642 related articles for article (PubMed ID: 19278620)
21. 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]
22. 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]
23. Seipinopathy: a novel endoplasmic reticulum stress-associated disease.
Ito D; Suzuki N
Brain; 2009 Jan; 132(Pt 1):8-15. PubMed ID: 18790819
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. Lipodystrophies: disorders of adipose tissue biology.
Garg A; Agarwal AK
Biochim Biophys Acta; 2009 Jun; 1791(6):507-13. PubMed ID: 19162222
[TBL] [Abstract][Full Text] [Related]
28. Tissue-autonomous function of Drosophila seipin in preventing ectopic lipid droplet formation.
Tian Y; Bi J; Shui G; Liu Z; Xiang Y; Liu Y; Wenk MR; Yang H; Huang X
PLoS Genet; 2011 Apr; 7(4):e1001364. PubMed ID: 21533227
[TBL] [Abstract][Full Text] [Related]
29. Seipin Deficiency as a Model of Severe Adipocyte Dysfunction: Lessons from Rodent Models and Teaching for Human Disease.
Magré J; Prieur X
Int J Mol Sci; 2022 Jan; 23(2):. PubMed ID: 35054926
[TBL] [Abstract][Full Text] [Related]
30. Membrane topology of the human seipin protein.
Lundin C; Nordström R; Wagner K; Windpassinger C; Andersson H; von Heijne G; Nilsson I
FEBS Lett; 2006 Apr; 580(9):2281-4. PubMed ID: 16574104
[TBL] [Abstract][Full Text] [Related]
31. Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes.
Simha V; Garg A
J Clin Endocrinol Metab; 2003 Nov; 88(11):5433-7. PubMed ID: 14602785
[TBL] [Abstract][Full Text] [Related]
32. Molecular mechanisms of hepatic steatosis and insulin resistance in the AGPAT2-deficient mouse model of congenital generalized lipodystrophy.
Cortés VA; Curtis DE; Sukumaran S; Shao X; Parameswara V; Rashid S; Smith AR; Ren J; Esser V; Hammer RE; Agarwal AK; Horton JD; Garg A
Cell Metab; 2009 Feb; 9(2):165-76. PubMed ID: 19187773
[TBL] [Abstract][Full Text] [Related]
33. A new seipin-associated neurodegenerative syndrome.
Guillén-Navarro E; Sánchez-Iglesias S; Domingo-Jiménez R; Victoria B; Ruiz-Riquelme A; Rábano A; Loidi L; Beiras A; González-Méndez B; Ramos A; López-González V; Ballesta-Martínez MJ; Garrido-Pumar M; Aguiar P; Ruibal A; Requena JR; Araújo-Vilar D
J Med Genet; 2013 Jun; 50(6):401-9. PubMed ID: 23564749
[TBL] [Abstract][Full Text] [Related]
34. Berardinelli-Seip congenital lipodystrophy.
Mandal K; Aneja S; Seth A; Khan A
Indian Pediatr; 2006 May; 43(5):440-5. PubMed ID: 16735770
[TBL] [Abstract][Full Text] [Related]
35. Berardinelli-Seip congenital lipodystrophy 2/SEIPIN determines brown adipose tissue maintenance and thermogenic programing.
Zhou H; Xu C; Lee H; Yoon Y; Chen W
Mol Metab; 2020 Jun; 36():100971. PubMed ID: 32246911
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Acyl-coenzyme A binding protein expression alters liver fatty acyl-coenzyme A metabolism.
Huang H; Atshaves BP; Frolov A; Kier AB; Schroeder F
Biochemistry; 2005 Aug; 44(30):10282-97. PubMed ID: 16042405
[TBL] [Abstract][Full Text] [Related]
39. Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel
Ceccarini G; Magno S; Pelosini C; Ferrari F; Sessa MR; Scabia G; Maffei M; Jéru I; Lascols O; Vigouroux C; Santini F
Front Endocrinol (Lausanne); 2020; 11():39. PubMed ID: 32117065
[TBL] [Abstract][Full Text] [Related]
40. GPAT3 deficiency alleviates insulin resistance and hepatic steatosis in a mouse model of severe congenital generalized lipodystrophy.
Gao M; Liu L; Wang X; Mak HY; Liu G; Yang H
Hum Mol Genet; 2020 Feb; 29(3):432-443. PubMed ID: 31873720
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]