| human | Q5 |
| P11886 | CNR ExploRA author ID | cristina.capanni |
| P10058 | IRIS UNIBO author ID | 11314 |
| P496 | ORCID iD | 0000-0001-8030-2508 |
| P1053 | ResearcherID | C-6995-2019 |
| P69 | educated at | University of Bologna | Q131262 |
| P108 | employer | Consiglio Nazionale delle Ricerche | Q902464 |
| P734 | family name | Capanni | Q100255548 |
| Capanni | Q100255548 | ||
| Capanni | Q100255548 | ||
| P735 | given name | Cristina | Q12899499 |
| Cristina | Q12899499 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q56996026 | A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome |
| Q36557465 | All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype. |
| Q46620985 | Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy |
| Q36205365 | Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment. |
| Q42815664 | Altered pre-lamin A processing is a common mechanism leading to lipodystrophy. |
| Q92713440 | Ankrd2 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies |
| Q28187977 | Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts |
| Q35771419 | Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. |
| Q37085852 | Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes |
| Q50854668 | Changes in vimentin, lamin A/C and mitofilin induce aberrant cell organization in fibroblasts from Fanconi anemia complementation group A (FA-A) patients. |
| Q57006982 | Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts |
| Q37211621 | Detection of mesenchymal stem cells senescence by prelamin A accumulation at the nuclear level. |
| Q47100171 | Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria. |
| Q51730936 | Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria. |
| Q38284300 | Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathies |
| Q46841230 | Drugs affecting prelamin A processing: effects on heterochromatin organization |
| Q28241359 | Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition |
| Q104801342 | Ectopic Expression of Ankrd2 Affects Proliferation, Motility and Clonogenic Potential of Human Osteosarcoma Cells |
| Q96226421 | Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization |
| Q56999311 | Emerin increase in regenerating muscle fibers |
| Q28144946 | Emerin presence in platelets |
| Q24309728 | Emerin-prelamin A interplay in human fibroblasts |
| Q38770767 | Emery-Dreifuss Muscular Dystrophy-Associated Mutant Forms of Lamin A Recruit the Stress Responsive Protein Ankrd2 into the Nucleus, Affecting the Cellular Response to Oxidative Stress. |
| Q34198632 | Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation |
| 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 |
| Q35559998 | Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene |
| Q36338746 | Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution |
| Q35103245 | Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology. |
| Q57000570 | Implications for nuclear organization and gene transcription of lamin A/C specific mutations |
| Q61819072 | Increase of Neuronal Nitric Oxide Synthase in Rat Skeletal Muscle during Ageing |
| Q57590763 | Inhibition of Metalloproteinase Activity in FANCA Is Linked to Altered Oxygen Metabolism |
| Q53316358 | Lamin A precursor induces barrier-to-autointegration factor nuclear localization. |
| Q34170514 | Laminopathies and lamin-associated signaling pathways |
| Q36542162 | Laminopathies: a chromatin affair |
| Q35897196 | Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases |
| Q44421915 | Lamins are rapamycin targets that impact human longevity: a study in centenarians |
| Q42912005 | Leupeptin preserves cardiac nitric oxide synthase 3 during reperfusion following long-term cardioplegia |
| Q43556782 | Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A. |
| Q46778702 | Muscular laminopathies: role of prelamin A in early steps of muscle differentiation |
| Q57007663 | Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy |
| Q36439430 | Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies. |
| Q57640118 | Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers |
| Q56985192 | Osteoblasts from a mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts |
| Q97651371 | PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation |
| Q60641354 | Phosphatidylinositol 3-Kinase Is Required for the Induction of Ornithine Decarboxylase in Leukemia Cells Stimulated to Growth |
| Q53538268 | Pre-Lamin A processing is linked to heterochromatin organization. |
| Q46296157 | Prelamin A is involved in early steps of muscle differentiation. |
| Q36753080 | Prelamin A processing and heterochromatin dynamics in laminopathies. |
| Q42735850 | Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle. |
| Q34520717 | Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics |
| Q56993478 | Remodelling of the nuclear lamina during human cytomegalovirus infection: role of the viral proteins pUL50 and pUL53 |
| Q42013273 | Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment |
| Q42818973 | SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies |
| Q51496986 | Slug transcription factor and nuclear Lamin B1 are upregulated in osteoarthritic chondrocytes. |
| Q36281672 | The empowerment of translational research: lessons from laminopathies. |
| Q28541992 | Treatment of FANCA cells with resveratrol and N-acetylcysteine: a comparative study |
| Q56998901 | Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains |
| Q41902731 | p44/42 mitogen-activated protein kinase is involved in the expression of ornithine decarboxylase in leukaemia L1210 cells |
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