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 *

236 related articles for article (PubMed ID: 21235735)

  • 1. Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease).
    Georges A; Bonneau J; Bonnefont-Rousselot D; Champigneulle J; Rabès JP; Abifadel M; Aparicio T; Guenedet JC; Bruckert E; Boileau C; Morali A; Varret M; Aggerbeck LP; Samson-Bouma ME
    Orphanet J Rare Dis; 2011 Jan; 6():1. PubMed ID: 21235735
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Anderson's disease/chylomicron retention disease in a Japanese patient with uniparental disomy 7 and a normal SAR1B gene protein coding sequence.
    Okada T; Miyashita M; Fukuhara J; Sugitani M; Ueno T; Samson-Bouma ME; Aggerbeck LP
    Orphanet J Rare Dis; 2011 Nov; 6():78. PubMed ID: 22104167
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Understanding Chylomicron Retention Disease Through Sar1b Gtpase Gene Disruption: Insight From Cell Culture.
    Sané AT; Seidman E; Peretti N; Kleme ML; Delvin E; Deslandres C; Garofalo C; Spahis S; Levy E
    Arterioscler Thromb Vasc Biol; 2017 Dec; 37(12):2243-2251. PubMed ID: 28982670
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia.
    Magnolo L; Najah M; Fancello T; Di Leo E; Pinotti E; Brini I; Gueddiche NM; Calandra S; Slimene NM; Tarugi P
    Gene; 2013 Jan; 512(1):28-34. PubMed ID: 23043934
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chylomicron retention disease: genetics, biochemistry, and clinical spectrum.
    Levy E; Poinsot P; Spahis S
    Curr Opin Lipidol; 2019 Apr; 30(2):134-139. PubMed ID: 30640893
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Chylomicron retention disease caused by SAR1B gene variations in 2 cases and literatures review].
    Zhang YQ; Wu LT; Cheng Y; Lu Y; Li YC; Feng JY; Xing QH; Li WJ; Wang JS
    Zhonghua Er Ke Za Zhi; 2024 Jun; 62(6):565-570. PubMed ID: 38763880
    [No Abstract]   [Full Text] [Related]  

  • 7. Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson disease.
    Levic DS; Minkel JR; Wang WD; Rybski WM; Melville DB; Knapik EW
    J Mol Med (Berl); 2015 Feb; 93(2):165-76. PubMed ID: 25559265
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutations of SAR1B gene in four children with chylomicron retention disease.
    Simone ML; Rabacchi C; Kuloglu Z; Kansu A; Ensari A; Demir AM; Hizal G; Di Leo E; Bertolini S; Calandra S; Tarugi P
    J Clin Lipidol; 2019; 13(4):554-562. PubMed ID: 31253576
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SAR1B GTPase is necessary to protect intestinal cells from disorders of lipid homeostasis, oxidative stress, and inflammation.
    Sané A; Ahmarani L; Delvin E; Auclair N; Spahis S; Levy E
    J Lipid Res; 2019 Oct; 60(10):1755-1764. PubMed ID: 31409740
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chylomicron retention disease caused by a new pathogenic variant in sar1b protein: a rare case report from Syria.
    Doya LJ; Mohammad L; Omran R; Ibrahim AA; Yousef N; Ibrahim A; Houreih MA
    BMC Pediatr; 2021 Oct; 21(1):449. PubMed ID: 34629076
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sar1b mutant mice recapitulate gastrointestinal abnormalities associated with chylomicron retention disease.
    Auclair N; Sané AT; Ahmarani L; Patey N; Beaulieu JF; Peretti N; Spahis S; Levy E
    J Lipid Res; 2021; 62():100085. PubMed ID: 33964306
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The endoplasmic reticulum coat protein II transport machinery coordinates cellular lipid secretion and cholesterol biosynthesis.
    Fryer LG; Jones B; Duncan EJ; Hutchison CE; Ozkan T; Williams PA; Alder O; Nieuwdorp M; Townley AK; Mensenkamp AR; Stephens DJ; Dallinga-Thie GM; Shoulders CC
    J Biol Chem; 2014 Feb; 289(7):4244-61. PubMed ID: 24338480
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities.
    Silvain M; Bligny D; Aparicio T; Laforêt P; Grodet A; Peretti N; Ménard D; Djouadi F; Jardel C; Bégué JM; Walker F; Schmitz J; Lachaux A; Aggerbeck LP; Samson-Bouma ME
    Clin Genet; 2008 Dec; 74(6):546-52. PubMed ID: 18786134
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional overlap between the mammalian
    Tang VT; Xiang J; Chen Z; McCormick J; Abbineni PS; Chen XW; Hoenerhoff M; Emmer BT; Khoriaty R; Lin JD; Ginsburg D
    Proc Natl Acad Sci U S A; 2024 May; 121(19):e2322164121. PubMed ID: 38687799
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inhibition of Sar1b, the Gene Implicated in Chylomicron Retention Disease, Impairs Migration and Morphogenesis of Developing Cortical Neurons.
    Li X; Yan M; Guo Z; Yan L; Feng R; Zhu H; Tu X; Yu S; Chen JG
    Neuroscience; 2020 Nov; 449():228-240. PubMed ID: 33002559
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Small GTPases SAR1A and SAR1B regulate the trafficking of the cardiac sodium channel Na
    Wang Z; Yu G; Liu Y; Liu S; Aridor M; Huang Y; Hu Y; Wang L; Li S; Xiong H; Tang B; Li X; Cheng C; Chakrabarti S; Wang F; Wu Q; Karnik SS; Xu C; Chen Q; Wang QK
    Biochim Biophys Acta Mol Basis Dis; 2018 Nov; 1864(11):3672-3684. PubMed ID: 30251687
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Small sequence variations between two mammalian paralogs of the small GTPase SAR1 underlie functional differences in coat protein complex II assembly.
    Melville DB; Studer S; Schekman R
    J Biol Chem; 2020 Jun; 295(25):8401-8412. PubMed ID: 32358066
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein.
    Charcosset M; Sassolas A; Peretti N; Roy CC; Deslandres C; Sinnett D; Levy E; Lachaux A
    Mol Genet Metab; 2008 Jan; 93(1):74-84. PubMed ID: 17945526
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genes.
    Dannoura AH; Berriot-Varoqueaux N; Amati P; Abadie V; Verthier N; Schmitz J; Wetterau JR; Samson-Bouma ME; Aggerbeck LP
    Arterioscler Thromb Vasc Biol; 1999 Oct; 19(10):2494-508. PubMed ID: 10521380
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Functional overlap between the mammalian
    Tang VT; Xiang J; Chen Z; McCormick J; Abbineni PS; Chen XW; Hoenerhoff M; Emmer BT; Khoriaty R; Lin JD; Ginsburg D
    bioRxiv; 2024 Feb; ():. PubMed ID: 38463989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.