Li T - Search Results

1

Serum Metabolic Profiling Analysis of Gout Patients Treated with Traditional Chinese Medicine Tongfengtai Granules Based on Gas Chromatography-Mass Spectrometry.

Zhang J, Pan H, Xie J, Wang J, Wang R, Qiu X, Zhong L, Li T, Xiao Y, Xiao M, Zhang Y, Jia E, Jiang Y, Wang B. Zhang J, et al. Among authors: li t. Evid Based Complement Alternat Med. 2020 Apr 26;2020:7404983. doi: 10.1155/2020/7404983. eCollection 2020. Evid Based Complement Alternat Med. 2020. PMID: 32419822 Free PMC article.

2

A novel variation of GDF3 in Chinese Han children with a broad phenotypic spectrum of non-syndromic CHDs.

Xiao J, Kang G, Wang J, Li T, Chen J, Wang J, Li W, Wang B. Xiao J, et al. Among authors: li t, li w. Cardiol Young. 2015 Oct;25(7):1263-7. doi: 10.1017/S1047951114002170. Epub 2014 Nov 5. Cardiol Young. 2015. PMID: 25372014

3

Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy.

Chen H, Zhou X, Wang J, Wang X, Liu L, Wu S, Li T, Chen S, Yang J, Sham PC, Zhu G, Zhang X, Wang B. Chen H, et al. Among authors: li t. Sci Rep. 2016 May 23;6:26362. doi: 10.1038/srep26362. Sci Rep. 2016. PMID: 27212199 Free PMC article.

4

Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.

Wang B, Li L, Zhu Y, Zhang W, Wang X, Chen B, Li T, Pan H, Wang J, Kee K, Cao Y. Wang B, et al. Among authors: li t, li l. Hum Reprod. 2017 Oct 1;32(10):2138-2146. doi: 10.1093/humrep/dex263. Hum Reprod. 2017. PMID: 28938739

5

A novel homozygous mutation of bone morphogenetic protein 15 identified in a consanguineous marriage family with primary ovarian insufficiency.

Zhang W, Wang J, Wang X, Li L, Pan H, Chen B, Zhu Y, Li T, Cao Y, Wang B. Zhang W, et al. Among authors: li t, li l. Reprod Biomed Online. 2018 Feb;36(2):206-209. doi: 10.1016/j.rbmo.2017.10.104. Epub 2017 Oct 26. Reprod Biomed Online. 2018. PMID: 29169851

6

Retrospective investigation of retinoblastoma in Chinese patients.

Jin L, Zhang W, Pan H, Li T, Liu B, Zhao J, Wang B. Jin L, et al. Among authors: li t. Oncotarget. 2017 May 23;8(65):108492-108497. doi: 10.18632/oncotarget.18174. eCollection 2017 Dec 12. Oncotarget. 2017. PMID: 29312545 Free PMC article.

7

Identification of LBX2 as a novel causal gene of atrial septal defect.

Wang J, Luo J, Chen Q, Wang X, He J, Zhang W, Yin Z, Zheng F, Pan H, Li T, Lou Q, Wang B. Wang J, et al. Among authors: li t. Int J Cardiol. 2018 Aug 15;265:188-194. doi: 10.1016/j.ijcard.2018.04.038. Epub 2018 Apr 11. Int J Cardiol. 2018. PMID: 29669692

8

Novel mutation in SP2 in a Chinese pedigree with Neural tube defects.

Liu BH, Wang J, Li CM, Qi L, Song YH, Pan H, Li TY, Wang BB. Liu BH, et al. CNS Neurosci Ther. 2018 Oct;24(10):978-980. doi: 10.1111/cns.12988. Epub 2018 May 31. CNS Neurosci Ther. 2018. PMID: 29855149 Free PMC article. No abstract available.

9

Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency.

Chen B, Li L, Wang J, Li T, Pan H, Liu B, Zhou Y, Cao Y, Wang B. Chen B, et al. Among authors: li t, li l. J Ovarian Res. 2018 Jun 18;11(1):48. doi: 10.1186/s13048-018-0413-0. J Ovarian Res. 2018. PMID: 29914564 Free PMC article.

10

Application of a deep convolutional neural network in the diagnosis of neonatal ocular fundus hemorrhage.

Wang B, Xiao L, Liu Y, Wang J, Liu B, Li T, Ma X, Zhao Y. Wang B, et al. Among authors: li t. Biosci Rep. 2018 Dec 7;38(6):BSR20180497. doi: 10.1042/BSR20180497. Print 2018 Dec 21. Biosci Rep. 2018. PMID: 30333258 Free PMC article.

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