Ma T - Search Results

1

Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy.

Du S, Zeng S, Song L, Ma H, Chen R, Luo J, Wang X, Ma T, Xu X, Sun H, Yi P, Guo J, Huang Y, Liu M, Wang T, Liao WP, Zhang L, Liu JY, Tang B. Du S, et al. Among authors: ma t, ma h. Sci China Life Sci. 2023 Sep;66(9):2152-2166. doi: 10.1007/s11427-022-2313-1. Epub 2023 Apr 12. Sci China Life Sci. 2023. PMID: 37071290

2

A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate.

Du S, Yang Y, Yi P, Luo J, Liu T, Chen R, Liu CJ, Ma T, Li Y, Wang C, Weng J, Liu M, Zhang L, Yang B, Zeng X, Liu JY. Du S, et al. Among authors: ma t. Genet Test Mol Biomarkers. 2019 Nov;23(11):759-765. doi: 10.1089/gtmb.2019.0092. Epub 2019 Oct 22. Genet Test Mol Biomarkers. 2019. PMID: 31638429

3

Severe brain calcification and migraine headache caused by SLC20A2 and PDGFRB heterozygous mutations in a five-year-old Chinese girl.

Sun H, Cao Z, Gao R, Li Y, Chen R, Du S, Ma T, Wang J, Xu X, Liu JY. Sun H, et al. Among authors: ma t. Mol Genet Genomic Med. 2021 May;9(5):e1670. doi: 10.1002/mgg3.1670. Epub 2021 Apr 1. Mol Genet Genomic Med. 2021. PMID: 33793087 Free PMC article.

4

Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9.

Ma T, Li L, Chen R, Yang L, Sun H, Du S, Xu X, Cao Z, Zhang X, Zhang L, Shi X, Liu JY. Ma T, et al. Pain. 2022 Apr 1;163(4):753-764. doi: 10.1097/j.pain.0000000000002421. Pain. 2022. PMID: 34326297 Free PMC article.

5

Mechanisms of PiT2-loop7 Missense Mutations Induced Pi Dyshomeostasis.

Sun H, Xu X, Luo J, Ma T, Cui J, Liu M, Xiong B, Zhu S, Liu JY. Sun H, et al. Among authors: ma t. Neurosci Bull. 2023 Jan;39(1):57-68. doi: 10.1007/s12264-022-00893-y. Epub 2022 Jun 17. Neurosci Bull. 2023. PMID: 35713844 Free PMC article.

6

Impaired fertility in 4930590J08Rik mutant male mice is associated with defective sperm energy metabolism.

Chen R, Ma T, Du S, Luo J, Zhang H, Xu X, Cao Z, Yuan Z, Sun H, Liu M, Xiong B, Shi Q, Liu JY. Chen R, et al. Among authors: ma t. FASEB J. 2022 Dec;36(12):e22634. doi: 10.1096/fj.202200805RR. FASEB J. 2022. PMID: 36331537

7

Murine Placental-Fetal Phosphate Dyshomeostasis Caused by an Xpr1 Deficiency Accelerates Placental Calcification and Restricts Fetal Growth in Late Gestation.

Xu X, Li X, Sun H, Cao Z, Gao R, Niu T, Wang Y, Ma T, Chen R, Wang C, Yang Z, Liu JY. Xu X, et al. Among authors: ma t. J Bone Miner Res. 2020 Jan;35(1):116-129. doi: 10.1002/jbmr.3866. Epub 2019 Oct 25. J Bone Miner Res. 2020. PMID: 31498925 Free article.

8

Germline Mutation of PLCD1 Contributes to Human Multiple Pilomatricomas through Protein Kinase D/Extracellular Signal-Regulated Kinase1/2 Cascade and TRPV6.

Liu K, Luo J, Ma T, Fang M, Xu Z, Wang L, Zhang XY, Wen J, Liu C, Cao Y, Li X, Zhang L, Guo A, Wang N, Yi P, Liu JY. Liu K, et al. Among authors: ma t. J Invest Dermatol. 2021 Mar;141(3):533-544. doi: 10.1016/j.jid.2020.05.121. Epub 2020 Aug 11. J Invest Dermatol. 2021. PMID: 32795530 Free article.

9

Novel SCN9A missense mutations contribute to congenital insensitivity to pain: Unexpected correlation between electrophysiological characterization and clinical phenotype.

Sun J, Li L, Yang L, Duan G, Ma T, Li N, Liu Y, Yao J, Liu JY, Zhang X. Sun J, et al. Among authors: ma t. Mol Pain. 2020 Jan-Dec;16:1744806920923881. doi: 10.1177/1744806920923881. Mol Pain. 2020. PMID: 32420800 Free PMC article.

10

Alcohol-aggravated episodic pain in humans with SCN11A mutation and ALDH2 polymorphism.

Yang L, Li L, Tang H, Ma T, Li Y, Zhang X, Shi X, Liu JY. Yang L, et al. Among authors: ma t. Pain. 2020 Jul;161(7):1470-1482. doi: 10.1097/j.pain.0000000000001853. Pain. 2020. PMID: 32132394

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