Thematic review series: Adipocyte Biology. Lipodystrophies: windows on adipose biology and metabolism (Q34610713)

3 August 2017

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title

Thematic review series: Adipocyte Biology. Lipodystrophies: windows on adipose biology and metabolism (English)

1 reference

3 August 2017

1 reference

1

Robert A Hegele

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Brian Rutt

series ordinal

4

object named as

Brian K Rutt

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3 August 2017

Tisha R Joy

2

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PubMed ID

17374881

3 August 2017

Salam A Al-Attar

series ordinal

3

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3 August 2017

20 March 2007

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Journal of Lipid Research

3 August 2017

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3 August 2017

48

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3 August 2017

7

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3 August 2017

1433-1444

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Acquired and inherited lipodystrophies

3 August 2017

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Lipodystrophy: lessons in lipid and energy metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Monogenic forms of insulin resistance: apertures that expose the common metabolic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Phenomics, lipodystrophy, and the metabolic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

An undiagnosed endocrinometabolic syndrome: report of 2 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Genetic basis of lipodystrophies and management of metabolic complications

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

A gene for congenital generalized lipodystrophy maps to human chromosome 9q34.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Congenital generalized lipodystrophy: significance of triglyceride biosynthetic pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Agpat6 deficiency causes subdermal lipodystrophy and resistance to obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Congenital Generalized Lipodystrophy Accompanied by Cystic Angiomatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli-Seip congenital lipodystrophy patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Phenotypic Heterogeneity in Body Fat Distribution in Patients with Congenital Generalized Lipodystrophy Caused by Mutations in the AGPAT2 or Seipin Genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Lipodystrophy of the extremities. A dominantly inherited syndrome associated with lipatrophic diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Hepatic steatosis in Dunnigan-type familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Risk factors for diabetes in familial partial lipodystrophy, Dunnigan variety.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Köbberling type of familial partial lipodystrophy: an underrecognized syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Human laminopathies: nuclei gone genetically awry

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Prelamin A farnesylation and progeroid syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

A novel heterozygous mutation in peroxisome proliferator-activated receptor-gamma gene in a patient with familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Non-DNA binding, dominant-negative, human PPARgamma mutations cause lipodystrophic insulin resistance

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

A single-base mutation in the peroxisome proliferator-activated receptor gamma4 promoter associated with altered in vitro expression and partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Peroxisomal proliferator activated receptor-gamma deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3)

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

PPARG F388L, a transactivation-deficient mutant, in familial partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Familial partial lipodystrophy phenotype resulting from a single-base mutation in deoxyribonucleic acid-binding domain of peroxisome proliferator-activated receptor-gamma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferator-activated receptor-gamma

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Premature atherosclerosis associated with monogenic insulin resistance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Genome-wide analysis of mouse transcripts using exon microarrays and factor graphs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Clinical features and metabolic derangements in acquired generalized lipodystrophy: case reports and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Clinical review 153: Lipodystrophy in human immunodeficiency virus-infected patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

"Buffalo hump" in men with HIV-1 infection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Pseudo-Cushing's syndrome in human immunodeficiency virus-infected patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Development of cervical fat pads following therapy with human immunodeficiency virus type 1 protease inhibitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Fat distribution in men with HIV infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Incidence of lipoatrophy and lipohypertrophy in the women's interagency HIV study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Cardiovascular risk and body-fat abnormalities in HIV-infected adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Hepatic steatosis and HIV infection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Absence of polycystic ovary syndrome features in human immunodeficiency virus-infected women despite significant hyperinsulinemia and truncal adiposity

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Adiponectin and leptin levels in HIV-infected subjects with insulin resistance and body fat redistribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Insulin-resistant diabetes mellitus and hypermetabolism in mandibuloacral dysplasia: a newly recognized form of partial lipodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Body fat distribution and metabolic derangements in patients with familial partial lipodystrophy associated with mandibuloacral dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Hutchinson-Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Molecular bases of progeroid syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Human Genome and Diseases: A new series of reviews in CMLS Werner Syndrome: genetic and molecular basis of a premature aging disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Semi-automated segmentation and quantification of adipose tissue in calf and thigh by MRI: a preliminary study in patients with monogenic metabolic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Quantitative and qualitative differences in subcutaneous adipose tissue stores across lipodystrophy types shown by magnetic resonance imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

Membrane topology of the human seipin protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

ALMNASplicing Mutation in Two Sisters with Severe Dunnigan-Type Familial Partial Lipodystrophy Type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.R700004-JLR200

10.1194/JLR.R700004-JLR200

21 January 2018

Identifiers

DOI

1 reference

3 August 2017

1 reference

PubMed ID

17374881