| scholarly article | Q13442814 |
| P50 | author | Caroline Le Dour | Q83465355 |
| P2093 | author name string | Wei Wu | |
| Howard J Worman | |||
| Corinne Vigouroux | |||
| Jacqueline Capeau | |||
| Véronique Béréziat | |||
| P2860 | cites work | Real-time PCR based on SYBR-Green I fluorescence: an alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions | Q21256663 |
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| An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy | Q24295141 | ||
| Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C | Q24612380 | ||
| Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse | Q24632769 | ||
| Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
| Structure of the globular tail of nuclear lamin | Q27638385 | ||
| The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy | Q27639152 | ||
| Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease | Q28139053 | ||
| Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy | Q28139598 | ||
| Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B) | Q28144565 | ||
| Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome | Q28201199 | ||
| Nuclear envelope-related lipodystrophies | Q28305014 | ||
| Matrix metalloproteinases and the regulation of tissue remodelling | Q29618747 | ||
| TGF-beta signaling and the fibrotic response | Q29620099 | ||
| Narrative review: fibrotic diseases: cellular and molecular mechanisms and novel therapies | Q34096270 | ||
| Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C | Q34145499 | ||
| Lamin a truncation in Hutchinson-Gilford progeria. | Q34191501 | ||
| Fibrosis in human adipose tissue: composition, distribution, and link with lipid metabolism and fat mass loss | Q34237665 | ||
| "Laminopathies": a wide spectrum of human diseases | Q34242119 | ||
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| Acquired and inherited lipodystrophies | Q34306820 | ||
| Hepatic steatosis in Dunnigan-type familial partial lipodystrophy | Q34453418 | ||
| Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy | Q35102865 | ||
| LMNA mutations induce a non-inflammatory fibrosis and a brown fat-like dystrophy of enlarged cervical adipose tissue | Q35474290 | ||
| Adipose tissue transcriptomic signature highlights the pathological relevance of extracellular matrix in human obesity | Q36673494 | ||
| Metabolic dysregulation and adipose tissue fibrosis: role of collagen VI. | Q37110569 | ||
| Perilipin deficiency and autosomal dominant partial lipodystrophy | Q37173608 | ||
| The role of LMNA in adipose: a novel mouse model of lipodystrophy based on the Dunnigan-type familial partial lipodystrophy mutation. | Q37190360 | ||
| Stimulation of adipogenesis of adult adipose-derived stem cells using substrates that mimic the stiffness of adipose tissue. | Q37206807 | ||
| Fibrosis and adipose tissue dysfunction | Q37227722 | ||
| ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene | Q37367994 | ||
| Adipose tissue expandability, lipotoxicity and the Metabolic Syndrome--an allostatic perspective | Q37670371 | ||
| Nuclear lamin-A scales with tissue stiffness and enhances matrix-directed differentiation | Q37686106 | ||
| Matrix metalloproteinases in metabolic syndrome | Q37979368 | ||
| Transforming growth factor-β signalling: role and consequences of Smad linker region phosphorylation. | Q38114728 | ||
| Decorin-binding Sites for Collagen Type I Are Mainly Located in Leucine-rich Repeats 4-5 | Q38291995 | ||
| The genetics of lipid storage and human lipodystrophies | Q38483874 | ||
| Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins | Q38893099 | ||
| Picrosirius staining plus polarization microscopy, a specific method for collagen detection in tissue sections | Q39572948 | ||
| Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy | Q42489401 | ||
| Fibronectin modulation of cell shape and lipogenic gene expression in 3T3-adipocytes | Q42820082 | ||
| The mechanical properties of human adipose tissues and their relationships to the structure and composition of the extracellular matrix | Q44306285 | ||
| Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome | Q44550613 | ||
| Characterization of adiposity and metabolism in Lmna-deficient mice | Q45713457 | ||
| Altered fat differentiation and adipocytokine expression are inter-related and linked to morphological changes and insulin resistance in HIV-1-infected lipodystrophic patients. | Q50785190 | ||
| Needle and surgical biopsy techniques differentially affect adipose tissue gene expression profiles. | Q51670985 | ||
| Histological and molecular features of lipomatous and nonlipomatous adipose tissue in familial partial lipodystrophy caused by LMNA mutations. | Q53222335 | ||
| New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome. | Q53230531 | ||
| LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. | Q54064162 | ||
| Familial lipoatrophic diabetes with dominant transmission. A new syndrome. | Q54544860 | ||
| Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy | Q57149453 | ||
| Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement | Q59461161 | ||
| Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies | Q60535383 | ||
| Mid-myocardial fibrosis by cardiac magnetic resonance in patients with lamin A/C cardiomyopathy: possible substrate for diastolic dysfunction | Q80164268 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 1 | |
| P304 | page(s) | 151-163 | |
| P577 | publication date | 2016-11-14 | |
| P1433 | published in | Journal of Lipid Research | Q6295449 |
| P1476 | title | Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy | |
| P478 | volume | 58 |
| Q48019389 | A lipodystrophy-causing lamin A mutant alters conformation and epigenetic regulation of the anti-adipogenic MIR335 locus. |
| Q92038784 | Ablation of SUN2-containing LINC complexes drives cardiac hypertrophy without interstitial fibrosis |
| Q41616038 | Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective. |
| Q57029307 | Fat fibrosis: friend or foe? |
| Q33799816 | LMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 Diabetes |
| Q90601728 | Lamin A, Chromatin and FPLD2: Not Just a Peripheral Ménage-à-Trois |
| 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. |
| Q51759528 | Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives. |
| Q47227302 | Messages from the voices within: regulation of signaling by proteins of the nuclear lamina. |
| Q55515543 | TGF-β Sustains Tumor Progression through Biochemical and Mechanical Signal Transduction. |
| Q91883618 | The structural and gene expression hypotheses in laminopathic diseases-not so different after all |
| Q91782097 | Towards precision medicine: defining and characterizing adipose tissue dysfunction to identify early immunometabolic risk in symptom-free adults from the GEMM family study |
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