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1976 1
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2001 6
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2003 12
2004 6
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99 results

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Page 1
ABC Family Transporters.
Liu X. Liu X. Adv Exp Med Biol. 2019;1141:13-100. doi: 10.1007/978-981-13-7647-4_2. Adv Exp Med Biol. 2019. PMID: 31571164 Review.
Some ABC transporters are also involved in diverse cellular processes such as maintenance of osmotic homeostasis, antigen processing, cell division, immunity, cholesterol, and lipid trafficking. Several human diseases such as cystic fibrosis, sitosterolemia, Tangier diseas …
Some ABC transporters are also involved in diverse cellular processes such as maintenance of osmotic homeostasis, antigen processing, cell d …
Familial Hypercholesterolemia: The Most Frequent Cholesterol Metabolism Disorder Caused Disease.
Benito-Vicente A, Uribe KB, Jebari S, Galicia-Garcia U, Ostolaza H, Martin C. Benito-Vicente A, et al. Int J Mol Sci. 2018 Nov 1;19(11):3426. doi: 10.3390/ijms19113426. Int J Mol Sci. 2018. PMID: 30388787 Free PMC article. Review.
Malfunctioning of cholesterol metabolism is caused by multiple hereditary diseases, including Familial Hypercholesterolemia, Sitosterolemia Type C and Niemann-Pick Type C1. Of these, familial hypercholesterolemia (FH) is a common inherited autosomal co-dominant disorder ch …
Malfunctioning of cholesterol metabolism is caused by multiple hereditary diseases, including Familial Hypercholesterolemia, Sitosterolem
The Inherited Hypercholesterolemias.
Loh WJ, Watts GF. Loh WJ, et al. Endocrinol Metab Clin North Am. 2022 Sep;51(3):511-537. doi: 10.1016/j.ecl.2022.02.006. Epub 2022 Jul 4. Endocrinol Metab Clin North Am. 2022. PMID: 35963626 Review.
In this review, we discuss familial hypercholesterolemia (FH), FH-mimics (eg, polygenic hypercholesterolemia [PH], FCH, sitosterolemia), and other inherited forms of hypercholesterolemia (eg, hyper-lipoprotein(a) levels [hyper-Lp(a)]). ...
In this review, we discuss familial hypercholesterolemia (FH), FH-mimics (eg, polygenic hypercholesterolemia [PH], FCH, sitosterolemia
Update on Sitosterolemia and Atherosclerosis.
Rocha VZ, Tada MT, Chacra APM, Miname MH, Mizuta MH. Rocha VZ, et al. Curr Atheroscler Rep. 2023 May;25(5):181-187. doi: 10.1007/s11883-023-01092-4. Epub 2023 Mar 10. Curr Atheroscler Rep. 2023. PMID: 36897412 Review.
PURPOSE OF REVIEW: The purpose of this review was to summarize important and updated information on sitosterolemia. Sitosterolemia is an inherited lipid disorder consisting of high levels of plasma plant sterols. ...RECENT FINDINGS: Since hypercholesterolemia is oft …
PURPOSE OF REVIEW: The purpose of this review was to summarize important and updated information on sitosterolemia. Sitosterolemia
[Sitosterolemia (phytosterolemia)].
Lütjohann D. Lütjohann D. Internist (Berl). 2019 Aug;60(8):871-877. doi: 10.1007/s00108-019-0635-2. Internist (Berl). 2019. PMID: 31254003 Review. German.
Sitosterolemia or phytosterolemia is a rare autosomal recessive hereditary lipid storage disorder. ...Phytosterols are found mainly in vegetable oils, margarine, nuts, grains, soybeans and avocados. Patients with sitosterolemia show extreme phenotypic heterogeneity
Sitosterolemia or phytosterolemia is a rare autosomal recessive hereditary lipid storage disorder. ...Phytosterols are found mainly i
Sitosterolemia, Hypercholesterolemia, and Coronary Artery Disease.
Tada H, Nohara A, Inazu A, Sakuma N, Mabuchi H, Kawashiri MA. Tada H, et al. J Atheroscler Thromb. 2018 Sep 1;25(9):783-789. doi: 10.5551/jat.RV17024. Epub 2018 Jul 20. J Atheroscler Thromb. 2018. PMID: 30033951 Free PMC article. Review.
Sitosterolemia is a rare inherited disease characterized by increased levels of plant sterols, such as sitosterol. ...Regarding therapies, LDL apheresis, as well as proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, could be useful for sitosterolemia,
Sitosterolemia is a rare inherited disease characterized by increased levels of plant sterols, such as sitosterol. ...Regarding thera
The ABCs of Sterol Transport.
Plummer AM, Culbertson AT, Liao M. Plummer AM, et al. Annu Rev Physiol. 2021 Feb 10;83:153-181. doi: 10.1146/annurev-physiol-031620-094944. Epub 2020 Nov 3. Annu Rev Physiol. 2021. PMID: 33141631 Review.
ATP-binding cassette (ABC) transporters play several critical roles in this process, and mutations in these sterol transporters lead to disorders such as Tangier disease and sitosterolemia. Biochemical and structural information on ABC sterol transporters is beginning to e …
ATP-binding cassette (ABC) transporters play several critical roles in this process, and mutations in these sterol transporters lead to diso …
Sitosterolemia.
Salen G, Patel S, Batta AK. Salen G, et al. Cardiovasc Drug Rev. 2002 Winter;20(4):255-70. doi: 10.1111/j.1527-3466.2002.tb00096.x. Cardiovasc Drug Rev. 2002. PMID: 12481199 Review.
Sitosterolemia was first described 28 years ago in two sisters. They had tendonxanthomas, normal plasma cholesterol levels, and elevated plant sterol levels. ...Bile acid binding resins and ileal bypass surgery are effective treatments for sitosterolemic patients, whereas
Sitosterolemia was first described 28 years ago in two sisters. They had tendonxanthomas, normal plasma cholesterol levels, and eleva
Plant Sterols, Stanols, and Sitosterolemia.
Ajagbe BO, Othman RA, Myrie SB. Ajagbe BO, et al. J AOAC Int. 2015 May-Jun;98(3):716-723. doi: 10.5740/jaoacint.SGEAjagbe. Epub 2015 May 4. J AOAC Int. 2015. PMID: 25941971 Free PMC article. Review.
Hematologic abnormalities including macrothrombocytopenia, stomatocytosis and hemolysis are frequently observed in sitosterolemia patients. Currently, ezetimibe, a sterol absorption inhibitor, is used as the routine treatment for sitosterolemia, with reported improv …
Hematologic abnormalities including macrothrombocytopenia, stomatocytosis and hemolysis are frequently observed in sitosterolemia pat …
Features of chinese patients with sitosterolemia.
Zhou Z, Su X, Cai Y, Ting TH, Zhang W, Lin Y, Xu A, Mao X, Zeng C, Liu L, Li X. Zhou Z, et al. Lipids Health Dis. 2022 Jan 18;21(1):11. doi: 10.1186/s12944-021-01619-1. Lipids Health Dis. 2022. PMID: 35042526 Free PMC article. Review.
BACKGROUND: Sitosterolemia is a lipid disorder characterized by the accumulation of phytosterols in plasma and organs, caused by mutations in the ABCG5 and/or ABCG8 genes. ...The clinical features and molecular characteristics of Chinese patients with sitosterolemia
BACKGROUND: Sitosterolemia is a lipid disorder characterized by the accumulation of phytosterols in plasma and organs, caused by muta …
99 results