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Items: 3

1.

A progeria-associated BAF-1 mutation modulates gene expression and accelerates aging in C. elegans II

(Submitter supplied) Alterations in the nuclear envelope are linked to a variety of rare diseases termed laminopathies. These include both tissue specific and systemic diseases. A single amino acid substitution in human barrier to autointegration factor (BAF) at position 12 (A12T) causes Néstor-Guillermo Progeria Syndrome (NGPS). This premature ageing condition affects a variety of tissues, leading to growth retardation and severe skeletal defects, including scoliosis. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19757
24 Samples
Download data: TXT
Series
Accession:
GSE261820
ID:
200261820
2.

Illumina NextSeq 500 (Caenorhabditis elegans)

Organism:
Caenorhabditis elegans
210 Series
3371 Samples
Download data
Platform
Accession:
GPL19757
ID:
100019757
3.

BN1047, Rep1, Dam::BAF-1

Organism:
Caenorhabditis elegans
Source name:
Hypodermis
Platform:
GPL19757
Series:
GSE261820
Download data
Sample
Accession:
GSM8152548
ID:
308152548
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db=gds|term=GSM8152548[Accession]|query=1|qty=2|blobid=MCID_6676f7608c5d4760e2daa5ef|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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