BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

394 related articles for article (PubMed ID: 19162222)

  • 21. Genetic basis of congenital generalized lipodystrophy.
    Agarwal AK; Barnes RI; Garg A
    Int J Obes Relat Metab Disord; 2004 Feb; 28(2):336-9. PubMed ID: 14557833
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Targeting ATGL to rescue BSCL2 lipodystrophy and its associated cardiomyopathy.
    Zhou H; Lei X; Yan Y; Lydic T; Li J; Weintraub NL; Su H; Chen W
    JCI Insight; 2019 Jun; 5(14):. PubMed ID: 31185001
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.
    Kim CA; Delépine M; Boutet E; El Mourabit H; Le Lay S; Meier M; Nemani M; Bridel E; Leite CC; Bertola DR; Semple RK; O'Rahilly S; Dugail I; Capeau J; Lathrop M; Magré J
    J Clin Endocrinol Metab; 2008 Apr; 93(4):1129-34. PubMed ID: 18211975
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Novel subtype of congenital generalized lipodystrophy associated with muscular weakness and cervical spine instability.
    Simha V; Agarwal AK; Aronin PA; Iannaccone ST; Garg A
    Am J Med Genet A; 2008 Sep; 146A(18):2318-26. PubMed ID: 18698612
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy.
    Agarwal AK; Simha V; Oral EA; Moran SA; Gorden P; O'Rahilly S; Zaidi Z; Gurakan F; Arslanian SA; Klar A; Ricker A; White NH; Bindl L; Herbst K; Kennel K; Patel SB; Al-Gazali L; Garg A
    J Clin Endocrinol Metab; 2003 Oct; 88(10):4840-7. PubMed ID: 14557463
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel BSCL2 gene mutation E189X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus.
    Jin J; Cao L; Zhao Z; Shen S; Kiess W; Zhi D; Ye R; Cheng R; Chen L; Yang Y; Luo F
    Eur J Endocrinol; 2007 Dec; 157(6):783-7. PubMed ID: 18057387
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. Function of seipin: new insights from Bscl2/seipin knockout mouse models.
    Dollet L; Magré J; Cariou B; Prieur X
    Biochimie; 2014 Jan; 96():166-72. PubMed ID: 23831461
    [TBL] [Abstract][Full Text] [Related]  

  • 31. FPLD2 LMNA mutation R482W dysregulates iPSC-derived adipocyte function and lipid metabolism.
    Friesen M; Cowan CA
    Biochem Biophys Res Commun; 2018 Jan; 495(1):254-260. PubMed ID: 29108996
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Mouse models of lipodystrophy and their significance in understanding fat regulation.
    Rochford JJ
    Curr Top Dev Biol; 2014; 109():53-96. PubMed ID: 24947236
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome.
    Miranda DM; Wajchenberg BL; Calsolari MR; Aguiar MJ; Silva JM; Ribeiro MG; Fonseca C; Amaral D; Boson WL; Resende BA; De Marco L
    Clin Endocrinol (Oxf); 2009 Oct; 71(4):512-7. PubMed ID: 19226263
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinical review#: Lipodystrophies: genetic and acquired body fat disorders.
    Garg A
    J Clin Endocrinol Metab; 2011 Nov; 96(11):3313-25. PubMed ID: 21865368
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Identification of genetic suppressors for a BSCL2 lipodystrophy pathogenic variant in Caenorhabditis elegans.
    Bai X; Smith HE; Golden A
    Dis Model Mech; 2024 Jun; 17(6):. PubMed ID: 38454882
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Seipin ablation in mice results in severe generalized lipodystrophy.
    Cui X; Wang Y; Tang Y; Liu Y; Zhao L; Deng J; Xu G; Peng X; Ju S; Liu G; Yang H
    Hum Mol Genet; 2011 Aug; 20(15):3022-30. PubMed ID: 21551454
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Seipin: from human disease to molecular mechanism.
    Cartwright BR; Goodman JM
    J Lipid Res; 2012 Jun; 53(6):1042-55. PubMed ID: 22474068
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.