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Items: 1 to 20 of 29

1.

Tyrosine and Glutamine-Leucine Are Metabolic Markers of Early-Stage Colorectal Cancers.

Li J, Li J, Wang H, Qi LW, Zhu Y, Lai M.

Gastroenterology. 2019 Jul;157(1):257-259.e5. doi: 10.1053/j.gastro.2019.03.020. Epub 2019 Mar 15. No abstract available.

PMID:
30885779
2.

Metabolomics Study on the Effects of Salvianolic Acid B and Borneol for Treating Cerebral Ischemia in Rats by Ultra-Performance Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry.

Duan W, Wang L, Lv J, Gao K, Lu Y, Qin S, Ma X, Li J, Ge X.

Rejuvenation Res. 2019 Aug;22(4):313-324. doi: 10.1089/rej.2018.2099. Epub 2018 Dec 28.

PMID:
30411995
3.

Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures.

Cassatella D, Howard SR, Acierno JS, Xu C, Papadakis GE, Santoni FA, Dwyer AA, Santini S, Sykiotis GP, Chambion C, Meylan J, Marino L, Favre L, Li J, Liu X, Zhang J, Bouloux PM, Geyter C, Paepe A, Dhillo WS, Ferrara JM, Hauschild M, Lang-Muritano M, Lemke JR, Flück C, Nemeth A, Phan-Hug F, Pignatelli D, Popovic V, Pekic S, Quinton R, Szinnai G, l'Allemand D, Konrad D, Sharif S, Iyidir ÖT, Stevenson BJ, Yang H, Dunkel L, Pitteloud N.

Eur J Endocrinol. 2018 Apr;178(4):377-388. doi: 10.1530/EJE-17-0568. Epub 2018 Feb 1.

4.

Revealing Alzheimer's disease genes spectrum in the whole-genome by machine learning.

Huang X, Liu H, Li X, Guan L, Li J, Tellier LCAM, Yang H, Wang J, Zhang J.

BMC Neurol. 2018 Jan 10;18(1):5. doi: 10.1186/s12883-017-1010-3.

5.

Next-generation sequencing reveals a novel NDP gene mutation in a Chinese family with Norrie disease.

Huang X, Tian M, Li J, Cui L, Li M, Zhang J.

Indian J Ophthalmol. 2017 Nov;65(11):1161-1165. doi: 10.4103/ijo.IJO_442_17.

6.

Implementing targeted region capture sequencing for the clinical detection of Alagille syndrome: An efficient and cost‑effective method.

Huang T, Yang G, Dang X, Ao F, Li J, He Y, Tang Q, He Q.

Mol Med Rep. 2017 Nov;16(5):6876-6881. doi: 10.3892/mmr.2017.7429. Epub 2017 Sep 7.

PMID:
28901437
7.

Screening Hepatotoxic Components in Euodia rutaecarpa by UHPLC-QTOF/MS Based on the Spectrum-Toxicity Relationship.

Liang J, Chen Y, Ren G, Dong W, Shi M, Xiong L, Li J, Dong J, Li F, Yuan J.

Molecules. 2017 Jul 27;22(8). pii: E1264. doi: 10.3390/molecules22081264.

8.

Impulsive stabilization of fractional differential systems.

Xu L, Li J, Ge SS.

ISA Trans. 2017 Sep;70:125-131. doi: 10.1016/j.isatra.2017.06.009. Epub 2017 Jun 20.

PMID:
28641815
9.

Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing.

Guo Y, Hwang LD, Li J, Eades J, Yu CW, Mansfield C, Burdick-Will A, Chang X, Chen Y, Duke FF, Zhang J, Fakharzadeh S, Fennessey P, Keating BJ, Jiang H, Hakonarson H, Reed DR, Preti G.

BMC Med Genet. 2017 Feb 15;18(1):11. doi: 10.1186/s12881-017-0369-8.

10.

Comparative studies on the multi-component pharmacokinetics of Aristolochiae Fructus and honey-fried Aristolochiae Fructus extracts after oral administration in rats.

Yuan J, Ren G, Liang J, Wang CZ, Yan Z, Huang Q, Li J, Chen Y, Tang Y, Liu X, Yuan CS.

BMC Complement Altern Med. 2017 Feb 10;17(1):107. doi: 10.1186/s12906-017-1626-2.

11.

Component analysis and target cell-based neuroactivity screening of Panax ginseng by ultra-performance liquid chromatography coupled with quadrupole-time-of-flight mass spectrometry.

Yuan J, Chen Y, Liang J, Wang CZ, Liu X, Yan Z, Tang Y, Li J, Yuan CS.

J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Dec 1;1038:1-11. doi: 10.1016/j.jchromb.2016.10.014. Epub 2016 Oct 17.

12.

A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese family.

Bu J, He S, Wang L, Li J, Liu J, Zhang X.

Indian J Ophthalmol. 2016 May;64(5):364-8. doi: 10.4103/0301-4738.185597.

13.

Protective effects of ethanol extract from Portulaca oleracea L on dextran sulphate sodium-induced mice ulcerative colitis involving anti-inflammatory and antioxidant.

Yang X, Yan Y, Li J, Tang Z, Sun J, Zhang H, Hao S, Wen A, Liu L.

Am J Transl Res. 2016 May 15;8(5):2138-48. eCollection 2016.

14.

Whole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial Disorder.

Nafisinia M, Guo Y, Dang X, Li J, Chen Y, Zhang J, Lake NJ, Gold WA, Riley LG, Thorburn DR, Keating B, Xu X, Hakonarson H, Christodoulou J.

JIMD Rep. 2017;32:117-124. doi: 10.1007/8904_2016_541. Epub 2016 Jun 26.

15.

An improved hydrothermal diamond anvil cell.

Li J, Bassett WA, Chou IM, Ding X, Li S, Wang X.

Rev Sci Instrum. 2016 May;87(5):053108. doi: 10.1063/1.4947506.

PMID:
27250393
16.

CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids.

Eichler FS, Li J, Guo Y, Caruso PA, Bjonnes AC, Pan J, Booker JK, Lane JM, Tare A, Vlasac I, Hakonarson H, Gusella JF, Zhang J, Keating BJ, Saxena R.

Brain. 2016 Jun;139(Pt 6):1666-72. doi: 10.1093/brain/aww066. Epub 2016 May 5.

17.

Safflower yellow B suppresses HepG2 cell injury induced by oxidative stress through the AKT/Nrf2 pathway.

Ma Z, Li C, Qiao Y, Lu C, Li J, Song W, Sun J, Zhai X, Niu J, Ren Q, Wen A.

Int J Mol Med. 2016 Mar;37(3):603-12. doi: 10.3892/ijmm.2016.2462. Epub 2016 Jan 21.

18.

Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction.

Matera I, Rusmini M, Guo Y, Lerone M, Li J, Zhang J, Di Duca M, Nozza P, Mosconi M, Pini Prato A, Martucciello G, Barabino A, Morandi F, De Giorgio R, Stanghellini V, Ravazzolo R, Devoto M, Hakonarson H, Ceccherini I.

Eur J Hum Genet. 2016 Aug;24(8):1211-5. doi: 10.1038/ejhg.2015.275. Epub 2016 Jan 27.

19.

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Liu Y, Li Y, March ME, Nguyen K, Xu K, Wang F, Guo Y, Keating B, Glessner J, Li J, Ganley TJ, Zhang J, Deardorff MA, Xu X, Hakonarson H.

Hum Genomics. 2016 Jan 18;10:5. doi: 10.1186/s40246-016-0060-8. No abstract available.

20.

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Liu Y, Li Y, March ME, Nguyen K, Xu K, Wang F, Guo Y, Keating B, Glessner J, Li J, Ganley TJ, Zhang J, Deardorff MA, Xu X, Hakonarson H.

Hum Genomics. 2015 Nov 11;9:31. doi: 10.1186/s40246-015-0053-z. Erratum in: Hum Genomics. 2016;10:5. Kenny, Nguyen [corrected to Nguyen, Kenny].

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