123 related articles for article (PubMed ID: 37640005)
1. Identification of molecular signatures and molecular dynamics simulation of highly deleterious missense variants of key autophagy regulator beclin 1: a computational based approach.
Kaur S; Vashistt J; Changotra H
J Biomol Struct Dyn; 2023 Aug; ():1-14. PubMed ID: 37640005
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Comprehensive
Hoda A; Berisha B; Bixheku X; Zanchi FB
J Biomol Struct Dyn; 2024 Apr; ():1-17. PubMed ID: 38656135
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. In silico analyses of Wnt1 nsSNPs reveal structurally destabilizing variants, altered interactions with Frizzled receptors and its deregulation in tumorigenesis.
Mondal A; Paul D; Dastidar SG; Saha T; Goswami AM
Sci Rep; 2022 Sep; 12(1):14934. PubMed ID: 36056132
[TBL] [Abstract][Full Text] [Related]
6. Computational screening and analysis of deleterious nsSNPs in human
Ahmad SU; Ali Y; Jan Z; Rasheed S; Nazir NUA; Khan A; Rukh Abbas S; Wadood A; Rehman AU
J Biomol Struct Dyn; 2023 Jun; 41(9):3964-3975. PubMed ID: 35446184
[TBL] [Abstract][Full Text] [Related]
7. Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis.
Shinwari K; Guojun L; Deryabina SS; Bolkov MA; Tuzankina IA; Chereshnev VA
ScientificWorldJournal; 2021; 2021():6642626. PubMed ID: 34234628
[TBL] [Abstract][Full Text] [Related]
8. Identification of deleterious nsSNPs in human HGF gene: in silico approach.
Hoda A; Lika Çekani M; Kolaneci V
J Biomol Struct Dyn; 2023; 41(21):11889-11903. PubMed ID: 36598356
[TBL] [Abstract][Full Text] [Related]
9. Assessment of structurally and functionally high-risk nsSNPs impacts on human bone morphogenetic protein receptor type IA (BMPR1A) by computational approach.
Islam MJ; Parves MR; Mahmud S; Tithi FA; Reza MA
Comput Biol Chem; 2019 Jun; 80():31-45. PubMed ID: 30884445
[TBL] [Abstract][Full Text] [Related]
10. Beclin 1 is required for neuron viability and regulates endosome pathways via the UVRAG-VPS34 complex.
McKnight NC; Zhong Y; Wold MS; Gong S; Phillips GR; Dou Z; Zhao Y; Heintz N; Zong WX; Yue Z
PLoS Genet; 2014 Oct; 10(10):e1004626. PubMed ID: 25275521
[TBL] [Abstract][Full Text] [Related]
11. A computational study on structural and functional consequences of nsSNPs in human dopa decarboxylase.
Kumar SB; Girish A; Sutar S; Premanand SA; Garg V; Yadav AK; Shukla R; Murthy TPK; Singh TR
J Biomol Struct Dyn; 2024 Jan; ():1-15. PubMed ID: 38193892
[TBL] [Abstract][Full Text] [Related]
12. Deleterious single nucleotide polymorphisms (SNPs) of human IFNAR2 gene facilitate COVID-19 severity in patients: a comprehensive
Akter S; Roy AS; Tonmoy MIQ; Islam MS
J Biomol Struct Dyn; 2022; 40(21):11173-11189. PubMed ID: 34355676
[TBL] [Abstract][Full Text] [Related]
13. Prediction of functionally significant single nucleotide polymorphisms in PTEN tumor suppressor gene: An in silico approach.
Khan I; Ansari IA; Singh P; Dass J FP
Biotechnol Appl Biochem; 2017 Sep; 64(5):657-666. PubMed ID: 26800850
[TBL] [Abstract][Full Text] [Related]
14. Computational screening of pathogenic missense nsSNPs in heme oxygenase 1 (HMOX1) gene and their structural and functional consequences.
Yadav AK; Murthy TPK; Divyashri G; Prasad N D; Prakash S; Vaishnavi V V; Shukla R; Singh TR
J Biomol Struct Dyn; 2024 Jul; 42(10):5072-5091. PubMed ID: 37434323
[TBL] [Abstract][Full Text] [Related]
15. Beclin 1 forms two distinct phosphatidylinositol 3-kinase complexes with mammalian Atg14 and UVRAG.
Itakura E; Kishi C; Inoue K; Mizushima N
Mol Biol Cell; 2008 Dec; 19(12):5360-72. PubMed ID: 18843052
[TBL] [Abstract][Full Text] [Related]
16. Prediction and evaluation of deleterious and disease causing non-synonymous SNPs (nsSNPs) in human NF2 gene responsible for neurofibromatosis type 2 (NF2).
Havranek B; Islam SM
J Biomol Struct Dyn; 2021 Nov; 39(18):7044-7055. PubMed ID: 32787631
[TBL] [Abstract][Full Text] [Related]
17. Targeting the potent Beclin 1-UVRAG coiled-coil interaction with designed peptides enhances autophagy and endolysosomal trafficking.
Wu S; He Y; Qiu X; Yang W; Liu W; Li X; Li Y; Shen HM; Wang R; Yue Z; Zhao Y
Proc Natl Acad Sci U S A; 2018 Jun; 115(25):E5669-E5678. PubMed ID: 29866835
[TBL] [Abstract][Full Text] [Related]
18.
Khan A; Waqas M; Tufail M; Halim SA; Murad W; Ahmad SU; Faheem M; Uddin J; Khalid A; Abdalla AN; Khan A; Al-Harrasi A
J Biomol Struct Dyn; 2023; 41(21):11629-11646. PubMed ID: 36734218
[TBL] [Abstract][Full Text] [Related]
19. Computational SNP Analysis and Molecular Simulation Revealed the Most Deleterious Missense Variants in the NBD1 Domain of Human ABCA1 Transporter.
Dash R; Ali MC; Rana ML; Munni YA; Barua L; Jahan I; Haque MF; Hannan MA; Moon IS
Int J Mol Sci; 2020 Oct; 21(20):. PubMed ID: 33066695
[TBL] [Abstract][Full Text] [Related]
20. Computational identification of pathogenic associated nsSNPs and its structural impact in UROD gene: a molecular dynamics approach.
Doss CG; Magesh R
Cell Biochem Biophys; 2014 Nov; 70(2):735-46. PubMed ID: 24777812
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
