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

8,856 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Segawa syndrome caused by TH gene mutation and its mechanism.
Wang Y, Wang C, Liu M, Xu W, Wang S, Yuan F, Luo X, Xu Q, Yin R, Wang A, Guo M, Lin L, Wang C, Cheng H, Liu Z, Zhang Y, Zeng F, Yan J, Chen Y. Wang Y, et al. Among authors: guo m. Front Genet. 2022 Dec 8;13:1004307. doi: 10.3389/fgene.2022.1004307. eCollection 2022. Front Genet. 2022. PMID: 36568392 Free PMC article.
Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency.
Yuan F, Wang S, Wang Y, Wang A, Wang C, Luo X, Xu Q, Yin R, Cheng H, Wang C, Guo M, Zhang Y, Xi J, Yang J, Sun X, Yan J, Zeng F, Chen Y. Yuan F, et al. Among authors: guo m. Stem Cell Res. 2021 May;53:102292. doi: 10.1016/j.scr.2021.102292. Epub 2021 Mar 17. Stem Cell Res. 2021. PMID: 33774333 Free article.
Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene.
Luo X, Wang Y, Yuan F, Lin L, Wang A, Wang C, Guo M, Wang S, Wang C, Xu Q, Yin R, Cheng H, Zhang Y, Liu Z, Xu W, Yan J, Zeng F, Chen Y. Luo X, et al. Among authors: guo m. Stem Cell Res. 2022 Jul;62:102798. doi: 10.1016/j.scr.2022.102798. Epub 2022 May 2. Stem Cell Res. 2022. PMID: 35537242 Free article.
The Study on the Clinical Phenotype and Function of HPRT1 Gene.
Guo M, Chen Y, Lin L, Wang Y, Wang A, Yuan F, Wang C, Wang S, Zhang Y. Guo M, et al. Child Neurol Open. 2022 Jul 19;9:2329048X221108821. doi: 10.1177/2329048X221108821. eCollection 2022 Jan-Dec. Child Neurol Open. 2022. PMID: 35875183 Free PMC article.
8,856 results