Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.
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Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?Spectrin tetramer formation is not required for viable development in DrosophilaBinding of polarity-sensitive hydrophobic ligands to erythroid and nonerythroid spectrin: fluorescence and molecular modeling studies.Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site.Erythrocyte disorders in the perinatal periodSpectrin Breakdown Products (SBDPs) as Potential Biomarkers for Neurodegenerative DiseasesHow we decide when a neonate needs a transfusion.Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site.Organization and dynamics of tryptophan residues in erythroid spectrin: novel structural features of denatured spectrin revealed by the wavelength-selective fluorescence approachChaperone activity and prodan binding at the self-associating domain of erythroid spectrin.Oxidative crosslinking, spectrin and membrane interactions of hemoglobin mixtures in HbEbeta-thalassemia.
P2860
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P2860
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.
description
article científic
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article scientifique
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articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 1997
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mutation of a highly conserved ...... tal neonatal hemolytic anemia.
@en
Mutation of a highly conserved ...... tal neonatal hemolytic anemia.
@nl
type
label
Mutation of a highly conserved ...... tal neonatal hemolytic anemia.
@en
Mutation of a highly conserved ...... tal neonatal hemolytic anemia.
@nl
prefLabel
Mutation of a highly conserved ...... tal neonatal hemolytic anemia.
@en
Mutation of a highly conserved ...... tal neonatal hemolytic anemia.
@nl
P2093
P2860
P356
P1476
Mutation of a highly conserved ...... tal neonatal hemolytic anemia.
@en
P2093
Gallagher PG
Marchesi SL
Mohandas N
Petruzzi MJ
P2860
P304
P356
10.1172/JCI119155
P407
P577
1997-01-01T00:00:00Z