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

Promoter analysis of the human centromeric and telomeric survival motor neuron genes (SMNC and SMNT)

1 Jun 1999

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 Muscle Physiology and Disorders
Share to Neurogenetic and Muscular Disorders Research
Share to RNA modifications and cancer

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 10366716
DOI: 10.1016/s0167-4781(99)00060-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Promoter analysis of the human centromeric and telomeric survival motor neuron genes (SMNC and SMNT)PMID 10366716Read ↗

Structure and Organization of the Human Survival Motor Neurone (SMN) GeneSemantic proximity Read ↗

Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron diseaseSemantic proximity Read ↗

Identification and characterization of a spinal muscular atrophy-determining gene.Semantic proximity Read ↗

Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy.Semantic proximity Read ↗

A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2.Semantic proximity Read ↗

The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy.Semantic proximity Read ↗

The survival motor neuron protein in spinal muscular atrophySemantic proximity Read ↗

Association between centromeric deletions of the SMN gene and sporadic adult‐onset lower motor neuron diseaseSemantic proximity Read ↗

Comprehensive Analysis of Retrotransposon Insertions within the Survival Motor Neuron Genes Involved in Spinal Muscular AtrophySemantic proximity Read ↗

SMNΔ7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMNSemantic proximity Read ↗

Human promoter analysis of the Programmed Axon Death genes <i>NMNAT2</i> and <i>SARM1</i>Semantic proximity Read ↗

Cloning and characterization of human and mouse telomerase RNA gene promoter sequencesSemantic proximity Read ↗

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