Yin CH - Search Results

1

SEC24D depletion induces osteogenic differentiation deficiency by inactivating the ATF6/TGF-β/Runx2 regulatory loop.

Zhang J, Yang K, Chen WQ, Sun DL, Hu HY, Li Q, Yan YS, Li YZ, Yin CH, Guo Q. Zhang J, et al. Among authors: yin ch. Commun Biol. 2025 May 15;8(1):758. doi: 10.1038/s42003-025-08175-9. Commun Biol. 2025. PMID: 40374976 Free PMC article.

2

[Progress of research on clinical use of non-invasive prenatal screening for special groups of pregnant women].

Yan Y, Wang Y, Liu Y, Yin C. Yan Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jul 10;38(7):694-698. doi: 10.3760/cma.j.cn511374-20201103-00772. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34247381 Chinese.

3

Identification of novel deep intronic PAH gene variants in patients diagnosed with phenylketonuria.

Jin X, Yan Y, Zhang C, Tai Y, An L, Yu X, Zhang L, Hao S, Cao X, Yin C, Ma X. Jin X, et al. Hum Mutat. 2022 Jan;43(1):56-66. doi: 10.1002/humu.24292. Epub 2021 Nov 16. Hum Mutat. 2022. PMID: 34747549

4

Metabolic and biophysical study of the MFN2^Ile213Thr mutant causing Hereditary Motor and Sensory Neuropathy (HMSN).

Yang K, Hu HY, Zhang J, Yan YS, Chen WQ, Liu Y, Sun YQ, Guo Q, Yin CH. Yang K, et al. Among authors: yin ch. Am J Transl Res. 2021 Oct 15;13(10):11501-11512. eCollection 2021. Am J Transl Res. 2021. PMID: 34786076 Free PMC article.

5

Investigation of a Novel NTRK1 Variation Causing Congenital Insensitivity to Pain With Anhidrosis.

Yang K, Xu YC, Hu HY, Li YZ, Li Q, Luan YY, Liu Y, Sun YQ, Feng ZK, Yan YS, Yin CH. Yang K, et al. Among authors: yin ch. Front Genet. 2021 Dec 6;12:763467. doi: 10.3389/fgene.2021.763467. eCollection 2021. Front Genet. 2021. PMID: 34938316 Free PMC article.

6

Protective Effect of Maternal First-Trimester Low Body Mass Index Against Macrosomia: A 10-Year Cross-Sectional Study.

Sun Y, Zhang M, Liu R, Wang J, Yang K, Wu Q, Yue W, Yin C. Sun Y, et al. Front Endocrinol (Lausanne). 2022 Feb 10;13:805636. doi: 10.3389/fendo.2022.805636. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35222271 Free PMC article.

7

Investigation of an inherited PCGF2: p.Pro65Leu mutation causing Turnpenny-Fry syndrome.

Qi KY, Shen M, Yang K, Yan YS, Wu J, Wang YP, Yin CH. Qi KY, et al. Among authors: yin ch. Am J Transl Res. 2022 Aug 15;14(8):5591-5597. eCollection 2022. Am J Transl Res. 2022. PMID: 36105049 Free PMC article.

8

Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta.

Yang K, Liu Y, Wu J, Zhang J, Hu HY, Yan YS, Chen WQ, Yang SF, Sun LJ, Sun YQ, Wu QQ, Yin CH. Yang K, et al. Among authors: yin ch. Genes (Basel). 2022 Sep 2;13(9):1578. doi: 10.3390/genes13091578. Genes (Basel). 2022. PMID: 36140746 Free PMC article.

9

Potential impact of ambient temperature on maternal blood pressure and hypertensive disorders of pregnancy: A nationwide multicenter study based on the China birth cohort.

Sun Y, Zhang M, Chen S, Zhang W, Zhang Y, Su S, Zhang E, Sun L, Yang K, Wang J, Yue W, Wu Q, Liu R, Yin C. Sun Y, et al. Environ Res. 2023 Jun 15;227:115733. doi: 10.1016/j.envres.2023.115733. Epub 2023 Mar 23. Environ Res. 2023. PMID: 36965789 Free article.

10

Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population.

Yang K, Fu LM, Chu XY, Zhang J, Chen WQ, Yan YS, Wang YP, Zhang DL, Yin CH, Guo Q. Yang K, et al. Among authors: yin ch. Mol Genet Genomic Med. 2023 Jul;11(7):e2186. doi: 10.1002/mgg3.2186. Epub 2023 Apr 30. Mol Genet Genomic Med. 2023. PMID: 37120754 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

365 results

Search Page

Filters