Lipoatrophy revisited (Q34089005)

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Language	Label	Description	Also known as
English	Lipoatrophy revisited	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

Europe PubMed Central

Lipoatrophy revisited (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

based on heuristic

inferred from title

author name string

Reitman ML

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Arioglu E

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Gavrilova O

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Taylor SI

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

publication date

1 December 2000

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Trends in Endocrinology and Metabolism

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

410-416

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

The Search for Human Obesity Genes

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7 January 2021

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Environmental contributions to the obesity epidemic

1 reference

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7 January 2021

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Disappearance of body fat in normal rats induced by adenovirus-mediated leptin gene therapy

1 reference

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7 January 2021

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Physiological response to long-term peripheral and central leptin infusion in lean and obese mice

1 reference

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Increased glucose metabolism and insulin sensitivity in transgenic skinny mice overexpressing leptin.

1 reference

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Regulating adipogenesis

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7 January 2021

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Transcriptional activation of adipogenesis

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

1 reference

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7 January 2021

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Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C

1 reference

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Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

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7 January 2021

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Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

1 reference

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

1 reference

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7 January 2021

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

1 reference

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Partial lipodystrophy associated with juvenile dermatomyositis: report of two cases

1 reference

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The Complement Abnormalities of Lipodystrophy

1 reference

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7 January 2021

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A syndrome of peripheral lipodystrophy, hyperlipidaemia and insulin resistance in patients receiving HIV protease inhibitors

1 reference

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Endocrine and metabolic evaluation of human immunodeficiency virus-infected patients with evidence of protease inhibitor-associated lipodystrophy

1 reference

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HIV protease inhibitors block human preadipocyte differentiation, but not via the PPARgamma/RXR heterodimer

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Lipodystrophy in patients naive to HIV protease inhibitors

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac and adipose tissue abnormalities but not diabetes in mice deficient in GLUT4

1 reference

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7 January 2021

based on heuristic

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Expression of the mitochondrial uncoupling protein gene from the aP2 gene promoter prevents genetic obesity

1 reference

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7 January 2021

based on heuristic

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Targeted expression of a toxin gene to adipose tissue: transgenic mice resistant to obesity.

1 reference

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7 January 2021

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Troglitazone action is independent of adipose tissue

1 reference

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7 January 2021

based on heuristic

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Life without white fat: a transgenic mouse

1 reference

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7 January 2021

based on heuristic

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Insulin resistance and diabetes mellitus in transgenic mice expressing nuclear SREBP-1c in adipose tissue: model for congenital generalized lipodystrophy

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Surgical implantation of adipose tissue reverses diabetes in lipoatrophic mice

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanism of insulin resistance in A-ZIP/F-1 fatless mice

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Leptin reverses insulin resistance and diabetes mellitus in mice with congenital lipodystrophy.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Leptin and diabetes in lipoatrophic mice

1 reference

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7 January 2021

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The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus

1 reference

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What if Minkowski had been ageusic? An alternative angle on diabetes

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Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors alpha and gamma

1 reference

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7 January 2021

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inferred from DOI database lookup

Leptin and the regulation of body weight in mammals

1 reference

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7 January 2021

based on heuristic

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Direct antidiabetic effect of leptin through triglyceride depletion of tissues.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Torpor in mice is induced by both leptin-dependent and -independent mechanisms

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Efficacy and safety of troglitazone in the treatment of lipodystrophy syndromes.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Late-onset lipoatrophic diabetes. Phenotypic and genotypic familial studies and effect of treatment with metformin and lispro insulin analog

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Familial partial lipodystrophy: two types of an X linked dominant syndrome, lethal in the hemizygous state

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Early manifestations of the carbohydrate-deficient glycoprotein syndrome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant partial lipodystrophy associated with Rieger anomaly, short stature, and insulinopenic diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2800%2900309-X

7 January 2021

based on heuristic

inferred from DOI database lookup

SHORT syndrome and insulin resistance

1 reference

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7 January 2021

based on heuristic

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LIPODYSTROPHY AND HEPATOMEGALY WITH DIABETES, LIPÆMIA, AND OTHER METABOLIC DISTURBANCES

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Dysregulation of insulin-like growth factors in a case of generalized acquired lipoatrophic diabetes mellitus (Lawrence Syndrome) connected with autoantibodies against adipocyte membranes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Barraquer-Simons syndrome (with sensorineural deafness): a contribution to the differential diagnosis of lipodystrophy syndromes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

A case of acquired partial lipodystrophy associated with localized scleroderma and undifferentiated connective tissue disease

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2800%2900309-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Partial Lipodystrophy and Dermatomyositis

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2800%2900309-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Partial lipodystrophy and familial C3 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2800%2900309-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Annular and semicircular lipoatrophies. Report of three cases and review of the literature

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Mesenteric Lipodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1043-2760%2800%2900309-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Localized lipoatrophy due to recombinant growth hormone therapy in a child with 6.7 kilobase gene deletion isolated growth hormone deficiency

1 reference

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7 January 2021

based on heuristic

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Identifiers

10.1016/S1043-2760(00)00309-X

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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