Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 88 Records) |
Query Trace: MYH9[original query] |
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Targeted next-generation sequencing identifies clinically relevant somatic mutations in a large cohort of inflammatory breast cancer. Breast cancer research : BCR 2018 Aug 20 (1): 88. Liang Xu, Vacher Sophie, Boulai Anais, Bernard Virginie, Baulande Sylvain, Bohec Mylene, Bièche Ivan, Lerebours Florence, Callens Céli |
Low-grade myofibroblastic sarcoma arising in the tip of the tongue with intravascular invasion: A case report. Oncology letters 2018 8 16 (3): 3889-3894. Mikami Yurie, Fujii Shinsuke, Kohashi Ken-Ichi, Yamada Yuichi, Moriyama Masafumi, Kawano Shintaro, Nakamura Seiji, Oda Yoshinao, Kiyoshima Tamot |
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD). Journal of human genetics 2018 Aug . Wang Kun, Zhao Sen, Zhang Qianqian, Yuan Jian, Liu Jiaqi, Ding Xinghuan, Song Xiaofei, Lin Jiachen, Du Renqian, Zhou Yangzhong, Sugimoto Michihiko, Chen Weisheng, Yuan Bo, Liu Jian, Yan Zihui, Liu Bowen, Zhang Yisen, Li Xiaoxin, Niu Yuchen, Long Bo, Shen Yiping, Zhang Shuyang, Abe Kuniya, Su Jianzhong, Wu Zhihong, Wu Nan, Liu Pengfei, Yang Xinjian, |
Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis. Haemophilia : the official journal of the World Federation of Hemophilia 2018 11 25 (1): 127-135. Saes Joline L, Simons Annet, de Munnik Sonja A, Nijziel Marten R, Blijlevens Nicole M A, Jongmans Marjolijn C, van der Reijden Bert A, Smit Yolba, Brons Paul P, van Heerde Waander L, Schols Saskia E |
An African perspective on the genetic risk of chronic kidney disease: a systematic review. BMC medical genetics 2018 10 19 (1): 187. George Cindy, Yako Yandiswa Y, Okpechi Ikechi G, Matsha Tandi E, Kaze Folefack Francois J, Kengne Andre |
Novel Haplotype Indicator for End-Stage Renal Disease Progression among Saudi Patients. International journal of nephrology 2019 9 2019 1095215. Cyrus Cyril, Chathoth Shahanas, Vatte Chittibabu, Alrubaish Nafie, Almuhanna Othman, Borgio J Francis, Al-Mueilo Samir, Al Muhanna Fahd, Al Ali Amein |
Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation. Ear and hearing 2019 5 41 (1): 114-124. Song Mee Hyun, Jung Jinsei, Rim John Hoon, Choi Hye Ji, Lee Hack June, Noh Byunghwa, Lee Jun Suk, Gee Heon Yung, Choi Jae You |
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in children. Genes, chromosomes & cancer 2019 May . de Smith Adam J, Lavoie Geneviève, Walsh Kyle M, Aujla Sumeet, Evans Erica, Hansen Helen M, Smirnov Ivan, Kang Alice Y, Zenker Martin, Ceremsak John J, Stieglitz Elliot, Muskens Ivo S, Roberts William, McKean-Cowdin Roberta, Metayer Catherine, Roux Philippe P, Wiemels Joseph |
Association between polymorphism rs2032487 in the non-muscle myosin heavy chain IIA gene (MHY9) and chronic kidney disease secondary to type 2 diabetes mellitus in a population of the Canary Islands. Endocrinologia, diabetes y nutricion 2019 Apr . Boronat Mauro, Tugores Antonio, Saavedra Pedro, Garay Paloma, Bosch Elvira, Lorenzo Dionisio, García-Cantón Cés |
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A.
Annals of neurology 2019 Mar 85 (3): 316-330. Tao Feifei, Beecham Gary W, Rebelo Adriana P, Svaren John, Blanton Susan H, Moran John J, Lopez-Anido Camila, Morrow Jasper M, Abreu Lisa, Rizzo Devon, Kirk Callyn A, Wu Xingyao, Feely Shawna, Verhamme Camiel, Saporta Mario A, Herrmann David N, Day John W, Sumner Charlotte J, Lloyd Thomas E, Li Jun, Yum Sabrina W, Taroni Franco, Baas Frank, Choi Byung-Ok, Pareyson Davide, Scherer Steven S, Reilly Mary M, Shy Michael E, Züchner Stephan, |
Effect of donor non-muscle myosin heavy chain (MYH9) gene polymorphisms on clinically relevant kidney allograft dysfunction. BMC nephrology 2020 Sep 21 (1): 380. Pazik Joanna, Oldak Monika, Ozi?b?o Dominika, Materkowska Dominika D?borska, Sadowska Anna, Malejczyk Jacek, Durlik Magdale |
Molecular and clinicopathological characteristics of ROS1-rearranged non-small-cell lung cancers identified by next-generation sequencing. Molecular oncology 2020 Sep . Cui Meiying, Han Yuchen, Li Pan, Zhang Jianying, Ou Qiuxiang, Tong Xiaoling, Zhao Ruiying, Dong Nan, Wu Xue, Li Wencai, Jiang Guozho |
Association of MYH9-rs3752462 polymorphisms with chronic kidney disease among clinically diagnosed hypertensive patients: a case-control study in a Ghanaian population. Clinical hypertension 2020 26 15. Owiredu William K B A, Appiah Michael, Obirikorang Christian, Adu Evans Asamoah, Boima Vincent, Amos-Abanyie Ernestine Kubi, Akyaw Priscilla Abena, Owiredu Eddie-Williams, Acheampong Emmanu |
MYH9 promotes cell metastasis via inducing Angiogenesis and Epithelial Mesenchymal Transition in Esophageal Squamous Cell Carcinoma. International journal of medical sciences 2020 8 17 (13): 2013-2023. Yang Bin, Liu Huijuan, Bi Yanghui, Cheng Caixia, Li Guodong, Kong Pengzhou, Zhang Ling, Shi Ruyi, Zhang Yunkui, Zhang Rongsheng, Cheng Xiaolo |
Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene. Medicine 2020 Jan 99 (3): e18722. Adam Khalid Mohamed, Mohammed Ali Mahmoud, Elamin Abubakr A |
Kidney podocyte-associated gene polymorphisms affect tacrolimus concentration in pediatric patients with refractory nephrotic syndrome. The pharmacogenomics journal 2020 Jan . Mo Xiaolan, Li Jiali, Liu Yunfeng, Liao Xin, Tan Mei, Chen Yilu, He Fan, He Yanling, Li Yingjie, Huang M |
[Molecular diagnosis of a family with May-Hegglin anomaly]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 1 37 (1): 60-63. Wu Chaoli, Mo Wuni |
MYH9 disorder: Identification and a novel mutation in patients with macrothrombocytopenia. Pediatric blood & cancer 2021 4 68 (7): e29055. Natesirinilkul Rungrote, Sosothikul Darintr, Komwilaisak Patcharee, Pongtanakul Bunchoo, Narkbunnum Nattee, Yudhasompop Najwa, Mekjarusgool Pimsiri, Niparuck Pimjai, Boonyawat Kochawan, Kunishima Shinji, Sirachainan Nongnuch, |
A Custom Target Next-Generation Sequencing 70-Gene Panel and Replication Study to Identify Genetic Markers of Diabetic Kidney Disease. Genes 2021 12 12 (12): . Mota-Zamorano Sonia, González Luz María, Robles Nicolás Roberto, Valdivielso José Manuel, Cancho Bárbara, López-Gómez Juan, Gervasini Guiller |
Association of the myosin heavy chain 9 gene single nucleotide polymorphism with inflammatory bowel disease. Biochemistry and biophysics reports 2021 Dec 28 101113. Abd Al-Aliem Ahmed Ezz El-Arab, Badr Eman A E, El-Shayeb Elsayed Ibrahem, Taman Ahmed Megahed Ahmed, Gadallah Abd El-Naser Abd El-At |
Genomic Sequencing of Cancer-related Genes in Sinonasal Squamous Cell Carcinoma and Coexisting Inverted Papilloma. Anticancer research 2021 Jan 41 (1): 71-79. Uchi Ryutaro, Jiromaru Rina, Yasumatsu Ryuji, Yamamoto Hidetaka, Hongo Takahiro, Manako Tomomi, Sato Kuniaki, Hashimoto Kazuki, Wakasaki Takahiro, Matsuo Mioko, Nakagawa Takas |
Development and verification of a hypoxia- and immune-associated prognosis signature for esophageal squamous cell carcinoma. Journal of gastrointestinal oncology 2022 Apr 13 (2): 462-477. Lian Lian, Teng Shi-Bing, Xia You-You, Shen Xiao-Ming, Zheng Yan, Han Shu-Guang, Wang Wen-Jie, Xu Xue-Fei, Zhou Cho |
Prediction of Tacrolimus Dose/Weight-Adjusted Trough Concentration in Pediatric Refractory Nephrotic Syndrome: A Machine Learning Approach. Pharmacogenomics and personalized medicine 2022 3 15 143-155. Mo Xiaolan, Chen Xiujuan, Wang Xianggui, Zhong Xiaoli, Liang Huiying, Wei Yuanyi, Deng Houliang, Hu Rong, Zhang Tao, Chen Yilu, Gao Xia, Huang Min, Li Jia |
Tacrolimus pharmacokinetics in pediatric nephrotic syndrome: A combination of population pharmacokinetic modelling and machine learning approaches to improve individual prediction. Frontiers in pharmacology 2022 12 13 942129. Huang Qiongbo, Lin Xiaobin, Wang Yang, Chen Xiujuan, Zheng Wei, Zhong Xiaoli, Shang Dewei, Huang Min, Gao Xia, Deng Hui, Li Jiali, Zeng Fangling, Mo Xiaol |
The Potential Impact of MYH9 (rs3752462) and ELMO1 (rs741301) Genetic Variants on the Risk of Nephrotic Syndrome Incidence. Biochemical genetics 2023 8 . Eglal A Hassan, Afaf M Elsaid, M M Abou-Elzahab, Ahmed M El-Refaey, Rehab Elmougy, Magdy M Youss |
A non-muscle myosin heavy chain 9 genetic variant is associated with graft failure following kidney transplantation. Kidney research and clinical practice 2023 6 42 (3): 389-402. Felix Poppelaars, Siawosh K Eskandari, Jeffrey Damman, Marc A Seelen, Bernardo Faria, Mariana Gaya da Cos |
Genetic features and kidney morphological changes in women with X-linked Alport syndrome. Journal of medical genetics 2023 5 . Hongling Di, Qing Wang, Dandan Liang, Jiahui Zhang, Erzhi Gao, Chunxia Zheng, Xiaomin Yu, Zhihong L |
[Unexpected diagnosis of nephronopthisis in the genetic study of hypertension due to histological diagnosis of benign nephroangioesclerosis evolved in a young caucasian patient]. Hipertension y riesgo vascular 2023 3 . Heras Benito M, Pérez García M L, Antúnez Plaza P, Montero Mateos |
Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population. Kidney international 2023 12 . Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch |
Genetic predisposition to differentiated thyroid cancer among Polish population. Polish archives of internal medicine 2024 1 . Martyna Borowczyk, Mateusz Sypniewski, Joanna Szyda, Ma?gorzata Braszka, Katarzyna Ziemnicka, Marek Rucha?a, Michalina Oszywa, Zbigniew J Król, Paula Dobo |
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- Page last updated:Apr 16, 2024
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