257 related articles for article (PubMed ID: 21533227)
21. 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]
22. 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]
23. Seipin, adipogenesis and lipid droplets.
Fei W; Du X; Yang H
Trends Endocrinol Metab; 2011 Jun; 22(6):204-10. PubMed ID: 21497513
[TBL] [Abstract][Full Text] [Related]
24. Ablation of
Mcilroy GD; Mitchell SE; Han W; Delibegović M; Rochford JJ
Dis Model Mech; 2020 Jan; 13(1):. PubMed ID: 31848133
[TBL] [Abstract][Full Text] [Related]
25. Dissecting seipin function: the localized accumulation of phosphatidic acid at ER/LD junctions in the absence of seipin is suppressed by Sei1p(ΔNterm) only in combination with Ldb16p.
Han S; Binns DD; Chang YF; Goodman JM
BMC Cell Biol; 2015 Dec; 16():29. PubMed ID: 26637296
[TBL] [Abstract][Full Text] [Related]
26. 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]
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. SEIPIN: A Key Factor for Nuclear Lipid Droplet Generation and Lipid Homeostasis.
Jin Y; Tan Y; Zhao P; Ren Z
Int J Mol Sci; 2020 Nov; 21(21):. PubMed ID: 33147895
[TBL] [Abstract][Full Text] [Related]
29. Severe cardiac phenotype of Berardinelli-Seip congenital lipodystrophy in an infant with homozygous E189X BSCL2 mutation.
Friguls B; Coroleu W; del Alcazar R; Hilbert P; Van Maldergem L; Pintos-Morell G
Eur J Med Genet; 2009; 52(1):14-6. PubMed ID: 19041432
[TBL] [Abstract][Full Text] [Related]
30. Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice.
Prieur X; Dollet L; Takahashi M; Nemani M; Pillot B; Le May C; Mounier C; Takigawa-Imamura H; Zelenika D; Matsuda F; Fève B; Capeau J; Lathrop M; Costet P; Cariou B; Magré J
Diabetologia; 2013 Aug; 56(8):1813-25. PubMed ID: 23680914
[TBL] [Abstract][Full Text] [Related]
31. Promethin Is a Conserved Seipin Partner Protein.
Castro IG; Eisenberg-Bord M; Persiani E; Rochford JJ; Schuldiner M; Bohnert M
Cells; 2019 Mar; 8(3):. PubMed ID: 30901948
[TBL] [Abstract][Full Text] [Related]
32. Type 2 Congenital Generalized Lipodystrophy: The Diagnosis is in Your Hands.
Montenegro RM; Fernandes VO; Penaforte Saboia JG; Montenegro APDR; Lima JG
J Pediatr; 2019 Apr; 207():257-257.e1. PubMed ID: 30579587
[No Abstract] [Full Text] [Related]
33. 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]
34. Higher adiponectin levels in patients with Berardinelli-Seip congenital lipodystrophy due to seipin as compared with 1-acylglycerol-3-phosphate-o-acyltransferase-2 deficiency.
Antuna-Puente B; Boutet E; Vigouroux C; Lascols O; Slama L; Caron-Debarle M; Khallouf E; Lévy-Marchal C; Capeau J; Bastard JP; Magré J
J Clin Endocrinol Metab; 2010 Mar; 95(3):1463-8. PubMed ID: 20097706
[TBL] [Abstract][Full Text] [Related]
35. Molecular characterization of seipin and its mutants: implications for seipin in triacylglycerol synthesis.
Fei W; Li H; Shui G; Kapterian TS; Bielby C; Du X; Brown AJ; Li P; Wenk MR; Liu P; Yang H
J Lipid Res; 2011 Dec; 52(12):2136-2147. PubMed ID: 21957196
[TBL] [Abstract][Full Text] [Related]
36. BSCL2/Seipin deficiency in hearts causes cardiac energy deficit and dysfunction via inducing excessive lipid catabolism.
Zhou H; Li J; Su H; Li J; Lydic TA; Young ME; Chen W
Clin Transl Med; 2022 Apr; 12(4):e736. PubMed ID: 35384404
[TBL] [Abstract][Full Text] [Related]
37. Complementary mutations in seipin gene in a patient with Berardinelli-Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin gene.
Wu YR; Hung SI; Chang YC; Chen ST; Lin YL; Chung WH
J Neurol Neurosurg Psychiatry; 2009 Oct; 80(10):1180-1. PubMed ID: 19762912
[No Abstract] [Full Text] [Related]
38. Molecular mechanisms underlying fasting modulated liver insulin sensitivity and metabolism in male lipodystrophic Bscl2/Seipin-deficient mice.
Chen W; Zhou H; Saha P; Li L; Chan L
Endocrinology; 2014 Nov; 155(11):4215-25. PubMed ID: 25093462
[TBL] [Abstract][Full Text] [Related]
39. Focus on progressive myoclonic epilepsy in Berardinelli-Seip syndrome.
Ferranti S; Lo Rizzo C; Renieri A; Galluzzi P; Grosso S
Neurol Sci; 2020 Nov; 41(11):3345-3348. PubMed ID: 32440981
[TBL] [Abstract][Full Text] [Related]
40. Seipin regulates ER-lipid droplet contacts and cargo delivery.
Salo VT; Belevich I; Li S; Karhinen L; Vihinen H; Vigouroux C; Magré J; Thiele C; Hölttä-Vuori M; Jokitalo E; Ikonen E
EMBO J; 2016 Dec; 35(24):2699-2716. PubMed ID: 27879284
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
