Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis
about
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple heSpectrin tetramer formation is not required for viable development in DrosophilaStructural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site.Flexibility of the alpha-spectrin N-terminus by EPR and fluorescence polarization.Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosisDrosophila development requires spectrin network formation.Spectrin Tunis (Sp alpha (I/78)) in a Korean family with hereditary elliptocytosis.Interactions within the coiled-coil domain of RetGC-1 guanylyl cyclase are optimized for regulation rather than for high affinity.A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency.Laboratory method to study mutational effects on human erythrocyte spectrin tetramerization.
P2860
Q24564889-12188C40-E91A-40B8-96B9-01B40C7BEA3AQ27314007-4B265086-9AAB-4FC9-8F41-07AA96FC2DA9Q33316438-BAADFAF9-EF4D-4983-9FB3-E184741BBEA9Q34173543-0DA6CEDA-84FE-4A3E-9734-0D56254613FAQ35881989-838F8A00-8A1E-478B-A53B-87A075F9ECC2Q36235170-3D8D967C-D22B-43FB-BEC0-E0C6D82B6A30Q37129465-92E2C776-A844-41BF-8385-7A553F28D69BQ43578129-D270011C-BD55-45CB-AB6B-20AEF9873506Q46089959-C9A98872-22A2-477D-B9A5-013D74541A25Q50504712-5C2861D4-B985-4E1A-A42F-F443BE03391B
P2860
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis
description
1991 nî lūn-bûn
@nan
1991 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Four different mutations in co ...... 4 in hereditary elliptocytosis
@ast
Four different mutations in co ...... 4 in hereditary elliptocytosis
@en
Four different mutations in co ...... 4 in hereditary elliptocytosis
@nl
type
label
Four different mutations in co ...... 4 in hereditary elliptocytosis
@ast
Four different mutations in co ...... 4 in hereditary elliptocytosis
@en
Four different mutations in co ...... 4 in hereditary elliptocytosis
@nl
prefLabel
Four different mutations in co ...... 4 in hereditary elliptocytosis
@ast
Four different mutations in co ...... 4 in hereditary elliptocytosis
@en
Four different mutations in co ...... 4 in hereditary elliptocytosis
@nl
P2093
P2860
P356
P1476
Four different mutations in co ...... 4 in hereditary elliptocytosis
@en
P2093
H Blacklock
J Manaster
L Peterson
T L Coetzer
P2860
P356
10.1172/JCI115371
P407
P577
1991-09-01T00:00:00Z