Seipin is necessary for normal brain development and spermatogenesis in addition to adipogenesis
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Seipin is necessary for normal brain development and spermatogenesis in addition to adipogenesis
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 24, Issue 15, Pages 4238-4249
Publisher
Oxford University Press (OUP)
Online
2015-05-03
DOI
10.1093/hmg/ddv156
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Lack of seipin in neurons results in anxiety- and depression-like behaviors via down regulation of PPARγ
- (2014) Libin Zhou et al. HUMAN MOLECULAR GENETICS
- Lack of testicular seipin causes teratozoospermia syndrome in men
- (2014) M. Jiang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice
- (2013) X. Prieur et al. DIABETOLOGIA
- Generation of leptin-deficient Lepmkyo/Lepmkyo rats and identification of leptin-responsive genes in the liver
- (2013) Megumi Aizawa-Abe et al. PHYSIOLOGICAL GENOMICS
- Functional Magnetic Resonance Imaging Analysis of Food-Related Brain Activity in Patients with Lipodystrophy Undergoing Leptin Replacement Therapy
- (2012) Daisuke Aotani et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Seipin: from human disease to molecular mechanism
- (2012) Bethany R. Cartwright et al. JOURNAL OF LIPID RESEARCH
- Berardinelli-Seip Congenital Lipodystrophy 2/Seipin Is a Cell-Autonomous Regulator of Lipolysis Essential for Adipocyte Differentiation
- (2012) W. Chen et al. MOLECULAR AND CELLULAR BIOLOGY
- Seipin ablation in mice results in severe generalized lipodystrophy
- (2011) X. Cui et al. HUMAN MOLECULAR GENETICS
- Lipodystrophies: Genetic and Acquired Body Fat Disorders
- (2011) Abhimanyu Garg JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Selective white matter abnormalities in a novel rat model of vascular dementia
- (2011) Akihiro Kitamura et al. NEUROBIOLOGY OF AGING
- The Human Lipodystrophy Gene Product Berardinelli-Seip Congenital Lipodystrophy 2/Seipin Plays a Key Role in Adipocyte Differentiation
- (2009) Weiqin Chen et al. ENDOCRINOLOGY
- Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy
- (2009) Yukiko K. Hayashi et al. JOURNAL OF CLINICAL INVESTIGATION
- Leptin signaling in brain: A link between nutrition and cognition?
- (2008) Christopher D. Morrison BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Seipinopathy: a novel endoplasmic reticulum stress-associated disease
- (2008) Daisuke Ito et al. BRAIN
- Caveolin-1: A New Locus for Human Lipodystrophy
- (2008) Abhimanyu Garg et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy
- (2008) C. A. Kim et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- An ENU-induced mutant archive for gene targeting in rats
- (2008) Tomoji Mashimo et al. NATURE GENETICS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started