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Page 1
Identification of a Gain-of-Function LIPC Variant as a Novel Cause of Familial Combined Hypocholesterolemia.
Dijk W, Di Filippo M, Kooijman S, van Eenige R, Rimbert A, Caillaud A, Thedrez A, Arnaud L, Pronk A, Garçon D, Sotin T, Lindenbaum P, Ozcariz Garcia E, Pais de Barros JP, Duvillard L, Si-Tayeb K, Amigo N, Le Questel JY, Rensen PCN, Le May C, Moulin P, Cariou B. Dijk W, et al. Among authors: si tayeb k. Circulation. 2022 Sep 6;146(10):724-739. doi: 10.1161/CIRCULATIONAHA.121.057978. Epub 2022 Jul 28. Circulation. 2022. PMID: 35899625 Free PMC article.
PCSK9 Inhibition: Does Lipoprotein Size Matter?
Si-Tayeb K, Cariou B. Si-Tayeb K, et al. J Am Heart Assoc. 2015 Nov 19;4(11):e002806. doi: 10.1161/JAHA.115.002806. J Am Heart Assoc. 2015. PMID: 26586733 Free PMC article. No abstract available.
Role of PCSK9 beyond liver involvement.
Cariou B, Si-Tayeb K, Le May C. Cariou B, et al. Curr Opin Lipidol. 2015 Jun;26(3):155-61. doi: 10.1097/MOL.0000000000000180. Curr Opin Lipidol. 2015. PMID: 25887680 Review.
PCSK9 regulates the NODAL signaling pathway and cellular proliferation in hiPSCs.
Roudaut M, Idriss S, Caillaud A, Girardeau A, Rimbert A, Champon B, David A, Lévêque A, Arnaud L, Pichelin M, Prieur X, Prat A, Seidah NG, Zibara K, Le May C, Cariou B, Si-Tayeb K. Roudaut M, et al. Among authors: si tayeb k. Stem Cell Reports. 2021 Dec 14;16(12):2958-2972. doi: 10.1016/j.stemcr.2021.10.004. Epub 2021 Nov 4. Stem Cell Reports. 2021. PMID: 34739847 Free PMC article.
FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells.
Caillaud A, Lévêque A, Thédrez A, Girardeau A, Canac R, Bray L, Baudic M, Barc J, Gaborit N, Lamirault G, Gardie B, Idriss S, Rimbert A, Le May C, Cariou B, Si-Tayeb K. Caillaud A, et al. Among authors: si tayeb k. STAR Protoc. 2022 Dec 16;3(4):101680. doi: 10.1016/j.xpro.2022.101680. Epub 2022 Sep 16. STAR Protoc. 2022. PMID: 36115027 Free PMC article.
[Hepatic organoids: What are the challenges?].
Luce E, Messina A, Caillaud A, Si-Tayeb K, Cariou B, Bur E, Dubart-Kupperschmitt A, Duclos-Vallée JC. Luce E, et al. Among authors: si tayeb k. Med Sci (Paris). 2021 Oct;37(10):902-909. doi: 10.1051/medsci/2021119. Epub 2021 Oct 14. Med Sci (Paris). 2021. PMID: 34647879 Free article. French.
A dominant vimentin variant causes a rare syndrome with premature aging.
Cogné B, Bouameur JE, Hayot G, Latypova X, Pattabiraman S, Caillaud A, Si-Tayeb K, Besnard T, Küry S, Chariau C, Gaignerie A, David L, Bordure P, Kaganovich D, Bézieau S, Golzio C, Magin TM, Isidor B. Cogné B, et al. Among authors: si tayeb k. Eur J Hum Genet. 2020 Sep;28(9):1218-1230. doi: 10.1038/s41431-020-0583-2. Epub 2020 Feb 17. Eur J Hum Genet. 2020. PMID: 32066935 Free PMC article.
Toward Personalized Medicine: Using Cardiomyocytes Differentiated From Urine-Derived Pluripotent Stem Cells to Recapitulate Electrophysiological Characteristics of Type 2 Long QT Syndrome.
Jouni M, Si-Tayeb K, Es-Salah-Lamoureux Z, Latypova X, Champon B, Caillaud A, Rungoat A, Charpentier F, Loussouarn G, Baró I, Zibara K, Lemarchand P, Gaborit N. Jouni M, et al. J Am Heart Assoc. 2015 Sep 1;4(9):e002159. doi: 10.1161/JAHA.115.002159. J Am Heart Assoc. 2015. PMID: 26330336 Free PMC article.
30 results