Deng SL - Search Results

1

Prognostic effect of high-flux hemodialysis in patients with chronic kidney disease.

Li X, Xu H, Xiao XC, Deng SL, Wang W, Tang R. Li X, et al. Among authors: deng sl. Braz J Med Biol Res. 2016 Jan;49(1):e4708. doi: 10.1590/1414-431X20154708. Epub 2015 Nov 27. Braz J Med Biol Res. 2016. PMID: 26628394 Free PMC article. Review.

2

Genetic analysis of the NEUROG2 gene in patients with Parkinson's disease.

Deng S, Deng H, Le W, Xu H, Yang H, Deng X, Lv H, Xie W, Zhu S, Jankovic J. Deng S, et al. Neurosci Lett. 2010 Jan 14;468(3):195-7. doi: 10.1016/j.neulet.2009.10.078. Epub 2009 Oct 29. Neurosci Lett. 2010. PMID: 19879328

3

The rs1142345 in TPMT Affects the Therapeutic Effect of Traditional Hypoglycemic Herbs in Prediabetes.

Li X, Lian FM, Guo D, Fan L, Tang J, Peng JB, Deng HW, Liu ZQ, Xiao XH, Wang YR, Qu KY, Deng S, Zhong Q, Sha YL, Zhu Y, Bai YJ, Chen XY, Zhou Q, Zhou HH, Tong XL, Zhang W. Li X, et al. Evid Based Complement Alternat Med. 2013;2013:327629. doi: 10.1155/2013/327629. Epub 2013 Apr 29. Evid Based Complement Alternat Med. 2013. PMID: 23737827 Free PMC article.

4

Genetic analysis of the S100B gene in Chinese patients with Parkinson disease.

Guo Y, Yang H, Deng X, Song Z, Yang Z, Xiong W, Yuan L, Xu H, Deng S, Deng H. Guo Y, et al. Neurosci Lett. 2013 Oct 25;555:134-6. doi: 10.1016/j.neulet.2013.09.037. Epub 2013 Sep 25. Neurosci Lett. 2013. PMID: 24076007

5

A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing.

Xiu X, Yuan J, Deng X, Xiao J, Xu H, Zeng Z, Guan L, Xu F, Deng S. Xiu X, et al. Biomed Res Int. 2014;2014:186048. doi: 10.1155/2014/186048. Epub 2014 Jul 6. Biomed Res Int. 2014. PMID: 25110662 Free PMC article.

6

Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

Deng H, Deng S, Xu H, Deng HX, Chen Y, Yuan L, Deng X, Yang S, Guan L, Zhang J, Yuan H, Guo Y. Deng H, et al. PLoS One. 2016 May 25;11(5):e0155180. doi: 10.1371/journal.pone.0155180. eCollection 2016. PLoS One. 2016. PMID: 27223613 Free PMC article.

7

Identification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing.

Deng S, Xu H, Yuan J, Xiao J, Yuan L, Deng X, Guan L, Zhu A, Rong P, Zhang J, Deng H. Deng S, et al. Indian J Med Res. 2016 Aug;144(2):200-205. doi: 10.4103/0971-5916.195026. Indian J Med Res. 2016. PMID: 27934798 Free PMC article.

8

A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus.

Wu S, Deng S, Song Z, Xu H, Yang Z, Liu X, Qi L, Deng H, Yuan L. Wu S, et al. J Mol Neurosci. 2019 Mar;67(3):418-423. doi: 10.1007/s12031-018-1245-5. Epub 2019 Jan 8. J Mol Neurosci. 2019. PMID: 30618027

9

Hemizygous F8 p.G201E mutation identified in a Chinese family with haemophilia A.

Wang P, Yuan L, Chen H, Xu H, Yang Z, Deng S, Deng H. Wang P, et al. J Chin Med Assoc. 2019 Jan;82(1):25-29. doi: 10.1097/JCMA.0000000000000002. J Chin Med Assoc. 2019. PMID: 30839399

10

Polytropic Influence of TRIB3 rs2295490 Genetic Polymorphism on Response to Antihypertensive Agents in Patients With Essential Hypertension.

Zhou J, He F, Sun B, Liu R, Gao Y, Ren H, Shu Y, Chen X, Liu Z, Zhou H, Deng S, Xu H, Li J, Xu L, Zhang W. Zhou J, et al. Front Pharmacol. 2019 Mar 27;10:236. doi: 10.3389/fphar.2019.00236. eCollection 2019. Front Pharmacol. 2019. PMID: 30971918 Free PMC article.

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