Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Anja R. Oldenburg"'
Autor:
Marie Garcia, Anne-Claire Guénantin, Anja R. Oldenburg, Emilie Capel, Jean-Sébastien Hulot, Jonas Paulsen, Nolwenn Briand, Akshay Shah, Corinne Vigouroux, Matthieu Mantecon, Philippe Collas, Dorota Jeziorowska
Publikováno v:
Human Molecular Genetics. 27:1447-1459
The p.R482W hotspot mutation in A-type nuclear lamins causes familial partial lipodystrophy of Dunnigan-type (FPLD2), a lipodystrophic syndrome complicated by early onset atherosclerosis. Molecular mechanisms underlying endothelial cell dysfunction c
Autor:
Jan Øivind Moskaug, Anita L. Sørensen, Anja R. Oldenburg, Philippe Collas, Nolwenn Briand, Inswasti Cahyani, Akshay Shah
Publikováno v:
Journal of Cell Biology. 216:2731-2743
Mutations in the Lamin A/C (LMNA) gene-encoding nuclear LMNA cause laminopathies, which include partial lipodystrophies associated with metabolic syndromes. The lipodystrophy-associated LMNA p.R482W mutation is known to impair adipogenic differentiat
Publikováno v:
BioEssays. 36:75-83
The nuclear envelope shapes the functional organization of the nucleus. Increasing evidence indicates that one of its main components, the nuclear lamina, dynamically interacts with the genome, including the promoter region of specific genes. This se
Publikováno v:
Human Molecular Genetics. 23:1151-1162
The nuclear lamina is implicated in the regulation of various nuclear functions. Several laminopathy-causing mutations in the LMNA gene, notably the p.R482W substitution linked to familial partial lipodystrophy type 2 (FPLD2), are clustered in the im
Autor:
Jonas Paulsen, Monika Sekelja, Corinne Vigouroux, Anja R. Oldenburg, Anita L. Sørensen, Akshay Shah, Nolwenn Briand, Erwan Delbarre, Alice Barateau, Brigitte Buendia, Philippe Collas
Publikováno v:
Genome Biology
Genome Biology, 2017, 18, pp.21. ⟨10.1186/s13059-016-1146-2⟩
Genome Biology, BioMed Central, 2017, 18, pp.21. ⟨10.1186/s13059-016-1146-2⟩
Genome Biology, 2017, 18, pp.21. ⟨10.1186/s13059-016-1146-2⟩
Genome Biology, BioMed Central, 2017, 18, pp.21. ⟨10.1186/s13059-016-1146-2⟩
Current three-dimensional (3D) genome modeling platforms are limited by their inability to account for radial placement of loci in the nucleus. We present Chrom3D, a user-friendly whole-genome 3D computational modeling framework that simulates positi
Autor:
Anja R, Oldenburg, Philippe, Collas
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1411
The nuclear lamina is a meshwork of A- and B-type lamins which interact with chromatin and regulate many nuclear functions. Recent studies have reported the discovery of chromatin domains interacting with nuclear lamins by chromatin immunoprecipitati
Autor:
Philippe Collas, Anja R. Oldenburg
Publikováno v:
Methods in Molecular Biology ISBN: 9781493935284
The nuclear lamina is a meshwork of A- and B-type lamins which interact with chromatin and regulate many nuclear functions. Recent studies have reported the discovery of chromatin domains interacting with nuclear lamins by chromatin immunoprecipitati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94362cab556c31474b0c75e4d5423a3a
https://doi.org/10.1007/978-1-4939-3530-7_20
https://doi.org/10.1007/978-1-4939-3530-7_20
Autor:
Torunn Rønningen, Akshay Shah, Philippe Collas, Anja R. Oldenburg, Kristin Vekterud, Erwan Delbarre, Jan Øivind Moskaug
Publikováno v:
Genome research. 25(12)
Dynamic interactions of nuclear lamins with chromatin through lamin-associated domains (LADs) contribute to spatial arrangement of the genome. Here, we provide evidence for prepatterning of differentiation-driven formation of lamin A/C LADs by domain
The nuclear lamina has been shown to interact with the genome through lamina-associated domains (LADs). LADs have been identified by DamID, a proximity labeling assay, and more recently by chromatin immunoprecipitation-sequencing (ChIP-seq) of A- and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9adda348fd4375cfd29d97bf6cb320e
https://europepmc.org/articles/PMC4615303/
https://europepmc.org/articles/PMC4615303/
Autor:
Philippe Collas, Nathalie Vadrot, Nolwenn Briand, Wikayatou Attanda, Anja R. Oldenburg, Brigitte Buendia, Eva Cabet, Patrick Vicart, Isabelle Duband-Goulet, Alice Barateau, Eivind G. Lund, Corinne Vigouroux, Fabien Gerbal
Publikováno v:
Human molecular genetics. 24(7)
Nuclear lamins are involved in many cellular functions due to their ability to bind numerous partners including chromatin and transcription factors, and affect their properties. Dunnigan type familial partial lipodystrophy (FPLD2; OMIM#151660) is cau