263 related articles for article (PubMed ID: 10940349)
1. The role of the microsomal triglygeride transfer protein in abetalipoproteinemia.
Berriot-Varoqueaux N; Aggerbeck LP; Samson-Bouma M; Wetterau JR
Annu Rev Nutr; 2000; 20():663-97. PubMed ID: 10940349
[TBL] [Abstract][Full Text] [Related]
2. [Microsomal triglyceride transfer protein and abetalipoproteinemia].
Berriot-Varoqueaux N; Aggerbeck LP; Samson-Bouma M
Ann Endocrinol (Paris); 2000 May; 61(2):125-9. PubMed ID: 10891663
[TBL] [Abstract][Full Text] [Related]
3. The molecular basis of abetalipoproteinemia.
Gregg RE; Wetterau JR
Curr Opin Lipidol; 1994 Apr; 5(2):81-6. PubMed ID: 8044420
[TBL] [Abstract][Full Text] [Related]
4. Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein.
Shoulders CC; Brett DJ; Bayliss JD; Narcisi TM; Jarmuz A; Grantham TT; Leoni PR; Bhattacharya S; Pease RJ; Cullen PM
Hum Mol Genet; 1993 Dec; 2(12):2109-16. PubMed ID: 8111381
[TBL] [Abstract][Full Text] [Related]
5. Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia.
Sharp D; Blinderman L; Combs KA; Kienzle B; Ricci B; Wager-Smith K; Gil CM; Turck CW; Bouma ME; Rader DJ
Nature; 1993 Sep; 365(6441):65-9. PubMed ID: 8361539
[TBL] [Abstract][Full Text] [Related]
6. Contemporary aspects of the biology and therapeutic regulation of the microsomal triglyceride transfer protein.
Hooper AJ; Burnett JR; Watts GF
Circ Res; 2015 Jan; 116(1):193-205. PubMed ID: 25552696
[TBL] [Abstract][Full Text] [Related]
7. Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjects.
Walsh MT; Di Leo E; Okur I; Tarugi P; Hussain MM
Biochim Biophys Acta; 2016 Nov; 1861(11):1623-1633. PubMed ID: 27487388
[TBL] [Abstract][Full Text] [Related]
8. A 30-amino acid truncation of the microsomal triglyceride transfer protein large subunit disrupts its interaction with protein disulfide-isomerase and causes abetalipoproteinemia.
Ricci B; Sharp D; O'Rourke E; Kienzle B; Blinderman L; Gordon D; Smith-Monroy C; Robinson G; Gregg RE; Rader DJ
J Biol Chem; 1995 Jun; 270(24):14281-5. PubMed ID: 7782284
[TBL] [Abstract][Full Text] [Related]
9. A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase.
Rehberg EF; Samson-Bouma ME; Kienzle B; Blinderman L; Jamil H; Wetterau JR; Aggerbeck LP; Gordon DA
J Biol Chem; 1996 Nov; 271(47):29945-52. PubMed ID: 8939939
[TBL] [Abstract][Full Text] [Related]
10. Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function.
Walsh MT; Iqbal J; Josekutty J; Soh J; Di Leo E; Özaydin E; Gündüz M; Tarugi P; Hussain MM
Circ Cardiovasc Genet; 2015 Oct; 8(5):677-87. PubMed ID: 26224785
[TBL] [Abstract][Full Text] [Related]
11. [The role of microsomal triglyceride transfer protein in metabolism of apo B-containing lipoprotein].
Sugimoto T; Yamashita S; Matsuzawa Y
Nihon Rinsho; 1999 Dec; 57(12):2684-9. PubMed ID: 10638197
[TBL] [Abstract][Full Text] [Related]
12. The assembly of triacylglycerol-rich lipoproteins: an essential role for the microsomal triacylglycerol transfer protein.
White DA; Bennett AJ; Billett MA; Salter AM
Br J Nutr; 1998 Sep; 80(3):219-29. PubMed ID: 9875061
[TBL] [Abstract][Full Text] [Related]
13. Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia.
Wetterau JR; Aggerbeck LP; Bouma ME; Eisenberg C; Munck A; Hermier M; Schmitz J; Gay G; Rader DJ; Gregg RE
Science; 1992 Nov; 258(5084):999-1001. PubMed ID: 1439810
[TBL] [Abstract][Full Text] [Related]
14. Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic families.
Di Filippo M; Varret M; Boehm V; Rabès JP; Ferkdadji L; Abramowitz L; Dumont S; Lenaerts C; Boileau C; Joly F; Schmitz J; Samson-Bouma ME; Bonnefont-Rousselot D
J Clin Lipidol; 2019; 13(1):201-212. PubMed ID: 30522860
[TBL] [Abstract][Full Text] [Related]
15. Microsomal triglyceride transfer protein, the abetalipoproteinemia gene product, mediates the secretion of apolipoprotein B-containing lipoproteins from heterologous cells.
Leiper JM; Bayliss JD; Pease RJ; Brett DJ; Scott J; Shoulders CC
J Biol Chem; 1994 Sep; 269(35):21951-4. PubMed ID: 8071315
[TBL] [Abstract][Full Text] [Related]
16. Using genetically engineered mice to understand apolipoprotein-B deficiency syndromes in humans.
Raabe M; Kim E; Véniant M; Nielsen LB; Young SG
Proc Assoc Am Physicians; 1998; 110(6):521-30. PubMed ID: 9824535
[TBL] [Abstract][Full Text] [Related]
17. Loss of both phospholipid and triglyceride transfer activities of microsomal triglyceride transfer protein in abetalipoproteinemia.
Khatun I; Walsh MT; Hussain MM
J Lipid Res; 2013 Jun; 54(6):1541-1549. PubMed ID: 23475612
[TBL] [Abstract][Full Text] [Related]
18. Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia.
Wang J; Hegele RA
Hum Mutat; 2000 Mar; 15(3):294-5. PubMed ID: 10679949
[TBL] [Abstract][Full Text] [Related]
19. A severe form of abetalipoproteinemia caused by new splicing mutations of microsomal triglyceride transfer protein (MTTP).
Pons V; Rolland C; Nauze M; Danjoux M; Gaibelet G; Durandy A; Sassolas A; Lévy E; Tercé F; Collet X; Mas E
Hum Mutat; 2011 Jul; 32(7):751-9. PubMed ID: 21394827
[TBL] [Abstract][Full Text] [Related]
20. Mouse microsomal triglyceride transfer protein large subunit: cDNA cloning, tissue-specific expression and chromosomal localization.
Nakamuta M; Chang BH; Hoogeveen R; Li WH; Chan L
Genomics; 1996 Apr; 33(2):313-6. PubMed ID: 8660984
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
