Panarach C, Netsawang C, Nuchprayoon I, Leecharoenkiat K
Sci Rep. 2024; 14(1):27362.
PMID: 39521890
PMC: 11550412.
DOI: 10.1038/s41598-024-78622-w.
More T, Devendra R, Dongerdiye R, Warang P, Kedar P
Mol Genet Genomics. 2023; 298(2):427-439.
PMID: 36598564
DOI: 10.1007/s00438-022-01984-1.
Wang X, Mao L, Shen N, Peng J, Zhu Y, Hu Q
Oncotarget. 2018; 8(68):113282-113286.
PMID: 29348906
PMC: 5762591.
DOI: 10.18632/oncotarget.22936.
Chowdhury S, Fang J, Sitharaman B
Future Sci OA. 2016; 1(3).
PMID: 26925250
PMC: 4765390.
DOI: 10.4155/fso.15.17.
Huang H, Zhao P, Arimatsu K, Tabeta K, Yamazaki K, Krieg L
G3 (Bethesda). 2013; 3(10):1687-95.
PMID: 23934996
PMC: 3789793.
DOI: 10.1534/g3.113.007013.
Suppression of hepcidin expression and iron overload mediate Salmonella susceptibility in ankyrin 1 ENU-induced mutant.
Yuki K, Eva M, Richer E, Chung D, Paquet M, Cellier M
PLoS One. 2013; 8(2):e55331.
PMID: 23390527
PMC: 3563626.
DOI: 10.1371/journal.pone.0055331.
Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant.
Rank G, Sutton R, Marshall V, Lundie R, Caddy J, Romeo T
Blood. 2009; 113(14):3352-62.
PMID: 19179303
PMC: 2665900.
DOI: 10.1182/blood-2008-08-172841.
Ankyrin-linked hereditary spherocytosis in an African-American kindred.
Sangerman J, Maksimova Y, Edelman E, Morrow J, Forget B, Gallagher P
Am J Hematol. 2008; 83(10):789-94.
PMID: 18704959
PMC: 11304496.
DOI: 10.1002/ajh.21254.
Hyaluronan-CD44 interaction activates stem cell marker Nanog, Stat-3-mediated MDR1 gene expression, and ankyrin-regulated multidrug efflux in breast and ovarian tumor cells.
Bourguignon L, Peyrollier K, Xia W, Gilad E
J Biol Chem. 2008; 283(25):17635-51.
PMID: 18441325
PMC: 2427357.
DOI: 10.1074/jbc.M800109200.
Chlorella viruses.
Yamada T, Onimatsu H, Van Etten J
Adv Virus Res. 2006; 66:293-336.
PMID: 16877063
PMC: 1955756.
DOI: 10.1016/S0065-3527(06)66006-5.
Group VIA phospholipase A2 forms a signaling complex with the calcium/calmodulin-dependent protein kinase IIbeta expressed in pancreatic islet beta-cells.
Wang Z, Ramanadham S, Ma Z, Bao S, Mancuso D, Gross R
J Biol Chem. 2004; 280(8):6840-9.
PMID: 15576376
PMC: 3716912.
DOI: 10.1074/jbc.M405287200.
Ankyrin gene mutations in japanese patients with hereditary spherocytosis.
Nakanishi H, Kanzaki A, Yawata A, Yamada O, Yawata Y
Int J Hematol. 2001; 73(1):54-63.
PMID: 11372755
DOI: 10.1007/BF02981903.
ankA: an Ehrlichia phagocytophila group gene encoding a cytoplasmic protein antigen with ankyrin repeats.
Caturegli P, Asanovich K, WALLS J, Bakken J, Madigan J, Popov V
Infect Immun. 2000; 68(9):5277-83.
PMID: 10948155
PMC: 101789.
DOI: 10.1128/IAI.68.9.5277-5283.2000.
Ankyrin-Tiam1 interaction promotes Rac1 signaling and metastatic breast tumor cell invasion and migration.
Bourguignon L, Zhu H, Shao L, Chen Y
J Cell Biol. 2000; 150(1):177-91.
PMID: 10893266
PMC: 2185563.
DOI: 10.1083/jcb.150.1.177.
Mapping of a palmitoylatable band 3-binding domain of human erythrocyte membrane protein 4.2.
Bhattacharyya R, Das A, Moitra P, Pal B, Mandal I, Basu J
Biochem J. 1999; 340 ( Pt 2):505-12.
PMID: 10333496
PMC: 1220278.
Nervous system defects of AnkyrinB (-/-) mice suggest functional overlap between the cell adhesion molecule L1 and 440-kD AnkyrinB in premyelinated axons.
Scotland P, Zhou D, Benveniste H, Bennett V
J Cell Biol. 1998; 143(5):1305-15.
PMID: 9832558
PMC: 2133070.
DOI: 10.1083/jcb.143.5.1305.
Small, membrane-bound, alternatively spliced forms of ankyrin 1 associated with the sarcoplasmic reticulum of mammalian skeletal muscle.
Zhou D, Birkenmeier C, Williams M, Sharp J, Barker J, Bloch R
J Cell Biol. 1997; 136(3):621-31.
PMID: 9024692
PMC: 2134284.
DOI: 10.1083/jcb.136.3.621.
Distance between Cys-201 in erythrocyte band 3 and the bilayer measured by single-photon radioluminescence.
Thevenin B, Bicknese S, Park J, Verkman A, SHOHET S
Biophys J. 1996; 71(5):2645-55.
PMID: 8913602
PMC: 1233751.
DOI: 10.1016/S0006-3495(96)79456-0.
Localization of the gene encoding the erythrocyte membrane protein p55 (Mpp1) on the mouse X Chromosome.
Peters L, Kirley L, Kim A, Chishti A
Mamm Genome. 1996; 7(3):245-6.
PMID: 8833260
DOI: 10.1007/s003359900279.
A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis.
Jarolim P, RUBIN H, Brabec V, PALEK J
J Clin Invest. 1995; 95(3):941-7.
PMID: 7883994
PMC: 441425.
DOI: 10.1172/JCI117802.
