Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: ESRRB[original query] |
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Evidence of genetic variations associated with rotator cuff disease. Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2014 Feb 23 (2): 227-35. Motta Geraldo da Rocha, Amaral Marcus Vinícius, Rezende Eduardo, Pitta Rafael, Vieira Thays Cristine dos Santos, Duarte Maria Eugenia Leite, Vieira Alexandre Rezende, Casado Priscila Ladei |
Significant association of full-thickness rotator cuff tears and estrogen-related receptor-ß (ESRRB). Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2015 Feb 24 (2): e31-5. Teerlink Craig C, Cannon-Albright Lisa A, Tashjian Robert |
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay. BMC medical genetics 2014 15 81. Weber Megan L, Hsin Hong-Yuan, Kalay Ersan, BroĊ½ková Dana S, Shimizu Takehiko, Bayram Merve, Deeley Kathleen, Küchler Erika C, Forella Jessalyn, Ruff Timothy D, Trombetta Vanessa M, Sencak Regina C, Hummel Michael, Briseño-Ruiz Jessica, Revu Shankar K, Granjeiro José M, Antunes Leonardo S, Antunes Livia A, Abreu Fernanda V, Costa Marcelo C, Tannure Patricia N, Koruyucu Mine, Patir Asli, Poletta Fernando A, Mereb Juan C, Castilla Eduardo E, Orioli Iêda M, Marazita Mary L, Ouyang Hongjiao, Jayaraman Thottala, Seymen Figen, Vieira Alexandre |
ESRRB polymorphisms are associated with comorbidity of temporomandibular disorders and rotator cuff disease. International journal of oral and maxillofacial surgery 2015 Nov . Bonato L L, Quinelato V, Pinheiro A daR, Amaral M V G, de Souza F N, Lobo J C, Aguiar D P, Augusto L M M, Vieira A R, Salles J I, Cossich V R A, Guimarães J A M, de Gouvêa C V D, Granjeiro J M, Casado P |
Identification of a genetic variant associated with rotator cuff repair healing. Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2016 Apr . Tashjian Robert Z, Granger Erin K, Zhang Yue, Teerlink Craig C, Cannon-Albright Lisa |
Association Between Polymorphisms in the Genes of Estrogen Receptors and the Presence of Temporomandibular Disorders and Chronic Arthralgia. Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons 2017 Nov . Quinelato Valquiria, Bonato Letícia Ladeira, Vieira Alexandre Rezende, Granjeiro José Mauro, Tesch Ricardo, Casado Priscila Ladei |
Estrogen receptor gene is associated with dental fluorosis in Brazilian children. Clinical oral investigations 2018 Dec . Dalledone M, Cunha A S, Ramazzotto L A, Pecharki G D, Nelson-Filho P, Scariot R, Trevilatto P C, Vieira A R, Küchler Erika C, Brancher João |
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese.
Nature communications 2018 Oct 9 (1): 4072. Zheng Ruijuan, Li Zhiqiang, He Fusheng, Liu Haipeng, Chen Jianhua, Chen Jiayu, Xie Xuefeng, Zhou Juan, Chen Hao, Wu Xiangyang, Wu Juehui, Chen Boyu, Liu Yahui, Cui Haiyan, Fan Lin, Sha Wei, Liu Yin, Wang Jiqiang, Huang Xiaochen, Zhang Linfeng, Xu Feifan, Wang Jie, Feng Yonghong, Qin Lianhua, Yang Hua, Liu Zhonghua, Cui Zhenglin, Liu Feng, Chen Xinchun, Gao Shaorong, Sun Silong, Shi Yongyong, Ge Baox |
Genetic basis of rotator cuff injury: a systematic review. BMC medical genetics 2019 9 20 (1): 149. Longo Umile Giuseppe, Candela Vincenzo, Berton Alessandra, Salvatore Giuseppe, Guarnieri Andrea, DeAngelis Joseph, Nazarian Ara, Denaro Vincen |
Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease. Frontiers in genetics 2019 10 76. Gallego-Martinez Alvaro, Requena Teresa, Roman-Naranjo Pablo, Lopez-Escamez Jose |
Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan. Scientific reports 2020 7 10 (1): 11902. Ramzan Memoona, Bashir Rasheeda, Salman Midhat, Mujtaba Ghulam, Sobreira Nara, Witmer P Dane, , Naz Sad |
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul . Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A |
Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population. Journal of advanced research 2021 7 31 13-24. Souissi Amal, Ben Said Mariem, Ben Ayed Ikhlas, Elloumi Ines, Bouzid Amal, Mosrati Mohamed Ali, Hasnaoui Mehdi, Belcadhi Malek, Idriss Nabil, Kamoun Hassen, Gharbi Nourhene, Gibriel Abdullah A, Tlili Abdelaziz, Masmoudi Sab |
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax |
A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case. BMC medical genomics 2022 2 15 (1): 18. Ghasemnejad Tohid, Shekari Khaniani Mahmoud, Nouri Nojadeh Jafar, Mansoori Derakhshan Si |
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- Page last updated:May 06, 2024
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