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Showing results for
yu chih chuan
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Yi-Chieh Chuang
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PKD2 founder mutation is the most common mutation of polycystic kidney disease in Taiwan.
NPJ Genom Med. 2022 Jul 1;7(1):40. doi: 10.1038/s41525-022-00309-w.
NPJ Genom Med. 2022.
PMID: 35778421
Free PMC article.
UMOD Mutations in Chronic Kidney Disease in Taiwan.
Chen HD, Yu CC, Yang IH, Hung CC, Kuo MC, Tarng DC, Chang JM, Hwang DY.
Chen HD, et al. Among authors: yu cc.
Biomedicines. 2022 Sep 13;10(9):2265. doi: 10.3390/biomedicines10092265.
Biomedicines. 2022.
PMID: 36140366
Free PMC article.
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Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation.
Lim LM, Chung WY, Hwang DY, Yu CC, Ke HL, Liang PI, Lin TW, Cheng SM, Huang AM, Kuo HT.
Lim LM, et al. Among authors: yu cc.
J Transl Med. 2022 Jul 21;20(1):324. doi: 10.1186/s12967-022-03522-4.
J Transl Med. 2022.
PMID: 35864526
Free PMC article.
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Abatacept in B7-1-positive proteinuric kidney disease.
Yu CC, Fornoni A, Weins A, Hakroush S, Maiguel D, Sageshima J, Chen L, Ciancio G, Faridi MH, Behr D, Campbell KN, Chang JM, Chen HC, Oh J, Faul C, Arnaout MA, Fiorina P, Gupta V, Greka A, Burke GW 3rd, Mundel P.
Yu CC, et al.
N Engl J Med. 2013 Dec 19;369(25):2416-23. doi: 10.1056/NEJMoa1304572. Epub 2013 Nov 8.
N Engl J Med. 2013.
PMID: 24206430
Free PMC article.
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Role of podocyte B7-1 in diabetic nephropathy.
Fiorina P, Vergani A, Bassi R, Niewczas MA, Altintas MM, Pezzolesi MG, D'Addio F, Chin M, Tezza S, Ben Nasr M, Mattinzoli D, Ikehata M, Corradi D, Schumacher V, Buvall L, Yu CC, Chang JM, La Rosa S, Finzi G, Solini A, Vincenti F, Rastaldi MP, Reiser J, Krolewski AS, Mundel PH, Sayegh MH.
Fiorina P, et al. Among authors: yu cc.
J Am Soc Nephrol. 2014 Jul;25(7):1415-29. doi: 10.1681/ASN.2013050518. Epub 2014 Mar 27.
J Am Soc Nephrol. 2014.
PMID: 24676639
Free PMC article.
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