These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 36197641)

  • 1. Molecular Dynamic Simulation of Neurexin1α Mutations Associated with Mental Disorder.
    Hendam A; Al-Sadek AF; Hefny HA
    J Mol Neurosci; 2022 Nov; 72(11):2252-2272. PubMed ID: 36197641
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dynamics and structural stability effects of germline PTEN mutations associated with cancer versus autism phenotypes.
    Smith IN; Thacker S; Jaini R; Eng C
    J Biomol Struct Dyn; 2019 Apr; 37(7):1766-1782. PubMed ID: 29663862
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neurexin1α knockout in rats causes aberrant social behaviour: relevance for autism and schizophrenia.
    Achterberg EJM; Biemans B; Vanderschuren LJMJ
    Psychopharmacology (Berl); 2024 Feb; ():. PubMed ID: 38418646
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.
    Kim HG; Rosenfeld JA; Scott DA; Bénédicte G; Labonne JD; Brown J; McGuire M; Mahida S; Naidu S; Gutierrez J; Lesca G; des Portes V; Bruel AL; Sorlin A; Xia F; Capri Y; Muller E; McKnight D; Torti E; Rüschendorf F; Hummel O; Islam Z; Kolatkar PR; Layman LC; Ryu D; Kong IK; Madan-Khetarpal S; Kim CH
    Mol Autism; 2019; 10():35. PubMed ID: 31649809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of ARX and non-syndromic intellectual disability in Chinese population.
    Wu Y; Zhang H; Liu X; Shi Z; Li H; Wang Z; Jie X; Huang S; Zhang F; Li J; Zhang K; Gao X
    Genes Genomics; 2019 Jan; 41(1):125-131. PubMed ID: 30255221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dynamic Play between Human N-α-acetyltransferase D and H4-mutant Histones: Molecular Dynamics Study.
    Rathod SB; Srivastava KR
    Curr Protein Pept Sci; 2023; 24(4):339-354. PubMed ID: 36924088
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Macromolecular crowding: chemistry and physics meet biology (Ascona, Switzerland, 10-14 June 2012).
    Foffi G; Pastore A; Piazza F; Temussi PA
    Phys Biol; 2013 Aug; 10(4):040301. PubMed ID: 23912807
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic Variants of the
    Shi Z; Jia X; Tian Y; Liu X; Bai J; Liu Y; Zhang F; Li J; Gao X; Zhang K
    Genet Test Mol Biomarkers; 2020 Oct; 24(10):625-631. PubMed ID: 32991201
    [No Abstract]   [Full Text] [Related]  

  • 10. In silico analysis of the tryptophan hydroxylase 2 (TPH2) protein variants related to psychiatric disorders.
    Pereira GRC; Tavares GDB; de Freitas MC; De Mesquita JF
    PLoS One; 2020; 15(3):e0229730. PubMed ID: 32119710
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In silico functional, structural and pathogenicity analysis of missense single nucleotide polymorphisms in human MCM6 gene.
    Kamal MM; Mia MS; Faruque MO; Rabby MG; Islam MN; Talukder MEK; Wani TA; Rahman MA; Hasan MM
    Sci Rep; 2024 May; 14(1):11607. PubMed ID: 38773180
    [TBL] [Abstract][Full Text] [Related]  

  • 12. In Silico Elucidation of Deleterious Non-synonymous SNPs in SHANK3, the Autism Spectrum Disorder Gene.
    Owji H; Eslami M; Nezafat N; Ghasemi Y
    J Mol Neurosci; 2020 Oct; 70(10):1649-1667. PubMed ID: 32519210
    [TBL] [Abstract][Full Text] [Related]  

  • 13. In silico screening, molecular docking, and molecular dynamics studies of SNP-derived human P5CR mutants.
    Sang P; Hu W; Ye YJ; Li LH; Zhang C; Xie YH; Meng ZH
    J Biomol Struct Dyn; 2017 Aug; 35(11):2441-2453. PubMed ID: 27677826
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structural analysis and conformational dynamics of SOCS1 gene mutations involved in diffuse large B-cell lymphoma.
    Dristy TT; Noor AR; Dey P; Saha A
    Gene; 2023 May; 864():147293. PubMed ID: 36813059
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Computational identification and analysis of deleterious non-synonymous single nucleotide polymorphisms (nsSNPs) in the human
    Kumar R; Jayaraman M; Ramadas K; Chandrasekaran A
    J Biomol Struct Dyn; 2024; 42(3):1518-1532. PubMed ID: 37173831
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Extrapolating the effect of deleterious nsSNPs in the binding adaptability of flavopiridol with CDK7 protein: a molecular dynamics approach.
    George Priya Doss C; Nagasundaram N; Chakraborty C; Chen L; Zhu H
    Hum Genomics; 2013 Apr; 7(1):10. PubMed ID: 23561625
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.
    Hamdan FF; Gauthier J; Araki Y; Lin DT; Yoshizawa Y; Higashi K; Park AR; Spiegelman D; Dobrzeniecka S; Piton A; Tomitori H; Daoud H; Massicotte C; Henrion E; Diallo O; ; Shekarabi M; Marineau C; Shevell M; Maranda B; Mitchell G; Nadeau A; D'Anjou G; Vanasse M; Srour M; Lafrenière RG; Drapeau P; Lacaille JC; Kim E; Lee JR; Igarashi K; Huganir RL; Rouleau GA; Michaud JL
    Am J Hum Genet; 2011 Mar; 88(3):306-16. PubMed ID: 21376300
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autism Spectrum Disorder/Intellectual Disability-Associated Mutations in Trio Disrupt Neuroligin 1-Mediated Synaptogenesis.
    Tian C; Paskus JD; Fingleton E; Roche KW; Herring BE
    J Neurosci; 2021 Sep; 41(37):7768-7778. PubMed ID: 34353896
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Computational repurposing approach for targeting the critical spike mutations in B.1.617.2 (delta), AY.1 (delta plus) and C.37 (lambda) SARS-CoV-2 variants using exhaustive structure-based virtual screening, molecular dynamic simulations and MM-PBSA methods.
    Ebrahimi M; Karami L; Alijanianzadeh M
    Comput Biol Med; 2022 Aug; 147():105709. PubMed ID: 35728285
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identifying and elucidating the roles of Y198N and Y204F mutations in the PAH enzyme through molecular dynamic simulations.
    Aslan T; Yenenler-Kutlu A; Gerlevik U; Aktuğlu Zeybek AÇ; Kıykım E; Sezerman OU; Birgul Iyison N
    J Biomol Struct Dyn; 2022; 40(19):9018-9029. PubMed ID: 33970801
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.