Found: 5
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The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophy.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 7, p. 2096, doi. 10.1093/hmg/ddu728
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- Publication type:
- Article
Deregulation of Fragile X-related protein 1 by the lipodystrophic lamin A p.R482W mutation elicits a myogenic gene expression program in preadipocytes.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1151, doi. 10.1093/hmg/ddt509
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- Publication type:
- Article
Enriched domain detector: a program for detection of wide genomic enrichment domains robust against local variations.
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. 11, p. e92, doi. 10.1093/nar/gku324
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- Publication type:
- Article
Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts.
- Published in:
- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-016-1146-2
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- Publication type:
- Article
Closing the (nuclear) envelope on the genome: How nuclear lamins interact with promoters and modulate gene expression.
- Published in:
- BioEssays, 2014, v. 36, n. 1, p. 75, doi. 10.1002/bies.201300138
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- Publication type:
- Article