Computational study of peptide interaction with mutant γ-crystallin with the aim of preventing dimerization
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[1] Yu Zhou,et al. A Novel CRYBB2 Stopgain Mutation Causing Congenital Autosomal Dominant Cataract in a Chinese Family , 2016, Journal of ophthalmology.
[2] Xiaohang Wu,et al. Prevalence and epidemiological characteristics of congenital cataract: a systematic review and meta-analysis , 2016, Scientific Reports.
[3] E. Souzeau,et al. Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract , 2016, BMC Research Notes.
[4] X. Kong,et al. A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract. , 2015, Genetics and molecular research : GMR.
[5] Yi-Bo Xi,et al. Cataract-linked mutation R188H promotes βB2-crystallin aggregation and fibrillization during acid denaturation. , 2014, Biochemical and biophysical research communications.
[6] Xu Ma,et al. A R54L Mutation of CRYAA Associated with Autosomal Dominant Nuclear Cataracts in a Chinese Family , 2013, Current eye research.
[7] M. Gur,et al. Computational Design of New Peptide Inhibitors for Amyloid Beta (Aβ) Aggregation in Alzheimer's Disease: Application of a Novel Methodology , 2013, PloS one.
[8] E. Souzeau,et al. Identification of a Novel Oligomerization Disrupting Mutation in CRYΑA Associated with Congenital Cataract in a South Australian Family , 2013, Human mutation.
[9] Rachel W. Martin,et al. 1H, 13C, and 15N assignments of wild-type human γS-crystallin and its cataract-related variant γS-G18V , 2012, Biomolecular NMR assignments.
[10] Xiyuan Zhou,et al. Prevalence of Eye Diseases and Causes of Visual Impairment in School-Aged Children in Western China , 2011, Journal of epidemiology.
[11] Thomas M. Bennett,et al. Cat-Map: putting cataract on the map , 2010, Molecular vision.
[12] Pierre Tufféry,et al. PEP-FOLD: an online resource for de novo peptide structure prediction , 2009, Nucleic Acids Res..
[13] Susan Vitale,et al. Clinical detection of precataractous lens protein changes using dynamic light scattering. , 2008, Archives of ophthalmology.
[14] Ruth Nussinov,et al. FireDock: a web server for fast interaction refinement in molecular docking† , 2008, Nucleic Acids Res..
[15] J. Hejtmancik. Congenital cataracts and their molecular genetics. , 2008, Seminars in cell & developmental biology.
[16] Carsten Kutzner,et al. GROMACS 4: Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation. , 2008, Journal of chemical theory and computation.
[17] Arif O. Khan,et al. Recessive congenital total cataract with microcornea and heterozygote carrier signs caused by a novel missense CRYAA mutation (R54C). , 2007, American journal of ophthalmology.
[18] T. Rosenberg,et al. Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8. , 2007, Investigative ophthalmology & visual science.
[19] J. Hejtmancik,et al. Genetic origins of cataract. , 2007, Archives of ophthalmology.
[20] T. Shinohara,et al. Role of the unfolded protein response (UPR) in cataract formation. , 2006, Experimental eye research.
[21] N. Klopp,et al. Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family. , 2006, Molecular vision.
[22] Gerrit Groenhof,et al. GROMACS: Fast, flexible, and free , 2005, J. Comput. Chem..
[23] D. J. Price,et al. A modified TIP3P water potential for simulation with Ewald summation. , 2004, The Journal of chemical physics.
[24] Jack Liang,et al. Alteration of protein-protein interactions of congenital cataract crystallin mutants. , 2003, Investigative ophthalmology & visual science.
[25] K. Lampi,et al. A nonsense mutation in CRYBB1 associated with autosomal dominant cataract linked to human chromosome 22q. , 2002, American journal of human genetics.
[26] R. Friesner,et al. Evaluation and Reparametrization of the OPLS-AA Force Field for Proteins via Comparison with Accurate Quantum Chemical Calculations on Peptides† , 2001 .
[27] D. Balasubramanian,et al. Molecular genetics of cataract. , 2000, Indian journal of ophthalmology.
[28] S. Bhattacharya,et al. Clinical and genetic heterogeneity in autosomal dominant cataract , 1999 .
[29] P. Kramer,et al. Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2. , 1997, Human molecular genetics.
[30] Payne,et al. Periodic boundary conditions in ab initio calculations. , 1995, Physical review. B, Condensed matter.
[31] M. Kaiser-Kupfer,et al. Autosomal dominant congenital cataract. Interocular phenotypic variability. , 1994, Ophthalmology.
[32] U. Andley,et al. Autophagy and UPR in alpha-crystallin mutant knock-in mouse models of hereditary cataracts. , 2016, Biochimica et biophysica acta.
[33] W. D. de Jong,et al. Structure and modifications of the junior chaperone alpha-crystallin. From lens transparency to molecular pathology. , 1994, European journal of biochemistry.