Detalhe da pesquisa
1.
The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophy.
Hum Mol Genet
; 24(7): 2096-109, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25524705
2.
A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus.
PLoS One
; 12(1): e0169189, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28125586
3.
Distinct Fiber Type Signature in Mouse Muscles Expressing a Mutant Lamin A Responsible for Congenital Muscular Dystrophy in a Patient.
Cells
; 6(2)2017 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-28441765
4.
Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts.
Genome Biol
; 18(1): 21, 2017 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28137286
5.
In Situ Detection of Interactions Between Nuclear Envelope Proteins and Partners.
Methods Mol Biol
; 1411: 147-58, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27147040