Yu T - Search Results

1

SUMO-specific protease 1 regulates mitochondrial biogenesis through PGC-1α.

Cai R, Yu T, Huang C, Xia X, Liu X, Gu J, Xue S, Yeh ET, Cheng J. Cai R, et al. Among authors: yu t. J Biol Chem. 2012 Dec 28;287(53):44464-70. doi: 10.1074/jbc.M112.422626. Epub 2012 Nov 14. J Biol Chem. 2012. PMID: 23152500 Free PMC article.

2

SENP1 regulates IFN-γ-STAT1 signaling through STAT3-SOCS3 negative feedback loop.

Yu T, Zuo Y, Cai R, Huang X, Wu S, Zhang C, Chin YE, Li D, Zhang Z, Xia N, Wang Q, Shen H, Yao X, Zhang ZY, Xue S, Shen L, Cheng J. Yu T, et al. J Mol Cell Biol. 2017 Apr 1;9(2):144-153. doi: 10.1093/jmcb/mjw042. J Mol Cell Biol. 2017. PMID: 27702761 Free PMC article.

3

Further delineation of bone marrow failure syndrome caused by novel compound heterozygous variants of MYSM1.

Li N, Xu Y, Yu T, Yao R, Chen J, Luo C, Wang J. Li N, et al. Among authors: yu t. Gene. 2020 Oct 5;757:144938. doi: 10.1016/j.gene.2020.144938. Epub 2020 Jul 5. Gene. 2020. PMID: 32640305

4

Targeted exome sequencing identified a novel mutation hotspot and a deletion in Chinese primary hypertrophic osteoarthropathy patients.

Chen Y, Li G, Xu Y, Yu T, Zhang Y, Li N, Yao RE, Zhou Y, Wang X, Shen Y, Yin L, Wang J. Chen Y, et al. Among authors: yu t. Clin Chim Acta. 2018 Dec;487:264-269. doi: 10.1016/j.cca.2018.10.005. Epub 2018 Oct 4. Clin Chim Acta. 2018. PMID: 30292630

5

Selective degradation of tRNASer(AGY) is the primary driver for mitochondrial seryl-tRNA synthetase-related disease.

Yu T, Zhang Y, Zheng WQ, Wu S, Li G, Zhang Y, Li N, Yao R, Fang P, Wang J, Zhou XL. Yu T, et al. Nucleic Acids Res. 2022 Nov 11;50(20):11755-11774. doi: 10.1093/nar/gkac1028. Nucleic Acids Res. 2022. PMID: 36350636 Free PMC article.

6

X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism: Identification and in vitro study of a novel small indel in the NR0B1 gene.

Yu T, Wang J, Yu Y, Huang X, Fu Q, Shen Y, Chen F. Yu T, et al. Among authors: yu y. Mol Med Rep. 2016 May;13(5):4039-45. doi: 10.3892/mmr.2016.5006. Epub 2016 Mar 18. Mol Med Rep. 2016. PMID: 27035099

7

Assessment of Rare Genetic Variants to Identify Candidate Modifier Genes Underlying Neurological Manifestations in Neurofibromatosis 1 Patients.

Tang J, Li N, Li G, Wang J, Yu T, Yao R. Tang J, et al. Among authors: yu t. Genes (Basel). 2022 Nov 26;13(12):2218. doi: 10.3390/genes13122218. Genes (Basel). 2022. PMID: 36553485 Free PMC article. Review.

8

[The molecular mechanism of haemophilia B caused by the Arg327Ile novel mutation in FIX gene in vitro expression].

Zhou JW, Dai J, Ding QL, Yu TT, Lu YL, Wang XF, Wang HL. Zhou JW, et al. Zhonghua Xue Ye Xue Za Zhi. 2012 Aug;33(8):642-7. Zhonghua Xue Ye Xue Za Zhi. 2012. PMID: 23134860 Chinese.

9

Zebrafish mafbb Mutants Display Osteoclast Over-Activation and Bone Deformity Resembling Osteolysis in MCTO Patients.

Han Y, Shao W, Zhong D, Ma C, Wei X, Ahmed A, Yu T, Jing W, Jing L. Han Y, et al. Among authors: yu t. Biomolecules. 2021 Mar 23;11(3):480. doi: 10.3390/biom11030480. Biomolecules. 2021. PMID: 33806930 Free PMC article.

10

Novel pathogenic ACAN variants in non-syndromic short stature patients.

Hu X, Gui B, Su J, Li H, Li N, Yu T, Zhang Q, Xu Y, Li G, Chen Y, Qing Y; Chinese Genetic Short Stature Consortium; Li C, Luo J, Fan X, Ding Y, Li J, Wang J, Wang X, Chen S, Shen Y. Hu X, et al. Among authors: yu t. Clin Chim Acta. 2017 Jun;469:126-129. doi: 10.1016/j.cca.2017.04.004. Epub 2017 Apr 7. Clin Chim Acta. 2017. PMID: 28396070

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

10,145 results

Search Page

Filters