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 *

233 related articles for article (PubMed ID: 27632409)

  • 21. 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]  

  • 22. 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]  

  • 23. Lafora's disease: towards a clinical, pathologic, and molecular synthesis.
    Minassian BA
    Pediatr Neurol; 2001 Jul; 25(1):21-9. PubMed ID: 11483392
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene.
    Huang HH; Chen TH; Hsiao HP; Huang CT; Wang CC; Shiau YH; Chao MC
    Kaohsiung J Med Sci; 2010 Nov; 26(11):615-20. PubMed ID: 21126715
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy.
    Schuster J; Khan TN; Tariq M; Shaiq PA; Mäbert K; Baig SM; Klar J
    BMC Med Genet; 2014 Jun; 15():71. PubMed ID: 24961962
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Congenital generalized lipodystrophy in an Indian patient with a novel mutation in BSCL2 gene.
    Shirwalkar HU; Patel ZM; Magre J; Hilbert P; Van Maldergem L; Mukhopadhyay RR; Maitra A
    J Inherit Metab Dis; 2008 Dec; 31 Suppl 2():S317-22. PubMed ID: 18690553
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. 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]  

  • 30. 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]  

  • 31. Clinical and electrophysiological features in a French family presenting with seipinopathy.
    Ollivier Y; Magot A; Latour P; Perrier J; Mercier S; Maisonobe T; Péréon Y
    Neuromuscul Disord; 2015 Feb; 25(2):161-4. PubMed ID: 25454168
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. Accelerated epigenetic aging and DNA methylation alterations in Berardinelli-Seip congenital lipodystrophy.
    Qannan A; Bejaoui Y; Izadi M; Yousri NA; Razzaq A; Christiansen C; Martin GM; Bell JT; Horvath S; Oshima J; Megarbane A; Ericsson J; Pourkarimi E; El Hajj N
    Hum Mol Genet; 2023 May; 32(11):1826-1835. PubMed ID: 36715159
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy.
    Boutet E; El Mourabit H; Prot M; Nemani M; Khallouf E; Colard O; Maurice M; Durand-Schneider AM; Chrétien Y; Grès S; Wolf C; Saulnier-Blache JS; Capeau J; Magré J
    Biochimie; 2009 Jun; 91(6):796-803. PubMed ID: 19278620
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Seipin/BSCL2-related motor neuron disease: Seipinopathy is a novel conformational disease associated with endoplasmic reticulum stress].
    Ito D; Suzuki N
    Rinsho Shinkeigaku; 2007 Jun; 47(6):329-35. PubMed ID: 17633104
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Talon cusps, macrodontia, and aberrant tooth morphology in Berardinelli-Seip syndrome.
    Solanki M; Patil SS; Baweja DK; Noorani H; Pk S
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Jan; 105(1):e41-7. PubMed ID: 18155601
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Lafora's disease presenting with progressive myoclonus epilepsy].
    Béjot Y; Lemesle-Martin M; Contégal F; Graule-Petot A; Thauvin C; Aubriot-Lorton MH; Moreau T; Giroud M
    Rev Neurol (Paris); 2007 Oct; 163(10):975-8. PubMed ID: 18033035
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.