Zobrazeno 1 - 10
of 4 825
pro vyhledávání: '"AS, Alport syndrome"'
Autor:
Mabillard, Holly1,2, Ryan, Rebecca1, Tzoumas, Nik3,4, Gear, Susie5, Sayer, John A.1,2,6 john.sayer@newcastle.ac.uk
Publikováno v:
Journal of Rare Diseases. 5/13/2024, Vol. 3 Issue 1, p1-26. 26p.
Autor:
Pearce, Helen1, Mabillard, Holly1,2,3 Holly.Mabillard2@newcastle.ac.uk
Publikováno v:
Journal of Rare Diseases. 11/8/2023, Vol. 2 Issue 1, p1-8. 8p.
Autor:
Jabbar, Maryam1, Rashid, Faisal2 optometristfaisalrasheed@gmail.com, Fatima, Naseer1, Ahmad, Hafiz Masood1
Publikováno v:
Pakistan Journal of Ophthalmology. 2023, Vol. 39 Issue 1, p72-74. 3p.
Autor:
Wang, Xiaoyuan1, Zhang, Yanqin1, Ding, Jie1 djnc_5855@126.com, Wang, Fang1 wangfangped@163.com
Publikováno v:
Scientific Reports. 9/10/2021, Vol. 11 Issue 1, p1-13. 13p.
Autor:
Tecellioglu, Fahriye Secil1 f.seciltecellioglu@gmail.com, Akpolat, Nusret2, Tabel, Yilmaz3, Gul, Mehmet4
Publikováno v:
Annals of Medical of Research. Sep2021, Vol. 28 Issue 9, p1791-1794. 4p.
Autor:
Omachi, Kohei1,2,3, Kaseda, Shota1,2, Yokota, Tsubasa1, Kamura, Misato1,2, Teramoto, Keisuke1,2, Kuwazuru, Jun1, Kojima, Haruka1, Nohara, Hirofumi1,2, Koyama, Kosuke1, Ohtsuki, Sumio4, Misumi, Shogo5, Takeo, Toru6, Nakagata, Naomi6, Li, Jian-Dong7, Shuto, Tsuyoshi1, Suico, Mary Ann1, Miner, Jeffrey H.3, Kai, Hirofumi1,2 hirokai@gpo.kumamoto-u.ac.jp
Publikováno v:
Scientific Reports. 3/29/2021, Vol. 11 Issue 1, p1-16. 16p.
Autor:
Adele Tanzi, Lola Buono, Cristina Grange, Corinne Iampietro, Alessia Brossa, Fanny Oliveira Arcolino, Maddalena Arigoni, Raffaele Calogero, Laura Perin, Silvia Deaglio, Elena Levtchenko, Licia Peruzzi, Benedetta Bussolati
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-16 (2024)
Abstract Background Personalized disease models are crucial for evaluating how diseased cells respond to treatments, especially in case of innovative biological therapeutics. Extracellular vesicles (EVs), nanosized vesicles released by cells for inte
Externí odkaz:
https://doaj.org/article/1d0980a33a23454f942994924d92a61f
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-13 (2024)
Abstract Background Alport syndrome (AS) is an inherited nephropathy caused by mutations in the type IV collagen genes. It is clinically characterized by damage to the eyes, ears and kidneys. Diagnosis of AS is hampered by its atypical clinical pictu
Externí odkaz:
https://doaj.org/article/283f0dd7decc4dab9d37f2359fa94223
Publikováno v:
International Journal of Nephrology and Renovascular Disease, Vol Volume 17, Pp 167-174 (2024)
Yang Li,1 Xue Yan,2 Zhen Luo,1 Xianxian Fu,1 Zhongju Li,1 Qiuzhu Xu,3 Juanjuan Chen,1 Jingmin Yang,2,4,5 Daru Lu4,5 1Department of Nephropathy, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Hainan, People’s Republ
Externí odkaz:
https://doaj.org/article/5475199c1894485584247425931c747a
Publikováno v:
International Multidisciplinary Scientific Conference on Social Sciences & Arts SGEM. 2019, Vol. 6, p383-391. 9p.