305 related articles for article (PubMed ID: 17200716)
1. Disruption of LDL but not VLDL clearance in autosomal recessive hypercholesterolemia.
Jones C; Garuti R; Michaely P; Li WP; Maeda N; Cohen JC; Herz J; Hobbs HH
J Clin Invest; 2007 Jan; 117(1):165-74. PubMed ID: 17200716
[TBL] [Abstract][Full Text] [Related]
2. Disruption of autosomal recessive hypercholesterolemia gene shows different phenotype in vitro and in vivo.
Harada-Shiba M; Takagi A; Marutsuka K; Moriguchi S; Yagyu H; Ishibashi S; Asada Y; Yokoyama S
Circ Res; 2004 Oct; 95(9):945-52. PubMed ID: 15472122
[TBL] [Abstract][Full Text] [Related]
3. Normal sorting but defective endocytosis of the low density lipoprotein receptor in mice with autosomal recessive hypercholesterolemia.
Jones C; Hammer RE; Li WP; Cohen JC; Hobbs HH; Herz J
J Biol Chem; 2003 Aug; 278(31):29024-30. PubMed ID: 12746448
[TBL] [Abstract][Full Text] [Related]
4. S-nitrosylation of ARH is required for LDL uptake by the LDL receptor.
Zhao Z; Pompey S; Dong H; Weng J; Garuti R; Michaely P
J Lipid Res; 2013 Jun; 54(6):1550-1559. PubMed ID: 23564733
[TBL] [Abstract][Full Text] [Related]
5. In the absence of the low density lipoprotein receptor, human apolipoprotein C1 overexpression in transgenic mice inhibits the hepatic uptake of very low density lipoproteins via a receptor-associated protein-sensitive pathway.
Jong MC; Dahlmans VE; van Gorp PJ; van Dijk KW; Breuer ML; Hofker MH; Havekes LM
J Clin Invest; 1996 Nov; 98(10):2259-67. PubMed ID: 8941642
[TBL] [Abstract][Full Text] [Related]
6. A combined LDL receptor/LDL receptor adaptor protein 1 mutation as the cause for severe familial hypercholesterolemia.
Soufi M; Rust S; Walter M; Schaefer JR
Gene; 2013 May; 521(1):200-3. PubMed ID: 23510778
[TBL] [Abstract][Full Text] [Related]
7. Endocytic adaptors Arh and Dab2 control homeostasis of circulatory cholesterol.
Tao W; Moore R; Meng Y; Smith ER; Xu XX
J Lipid Res; 2016 May; 57(5):809-17. PubMed ID: 27005486
[TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive hypercholesterolemia: a mild phenotype of familial hypercholesterolemia: insight from the kinetic study using stable isotope and animal studies.
Tada H; Kawashiri MA; Nohara A; Inazu A; Kobayashi J; Mabuchi H; Yamagishi M
J Atheroscler Thromb; 2015; 22(1):1-9. PubMed ID: 25399932
[TBL] [Abstract][Full Text] [Related]
9. Clinical and biochemical characterisation of patients with autosomal recessive hypercholesterolemia (ARH).
Fellin R; Zuliani G; Arca M; Pintus P; Pacifico A; Montali A; Corsini A; Maioli M
Nutr Metab Cardiovasc Dis; 2003 Oct; 13(5):278-86. PubMed ID: 14717060
[TBL] [Abstract][Full Text] [Related]
10. Altered metabolism of low-density lipoprotein and very-low-density lipoprotein remnant in autosomal recessive hypercholesterolemia: results from stable isotope kinetic study in vivo.
Tada H; Kawashiri MA; Ikewaki K; Terao Y; Noguchi T; Nakanishi C; Tsuchida M; Takata M; Miwa K; Konno T; Hayashi K; Nohara A; Inazu A; Kobayashi J; Mabuchi H; Yamagishi M
Circ Cardiovasc Genet; 2012 Feb; 5(1):35-41. PubMed ID: 22157599
[TBL] [Abstract][Full Text] [Related]
11. LDL-receptor mutations in Europe.
Dedoussis GV; Schmidt H; Genschel J
Hum Mutat; 2004 Dec; 24(6):443-59. PubMed ID: 15523646
[TBL] [Abstract][Full Text] [Related]
12. Spectrum of LDLR gene mutations, including a novel mutation causing familial hypercholesterolaemia, in North-western Greece.
Diakou M; Miltiadous G; Xenophontos SL; Manoli P; Cariolou MA; Elisaf M
Eur J Intern Med; 2011 Oct; 22(5):e55-9. PubMed ID: 21925044
[TBL] [Abstract][Full Text] [Related]
13. Lack of phosphatidylethanolamine N-methyltransferase alters plasma VLDL phospholipids and attenuates atherosclerosis in mice.
Zhao Y; Su B; Jacobs RL; Kennedy B; Francis GA; Waddington E; Brosnan JT; Vance JE; Vance DE
Arterioscler Thromb Vasc Biol; 2009 Sep; 29(9):1349-55. PubMed ID: 19520976
[TBL] [Abstract][Full Text] [Related]
14. LR11/SorLA links triglyceride-rich lipoproteins to risk of developing cardiovascular disease in FH patients.
Vongpromek R; Bujo H; Hoekstra M; Schneider WJ; van der Zee L; Schinkel AF; Korporaal SJ; Dik WA; Ebinuma H; Jiang M; Verhoeven AJ; Sijbrands EJ; Mulder MT
Atherosclerosis; 2015 Dec; 243(2):429-37. PubMed ID: 26520897
[TBL] [Abstract][Full Text] [Related]
15. Increased sphingomyelin content of plasma lipoproteins in apolipoprotein E knockout mice reflects combined production and catabolic defects and enhances reactivity with mammalian sphingomyelinase.
Jeong Ts; Schissel SL; Tabas I; Pownall HJ; Tall AR; Jiang X
J Clin Invest; 1998 Feb; 101(4):905-12. PubMed ID: 9466986
[TBL] [Abstract][Full Text] [Related]
16. Autosomal recessive hypercholesterolemia.
Soutar AK; Naoumova RP
Semin Vasc Med; 2004 Aug; 4(3):241-8. PubMed ID: 15630633
[TBL] [Abstract][Full Text] [Related]
17. The modular adaptor protein ARH is required for low density lipoprotein (LDL) binding and internalization but not for LDL receptor clustering in coated pits.
Michaely P; Li WP; Anderson RG; Cohen JC; Hobbs HH
J Biol Chem; 2004 Aug; 279(32):34023-31. PubMed ID: 15166224
[TBL] [Abstract][Full Text] [Related]
18. Replacement of cysteine at position 46 in the first cysteine-rich repeat of the LDL receptor impairs apolipoprotein recognition.
Benito-Vicente A; Uribe KB; Siddiqi H; Jebari S; Galicia-Garcia U; Larrea-Sebal A; Cenarro A; Stef M; Ostolaza H; Civeira F; Palacios L; Martin C
PLoS One; 2018; 13(10):e0204771. PubMed ID: 30332439
[TBL] [Abstract][Full Text] [Related]
19. Atomic structure of the autosomal recessive hypercholesterolemia phosphotyrosine-binding domain in complex with the LDL-receptor tail.
Dvir H; Shah M; Girardi E; Guo L; Farquhar MG; Zajonc DM
Proc Natl Acad Sci U S A; 2012 May; 109(18):6916-21. PubMed ID: 22509010
[TBL] [Abstract][Full Text] [Related]
20. In LDL receptor-deficient mice, catabolism of remnant lipoproteins requires a high level of apoE but is inhibited by excess apoE.
van Dijk KW; van Vlijmen BJ; van't Hof HB; van der Zee A; Santamarina-Fojo S; van Berkel TJ; Havekes LM; Hofker MH
J Lipid Res; 1999 Feb; 40(2):336-44. PubMed ID: 9925664
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
