| 2024 |
Zheng SM, Feng YC, Zhu Q, Li RQ, Yan QQ, Teng L, et al., 'MILIP Binding to tRNAs Promotes Protein Synthesis to Drive Triple-Negative Breast Cancer.', Cancer Res, OF1-OF15 (2024)
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| 2024 |
Xu L, Xiang W, Yang J, Gao J, Wang X, Meng L, et al., 'PHB2 promotes SHIP2 ubiquitination via the E3 ligase NEDD4 to regulate AKT signaling in gastric cancer', JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 43 (2024) [C1]
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Nova |
| 2023 |
Li RQ, Zhao XH, Zhu Q, Liu T, Hondermarck H, Thorne RF, et al., 'Exploring neurotransmitters and their receptors for breast cancer prevention and treatment.', Theranostics, 13 1109-1129 (2023) [C1]
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Nova |
| 2023 |
La T, Chen S, Zhao XH, Zhou S, Xu R, Teng L, et al., 'LncRNA LIMp27 Regulates the DNA Damage Response through p27 in p53-Defective Cancer Cells.', Adv Sci (Weinh), 10 e2204599 (2023) [C1]
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Nova |
| 2022 |
Wang PL, Teng L, Feng YC, Yue YM, Han MM, Yan Q, et al., 'The N-Myc-responsive lncRNA MILIP promotes DNA double-strand break repair through non-homologous end joining', PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 119 (2022) [C1]
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Nova |
| 2021 |
Teng L, Feng YC, Guo ST, Wang PL, Qi TF, Yue YM, et al., 'The pan-cancer lncRNA PLANE regulates an alternative splicing program to promote cancer pathogenesis', NATURE COMMUNICATIONS, 12 (2021) [C1]
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Nova |
| 2021 |
La T, Chen S, Guo T, Zhao XH, Teng L, Li D, et al., 'Visualization of endogenous p27 and Ki67 reveals the importance of a c-Myc-driven metabolic switch in promoting survival of quiescent cancer cells', THERANOSTICS, 11 9605-9622 (2021) [C1]
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Nova |
| 2021 |
Feng YC, Zhao XH, Teng L, Thorne RF, Jin L, Zhang XD, 'The pan-cancer lncRNA MILIP links c-Myc to p53 repression', MOLECULAR & CELLULAR ONCOLOGY, 8 (2021)
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| 2018 |
Zhang S, Zhu Q, Chen X, Zhao Y, Zhao X, Yang Y, et al., 'Forensic applicability of multi-allelic InDels with mononucleotide homopolymer structures', ELECTROPHORESIS, 39 2136-2143 (2018)
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| 2018 |
Zhao Y, Chen X, Yang Y, Zhao X, Zhang S, Gao Z, et al., 'Potential forensic biogeographic application of diatom colony consistency analysis employing pyrosequencing profiles of the 18S rDNA V7 region', INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 132 1611-1620 (2018)
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| 2018 |
Zhao Y, Mao Z, Pang H, Zhao X, Zhang S, Gao Z, et al., 'Association of programmed cell death 1 (PDCD1 ) gene polymorphisms with colorectal cancer among Han Chinese population', Chinese Journal of Medical Genetics, 35 219-223 (2018)
Objective To assess the association of programmed cell death 1 (PDCD1) gene polymorphisms with the susceptibility and/or progression of colorectal cancer. Methods A hospital-based... [more] Objective To assess the association of programmed cell death 1 (PDCD1) gene polymorphisms with the susceptibility and/or progression of colorectal cancer. Methods A hospital-based case-control study was carried out, which recruited 426 colorectal cancer patients and 500 healthy individuals. Five single nucleotide polymorphisms, namely rs36084323, rsll568821, rs2227981, rs2227982 and rsl0204525, were selected for the study and genotyped with a polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) assay. Results The G allele of rs36084323 under a dominant model was associated with increased risk of advanced TNM staging of colorectal cancer progression (OR = 1.59, 95% CI = 1.02-2.48). Haplotypes G-G-C-T-A and A-G-C-C-G of the rs36084323, rsll568821, rs2227981, rs2227982, and rsl0204525 were negatively associated with the occurrence of colorectal cancer. Conclusion The G allele of rs36084323 is associated with increased risk of advanced TNM staging of colorectal cancer. Conversely, the incidence of colorectal cancer is negatively associated with the haplotypes G-G-C-T-A and A-G-C-C-G of rs36084323, rsll568821, rs2227981, rs2227982, and rs10204525.
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| 2018 |
Gao Z, Chen X, Zhao Y, Zhao X, Zhang S, Yang Y, et al., 'Forensic genetic informativeness of an SNP panel consisting of 19 multi-allelic SNPs', FORENSIC SCIENCE INTERNATIONAL-GENETICS, 34 49-56 (2018)
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| 2018 |
Zhao X, Chen X, Zhao Y, Zhang S, Gao Z, Yang Y, et al., 'Construction and forensic genetic characterization of 11 autosomal haplotypes consisting of 22 tri-allelic indels', FORENSIC SCIENCE INTERNATIONAL-GENETICS, 34 71-80 (2018)
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| 2017 |
Zhao Y, Zhao X, Zhang S, Gao Z, Yang Y, Fang T, et al., 'A short unix shell script for vcftools commands iteration to obtain the genotypes of variations for forensic purpose', Forensic Science International: Genetics Supplement Series, 6 e49-e51 (2017)
The release of 1000 Genomes Project has provided a great variety of genome-wide variations spanning major populations worldwide, which offered a convenient path to the study of hu... [more] The release of 1000 Genomes Project has provided a great variety of genome-wide variations spanning major populations worldwide, which offered a convenient path to the study of human genetic structure. VCFtools, a suite of functions dedicated to loci details summarizing, calculating, filtering, and genotype outputting can act as a powerful utility for genetic markers hunting and evaluating in the context of forensic purpose. While it is a labor-intensive and error-prone job involving repeating of multiple VCFtools commands step by step. Hence, we introduced a short UNIX-based bash shell script which contains an iteration structure to call VCFtools commands repeatedly for summarizing genotypes in different variation loci of different populations automatically. By setting up variations list and groups list, VCFtools commands with different arguments can be executed consecutively. Consequently, this process can be realized automatically with high efficiency and precision in the study of forensic genetics.
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