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 *

134 related articles for article (PubMed ID: 12364545)

  • 21. Common and rare ABCA1 variants affecting plasma HDL cholesterol.
    Wang J; Burnett JR; Near S; Young K; Zinman B; Hanley AJ; Connelly PW; Harris SB; Hegele RA
    Arterioscler Thromb Vasc Biol; 2000 Aug; 20(8):1983-9. PubMed ID: 10938021
    [TBL] [Abstract][Full Text] [Related]  

  • 22. ABCA1-mediated transport of cellular cholesterol and phospholipids to HDL apolipoproteins.
    Oram JF; Vaughan AM
    Curr Opin Lipidol; 2000 Jun; 11(3):253-60. PubMed ID: 10882340
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The role of the ABCA1 transporter and cholesterol efflux in familial hypoalphalipoproteinemia.
    Hovingh GK; Van Wijland MJ; Brownlie A; Bisoendial RJ; Hayden MR; Kastelein JJ; Groen AK
    J Lipid Res; 2003 Jun; 44(6):1251-5. PubMed ID: 12700344
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Adenosine-triphosphate-binding cassette transporter-1 trafficking and function.
    Kang MH; Singaraja R; Hayden MR
    Trends Cardiovasc Med; 2010 Feb; 20(2):41-9. PubMed ID: 20656214
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Naturally occurring mutations in the largest extracellular loops of ABCA1 can disrupt its direct interaction with apolipoprotein A-I.
    Fitzgerald ML; Morris AL; Rhee JS; Andersson LP; Mendez AJ; Freeman MW
    J Biol Chem; 2002 Sep; 277(36):33178-87. PubMed ID: 12084722
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Tangier disease: epidemiology, pathophysiology, and management.
    Puntoni M; Sbrana F; Bigazzi F; Sampietro T
    Am J Cardiovasc Drugs; 2012 Oct; 12(5):303-11. PubMed ID: 22913675
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [The role of transmembrane lipidtransporter molecules in the atherosclerotic process].
    Harangi M; Köbling T; Paragh G
    Orv Hetil; 2006 Feb; 147(6):251-7. PubMed ID: 16610615
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel mutation in the ABCA1 gene causing an atypical phenotype of Tangier disease.
    Negi SI; Brautbar A; Virani SS; Anand A; Polisecki E; Asztalos BF; Ballantyne CM; Schaefer EJ; Jones PH
    J Clin Lipidol; 2013; 7(1):82-7. PubMed ID: 23351586
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Do DNA sequence variants in ABCA1 contribute to HDL cholesterol levels in the general population?
    Pajukanta P
    J Clin Invest; 2004 Nov; 114(9):1244-7. PubMed ID: 15520856
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis.
    Ishii J; Nagano M; Kujiraoka T; Ishihara M; Egashira T; Takada D; Tsuji M; Hattori H; Emi M
    J Hum Genet; 2002; 47(7):366-9. PubMed ID: 12111371
    [TBL] [Abstract][Full Text] [Related]  

  • 31. ATP-binding cassette transporter A1 and cholesterol trafficking.
    Oram JF
    Curr Opin Lipidol; 2002 Aug; 13(4):373-81. PubMed ID: 12151852
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease.
    Bodzioch M; Orsó E; Klucken J; Langmann T; Böttcher A; Diederich W; Drobnik W; Barlage S; Büchler C; Porsch-Ozcürümez M; Kaminski WE; Hahmann HW; Oette K; Rothe G; Aslanidis C; Lackner KJ; Schmitz G
    Nat Genet; 1999 Aug; 22(4):347-51. PubMed ID: 10431237
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Serum amyloid A promotes ABCA1-dependent and ABCA1-independent lipid efflux from cells.
    Stonik JA; Remaley AT; Demosky SJ; Neufeld EB; Bocharov A; Brewer HB
    Biochem Biophys Res Commun; 2004 Sep; 321(4):936-41. PubMed ID: 15358117
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Apolipoprotein A-I activates cellular cAMP signaling through the ABCA1 transporter.
    Haidar B; Denis M; Marcil M; Krimbou L; Genest J
    J Biol Chem; 2004 Mar; 279(11):9963-9. PubMed ID: 14701824
    [TBL] [Abstract][Full Text] [Related]  

  • 35. ATP-binding cassette transporter A1 mediates cellular secretion of alpha-tocopherol.
    Oram JF; Vaughan AM; Stocker R
    J Biol Chem; 2001 Oct; 276(43):39898-902. PubMed ID: 11546785
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel ABCA1 nonsense mutation, R1270X, in Tangier disease associated with an unrecognised bleeding tendency.
    Hooper AJ; Robertson K; Ng L; Kattampallil JS; Latchem D; Willsher PC; Thom J; Baker RI; Burnett JR
    Clin Chim Acta; 2009 Nov; 409(1-2):136-9. PubMed ID: 19723515
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency.
    Nishida Y; Hirano K; Tsukamoto K; Nagano M; Ikegami C; Roomp K; Ishihara M; Sakane N; Zhang Z; Tsujii Ki K; Matsuyama A; Ohama T; Matsuura F; Ishigami M; Sakai N; Hiraoka H; Hattori H; Wellington C; Yoshida Y; Misugi S; Hayden MR; Egashira T; Yamashita S; Matsuzawa Y
    Biochem Biophys Res Commun; 2002 Jan; 290(2):713-21. PubMed ID: 11785958
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol.
    Candini C; Schimmel AW; Peter J; Bochem AE; Holleboom AG; Vergeer M; Dullaart RP; Dallinga-Thie GM; Hovingh GK; Khoo KL; Fasano T; Bocchi L; Calandra S; Kuivenhoven JA; Motazacker MM
    Atherosclerosis; 2010 Dec; 213(2):492-8. PubMed ID: 20880529
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family.
    Maranghi M; Truglio G; Gallo A; Grieco E; Verrienti A; Montali A; Gallo P; Alesini F; Arca M; Lucarelli M
    Biochem Biophys Res Commun; 2019 Jan; 508(2):487-493. PubMed ID: 30503498
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 ( ABCA1) gene in Japanese patients with Tangier disease.
    Guo Z; Inazu A; Yu W; Suzumura T; Okamoto M; Nohara A; Higashikata T; Sano R; Wakasugi K; Hayakawa T; Yoshida K; Suehiro T; Schmitz G; Mabuchi H
    J Hum Genet; 2002; 47(6):325-9. PubMed ID: 12111381
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.