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"Laminopathies": a wide spectrum of human diseases

published in: Experimental Cell Research

date of publication: 2007-03-30

language: English

Cites articles 148

Date

Title

Authors

2007-02

Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis

Michael P. Whyte, William H. McAlister, Steven Mumm
2006-11-03

Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins

Antoine Muchir, Gisèle Bonne, Martin Lammens
2006-10-26

Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes

James M Holaska, Soroush Rais-Bahrami
2006-10-24

DNA damage responses in progeroid syndromes arise from defective maturation of prelamin A.
2006-10

Lamin B1 duplications cause autosomal dominant leukodystrophy
2006-10-01

Man1, an inner nuclear membrane protein, regulates vascular remodeling by modulating transforming growth factor beta signaling
2006-08-31

Karyopherin-mediated import of integral inner nuclear membrane proteins

Günter Blobel
2006-08-15

Farnesylated lamins, progeroid syndromes and farnesyl transferase inhibitors
2006-08-01

A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation

Stephen G. Young
2006-08

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

Valentine Charlton-Menys, Robert A. Hegele
2006-06-26

Distinct structural and mechanical properties of the nuclear lamina in Hutchinson-Gilford progeria syndrome

Tom Misteli
2006-03-16

A mitotic lamin B matrix induced by RanGTP required for spindle assembly
2006-03-01

Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles
2006-02-16

A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria

Stephen G. Young
2006-02-15

The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers
2006-02-14

Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration

Corrado Angelini, Ben Shneiderman, Eric Hoffman
2006-01-13

Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy
2006-01-10

Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration

Dedra Cutler, Eric Hoffman
2006-12-10

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

Michael A. Fox, Guy A. Rouleau, Jean-Pierre Bouchard, Nicolas Dupré, Joshua R. Sanes, Sandra B. Laurent, Patrick A Dion
2006-07-05

Lamins A and C but not lamin B1 regulate nuclear mechanics.

Julie Ji, Karen Reue
2006-04-03

Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.

Gisèle Bonne, Aleksey Shatunov, Sue Brown
2006-03-01

Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis.

Andreas Janecke
2006-01-01

Primary prevention of sudden death in patients with lamin A/C gene mutations.

Jop H van Berlo, Gisèle Bonne
2006-07-06

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy
2006-04-28

The carboxyl-terminal nucleoplasmic region of MAN1 exhibits a DNA binding winged helix domain

Sandrine Caputo, Joël Couprie, Muriel Gondry
2006-01-06

Here come the SUNs: a nucleocytoskeletal missing link
2005-10-05

Prelamin A, Zmpste24, misshapen cell nuclei, and progeria--new evidence suggesting that protein farnesylation could be important for disease pathogenesis
2005-09-26

Inhibiting farnesylation reverses the nuclear morphology defect in a HeLa cell model for Hutchinson-Gilford progeria syndrome
2005-08-29

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

Stephen G. Young, Jeffrey H Miner, Casey L Moulson, Anne P Beigneux, Loren G Fong
2005-09-06

Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome

Francis Collins, Brian C Capell, Channing Der, Leslie B Gordon
2005-08-26

Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition
2005-08-29

Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cells

Article - wd:Q34242119

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