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Cited by in CrossRef
For: Katayama K, Nomura S, Tryggvason K, Ito M. Searching for a treatment for Alport syndrome using mouse models. World J Nephrol 2014; 3(4): 230-236 [PMID: 25374816 DOI: 10.5527/wjn.v3.i4.230]
URL: https://www.wjgnet.com/2220-6124/full/v3/i4/230.htm
Number Citing Articles
1
Manami Iida, Shuichi Ohtomo, Naoko A. Wada, Otoya Ueda, Yoshinori Tsuboi, Atsuo Kurata, Kou-ichi Jishage, Naoshi Horiba, Franziska Theilig. TNF-α induces Claudin-1 expression in renal tubules in Alport micePLOS ONE 2022; 17(3): e0265081 doi: 10.1371/journal.pone.0265081
2
Emilia Anouk Margo Firat, Eva Miriam Buhl, Nassim Bouteldja, Bart Smeets, Ulf Eriksson, Peter Boor, Barbara Mara Klinkhammer. PDGF-D Is Dispensable for the Development and Progression of Murine Alport SyndromeThe American Journal of Pathology 2024; 194(5): 641 doi: 10.1016/j.ajpath.2023.12.009
3
Avanti Adone, Ashish Anjankar. Alport Syndrome: A Comprehensive ReviewCureus 2023;  doi: 10.7759/cureus.47129
4
Matthew J. Williams, Toshifumi Sugatani, Olga A. Agapova, Yifu Fang, Joseph P. Gaut, Marie-Claude Faugere, Hartmut H. Malluche, Keith A. Hruska. The activin receptor is stimulated in the skeleton, vasculature, heart, and kidney during chronic kidney diseaseKidney International 2018; 93(1): 147 doi: 10.1016/j.kint.2017.06.016
5
Examining the Causal Relationship Between Genes, Epigenetics, and Human HealthAdvances in Bioinformatics and Biomedical Engineering 2019; : 361 doi: 10.4018/978-1-5225-8066-9.ch015
6
Andreas F. Hofmeister, Martin Kömhoff, Stefanie Weber, Ivica Grgic. Disease modeling in genetic kidney diseases: miceCell and Tissue Research 2017; 369(1): 159 doi: 10.1007/s00441-017-2639-3
7
S. Pinto, M. Hoek, Y. Huang, P. Costet, L. Ma, J.E. Imbriglio. Comprehensive Medicinal Chemistry III2017; : 694 doi: 10.1016/B978-0-12-409547-2.12432-1
8
Tomohiro Murata, Kan Katayama, Toshitaka Oohashi, Timo Jahnukainen, Tomoko Yonezawa, Yoshikazu Sado, Eiji Ishikawa, Shinsuke Nomura, Karl Tryggvason, Masaaki Ito. COL4A6 is dispensable for autosomal recessive Alport syndromeScientific Reports 2016; 6(1) doi: 10.1038/srep29450
9
Camila I. Irion, Monique Williams, Jose Condor Capcha, Trevor Eisenberg, Guerline Lambert, Lauro M. Takeuchi, Grace Seo, Keyvan Yousefi, Rosemeire Kanashiro-Takeuchi, Keith A. Webster, Karen C. Young, Joshua M. Hare, Lina A. Shehadeh. Col4a3-/- Mice on Balb/C Background Have Less Severe Cardiorespiratory Phenotype and SGLT2 Over-Expression Compared to 129x1/SvJ and C57Bl/6 BackgroundsInternational Journal of Molecular Sciences 2022; 23(12): 6674 doi: 10.3390/ijms23126674
10
Jifan Guo, Wenping Song, Joseph Boulanger, Ethan Y. Xu, Fang Wang, Yanqin Zhang, Qun He, Suxia Wang, Li Yang, Cynthia Pryce, Lucy Phillips, Deidre MacKenna, Ekkehard Leberer, Oxana Ibraghimov-Beskrovnaya, Jie Ding, Shiguang Liu. Dysregulated Expression of microRNA-21 and Disease-Related Genes in Human Patients and in a Mouse Model of Alport SyndromeHuman Gene Therapy 2019; 30(7): 865 doi: 10.1089/hum.2018.205
11
Yuan Wu, Yi Guo, Jinzhong Yuan, Hongbo Xu, Yong Chen, Hao Zhang, Mingyang Yuan, Hao Deng, Lamei Yuan. A COL4A5 Missense Variant in a Han-Chinese Family with X-linked Alport SyndromeCurrent Molecular Medicine 2019; 19(10): 758 doi: 10.2174/1566524019666190906144214
12
Jianqing Liang, Youhua Liu. Animal Models of Kidney Disease: Challenges and PerspectivesKidney360 2023; 4(10): 1479 doi: 10.34067/KID.0000000000000227
13
Valerie S LeBleu, Keizo Kanasaki, Sara Lovisa, Joseph L Alge, Jiha Kim, Yang Chen, Yingqi Teng, Behzad Gerami-Naini, Hikaru Sugimoto, Noritoshi Kato, Ignacio Revuelta, Nicole Grau, Jonathan P Sleeman, Gangadhar Taduri, Akane Kizu, Shahin Rafii, Konrad Hochedlinger, Susan E Quaggin, Raghu Kalluri. Genetic reprogramming with stem cells regenerates glomerular epithelial podocytes in Alport syndromeLife Science Alliance 2024; 7(6): e202402664 doi: 10.26508/lsa.202402664