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Links from Nucleotide

Items: 4

1.
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
W T Tse, M C Lecomte, F F Costa, M Garbarz, C Feo, P Boivin, D Dhermy, B G Forget
J Clin Invest. 1990 Sep; 86(3): 909–916. doi: 10.1172/JCI114792
PMCID:
PMC296810
SummaryPage BrowsePDF–1.8M
2.
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.
M Garbarz, W T Tse, P G Gallagher, C Picat, M C Lecomte, F Galibert, D Dhermy, B G Forget
J Clin Invest. 1991 Jul; 88(1): 76–81. doi: 10.1172/JCI115307
PMCID:
PMC296005
SummaryPage BrowsePDF–1.3M
3.
The carboxyterminal EF domain of erythroid α-spectrin is necessary for optimal spectrin-actin binding
Catherine Korsgren, Samuel E. Lux
Blood. 2010 Oct 7; 116(14): 2600–2607. Prepublished online 2010 Jun 28. doi: 10.1182/blood-2009-12-260612
PMCID:
PMC2953892
AbstractArticle
4.
Protein 4.2 Binds to the Carboxyl-terminal EF-hands of Erythroid α-Spectrin in a Calcium- and Calmodulin-dependent Manner
Catherine Korsgren, Luanne L. Peters, Samuel E. Lux
J Biol Chem. 2010 Feb 12; 285(7): 4757–4770. Published online 2009 Sep 11. doi: 10.1074/jbc.M109.056200
PMCID:
PMC2836081
AbstractArticlePDF–2.3M

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