Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 31


Diffusion of glycophorin A in human erythrocytes.

Giger K, Habib I, Ritchie K, Low PS.

Biochim Biophys Acta. 2016 Nov;1858(11):2839-2845. doi: 10.1016/j.bbamem.2016.08.012.


Identification of adducin-binding residues on the cytoplasmic domain of erythrocyte membrane protein, band 3.

Franco T, Chu H, Low PS.

Biochem J. 2016 Oct 1;473(19):3147-58. doi: 10.1042/BCJ20160328.


Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts.

Satchwell TJ, Bell AJ, Hawley BR, Pellegrin S, Mordue KE, van Deursen CT, Braak NH, Huls G, Leers MP, Overwater E, Tamminga RY, van der Zwaag B, Fermo E, Bianchi P, van Wijk R, Toye AM.

Haematologica. 2016 Sep;101(9):1018-27. doi: 10.3324/haematol.2016.146209.


Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.

Han JH, Kim S, Jang H, Kim SW, Lee MG, Koh H, Lee JH.

PLoS One. 2015 Jun 24;10(6):e0131251. doi: 10.1371/journal.pone.0131251.


The cytoskeletal binding domain of band 3 is required for multiprotein complex formation and retention during erythropoiesis.

Satchwell TJ, Hawley BR, Bell AJ, Ribeiro ML, Toye AM.

Haematologica. 2015 Jan;100(1):133-42. doi: 10.3324/haematol.2014.114538.


Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives.

Caignard G, Eva MM, van Bruggen R, Eveleigh R, Bourque G, Malo D, Gros P, Vidal SM.

Genes (Basel). 2014 Sep 29;5(4):887-925. doi: 10.3390/genes5040887. Review.


Characterization of ENU-induced Mutations in Red Blood Cell Structural Proteins.

Kildey K, Flower RL, Tran TV, Tunningley R, Harris J, Dean MM.

Comput Struct Biotechnol J. 2013 Sep 23;6:e201303012. doi: 10.5936/csbj.201303012.


A deep intronic mutation in the ankyrin-1 gene causes diminished protein expression resulting in hemolytic anemia in mice.

Huang H, Zhao P, Arimatsu K, Tabeta K, Yamazaki K, Krieg L, Fu E, Zhang T, Du X.

G3 (Bethesda). 2013 Oct 3;3(10):1687-95. doi: 10.1534/g3.113.007013.


Protective effects of stem bark of Harungana madgascariensis on the red blood cell membrane.

Biapa PC, Matei H, Bâlici Ş, Oben JE, Ngogang JY.

BMC Complement Altern Med. 2013 May 10;13:98. doi: 10.1186/1472-6882-13-98.


Suppression of hepcidin expression and iron overload mediate Salmonella susceptibility in ankyrin 1 ENU-induced mutant.

Yuki KE, Eva MM, Richer E, Chung D, Paquet M, Cellier M, Canonne-Hergaux F, Vaulont S, Vidal SM, Malo D.

PLoS One. 2013;8(2):e55331. doi: 10.1371/journal.pone.0055331.


A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter.

Yocum AO, Steiner LA, Seidel NE, Cline AP, Rout ED, Lin JY, Wong C, Garrett LJ, Gallagher PG, Bodine DM.

Blood. 2012 Oct 25;120(17):3586-93. doi: 10.1182/blood-2012-08-450262.


A novel ENU-mutation in ankyrin-1 disrupts malaria parasite maturation in red blood cells of mice.

Greth A, Lampkin S, Mayura-Guru P, Rodda F, Drysdale K, Roberts-Thomson M, McMorran BJ, Foote SJ, Burgio G.

PLoS One. 2012;7(6):e38999. doi: 10.1371/journal.pone.0038999.


Obscurin and KCTD6 regulate cullin-dependent small ankyrin-1 (sAnk1.5) protein turnover.

Lange S, Perera S, Teh P, Chen J.

Mol Biol Cell. 2012 Jul;23(13):2490-504. doi: 10.1091/mbc.E12-01-0052.


Structurally similar but functionally diverse ZU5 domains in human erythrocyte ankyrin.

Yasunaga M, Ipsaro JJ, Mondragón A.

J Mol Biol. 2012 Apr 6;417(4):336-50. doi: 10.1016/j.jmb.2012.01.041.


β-III spectrin is critical for development of purkinje cell dendritic tree and spine morphogenesis.

Gao Y, Perkins EM, Clarkson YL, Tobia S, Lyndon AR, Jackson M, Rothstein JD.

J Neurosci. 2011 Nov 16;31(46):16581-90. doi: 10.1523/JNEUROSCI.3332-11.2011.


Coordinating electrical activity of the heart: ankyrin polypeptides in human cardiac disease.

Curran J, Mohler PJ.

Expert Opin Ther Targets. 2011 Jul;15(7):789-801. doi: 10.1517/14728222.2011.575363. Review.


Mutant GlialCAM causes megalencephalic leukoencephalopathy with subcortical cysts, benign familial macrocephaly, and macrocephaly with retardation and autism.

López-Hernández T, Ridder MC, Montolio M, Capdevila-Nortes X, Polder E, Sirisi S, Duarri A, Schulte U, Fakler B, Nunes V, Scheper GC, Martínez A, Estévez R, van der Knaap MS.

Am J Hum Genet. 2011 Apr 8;88(4):422-32. doi: 10.1016/j.ajhg.2011.02.009.


A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.

Hughes MR, Anderson N, Maltby S, Wong J, Berberovic Z, Birkenmeier CS, Haddon DJ, Garcha K, Flenniken A, Osborne LR, Adamson SL, Rossant J, Peters LL, Minden MD, Paulson RF, Wang C, Barber DL, McNagny KM, Stanford WL.

Exp Hematol. 2011 Mar;39(3):305-20, 320.e1-2. doi: 10.1016/j.exphem.2010.12.009. Erratum in: Exp Hematol. 2011 May 39(5):601.


Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis.

Gallagher PG, Steiner LA, Liem RI, Owen AN, Cline AP, Seidel NE, Garrett LJ, Bodine DM.

J Clin Invest. 2010 Dec;120(12):4453-65. doi: 10.1172/JCI42240.


Defining new insight into atypical arrhythmia: a computational model of ankyrin-B syndrome.

Wolf RM, Mitchell CC, Christensen MD, Mohler PJ, Hund TJ.

Am J Physiol Heart Circ Physiol. 2010 Nov;299(5):H1505-14. doi: 10.1152/ajpheart.00503.2010.

Items per page

Supplemental Content

Support Center