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科学研究

2020年实验室发表的学术论文
日期:2021-01-23

1. Sun et al. Comparative Transcriptome Analysis Reveals the Intensive Early Stage Responses of Host Cells to SARS-CoV-2 Infection. Front Microbiol. 2020 Nov 25;11: 593857.

2. Wang et al. TAF1A and ZBTB41 serve as novel key genes in cervical cancer identified by integrated approaches. Cancer Gene Ther. 2020 Dec 12.

3. Yuan et al. A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient. Front Cardiovasc Med. 2020 Nov 9;7: 582350.

4. Wang et al. Integrated Analysis of the Functions and Prognostic Values of RNA-Binding Proteins in Colorectal Cancer. Front Cell Dev Biol. 2020 Nov 5;8: 595605.

5. Wu et al. Venous thromboembolic events in patients with COVID-19: A systematic review and meta-analysis. Age Ageing. 2020 Nov 17: afaa259.

6. Li et al. ZLM-7 inhibits the occurrence and angiogenesis of breast cancer through miR-212-3p/Sp1/VEGFA signal axis. Mol Med. 2020 Nov 13;26(1): 109.

7. Guo et al. NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism. Am J Hum Genet. 2020 Nov 5;107(5): 963-976.

8. Ming et al. ARG1 functions as a tumor suppressor in breast cancer. Acta Biochim Biophys Sin (Shanghai). 2020 Dec 11;52(11): 1257-1264.

9. Zhang et al. A longitudinal study reveals the alterations of the Microtus fortis colonic microbiota during the natural resistance to Schistosoma japonicum infection. Exp Parasitol. 2020 Dec;219: 108030.

10. Ahmed et al. Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy. Hum Genet. 2020 Oct 13. doi: 10.1007/s00439-020-02226-3.

11. Shen et al. Mechanisms of Resistance to Schistosoma japonicum Infection in Microtus fortis, the Natural Non-permissive Host. Front Microbiol. 2020 Sep 3;11: 2092.

12. Wang et al. Evaluation of current medical approaches for COVID-19: a systematic review and meta-analysis. BMJ Support Palliat Care. 2020 Sep 21: bmjspcare-2020-002554.

13. Ding et al. Transcription factor POU3F2 regulates TRIM8 expression contributing to cellular functions implicated in schizophrenia. Mol Psychiatry. 2020 Sep 14. doi: 10.1038/s41380-020-00877-2.

14. Lv et al. The relationships of vitamin D, vitamin D receptor gene polymorphisms, and vitamin D supplementation with Parkinson's disease. Transl Neurodegener. 2020 Sep 1;9(1): 34.

15. Shah et al. Excess of RALGAPB de novo variants in neurodevelopmental disorders. Eur J Med Genet. 2020 Nov;63(11): 104041.

16. Meng et al. Integrative analyses prioritize GNL3 as a risk gene for bipolar disorder. Mol Psychiatry. 2020 Nov;25(11): 2672-2684.

17. Luo et al. The Functional Role of Voltage-Gated Sodium Channel Nav1.5 in Metastatic Breast Cancer. Front Pharmacol. 2020 Jul 23;11: 1111.

18. Lu et al. Necdin regulates BMAL1 stability and circadian clock through SGT1-HSP90 chaperone machinery. Nucleic Acids Res. 2020 Aug 20;48(14): 7944-7957.

19. Lin et al. Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima. Neurobiol Dis. 2020 Sep;143: 105013.

20. Quan et al. Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders. J Mol Neurosci. 2020 Dec;70(12): 2085-2092.

21. Hou et al. Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism. Eur J Endocrinol. 2020 Sep;183(3): 245-254.

22. Men et al. Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism. J Med Genet. 2021 Jan;58(1): 66-72.

23. Change et al. Targeting PIK3CG in Combination with Paclitaxel as a Potential Therapeutic Regimen in Claudin-Low Breast Cancer. Cancer Manag Res. 2020 Apr 20;12: 2641-2651.

24. Wang et al. Systematic prediction of key genes for ovarian cancer by co-expression network analysis. J Cell Mol Med. 2020 Jun;24(11): 6298-6307.

25. Gao et al. Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy. Mol Genet Genomic Med. 2020 Jun;8(6): e1236.

26. Dai et al. Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism. Clin Genet. 2020 May;97(5): 696-703.

27. Pielnaaet al. Zika virus-spread, epidemiology, genome, transmission cycle, clinical manifestation, associated challenges, vaccine and antiviral drug development. Virology. 2020 Apr;543: 34-42.

28. Wu et al. Genome Composition and Divergence of the Novel Coronavirus (2019-nCoV) Originating in China. Cell Host Microbe. 2020 Mar 11;27(3): 325-328.

29. Chen et al. The relationship between the minor allele content and Alzheimer's disease. Genomics. 2020 May;112(3): 2426-2432.

30. Yu et al. The UFM1 cascade times mitosis entry associated with microcephaly. FASEB J. 2020 Jan;34(1): 1319-1330.

31. Xing et al. Hyperactive Akt-mTOR pathway as a therapeutic target for pain hypersensitivity in Cntnap2-deficient mice. Neuropharmacology. 2020 Mar 15;165: 107816.

32. Men et al. Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism. Fertil Steril. 2020 Jan;113(1): 158-166.

33. Zhou et al. The NALCN Channel Regulator UNC-80 Functions in a Subset of Interneurons To Regulate Caenorhabditis elegans Reversal Behavior. G3 (Bethesda). 2020 Jan 7;10(1): 199-210.

34. Li et al. Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort. J Clin Endocrinol Metab. 2020 May 1;105(5): dgz182.

35. Wu et al. Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort. Clin Genet. 2020 Feb;97(2): 338-346.

36. Men et al. Identification of a Novel CNV at 8q13 in a Family With Branchio-Oto-Renal Syndrome and Epilepsy. Laryngoscope. 2020 Feb;130(2): 526-532.

37. Lu et al. Locus-specific DNA methylation of Mecp2 promoter leads to autism-like phenotypes in mice. Cell Death Dis. 2020 Feb 3; 11(2): 85.