Nuclear envelope, nuclear lamina, and inherited disease (Q36258265)

13 August 2017

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title

Nuclear envelope, nuclear lamina, and inherited disease (English)

1 reference

13 August 2017

Howard J Worman

1

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13 August 2017

Jean-Claude Courvalin

series ordinal

2

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13 August 2017

publication date

1 January 2005

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International Review of Cytology

13 August 2017

published in

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13 August 2017

volume

246

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13 August 2017

page(s)

231-279

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Isolation of nuclear pore complexes in association with a lamina

13 August 2017

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The gene for a novel human lamin maps at a highly transcribed locus of chromosome 19 which replicates at the onset of S-phase.

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

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

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7 January 2021

The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells.

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Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement

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

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7 January 2021

Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.

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7 January 2021

Human mutations affecting aging — a review

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7 January 2021

Domain-specific disassembly and reassembly of nuclear membranes during mitosis

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7 January 2021

Life at the edge: the nuclear envelope and human disease

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7 January 2021

Solution structure of the constant region of nuclear envelope protein LAP2 reveals two LEM-domain structures: one binds BAF and the other binds DNA

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7 January 2021

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

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7 January 2021

LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).

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7 January 2021

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

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7 January 2021

A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy

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7 January 2021

Stepwise reassembly of the nuclear envelope at the end of mitosis

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7 January 2021

LMNA mutations in atypical Werner's syndrome

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7 January 2021

Symmetry of bone lesions in osteopoikilosis. Report of 4 cases

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7 January 2021

Chromatin motion is constrained by association with nuclear compartments in human cells.

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7 January 2021

Direct interaction between emerin and lamin A

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7 January 2021

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

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7 January 2021

Molecular basis of muscular dystrophies.

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7 January 2021

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7 January 2021

Proteomic analysis of the mammalian nuclear pore complex

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7 January 2021

The nuclear pore complex: disease associations and functional correlations.

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7 January 2021

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes

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7 January 2021

Genome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis

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7 January 2021

Characterization of adiposity and metabolism in Lmna-deficient mice

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7 January 2021

Insulin-resistant diabetes mellitus and hypermetabolism in mandibuloacral dysplasia: a newly recognized form of partial lipodystrophy

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7 January 2021

Nuclear pore complexes form immobile networks and have a very low turnover in live mammalian cells

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7 January 2021

Muscular dystrophies: genes to pathogenesis

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7 January 2021

Paternal origin of LMNA mutations in Hutchinson-Gilford progeria

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7 January 2021

The Hutchinson-Gilford progeria syndrome. Report of 4 cases and review of the literature

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7 January 2021

Lamin a truncation in Hutchinson-Gilford progeria.

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7 January 2021

Structure of the globular tail of nuclear lamin

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7 January 2021

The spatio-temporal organization of DNA replication sites is identical in primary, immortalized and transformed mammalian cells

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7 January 2021

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7 January 2021

In vivo and in vitro interaction between human transcription factor MOK2 and nuclear lamin A/C.

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7 January 2021

Inner nuclear membrane protein LBR preferentially interacts with DNA secondary structures and nucleosomal linker

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7 January 2021

A modified procedure for the isolation of a pore complex-lamina fraction from rat liver nuclei

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7 January 2021

Nuclear membrane dynamics and reassembly in living cells: targeting of an inner nuclear membrane protein in interphase and mitosis

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7 January 2021

Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked Emery-Dreifuss muscular dystrophy

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7 January 2021

Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expression

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7 January 2021

Unusual type of benign x-linked muscular dystrophy

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7 January 2021

Emery-Dreifuss syndrome

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7 January 2021

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

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7 January 2021

The nuclear pore complex: nucleocytoplasmic transport and beyond

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7 January 2021

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

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7 January 2021

Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy

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7 January 2021

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

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7 January 2021

On the occurrence of a fibrous lamina on the inner aspect of the nuclear envelope in certain cells of vertebrates

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7 January 2021

An autosomal-dominant dystrophy with humeropelvic distribution and cardiomyopathy

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7 January 2021

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

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7 January 2021

cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins

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7 January 2021

Isolation and characterization of a proteinaceous subnuclear fraction composed of nuclear matrix, peripheral lamina, and nuclear pore complexes from embryos of Drosophila melanogaster

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7 January 2021

Integral membrane proteins of the nuclear envelope interact with lamins and chromosomes, and binding is modulated by mitotic phosphorylation

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7 January 2021

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

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7 January 2021

Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation

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Matefin, a Caenorhabditis elegans germ line-specific SUN-domain nuclear membrane protein, is essential for early embryonic and germ cell development

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7 January 2021

cDNA cloning of a germ cell specific lamin B3 from mouse spermatocytes and analysis of its function by ectopic expression in somatic cells.

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7 January 2021

Identification and cloning of an mRNA coding for a germ cell-specific A-type lamin in mice

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7 January 2021

Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene

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7 January 2021

Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene

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7 January 2021

Immunocytochemical localization of the major polypeptides of the nuclear pore complex-lamina fraction. Interphase and mitotic distribution

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7 January 2021

The nuclear envelope lamina is reversibly depolymerized during mitosis.

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7 January 2021

TorsinA and torsion dystonia: Unraveling the architecture of the nuclear envelope

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7 January 2021

Altered protein dynamics of disease-associated lamin A mutants

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7 January 2021

Buschke-Ollendorff Syndrome Associated with Elevated Elastin Production by Affected Skin Fibroblasts in Culture

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7 January 2021

The tail domain of lamin Dm0 binds histones H2A and H2B

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7 January 2021

Keratin-like proteins that coisolate with intermediate filaments of BHK-21 cells are nuclear lamins

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7 January 2021

Nuclear lamins: building blocks of nuclear architecture

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7 January 2021

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

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7 January 2021

Aberrant cellular behavior of mutant torsinA implicates nuclear envelope dysfunction in DYT1 dystonia.

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7 January 2021

Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation.

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7 January 2021

The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein

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7 January 2021

A new autosomal recessive lethal chondrodystrophy with congenital hydrops

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7 January 2021

RNAi of FACE1 protease results in growth inhibition of human cells expressing lamin A: implications for Hutchinson-Gilford progeria syndrome.

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7 January 2021

Lamins A and C are not expressed at early stages of human lymphocyte differentiation

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7 January 2021

An integral membrane protein of the pore membrane domain of the nuclear envelope contains a nucleoporin-like region

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7 January 2021

Emerin binding to Btf, a death-promoting transcriptional repressor, is disrupted by a missense mutation that causes Emery-Dreifuss muscular dystrophy

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7 January 2021

Vertebrate Nup53 interacts with the nuclear lamina and is required for the assembly of a Nup93-containing complex

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7 January 2021

Mutations of phosphorylation sites in lamin A that prevent nuclear lamina disassembly in mitosis

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7 January 2021

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

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7 January 2021

Intermediate filaments: molecular structure, assembly mechanism, and integration into functionally distinct intracellular Scaffolds

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7 January 2021

Sun2 is a novel mammalian inner nuclear membrane protein

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7 January 2021

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

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7 January 2021

Characterization of a second highly conserved B-type lamin present in cells previously thought to contain only a single B-type lamin

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7 January 2021

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

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7 January 2021

Emerin caps the pointed end of actin filaments: evidence for an actin cortical network at the nuclear inner membrane

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7 January 2021

The human lamin B receptor/sterol reductase multigene family

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7 January 2021

Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo

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7 January 2021

A-type lamins: guardians of the soma?

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7 January 2021

Dissociation of Oct-1 from the nuclear peripheral structure induces the cellular aging-associated collagenase gene expression

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7 January 2021

Dunnigan-Kobberling syndrome: an autosomal dominant form of partial lipodystrophy.

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7 January 2021

A defect in the regional deposition of adipose tissue (partial lipodystrophy) is encoded by a gene at chromosome 1q.

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7 January 2021

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

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7 January 2021

Nuclear organization of DNA replication in primary mammalian cells.

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7 January 2021

In vitro assay and characterization of the farnesylation-dependent prelamin A endoprotease

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7 January 2021

Pelger-Huët anomaly of the leukocytes

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7 January 2021

Lipodystrophy of the extremities. A dominantly inherited syndrome associated with lipatrophic diabetes

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7 January 2021

A Drosophila model of early onset torsion dystonia suggests impairment in TGF-beta signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

A monoclonal antibody against nuclear lamina proteins reveals cell type-specificity in Xenopus laevis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Lamin A/C speckles mediate spatial organization of splicing factor compartments and RNA polymerase II transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Structural characterization of the LEM motif common to three human inner nuclear membrane proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Lamins A and C appear during retinoic acid-induced differentiation of mouse embryonal carcinoma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Biochemical studies of Zmpste24-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Structural organization of the human gene (LMNB1) encoding nuclear lamin B1

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

MAN1, an inner nuclear membrane protein that shares the LEM domain with lamina-associated polypeptide 2 and emerin

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Binding of matrix attachment regions to lamin B1

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Binding of matrix attachment regions to lamin polymers involves single-stranded regions and the minor groove

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

An alternative splicing product of the lamin A/C gene lacks exon 10.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The C. elegans hook protein, ZYG-12, mediates the essential attachment between the centrosome and nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The retinoblastoma gene product is a cell cycle-dependent, nuclear matrix-associated protein

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Increased solubility of lamins and redistribution of lamin C in X-linked Emery-Dreifuss muscular dystrophy fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Remodelling of the nuclear lamina and nucleoskeleton is required for skeletal muscle differentiation in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Interphase chromosomes undergo constrained diffusional motion in living cells

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

A carboxyl-terminal interaction of lamin B1 is dependent on the CAAX endoprotease Rce1 and carboxymethylation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Disruption of nuclear lamin organization blocks the elongation phase of DNA replication

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

TorsinA in the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Mandibuloacral dysplasia: a rare progeroid syndrome. Two brothers confirm autosomal recessive inheritance.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The integral inner nuclear membrane protein MAN1 physically interacts with the R-Smad proteins to repress signaling by the transforming growth factor-{beta} superfamily of cytokines

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The Functions of Klarsicht and Nuclear Lamin in Developmentally Regulated Nuclear Migrations of Photoreceptor Cells in theDrosophilaEye

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The MAN antigens are non-lamin constituents of the nuclear lamina in vertebrate cells

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

In vitro disassembly of the nuclear lamina and M phase-specific phosphorylation of lamins by cdc2 kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21–22

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The lamin CxxM motif promotes nuclear membrane growth

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Dynamics of nuclear pore complex organization through the cell cycle.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Intranuclear membrane structure formations by CaaX-containing nuclear proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

SANE, a novel LEM domain protein, regulates bone morphogenetic protein signaling through interaction with Smad1.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Lipoatrophy revisited

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The yeast nuclear pore complex: composition, architecture, and transport mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Emery-dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Interaction between emerin and nuclear lamins

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Cytoplasmic dynein as a facilitator of nuclear envelope breakdown

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Experimental disintegration of the nuclear envelope. Evidence for pore-connecting fibrils

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Nuclear membrane proteins with potential disease links found by subtractive proteomics

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The stability of the nuclear lamina polymer changes with the composition of lamin subtypes according to their individual binding strengths

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Integral membrane proteins specific to the inner nuclear membrane and associated with the nuclear lamina

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Tight skin and limited joint movements as early presentation of Hutchinson-Gilford progeria in a 7-week-old infant.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Immunocytochemical analysis of human muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Transgenic mouse model of early-onset DYT1 dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Mandibuloacral dysplasia caused by homozygosity for the R527H mutation in lamin A/C.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Human lamin B receptor exhibits sterol C14-reductase activity in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Body fat distribution and metabolic derangements in patients with familial partial lipodystrophy associated with mandibuloacral dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Genetic and phenotypic heterogeneity in patients with mandibuloacral dysplasia-associated lipodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Incorporation of the nuclear pore basket protein nup153 into nuclear pore structures is dependent upon lamina assembly: evidence from cell-free extracts of Xenopus eggs

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The amino-terminal domain of the lamin B receptor is a nuclear envelope targeting signal

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Disruption of nuclear lamin organization alters the distribution of replication factors and inhibits DNA synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Role of ANC-1 in tethering nuclei to the actin cytoskeleton.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

ANChors away: an actin based mechanism of nuclear positioning

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The gene structure of Xenopus nuclear lamin A: a model for the evolution of A-type from B-type lamins by exon shuffling

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The gene structure of B-type nuclear lamins of Xenopus laevis: implications for the evolution of the vertebrate lamin family

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Peering through the Pore

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Distinct regions specify the nuclear membrane targeting of emerin, the responsible protein for Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

CDNA microarray analysis of gene expression in fibroblasts of patients with X-linked Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The lethal phenotype of a homozygous nonsense mutation in the lamin A/C gene

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Formation of nuclear splicing factor compartments is independent of lamins A/C.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Lamin B1 is required for mouse development and nuclear integrity

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery–Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Identification of cell cycle-regulated phosphorylation sites on nuclear lamin C

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The lamin B receptor of Drosophila melanogaster

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Maturation of nuclear lamin A involves a specific carboxy-terminal trimming, which removes the polyisoprenylation site from the precursor; implications for the structure of the nuclear lamina

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Köbberling-Dunnigan syndrome: a rare cause of generalized muscular hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Emerin interacts in vitro with the splicing-associated factor, YT521-B

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The inner nuclear membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The nuclear lamina and inherited disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

How do mutations in lamins A and C cause disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

A lamin B receptor in the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

The lamin B receptor of the nuclear envelope inner membrane: a polytopic protein with eight potential transmembrane domains

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Primary structure analysis of an integral membrane glycoprotein of the nuclear pore

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

POM152 is an integral protein of the pore membrane domain of the yeast nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Chromosomal assignment of human nuclear envelope protein genes LMNA, LMNB1, and LBR by fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Integral membrane proteins of the nuclear envelope are dispersed throughout the endoplasmic reticulum during mitosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Protein-protein interactions between human nuclear lamins expressed in yeast

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Interaction between an integral protein of the nuclear envelope inner membrane and human chromodomain proteins homologous to Drosophila HP1

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Domain-specific interactions of human HP1-type chromodomain proteins and inner nuclear membrane protein LBR

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Spectrin repeat proteins in the nucleus.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

Familial mandibuloacral dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2805%2946006-4

7 January 2021

10.1016/S0074-7696(05)46006-4

Identifiers

DOI

1 reference

13 August 2017

1 reference