Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
about
Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissuesObscurin targets ankyrin-B and protein phosphatase 2A to the cardiac M-linePrimary structure and domain organization of human alpha and beta adducinAn alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 geneAn isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cellsSmall, membrane-bound, alternatively spliced forms of ankyrin 1 associated with the sarcoplasmic reticulum of mammalian skeletal muscleCloning of the alpha-adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplificationThe murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) geneGenetic disorders of the red cell membranesAnk3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domainIsoforms of ankyrin-3 that lack the NH2-terminal repeats associate with mouse macrophage lysosomesCharacterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice.Analysis of the mobilities of band 3 populations associated with ankyrin protein and junctional complexes in intact murine erythrocytes.Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivoHereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleationAnkyrins.Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing.Weighing in on molecular anchors: the role of ankyrin polypeptides in human arrhythmia.A hierarchy of ankyrin-spectrin complexes clusters sodium channels at nodes of RanvierSingle-cell electrical lysis of erythrocytes detects deficiencies in the cytoskeletal protein networkHereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins.A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.Distinct ankyrin isoforms at neuron cell bodies and nodes of Ranvier resolved using erythrocyte ankyrin-deficient miceA new 440-kD isoform is the major ankyrin in neonatal rat brain.Tissue plasminogen activator regulates Purkinje neuron development and survival.Ankyrin protein networks in membrane formation and stabilization.Perspectives in Pediatric Pathology, Chapter 17. Other Hypergonadotropic Hypogonadisms.Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations.Of mice and men: the mice were right.Molecular and functional characterization of protein 4.1B, a novel member of the protein 4.1 family with high level, focal expression in brain.β-III-spectrin spinocerebellar ataxia type 5 mutation reveals a dominant cytoskeletal mechanism that underlies dendritic arborization.Expression of antisense or sense RNA of an ankyrin repeat-containing gene blocks chloroplast differentiation in arabidopsis.
P2860
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P2860
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
description
1991 nî lūn-bûn
@nan
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
1991年论文
@zh
1991年论文
@zh-cn
name
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
@en
type
label
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
@en
prefLabel
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
@en
P2093
P2860
P356
P1476
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
@en
P2093
Birkenmeier CS
Bronson RT
P2860
P304
P356
10.1083/JCB.114.6.1233
P407
P577
1991-09-01T00:00:00Z