(Q28189195)

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

A visual screen of a GFP-fusion library identifies a new type of nuclear envelope membrane protein

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

Direct interaction between emerin and lamin A

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

Emery-Dreifuss muscular dystrophy - a 40 year retrospective

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

Mutations in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expression

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

Mutations in the LMNA gene encoding lamin A/C

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

cDNA cloning and characterization of lamina-associated polypeptide 1C (LAP1C), an integral protein of the inner nuclear membrane

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

Structure and mapping of the human thymopoietin (TMPO) gene and relationship of human TMPO beta to rat lamin-associated polypeptide 2

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1600-0854.2001.21001.X

The nuclear envelope, muscular dystrophy and gene expression

21 April 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

Nuclear lamins: their structure, assembly, and interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

Essential roles for Caenorhabditis elegans lamin gene in nuclear organization, cell cycle progression, and spatial organization of nuclear pore complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

Insertional mutation of the Drosophila nuclear lamin Dm0 gene results in defective nuclear envelopes, clustering of nuclear pore complexes, and accumulation of annulate lamellae

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

Interaction between emerin and nuclear lamins

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

Ultrastructural abnormality of sarcolemmal nuclei in Emery-Dreifuss muscular dystrophy (EDMD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

The ER-overload response: activation of NF-kappa B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

Functional organization of the nuclear envelope

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

The nuclear lamina is a meshwork of intermediate-type filaments

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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/10.1034%2FJ.1600-0854.2001.21001.X

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.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

The conserved carboxy-terminal cysteine of nuclear lamins is essential for lamin association with the nuclear envelope

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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/10.1034%2FJ.1600-0854.2001.21001.X

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/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Three distinct human thymopoietins are derived from alternatively spliced mRNAs

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced products

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Free diffusion to and from the inner nuclear membrane of newly synthesized plasma membrane glycoproteins

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Immunocytochemical study of the partition and distribution of Sindbis virus glycoproteins in freeze-fractured membranes of infected baby hamster kidney cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Immunoelectron microscopic studies of the intracellular transport of the membrane glycoprotein (G) of vesicular stomatitis virus in infected Chinese hamster ovary cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Unusual type of benign x-linked muscular dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Emery-Dreifuss muscular dystrophy and other related disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

The Emery-Dreifuss Muscular Dystrophy Mutation Database

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021

Partial lipoatrophy with insulin resistant diabetes and hyperlipidaemia (Dunnigan syndrome).

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0854.2001.21001.X

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/10.1034%2FJ.1600-0854.2001.21001.X

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/10.1034%2FJ.1600-0854.2001.21001.X

7 January 2021