4.7 Article

Mutational analysis of FUS gene and its structural and functional role in amyotrophic lateral sclerosis 6

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Untitled

HUMAN MUTATION (2018)

Article Genetics & Heredity

Untitled

HUMAN MUTATION (2018)

Article Neurosciences

Untitled

EUROPEAN JOURNAL OF NEUROLOGY (2016)

Article Biochemistry & Molecular Biology

Computational Screening of Disease-Associated Mutations in OCA2 Gene

Balu Kamaraj et al.

CELL BIOCHEMISTRY AND BIOPHYSICS (2014)

Article Biochemistry & Molecular Biology

Drug resistance mechanism of PncA in Mycobacterium tuberculosis

Vidya Rajendran et al.

JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2014)

Article Biochemistry & Molecular Biology

Role of ELA region in auto-activation of mutant KIT receptor: a molecular dynamics simulation insight

Rituraj Purohit

JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2014)

Article Biochemistry & Molecular Biology

Investigation of Binding Phenomenon of NSP3 and p130Cas Mutants and Their Effect on Cell Signalling

K. Balu et al.

CELL BIOCHEMISTRY AND BIOPHYSICS (2013)

Review Biochemistry & Molecular Biology

Molecular Mechanisms of Disease-Causing Missense Mutations

Shannon Stefl et al.

JOURNAL OF MOLECULAR BIOLOGY (2013)

Article Biochemistry & Molecular Biology

In-silico screening of cancer associated mutation on PLK1 protein and its structural consequences

Balu Kamaraj et al.

JOURNAL OF MOLECULAR MODELING (2013)

Article Biotechnology & Applied Microbiology

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)

Review Biochemistry & Molecular Biology

Nuclear import by karyopherin-βs: Recognition and inhibition

Yuh Min Chook et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)

Review Biochemistry & Molecular Biology

Molecular basis for specificity of nuclear import and prediction of nuclear localization

Mary Marfori et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)

Article Geriatrics & Gerontology

A de novo missense mutation of the FUS gene in a true sporadic ALS case

Adriano Chio et al.

NEUROBIOLOGY OF AGING (2011)

Article Geriatrics & Gerontology

FUS mutations in sporadic amyotrophic lateral sclerosis

Shiao-Lin Lai et al.

NEUROBIOLOGY OF AGING (2011)

Article Multidisciplinary Sciences

In Silico Analysis of Single Nucleotide Polymorphism (SNPs) in Human β-Globin Gene

Mohammed Alanazi et al.

PLOS ONE (2011)

Article Biochemistry & Molecular Biology

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)

Review Neurosciences

TDP-43 and FUS: a nuclear affair

Dorothee Dormann et al.

TRENDS IN NEUROSCIENCES (2011)

Article Biochemistry & Molecular Biology

Recognition of nuclear targeting signals by Karyopherin-β proteins

Darui Xu et al.

CURRENT OPINION IN STRUCTURAL BIOLOGY (2010)

Article Biochemistry & Molecular Biology

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

Dorothee Dormann et al.

EMBO JOURNAL (2010)

Article Genetics & Heredity

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis

Lucia Corrado et al.

JOURNAL OF MEDICAL GENETICS (2010)

Article Clinical Neurology

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)

Letter Biochemical Research Methods

A method and server for predicting damaging missense mutations

Ivan A. Adzhubei et al.

NATURE METHODS (2010)

Article Biochemical Research Methods

Automated inference of molecular mechanisms of disease from amino acid substitutions

Biao Li et al.

BIOINFORMATICS (2009)

Article Biochemical Research Methods

Next generation tools for the annotation of human SNPs

Rachel Karchin

BRIEFINGS IN BIOINFORMATICS (2009)

Article Biotechnology & Applied Microbiology

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)

Article Biochemical Research Methods

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

Prateek Kumar et al.

NATURE PROTOCOLS (2009)

Article Biochemical Research Methods

A three-state prediction of single point mutations on protein stability changes

Emidio Capriotti et al.

BMC BIOINFORMATICS (2008)

Article Chemistry, Physical

GROMACS 4: Algorithms for highly efficient, load-balanced, and scalable molecular simulation

Berk Hess et al.

JOURNAL OF CHEMICAL THEORY AND COMPUTATION (2008)

Article Biochemistry & Molecular Biology

Rules for nuclear localization sequence recognition by karyopherinβ2

Brittany J. Lee et al.

Article Biochemical Research Methods

PMUT:: a web-based tool for the annotation of pathological mutations on proteins

C Ferrer-Costa et al.

BIOINFORMATICS (2005)

Article Genetics & Heredity

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)

Article Biochemistry & Molecular Biology

The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003

B Boeckmann et al.

NUCLEIC ACIDS RESEARCH (2003)

Article Biochemistry & Molecular Biology

The Protein Data Bank

HM Berman et al.

NUCLEIC ACIDS RESEARCH (2000)