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 *

119 related articles for article (PubMed ID: 25572701)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Chylomicron retention disease.
    Desaldeleer C; Henno S; Bruneau B; Dabadie A
    Dig Liver Dis; 2013 Feb; 45(2):e3. PubMed ID: 22959141
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Chylomicron retention disease: A rare cause of chronic diarrhea.
    Ben Ameur S; Aloulou H; Jlidi N; Kamoun F; Chabchoub I; Di Filippo M; Sfaihi L; Hachicha M
    Arch Pediatr; 2016 Jul; 23(7):735-7. PubMed ID: 27266643
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Inherited hematological disorders due to defects in coat protein (COP)II complex.
    Russo R; Esposito MR; Iolascon A
    Am J Hematol; 2013 Feb; 88(2):135-40. PubMed ID: 22764119
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Novel missense mutations of SAR1B gene in an infant with chylomicron retention disease.
    Treepongkaruna S; Chongviriyaphan N; Suthutvoravut U; Charoenpipop D; Choubtum L; Wattanasirichaigoon D
    J Pediatr Gastroenterol Nutr; 2009 Mar; 48(3):370-3. PubMed ID: 19274794
    [No Abstract]   [Full Text] [Related]  

  • 16. The role of ANGPTL3 in controlling lipoprotein metabolism.
    Tikka A; Jauhiainen M
    Endocrine; 2016 May; 52(2):187-93. PubMed ID: 26754661
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Establishment of reference values of α-tocopherol in plasma, red blood cells and adipose tissue in healthy children to improve the management of chylomicron retention disease, a rare genetic hypocholesterolemia.
    Cuerq C; Restier L; Drai J; Blond E; Roux A; Charriere S; Michalski MC; Di Filippo M; Levy E; Lachaux A; Peretti N
    Orphanet J Rare Dis; 2016 Aug; 11(1):114. PubMed ID: 27520363
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chylomicron retention disease--the role of ultrastructural examination in differential diagnosis.
    Boldrini R; Biselli R; Bosman C
    Pathol Res Pract; 2001; 197(11):753-7. PubMed ID: 11770019
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene.
    Cefalù AB; Calvo PL; Noto D; Baldi M; Valenti V; Lerro P; Tramuto F; Lezo A; Morra I; Cenacchi G; Barbera C; Averna MR
    Metabolism; 2010 Apr; 59(4):463-7. PubMed ID: 19846172
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.