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Items: 4

1.
A novel FOXP3 mutation in a Chinese child with IPEX‐associated membranous nephropathy
Liwen Tan, Yunfei An, Qin Yang, Haiping Yang, Gaofu Zhang, Qiu Li, Mo Wang
Mol Genet Genomic Med. 2022 Jun; 10(6): e1945. Published online 2022 Apr 18. doi: 10.1002/mgg3.1945
PMCID:
PMC9184667
AbstractArticlePDF–2.2M
2.
Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney disease
Fujun Lin, Fan Bian, Jun Zou, Xiangru Wu, Jianping Shan, Wei Lu, Yao Yao, Gengru Jiang, Daniel Philip Gale
BMC Nephrol. 2014; 15: 175. Published online 2014 Nov 7. doi: 10.1186/1471-2369-15-175
PMCID:
PMC4233041
AbstractArticlePDF–1.3M
3.
Systemic autoimmunity and defective Fas ligand secretion in the absence of the Wiskott-Aldrich syndrome protein
Nikolay P. Nikolov, Masaki Shimizu, Sophia Cleland, Daniel Bailey, Joseph Aoki, Ted Strom, Pamela L. Schwartzberg, Fabio Candotti, Richard M. Siegel
Blood. 2010 Aug 5; 116(5): 740–747. Prepublished online 2010 May 10. doi: 10.1182/blood-2009-08-237560
PMCID:
PMC2918330
AbstractArticle
4.
Comparative distribution of the alpha 1(IV), alpha 5(IV), and alpha 6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patients.
B Peissel, L Geng, R Kalluri, C Kashtan, H G Rennke, G R Gallo, K Yoshioka, M J Sun, B G Hudson, E G Neilson, et al.
J Clin Invest. 1995 Oct; 96(4): 1948–1957. doi: 10.1172/JCI118241
PMCID:
PMC185832
SummaryPage BrowsePDF–4.2M

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