(Q36249005)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

review article

1 reference

title

A-type lamin complexes and regenerative potential: a step towards understanding laminopathic diseases? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

publication date

2 September 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

Histochemistry and Cell Biology

6 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

volume

125

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

page(s)

33-41

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

Cell cycle dynamics of the nuclear envelope.

6 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00418-005-0050-8

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

21 January 2018

1 reference

12 December 2020

Lamin a truncation in Hutchinson-Gilford progeria.

1 reference

12 December 2020

Crystal structure of the human lamin A coil 2B dimer: implications for the head-to-tail association of nuclear lamins

1 reference

12 December 2020

Circulating stem cells and tissue repair.

1 reference

12 December 2020

A-type lamins: guardians of the soma?

1 reference

12 December 2020

Structure of the globular tail of nuclear lamin

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

MAN1 and emerin have overlapping function(s) essential for chromosome segregation and cell division in Caenorhabditis elegans

1 reference

12 December 2020

Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.

1 reference

12 December 2020

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

1 reference

12 December 2020

Differential timing of nuclear lamin A/C expression in the various organs of the mouse embryo and the young animal: a developmental study.

1 reference

12 December 2020

BAF: roles in chromatin, nuclear structure and retrovirus integration

1 reference

12 December 2020

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

1 reference

12 December 2020

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Energy- and temperature-dependent transport of integral proteins to the inner nuclear membrane via the nuclear pore

1 reference

12 December 2020

Proteins that bind A-type lamins: integrating isolated clues

1 reference

12 December 2020

Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

1 reference

12 December 2020

Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome

1 reference

12 December 2020

Syne proteins anchor muscle nuclei at the neuromuscular junction

1 reference

12 December 2020

Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene

1 reference

12 December 2020

Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction.

1 reference

12 December 2020

Generation of different fates from multipotent muscle stem cells

1 reference

12 December 2020

Lamin-dependent localization of UNC-84, a protein required for nuclear migration in Caenorhabditis elegans

1 reference

12 December 2020

Stem and progenitor cells: origins, phenotypes, lineage commitments, and transdifferentiations

1 reference

12 December 2020

A progeroid syndrome in mice is caused by defects in A-type lamins

1 reference

12 December 2020

Stem cells in the dog heart are self-renewing, clonogenic, and multipotent and regenerate infarcted myocardium, improving cardiac function

1 reference

12 December 2020

Lamin B1 is required for mouse development and nuclear integrity

1 reference

12 December 2020

Lamin proteins form an internal nucleoskeleton as well as a peripheral lamina in human cells

1 reference

12 December 2020

Cellular and molecular regulation of muscle regeneration

1 reference

12 December 2020

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

1 reference

12 December 2020

Cells of the cellular immune and hemopoietic system of the mouse lack lamins A/C: distinction versus other somatic cells

1 reference

12 December 2020

Life at the edge: the nuclear envelope and human disease

1 reference

12 December 2020

E2Fs regulate adipocyte differentiation

1 reference

12 December 2020

The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

1 reference

12 December 2020

ANChors away: an actin based mechanism of nuclear positioning

1 reference

12 December 2020

Adult murine skeletal muscle contains cells that can differentiate into beating cardiomyocytes in vitro

1 reference

12 December 2020

Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant.

1 reference

12 December 2020

Molecular characterization of protein kinase C-alpha binding to lamin A.

1 reference

12 December 2020

XMAN1, an inner nuclear membrane protein, antagonizes BMP signaling by interacting with Smad1 in Xenopus embryos

1 reference

12 December 2020

The inner nuclear membrane protein Sun1 mediates the anchorage of Nesprin-2 to the nuclear envelope

1 reference

12 December 2020

108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands

1 reference

12 December 2020

Direct binding of nuclear membrane protein MAN1 to emerin in vitro and two modes of binding to barrier-to-autointegration factor

1 reference

12 December 2020

The nuclear lamina comes of age.

1 reference

12 December 2020

Unusual expression of emerin in a patient with X-linked Emery–Dreifuss muscular dystrophy

1 reference

12 December 2020

Retinoblastoma protein functions as a molecular switch determining white versus brown adipocyte differentiation.

1 reference

12 December 2020

A chromatin binding site in the tail domain of nuclear lamins that interacts with core histones

1 reference

12 December 2020

Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype

1 reference

12 December 2020

Nuclear lamins: building blocks of nuclear architecture

1 reference

12 December 2020

Transcriptional repression, apoptosis, human disease and the functional evolution of the nuclear lamina

1 reference

12 December 2020

MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-beta signaling.

1 reference

12 December 2020

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

1 reference

12 December 2020

Rb is required for progression through myogenic differentiation but not maintenance of terminal differentiation.

1 reference

12 December 2020

Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice

1 reference

12 December 2020

Signals and structural features involved in integral membrane protein targeting to the inner nuclear membrane

1 reference

12 December 2020

Myocardial regeneration by activation of multipotent cardiac stem cells in ischemic heart failure

1 reference

12 December 2020

Inner nuclear membrane proteins and the nuclear lamina

1 reference

12 December 2020

Alteration of nuclear lamin organization inhibits RNA polymerase II-dependent transcription

1 reference

12 December 2020

Distinct functional domains in emerin bind lamin A and DNA-bridging protein BAF

1 reference

12 December 2020

Nuclear envelope and nuclear matrix: interactions and dynamics

1 reference

12 December 2020

Architectural abnormalities in muscle nuclei. Ultrastructural differences between X-linked and autosomal dominant forms of EDMD

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

The carboxyl-terminal region common to lamins A and C contains a DNA binding domain.

1 reference

12 December 2020

Transcriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitro

1 reference

12 December 2020

Teratocarcinoma stem cells and early mouse embryos contain only a single major lamin polypeptide closely resembling lamin B

1 reference

12 December 2020

Postnatal isl1+ cardioblasts enter fully differentiated cardiomyocyte lineages

1 reference

12 December 2020

The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane.

1 reference

12 December 2020

Skeletal muscle satellite cells can spontaneously enter an alternative mesenchymal pathway.

1 reference

12 December 2020

Nuclear lamins A and B1: different pathways of assembly during nuclear envelope formation in living cells

1 reference

12 December 2020

Plasticity of adult stem cells

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

Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene

1 reference

12 December 2020

Organization of synaptic myonuclei by Syne proteins and their role during the formation of the nerve-muscle synapse

1 reference

12 December 2020

10.1007/S00418-005-0050-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16142451%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference