Chen HT - Search Results

1

Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification.

Guo XX, Zou XH, Wang C, Yao XP, Su HZ, Lai LL, Chen HT, Lai JH, Liu YB, Chen DP, Deng YC, Lin P, Lin HS, Hong BC, Yao QY, Chen XJ, Huang DQ, Fu HX, Peng JD, Niu YF, Zhao YY, Zhu XQ, Lu XP, Lin HL, Li YK, Liu CY, Huang GB, Wang N, Chen WJ. Guo XX, et al. Among authors: chen xj, chen wj, chen ht, chen dp. Hum Mutat. 2019 Apr;40(4):392-403. doi: 10.1002/humu.23703. Epub 2019 Jan 15. Hum Mutat. 2019. PMID: 30609140

2

Mutation screening of PDGFB gene in Chinese population with primary familial brain calcification.

Yao XP, Wang C, Su HZ, Guo XX, Lu YQ, Zhao M, Liu YB, Lai JH, Chen HT, Wang N, Chen WJ. Yao XP, et al. Among authors: chen wj, chen ht. Gene. 2016 Oct 28:S0378-1119(16)30826-5. doi: 10.1016/j.gene.2016.10.037. Online ahead of print. Gene. 2016. PMID: 27984190

3

Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families.

Wang C, Yao XP, Chen HT, Lai JH, Guo XX, Su HZ, Dong EL, Zhang QJ, Wang N, Chen WJ. Wang C, et al. Among authors: chen wj, chen ht. J Hum Genet. 2017 Jul;62(7):697-701. doi: 10.1038/jhg.2017.25. Epub 2017 Mar 16. J Hum Genet. 2017. PMID: 28298627

4

Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcification.

Yao XP, Zhao M, Wang C, Guo XX, Su HZ, Dong EL, Chen HT, Lai JH, Liu YB, Wang N, Chen WJ. Yao XP, et al. Among authors: chen wj, chen ht. Cell Tissue Res. 2017 Nov;370(2):267-273. doi: 10.1007/s00441-017-2663-3. Epub 2017 Aug 2. Cell Tissue Res. 2017. PMID: 28766044

5

Correlation of clinical and ultrasonographic features in congenital muscular torticollis.

Hsu TC, Wang CL, Wong MK, Hsu KH, Tang FT, Chen HT. Hsu TC, et al. Among authors: chen ht. Arch Phys Med Rehabil. 1999 Jun;80(6):637-41. doi: 10.1016/s0003-9993(99)90165-x. Arch Phys Med Rehabil. 1999. PMID: 10378488

6

Successful separation of ischiopagus tripus conjoined twins.

Hung WT, Chen WJ, Chen HT, Hsu TC, Chao CC, Wu TT. Hung WT, et al. Among authors: chen wj, chen ht. J Pediatr Surg. 1986 Nov;21(11):920-3. doi: 10.1016/s0022-3468(86)80088-4. J Pediatr Surg. 1986. PMID: 2947986

7

Transcriptomic Redox Dysregulation in a Rat Model of Metabolic Syndrome-Associated Kidney Injury.

Lu CL, Wang YY, Tsai YJ, Chen HT, Ma MC, Wu WB. Lu CL, et al. Among authors: chen ht. Antioxidants (Basel). 2025 Jun 17;14(6):746. doi: 10.3390/antiox14060746. Antioxidants (Basel). 2025. PMID: 40563378 Free PMC article.

8

Allogeneic Stem Cell Transplantation: The Relevance of Conditioning Regime Intensity for Myelodysplastic Syndromes (MDS).

Berg T, Salter B, Radford M, Chen HTT, Leber B. Berg T, et al. Among authors: chen htt. Curr Oncol. 2025 May 30;32(6):319. doi: 10.3390/curroncol32060319. Curr Oncol. 2025. PMID: 40558262 Free PMC article. Review.

9

Disorder-Induced Spectral Splitting versus Rabi Splitting under Strong Light-Matter Coupling.

Li WK, Chen HT. Li WK, et al. Among authors: chen ht. J Phys Chem Lett. 2025 Jun 24:6728-6733. doi: 10.1021/acs.jpclett.5c01302. Online ahead of print. J Phys Chem Lett. 2025. PMID: 40552751

10

Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers.

Liao Y, Chan YT, Lin YK, Molakaseema V, Selvaraj A, Chen HT, Wang YM, Choo YM, Kao CL. Liao Y, et al. Among authors: chen ht. Methods Mol Biol. 2025;2931:177-186. doi: 10.1007/978-1-0716-4562-8_14. Methods Mol Biol. 2025. PMID: 40531457

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