Article

In silico analysis of detrimental mutation in EPHB2 gene causing Alzheimer’s disease

2014-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: b7287605-8501-5952-a0af-c2830181dbfa
DOI: 10.1186/1471-2164-15-s2-p46
PMCID: PMC4075625

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

In silico analysis of detrimental mutation in EPHB2 gene causing Alzheimer’s diseaseDOI 10.1186/1471-2164-15-s2-p46Read

In-silico predictions of deleterious SNPs in Human ephrin type-A receptor 3 (EPHA3) geneSemantic proximity Read

Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's diseaseSemantic proximity Read

De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer diseaseSemantic proximity Read

Variant TREM2 Signaling in Alzheimer's DiseaseSemantic proximity Read

Familial Alzheimer's chromosome 14 mutationsSemantic proximity Read

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseSemantic proximity Read

A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature.Semantic proximity Read

EphA4 regulates Aβ production via BACE1 expression in neuronsSemantic proximity Read

Mutation analysis of the MS4A and TREM gene clusters in a case-control Alzheimer's disease data set.Semantic proximity Read

Molecular Modelling of nsSNPs in GABRA2 Gene in Epilepsy and Study of Their Impact On Structure and Stability of GABRA2 ProteinSemantic proximity Read

Sequence analysis and bioinformatics analysis of chromosome 17q25 in familial moyamoya diseaseSemantic proximity Read

Classification of <i>ACE</i> variants related to Alzheimer’s disease (AD): the <i>ACE</i> mutations — AD browserSemantic proximity Read