Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A microdeletion in Alzheimer's disease disrupts NAMPT gene.

Journal of genetics - 1 Aug 2014

Villela Darine, Schlesinger David, Suemoto Claudia K, Grinberg Lea T, Rosenberg Carla

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alzheimer Disease
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 7
Share to Comparative Genomic Hybridization

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytokines

Share to DNA Copy Number Variations

Share to Genetic Association Studies

Share to Nicotinamide Phosphoribosyltransferase

Source

Identifiers

PMID: 25189255
DOI: 10.1007/s12041-014-0399-3

Genes

NAMPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A microdeletion in Alzheimer's disease disrupts NAMPT gene.PMID 25189255Read ↗

<i>TMEM230</i> is not a gene for Parkinson’s diseaseSemantic proximity Read ↗

Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2.Semantic proximity Read ↗

TMEM106B is a susceptibility locus for Ftld.Semantic proximity Read ↗

A sensory and motor neuropathy caused by a genetic variant of NAMPT.Semantic proximity Read ↗

NAMPT and NAPRT1: novel polymorphisms and distribution of variants between normal tissues and tumor samples.Semantic proximity Read ↗

Programmed axon degeneration gene variants in human disease.Semantic proximity Read ↗

DNA Methyltransferase 1 Is Dysregulated in Parkinson’s Disease via Mediation of miR-17Semantic proximity Read ↗

Characterisation of a novel NR4A2 mutation in Parkinson's disease brain.Semantic proximity Read ↗

A novel genomic mutation in ADNP leading to intellectual disability.Semantic proximity Read ↗

Downregulation of lncRNA MEG3 is involved in Parkinson’s diseaseSemantic proximity Read ↗

From a single nucleotide polymorphism to tau pathology: Appoptosin is the missing link.Semantic proximity Read ↗

Alzheimer’s disease-associated <i>TM2D</i> genes regulate Notch signaling and neuronal function in <i>Drosophila</i>Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.