(Q37383083)

20 August 2017

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title

Fraying at the edge mouse models of diseases resulting from defects at the nuclear periphery (English)

1 reference

20 August 2017

Tatiana V Cohen

1

1 reference

20 August 2017

Colin L Stewart

series ordinal

2

1 reference

20 August 2017

publication date

1 January 2008

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Current Topics in Developmental Biology

20 August 2017

published in

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20 August 2017

volume

84

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20 August 2017

page(s)

351-384

1 reference

Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia

20 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

What MAN1 does to the Smads. TGFbeta/BMP signaling and the nuclear envelope.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

LEM2 is a novel MAN1-related inner nuclear membrane protein associated with A-type lamins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Early sorting of inner nuclear membrane proteins is conserved

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Identification and characterization of cDNAs encoding four novel proteins that interact with translin associated factor-X

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

The dual-specificity phosphatase MKP-1 limits the cardiac hypertrophic response in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Life at the edge: the nuclear envelope and human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The laminopathies: the functional architecture of the nucleus and its contribution to disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Identification of phosphatases for Smad in the BMP/DPP pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

LMNA mutations in atypical Werner's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The nuclear envelope protein MAN1 regulates TGFbeta signaling and vasculogenesis in the embryonic yolk sac.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Dystonia and the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The nuclear envelope as an integrator of nuclear and cytoplasmic architecture

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Coupling of the nucleus and cytoplasm: role of the LINC complex

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Characterization of adiposity and metabolism in Lmna-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Generation and characterization of Dyt1 DeltaGAG knock-in mouse as a model for early-onset dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Motor deficits and hyperactivity in Dyt1 knockdown mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Lamin a truncation in Hutchinson-Gilford progeria.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Alterations in mitosis and cell cycle progression caused by a mutant lamin A known to accelerate human aging

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

SUN1 is required for telomere attachment to nuclear envelope and gametogenesis in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nucleoplasmic lamins and their interaction partners, LAP2alpha, Rb, and BAF, in transcriptional regulation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Hutchinson-Gilford progeria syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Biology of the striated muscle dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Recruitment to the nuclear periphery can alter expression of genes in human cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Lamin A/C and emerin are critical for skeletal muscle satellite cell differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Overview of adipose tissue and its role in obesity and metabolic disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The Werner Syndrome Helicase-Nuclease--One Protein, Many Mysteries

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nuclear lamins: building blocks of nuclear architecture

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Toward therapy for DYT1 dystonia: allele-specific silencing of mutant TorsinA

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Reduced adiponectin and HDL cholesterol without elevated C-reactive protein: clues to the biology of premature atherosclerosis in Hutchinson-Gilford Progeria Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Disease progression in Hutchinson-Gilford progeria syndrome: impact on growth and development.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The dystonia-associated protein torsinA modulates synaptic vesicle recycling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The inner nuclear envelope as a transcription factor resting place

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Familial cutaneous collagenomas resulting from a novel mutation in LEMD3

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

RecQ helicases: caretakers of the genome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Multiple roles for emerin: implications for Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

An emerin "proteome": purification of distinct emerin-containing complexes from HeLa cells suggests molecular basis for diverse roles including gene regulation, mRNA splicing, signaling, mechanosensing, and nuclear architecture.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The human lamin B receptor/sterol reductase multigene family

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Signaling of transforming growth factor-beta family members through Smad proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The inner-nuclear-envelope protein emerin regulates HIV-1 infectivity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Organelle proteome variation among different cell types: lessons from nuclear membrane proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Unique players in the BMP pathway: small C-terminal domain phosphatases dephosphorylate Smad1 to attenuate BMP signaling.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

A genetic locus targeted to the nuclear periphery in living cells maintains its transcriptional competence

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nuclear lamin A/C deficiency induces defects in cell mechanics, polarization, and migration

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The role of C/EBP(epsilon) in the terminal stages of granulocyte differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Sequence and expression of a type II keratin, K5, in human epidermal cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Origin of nuclear buds and micronuclei in normal and folate-deprived human lymphocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Genomic instability in laminopathy-based premature aging

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Lamin B receptor plays a role in stimulating nuclear envelope production and targeting membrane vesicles to chromatin during nuclear envelope assembly through direct interaction with importin beta

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Defects in lamin B1 expression or processing affect interphase chromosome position and gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

The inner nuclear membrane protein emerin regulates beta-catenin activity by restricting its accumulation in the nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Phenotype and course of Hutchinson-Gilford progeria syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The LEM domain proteins emerin and LAP2alpha are dispensable for human immunodeficiency virus type 1 and murine leukemia virus infections.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Transforming growth factor beta and mouse development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Loss of nucleoplasmic LAP2alpha-lamin A complexes causes erythroid and epidermal progenitor hyperproliferation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

TorsinA in the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Mitotic phosphorylation of the lamin B receptor by a serine/arginine kinase and p34(cdc2)

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

A nuclear envelope-associated kinase phosphorylates arginine-serine motifs and modulates interactions between the lamin B receptor and other nuclear proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

The Werner syndrome protein: an update

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Dependence of diffusional mobility of integral inner nuclear membrane proteins on A-type lamins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Lamin B1 duplications cause autosomal dominant leukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

The human lipodystrophy gene BSCL2/seipin may be essential for normal adipocyte differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nucleoplasmic LAP2alpha-lamin A complexes are required to maintain a proliferative state in human fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Transcriptional repression mediated by repositioning of genes to the nuclear lamina

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Signaling pathways in vascular development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

A novel role for the nuclear membrane protein emerin in association of the centrosome to the outer nuclear membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nuclear membrane proteins with potential disease links found by subtractive proteomics

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

ER Biogenesis: Self-Assembly of Tubular Topology by Protein Hairpins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Wild-type levels of human immunodeficiency virus type 1 infectivity in the absence of cellular emerin protein

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The lamin B receptor-associated protein p34 shares sequence homology and antigenic determinants with the splicing factor 2-associated protein p32

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Smooth muscle cell depletion and collagen types in progeric arteries

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Blurring the boundary: the nuclear envelope extends its reach.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Structural requirements for the assembly of LINC complexes and their function in cellular mechanical stiffness

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Rb and N-ras function together to control differentiation in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

SUN-domain proteins: 'Velcro' that links the nucleoskeleton to the cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

The inner nuclear membrane protein Lem2 is critical for normal nuclear envelope morphology

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

A-type lamins are essential for TGF-beta1 induced PP2A to dephosphorylate transcription factors

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Lamin B1 is required for mouse development and nuclear integrity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

LEM-Domain proteins: new insights into lamin-interacting proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Distinct functional domains in nesprin-1alpha and nesprin-2beta bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

"Laminopathies": a wide spectrum of human diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nuclear envelope, nuclear lamina, and inherited disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

A lamin B receptor in the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson-Gilford progeria syndrome mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Treatment with a farnesyltransferase inhibitor improves survival in mice with a Hutchinson-Gilford progeria syndrome mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

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%2FS0070-2153%2808%2900607-8

7 January 2021

Motor deficits and hyperactivity in cerebral cortex-specific Dyt1 conditional knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Syne-1 and Syne-2 play crucial roles in myonuclear anchorage and motor neuron innervation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Abnormal motor function and dopamine neurotransmission in DYT1 DeltaGAG transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

Organization and modulation of nuclear lamina structure

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900607-8

7 January 2021

10.1016/S0070-2153(08)00607-8

Identifiers

DOI

1 reference

20 August 2017

1 reference