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[PDF] The human obesity gene map: the 2005 update


T Rankinen, A Zuberi, YC Chagnon, SJ Weisnagel, G … - Obesity, 2006 - pbrc.edu
Abstract RANKINEN, TUOMO, AAMIR ZUBERI, YVON C. CHAGNON, S. JOHN
WEISNAGEL, GEORGE ARGYROPOULOS, BRANDON WALTS, LOUIS PE´RUSSE, AND CLAUDE
BOUCHARD. The human obesity gene map: the 2005 update. Obesity. 2006;14: ...
Cited by 335 - Related articles - View as HTML - All 6 versions

Acquired and inherited lipodystrophies

- shouxi.net
A Garg - The New England journal of medicine, 2004 - nejm.org
Lipodystrophies are clinically heterogeneous acquired or inherited disorders characterized by
the selective loss of adipose tissue. Affected patients are predisposed to insulin resistance and
its attendant complications, including diabetes mellitus, dyslipidemia, hepatic steatosis, ...
Cited by 251 - Related articles - BL Direct - All 10 versions

[PDF] The human obesity gene map: the 2003 update


EE Snyder, B Walts, L Pérusse, YC Chagnon, SJ … - update, 2004 - Citeseer
WEISNAGEL, TUOMO RANKINEN, AND CLAUDE BOUCHARD. The human obesity gene
map: the 2003 update. Obes Res. 2004;12:369–439. This is the tenth update of the human obesity
gene map, incorporating published results up to the end of October 2003 and continuing ...
Cited by 240 - Related articles - View as HTML - BL Direct - All 7 versions

[PDF] The human obesity gene map: the 2004 update


L Perusse, T Rankinen, A Zuberi, YC Chagnon, … - Obesity …, 2005 - informatik.hu-berlin.de
Abstract PE´ RUSSE, LOUIS, TUOMO RANKINEN, AAMIR ZUBERI, YVON C. CHAGNON, S.
JOHN WEISNAGEL, GEORGE ARGYROPOULOS, BRANDON WALTS, ERIC E. SNYDER, AND
CLAUDE BOUCHARD. The human obesity gene map: the 2004 update. Obes Res. 2005; ...
Cited by 210 - Related articles - View as HTML - All 6 versions

Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

- bmj.com [PDF] 
L Van Maldergem, J Magre, TE Khallouf, T Gedde- … - British Medical …, 2002 - jmg.bmj.com
A correction has been published for this article. The contents of the ... L Van Maldergem, J
Magré, TE Khallouf, T Gedde-Dahl Jr, M Delépine, O Trygstad, E Seemanova, T
Stephenson, CS Albott, F Bonnici, VR Panz, JL Medina, P Bogalho, F Huet, S Savasta, A ...
Cited by 72 - Related articles - BL Direct - All 8 versions

Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy

- endojournals.org
AK Agarwal, V Simha, EA Oral, SA Moran, P … - Journal of Clinical …, 2003 - Endocrine Soc
CONGENITAL GENERALIZED LIPODYSTROPHY [CGL; Berardinelli-Seip syndrome, Online
Mendelian Inheritance in Man (OMIM) no. 269700; http://www.ncbi.nlm.nih.gov/Omim/] is a rare
autosomal recessive disorder characterized by near complete absence of adipose tissue ...
Cited by 63 - Related articles - BL Direct - All 5 versions

Prevalence of mutations in AGPAT2 among human lipodystrophies


J Magré, M Delépine, L Van Maldergem, JJ Robert, J … - Diabetes, 2003 - Am Diabetes Assoc
Berardinelli-Seip congenital lipodystrophy (BSCL) is a heterogeneous genetic disease characterized
by near absence of adipose tissue and severe insulin resistance. We have previously identified
mutations in the seipin gene in a subset of our patients' cohort. Recently, disease-causing ...
Cited by 38 - Related articles - BL Direct - All 5 versions

Genetic basis of congenital generalized lipodystrophy


AK Agarwal, RI Barnes, A Garg - International Journal of Obesity, 2003 - nature.com
Congenital generalized lipodystrophy (CGL) is an autosomal recessive disorder characterized
by extreme lack of body fat and severe insulin resistance since birth. Recently, mutations have
been reported in 1-acylglycerol-3-phosphate-O-acyltransferase 2 (AGPAT2) and ...
Cited by 18 - Related articles - BL Direct - All 4 versions

Differential Gene Expression in Liposarcoma, Lipoma, and Adipose Tissue#


KM Skubitz, EY Cheng, DR Clohisy, RC … - Cancer …, 2005 - informahealthcare.com
Malignant transformation is thought to be associated with changes in the expression of a number
of genes, and this alteration in gene expression is felt to be critical to the development of the
malignant phenotype. Sarcomas represent a diverse group of tumors derived from cells of ...
Cited by 17 - Related articles - All 7 versions

Gene and phenotype analysis of congenital generalized lipodystrophy in Japanese …

- endojournals.org
K Ebihara, T Kusakabe, H Masuzaki, N … - Journal of Clinical …, 2004 - Endocrine Soc
Congenital generalized lipodystrophy (CGL), Berardinelli-Seip syndrome, is a rare metabolic
disorder characterized by a near total lack of adipose tissue from birth or early infancy.
Recently, seipin, encoding a 398-amino acid protein of unknown function, and AGPAT2, ...
Cited by 19 - Related articles - BL Direct - All 5 versions


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