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.
168 related articles for article (PubMed ID: 25559265)
1. 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]
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]
5. Studying lipoprotein trafficking in zebrafish, the case of chylomicron retention disease. Schlegel A J Mol Med (Berl); 2015 Feb; 93(2):115-8. PubMed ID: 25572701 [No 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. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. High-fat diet reveals the impact of Sar1b defects on lipid and lipoprotein profile and cholesterol metabolism. Auclair N; Sané AT; Ahmarani L; Ould-Chikh NE; Patey N; Beaulieu JF; Delvin E; Spahis S; Levy E J Lipid Res; 2023 Sep; 64(9):100423. PubMed ID: 37558128 [TBL] [Abstract][Full Text] [Related]
16. Sar1b transgenic male mice are more susceptible to high-fat diet-induced obesity, insulin insensitivity and intestinal chylomicron overproduction. Levy E; Spahis S; Garofalo C; Marcil V; Montoudis A; Sinnet D; Sanchez R; Peretti N; Beaulieu JF; Sane A J Nutr Biochem; 2014 May; 25(5):540-8. PubMed ID: 24657056 [TBL] [Abstract][Full Text] [Related]
17. New Insights In Intestinal Sar1B GTPase Regulation and Role in Cholesterol Homeostasis. Sané A; Seidman E; Spahis S; Lamantia V; Garofalo C; Montoudis A; Marcil V; Levy E J Cell Biochem; 2015 Oct; 116(10):2270-82. PubMed ID: 25826777 [TBL] [Abstract][Full Text] [Related]
18. Low rate of production of apolipoproteins B100 and AI in 2 patients with Anderson disease (chylomicron retention disease). Ouguerram K; Zaïr Y; Kasbi-Chadli F; Nazih H; Bligny D; Schmitz J; Aparicio T; Chétiveaux M; Magot T; Aggerbeck LP; Samson-Bouma ME; Krempf M Arterioscler Thromb Vasc Biol; 2012 Jun; 32(6):1520-5. PubMed ID: 22441101 [TBL] [Abstract][Full Text] [Related]
19. The intracellular transport of chylomicrons requires the small GTPase, Sar1b. Shoulders CC; Stephens DJ; Jones B Curr Opin Lipidol; 2004 Apr; 15(2):191-7. PubMed ID: 15017362 [TBL] [Abstract][Full Text] [Related]
20. Validation of Knock-Out Caco-2 TC7 Cells as Models of Enterocytes of Patients with Familial Genetic Hypobetalipoproteinemias. Bordat C; Vairo D; Cuerq C; Halimi C; Peiretti F; Penhoat A; Vieille-Marchiset A; Gonzalez T; Michalski MC; Nowicki M; Peretti N; Reboul E Nutrients; 2023 Jan; 15(3):. PubMed ID: 36771214 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]