A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families-Reference-Cited by-同舟云学术

A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families

Published:2013-04-18 Issue:7 Volume:58 Page:480-489
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Al-Hamed Mohamed H,Al-Sabban Essam,Al-Mojalli Hamad,Al-Harbi Naffaa,Faqeih Eissa,Al Shaya Hammad,Alhasan Khalid,Al-Hissi Safaa,Rajab Mohamed,Edwards Noel,Al-Abbad Abbas,Al-Hassoun Ibrahim,Sayer John A,Meyer Brian F

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg201327.pdf

Reference60 articles.

1. Franceschini, N., North, K. E., Kopp, J. B., McKenzie, L. & Winkler, C. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review. Genet. Med. 8, 63–75 (2006).

2. Mundel, P. & Shankland, S. J. Podocyte biology and response to injury. J. Am. Soc. Nephrol. 13, 3005–3015 (2002).

3. Machuca, E., Benoit, G. & Antignac, C. Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology. Hum. Mol. Genet. 18, R185–R194 (2009).

4. Godefroid, N. & Dahan, K. Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations. Nephrol. Dial. Transplant. 25, 2837–2839 (2010).

5. Hinkes, B. G., Mucha, B., Vlangos, C. N., Gbadegesin, R., Liu, J., Hasselbacher, K. et al. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2). Pediatrics 119, e907–e919 (2007).

Cited by 39 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Roles of myosin 1e and the actin cytoskeleton in kidney functions and familial kidney disease;Cytoskeleton;2024-05-06

2. Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis?;Pediatric Nephrology;2023-09-20

3. Genetic analysis and outcomes of Omani children with steroid‐resistant nephrotic syndrome;Molecular Genetics & Genomic Medicine;2023-05-19

4. Hereditable variants of classical protein tyrosine phosphatase genes: Will they prove innocent or guilty?;Frontiers in Cell and Developmental Biology;2023-01-23

5. Unconventional Myosins from Caenorhabditis elegans as a Probe to Study Human Orthologues;Biomolecules;2022-12-16