Sun L - Search Results

1

Transplantation for infantile nephronophthisis with loss-of-function mutation in NPHP3: Lesson from a case.

Zhang H, Luo J, Liu L, Li J, Fu Q, Chen W, Yang S, Shang W, Wang H, Deng R, Sun L, Zhu X, Wang C. Zhang H, et al. Among authors: sun l. Pediatr Transplant. 2018 Jun 4:e13233. doi: 10.1111/petr.13233. Online ahead of print. Pediatr Transplant. 2018. PMID: 29869359

2

Clinical and pathological characteristics of 5 children with HBV surface antigen (HBsAg)-negative hepatitis B virus-associated glomerulonephritis.

Liu T, Yang S, Yue Z, Kuang Y, Guan W, Sun L. Liu T, et al. Among authors: sun l. J Clin Virol. 2015 May;66:1-5. doi: 10.1016/j.jcv.2015.02.012. Epub 2015 Feb 20. J Clin Virol. 2015. PMID: 25866326

3

High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients.

Sun L, Tong H, Wang H, Yue Z, Liu T, Lin H, Li J, Wang C. Sun L, et al. Nephrology (Carlton). 2016 Mar;21(3):209-16. doi: 10.1111/nep.12563. Nephrology (Carlton). 2016. PMID: 26184788

4

Two Chinese nephronophthisis pedigrees harbored a compound heterozygous deletion with a point mutation in NPHP1.

Chen H, Lin H, Yue Z, Wang H, Yang J, Sun L. Chen H, et al. Among authors: sun l. Int J Mol Epidemiol Genet. 2019 Aug 15;10(4):53-58. eCollection 2019. Int J Mol Epidemiol Genet. 2019. PMID: 31523374 Free PMC article.

5

Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis.

Yue Z, Lin H, Li M, Wang H, Liu T, Hu M, Chen H, Tong H, Sun L. Yue Z, et al. Among authors: sun l. Clin Chim Acta. 2020 Jul;506:136-144. doi: 10.1016/j.cca.2020.03.015. Epub 2020 Mar 12. Clin Chim Acta. 2020. PMID: 32173348

6

Novel mutation of TCIRG1 and clinical pictures of two infantile malignant osteopetrosis patients.

Yuan P, Yue Z, Sun L, Huang W, Hu B, Yang Z, Hu Y, Xiao H, Shi H, Zhou Q, Wang Y. Yuan P, et al. Among authors: sun l. J Bone Miner Metab. 2011 Mar;29(2):251-6. doi: 10.1007/s00774-010-0228-6. Epub 2010 Nov 2. J Bone Miner Metab. 2011. PMID: 21042819

7

COQ2 mutation associated isolated nephropathy in two siblings from a Chinese pedigree.

Li M, Yue Z, Lin H, Wang H, Chen H, Sun L. Li M, et al. Among authors: sun l. Ren Fail. 2021 Dec;43(1):97-101. doi: 10.1080/0886022X.2020.1864402. Ren Fail. 2021. PMID: 33397173 Free PMC article.

8

Clinical features and mutation of NPHP5 in two Chinese siblings with Senior-Løken syndrome.

Tong H, Yue Z, Sun L, Chen H, Wang W, Wang H. Tong H, et al. Among authors: sun l. Nephrology (Carlton). 2013 Dec;18(12):838-42. doi: 10.1111/nep.12156. Nephrology (Carlton). 2013. PMID: 24674142

9

Novel mutation of OCRL1 in Lowe syndrome.

Liu T, Yue Z, Wang H, Tong H, Sun L. Liu T, et al. Among authors: sun l. Indian J Pediatr. 2015 Jan;82(1):89-92. doi: 10.1007/s12098-014-1581-6. Epub 2014 Oct 10. Indian J Pediatr. 2015. PMID: 25297642

10

An Nphp1 knockout mouse model targeting exon 2-20 demonstrates characteristic phenotypes of human nephronophthisis.

Li D, Hu M, Chen H, Wu X, Wei X, Lin H, Gao X, Wang H, Li M, Ong ACM, Yue Z, Sun L. Li D, et al. Among authors: sun l. Hum Mol Genet. 2021 Dec 27;31(2):232-243. doi: 10.1093/hmg/ddab239. Hum Mol Genet. 2021. PMID: 34415307 Free article.

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