Nucleoplasmic lamins define growth-regulating functions of lamina-associated polypeptide 2α in progeria cells.

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Nucleoplasmic lamins define growth-regulating functions of lamina-associated polypeptide 2α in progeria cells.

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Nucleoplasmic lamins define gr ...... ypeptide 2α in progeria cells.

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Nucleoplasmic lamins define gr ...... ypeptide 2α in progeria cells.

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Nucleoplasmic lamins define gr ...... ypeptide 2α in progeria cells.

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Nucleoplasmic lamins define gr ...... ypeptide 2α in progeria cells.

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Nucleoplasmic lamins define gr ...... ypeptide 2α in progeria cells.

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Nucleoplasmic lamins define gr ...... ypeptide 2α in progeria cells.

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P1476

Nucleoplasmic lamins define gr ...... ypeptide 2α in progeria cells.

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P2093

Konstantina Georgiou

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

Nana Naetar

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Petra Fichtinger

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Sandra Vidak

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Thomas Dechat

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P2860

The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin

LAP2alpha-binding protein LINT-25 is a novel chromatin-associated protein involved in cell cycle exit

Detergent-salt resistance of LAP2alpha in interphase nuclei and phosphorylation-dependent association with chromosomes early in nuclear assembly implies functions in nuclear structure dynamics.

Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome

Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma protein

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

Lamin A-dependent nuclear defects in human aging

Molecular insights into the premature aging disease progeria

Lamina-associated polypeptide 2alpha binds intranuclear A-type lamins

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

P31

scholarly article

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10.1242/JCS.208462

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P407

English

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P478

131

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Roland Foisner

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2018-02-08T00:00:00Z

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29361532

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P932

5826045

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