Toyota Tomoko, Iwata Yasuhide, Suzuki Katsuaki, Kikuchi Mitsuru, Hashimoto Tasuku, Kanahara Nobuhisa, Mori Norio, Itokawa Masanari, Stork Oliver, Yoshikawa Tak |
Role of glyoxalase I gene polymorphisms in late-onset epilepsy and drug-resistant epilepsy. Journal of the neurological sciences 2016 Apr 363 200-6. Tao Hua, Si Ligang, Zhou Xu, Liu Zhou, Ma Zhonghua, Zhou Haihong, Zhong Wangtao, Cui Lili, Zhang Shuyan, Li You, Ma Guoda, Zhao Jianghao, Huang Wenhui, Yao Lifen, Xu Zhien, Zhao Bin, Li Kesh |
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case-control study in a Sicilian population. Molecular biology reports 2018 Aug . Donato Luigi, Scimone Concetta, Nicocia Giacomo, Denaro Lucia, Robledo Renato, Sidoti Antonina, D'Angelo Rosal |
Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia. Psychiatric genetics 2018 Jul . Ishizuka Kanako, Kimura Hiroki, Kushima Itaru, Inada Toshiya, Okahisa Yuko, Ikeda Masashi, Iwata Nakao, Mori Daisuke, Aleksic Branko, Ozaki Nor |
The influence of glyoxalase 1 gene polymorphism on its expression at different stages of breast cancer in Egyptian women. Genes & cancer 2017 Nov 8 (11-12): 799-807. Abdul-Maksoud Rehab S, Elsayed Walid Sh, Elsayed Rasha |
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. Annals of neurology 2019 Dec . Tilch Erik, Schormair Barbara, Zhao Chen, Salminen Aaro V, Antic Nikolic Ana, Holzknecht Evi, Högl Birgit, Poewe Werner, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Fietze Ingo, Berger Klaus, Lichtner Peter, Gieger Christian, Peters Annette, Müller-Myhsok Bertram, Hoischen Alexander, Winkelmann Juliane, Oexle Konr |
Common variants in glyoxalase I do not increase chronic pancreatitis risk. PloS one 2019 14 (10): e0222927. Kaune Tom, Hollenbach Marcus, Keil Bettina, Chen Jian-Min, Masson Emmanuelle, Becker Carla, Damm Marko, Ruffert Claudia, Grützmann Robert, Hoffmeister Albrecht, Te Morsche Rene H M, Cavestro Giulia Martina, Zuppardo Raffaella Alessia, Saftoiu Adrian, Malecka-Panas Ewa, G?uszek Stanislaw, Bugert Peter, Lerch Markus M, Weiss Frank Ulrich, Zou Wen-Bin, Liao Zhuan, Hegyi Peter, Drenth Joost Ph, Riedel Jan, Férec Claude, Scholz Markus, Kirsten Holger, Tóth Andrea, Ewers Maren, Witt Heiko, Griesmann Heidi, Michl Patrick, Rosendahl Jon |
Loci associated with genomic damage levels in chronic kidney disease patients and controls. Mutation research 2020 04 852 503167. Corredor Zuray, da Silva Filho Miguel Inácio, Rodríguez-Ribera Lara, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José Aurelio, Henández Alba, Försti Asta, Marcos Ricard, Pastor Susa |
The genetic map of diabetic nephropathy: evidence from a systematic review and meta-analysis of genetic association studies. Clinical kidney journal 2020 10 13 (5): 768-781. Tziastoudi Maria, Stefanidis Ioannis, Zintzaras Eli |
Associations of dicarbonyl stress with complement activation: the CODAM study. Diabetologia 2020 1 63 (5): 1032-1042. Xin Ying, Hertle Elisabeth, van der Kallen Carla J H, Schalkwijk Casper G, Stehouwer Coen D A, van Greevenbroek Marleen M |
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. Scientific reports 2020 Jan 10 (1): 144. Corredor Zuray, Filho Miguel Inácio da Silva, Rodríguez-Ribera Lara, Velázquez Antonia, Hernández Alba, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José, Vallés Prats Martí, Calabia Martínez Jordi, Försti Asta, Marcos Ricard, Pastor Susa |
Polymorphisms in Glyoxalase I Gene Are Not Associated with Glyoxalase I Expression in Whole Blood or Markers of Methylglyoxal Stress: The CODAM Study. Antioxidants (Basel, Switzerland) 2021 Feb 10 (2): . Maasen Kim, Hanssen Nordin M J, van der Kallen Carla J H, Stehouwer Coen D A, van Greevenbroek Marleen M J, Schalkwijk Casper |
Multiplex Protein Biomarker Profiling in Patients with Familial Hypercholesterolemia. Genes 2021 10 12 (10): . Dlouha Dana, Blaha Milan, Rohlova Eva, Hubacek Jaroslav A, Lanska Vera, Visek Jakub, Blaha Vladim |
Clinical Implications of Glyoxalase1 Gene Polymorphism and Elevated Levels of the Reactive Metabolite Methylglyoxal in the Susceptibility of Type 2 Diabetes Mellitus in the Patients from Asir and Tabuk Regions of Saudi Arabia. Journal of personalized medicine 2022 4 12 (4): . Alhujaily Muhanad, Mir Mohammad Muzaffar, Mir Rashid, Alghamdi Mushabab Ayed Abdullah, Wani Javed Iqbal, Sabah Zia Ul, Elfaki Imadeldin, Alnour Tarig Mohammad Saad, Jeelani Mohammed, Abomughaid Mosleh Mohammad, Alharbi Samir Abdulkar |
Gene- and Gender-Related Decrease in Serum BDNF Levels in Alzheimer's Disease. International journal of molecular sciences 2022 12 23 (23): . Piancatelli Daniela, Aureli Anna, Sebastiani Pierluigi, Colanardi Alessia, Del Beato Tiziana, Del Cane Lorenza, Sucapane Patrizia, Marini Carmine, Di Loreto Silv |
The genetic polymorphisms and activity of glyoxalase 1 as a risk factor for acute coronary syndrome in South Indians with type 2 diabetes mellitus. Gene 2023 8 885 147701. Sushmita Bora, Prashant Shankarrao Adole, Kolar Vishwanath Vinod, Ajith Ananthakrishna Pillai, Shaheer Ahm |
Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study. Frontiers in endocrinology 2023 11 14 1235581. Qiaoli Zeng, Taili Yang, Wenfeng Wei, Dehua Zou, Yue Wei, Fengqiong Han, Jieyun He, Jinzhi Huang, Runmin G |
Genomic analysis identifies risk factors in restless legs syndrome. medRxiv : the preprint server for health sciences 2024 1 . Fulya Akçimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Trayn |
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