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Items: 1 to 20 of 46

1.
The complicated clinical course in a case of atypical lipodystrophy after development of neutralizing antibody to metreleptin: treatment with setmelanotide
Baris Akinci, Rasimcan Meral, Diana Rus, Rita Hench, Adam H Neidert, Frank DiPaola, Maria Westerhoff, Simeon I Taylor, Elif A Oral
Endocrinol Diabetes Metab Case Rep. 2020; 2020: 19-0139. Published online 2020 Mar 25. doi: 10.1530/EDM-19-0139
PMCID:
PMC7159256
AbstractArticlePDF–1.1M
2.
Myositis associated with localized lipodystrophy: an unrecognized condition?
H-J Gdynia, P Weydt, A Ernst, S Klein, A-D Sperfeld, A Riecker
Eur J Med Res. 2009; 14(5): 228–230. Published online 2009 May 14. doi: 10.1186/2047-783X-14-5-228
PMCID:
PMC3351983
AbstractArticlePDF–1.4M
3.
Drug-Induced Atypical Lipodystrophy
Priyadarshini Rajakumar, Shriraam Mahadevan, Adlyne Reena Asirvatham, Asha Ranjan
JCEM Case Rep. 2024 Apr; 2(4): luae067. Published online 2024 Apr 18. doi: 10.1210/jcemcr/luae067
PMCID:
PMC11025636
AbstractArticlePDF–383K
4.
Diphlorethohydroxycarmalol of Ishige okamurae and Caffeine Modified the Expression of Extracellular Fibrillars during Adipogenesis of Mouse Subcutaneous Adipose Derived Stem Cell
Younmi Jeon, Siyoung Song, Hagju Kim, Yong-Pil Cheon
Dev Reprod. 2013 Sep; 17(3): 275–287. doi: 10.12717/DR.2013.17.3.275
PMCID:
PMC4282291
AbstractArticlePDF–806K
5.
Electrolyte and Haemogram changes post large volume liposuction comparing two different tumescent solutions
Kumar Vivek, Shah Amiti, Saha Shivshankar, Choudhary Lalit
Indian J Plast Surg. 2014 Sep-Dec; 47(3): 386–393. doi: 10.4103/0970-0358.146604
PMCID:
PMC4292117
AbstractArticlePDF–1.0M
6.
Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia
Henian Cao, Lindsay Alston, Jennifer Ruschman, Robert A Hegele
Lipids Health Dis. 2008; 7: 3. Published online 2008 Jan 31. doi: 10.1186/1476-511X-7-3
PMCID:
PMC2276215
AbstractArticlePDF–386K
7.
Lipodystrophy Syndromes
Iram Hussain, Abhimanyu Garg
Endocrinol Metab Clin North Am. Author manuscript; available in PMC 2020 Oct 27.
Published in final edited form as: Endocrinol Metab Clin North Am. 2016 Dec; 45(4): 783–797. Published online 2016 Oct 6. doi: 10.1016/j.ecl.2016.06.012
PMCID:
PMC7590232
ArticlePDF–519K
8.
Coatomer-dependent protein delivery to lipid droplets
Krishnakant G. Soni, Gonzalo A. Mardones, Rachid Sougrat, Elena Smirnova, Catherine L. Jackson, Juan S. Bonifacino
J Cell Sci. 2009 Jun 1; 122(11): 1834–1841. Published online 2009 May 20. doi: 10.1242/jcs.045849
PMCID:
PMC2684835
AbstractArticle
9.
DNA damage triggers a chronic auto-inflammatory response leading to fat depletion in NER progeria
Ismene Karakasilioti, Irene Kamileri, Georgia Chatzinikolaou, Theodoros Kosteas, Eleni Vergadi, Andria Rasile Robinson, Iannis Tsamardinos, Tania A Rozgaja, Sandra Siakouli, Christos Tsatsanis, Laura J. Niedernhofer, George A. Garinis
Cell Metab. Author manuscript; available in PMC 2014 Jul 31.
Published in final edited form as: Cell Metab. 2013 Sep 3; 18(3): 403–415. doi: 10.1016/j.cmet.2013.08.011
PMCID:
PMC4116679
AbstractArticlePDF–2.1M
10.
Analysis of naturally occurring mutations in the human lipodystrophy protein seipin reveals multiple potential pathogenic mechanisms
M. F. Michelle Sim, M. Mesbah Uddin Talukder, Rowena J. Dennis, Stephen O’Rahilly, J. Michael Edwardson, Justin J. Rochford
Diabetologia. 2013; 56(11): 2498–2506. Published online 2013 Aug 30. doi: 10.1007/s00125-013-3029-3
PMCID:
PMC3824349
AbstractArticlePDF–437K
11.
Expression of Fibroblast Growth Factor-21 in Muscle Is Associated with Lipodystrophy, Insulin Resistance and Lipid Disturbances in Patients with HIV
Birgitte Lindegaard, Thine Hvid, Thomas Grøndahl, Christian Frosig, Jan Gerstoft, Pernille Hojman, Bente Klarlund Pedersen
PLoS One. 2013; 8(3): e55632. Published online 2013 Mar 22. doi: 10.1371/journal.pone.0055632
Correction in:
PLoS One. 2015; 10(4): e0127249.
PMCID:
PMC3606412
AbstractArticlePDF–414K
12.
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment
Daria Camozzi, Maria Rosaria D’Apice, Elisa Schena, Vittoria Cenni, Marta Columbaro, Cristina Capanni, Nadir M. Maraldi, Stefano Squarzoni, Michela Ortolani, Giuseppe Novelli, Giovanna Lattanzi
Histochem Cell Biol. 2012; 138(4): 643–651. Published online 2012 Jun 17. doi: 10.1007/s00418-012-0977-5
PMCID:
PMC3432780
AbstractArticlePDF–511K
13.
Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins
Isabelle Duband-Goulet, Stephanie Woerner, Sylvaine Gasparini, Wikayatou Attanda, Emilie Kondé, Carine Tellier-Lebègue, Constantin T. Craescu, Aurélie Gombault, Pascal Roussel, Nathalie Vadrot, Patrick Vicart, Cecilia Östlund, Howard J. Worman, Sophie Zinn-Justin, Brigitte Buendia
Exp Cell Res. Author manuscript; available in PMC 2012 Dec 10.
Published in final edited form as: Exp Cell Res. 2011 Dec 10; 317(20): 2800–2813. Published online 2011 Oct 4. doi: 10.1016/j.yexcr.2011.09.012
PMCID:
PMC3215798
AbstractArticlePDF–2.4M
14.
Human 1-Acylglycerol-3-phosphate O-Acyltransferase Isoforms 1 and 2: BIOCHEMICAL CHARACTERIZATION AND INABILITY TO RESCUE HEPATIC STEATOSIS IN Agpat2−/− GENE LIPODYSTROPHIC MICE
Anil K. Agarwal, Suja Sukumaran, Víctor A. Cortés, Katie Tunison, Dario Mizrachi, Shireesha Sankella, Robert D. Gerard, Jay D. Horton, Abhimanyu Garg
J Biol Chem. 2011 Oct 28; 286(43): 37676–37691. Published online 2011 Aug 27. doi: 10.1074/jbc.M111.250449
PMCID:
PMC3199511
AbstractArticlePDF–4.1M
15.
Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations
Anna Rajab, Volker Straub, Liza J. McCann, Dominik Seelow, Raymonda Varon, Rita Barresi, Anne Schulze, Barbara Lucke, Susanne Lützkendorf, Mohsen Karbasiyan, Sebastian Bachmann, Simone Spuler, Markus Schuelke
PLoS Genet. 2010 Mar; 6(3): e1000874. Published online 2010 Mar 12. doi: 10.1371/journal.pgen.1000874
PMCID:
PMC2837386
AbstractArticlePDF–5.3M
16.
The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development
Mao Mao, Daniel R. Thedens, Bo Chang, Belinda S. Harris, Qing Yin Zheng, Kenneth R. Johnson, Leah Rae Donahue, Michael G. Anderson
Mamm Genome. Author manuscript; available in PMC 2010 Aug 1.
Published in final edited form as: Mamm Genome. 2009 Aug; 20(8): 462–475. Published online 2009 Aug 8. doi: 10.1007/s00335-009-9210-9
PMCID:
PMC2759419
AbstractArticlePDF–4.0M
17.
Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy
Yukiko K. Hayashi, Chie Matsuda, Megumu Ogawa, Kanako Goto, Kayo Tominaga, Satomi Mitsuhashi, Young-Eun Park, Ikuya Nonaka, Naomi Hino-Fukuyo, Kazuhiro Haginoya, Hisashi Sugano, Ichizo Nishino
J Clin Invest. 2009 Sep 1; 119(9): 2623–2633. Published online 2009 Aug 10. doi: 10.1172/JCI38660
PMCID:
PMC2735915
AbstractArticlePDF–4.9M
18.
Local regulation of fat metabolism in peripheral nerves
Mark H.G. Verheijen, Roman Chrast, Patrick Burrola, Greg Lemke
Genes Dev. 2003 Oct 1; 17(19): 2450–2464. doi: 10.1101/gad.1116203
PMCID:
PMC218081
AbstractArticlePDF–701K
19.
Brief Genetic Analysis: Effects of Ritonavir on Adipocyte Gene Expression: Evidence for a Stress-Related Response
Diane C. Adler-Wailes, Evan L. Guiney, Jashin Koo, Jack A. Yanovski
Obesity (Silver Spring) Author manuscript; available in PMC 2009 Jan 6.
Published in final edited form as: Obesity (Silver Spring). 2008 Oct; 16(10): 2379–2387. Published online 2008 Jul 17. doi: 10.1038/oby.2008.350
Correction in:
volume 17 on page 616
PMCID:
PMC2614385
AbstractArticlePDF–718K
20.
The Human Lipodystrophy Gene BSCL2/Seipin May Be Essential for Normal Adipocyte Differentiation
Victoria A. Payne, Neil Grimsey, Antoinette Tuthill, Sam Virtue, Sarah L. Gray, Edoardo Dalla Nora, Robert K. Semple, Stephen O'Rahilly, Justin J. Rochford
Diabetes. 2008 Aug; 57(8): 2055–2060. doi: 10.2337/db08-0184
PMCID:
PMC2494687
AbstractArticlePDF–575K

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