Université Pierre-et-Marie-Curie
110 imported, source-linked research records. All imported publication dates.
110 matching research records
Topic: Nuclear architecture. Only records linked to Université Pierre-et-Marie-Curie are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.
Showing 1–50 of 110 matching records. Counts update as records arrive.
MYH7 -related myopathies: clinical, myopathological and genotypic spectrum in a multicentre French cohort
October 24, 2024 · 12 citations · Open access
Open original record →Nuclear Translocation of the LINE-1 Encoded ORF1 Protein Alters Nuclear Envelope Integrity in Human Neurons
January 1, 2024 · 0 citations · Open access
Open original record →Hutchinson-Gilford progeria syndrome: Rejuvenating old drugs to fight accelerated ageing
April 9, 2020 · 35 citations · Open access
Open original record →Autophagy-Dependent Ferroptosis: Machinery and Regulation
March 10, 2020 · 816 citations · Open access
Open original record →The mammalian LINC complex component SUN1 regulates muscle regeneration by modulating drosha activity.
November 5, 2019 · 0 citations · Open access
Open original record →Healthspan and lifespan extension by fecal microbiota transplantation into progeroid mice
July 22, 2019 · 685 citations · Open access
Open original record →Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies
June 3, 2019 · 279 citations · Open access
Open original record →Extracellular matrix mechanical cues regulate lipid metabolism through Lipin-1 and SREBP
February 4, 2019 · 236 citations · Open access
Open original record →Clinical Diagnosis, Imaging, and Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
August 1, 2018 · 273 citations · Open access
Open original record →Methionine Restriction Extends Lifespan in Progeroid Mice and Alters Lipid and Bile Acid Metabolism
August 1, 2018 · 188 citations · Open access
Open original record →Rescue of biosynthesis of nicotinamide adenine dinucleotide protects the heart in cardiomyopathy caused by lamin A/C gene mutation
July 23, 2018 · 57 citations · Open access
Open original record →KAP1 facilitates reinstatement of heterochromatin after DNA replication
June 25, 2018 · 52 citations · Open access
Open original record →Active fluctuations modulate gene expression in mouse oocytes
June 14, 2018 · 2 citations · Open access
Open original record →Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes
April 25, 2018 · 38 citations · Open access
Open original record →The lipodystrophic hotspot lamin A p.R482W mutation deregulates the mesodermal inducer T/Brachyury and early vascular differentiation gene networks
February 8, 2018 · 48 citations · Open access
Open original record →Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next‐generation human artificial chromosomes for Duchenne muscular dystrophy
December 14, 2017 · 33 citations · Open access
Open original record →The early pregnancy placenta foreshadows DNA methylation alterations of solid tumors
July 5, 2017 · 46 citations · Open access
Open original record →Molecular definitions of autophagy and related processes
June 8, 2017 · 1,643 citations · Open access
Open original record →Distinct Fiber Type Signature in Mouse Muscles Expressing a Mutant Lamin A Responsible for Congenital Muscular Dystrophy in a Patient
April 24, 2017 · 4 citations · Open access
Open original record →Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
March 15, 2017 · 111 citations · Open access
Open original record →Autophagie, bonne santé et longévité
March 1, 2017 · 3 citations · Open access
Open original record →A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus
January 26, 2017 · 27 citations · Open access
Open original record →Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care
December 12, 2016 · 21 citations
Open original record →Epigenetic studies of plasmodium falciparum pre-erythrocytic stages
December 1, 2016 · 0 citations · Open access
Open original record →Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy
November 15, 2016 · 46 citations · Open access
Open original record →Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene
November 8, 2016 · 66 citations · Open access
Open original record →Positioning nuclei at the periphery of skeletal muscle cells
September 27, 2016 · 0 citations · Open access
Open original record →Caractérisation morphologique et moléculaire du néphroblastome, du blastème et de la région chromosomique 11p15 en particulier
September 19, 2016 · 0 citations · Open access
Open original record →Clinical Utility Gene Card for: Familial partial lipodystrophy
August 3, 2016 · 18 citations · Open access
Open original record →Role of oxidised protein repair for skeletal muscle homeostasis
July 1, 2016 · 0 citations · Open access
Open original record →ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene
April 30, 2016 · 103 citations · Open access
Open original record →YAP-Mediated Mechanotransduction in Skeletal Muscle
February 16, 2016 · 140 citations · Open access
Open original record →The 3D folding of metazoan genomes correlates with the association of similar repetitive elements
November 24, 2015 · 116 citations · Open access
Open original record →One‐year metreleptin improves insulin secretion in patients with diabetes linked to genetic lipodystrophic syndromes
November 20, 2015 · 58 citations · Open access
Open original record →A common French-Italian laminopathy registry – update & future prospects
November 11, 2015 · 0 citations · Open access
Open original record →Gene Therapy for LMNA-related Congenital Muscular Dystrophy (L-CMD) by Trans-Splicing
November 11, 2015 · 3 citations · Open access
Open original record →Linking replication stress with heterochromatin formation
October 28, 2015 · 61 citations · Open access
Open original record →Spatial reorganization of telomeres in long-lived quiescent cells
September 23, 2015 · 106 citations · Open access
Open original record →Probing the target search of DNA-binding proteins in mammalian cells using TetR as model searcher
July 7, 2015 · 228 citations · Open access
Open original record →Dynamique des variants de l'histone H3 en réponse aux dommages de l'ADN induits par les UVC dans les cellules humaines
June 15, 2015 · 0 citations · Open access
Open original record →Refining the regulatory region upstream of SOX9 associated with 46,XX testicular disorders of Sex Development (DSD)
April 21, 2015 · 67 citations · Open access
Open original record →Blue‐light dependent reactive oxygen species formation by Arabidopsis cryptochrome may define a novel evolutionarily conserved signaling mechanism
February 26, 2015 · 122 citations · Open access
Open original record →Truncated prelamin A expression in HGPS-like patients: a transcriptional study
February 4, 2015 · 38 citations · Open access
Open original record →Cardiac involvement in laminopathies
January 1, 2015 · 3 citations · Open access
Open original record →An overview of new translational, clinical and therapeutic perspectives in laminopathies and other nuclear envelope-related diseases.
January 1, 2015 · 1 citations · Open access
Open original record →High-quality genome (re)assembly using chromosomal contact data
December 17, 2014 · 168 citations · Open access
Open original record →Nuclear volume differences between balanced and unbalanced spermatozoa in chromosomal translocation carriers
December 4, 2014 · 7 citations · Open access
Open original record →Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1
November 25, 2014 · 51 citations · Open access
Open original record →Altered cross-bridge properties in skeletal muscle dystrophies
October 14, 2014 · 9 citations · Open access
Open original record →Diagnostic approach to the congenital muscular dystrophies
January 9, 2014 · 347 citations · Open access
Open original record →