BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

375 related articles for article (PubMed ID: 21051554)

  • 21. Overexpression of a short human seipin/BSCL2 isoform in mouse adipose tissue results in mild lipodystrophy.
    Cui X; Wang Y; Meng L; Fei W; Deng J; Xu G; Peng X; Ju S; Zhang L; Liu G; Zhao L; Yang H
    Am J Physiol Endocrinol Metab; 2012 Mar; 302(6):E705-13. PubMed ID: 22234369
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutations in the seipin and AGPAT2 genes clustering in consanguineous families with Berardinelli-Seip congenital lipodystrophy from two separate geographical regions of Brazil.
    Gomes KB; Fernandes AP; Ferreira AC; Pardini H; Garg A; Magré J; Pardini VC
    J Clin Endocrinol Metab; 2004 Jan; 89(1):357-61. PubMed ID: 14715872
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations.
    Nishiyama A; Yagi M; Awano H; Okizuka Y; Maeda T; Yoshida S; Takeshima Y; Matsuo M
    Pediatr Int; 2009 Dec; 51(6):775-9. PubMed ID: 19438831
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects.
    Fu M; Kazlauskaite R; Baracho Mde F; Santos MG; Brandão-Neto J; Villares S; Celi FS; Wajchenberg BL; Shuldiner AR
    J Clin Endocrinol Metab; 2004 Jun; 89(6):2916-22. PubMed ID: 15181077
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Leptin ameliorates insulin resistance and hepatic steatosis in Agpat2-/- lipodystrophic mice independent of hepatocyte leptin receptors.
    Cortés VA; Cautivo KM; Rong S; Garg A; Horton JD; Agarwal AK
    J Lipid Res; 2014 Feb; 55(2):276-88. PubMed ID: 24293639
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Metabolic, Reproductive, and Neurologic Abnormalities in Agpat1-Null Mice.
    Agarwal AK; Tunison K; Dalal JS; Nagamma SS; Hamra FK; Sankella S; Shao X; Auchus RJ; Garg A
    Endocrinology; 2017 Nov; 158(11):3954-3973. PubMed ID: 28973305
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Difficult to manage diabetes mellitus associated with generalized congenital lipodystrophy. Report of two cases].
    Cardona-Hernández R; Suárez-Ortega L; Torres M
    An Pediatr (Barc); 2011 Feb; 74(2):126-30. PubMed ID: 21168376
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Absence of AGPAT2 impairs brown adipogenesis, increases IFN stimulated gene expression and alters mitochondrial morphology.
    Tapia PJ; Figueroa AM; Eisner V; González-Hódar L; Robledo F; Agarwal AK; Garg A; Cortés V
    Metabolism; 2020 Oct; 111():154341. PubMed ID: 32810486
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prevalence of mutations in AGPAT2 among human lipodystrophies.
    Magré J; Delépine M; Van Maldergem L; Robert JJ; Maassen JA; Meier M; Panz VR; Kim CA; Tubiana-Rufi N; Czernichow P; Seemanova E; Buchanan CR; Lacombe D; Vigouroux C; Lascols O; Kahn CR; Capeau J; Lathrop M
    Diabetes; 2003 Jun; 52(6):1573-8. PubMed ID: 12765973
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and molecular aspects of Berardinelli-Seip Congenital Lipodystrophy (BSCL).
    Gomes KB; Pardini VC; Fernandes AP
    Clin Chim Acta; 2009 Apr; 402(1-2):1-6. PubMed ID: 19167372
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Dysfunction of lipid metabolism in lipodystrophic Seipin-deficient mice.
    Wang M; Gao M; Liao J; Han Y; Wang Y; Liu G
    Biochem Biophys Res Commun; 2015 May; 461(2):206-10. PubMed ID: 25866184
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Congenital generalized lipodystrophy: significance of triglyceride biosynthetic pathways.
    Agarwal AK; Garg A
    Trends Endocrinol Metab; 2003 Jul; 14(5):214-21. PubMed ID: 12826327
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Inherited lipodystrophies and hypertriglyceridemia.
    Simha V; Garg A
    Curr Opin Lipidol; 2009 Aug; 20(4):300-8. PubMed ID: 19494770
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Induction of adipocyte differentiation by a thiazolidinedione in cultured, subepidermal, fibroblast-like cells of an infant with congenital generalized lipodystrophy.
    Fischer P; Möller P; Bindl L; Melzner I; Tornqvist H; Debatin KM; Wabitsch M
    J Clin Endocrinol Metab; 2002 May; 87(5):2384-90. PubMed ID: 11994391
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Resistance to high-fat diet-induced obesity and altered expression of adipose-specific genes in HSL-deficient mice.
    Harada K; Shen WJ; Patel S; Natu V; Wang J; Osuga J; Ishibashi S; Kraemer FB
    Am J Physiol Endocrinol Metab; 2003 Dec; 285(6):E1182-95. PubMed ID: 12954598
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Congenital generalized lipodystrophy: profile of the disease and gender differences in two siblings.
    Raygada M; Rennert O
    Clin Genet; 2005 Jan; 67(1):98-101. PubMed ID: 15617555
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.