Related references
Note: Only part of the references are listed.Computational Screening of Disease-Associated Mutations in OCA2 Gene
Balu Kamaraj et al.
CELL BIOCHEMISTRY AND BIOPHYSICS (2014)
Drug resistance mechanism of PncA in Mycobacterium tuberculosis
Vidya Rajendran et al.
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2014)
Role of ELA region in auto-activation of mutant KIT receptor: a molecular dynamics simulation insight
Rituraj Purohit
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2014)
Investigation of Binding Phenomenon of NSP3 and p130Cas Mutants and Their Effect on Cell Signalling
K. Balu et al.
CELL BIOCHEMISTRY AND BIOPHYSICS (2013)
Mutational analysis of TYR gene and its structural consequences in OCA1A
K. Balu et al.
GENE (2013)
Molecular Mechanisms of Disease-Causing Missense Mutations
Shannon Stefl et al.
JOURNAL OF MOLECULAR BIOLOGY (2013)
In-silico screening of cancer associated mutation on PLK1 protein and its structural consequences
Balu Kamaraj et al.
JOURNAL OF MOLECULAR MODELING (2013)
Molecular Dynamic Simulation Reveals Damaging Impact of RAC1 F28L Mutation in the Switch I Region
Ambuj Kumar et al.
PLOS ONE (2013)
In Silico Screening and Molecular Dynamics Simulation of Disease-Associated nsSNP in TYRP1 Gene and Its Structural Consequences in OCA3
Balu Kamaraj et al.
BIOMED RESEARCH INTERNATIONAL (2013)
In silico investigation of molecular mechanism of laminopathy caused by a point mutation (R482W) in lamin A/C protein
Vidya Rajendran et al.
AMINO ACIDS (2012)
Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2011)
Nuclear import by karyopherin-βs: Recognition and inhibition
Yuh Min Chook et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)
Molecular basis for specificity of nuclear import and prediction of nuclear localization
Mary Marfori et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)
A de novo missense mutation of the FUS gene in a true sporadic ALS case
Adriano Chio et al.
NEUROBIOLOGY OF AGING (2011)
FUS mutations in sporadic amyotrophic lateral sclerosis
Shiao-Lin Lai et al.
NEUROBIOLOGY OF AGING (2011)
In Silico Analysis of Single Nucleotide Polymorphism (SNPs) in Human β-Globin Gene
Mohammed Alanazi et al.
PLOS ONE (2011)
A missense mutation in CLIC2 associated with intellectual disability is predicted by in silico modeling to affect protein stability and dynamics
Shawn Witham et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2011)
TDP-43 and FUS: a nuclear affair
Dorothee Dormann et al.
TRENDS IN NEUROSCIENCES (2011)
Novel FUS/TLS Mutations and Pathology in Familial and Sporadic Amyotrophic Lateral Sclerosis
Christopher Hewitt et al.
ARCHIVES OF NEUROLOGY (2010)
Recognition of nuclear targeting signals by Karyopherin-β proteins
Darui Xu et al.
CURRENT OPINION IN STRUCTURAL BIOLOGY (2010)
ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
Dorothee Dormann et al.
EMBO JOURNAL (2010)
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
Lucia Corrado et al.
JOURNAL OF MEDICAL GENETICS (2010)
A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: A clinical, pathological and genetic report
Yukiko Yamamoto-Watanabe et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia
J. Yan et al.
NEUROLOGY (2010)
Automated inference of molecular mechanisms of disease from amino acid substitutions
Biao Li et al.
BIOINFORMATICS (2009)
Next generation tools for the annotation of human SNPs
Rachel Karchin
BRIEFINGS IN BIOINFORMATICS (2009)
Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1
Marcelo Carvalho et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2009)
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
Prateek Kumar et al.
NATURE PROTOCOLS (2009)
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
N. Ticozzi et al.
NEUROLOGY (2009)
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
Caroline Vance et al.
SCIENCE (2009)
A three-state prediction of single point mutations on protein stability changes
Emidio Capriotti et al.
BMC BIOINFORMATICS (2008)
GROMACS 4: Algorithms for highly efficient, load-balanced, and scalable molecular simulation
Berk Hess et al.
JOURNAL OF CHEMICAL THEORY AND COMPUTATION (2008)
Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis
Marcelo A. Carvalho et al.
CANCER RESEARCH (2007)
Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information
E. Capriotti et al.
BIOINFORMATICS (2006)
Rules for nuclear localization sequence recognition by karyopherinβ2
Brittany J. Lee et al.
CELL (2006)
PMUT:: a web-based tool for the annotation of pathological mutations on proteins
C Ferrer-Costa et al.
BIOINFORMATICS (2005)
Integrated evaluation of DNA sequence variants of unknown clinical significance:: Application to BRCA1 and BRCA2
DE Goldgar et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003
B Boeckmann et al.
NUCLEIC ACIDS RESEARCH (2003)
Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: Structure-based assessment of amino acid variation
D Chasman et al.
JOURNAL OF MOLECULAR BIOLOGY (2001)
The Protein Data Bank
HM Berman et al.
NUCLEIC ACIDS RESEARCH (2000)