Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells. - Wikidata - wikimedia - TriplyDB

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

http://www.wikidata.org/entity/Q37958960

about

Potential therapeutic effects of the MTOR inhibitors for preventing ageing and progeria-related disorders Recent advances in understanding the role of lamins in health and disease All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.Cell Mechanosensitivity is Enabled by the LINC Nuclear Complex.Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathies Concise Review: Plasma and Nuclear Membranes Convey Mechanical Information to Regulate Mesenchymal Stem Cell Lineage.Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins Lamins and bone disorders: current understanding and perspectives.

P2860

Q28067037-F54E380F-92F3-413D-A3F9-56AB2532AF03 Q28068068-7E5DD30C-4039-4A02-BE02-7E3F99A35CB2 Q36557465-98538E08-E94A-48AD-B70E-29DD1A2E6982 Q37016154-D06DC345-B568-4B29-96C3-03310576859C Q38284300-A22A18C7-2ACD-4689-A29C-923A6B799F25 Q38739307-C12B659A-C17A-4086-895C-7595BC36C8E0 Q38893099-19AEC8D0-1841-4984-A44C-7D766B1A2CA7 Q54945496-6258FD39-C6E5-48DA-9C8A-CEFA55BC0998

P2860

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

http://www.wikidata.org/entity/Q37958960

description

article científic

@ca

article scientifique

@fr

articol științific

@ro

articolo scientifico

@it

artigo científico

@gl

artigo científico

@pt

artigo científico

@pt-br

artikel ilmiah

@id

artikull shkencor

@sq

artículo científico

@es

name

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

@en

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

@nl

type

label

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

@en

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

@nl

prefLabel

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

@en

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

@nl

P1433

Q37958960-FEB02A6F-9DDF-4D04-84FE-B47042977D57

P1476

Q37958960-A8C4DD78-480F-4EC1-9B98-7DBBF698E997

P2860

Q37958960-03C76573-A66E-4766-A973-7B3E72A62F4A

Q37958960-08A66261-C4F2-4CB8-9889-2A5C921BECA1

Q37958960-0A19C3D0-494C-45B6-92E5-1A95E33F5756

Q37958960-20315E97-8B41-43F7-93D8-14DCE882622A

Q37958960-261D1334-E55B-48B6-AF5A-8B12473F2E00

Q37958960-2817F17F-F5E6-42A8-8345-315B31B00E56

Q37958960-29F334CC-3EB6-4943-842C-8C966A5D9C51

Q37958960-317D679F-CB08-462C-8805-607E8F655FF1

Q37958960-330113F1-306B-4A7A-9D83-C259DBE214C8

Q37958960-35E21A54-D57E-4BB8-8A31-E3BD7BEB825B

P304

Q37958960-B1806CAF-4777-49AA-99BA-73C4A1171EAC

P31

Q37958960-0BFF0590-3FB4-46B3-AB2B-79C72658CD2E

P356

Q37958960-1A3D1963-D820-48DC-ABA5-A8129A4EBA1E

P433

Q37958960-FDB3946D-EC7F-4FDB-A5D3-AA1876A7187F

P478

Q37958960-02216EB7-D5FD-485E-B387-352CCDC5D693

P50

Q37958960-EA7C0496-B315-4D45-9289-9C62C60419B8

P577

Q37958960-9951F9ED-D05C-4BC9-B3F6-21806D950125

P698

Q37958960-B561417F-D559-40C9-9D69-8AC25A7DEB70

P356

P1433

Biochemical Society Transactions

P1476

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

@en

P2860

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

Prenylated prelamin A interacts with Narf, a novel nuclear protein

Emerin-prelamin A interplay in human fibroblasts

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

Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes

Loss of a DNA binding site within the tail of prelamin A contributes to altered heterochromatin anchorage by progerin

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

Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome

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

Analysis of prelamin A biogenesis reveals the nucleus to be a CaaX processing compartment

P304

1698-1704

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1042/BST20110657

http://www.w3.org/2001/XMLSchema#string

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

39

http://www.w3.org/2001/XMLSchema#string

P50

Giovanna Lattanzi

P577

2011-12-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

22103510

http://www.w3.org/2001/XMLSchema#string