(Q35145852)

6 August 2017

1 reference

title

The laminopathies: nuclear structure meets disease (English)

1 reference

6 August 2017

Leslie Mounkes

1

1 reference

6 August 2017

Serguei Kozlov

series ordinal

2

1 reference

6 August 2017

Brian Burke

series ordinal

3

1 reference

6 August 2017

Colin L Stewart

series ordinal

4

1 reference

6 August 2017

publication date

1 June 2003

1 reference

Current Opinion in Genetics & Development

6 August 2017

published in

1 reference

6 August 2017

volume

13

1 reference

6 August 2017

issue

3

1 reference

6 August 2017

page(s)

223-230

1 reference

Transport into and out of the nucleus

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Functional organization of the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Nuclear lamins: their structure, assembly, and interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Review: the dynamics of the nuclear lamins during the cell cycle-- relationship between structure and function

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Change of karyoskeleton during mammalian spermatogenesis: expression pattern of nuclear lamin C2 and its regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

The CaaX motif of lamin A functions in conjunction with the nuclear localization signal to target assembly to the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

The CaaX motif is required for isoprenylation, carboxyl methylation, and nuclear membrane association of lamin B2.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

A- and B-type lamins are differentially expressed in normal human tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

Life at the edge: the nuclear envelope and human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

LAP2 binds to BAF.DNA complexes: requirement for the LEM domain and modulation by variable regions

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Barrier-to-autointegration factor (BAF) bridges DNA in a discrete, higher-order nucleoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Mouse germ cell-less as an essential component for nuclear integrity.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Emery-Dreifuss muscular dystrophy and other related disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

The nuclear muscular dystrophies.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Characterization of adiposity and metabolism in Lmna-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Demonstration of mechanical connections between integrins, cytoskeletal filaments, and nucleoplasm that stabilize nuclear structure

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Identification of IEX-1 as a biomechanically controlled nuclear factor-kappaB target gene that inhibits cardiomyocyte hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

LIS1: cellular function of a disease-causing gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

A nuclear lamin is required for cytoplasmic organization and egg polarity in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Syne-1, a dystrophin- and Klarsicht-related protein associated with synaptic nuclei at the neuromuscular junction

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

The nesprins are giant actin-binding proteins, orthologous to Drosophila melanogaster muscle protein MSP-300

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

Nuclear compartments and gene regulation.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Structure of the globular tail of nuclear lamin

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

The nuclear envelope, muscular dystrophy and gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

Lamin a truncation in Hutchinson-Gilford progeria.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900058-3

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%2FS0959-437X%2803%2900058-3

7 January 2021

10.1016/S0959-437X(03)00058-3

Identifiers

DOI

1 reference

6 August 2017

1 reference