Patients with Bardet-Biedl Syndrome Have Hyperleptinemia Suggestive of Leptin Resistance-Reference-Cited by-同舟云学术

Patients with Bardet-Biedl Syndrome Have Hyperleptinemia Suggestive of Leptin Resistance

Published:2011-03-01 Issue:3 Volume:96 Page:E528-E535
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Feuillan Penelope P.¹,Ng David¹,Han Joan C.²,Sapp Julie C.¹,Wetsch Katie¹,Spaulding Emma¹,Zheng Yuqian C.²,Caruso Rafael C.³,Brooks Brian P.³,Johnston Jennifer J.¹,Yanovski Jack A.²,Biesecker Leslie G.¹

Affiliation:

1. Genetic Disease Research Branch (P.P.F., D.N., J.C.S., K.W., E.S., J.J.J., L.G.B.), National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892;

2. Section on Growth and Obesity (J.C.H., Y.C.Z., J.A.Y.), Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892;

3. National Eye Institute (R.C.C., B.P.B.), National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/96/3/E528/9069765/jcemE528.pdf

Reference42 articles.

1. Sur un syndrome d'obésité congenitale avec poldactylie et rétinité pigmentaire (contribution a l'étude des formes cliniques de l'obésité hypophysaire);Bardet,1920

2. New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey.;Beales;J Med Genet,1999

3. Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome.;Ansley;Nature,2003

4. Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.;Badano;Am J Hum Genet,2003

5. Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).;Chiang;Proc Natl Acad Sci USA,2006

Cited by 98 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Spectrum of pathogenic variants and high prevalence of pathogenic BBS7 variants in Russian patients with Bardet–Biedl syndrome;Frontiers in Genetics;2024-07-18

2. Collaborative effort: managing Bardet-Biedl syndrome in pediatric patients. Case series and a literature review;Frontiers in Endocrinology;2024-07-18

3. Verbesserte Versorgungs-und Behandlungsoptionen für Patienten mit Hyperphagie-assoziierter Adipositas bei Bardet-Biedl-Syndrom;Klinische Pädiatrie;2024-03-08

4. Bardet‐Biedl syndrome: A clinical overview focusing on diagnosis, outcomes and best‐practice management;Diabetes, Obesity and Metabolism;2024-02-21

5. Emerging mechanistic understanding of cilia function in cellular signalling;Nature Reviews Molecular Cell Biology;2024-02-16