Ankirini (Serbo-Croatian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ankirini" in Serbo-Croatian language version.

refsWebsite

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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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780^th place

1archive.org

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1schizophreniaforum.org

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archive.org

Schott JJ, Charpentier F, Peltier S, et al. (November 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

dx.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. DOI:10.1093/emboj/cdf651. PMC 136955. PMID 12456646.
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. DOI:10.1038/345736a0. PMID 2141669.
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. DOI:10.1038/280468a0. PMID 379653.
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. DOI:10.1016/j.yexcr.2003.12.025. PMID 15051494.
Kapfhamer D, Miller DE, Lambert S, Bennett V, Glover TW, Burmeister M (May 1995). „Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10”. Genomics 27 (1): 189–91. DOI:10.1006/geno.1995.1023. PMID 7665168.
Ferreira MA, O'Donovan MC, Meng YA, et al. (August 2008). „Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder”. Nat. Genet. 40 (9): 1056. DOI:10.1038/ng.209. PMC 2703780. PMID 18711365.

jbc.org

Bennett V, Stenbuck PJ (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. DOI:10.1093/emboj/cdf651. PMC 136955. PMID 12456646.
Bennett V, Baines AJ (2001). „Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues”. Physiol. Rev. 81 (3): 1353–92. PMID 11427698. Arhivirano iz originala na datum 2010-05-13. Pristupljeno 2014-05-19.
Bennett V, Stenbuck PJ (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. DOI:10.1038/345736a0. PMID 2141669.
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. DOI:10.1038/280468a0. PMID 379653.
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. DOI:10.1016/j.yexcr.2003.12.025. PMID 15051494.
Schott JJ, Charpentier F, Peltier S, et al. (November 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 (May 1995). „Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10”. Genomics 27 (1): 189–91. DOI:10.1006/geno.1995.1023. PMID 7665168.
Ferreira MA, O'Donovan MC, Meng YA, et al. (August 2008). „Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder”. Nat. Genet. 40 (9): 1056. DOI:10.1038/ng.209. PMC 2703780. PMID 18711365.

physiology.org

physrev.physiology.org

Bennett V, Baines AJ (2001). „Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues”. Physiol. Rev. 81 (3): 1353–92. PMID 11427698. Arhivirano iz originala na datum 2010-05-13. Pristupljeno 2014-05-19.

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. DOI:10.1093/emboj/cdf651. PMC 136955. PMID 12456646.

schizophreniaforum.org

„Channeling Mental Illness: GWAS Links Ion Channels, Bipolar Disorder”. Schizophrenia Research Forum: News. schizophreniaforum.org. 19. 08. 2008.. Arhivirano iz originala na datum 2010-12-18. Pristupljeno 21. 08. 2008.

web.archive.org

Bennett V, Baines AJ (2001). „Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues”. Physiol. Rev. 81 (3): 1353–92. PMID 11427698. Arhivirano iz originala na datum 2010-05-13. Pristupljeno 2014-05-19.
„Channeling Mental Illness: GWAS Links Ion Channels, Bipolar Disorder”. Schizophrenia Research Forum: News. schizophreniaforum.org. 19. 08. 2008.. Arhivirano iz originala na datum 2010-12-18. Pristupljeno 21. 08. 2008.