LINCing lamin B2 to neuronal migration: growing evidence for cell-specific roles of B-type lamins. (Q34521711)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21278813%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

LINCing lamin B2 to neuronal migration: growing evidence for cell-specific roles of B-type lamins (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21278813%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Catherine Coffinier

series ordinal

1

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21 January 2020

publication date

1 September 2010

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21 January 2020

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21 January 2020

volume

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21278813%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

issue

5

1 reference

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21 January 2020

page(s)

407-411

1 reference

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LINC complexes in health and disease

21 January 2020

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7 July 2018

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7 July 2018

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SUN1/2 and Syne/Nesprin-1/2 complexes connect centrosome to the nucleus during neurogenesis and neuronal migration in mice

7 July 2018

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Laminopathies and the long strange trip from basic cell biology to therapy

7 July 2018

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SUN1 and SUN2 play critical but partially redundant roles in anchoring nuclei in skeletal muscle cells in mice

7 July 2018

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7 July 2018

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A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy.

7 July 2018

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SUN-domain and KASH-domain proteins during development, meiosis and disease.

7 July 2018

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Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin

7 July 2018

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

7 July 2018

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Blurring the boundary: the nuclear envelope extends its reach.

7 July 2018

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Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development

7 July 2018

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

7 July 2018

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Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue

7 July 2018

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Differential expression of nuclear lamin, the major component of nuclear lamina, during neurogenesis in two germinal regions of adult rat brain

7 July 2018

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

7 July 2018

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Neuronal polarity in CNS development

7 July 2018

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Lamin B1 duplications cause autosomal dominant leukodystrophy

7 July 2018

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

7 July 2018

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

7 July 2018

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The cellular roles of the lissencephaly gene LIS1, and what they tell us about brain development

7 July 2018

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A mitotic lamin B matrix induced by RanGTP required for spindle assembly

7 July 2018

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

7 July 2018

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Cortical neuronal migration mutants suggest separate but intersecting pathways

7 July 2018

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Lamin B1 is required for mouse development and nuclear integrity

7 July 2018

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

7 July 2018

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

7 July 2018

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

7 July 2018

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7 July 2018

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7 July 2018

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Life at the edge: the nuclear envelope and human disease

7 July 2018

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Life is a journey: a genetic look at neocortical development

7 July 2018

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7 July 2018

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Lamins and disease: insights into nuclear infrastructure

7 July 2018

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Lamins in disease: why do ubiquitously expressed nuclear envelope proteins give rise to tissue-specific disease phenotypes?

7 July 2018

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

7 July 2018

1 reference

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027074

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

7 July 2018

1 reference

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Differential timing of nuclear lamin A/C expression in the various organs of the mouse embryo and the young animal: a developmental study.

7 July 2018

1 reference

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027074

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

7 July 2018

1 reference

https://api.crossref.org/works/10.4161%2FNUCL.1.5.12830

A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.4161%2FNUCL.1.5.12830

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

21 January 2018

1 reference

https://api.crossref.org/works/10.4161%2FNUCL.1.5.12830

Drosophila klaroid encodes a SUN domain protein required for Klarsicht localization to the nuclear envelope and nuclear migration in the eye.

21 January 2018

1 reference

https://api.crossref.org/works/10.4161%2FNUCL.1.5.12830

Cell nuclei spin in the absence of lamin b1.

21 January 2018

1 reference

https://api.crossref.org/works/10.4161%2FNUCL.1.5.12830

The nuclear lamina is a meshwork of intermediate-type filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.4161%2FNUCL.1.5.12830

Genome instability in progeria: when repair gets old

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21278813

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21278813

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.4161/NUCL.1.5.12830

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21278813%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21278813%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

PubMed publication ID

21278813

1 reference