Connection

Emil Alexov to Humans

This is a "connection" page, showing publications Emil Alexov has written about Humans.
Connection Strength

0.745
  1. Opioid Addiction and Opioid Receptor Dimerization: Structural Modeling of the OPRD1 and OPRM1 Heterodimer and Its Signaling Pathways. Int J Mol Sci. 2021 Sep 24; 22(19).
    View in: PubMed
    Score: 0.030
  2. Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and Disease. Int J Mol Sci. 2021 Jul 31; 22(15).
    View in: PubMed
    Score: 0.030
  3. SAAMBE-SEQ: a sequence-based method for predicting mutation effect on protein-protein binding affinity. Bioinformatics. 2021 05 17; 37(7):992-999.
    View in: PubMed
    Score: 0.029
  4. SAAFEC-SEQ: A Sequence-Based Method for Predicting the Effect of Single Point Mutations on Protein Thermodynamic Stability. Int J Mol Sci. 2021 Jan 09; 22(2).
    View in: PubMed
    Score: 0.029
  5. An Ensemble Approach to Predict the Pathogenicity of Synonymous Variants. Genes (Basel). 2020 09 21; 11(9).
    View in: PubMed
    Score: 0.028
  6. SAAMBE-3D: Predicting Effect of Mutations on Protein-Protein Interactions. Int J Mol Sci. 2020 Apr 07; 21(7).
    View in: PubMed
    Score: 0.027
  7. Novel Genetic Markers for Early Detection of Elevated Breast Cancer Risk in Women. Int J Mol Sci. 2019 Sep 28; 20(19).
    View in: PubMed
    Score: 0.026
  8. Computational Investigation of the Missense Mutations in DHCR7 Gene Associated with Smith-Lemli-Opitz Syndrome. Int J Mol Sci. 2018 Jan 04; 19(1).
    View in: PubMed
    Score: 0.023
  9. Forces and Disease: Electrostatic force differences caused by mutations in kinesin motor domains can distinguish between disease-causing and non-disease-causing mutations. Sci Rep. 2017 08 15; 7(1):8237.
    View in: PubMed
    Score: 0.023
  10. Cofactors-loaded quaternary structure of lysine-specific demethylase 5C (KDM5C) protein: Computational model. Proteins. 2016 12; 84(12):1797-1809.
    View in: PubMed
    Score: 0.021
  11. SAAMBE: Webserver to Predict the Charge of Binding Free Energy Caused by Amino Acids Mutations. Int J Mol Sci. 2016 Apr 12; 17(4):547.
    View in: PubMed
    Score: 0.021
  12. Investigating the linkage between disease-causing amino acid variants and their effect on protein stability and binding. Proteins. 2016 Feb; 84(2):232-9.
    View in: PubMed
    Score: 0.020
  13. Revealing the Effects of Missense Mutations Causing Snyder-Robinson Syndrome on the Stability and Dimerization of Spermine Synthase. Int J Mol Sci. 2016 Jan 08; 17(1).
    View in: PubMed
    Score: 0.020
  14. Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease. Int J Mol Sci. 2015 Nov 13; 16(11):27270-87.
    View in: PubMed
    Score: 0.020
  15. Impact of Rett Syndrome Mutations on MeCP2 MBD Stability. Biochemistry. 2015 Oct 20; 54(41):6357-68.
    View in: PubMed
    Score: 0.020
  16. On human disease-causing amino acid variants: statistical study of sequence and structural patterns. Hum Mutat. 2015 May; 36(5):524-534.
    View in: PubMed
    Score: 0.019
  17. Structural, Dynamical, and Energetical Consequences of Rett Syndrome Mutation R133C in MeCP2. Comput Math Methods Med. 2015; 2015:746157.
    View in: PubMed
    Score: 0.019
  18. Structural and physico-chemical effects of disease and non-disease nsSNPs on proteins. Curr Opin Struct Biol. 2015 Jun; 32:18-24.
    View in: PubMed
    Score: 0.019
  19. Chronic Beryllium Disease: revealing the role of beryllium ion and small peptides binding to HLA-DP2. PLoS One. 2014; 9(11):e111604.
    View in: PubMed
    Score: 0.019
  20. ProBLM web server: protein and membrane placement and orientation package. Comput Math Methods Med. 2014; 2014:838259.
    View in: PubMed
    Score: 0.018
  21. Computational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnostics. Int J Mol Sci. 2014 May 30; 15(6):9670-717.
    View in: PubMed
    Score: 0.018
  22. Understanding molecular effects of naturally occurring genetic differences. J Mol Biol. 2013 Nov 01; 425(21):3911-3.
    View in: PubMed
    Score: 0.017
  23. Molecular mechanisms of disease-causing missense mutations. J Mol Biol. 2013 Nov 01; 425(21):3919-36.
    View in: PubMed
    Score: 0.017
  24. Protonation and pK changes in protein-ligand binding. Q Rev Biophys. 2013 May; 46(2):181-209.
    View in: PubMed
    Score: 0.017
  25. Enhancing human spermine synthase activity by engineered mutations. PLoS Comput Biol. 2013; 9(2):e1002924.
    View in: PubMed
    Score: 0.017
  26. A rational free energy-based approach to understanding and targeting disease-causing missense mutations. J Am Med Inform Assoc. 2013 Jul-Aug; 20(4):643-51.
    View in: PubMed
    Score: 0.017
  27. Analyzing effects of naturally occurring missense mutations. Comput Math Methods Med. 2012; 2012:805827.
    View in: PubMed
    Score: 0.016
  28. Predicting folding free energy changes upon single point mutations. Bioinformatics. 2012 Mar 01; 28(5):664-71.
    View in: PubMed
    Score: 0.015
  29. A missense mutation in CLIC2 associated with intellectual disability is predicted by in silico modeling to affect protein stability and dynamics. Proteins. 2011 Aug; 79(8):2444-54.
    View in: PubMed
    Score: 0.015
  30. In silico and in vitro investigations of the mutability of disease-causing missense mutation sites in spermine synthase. PLoS One. 2011; 6(5):e20373.
    View in: PubMed
    Score: 0.015
  31. On the role of electrostatics in protein-protein interactions. Phys Biol. 2011 Jun; 8(3):035001.
    View in: PubMed
    Score: 0.015
  32. Computational analysis of missense mutations causing Snyder-Robinson syndrome. Hum Mutat. 2010 Sep; 31(9):1043-9.
    View in: PubMed
    Score: 0.014
  33. Modeling effects of human single nucleotide polymorphisms on protein-protein interactions. Biophys J. 2009 Mar 18; 96(6):2178-88.
    View in: PubMed
    Score: 0.013
  34. Increased p53 signaling impairs neural differentiation in HUWE1-promoted intellectual disabilities. Cell Rep Med. 2021 04 20; 2(4):100240.
    View in: PubMed
    Score: 0.007
  35. Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. Nat Commun. 2020 07 23; 11(1):3698.
    View in: PubMed
    Score: 0.007
  36. Three additional patients with EED-associated overgrowth: potential mutation hotspots identified? J Hum Genet. 2019 Jun; 64(6):561-572.
    View in: PubMed
    Score: 0.006
  37. Structural Perspective on Revealing and Altering Molecular Functions of Genetic Variants Linked with Diseases. Int J Mol Sci. 2019 Jan 28; 20(3).
    View in: PubMed
    Score: 0.006
  38. Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects. Eur J Hum Genet. 2018 03; 26(3):420-427.
    View in: PubMed
    Score: 0.006
  39. Identification and characterization of a missense mutation in the O-linked ?-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability. J Biol Chem. 2017 05 26; 292(21):8948-8963.
    View in: PubMed
    Score: 0.005
  40. Binding Analysis of Methyl-CpG Binding Domain of MeCP2 and Rett Syndrome Mutations. ACS Chem Biol. 2016 10 21; 11(10):2706-2715.
    View in: PubMed
    Score: 0.005
  41. ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons. Hum Mol Genet. 2015 Sep 01; 24(17):4848-61.
    View in: PubMed
    Score: 0.005
  42. Rational design of small-molecule stabilizers of spermine synthase dimer by virtual screening and free energy-based approach. PLoS One. 2014; 9(10):e110884.
    View in: PubMed
    Score: 0.005
  43. A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease. J Alzheimers Dis. 2014; 39(1):23-7.
    View in: PubMed
    Score: 0.004
  44. A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation. Hum Mol Genet. 2014 Jan 15; 23(2):418-33.
    View in: PubMed
    Score: 0.004
  45. Cancer missense mutations alter binding properties of proteins and their interaction networks. PLoS One. 2013; 8(6):e66273.
    View in: PubMed
    Score: 0.004
  46. A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome. Hum Mol Genet. 2013 Sep 15; 22(18):3789-97.
    View in: PubMed
    Score: 0.004
  47. An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. Hum Mol Genet. 2012 Oct 15; 21(20):4497-507.
    View in: PubMed
    Score: 0.004
  48. Structural assessment of the effects of amino acid substitutions on protein stability and protein protein interaction. Int J Comput Biol Drug Des. 2010; 3(4):334-49.
    View in: PubMed
    Score: 0.004
  49. Electrostatic and lipid anchor contributions to the interaction of transducin with membranes: mechanistic implications for activation and translocation. J Biol Chem. 2008 Nov 07; 283(45):31197-207.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.