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PUBMED FOR HANDHELDS

Journal Abstract Search


313 related items for PubMed ID: 38594551

  • 1. Exploring key genes and pathways associated with sex differences in autism spectrum disorder: integrated bioinformatic analysis.
    Nautiyal H, Jaiswar A, Jha PK, Dwivedi S.
    Mamm Genome; 2024 Jun; 35(2):280-295. PubMed ID: 38594551
    [Abstract] [Full Text] [Related]

  • 2. Integrated genome-wide Alu methylation and transcriptome profiling analyses reveal novel epigenetic regulatory networks associated with autism spectrum disorder.
    Saeliw T, Tangsuwansri C, Thongkorn S, Chonchaiya W, Suphapeetiporn K, Mutirangura A, Tencomnao T, Hu VW, Sarachana T.
    Mol Autism; 2018 Jun; 9():27. PubMed ID: 29686828
    [Abstract] [Full Text] [Related]

  • 3. Identification of target hub genes and construction of a novel miRNA regulatory network in autism spectrum disorder by integrated analysis.
    Zhu J, Meng H, Li Y.
    Medicine (Baltimore); 2023 Jul 21; 102(29):e34420. PubMed ID: 37478258
    [Abstract] [Full Text] [Related]

  • 4. Integrated Analysis of Hub Genes and Pathways In Esophageal Carcinoma Based on NCBI's Gene Expression Omnibus (GEO) Database: A Bioinformatics Analysis.
    Yu-Jing T, Wen-Jing T, Biao T.
    Med Sci Monit; 2020 Aug 05; 26():e923934. PubMed ID: 32756534
    [Abstract] [Full Text] [Related]

  • 5. Gene network in pulmonary tuberculosis based on bioinformatic analysis.
    Li L, Lv J, He Y, Wang Z.
    BMC Infect Dis; 2020 Aug 18; 20(1):612. PubMed ID: 32811479
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  • 6. Integrated bioinformatics analysis for the screening of hub genes and therapeutic drugs in ovarian cancer.
    Yang D, He Y, Wu B, Deng Y, Wang N, Li M, Liu Y.
    J Ovarian Res; 2020 Jan 27; 13(1):10. PubMed ID: 31987036
    [Abstract] [Full Text] [Related]

  • 7. Screening and Bioinformatics Analysis of Differential Genes in Autism Spectrum Disorder Based on GEO Database.
    Zhu J, Meng H, Li Y.
    Stud Health Technol Inform; 2023 Nov 23; 308():280-288. PubMed ID: 38007751
    [Abstract] [Full Text] [Related]

  • 8. Identification of hub-methylated differentially expressed genes in patients with gestational diabetes mellitus by multi-omic WGCNA basing epigenome-wide and transcriptome-wide profiling.
    Chen M, Yan J, Han Q, Luo J, Zhang Q.
    J Cell Biochem; 2020 Jun 23; 121(5-6):3173-3184. PubMed ID: 31886571
    [Abstract] [Full Text] [Related]

  • 9. Identification of Potential Hub Genes and Signal Pathways Promoting the Distinct Biological Features of Cord Blood-Derived Endothelial Progenitor Cells Via Bioinformatics.
    Wang Q, Chen S, Wu J, Liu D, Jiang N, Wang B, Zhai J, Liu Z.
    Genet Test Mol Biomarkers; 2020 Sep 23; 24(9):549-561. PubMed ID: 32744910
    [Abstract] [Full Text] [Related]

  • 10. Integrated gene expression profiling and functional enrichment analyses to discover biomarkers and pathways associated with Guillain-Barré syndrome and autism spectrum disorder to identify new therapeutic targets.
    Hasib RA, Ali MC, Rahman MH, Ahmed S, Sultana S, Summa SZ, Shimu MSS, Afrin Z, Jamal MAHM.
    J Biomol Struct Dyn; 2024 Sep 23; 42(21):11299-11321. PubMed ID: 37776011
    [Abstract] [Full Text] [Related]

  • 11. Integrated Transcriptome Analyses Revealed Key Target Genes in Mouse Models of Autism.
    Duan W, Wang K, Duan Y, Chu X, Ma R, Hu P, Xiong B.
    Autism Res; 2020 Mar 23; 13(3):352-368. PubMed ID: 31743624
    [Abstract] [Full Text] [Related]

  • 12. Exploring the molecular mechanism of comorbidity of autism spectrum disorder and inflammatory bowel disease by combining multiple data sets.
    Zhu J, Meng H, Zhang L, Li Y.
    J Transl Med; 2023 Jun 08; 21(1):372. PubMed ID: 37291580
    [Abstract] [Full Text] [Related]

  • 13. Sex Differences in Osteoarthritis Pathogenesis: A Comprehensive Study Based on Bioinformatics.
    Yang Y, You X, Cohen JD, Zhou H, He W, Li Z, Xiong Y, Yu T.
    Med Sci Monit; 2020 Apr 07; 26():e923331. PubMed ID: 32255771
    [Abstract] [Full Text] [Related]

  • 14. Identification of key pathways and genes in polycystic ovary syndrome via integrated bioinformatics analysis and prediction of small therapeutic molecules.
    Devarbhavi P, Telang L, Vastrad B, Tengli A, Vastrad C, Kotturshetti I.
    Reprod Biol Endocrinol; 2021 Feb 23; 19(1):31. PubMed ID: 33622336
    [Abstract] [Full Text] [Related]

  • 15. Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes.
    Mordaunt CE, Jianu JM, Laufer BI, Zhu Y, Hwang H, Dunaway KW, Bakulski KM, Feinberg JI, Volk HE, Lyall K, Croen LA, Newschaffer CJ, Ozonoff S, Hertz-Picciotto I, Fallin MD, Schmidt RJ, LaSalle JM.
    Genome Med; 2020 Oct 14; 12(1):88. PubMed ID: 33054850
    [Abstract] [Full Text] [Related]

  • 16. De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types.
    Chen S, Wang J, Cicek E, Roeder K, Yu H, Devlin B.
    Mol Autism; 2020 Oct 08; 11(1):76. PubMed ID: 33032641
    [Abstract] [Full Text] [Related]

  • 17. DNA methylation biomarkers for nasopharyngeal carcinoma.
    Han B, Yang X, Zhang P, Zhang Y, Tu Y, He Z, Li Y, Yuan J, Dong Y, Hosseini DK, Zhou T, Sun H.
    PLoS One; 2020 Oct 08; 15(4):e0230524. PubMed ID: 32271791
    [Abstract] [Full Text] [Related]

  • 18. Bioinformatic Analysis of Key Genes and Pathways Related to Keloids.
    Bi S, Liu R, Wu B, He L, Gu J.
    Biomed Res Int; 2021 Oct 08; 2021():5897907. PubMed ID: 33860039
    [Abstract] [Full Text] [Related]

  • 19. Exploring the molecular mechanism of sepsis-associated encephalopathy by integrated analysis of multiple datasets.
    Zhang Q, Lu C, Fan W, Yin Y.
    Cytokine; 2024 Aug 08; 180():156609. PubMed ID: 38781871
    [Abstract] [Full Text] [Related]

  • 20. Transcriptome analysis identifies an ASD-Like phenotype in oligodendrocytes and microglia from C58/J amygdala that is dependent on sex and sociability.
    Dalton GD, Siecinski SK, Nikolova VD, Cofer GP, Hornburg KJ, Qi Y, Johnson GA, Jiang YH, Moy SS, Gregory SG.
    Behav Brain Funct; 2024 Jun 19; 20(1):14. PubMed ID: 38898502
    [Abstract] [Full Text] [Related]


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