Lamins, laminopathies and disease mechanisms: possible role for proteasomal degradation of key regulatory proteins. - Wikidata - wikimedia - TriplyDB

Lamins, laminopathies and disease mechanisms: possible role for proteasomal degradation of key regulatory proteins.

Lamins, laminopathies and disease mechanisms: possible role for proteasomal degradation of key regulatory proteins.

http://www.wikidata.org/entity/Q37907728

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Lamin A/C haploinsufficiency modulates the differentiation potential of mouse embryonic stem cells When lamins go bad: nuclear structure and disease Ubiquitin ligase RNF123 mediates degradation of heterochromatin protein 1α and β in lamin A/C knock-down cells.Sustained accumulation of prelamin A and depletion of lamin A/C both cause oxidative stress and mitochondrial dysfunction but induce different cell fates Breaking down protein degradation mechanisms in cardiac muscle.Use of Xenopus cell-free extracts to study size regulation of subcellular structures.Recent advances in understanding nuclear size and shape.Heart-specific expression of laminopathic mutations in transgenic zebrafish.Lamin misexpression upregulates three distinct ubiquitin ligase systems that degrade ATR kinase in HeLa cells.

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Lamins, laminopathies and disease mechanisms: possible role for proteasomal degradation of key regulatory proteins.

http://www.wikidata.org/entity/Q37907728

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artikel ilmiah

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Lamins, laminopathies and dise ...... on of key regulatory proteins.

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Lamins, laminopathies and dise ...... on of key regulatory proteins.

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type

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Lamins, laminopathies and dise ...... on of key regulatory proteins.

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Lamins, laminopathies and dise ...... on of key regulatory proteins.

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Lamins, laminopathies and dise ...... on of key regulatory proteins.

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Lamins, laminopathies and dise ...... on of key regulatory proteins.

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S12038-011-9085-2

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Journal of Biosciences

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Lamins, laminopathies and dise ...... on of key regulatory proteins.

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B Muralikrishna

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Pankaj Chaturvedi

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Veena K Parnaik

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P2860

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

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

Lamin B1 is required for mouse development and nuclear integrity

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

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

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

Lamin A-dependent nuclear defects in human aging

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

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

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

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s12038-011-9085-2

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471-479

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scholarly article

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10.1007/S12038-011-9085-2

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3

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36

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21799258

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