The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy - Test2 - elhamkhani - TriplyDB

The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

http://www.wikidata.org/entity/Q27639152

about

Conformational changes in the nuclear lamina induced by herpes simplex virus type 1 require genes U(L)31 and U(L)34 Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome Altered protein dynamics of disease-associated lamin A mutants Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD)Structural basis for heteromeric assembly and perinuclear organization of keratin filaments Implications and Assessment of the Elastic Behavior of Lamins in Laminopathies Regulation of lamin properties and functions: does phosphorylation do it all?Laminopathies and the long strange trip from basic cell biology to therapy Myopathic lamin mutations cause reductive stress and activate the nrf2/keap-1 pathway Monoclonal antibodies specific for disease-associated point-mutants: lamin A/C R453W and R482W SUMO regulates the assembly and function of a cytoplasmic intermediate filament protein in C. elegans A comparative study of Drosophila and human A-type lamins.Diseases of the nuclear envelope.LMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 Diabetes Functions and dysfunctions of the nuclear lamin Ig-fold domain in nuclear assembly, growth, and Emery-Dreifuss muscular dystrophy.Nuclear lamins.The different function of single phosphorylation sites of Drosophila melanogaster lamin Dm and lamin C The lamin protein family."Laminopathies": a wide spectrum of human diseases.Direct actin binding to A- and B-type lamin tails and actin filament bundling by the lamin A tail.The nucleoporin Nup88 is interacting with nuclear lamin A.Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin Nuclear lamins and chromatin: when structure meets function.Systematic identification of pathological lamin A interactors.LMNA cardiomyopathy: cell biology and genetics meet clinical medicine.Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases.Nuclear lamins: key regulators of nuclear structure and activities Nuclear membrane diversity: underlying tissue-specific pathologies in disease?Lamins at a glance.Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery-Dreifuss muscular dystrophy.Lamin A tail modification by SUMO1 is disrupted by familial partial lipodystrophy-causing mutations Regulation of nuclear lamin polymerization by importin alpha.BioID Identification of Lamin-Associated Proteins.Calcium causes a conformational change in lamin A tail domain that promotes farnesyl-mediated membrane association.From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.Laminopathies disrupt epigenomic developmental programs and cell fate Adult stem cell maintenance and tissue regeneration in the ageing context: the role for A-type lamins as intrinsic modulators of ageing in adult stem cells and their niches.

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P2860

The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

http://www.wikidata.org/entity/Q27639152

description

2002 nî lūn-bûn

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2002 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2002 թվականի հունիսին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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name

The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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The Ig-like structure of the C ...... thy, and partial lipodystrophy

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Bernard Gilquin

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Cecilia Ostlund

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Gisèle Bonne

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Howard J Worman

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Isabelle Krimm

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Jean-Claude Courvalin

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Jean-Paul Mornon

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Joël Couprie

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Paul Hossenlopp

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Sophie Zinn-Justin

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811-23

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scholarly article

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2002-06-01T00:00:00Z

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