Lin H - Search Results

1

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: lin h. 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

2

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. Among authors: lin h. Nephrology (Carlton). 2016 Mar;21(3):209-16. doi: 10.1111/nep.12563. Nephrology (Carlton). 2016. PMID: 26184788

3

WT1 mutation-associated nephropathy: a single-center experience .

Yue Z, Wang H, Lin H, Yang J, Liu T, Liu Y, Chen H, Sun L. Yue Z, et al. Among authors: lin h. Clin Nephrol. 2017 May;87 (2017)(5):245-254. doi: 10.5414/CN108948. Clin Nephrol. 2017. PMID: 28257282

4

[Clinical and pathological features and the misdiagnosis of childhood Alport syndrome: a retrospective analysis of 91 cases].

Chen YZ, Sun LZ, Wang HY, Jiang XY, Mo Y, Yue ZH, Chen HM, Liu T, Lin HR. Chen YZ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Apr;19(4):371-375. doi: 10.7499/j.issn.1008-8830.2017.04.001. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28407818 Free PMC article. Chinese.

5

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: lin h. 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.

6

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: lin h. Ren Fail. 2021 Dec;43(1):97-101. doi: 10.1080/0886022X.2020.1864402. Ren Fail. 2021. PMID: 33397173 Free PMC article.

7

Cyclosporine A relieved proteinuria and hypoproteinemia in DGKE nephropathy.

Fu W, Li M, Lin H, Xu Y, Han W, Chen H, Sun L. Fu W, et al. Among authors: lin h. Clin Chim Acta. 2021 Jul;518:78-82. doi: 10.1016/j.cca.2021.02.021. Epub 2021 Mar 17. Clin Chim Acta. 2021. PMID: 33741360

8

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: lin h. Hum Mol Genet. 2021 Dec 27;31(2):232-243. doi: 10.1093/hmg/ddab239. Hum Mol Genet. 2021. PMID: 34415307 Free article.

9

Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cells.

Wu X, Wang H, Chen H, Lin H, Li M, Yue Z, Sun L. Wu X, et al. Among authors: lin h. Biochem Biophys Res Commun. 2021 Dec 10;582:57-63. doi: 10.1016/j.bbrc.2021.10.037. Epub 2021 Oct 18. Biochem Biophys Res Commun. 2021. PMID: 34689106

10

A novel ITGA3 homozygous splice mutation in an ILNEB syndrome child with slow progression.

Liu Y, Yue Z, Wang H, Li M, Wu X, Lin H, Han W, Lan S, Sun L. Liu Y, et al. Among authors: lin h. Clin Chim Acta. 2021 Dec;523:430-436. doi: 10.1016/j.cca.2021.10.027. Epub 2021 Oct 28. Clin Chim Acta. 2021. PMID: 34751145

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

32,497 results

Search Page

Filters