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Acta Oto-Laryngologica Volume 128, 2008 - Issue 11
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Polymorphic analysis of the heat-shock protein 70 gene (HSPA1A) in Ménière's disease

Sachie Kawaguchi Department of Otorhinolaryngology, Tokyo Medical University, Tokyo, JapanCorrespondence[email protected]
,
Akira Hagiwara Department of Otorhinolaryngology, Tokyo Medical University, Tokyo, Japan
&
Mamoru Suzuki Department of Otorhinolaryngology, Tokyo Medical University, Tokyo, Japan
Pages 1173-1177 | Received 05 Nov 2007, Published online: 08 Jul 2009

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Giuseppe Chiarella, C Petrolo & E Cassandro. (2015) The genetics of Ménière’s disease. The Application of Clinical Genetics 8, pages 9-17.
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Masaaki Teranishi, Yasue Uchida, Naoki Nishio, Ken Kato, Hironao Otake, Tadao Yoshida, Hirokazu Suzuki, Michihiko Sone, Saiko Sugiura, Fujiko Ando, Hiroshi Shimokata & Tsutomu Nakashima. (2013) Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease. Free Radical Research 47:6-7, pages 498-506.
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Yang Huang, Masaaki Teranishi, Yasue Uchida, Naoki Nishio, Ken Kato, Hironao Otake, Tadao Yoshida, Michihiko Sone, Saiko Sugiura, Fujiko Ando, Hiroshi Shimokata & Tsutomu Nakashima. (2013) Association Between Polymorphisms in Genes Encoding Methylenetetrahydrofolate Reductase and the Risk of Ménière's Disease. Journal of Neurogenetics 27:1-2, pages 5-10.
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Elina Hietikko, Jouko Kotimäki, Annaleena Okuloff, Martti Sorri & Minna Männikkö. (2012) A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies. International Journal of Audiology 51:11, pages 841-845.
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Articles from other publishers (29)

Qingqing Dai, Lili Long, Hui Zhao, Ruikai Wang, Hong Zheng & Maoli Duan. (2022) Genetic advances in Meniere Disease. Molecular Biology Reports 50:3, pages 2901-2908.
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Faith O. Alele, John R. Otto, Bunmi S. Malau-Aduli & Aduli E. O. Malau-Aduli. (2022) Next Generation Sequencing of Genotype Variants and Genetic Association between Heat Shock Proteins HSPA1B Single Nucleotide Polymorphism at the g.31829044 Locus and Heat Tolerance: A Pilot Quasi-Experimental Study. Biomolecules 12:10, pages 1465.
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So Young Kim, Chang Ho Lee, Dae Myoung Yoo, Chanyang Min & Hyo Geun Choi. (2021) Association Between Asthma and Meniere's Disease: A Nested Case–Control Study. The Laryngoscope 132:4, pages 864-872.
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Brent A Wilkerson, Heather L Zebroski, Connor R Finkbeiner, Alex D Chitsazan, Kylie E Beach, Nilasha Sen, Renee C Zhang & Olivia Bermingham-McDonogh. (2021) Novel cell types and developmental lineages revealed by single-cell RNA-seq analysis of the mouse crista ampullaris. eLife 10.
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Eun Hye Oh, Jin-Hong Shin, Hyang-Sook Kim, Jae Wook Cho, Seo Young Choi, Kwang-Dong Choi, Je-Keun Rhee, Seowhang Lee, Changwook Lee & Jae-Hwan Choi. (2020) Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian Population. Frontiers in Neurology 10.
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Maria Scuto, Paola Di Mauro, Maria Laura Ontario, Chiara Amato, Sergio Modafferi, Domenico Ciavardelli, Angela Trovato Salinaro, Luigi Maiolino & Vittorio Calabrese. (2019) Nutritional Mushroom Treatment in Meniere’s Disease with Coriolus versicolor: A Rationale for Therapeutic Intervention in Neuroinflammation and Antineurodegeneration. International Journal of Molecular Sciences 21:1, pages 284.
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Nicola L. Yeo, Mathew P. White, Natalie Ronan, David J. Whinney, Alison Curnow & Jessica Tyrrell. (2018) Stress and Unusual Events Exacerbate Symptoms in Menière's Disease: A Longitudinal Study. Otology & Neurotology 39:1, pages 73-81.
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Sung-Il Nam. (2017) Recent Research Trend for Ménièreʼs Disease. Research in Vestibular Science 16:2, pages 39-46.
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Sebahattin Cureoglu, Rafael da Costa Monsanto & Michael M. Paparella. (2016) Histopathology of Meniere’s Disease. Operative Techniques in Otolaryngology-Head and Neck Surgery 27:4, pages 194-204.
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Yuan-Jun Li, Zhan-Guo Jin & Xian-Rong Xu. (2016) Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis. Journal of Vestibular Research 25:5-6, pages 211-218.
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Jeffrey D. Hasday, Christopher Thompson & Ishwar S. Singh. 2011. Comprehensive Physiology. Comprehensive Physiology 109 148 .
Shahira S. ElGemei, Noha M. Shaheen & Reham Emad Abu Khalil. (2012) The association between heat shock protein P2/P2 genotype with Egyptian hepatocellular carcinoma patients. Comparative Clinical Pathology 22:6, pages 1183-1188.
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Tai Wang, Pablo C. Echeverría & Didier Picard. 2013. Inhibitors of Molecular Chaperones as Therapeutic Agents. Inhibitors of Molecular Chaperones as Therapeutic Agents 1 36 .
Elina Hietikko, Jouko Kotimäki & Minna Männikkö. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences.
Naoki Nishio, Masaaki Teranishi, Yasue Uchida, Saiko Sugiura, Fujiko Ando, Hiroshi Shimokata, Michihiko Sone, Hironao Otake, Ken Kato, Tadao Yoshida, Mitsuhiko Tagaya, Tatsuya Hibi & Tsutomu Nakashima. (2013) Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Ménière's disease and sudden sensorineural hearing loss. Life Sciences 92:10, pages 541-546.
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Alberto J.L. Macario, Everly Conway de Macario & Francesco CappelloAlberto J.L Macario, Everly Conway de Macario & Francesco Cappello. 2013. The Chaperonopathies. The Chaperonopathies 63 69 .
S. Schmerber, J.-M. Lejeune & G. Dumas. (2012) Sordità autoimmune. EMC - Otorinolaringoiatria 11:4, pages 1-14.
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José Antonio López-Escamez. (2012) Papel de la medicina genómica en las enfermedades del oído medio e interno. Acta Otorrinolaringológica Española 63:6, pages 470-479.
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José Antonio López-Escamez. (2012) Role of Genomic Medicine in Middle and Inner Ear Diseases. Acta Otorrinolaringologica (English Edition) 63:6, pages 470-479.
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S. Schmerber, J.-M. Lejeune & G. Dumas. (2012) Hipoacusia autoinmunitaria. EMC - Otorrinolaringología 41:4, pages 1-16.
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Masaaki TeranishiYasue UchidaNaoki NishioKen KatoHironao OtakeTadao YoshidaHirokazu SuzukiMichihiko SoneSaiko SugiuraFujiko AndoHiroshi ShimokataTsutomu Nakashima. (2012) Polymorphisms in Genes Involved in Oxidative Stress Response in Patients with Sudden Sensorineural Hearing Loss and Ménière's Disease in a Japanese Population. DNA and Cell Biology 31:10, pages 1555-1562.
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S. Schmerber, J.-M. Lejeune & G. Dumas. (2012) Surdité auto-immune. EMC - Oto-rhino-laryngologie 7:3, pages 1-15.
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Yoshihiro Noguchi. (2012) Meniere's disease and gene. Equilibrium Research 71:4, pages 247-251.
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Robert W. Eppsteiner & Richard J.H. Smith. (2011) Genetic disorders of the vestibular system. Current Opinion in Otolaryngology & Head & Neck Surgery 19:5, pages 397-402.
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Irene GazquezJose A. Lopez-EscamezAntonia MorenoColleen A. CampbellNicole C. MeyerJohn P. CareyLloyd B. MinorBruce J. GantzMarlan R. HansenCharles C. Della SantinaIsmael AranAndres Soto-VarelaSofia SantosAngel BatuecasHerminio Perez-GarriguesAlicia Lopez-NevotRichard J.H. SmithMiguel A. Lopez-Nevot. (2011) Functional Variants in NOS1 and NOS2A Are Not Associated with Progressive Hearing Loss in Ménière's Disease in a European Caucasian Population . DNA and Cell Biology 30:9, pages 699-708.
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Vittorio Calabrese, C. Cornelius, L. Maiolino, M. Luca, R. Chiaramonte, M. A. Toscano & A. Serra. (2010) Oxidative Stress, Redox Homeostasis and Cellular Stress Response in Ménière’s Disease: Role of Vitagenes. Neurochemical Research 35:12, pages 2208-2217.
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Jeffrey T. Vrabec. (2010) Genetic Investigations of Meniere‘s Disease. Otolaryngologic Clinics of North America 43:5, pages 1121-1132.
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Yuzhen Wang, Fang Zhou, Yiming Wu, Dong Xu, Weihui Li & Shoupei Liang. (2010) The relationship between three heat shock protein 70 gene polymorphisms and susceptibility to lung cancer. Clinical Chemistry and Laboratory Medicine 48:11.
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