| scholarly article | Q13442814 |
| P356 | DOI | 10.1021/BI020704G |
| P698 | PubMed publication ID | 12718522 |
| P50 | author | Joël Couprie | Q58239952 |
| Isabelle Krimm | Q73003613 | ||
| P2093 | author name string | Howard J Worman | |
| Sophie Zinn-Justin | |||
| Jean-Claude Courvalin | |||
| Vérène Stierlé | |||
| Isabelle Duband-Goulet | |||
| Cecilia Ostlund | |||
| Paul Hossenlopp | |||
| P433 | issue | 17 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 4819-4828 | |
| P577 | publication date | 2003-05-01 | |
| P1433 | published in | Biochemistry | Q764876 |
| P1476 | title | The carboxyl-terminal region common to lamins A and C contains a DNA binding domain | |
| P478 | volume | 42 |
| Q58650523 | A Novel Mutation in Lamin A/C Gene: Phenotype and Consequences on the Protein Structure and Flexibility |
| Q28072459 | A Novel Role of Lamins from Genetic Disease to Cancer Biomarkers |
| Q47162408 | A Perspective on the Experimental Techniques for Studying Lamins |
| Q24671540 | A carboxyl-terminal interaction of lamin B1 is dependent on the CAAX endoprotease Rce1 and carboxymethylation |
| Q33512523 | A comparative study of Drosophila and human A-type lamins |
| Q48019389 | A lipodystrophy-causing lamin A mutant alters conformation and epigenetic regulation of the anti-adipogenic MIR335 locus. |
| Q39297135 | A truncated lamin A in the Lmna -/- mouse line: implications for the understanding of laminopathies |
| Q36249005 | A-type lamin complexes and regenerative potential: a step towards understanding laminopathic diseases? |
| Q35934217 | A-type lamins: guardians of the soma? |
| Q37352413 | A-type nuclear lamins act as transcriptional repressors when targeted to promoters. |
| Q42815664 | Altered pre-lamin A processing is a common mechanism leading to lipodystrophy. |
| Q24791233 | Altered protein dynamics of disease-associated lamin A mutants |
| Q41387611 | Atomic Force Microscopy micro-rheology reveals large structural inhomogeneities in single cell-nuclei. |
| Q21284190 | Bomapin is a redox-sensitive nuclear serpin that affects responsiveness of myeloid progenitor cells to growth environment |
| Q50775986 | Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization. |
| Q37612740 | Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts |
| Q24292954 | Conformational changes in the nuclear lamina induced by herpes simplex virus type 1 require genes U(L)31 and U(L)34 |
| Q64106731 | Deciphering Nuclear Mechanobiology in Laminopathy |
| Q36305787 | Differential basal-to-apical accessibility of lamin A/C epitopes in the nuclear lamina regulated by changes in cytoskeletal tension |
| Q40009819 | Differentiation of C2C12 myoblasts expressing lamin A mutated at a site responsible for Emery-Dreifuss muscular dystrophy is improved by inhibition of the MEK-ERK pathway and stimulation of the PI3-kinase pathway |
| Q33687043 | Diseases of the nuclear envelope |
| Q28651142 | Economy, speed and size matter: evolutionary forces driving nuclear genome miniaturization and expansion |
| Q36232795 | Expression of a mutant lamin A that causes Emery-Dreifuss muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts |
| Q39994086 | Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects |
| Q44641885 | Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription |
| Q38085610 | Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations |
| Q33649127 | Genome mapping and characterization of the Anopheles gambiae heterochromatin |
| Q33737760 | Identification of an essential domain in the herpes simplex virus 1 UL34 protein that is necessary and sufficient to interact with UL31 protein |
| Q38301171 | Interaction of a self-assembling peptide with oligonucleotides: complexation and aggregation |
| Q37958971 | LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations |
| Q40451474 | Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy. |
| Q28277676 | Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy |
| Q93386944 | Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation |
| Q52882876 | Lamin A reassembly at the end of mitosis is regulated by its SUMO-interacting motif. |
| Q90601728 | Lamin A, Chromatin and FPLD2: Not Just a Peripheral Ménage-à-Trois |
| Q39181367 | Lamin A/C Cardiomyopathies: Current Understanding and Novel Treatment Strategies |
| Q33752204 | Lamin-binding Proteins |
| Q54994621 | Laminopathy-causing lamin A mutations reconfigure lamina-associated domains and local spatial chromatin conformation. |
| Q64881706 | Lamins and Lamin-Associated Proteins in Gastrointestinal Health and Disease. |
| Q38698252 | Lamins in the nuclear interior - life outside the lamina |
| Q51759528 | Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives. |
| Q24336480 | Loss of a DNA binding site within the tail of prelamin A contributes to altered heterochromatin anchorage by progerin |
| Q40480429 | MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-beta signaling. |
| Q36237237 | Mapping of lamin A- and progerin-interacting genome regions |
| Q33895715 | Mechanobiology and the microcirculation: cellular, nuclear and fluid mechanics |
| Q34972521 | Mutations in LMNA modulate the lamin A--Nesprin-2 interaction and cause LINC complex alterations |
| Q58758731 | Nesprins and Lamins in Health and Diseases of Cardiac and Skeletal Muscles |
| Q52843884 | Non-farnesylated B-type lamin can tether chromatin inside the nucleus and its chromatin interaction requires the Ig-fold region. |
| Q39821362 | Novel roles for A-type lamins in telomere biology and the DNA damage response pathway. |
| Q35194606 | Nuclear envelope and genome interactions in cell fate |
| Q36258265 | Nuclear envelope, nuclear lamina, and inherited disease |
| Q34925545 | Nuclear lamins and chromatin: when structure meets function. |
| Q34766646 | Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin |
| Q41958139 | Nuclear lamins: making contacts with promoters |
| Q47799769 | Nuclear protein import is reduced in cells expressing nuclear envelopathy-causing lamin A mutants |
| Q37183946 | Nuclear shape, mechanics, and mechanotransduction |
| Q34574178 | Nucleoskeleton mechanics at a glance |
| Q26851708 | Overlapping syndromes in laminopathies: a meta-analysis of the reported literature |
| Q38087890 | Partners and post-translational modifications of nuclear lamins |
| Q41277814 | Phosphorylation of connexin43 on S279/282 may contribute to laminopathy-associated conduction defects. |
| Q28071818 | Physiological and Pathological Aging Affects Chromatin Dynamics, Structure and Function at the Nuclear Edge |
| Q42092692 | Prepatterning of differentiation-driven nuclear lamin A/C-associated chromatin domains by GlcNAcylated histone H2B. |
| Q40175421 | Primary laminopathy fibroblasts display altered genome organization and apoptosis. |
| Q35623475 | Proliferation-dependent positioning of individual centromeres in the interphase nucleus of human lymphoblastoid cell lines |
| Q35589666 | Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins |
| Q28083281 | Regulation of lamin properties and functions: does phosphorylation do it all? |
| Q42013273 | Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment |
| Q37663719 | Role of A-type lamins in signaling, transcription, and chromatin organization. |
| Q92937255 | SIRT7 mediates L1 elements transcriptional repression and their association with the nuclear lamina |
| Q92190852 | Spatial chromatin organization and gene regulation at the nuclear lamina |
| Q42133558 | Structure and stability of the lamin A tail domain and HGPS mutant |
| Q27646419 | Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD) |
| Q37296179 | The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress |
| Q34185976 | The different function of single phosphorylation sites of Drosophila melanogaster lamin Dm and lamin C |
| Q26859120 | The nuclear lamina is mechano-responsive to ECM elasticity in mature tissue |
| Q36815711 | The nuclear lamina. Both a structural framework and a platform for genome organization |
| Q28209433 | The strange case of the "lumper" lamin A/C gene and human premature ageing |
| Q53853271 | [Laminopathies: lipodystrophies, insulin resistance, syndromes of accelerated ageing... and others]. |
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