Xu Y - Search Results

1

Loss of astrocyte polarization in the tg-ArcSwe mouse model of Alzheimer's disease.

Yang J, Lunde LK, Nuntagij P, Oguchi T, Camassa LM, Nilsson LN, Lannfelt L, Xu Y, Amiry-Moghaddam M, Ottersen OP, Torp R. Yang J, et al. Among authors: xu y. J Alzheimers Dis. 2011;27(4):711-22. doi: 10.3233/JAD-2011-110725. J Alzheimers Dis. 2011. PMID: 21891870

2

BDNF gene polymorphisms are associated with Alzheimer's disease-related depression and antidepressant response.

Zhang L, Fang Y, Zeng Z, Lian Y, Wei J, Zhu H, Jia Y, Zhao X, Xu Y. Zhang L, et al. Among authors: xu y. J Alzheimers Dis. 2011;26(3):523-30. doi: 10.3233/JAD-2011-110113. J Alzheimers Dis. 2011. PMID: 21677379

3

Lentivirus-mediated APP695-RNAi reduces apoptosis in APP transgenic mouse neurons.

Zhao X, Wen L, Li G, Ba Q, Cui Y, Han Z, Jia Y, Xu Y. Zhao X, et al. Among authors: xu y. Neuroreport. 2011 Nov 16;22(16):804-8. doi: 10.1097/WNR.0b013e32834b6c92. Neuroreport. 2011. PMID: 21975314

4

Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations.

Mao CY, Yang J, Zhang SY, Luo HY, Song B, Liu YT, Wu J, Sun SL, Yang ZH, Du P, Wang YH, Shi CH, Xu YM. Mao CY, et al. Int J Neurosci. 2016 Dec;126(12):1071-6. doi: 10.3109/00207454.2015.1118628. Epub 2015 Dec 7. Int J Neurosci. 2016. PMID: 26643368

5

CHCHD2 gene mutations in familial and sporadic Parkinson's disease.

Shi CH, Mao CY, Zhang SY, Yang J, Song B, Wu P, Zuo CT, Liu YT, Ji Y, Yang ZH, Wu J, Zhuang ZP, Xu YM. Shi CH, et al. Among authors: xu ym. Neurobiol Aging. 2016 Feb;38:217.e9-217.e13. doi: 10.1016/j.neurobiolaging.2015.10.040. Epub 2015 Nov 6. Neurobiol Aging. 2016. PMID: 26705026

6

MC1R variants in Chinese Han patients with sporadic Parkinson's disease.

Shi CH, Wang H, Mao CY, Yang J, Song B, Liu YT, Yang ZH, Luo HY, Zhang SY, Wu J, Xu YM. Shi CH, et al. Neurobiol Aging. 2016 Jun;42:217.e5-6. doi: 10.1016/j.neurobiolaging.2016.02.026. Epub 2016 Mar 3. Neurobiol Aging. 2016. PMID: 27084066

7

Pseudo-dominant inheritance of a novel double GLA mutation associated with Fabry disease mimicking familial episodic pain.

Mao C, Luo H, Yang J, Qin J, Wang H, Song B, Sun S, Zhuang Z, Shi C, Xu Y. Mao C, et al. Among authors: xu y. Am J Med Genet A. 2016 Nov;170(11):3051-3053. doi: 10.1002/ajmg.a.37833. Epub 2016 Aug 17. Am J Med Genet A. 2016. PMID: 27531472 No abstract available.

8

Brain glucose metabolism changes in Parkinson's disease patients with CHCHD2 mutation based on (18)F-FDG PET imaging.

Mao CY, Wu P, Zhang SY, Yang J, Liu YT, Zuo CT, Zhuang ZP, Shi CH, Xu YM. Mao CY, et al. J Neurol Sci. 2016 Oct 15;369:303-305. doi: 10.1016/j.jns.2016.08.042. Epub 2016 Aug 21. J Neurol Sci. 2016. PMID: 27653913 No abstract available.

9

DNAJC6 mutations are not common causes of early onset Parkinson's disease in Chinese Han population.

Shi C, Li F, Yang J, Zhang S, Mao C, Wang H, Shi M, Liu Y, Song B, Xu Y. Shi C, et al. Among authors: xu y. Neurosci Lett. 2016 Nov 10;634:60-62. doi: 10.1016/j.neulet.2016.09.044. Epub 2016 Sep 26. Neurosci Lett. 2016. PMID: 27687717

10

SMPD1 variants in Chinese Han patients with sporadic Parkinson's disease.

Mao CY, Yang J, Wang H, Zhang SY, Yang ZH, Luo HY, Li F, Shi M, Liu YT, Zhuang ZP, Du P, Wang YH, Shi CH, Xu YM. Mao CY, et al. Parkinsonism Relat Disord. 2017 Jan;34:59-61. doi: 10.1016/j.parkreldis.2016.10.014. Epub 2016 Oct 19. Parkinsonism Relat Disord. 2017. PMID: 27814975

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