Ankirini (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ankirini" in Serbian language version.

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9nih.gov

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6doi.org

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2web.archive.org

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1rcsb.org

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1physiology.org

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1jbc.org

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1archive.org

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1schizophreniaforum.org

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archive.org

Schott JJ; Charpentier F; Peltier S; et al. (1995). „Mapping of a gene for long QT syndrome to chromosome 4q25-27”. Am. J. Hum. Genet. 57 (5): 1114—22. PMC 1801360 . PMID 7485162.

doi.org

PDB: 1N11; Michaely P, Tomchick DR, Machius M, Anderson RG (2002). „Crystal structure of a 12 ANK repeat stack from human ANK1”. EMBO J. 21 (23): 6387—96. PMC 136955 . PMID 12456646. doi:10.1093/emboj/cdf651. Текст „ankyrinR ” игнорисан (помоћ)
Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V (1990). „Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8”. Nature. 345 (6277): 736—9. PMID 2141669. doi:10.1038/345736a0.
Bennett V, Stenbuck PJ (1979). „The membrane attachment protein for spectrin is associated with band 3 in human erythrocyte membranes”. Nature. 280 (5722): 468—73. PMID 379653. doi:10.1038/280468a0.
Singleton PA, Bourguignon LY (2004). „CD44 interaction with ankyrin and IP3 receptor in lipid rafts promotes hyaluronan-mediated Ca2+ signaling leading to nitric oxide production and endothelial cell adhesion and proliferation”. Exp Cell Res. 295 (1): 102—18. PMID 15051494. doi:10.1016/j.yexcr.2003.12.025.
Kapfhamer D, Miller DE, Lambert S, Bennett V, Glover TW, Burmeister M (1995). „Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10”. Genomics. 27 (1): 189—91. PMID 7665168. doi:10.1006/geno.1995.1023.
Ferreira MA; O'Donovan MC; Meng YA; et al. (2008). „Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder”. Nat. Genet. 40 (9): 1056. PMC 2703780 . PMID 18711365. doi:10.1038/ng.209.

jbc.org

Bennett V, Stenbuck PJ (10. 4. 1979). „Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin”. J Biol Chem. 254 (7): 2533—41. PMID 372182.

nih.gov

ncbi.nlm.nih.gov

PDB: 1N11; Michaely P, Tomchick DR, Machius M, Anderson RG (2002). „Crystal structure of a 12 ANK repeat stack from human ANK1”. EMBO J. 21 (23): 6387—96. PMC 136955 . PMID 12456646. doi:10.1093/emboj/cdf651. Текст „ankyrinR ” игнорисан (помоћ)
Bennett V, Baines AJ (1. 7. 2001). „Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues”. Physiol. Rev. 81 (3): 1353—92. PMID 11427698. Архивирано из оригинала 13. 05. 2010. г. Приступљено 21. 03. 2010.
Bennett V, Stenbuck PJ (10. 4. 1979). „Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin”. J Biol Chem. 254 (7): 2533—41. PMID 372182.
Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V (1990). „Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8”. Nature. 345 (6277): 736—9. PMID 2141669. doi:10.1038/345736a0.
Bennett V, Stenbuck PJ (1979). „The membrane attachment protein for spectrin is associated with band 3 in human erythrocyte membranes”. Nature. 280 (5722): 468—73. PMID 379653. doi:10.1038/280468a0.
Singleton PA, Bourguignon LY (2004). „CD44 interaction with ankyrin and IP3 receptor in lipid rafts promotes hyaluronan-mediated Ca2+ signaling leading to nitric oxide production and endothelial cell adhesion and proliferation”. Exp Cell Res. 295 (1): 102—18. PMID 15051494. doi:10.1016/j.yexcr.2003.12.025.
Schott JJ; Charpentier F; Peltier S; et al. (1995). „Mapping of a gene for long QT syndrome to chromosome 4q25-27”. Am. J. Hum. Genet. 57 (5): 1114—22. PMC 1801360 . PMID 7485162.
Kapfhamer D, Miller DE, Lambert S, Bennett V, Glover TW, Burmeister M (1995). „Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10”. Genomics. 27 (1): 189—91. PMID 7665168. doi:10.1006/geno.1995.1023.
Ferreira MA; O'Donovan MC; Meng YA; et al. (2008). „Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder”. Nat. Genet. 40 (9): 1056. PMC 2703780 . PMID 18711365. doi:10.1038/ng.209.

physiology.org

physrev.physiology.org

Bennett V, Baines AJ (1. 7. 2001). „Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues”. Physiol. Rev. 81 (3): 1353—92. PMID 11427698. Архивирано из оригинала 13. 05. 2010. г. Приступљено 21. 03. 2010.

rcsb.org

PDB: 1N11; Michaely P, Tomchick DR, Machius M, Anderson RG (2002). „Crystal structure of a 12 ANK repeat stack from human ANK1”. EMBO J. 21 (23): 6387—96. PMC 136955 . PMID 12456646. doi:10.1093/emboj/cdf651. Текст „ankyrinR ” игнорисан (помоћ)

schizophreniaforum.org

„Channeling Mental Illness: GWAS Links Ion Channels, Bipolar Disorder”. Schizophrenia Research Forum: News. schizophreniaforum.org. 19. 8. 2008. Архивирано из оригинала 18. 12. 2010. г. Приступљено 21. 8. 2008.

web.archive.org

Bennett V, Baines AJ (1. 7. 2001). „Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues”. Physiol. Rev. 81 (3): 1353—92. PMID 11427698. Архивирано из оригинала 13. 05. 2010. г. Приступљено 21. 03. 2010.
„Channeling Mental Illness: GWAS Links Ion Channels, Bipolar Disorder”. Schizophrenia Research Forum: News. schizophreniaforum.org. 19. 8. 2008. Архивирано из оригинала 18. 12. 2010. г. Приступљено 21. 8. 2008.