Lang Y - Search Results

1

Minigene splicing assays reveal new insights into exonic variants of the SLC12A3 gene in Gitelman syndrome.

Shi X, Wang H, Zhang R, Liu Z, Guo W, Wang S, Liu X, Lang Y, Bottillo I, Dong B, Shao L. Shi X, et al. Among authors: lang y. Mol Genet Genomic Med. 2023 Apr;11(4):e2128. doi: 10.1002/mgg3.2128. Epub 2023 Jan 3. Mol Genet Genomic Med. 2023. PMID: 36597580 Free PMC article.

2

A novel SLC12A3 splicing mutation skipping of two exons and preliminary screening for alternative splice variants in human kidney.

Shao L, Liu L, Miao Z, Ren H, Wang W, Lang Y, Yue S, Chen N. Shao L, et al. Among authors: lang y. Am J Nephrol. 2008;28(6):900-7. doi: 10.1159/000141932. Epub 2008 Jun 26. Am J Nephrol. 2008. PMID: 18580052

3

Coexistence of normotensive primary aldosteronism in two patients with Gitelman's syndrome and novel thiazide-sensitive Na-Cl cotransporter mutations.

Miao Z, Gao Y, Bindels RJ, Yu W, Lang Y, Chen N, Ren H, Sun F, Li Y, Wang X, Shao L. Miao Z, et al. Among authors: lang y. Eur J Endocrinol. 2009 Aug;161(2):275-83. doi: 10.1530/EJE-09-0271. Epub 2009 May 18. Eur J Endocrinol. 2009. PMID: 19451210 Free article.

4

A novel SLC4A1 variant in an autosomal dominant distal renal tubular acidosis family with a severe phenotype.

Shao L, Xu Y, Dong Q, Lang Y, Yue S, Miao Z. Shao L, et al. Among authors: lang y. Endocrine. 2010 Jun;37(3):473-8. doi: 10.1007/s12020-010-9340-6. Epub 2010 Apr 17. Endocrine. 2010. PMID: 20960171

5

High-frequency variant p.T60M in NaCl cotransporter and blood pressure variability in Han Chinese.

Shao L, Lang Y, Wang Y, Gao Y, Zhang W, Niu H, Liu S, Chen N. Shao L, et al. Among authors: lang y. Am J Nephrol. 2012;35(6):515-9. doi: 10.1159/000339165. Epub 2012 May 23. Am J Nephrol. 2012. PMID: 22627394

6

Percutaneous Transluminal Revascularization following an Angiotensin Receptor Blocker: Successful Treatment for Flash Pulmonary Edema and Hyponatremic Hypertensive Syndrome.

Shao L, Gao Y, Xu Y, Lang Y. Shao L, et al. Among authors: lang y. Cardiorenal Med. 2012 Aug;2(3):184-189. doi: 10.1159/000339297. Epub 2012 Jun 14. Cardiorenal Med. 2012. PMID: 22969774 Free PMC article.

7

Mutation analysis and audiologic assessment in six Chinese children with primary distal renal tubular acidosis.

Gao Y, Xu Y, Li Q, Lang Y, Dong Q, Shao L. Gao Y, et al. Among authors: lang y. Ren Fail. 2014 Sep;36(8):1226-32. doi: 10.3109/0886022X.2014.930332. Epub 2014 Jun 30. Ren Fail. 2014. PMID: 24975934 Free article.

8

Two Novel HOGA1 Splicing Mutations Identified in a Chinese Patient with Primary Hyperoxaluria Type 3.

Wang X, Zhao X, Wang X, Yao J, Zhang F, Lang Y, Tuffery-Giraud S, Bottillo I, Shao L. Wang X, et al. Among authors: lang y. Am J Nephrol. 2015;42(1):78-84. doi: 10.1159/000439232. Am J Nephrol. 2015. PMID: 26340091

9

Genotype/Phenotype Analysis in 67 Chinese Patients with Gitelman's Syndrome.

Liu T, Wang C, Lu J, Zhao X, Lang Y, Shao L. Liu T, et al. Among authors: lang y. Am J Nephrol. 2016;44(2):159-68. doi: 10.1159/000448694. Epub 2016 Aug 17. Am J Nephrol. 2016. PMID: 27529443

10

Two novel AGXT mutations identified in primary hyperoxaluria type-1 and distinct morphological and structural difference in kidney stones.

Wang C, Lu J, Lang Y, Liu T, Wang X, Zhao X, Shao L. Wang C, et al. Among authors: lang y. Sci Rep. 2016 Sep 20;6:33652. doi: 10.1038/srep33652. Sci Rep. 2016. PMID: 27644547 Free PMC article.

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