Association of the myosin heavy chain 9 gene single nucleotide polymorphism with inflammatory bowel disease

by Ahmed Ezz El-Arab Abd Al-Aliem, Eman A.E. Badr, Elsayed Ibrahem El-Shayeb, Ahmed Megahed Ahmed Taman, Abd El-naser Abd El-atty Gadallah
Published 2021-12-01

MYH9 nephropathy

by Taehoon Oh, Hyun Jung Seo, Kyu Taek Lee, Han Jo Kim, Hwi Jun Kim, Ji-Hye Lee, Hae Il Cheong, Eun Young Lee
Published 2015-03-01

Myosin expression and podocyte function in kidney structure and function, in heterozygous MHY9 knockout mice

by Belghasem, Mostafa
Published 2019

The effects of mechanical strain on adhesion in Myh9-ablated podocytes

by Keller, Keith Hollis
Published 2017

Moyamoya-like vasculopathy associated to MYH9-related thrombocytopenia manifested by multiple cerebral ischemic lesions: a case report

by Athena Cristina Ribigan, Raluca Stefania Badea, Alida Ciocan, Dana Stefan, Bogdan Casaru, Patricia Ioan, Florina Antochi, Ovidiu Băjenaru
Published 2020-09-01

c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family

by Vitor G.L. Dantas, Karina Lezirovitz, Guilherme L. Yamamoto, Carolina Fischinger Moura de Souza, Simone Gomes Ferreira, Regina C. Mingroni-Netto
Published 2014-12-01

miR-6089/MYH9/β-catenin/c-Jun negative feedback loop inhibits ovarian cancer carcinogenesis and progression

by Longyang Liu, Yingxia Ning, Juanjuan Yi, Jianhuan Yuan, Weiyi Fang, Zhongqiu Lin, Zhaoyang Zeng
Published 2020-05-01

The E3 ligase Ubr3 regulates Usher syndrome and MYH9 disorder proteins in the auditory organs of Drosophila and mammals

by Tongchao Li, Nikolaos Giagtzoglou, Daniel F Eberl, Sonal Nagarkar Jaiswal, Tiantian Cai, Dorothea Godt, Andrew K Groves, Hugo J Bellen
Published 2016-06-01

Linking the Landscape of <i>MYH9</i>-Related Diseases to the Molecular Mechanisms that Control Non-Muscle Myosin II-A Function in Cells

by Gloria Asensio-Juárez, Clara Llorente-González, Miguel Vicente-Manzanares
Published 2020-06-01

R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura

by Chih-Chien Sung, Shih-Hua Lin, Tai-Kuang Chao, Yeu-Chin Chen
Published 2014-01-01

MYH9 Key Amino Acid Residues Identified by the Anti-Idiotypic Antibody to Porcine Reproductive and Respiratory Syndrome Virus Glycoprotein 5 Involve in the Virus Internalization by...

by Liangliang Li, Lu Zhang, Qifan Hu, Liang Zhao, Yuchen Nan, Gaopeng Hou, Yiyang Chen, Ximeng Han, Xiaolei Ren, Qin Zhao, Hu Tao, Zhenzhao Sun, Gaiping Zhang, Chunyan Wu, Jingfei Wang, En-Min Zhou
Published 2019-12-01

Hearing lessons from flies

by Yi-Nan Lee, Cheng-Ting Chien
Published 2016-08-01

Association of MYH9 Polymorphisms with Hypertension in Patients with Chronic Kidney Disease in China

by Liping Liu, Caili Wang, Yan Mi, Dan Liu, Li Li, Junying Fan, Lei Nan, Niya Jia, Yu Du
Published 2016-12-01

Identifying and Phenotyping an ENU Derived Mouse Model of MYH9 Related Disease

by Berndl, Elizabeth Sara Lefebvre
Published 2012

MYH9 Aggregation Induced by Direct Interaction With PRRSV GP5 Ectodomain Facilitates Viral Internalization by Permissive Cells

by Biyun Xue, Gaopeng Hou, Guixi Zhang, Jingjing Huang, Liangliang Li, Yuchen Nan, Yang Mu, Lizhen Wang, Lu Zhang, Ximeng Han, Xiaolei Ren, Qin Zhao, Chunyan Wu, Jingfei Wang, En-Min Zhou
Published 2019-10-01

Direct Interaction Between CD163 N-Terminal Domain and MYH9 C-Terminal Domain Contributes to Porcine Reproductive and Respiratory Syndrome Virus Internalization by Permissive Cells

by Gaopeng Hou, Biyun Xue, Liangliang Li, Yuchen Nan, Lu Zhang, Kuokuo Li, Qin Zhao, Julian A. Hiscox, James P. Stewart, Chunyan Wu, Jingfei Wang, En-Min Zhou
Published 2019-08-01

Identifying and Phenotyping an ENU Derived Mouse Model of MYH9 Related Disease

by Berndl, Elizabeth Sara Lefebvre
Published 2012

Nodular fasciitis occurring at the anterior abdominal wall in a 12-year-old female

by Tamotsu Kobayashi, Yutaka Kanamori, Mai Kutsukake, Masataka Takahashi, Motohiro Kano, Teizaburo Mori, Satoko Yamagishi, Ryoya Furugane, Akihiro Fujino, Takumi Shiobara, Yoshiyuki Tsutsumi, Osamu Miyazaki, Chizuko Haga, Takako Yoshioka
Published 2021-11-01

Clinical features and analysis of deafness genes in 2 patients from a Chinese family with MYH9 disorder

by CHEN Yinyi, ZHANG Ying'ai, GAO Xin
Published 2019-06-01

Case Report: Pathogenic MYH9 c.5797delC Mutation in a Patient With Apparent Thrombocytopenia and Nephropathy

by Pingping Ren, Pingping Ren, Pingping Ren, Hongjun Chen, Hongjun Chen, Hongjun Chen, Yucheng Wang, Yucheng Wang, Yucheng Wang, Cuili Wang, Cuili Wang, Cuili Wang, Shi Feng, Shi Feng, Shi Feng, Hong Jiang, Hong Jiang, Hong Jiang, Jianghua Chen, Jianghua Chen, Jianghua Chen
Published 2021-07-01