Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: HSPB1[original query] |
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Functional promoter -1271G>C variant of HSPB1 predicts lung cancer risk and survival. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2010 Apr 28 (11): 1928-35. Guo Huan, Bai Yun, Xu Ping, Hu Zhibin, Liu Li, Wang Fang, Jin Guangfu, Wang Feng, Deng Qifei, Tu Yixiao, Feng Maohui, Lu Daru, Shen Hongbing, Wu Tangch |
Functional promoter rs2868371 variant of HSPB1 associates with radiation-induced esophageal toxicity in patients with non-small-cell lung cancer treated with radio(chemo)therapy. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 2011 Nov 101 (2): 271-7. Lopez Guerra Jose Luis, Wei Qingyi, Yuan Xianglin, Gomez Daniel, Liu Zhensheng, Zhuang Yan, Yin Ming, Li Minghuan, Wang Li-E, Cox James D, Liao Zhongxi |
HSPB1 gene polymorphisms predict risk of mortality for US patients after radio(chemo)therapy for non-small cell lung cancer. International journal of radiation oncology, biology, physics 2012 Oct 84 (2): e229-35. Xu Ting, Wei Qingyi, Lopez Guerra Jose Luis, Wang Li-E, Liu Zhensheng, Gomez Daniel, O'Reilly Michael, Lin Steven Hsesheng, Zhuang Yan, Levy Lawrence B, Mohan Radhe, Zhou Honghao, Liao Zhongxi |
Functional promoter variant rs2868371 of HSPB1 is associated with risk of radiation pneumonitis after chemoradiation for non-small cell lung cancer. International journal of radiation oncology, biology, physics 2013 Jan . Pang Q, Wei Q, Xu T, Yuan X, Lopez Guerra JL, Levy LB, Liu Z, Gomez DR, Zhuang Y, Wang LE, Mohan R, Komaki R, Liao Z |
[The clinical presentation and gene mutation of probands in Chinese patients with Charcot-Marie-Tooth disease]. Zhonghua nei ke za zhi 2015 Jul 54 (7): 623-7. Liu Xiaoxuan, Fan Dongsheng, Song Shuju |
Associations of LIG4 and HSPB1 genetic polymorphisms with risk of radiation-induced lung injury in lung cancer patients treated with radiotherapy. BioMed research international 2015 2015 860373. Xu Feng, Han Ji-Chang, Zhang Ya-Jun, Zhang Yi-Jie, Liu Xiao-Chun, Qi Guan-Bin, Liu Dan, Chen Yan-Zhi, Zhao Yu-Xia, Bai |
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. Brain : a journal of neurology 2015 Nov . Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton |
The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy. Molecular genetics & genomic medicine 2014 Nov 2 (6): 522-9. DiVincenzo Christina, Elzinga Christopher D, Medeiros Adam C, Karbassi Izabela, Jones Jeremiah R, Evans Matthew C, Braastad Corey D, Bishop Crystal M, Jaremko Malgorzata, Wang Zhenyuan, Liaquat Khalida, Hoffman Carol A, York Michelle D, Batish Sat D, Lupski James R, Higgins Joseph |
HSPB1 polymorphisms might be associated with radiation-induced damage risk in lung cancer patients treated with radiotherapy. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2016 Feb . Li Xiaofeng, Xu Sheng, Cheng Yu, Shu J |
[Association and interaction of heat shock proteins B1 gene and tumor-suppressor protein p53 gene with chromosome damage levels among coke oven workers]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2016 Oct 50 (10): 900-906. Li X L, Deng Q F, Zhang X, Wang T, Chen Z W, Bai Y S, Wang S H, Wu T C, Guo |
Charcot-Marie-Tooth disease: genetic subtypes in the Sardinian population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2017 Mar . Lorena Lorefice, Rita Murru M, Giancarlo Coghe, Giuseppe Fenu, Daniela Corongiu, Jessica Frau, Stefania Tranquilli, Paolo Tacconi, Alessandro Vannelli, Giovanni Marrosu, Elena Mamusa, Eleonora Cocco, Giovanna Marrosu |
Screening for SH3TC2, PMP2, and BSCL2 Variants in a Cohort of Chinese Patients with Charcot-Marie-Tooth. Chinese medical journal 2018 Jan 131 (2): 151-155. Zhao Xin, Jiang Ming-Ming, Yan Yi-Zhou, Liu Lei, Xie Yong-Zhi, Li Xiao-Bo, Hu Zheng-Mao, Zi Xiao-Hong, Xia Kun, Tang Bei-Sha, Zhang Ru- |
HSPB1 rs2070804 polymorphism is associated with the depth of primary tumor. Journal of cellular biochemistry 2019 Jul . Hung Chin-Sheng, Huang Chien-Yu, Hsu Yu-Wen, Makondi Precious Takondwa, Chang Wei-Chiao, Chang Yu-Jia, Wang Jaw-Yuan, Wei Po- |
Association of single nucleotide polymorphisms at HSPB1 rs7459185 and TGFB1 rs11466353 with radiation esophagitis in lung cancer. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 2019 Mar 135 161-169. Delgado Blas David, Enguix-Riego María Valle, Fernández de Bobadilla Jon Cacicedo, Herrero Rivera Daniel, Nieto-Guerrero Gómez Jose María, Praena-Fernández Juan Manuel, Rivin Del Campo Eleonor, Ortiz Gordillo María José, Fernandez Fernandez María Del Carmen, Lopez Guerra Jose Lu |
The single nucleotide variant rs2868371 associates with the risk of mortality in non-small cell lung cancer patients: A multicenter prospective validation. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 2019 Apr 136 29-36. Enguix-Riego María Del Valle, Cacicedo Jon, Delgado León Blas David, Nieto-Guerrero Gómez Jose María, Herrero Rivera Daniel, Perez Marco, Praena-Fernández Juan Manuel, Sanchez Carmona Gerardo, Rivin Del Campo Eleonor, Ortiz Gordillo María José, Lopez Guerra Jose Lu |
MAPK pathway and B cells overactivation in multiple sclerosis revealed by phosphoproteomics and genomic analysis. Proceedings of the National Academy of Sciences of the United States of America 2019 Apr . Kotelnikova Ekaterina, Kiani Narsis A, Messinis Dimitris, Pertsovskaya Inna, Pliaka Vicky, Bernardo-Faura Marti, Rinas Melanie, Vila Gemma, Zubizarreta Irati, Pulido-Valdeolivas Irene, Sakellaropoulos Theodore, Faigle Wolfgang, Silberberg Gilad, Masso Mar, Stridh Pernilla, Behrens Janina, Olsson Tomas, Martin Roland, Paul Friedemann, Alexopoulos Leonidas G, Saez-Rodriguez Julio, Tegner Jesper, Villoslada Pab |
The Association Between Heat-Shock Protein Polymorphisms and Prognosis in Lung Cancer Patients Treated With Platinum-Based Chemotherapy. Frontiers in pharmacology 2020 11 1029. Zou Ting, Liu Jun-Yan, She Li, Yin Ji-Ye, Li Xi, Li Xiang-Ping, Zhou Hong-Hao, Chen Juan, Liu Zhao-Qi |
Prognostic value of the TGF?1 rs4803455 single nucleotide polymorphism in small cell lung cancer. Tumori 2020 Aug 300891620946841. Ayala de Miguel Pablo, Enguix-Riego María Valle, Cacicedo Jon, Delgado Blas David, Perez Marco, Praena-Fernández Juan Manuel, Quintana Cortés Laura, Borrega García Pablo, Del Campo Eleonor Rivin, Lopez Guerra Jose Lu |
Molecular analysis and clinical diversity of distal hereditary motor neuropathy. European journal of neurology 2020 4 27 (7): 1319-1326. Liu X, Duan X, Zhang Y, Sun A, Fan |
Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families. Frontiers in neurology 2020 12 11 603003. Xie Yongzhi, Lin Zhiqiang, Pakhrin Pukar Singh, Li Xiaobo, Wang Binghao, Liu Lei, Huang Shunxiang, Zhao Huadong, Cao Wanqian, Hu Zhengmao, Guo Jifeng, Shen Lu, Tang Beisha, Zhang Ru |
Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation. European journal of neurology 2020 Dec . Frasquet Marina, Rojas-García Ricard, Argente-Escrig Herminia, Vázquez-Costa Juan Francisco, Muelas Nuria, Vílchez Juan Jesús, Sivera Rafael, Millet Elvira, Barreiro Marisa, Díaz-Manera Jordi, Turon-Sans Janina, Cortés-Vicente Elena, Querol Luis, Ramírez-Jiménez Laura, Martínez-Rubio Dolores, Sánchez-Monteagudo Ana, Espinós Carmen, Sevilla Teresa, Lupo Vincen |
HSPA1A, HSPA1L and TRAP1 heat shock genes may be associated with prognosis in ovarian epithelial cancer. Oncology letters 2020 1 19 (1): 359-367. De Andrade Warne Pedro, Da Conceição Braga Letícia, Gonçales Nikole Gontijo, Silva Luciana Maria, Da Silva Filho Agnaldo Lop |
Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants. Frontiers in genetics 2021 8 12 682050. Ferese Rosangela, Campopiano Rosa, Scala Simona, D'Alessio Carmelo, Storto Marianna, Buttari Fabio, Centonze Diego, Logroscino Giancarlo, Zecca Chiara, Zampatti Stefania, Fornai Francesco, Cianci Vittoria, Manfroi Elisabetta, Giardina Emiliano, Magnani Mauro, Suppa Antonio, Novelli Giuseppe, Gambardella Stefa |
The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease. Turkish neurosurgery 2021 6 31 (6): 888-895. Yalcintepe Sinem, Gurkan Hakan, Dogan Ipek Gungor, Demir Selma, Sag Sebnem Ozemri, Kabayegit Zehra Manav, Atli Emine Ikbal, Atli Engin, Eker Damla, Temel Sehime Guls |
In silico screening and exploration into phenotypic alterations of deleterious oncogenic single nucleotide polymorphisms in HSPB1 gene. Genomics 2021 6 113 (4): 2812-2825. Bhattacharya Shreya, Ray Suj |
Validation of Polymorphisms Associated with the Risk of Radiation-Induced Oesophagitis in an Independent Cohort of Non-Small-Cell Lung Cancer Patients. Cancers 2021 Mar 13 (6): . Aguado-Barrera Miguel E, Martínez-Calvo Laura, Fernández-Tajes Juan, Calvo-Crespo Patricia, Taboada-Valladares Begoña, Lobato-Busto Ramón, Gómez-Caamaño Antonio, Vega A |
[Rare variants of HSPB1 are probably associated with amyotrophic lateral sclerosis]. Nan fang yi ke da xue xue bao = Journal of Southern Medical University 2021 Jan 41 (1): 75-78. Chen Junyi, Liu Xiangyi, Xu Yingsheng, Fan Dongshe |
HSPB1 Gene Variants and Schizophrenia: A Case-Control Study in a Polish Population. Disease markers 2022 3 2022 4933011. Kowalczyk Malgorzata, Kucia Krzysztof, Owczarek Aleksander, Suchanek-Raif Renata, Paul-Samojedny Monika, Choreza Piotr, Kowalski J |
[Genetic distribution in Chinese patients with hereditary peripheral neuropathy]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2022 10 54 (5): 874-883. Liu X X, Duan X H, Zhang S, Sun A P, Zhang Y S, Fan D |
Mutational screening of Greek patients with axonal Charcot-Marie-Tooth disease using targeted Next-Generation Sequencing: clinical & molecular spectrum delineation. Journal of the peripheral nervous system : JPNS 2023 9 . Zoi Kontogeorgiou, Chrisoula Kartanou, Michail Rentzos, Panagiotis Kokotis, Evangelos Anagnostou, Thomas Zambelis, Elisabeth Chroni, Argyris Dinopoulos, Marios Panas, Georgios Koutsis, Georgia Karadi |
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