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Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle

Cell death and differentiation, 2011-08, Vol.18 (8), p.1305-1315

2011

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Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

Cellular and molecular life sciences : CMLS, 2005-11, Vol.62 (22), p.2669-2678, Article 2669

2005

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Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

European journal of histochemistry, 2011-10, Vol.55 (4), p.e36-e36

2011

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Bent spine syndrome due to myofibrillar myopathy

Journal of the neurological sciences, 2013-10, Vol.333, p.e449-e449

2013

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Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy

Journal of medical genetics, 2009-01, Vol.46 (1), p.40-48

2009

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The Role of Autophagy in the Maintenance of Stemness and Differentiation of Mesenchymal Stem Cells

Stem Cell Reviews and Reports, 2016-12, Vol.12 (6), p.621-633

2016

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PO-435 Photoactivation of nanoparticles delivered by mesenchymal stem cells induces osteosarcoma cell death in in vitro 3D co-culture models

ESMO open, 2018-07, Vol.3 (Suppl 2), p.A193-A193

2018

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Mandibuloacral dysplasia: A premature ageing disease with aspects of physiological ageing

Ageing research reviews, 2018-03, Vol.42, p.1-13

2018

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Erratum - Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

European journal of histochemistry, 2013-12, Vol.57 (4), p.42-e42

2013

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Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy

Journal of medical genetics, 2005-03, Vol.42 (3), p.214-220

2005

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LOW-INTENSITY PULSED ULTRASOUND INDUCES CHONDROGENIC DIFFERENTIATION OF ADIPOSE-STROMAL CELLS IN 3D PIEZOELECTRIC HYDROGEL

Osteoarthritis and cartilage, 2022-04, Vol.30, p.S59-S59

2022

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Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplication

Neuromuscular disorders : NMD, 2010-08, Vol.20 (8), p.512-516

2010

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All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype

Oncotarget, 2015-10, Vol.6 (30), p.29914-29928

2015

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Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency

Nature genetics, 2003-12, Vol.35 (4), p.367-371

2003

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Altered pre-lamin A processing is a common mechanism leading to lipodystrophy

Human molecular genetics, 2005-06, Vol.14 (11), p.1489-1502

2005

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Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies

European journal of histochemistry, 2006-01, Vol.50 (1), p.1-8

2006

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Emerin increase in regenerating muscle fibers

European journal of histochemistry, 2005-10, Vol.49 (4), p.355-362

2005

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G.P.5.09 Pre-lamin A is modulated during muscle cell differentiation. Implications for Emery–Dreifuss muscular dystrophy

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.800-800

2007

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Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy

Physiological genomics, 2005-10, Vol.23 (2), p.150-158

2005

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Emerin expression at the early stages of myogenic differentiation

Differentiation (London), 2000-12, Vol.66 (4), p.208-217

2000

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H9c2 cardiac myoblasts undergo apoptosis in a model of ischemia consisting of serum deprivation and hypoxia: inhibition by PMA

FEBS letters, 2003-02, Vol.536 (1), p.85-91

2003

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Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology

European journal of histochemistry, 2003-01, Vol.47 (1), p.3-16

2003

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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

Experimental cell research, 2003-11, Vol.291 (1), p.122-134

2003

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Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2

Muscle & nerve, 2005-06, Vol.31 (6), p.764-767

2005

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Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts

Matrix biology, 2001-11, Vol.20 (7), p.475-486

2001

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Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

Bent spine syndrome due to myofibrillar myopathy

Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy

The Role of Autophagy in the Maintenance of Stemness and Differentiation of Mesenchymal Stem Cells

PO-435 Photoactivation of nanoparticles delivered by mesenchymal stem cells induces osteosarcoma cell death in in vitro 3D co-culture models

Mandibuloacral dysplasia: A premature ageing disease with aspects of physiological ageing

Erratum - Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy

LOW-INTENSITY PULSED ULTRASOUND INDUCES CHONDROGENIC DIFFERENTIATION OF ADIPOSE-STROMAL CELLS IN 3D PIEZOELECTRIC HYDROGEL

Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplication

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype

Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency

Altered pre-lamin A processing is a common mechanism leading to lipodystrophy

Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies

Emerin increase in regenerating muscle fibers

G.P.5.09 Pre-lamin A is modulated during muscle cell differentiation. Implications for Emery–Dreifuss muscular dystrophy

Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy

Emerin expression at the early stages of myogenic differentiation

H9c2 cardiac myoblasts undergo apoptosis in a model of ischemia consisting of serum deprivation and hypoxia: inhibition by PMA

Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology

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

Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2

Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts

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