(Q37827754)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

review article

1 reference

title

Laminopathies: the molecular background of the disease and the prospects for its treatment (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author

Magda Dubińska-Magiera

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Ryszard Rzepecki

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

Magdalena Zaremba-Czogalla

19 January 2020

series ordinal

1

object named as

Magdalena Zaremba-Czogalla

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

27 December 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

Cellular & Molecular Biology Letters

19 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

114-148

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.2478/s11658-010-0038-9

19 January 2020

exact match

0 references

cites work

Advances in mesenchymal stem cell-mediated gene therapy for cancer.

1 reference

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Atypical progeroid syndrome due to heterozygous missense LMNA mutations

21 January 2018

1 reference

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Lamins as cancer biomarkers

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin A/C and emerin are critical for skeletal muscle satellite cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD)

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Increased expression of the Hutchinson-Gilford progeria syndrome truncated lamin A transcript during cell aging

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Intermediate filaments: from cell architecture to nanomechanics

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Role of bone marrow cell trafficking in replenishing skeletal muscle SP and MP cell populations

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

The nuclear lamina. Both a structural framework and a platform for genome organization

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

A-type lamins and signaling: the PI 3-kinase/Akt pathway moves forward

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Phenomics and lamins: from disease to therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Tyrosine phosphorylation of nuclear-membrane protein emerin by Src, Abl and other kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Sumoylation regulates lamin A function and is lost in lamin A mutants associated with familial cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Heart-hand syndrome of Slovenian type: a new kind of laminopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

In vivo contribution of murine mesenchymal stem cells into multiple cell-types under minimal damage conditions.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Role of A-type lamins in signaling, transcription, and chromatin organization.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

A-type lamins: guardians of the soma?

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Laminopathies and the long strange trip from basic cell biology to therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Gone with the Wnt/Notch: stem cells in laminopathies, progeria, and aging

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

In the middle of it all: mutual mechanical regulation between the nucleus and the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

HIV protease inhibitors block the zinc metalloproteinase ZMPSTE24 and lead to an accumulation of prelamin A in cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Prelamin A and lamin A appear to be dispensable in the nuclear lamina

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Wnt signalling: variety at the core.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Blocking protein farnesyltransferase improves nuclear shape in fibroblasts from humans with progeroid syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

How cells read TGF-beta signals

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin B1 is required for mouse development and nuclear integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

An emerin "proteome": purification of distinct emerin-containing complexes from HeLa cells suggests molecular basis for diverse roles including gene regulation, mRNA splicing, signaling, mechanosensing, and nuclear architecture.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

De novo LMNA mutations cause a new form of congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

The nuclear envelope from basic biology to therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Barrier-to-autointegration factor--a BAFfling little protein

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Wnt/beta-catenin signaling: components, mechanisms, and diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Successful surgical repair for Emery-Dreifuss muscular dystrophy valvular disease with long-term follow-up.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Muscular dystrophies: an update on pathology and diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

LMNA mutations in atypical Werner's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Type A insulin resistance syndrome revealing a novel lamin A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Long-term efficacy of leptin replacement in patients with generalized lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Glucose induces de novo lipogenesis in rat muscle satellite cells through a sterol-regulatory-element-binding-protein-1c-dependent pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin a truncation in Hutchinson-Gilford progeria.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Activating the synthesis of progerin, the mutant prelamin A in Hutchinson-Gilford progeria syndrome, with antisense oligonucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Alterations in mitosis and cell cycle progression caused by a mutant lamin A known to accelerate human aging

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Nuclear lamins: key regulators of nuclear structure and activities

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Inhibiting farnesylation reverses the nuclear morphology defect in a HeLa cell model for Hutchinson-Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Marrow-isolated adult multilineage inducible (MIAMI) cells, a unique population of postnatal young and old human cells with extensive expansion and differentiation potential

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma protein

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

A-type lamins regulate retinoblastoma protein function by promoting subnuclear localization and preventing proteasomal degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin A-dependent nuclear defects in human aging

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Adipogenesis and WNT signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

New approaches to progeria

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Disruption of spermatogenesis in mice lacking A-type lamins.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

The inner nuclear membrane protein emerin regulates beta-catenin activity by restricting its accumulation in the nucleus

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin complexes in the nuclear interior control progenitor cell proliferation and tissue homeostasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Thematic review series: Adipocyte Biology. Lipodystrophies: windows on adipose biology and metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

No place like home: anatomy and function of the stem cell niche

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Unusual type of benign x-linked muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Mechanisms of action of mesenchymal stem cells in cardiac repair: potential influences on the cardiac stem cell niche.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Class I histone deacetylases sequentially interact with MyoD and pRb during skeletal myogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Nuclear envelope defects cause stem cell dysfunction in premature-aging mice

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Lamin B1 duplications cause autosomal dominant leukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Potential of mesenchymal stem cells for the therapy of autoimmune diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Dynamic complexes of A-type lamins and emerin influence adipogenic capacity of the cell via nucleocytoplasmic distribution of beta-catenin

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Progerin elicits disease phenotypes of progeria in mice whether or not it is farnesylated.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Molecular signatures of Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Long-term efficacy of leptin replacement in patients with Dunnigan-type familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Nuclear lamins: laminopathies and their role in premature ageing.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Biochemical studies of Zmpste24-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Integrase-defective lentiviral vectors: progress and applications.

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

beta-Catenin promotes self-renewal of skeletal-muscle satellite cells

21 January 2018

1 reference

https://api.crossref.org/works/10.2478%2FS11658-010-0038-9

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

12 December 2020

Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

1 reference

12 December 2020

Familial partial lipodystrophy associated with the heterozygous LMNA mutation 1445G>A (Arg482Gln) in a Polish family

1 reference

12 December 2020

Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutations

1 reference

12 December 2020

In vivo phosphorylation of Drosophila melanogaster nuclear lamins during both interphase and mitosis.

1 reference

12 December 2020

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations

1 reference

12 December 2020

Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors.

1 reference

12 December 2020

Lamin-binding Proteins

1 reference

12 December 2020

Cell-extrinsic defective lymphocyte development in Lmna(-/-) mice

1 reference

12 December 2020

Both emerin and lamin C depend on lamin A for localization at the nuclear envelope

1 reference

12 December 2020

Direct actin binding to A- and B-type lamin tails and actin filament bundling by the lamin A tail

1 reference

12 December 2020

Abnormal development of the cerebral cortex and cerebellum in the setting of lamin B2 deficiency.

1 reference

12 December 2020

Identification of essential genes in cultured mammalian cells using small interfering RNAs.

1 reference

12 December 2020

The role of mitotic vesicles in the nuclear assembly

1 reference

12 December 2020

Buschke–Ollendorff Syndrome with Striking Phenotypic Variation Resulting from a Novel c.2203C>T Nonsense Mutation in LEMD3

1 reference

12 December 2020

Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene

1 reference

12 December 2020

1 reference

12 December 2020

Genotype-phenotype correlations in laminopathies: how does fate translate?

1 reference

12 December 2020

The nuclear lamins and the nuclear envelope

1 reference

12 December 2020

Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cells

1 reference

12 December 2020

Defective lamin A-Rb signaling in Hutchinson-Gilford Progeria Syndrome and reversal by farnesyltransferase inhibition

1 reference

12 December 2020

Emery-Dreifuss muscular dystrophy

1 reference

12 December 2020

Dynamics of lamin-A processing following precursor accumulation

1 reference

12 December 2020

Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice

1 reference

12 December 2020

Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis

1 reference

12 December 2020

Pathological roles of MAPK signaling pathways in human diseases

1 reference

12 December 2020

Stem cell antigen-1 is necessary for cell-cycle withdrawal and myoblast differentiation in C2C12 cells

1 reference

12 December 2020

Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference

1 reference

12 December 2020

Fast regulation of AP-1 activity through interaction of lamin A/C, ERK1/2, and c-Fos at the nuclear envelope

1 reference

12 December 2020

Embryonic and adult isoforms of XLAP2 form microdomains associated with chromatin and the nuclear envelope.

1 reference

12 December 2020

Regeneration of skeletal muscle from transplanted immortalised myoblasts is oligoclonal

1 reference

12 December 2020

Treatment with a farnesyltransferase inhibitor improves survival in mice with a Hutchinson-Gilford progeria syndrome mutation.

1 reference

12 December 2020

Genetically modified mesenchymal stem cells and their clinical potential in acute cardiovascular disease

1 reference

12 December 2020

A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

1 reference

12 December 2020

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)

1 reference

12 December 2020

Recruitment of beta-catenin to cadherin-mediated intercellular adhesions is involved in myogenic induction.

1 reference

12 December 2020

A-type lamins are essential for TGF-beta1 induced PP2A to dephosphorylate transcription factors

1 reference

12 December 2020

The position of the mutation within the LMNA gene determines the type and extent of tissue involvement in laminopathies

1 reference

12 December 2020

Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities

1 reference

12 December 2020

Expression of a mutant lamin A that causes Emery-Dreifuss muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts

1 reference

12 December 2020

Reduced expression of A-type lamins and emerin activates extracellular signal-regulated kinase in cultured cells.

1 reference

12 December 2020

10.2478/S11658-010-0038-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21225470%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference