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Page 1
The power of zebrafish models for understanding the co-occurrence of craniofacial and limb disorders.
Genesis. 2021 Feb;59(1-2):e23407. doi: 10.1002/dvg.23407. Epub 2021 Jan 4.
Genesis. 2021.
PMID: 33393730
Free PMC article.
Review.
Loss of prdm1a accelerates melanoma onset and progression.
Iwanaga R, Truong BT, Hsu JY, Lambert KA, Vyas R, Orlicky D, Shellman YG, Tan AC, Ceol C, Artinger KB.
Iwanaga R, et al. Among authors: truong bt.
Mol Carcinog. 2020 Sep;59(9):1052-1063. doi: 10.1002/mc.23236. Epub 2020 Jun 20.
Mol Carcinog. 2020.
PMID: 32562448
Free PMC article.
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PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation.
Truong BT, Shull LC, Lencer E, Bend EG, Field M, Blue EE, Bamshad MJ, Skinner C, Everman D, Schwartz CE, Flanagan-Steet H, Artinger KB.
Truong BT, et al.
Dis Model Mech. 2023 Apr 1;16(4):dmm049977. doi: 10.1242/dmm.049977. Epub 2023 Apr 21.
Dis Model Mech. 2023.
PMID: 37083955
Free PMC article.
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Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.
Truong BT, Yarza TKL, Bootpetch Roberts T, Roberts S, Xu J, Steritz MJ, Tobias-Grasso CAM, Azamian M, Lalani SR, Mohlke KL, Lee NR, Cutiongco-de la Paz EM, Reyes-Quintos MRT, Santos-Cortez RLP, Chiong CM.
Truong BT, et al.
Clin Genet. 2019 May;95(5):634-636. doi: 10.1111/cge.13515. Epub 2019 Mar 4.
Clin Genet. 2019.
PMID: 30828794
Free PMC article.
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Human split hand/foot variants are not as functional as wildtype human PRDM1 in the rescue of craniofacial defects.
Truong BT, Shull LC, Zepeda BJ, Lencer E, Artinger KB.
Truong BT, et al.
Birth Defects Res. 2024 Mar;116(3):e2327. doi: 10.1002/bdr2.2327.
Birth Defects Res. 2024.
PMID: 38456586
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