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Items: 1 to 20 of 112


Crystal structure and functional interpretation of the erythrocyte spectrin tetramerization domain complex.

Ipsaro JJ, Harper SL, Messick TE, Marmorstein R, Mondragón A, Speicher DW.

Blood. 2010 Jun 10;115(23):4843-52. doi: 10.1182/blood-2010-01-261396. Epub 2010 Mar 2.


The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.

Harper SL, Sriswasdi S, Tang HY, Gaetani M, Gallagher PG, Speicher DW.

Blood. 2013 Oct 24;122(17):3045-53. doi: 10.1182/blood-2013-02-487702. Epub 2013 Aug 23.


Structural basis for spectrin recognition by ankyrin.

Ipsaro JJ, Mondragón A.

Blood. 2010 May 20;115(20):4093-101. doi: 10.1182/blood-2009-11-255604. Epub 2010 Jan 25.


Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?

Giorgi M, Cianci CD, Gallagher PG, Morrow JS.

Exp Mol Pathol. 2001 Jun;70(3):215-30.


Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variants.

Lecomte MC, Garbarz M, Gautero H, Bournier O, Galand C, Boivin P, Dhermy D.

Br J Haematol. 1993 Nov;85(3):584-95.


Spectrin self-association site: characterization and study of beta-spectrin mutations associated with hereditary elliptocytosis.

Nicolas G, Pedroni S, Fournier C, Gautero H, Craescu C, Dhermy D, Lecomte MC.

Biochem J. 1998 May 15;332 ( Pt 1):81-9.


Dynamic molecular modeling of pathogenic mutations in the spectrin self-association domain.

Zhang Z, Weed SA, Gallagher PG, Morrow JS.

Blood. 2001 Sep 15;98(6):1645-53.


Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis.

Coetzer T, Lawler J, Prchal JT, Palek J.

Blood. 1987 Sep;70(3):766-72.


Mutational effects at the tetramerization site of nonerythroid alpha spectrin.

Sumandea CA, Fung LW.

Brain Res Mol Brain Res. 2005 May 20;136(1-2):81-90. Epub 2005 Mar 2.


Laboratory method to study mutational effects on human erythrocyte spectrin tetramerization.

Ranganathan S, Menhart N, Topouzian N, Fung LW.

Am J Hematol. 2001 Aug;67(4):247-51.


Association studies of erythroid alpha-spectrin at the tetramerization site.

Lam VQ, Antoniou C, Rolius R, Fung LW.

Br J Haematol. 2009 Nov;147(3):392-5. doi: 10.1111/j.1365-2141.2009.07876.x. Epub 2009 Aug 31.


Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain.

Garbarz M, Lecomte MC, Féo C, Devaux I, Picat C, Lefebvre C, Galibert F, Gautero H, Bournier O, Galand C, et al.

Blood. 1990 Apr 15;75(8):1691-8.


Crystal structure of the nonerythroid alpha-spectrin tetramerization site reveals differences between erythroid and nonerythroid spectrin tetramer formation.

Mehboob S, Song Y, Witek M, Long F, Santarsiero BD, Johnson ME, Fung LW.

J Biol Chem. 2010 May 7;285(19):14572-84. doi: 10.1074/jbc.M109.080028. Epub 2010 Mar 14.


Novel exon 2 α spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct α spectrin defects.

Swierczek S, Agarwal AM, Naidoo K, Lorenzo FR, Whisenant J, Nussenzveig RH, Agarwal N, Coetzer TL, Prchal JT.

Haematologica. 2013 Dec;98(12):1972-9. doi: 10.3324/haematol.2013.086629. Epub 2013 Sep 27.

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