Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

22,451 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Loss of function of CMPK2 causes mitochondria deficiency and brain calcification.
Zhao M, Su HZ, Zeng YH, Sun Y, Guo XX, Li YL, Wang C, Zhao ZY, Huang XJ, Lin KJ, Ye ZL, Lin BW, Hong S, Zheng J, Liu YB, Yao XP, Yang D, Lu YQ, Chen HZ, Zuo E, Yang G, Wang HT, Huang CW, Lin XH, Cen Z, Lai LL, Zhang YK, Li X, Lai T, Lin J, Zuo DD, Lin MT, Liou CW, Kong QX, Yan CZ, Xiong ZQ, Wang N, Luo W, Zhao CP, Cheng X, Chen WJ. Zhao M, et al. Among authors: yang d, yang g. Cell Discov. 2022 Nov 29;8(1):128. doi: 10.1038/s41421-022-00475-2. Cell Discov. 2022. PMID: 36443312 Free PMC article.
LRP10 in autosomal-dominant Parkinson's disease.
Chen Y, Cen Z, Zheng X, Pan Q, Chen X, Zhu L, Chen S, Wu H, Xie F, Wang H, Yang D, Wang L, Zhang B, Luo W. Chen Y, et al. Among authors: yang d. Mov Disord. 2019 Jun;34(6):912-916. doi: 10.1002/mds.27693. Epub 2019 Apr 9. Mov Disord. 2019. PMID: 30964957
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from China.
Chen S, Cen Z, Fu F, Chen Y, Chen X, Yang D, Wang H, Wu H, Zheng X, Xie F, Ouyang Z, Tang W, Zhang S, Yin L, Zhang Y, Meng P, Zhu X, Zhang H, Jiang F, Zhang K, He J, Zhang D, Ming H, Song D, Zhou Z, Luo Y, Gu Q, Su Y, Wu X, Tang H, Wu C, Chen W, Liu JY, Luo W; Chinese PFBC Study Group. Chen S, et al. Among authors: yang d. Parkinsonism Relat Disord. 2019 Jul;64:211-219. doi: 10.1016/j.parkreldis.2019.04.009. Epub 2019 Apr 11. Parkinsonism Relat Disord. 2019. PMID: 31003906
Intronic (TTTGA)n insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy.
Cen Z, Chen Y, Yang D, Zhu Q, Chen S, Chen X, Wang B, Xie F, Ouyang Z, Jiang Z, Fu A, Hu B, Yin H, Qiu X, Yu F, Du X, Hao W, Liu Y, Wang H, Wang L, Yu X, Xiao Y, Liu C, Xiao J, Zhou Y, Yang W, Zhang B, Luo W. Cen Z, et al. Among authors: yang d, yang w. Mov Disord. 2019 Oct;34(10):1571-1576. doi: 10.1002/mds.27832. Epub 2019 Sep 4. Mov Disord. 2019. PMID: 31483537
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcification.
Cen Z, Chen Y, Chen S, Wang H, Yang D, Zhang H, Wu H, Wang L, Tang S, Ye J, Shen J, Wang H, Fu F, Chen X, Xie F, Liu P, Xu X, Cao J, Cai P, Pan Q, Li J, Yang W, Shan PF, Li Y, Liu JY, Zhang B, Luo W. Cen Z, et al. Among authors: yang d, yang w. Brain. 2020 Feb 1;143(2):491-502. doi: 10.1093/brain/awz392. Brain. 2020. PMID: 31851307
MYORG Mutation Heterozygosity Is Associated With Brain Calcification.
Chen Y, Cen Z, Chen X, Wang H, Chen S, Yang D, Fu F, Wang L, Liu P, Wu H, Zheng X, Xie F, Ouyang Z, Zhang Y, Zhou Y, Huang X, Wang F, Huang G, An H, Liang Y, Hong W, Wang A, Huang S, Chen W, Yin L, Yang Y, Huang H, Zeng R, Zhao N, Jiang B, Zhang B, Luo W; Chinese PFBC Study Group. Chen Y, et al. Among authors: yang d, yang y. Mov Disord. 2020 Apr;35(4):679-686. doi: 10.1002/mds.27973. Epub 2020 Jan 17. Mov Disord. 2020. PMID: 31951047
Genetic profile of Chinese patients with Charcot-Marie-Tooth disease.
Ouyang ZY, Chen Y, Qin DQ, Cen ZD, Zheng XS, Xie F, Chen S, Wang HT, Yang DH, Chen XH, Wang LB, Zhang BR, Luo W. Ouyang ZY, et al. Chin Med J (Engl). 2020 Nov 5;133(21):2633-2634. doi: 10.1097/CM9.0000000000001095. Chin Med J (Engl). 2020. PMID: 32941234 Free PMC article. No abstract available.
22,451 results
You have reached the last available page of results. Please see the User Guide for more information.