Tran VK - Search Results

1

Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children.

Nguyen HTT, Vu DC, Nguyen DM, Dang QD, Tran VK, Le H, Tong SM. Nguyen HTT, et al. Among authors: tran vk. Dent J (Basel). 2021 Apr 27;9(5):49. doi: 10.3390/dj9050049. Dent J (Basel). 2021. PMID: 33925433 Free PMC article.

2

Exon deletion patterns of the dystrophin gene in 82 Vietnamese Duchenne/Becker muscular dystrophy patients.

Tran VK, Ta VT, Vu DC, Nguyen ST, Do HN, Ta MH, Tran TH, Matsuo M. Tran VK, et al. Among authors: tran th. J Neurogenet. 2013 Dec;27(4):170-5. doi: 10.3109/01677063.2013.830616. Epub 2013 Oct 7. J Neurogenet. 2013. PMID: 24099565

3

Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene.

Niba ET, Tran VK, Tuan-Pham le A, Vu DC, Nguyen NK, Ta VT, Tran TH, Lee T, Takeshima Y, Matsuo M. Niba ET, et al. Among authors: tran th, tran vk. Clin Chim Acta. 2014 Sep 25;436:155-9. doi: 10.1016/j.cca.2014.05.018. Epub 2014 Jun 2. Clin Chim Acta. 2014. PMID: 24892813

4

Cryptic splice activation but not exon skipping is observed in minigene assays of dystrophin c.9361+1G>A mutation identified by NGS.

Niba ETE, Nishida A, Tran VK, Vu DC, Matsumoto M, Awano H, Lee T, Takeshima Y, Nishio H, Matsuo M. Niba ETE, et al. Among authors: tran vk. J Hum Genet. 2017 Apr;62(5):531-537. doi: 10.1038/jhg.2016.162. Epub 2017 Jan 19. J Hum Genet. 2017. PMID: 28100912

5

Acromesomelic dysplasia Maroteaux-type in patients from Vietnam.

Tran TH, Cao MH, Luong LH, Le PT, Vu DC, Ta TD, Bui TH, Nguyen DH, Van Ta T, Tran VK. Tran TH, et al. Among authors: tran vk. Am J Med Genet A. 2019 Aug;179(8):1420-1422. doi: 10.1002/ajmg.a.61192. Epub 2019 May 11. Am J Med Genet A. 2019. PMID: 31077548

6

Novel variants of CYP21A2 in Vietnamese patients with congenital adrenal hyperplasia.

Chi DV, Tran TH, Nguyen DH, Luong LH, Le PT, Ta MH, Ngo HTT, Nguyen MP, Le-Anh TP, Nguyen DP, Bui TH, Ta VT, Tran VK. Chi DV, et al. Among authors: tran th, tran vk. Mol Genet Genomic Med. 2019 May;7(5):e623. doi: 10.1002/mgg3.623. Epub 2019 Feb 27. Mol Genet Genomic Med. 2019. PMID: 30816000 Free PMC article.

7

A Novel Nonsense Mutation c.374C>G in CYP21A2 Gene of a Vietnamese Patient with Congenital Adrenal Hyperplasia.

Vu CD, Van Ta T, Nguyen NL, Nguyen HH, Nguyen TKL, Tran TH, Tran VK. Vu CD, et al. Among authors: tran th, tran vk. Adv Exp Med Biol. 2020;1292:27-35. doi: 10.1007/5584_2018_300. Adv Exp Med Biol. 2020. PMID: 30838541

8

Variation of Mitochondrial DNA HV1 AND HV2 of the Vietnamese Population.

Tran TTH, Nguyen DH, Tran VK, Nguyen QL, Trinh HA, Luong LH, Tran VA, Pham LAT, Nguyen TT, Nguyen VB, Tran TH, Van Ta T. Tran TTH, et al. Among authors: tran va, tran th, tran vk. Adv Exp Med Biol. 2020;1292:37-63. doi: 10.1007/5584_2018_301. Adv Exp Med Biol. 2020. PMID: 30838542

9

Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam.

Ngo TT, Tran TH, Ta TD, Le TP, Nguyen PD, Tran MA, Bui TH, Ta TV, Tran VK. Ngo TT, et al. Among authors: tran th, tran ma, tran vk. Anemia. 2022 Jul 5;2022:2653089. doi: 10.1155/2022/2653089. eCollection 2022. Anemia. 2022. PMID: 35845714 Free PMC article.

10

Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B.

Tuan Pham LA, Nguyen TT, Nga Le HB, Tran DQ, Ho CT, Tran TH, Ta VT, Bui TH, Tran VK. Tuan Pham LA, et al. Among authors: tran dq, tran th, tran vk. J Genet. 2017 Dec;96(6):933-939. doi: 10.1007/s12041-017-0857-9. J Genet. 2017. PMID: 29321352 Free article.

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