These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 23989774)

  • 1. Analysis of naturally occurring mutations in the human lipodystrophy protein seipin reveals multiple potential pathogenic mechanisms.
    Sim MF; Talukder MM; Dennis RJ; O'Rahilly S; Edwardson JM; Rochford JJ
    Diabetologia; 2013 Nov; 56(11):2498-506. PubMed ID: 23989774
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adipose specific disruption of seipin causes early-onset generalised lipodystrophy and altered fuel utilisation without severe metabolic disease.
    Mcilroy GD; Suchacki K; Roelofs AJ; Yang W; Fu Y; Bai B; Wallace RJ; De Bari C; Cawthorn WP; Han W; Delibegović M; Rochford JJ
    Mol Metab; 2018 Apr; 10():55-65. PubMed ID: 29459250
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Suppression of adipogenesis by pathogenic seipin mutant is associated with inflammatory response.
    Qiu W; Wee K; Takeda K; Lim X; Sugii S; Radda GK; Han W
    PLoS One; 2013; 8(3):e57874. PubMed ID: 23520483
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The human lipodystrophy gene BSCL2/seipin may be essential for normal adipocyte differentiation.
    Payne VA; Grimsey N; Tuthill A; Virtue S; Gray SL; Dalla Nora E; Semple RK; O'Rahilly S; Rochford JJ
    Diabetes; 2008 Aug; 57(8):2055-60. PubMed ID: 18458148
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analyzing the functions and structure of the human lipodystrophy protein seipin.
    Sim MF; Talukder MU; Dennis RJ; Edwardson JM; Rochford JJ
    Methods Enzymol; 2014; 537():161-75. PubMed ID: 24480346
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Towards a mechanistic understanding of lipodystrophy and seipin functions.
    Wee K; Yang W; Sugii S; Han W
    Biosci Rep; 2014 Oct; 34(5):. PubMed ID: 25195639
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology.
    Szymanski KM; Binns D; Bartz R; Grishin NV; Li WP; Agarwal AK; Garg A; Anderson RG; Goodman JM
    Proc Natl Acad Sci U S A; 2007 Dec; 104(52):20890-5. PubMed ID: 18093937
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lack of testicular seipin causes teratozoospermia syndrome in men.
    Jiang M; Gao M; Wu C; He H; Guo X; Zhou Z; Yang H; Xiao X; Liu G; Sha J
    Proc Natl Acad Sci U S A; 2014 May; 111(19):7054-9. PubMed ID: 24778225
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adipose transplantation improves metabolism and atherosclerosis but not perivascular adipose tissue abnormality or vascular dysfunction in lipodystrophic
    Meng Z; Liu C; Xu M; Tao Y; Li H; Wang X; Liao J; Wang M
    Am J Physiol Cell Physiol; 2024 May; 326(5):C1410-C1422. PubMed ID: 38525541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Impaired adipogenic capacity in induced pluripotent stem cells from lipodystrophic patients with BSCL2 mutations.
    Mori E; Fujikura J; Noguchi M; Nakao K; Matsubara M; Sone M; Taura D; Kusakabe T; Ebihara K; Tanaka T; Hosoda K; Takahashi K; Asaka I; Inagaki N; Nakao K
    Metabolism; 2016 Apr; 65(4):543-56. PubMed ID: 26975546
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The human lipodystrophy gene product Berardinelli-Seip congenital lipodystrophy 2/seipin plays a key role in adipocyte differentiation.
    Chen W; Yechoor VK; Chang BH; Li MV; March KL; Chan L
    Endocrinology; 2009 Oct; 150(10):4552-61. PubMed ID: 19574402
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Seipin oligomers can interact directly with AGPAT2 and lipin 1, physically scaffolding critical regulators of adipogenesis.
    Talukder MM; Sim MF; O'Rahilly S; Edwardson JM; Rochford JJ
    Mol Metab; 2015 Mar; 4(3):199-209. PubMed ID: 25737955
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adipose-specific knockout of SEIPIN/BSCL2 results in progressive lipodystrophy.
    Liu L; Jiang Q; Wang X; Zhang Y; Lin RC; Lam SM; Shui G; Zhou L; Li P; Wang Y; Cui X; Gao M; Zhang L; Lv Y; Xu G; Liu G; Zhao D; Yang H
    Diabetes; 2014 Jul; 63(7):2320-31. PubMed ID: 24622797
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuroanatomical characterisation of the expression of the lipodystrophy and motor-neuropathy gene Bscl2 in adult mouse brain.
    Garfield AS; Chan WS; Dennis RJ; Ito D; Heisler LK; Rochford JJ
    PLoS One; 2012; 7(9):e45790. PubMed ID: 23049863
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heterozygous deletion of Seipin in islet beta cells of male mice has an impact on insulin synthesis and secretion through reduced PPARγ expression.
    Xiong J; Sun P; Wang Y; Hua X; Song W; Wang Y; Wu J; Yu W; Liu G; Chen L
    Diabetologia; 2020 Feb; 63(2):338-350. PubMed ID: 31776610
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Oligomers of the lipodystrophy protein seipin may co-ordinate GPAT3 and AGPAT2 enzymes to facilitate adipocyte differentiation.
    Sim MFM; Persiani E; Talukder MMU; Mcilroy GD; Roumane A; Edwardson JM; Rochford JJ
    Sci Rep; 2020 Feb; 10(1):3259. PubMed ID: 32094408
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Effects of Seipin on Mouse Mesenchymal Stem Cell Osteo-Adipogenic Balance.
    Li Z; Jin S; Xu T; Chen H; Cai W; Du J; Qiu J; Zhuang S; Qi Y; Gu W; Pang L
    Stem Cells Dev; 2024 Apr; 33(7-8):177-188. PubMed ID: 38386508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A study of congenital generalized lipodystrophy (CGL) caused by BSCL2 gene mutation.
    Ye JY; Huang AJ; Fu ZZ; Gong YY; Yang HY; Zhou HW
    Yi Chuan; 2022 Oct; 44(10):926-936. PubMed ID: 36384728
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of Seipin in Human Diseases and Experimental Animal Models.
    Li Y; Yang X; Peng L; Xia Q; Zhang Y; Huang W; Liu T; Jia D
    Biomolecules; 2022 Jun; 12(6):. PubMed ID: 35740965
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gene and phenotype analysis of congenital generalized lipodystrophy in Japanese: a novel homozygous nonsense mutation in seipin gene.
    Ebihara K; Kusakabe T; Masuzaki H; Kobayashi N; Tanaka T; Chusho H; Miyanaga F; Miyazawa T; Hayashi T; Hosoda K; Ogawa Y; Nakao K
    J Clin Endocrinol Metab; 2004 May; 89(5):2360-4. PubMed ID: 15126564
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.