نتایج جستجو برای: bscl2

تعداد نتایج: 108  

2018
Vitor Teixeira Lisa Johnsen Fernando Martínez-Montañés Alexandra Grippa Laura Buxó Fatima-Zahra Idrissi Christer S Ejsing Pedro Carvalho

Storage and consumption of neutral lipids in lipid droplets (LDs) are essential for energy homeostasis and tightly coupled to cellular metabolism. However, how metabolic cues are integrated in the life cycle of LDs is unclear. In this study, we characterize the function of Ldo16 and Ldo45, two splicing isoforms of the same protein in budding yeast. We show that Ldo proteins interact with the se...

Journal: :Diabetes 2003
Jocelyne Magré Marc Delépine Lionel Van Maldergem Jean-Jacques Robert J Antonie Maassen Muriel Meier Vanessa R Panz Chong Ae Kim Nadia Tubiana-Rufi Paul Czernichow Eva Seemanova Charles R Buchanan Didier Lacombe Corinne Vigouroux Olivier Lascols C Ronald Kahn Jacqueline Capeau Mark Lathrop

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 mutations in AGPAT2 have been reported in BSCL patients. In this study, we have performed mutation screening in...

Journal: :The Journal of Cell Biology 2008
Weihua Fei Guanghou Shui Bruno Gaeta Ximing Du Lars Kuerschner Peng Li Andrew J. Brown Markus R. Wenk Robert G. Parton Hongyuan Yang

Lipid droplets (LDs) are emerging cellular organelles that are of crucial importance in cell biology and human diseases. In this study, we present our screen of approximately 4,700 Saccharomyces cerevisiae mutants for abnormalities in the number and morphology of LDs; we identify 17 fld (few LDs) and 116 mld (many LDs) mutants. One of the fld mutants (fld1) is caused by the deletion of YLR404W,...

2012
Xin-Gui Peng Shenghong Ju Fang Fang Yu Wang Ke Fang Xin Cui George Liu Peng Li Hui Mao Gao-Jun Teng

Xin-Gui Peng, Shenghong Ju, Fang Fang, Yu Wang, Ke Fang, Xin Cui, George Liu, Peng Li, Hui Mao, and Gao-Jun Teng Jiangsu Key Laboratory of Molecular and Functional Imaging, Department of Radiology, Zhongda Hospital, Medical School, Southeast University, Nanjing, China; Bruker BioSpin, Beijing, China; Institute of Cardiovascular Sciences and Key Laboratory of Molecular Cardiovascular Sciences, M...

Charcot-Marie-Tooth disease (CMT) is the most common hereditary neuropathy of the peripheral nervous system with a wide range of severity and age of onset. CMT patients share similar phenotypes which make it often impossible to identify the disease types based on clinical presentation and electrophysiological studies alone. In recent years, novel genetic diagnostic approaches such as whole exom...

Mohammad Ghofrani, Mohammad Keramatipour, Mohammad Reza Alaei, Mohsen Taghizadeh, Saeed Talebi,

Background: Progressive encephalopathy with or without lipodystrophy is a rare autosomal recessive childhood-onset seipin-associated neurodegenerative syndrome, leading to developmental regression of motor and cognitive skills. In this study, we introduce a patient with developmental regression and autism. The causative mutation was found by exome sequencing. Methods: The proband showed a gener...

Journal: :American journal of physiology. Endocrinology and metabolism 2013
Xin-Gui Peng Shenghong Ju Fang Fang Yu Wang Ke Fang Xin Cui George Liu Peng Li Hui Mao Gao-Jun Teng

Brown adipose tissue (BAT) plays a key role in thermogenesis to protect the body from cold and obesity. White adipose tissue (WAT) stores excess energy in the form of triglycerides. To better understand the genetic effect on regulation of WAT and BAT, we investigated the fat fraction (FF) in two types of adipose tissues in ob/ob, human BSCL2/seipin gene knockout (SKO), Fsp27 gene knockout (Fsp2...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید