LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations. - Wikidata - awgldk - TriplyDB

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

http://www.wikidata.org/entity/Q37958971

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Defects of Lipid Synthesis Are Linked to the Age-Dependent Demyelination Caused by Lamin B1 Overexpression Familial partial lipodystrophy, Dunnigan variety - challenges for patient care during pregnancy: a case report.Lamin A tail modification by SUMO1 is disrupted by familial partial lipodystrophy-causing mutations Role of Epicardial Adipose Tissue in Health and Disease: A Matter of Fat?Atomic force microscopy and lamins: A review study towards future, combined investigations.Itm2a silencing rescues lamin A mediated inhibition of 3T3-L1 adipocyte differentiation.Lipodystrophy and obesity are associated with decreased number of T cells with regulatory function and pro-inflammatory macrophage phenotype.Lipodystrophic laminopathies: Diagnostic clues.

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P2860

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

http://www.wikidata.org/entity/Q37958971

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article científic

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article scientifique

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articol științific

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articolo scientifico

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artigo científico

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artigo científico

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artigo científico

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artikel ilmiah

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artikull shkencor

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artículo científico

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name

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

@en

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

@nl

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label

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

@en

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

@nl

prefLabel

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

@en

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

@nl

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Biochemical Society Transactions

P1476

LMNA-linked lipodystrophies: from altered fat distribution to cellular alterations.

@en

P2093

Camille Vatier

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Corinne Vigouroux

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Guillaume Bidault

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Jacqueline Capeau

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Véronique Béréziat

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P2860

Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities

Phenotype and course of Hutchinson-Gilford progeria syndrome

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

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

A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy

Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia

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

A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

Genomic instability in laminopathy-based premature aging

Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice

P304

1752-1757

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scholarly article

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10.1042/BST20110675

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6

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39

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2011-12-01T00:00:00Z

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P698

22103520

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