Zhang T - Search Results

1

Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.

Ma J, Ma X, Lin K, Huang R, Bi X, Ming C, Li L, Li X, Li G, Zhao L, Yang T, Gao Y, Zhang T. Ma J, et al. Among authors: zhang t. Hum Genomics. 2023 Jan 4;17(1):1. doi: 10.1186/s40246-022-00449-1. Hum Genomics. 2023. PMID: 36597107 Free PMC article.

2

[Radiological research of maxillary sinus development of children and adolescent without sinusitis in Kunming of Yunnan].

Zhang T, Gao Y, Ruan B, Lu T, Shi H, Lin J. Zhang T, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 Dec;25(23):1081-3. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011. PMID: 22384568 Chinese.

3

[Diagnosis and treatment of faciocervical lymphatic malformations in infant].

Ma J, Mao Z, Lou F, Lin K, Zhang T. Ma J, et al. Among authors: zhang t. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Aug;49(8):687-9. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014. PMID: 25351128 Chinese.

4

[Diagnosis and surgical resection of faciocervical lipomas in children].

Ma J, Lou F, Lu T, Guo Y, Gao Y, Zhang T. Ma J, et al. Among authors: zhang t. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Dec;28(24):1960-3. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014. PMID: 25895316 Chinese.

5

Waardenburg syndrome type II in a Chinese patient caused by a novel nonsense mutation in the SOX10 gene.

Ma J, Zhang TS, Lin K, Sun H, Jiang HC, Yang YL, Low F, Gao YQ, Ruan B. Ma J, et al. Int J Pediatr Otorhinolaryngol. 2016 Jun;85:56-61. doi: 10.1016/j.ijporl.2016.03.043. Epub 2016 Apr 7. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27240497

6

Core‑shell lipid polymer nanoparticles for combined chemo and gene therapy of childhood head and neck cancers.

Zhang T, Ma J, Li C, Lin K, Lou F, Jiang H, Gao Y, Yang Y, Ming C, Ruan B. Zhang T, et al. Oncol Rep. 2017 Mar;37(3):1653-1661. doi: 10.3892/or.2017.5365. Epub 2017 Jan 13. Oncol Rep. 2017. PMID: 28098869

7

Diagnosis and surgical treatment of cervical macrocystic lymphatic malformations in infants.

Ma J, Biao R, Lou F, Lin K, Gao YQ, Wang ML, Yang YL, Zhang TS. Ma J, et al. Exp Ther Med. 2017 Aug;14(2):1293-1298. doi: 10.3892/etm.2017.4703. Epub 2017 Jun 28. Exp Ther Med. 2017. PMID: 28810590 Free PMC article.

8

Molecular characterization of genomic DNA in mycoplasma pneumoniae strains isolated from serious mycoplasma pneumonia cases in 2016, Yunnan, China.

Qiu L, Wang L, Tan L, Li M, Wu C, Li L, Zhang Z, Jiang H, Sun Q, Zhang T. Qiu L, et al. Among authors: zhang t, zhang z. Infect Genet Evol. 2018 Mar;58:125-134. doi: 10.1016/j.meegid.2017.12.020. Epub 2017 Dec 22. Infect Genet Evol. 2018. PMID: 29275190

9

A novel variant in MITF in a child from Yunnan-Guizhou Plateau with autosomal dominant inheritance of nonsyndromic hearing loss: A case report.

Zhang Z, Chen QD, Zhao LP, Ma J, Zhang TS, Pang JX, Li YF, Wang MF, Wang AP, Tang L, Li LJ, He WJ, Gu H. Zhang Z, et al. Mol Med Rep. 2018 Apr;17(4):6054-6058. doi: 10.3892/mmr.2018.8627. Epub 2018 Feb 22. Mol Med Rep. 2018. PMID: 29484430

10

A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II.

Ma J, Zhang Z, Jiang HC, Sun H, Ming C, Zhao LP, Gao YQ, Li ZC, Sun MH, Xiao Y, Wu GL, Zhang TS, Ruan B. Ma J, et al. Mol Med Rep. 2019 Mar;19(3):1775-1780. doi: 10.3892/mmr.2019.9815. Epub 2019 Jan 3. Mol Med Rep. 2019. PMID: 30628718

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