Chen H - Search Results

1

Case Report: Identification of a Novel Variant (m.8909T>C) of Human Mitochondrial ATP6 Gene and Its Functional Consequences on Yeast ATP Synthase.

Ding Q, Kucharczyk R, Zhao W, Dautant A, Xu S, Niedzwiecka K, Su X, Giraud MF, Gombeau K, Zhang M, Xie H, Zeng C, Bouhier M, di Rago JP, Liu Z, Tribouillard-Tanvier D, Chen H. Ding Q, et al. Among authors: chen h. Life (Basel). 2020 Sep 22;10(9):215. doi: 10.3390/life10090215. Life (Basel). 2020. PMID: 32971864 Free PMC article.

2

Identification of G8969>A in mitochondrial ATP6 gene that severely compromises ATP synthase function in a patient with IgA nephropathy.

Wen S, Niedzwiecka K, Zhao W, Xu S, Liang S, Zhu X, Xie H, Tribouillard-Tanvier D, Giraud MF, Zeng C, Dautant A, Kucharczyk R, Liu Z, di Rago JP, Chen H. Wen S, et al. Among authors: chen h. Sci Rep. 2016 Nov 4;6:36313. doi: 10.1038/srep36313. Sci Rep. 2016. PMID: 27812026 Free PMC article.

3

Molecular basis of diseases caused by the mtDNA mutation m.8969G>A in the subunit a of ATP synthase.

Skoczeń N, Dautant A, Binko K, Godard F, Bouhier M, Su X, Lasserre JP, Giraud MF, Tribouillard-Tanvier D, Chen H, di Rago JP, Kucharczyk R. Skoczeń N, et al. Among authors: chen h. Biochim Biophys Acta Bioenerg. 2018 Aug;1859(8):602-611. doi: 10.1016/j.bbabio.2018.05.009. Epub 2018 May 18. Biochim Biophys Acta Bioenerg. 2018. PMID: 29778688 Free article.

4

Deregulating mitochondrial metabolite and ion transport has beneficial effects in yeast and human cellular models for NARP syndrome.

Su X, Rak M, Tetaud E, Godard F, Sardin E, Bouhier M, Gombeau K, Caetano-Anollés D, Salin B, Chen H, di Rago JP, Tribouillard-Tanvier D. Su X, et al. Among authors: chen h. Hum Mol Genet. 2019 Nov 15;28(22):3792-3804. doi: 10.1093/hmg/ddz160. Hum Mol Genet. 2019. PMID: 31276579

5

Genetic analysis of the complement pathway in C3 glomerulopathy.

Zhao W, Ding Y, Lu J, Zhang T, Chen D, Zhang H, Zeng C, Liu Z, Chen H. Zhao W, et al. Among authors: chen d, chen h. Nephrol Dial Transplant. 2018 Nov 1;33(11):1919-1927. doi: 10.1093/ndt/gfy033. Nephrol Dial Transplant. 2018. PMID: 29566171

6

Roles of mast cells and monocyte chemoattractant protein-1 in the renal injury of obesity-related glomerulopathy.

Wang X, Chen H, Zhang M, Liu Z. Wang X, et al. Among authors: chen h. Am J Med Sci. 2013 Oct;346(4):295-301. doi: 10.1097/MAJ.0b013e31827559f8. Am J Med Sci. 2013. PMID: 23255244

7

Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic Syndrome.

Zhang T, Lu J, Liang S, Chen D, Zhang H, Zeng C, Liu Z, Chen H. Zhang T, et al. Among authors: chen d, chen h. Am J Nephrol. 2016;43(3):160-9. doi: 10.1159/000445127. Epub 2016 Apr 12. Am J Nephrol. 2016. PMID: 27064621 Free article.

8

A haplotype in CFH family genes confers high risk of rare glomerular nephropathies.

Ding Y, Zhao W, Zhang T, Qiang H, Lu J, Su X, Wen S, Xu F, Zhang M, Zhang H, Zeng C, Liu Z, Chen H. Ding Y, et al. Among authors: chen h. Sci Rep. 2017 Jul 20;7(1):6004. doi: 10.1038/s41598-017-05173-8. Sci Rep. 2017. PMID: 28729648 Free PMC article.

9

Podocyte lesions in patients with obesity-related glomerulopathy.

Chen HM, Liu ZH, Zeng CH, Li SJ, Wang QW, Li LS. Chen HM, et al. Am J Kidney Dis. 2006 Nov;48(5):772-9. doi: 10.1053/j.ajkd.2006.07.025. Am J Kidney Dis. 2006. PMID: 17059996

10

A non-invasive laboratory panel as a diagnostic and prognostic biomarker for thrombotic microangiopathy: development and application in a Chinese cohort study.

Zhang T, Chen H, Liang S, Chen D, Zheng C, Zeng C, Zhang H, Liu Z. Zhang T, et al. Among authors: chen d, chen h. PLoS One. 2014 Nov 5;9(11):e111992. doi: 10.1371/journal.pone.0111992. eCollection 2014. PLoS One. 2014. PMID: 25372665 Free PMC article.

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