Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Characterization of zebrafish merlot/chablis as non-mammalian vertebrate models for severe congenital anemia due to protein 4.1 deficiency.

Development (Cambridge, England) - 1 Sept 2002

Shafizadeh Ebrahim, Paw Barry H, Foott Helen, Liao Eric C, Barut Bruce A, Cope John J, Zon Leonard I, Lin Shuo

Abstract excerpt

The red blood cell membrane skeleton is an elaborate and organized network of structural proteins that interacts with the lipid bilayer and transmembrane proteins to maintain red blood cell morphology, membrane deformability and mechanical stability. A crucial component of red blood cell membrane skeleton is the erythroid specific protein 4.1R, which anchors the spectrin-actin based cytoskeleton to the plasma...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anemia, Hemolytic
Share to Codon, Nonsense

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cytoskeletal Proteins

Share to DNA, Complementary

Share to Erythrocyte Membrane

Share to Neuropeptides

Share to Sequence Deletion

Share to Zebrafish

Source

Identifiers

PMID: 12183387
DOI: 10.1242/dev.129.18.4359

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of zebrafish merlot/chablis as non-mammalian vertebrate models for severe congenital anemia due to protein 4.1 deficiency.PMID 12183387Read ↗

Hereditary spherocytosis in zebrafishrieslingillustrates evolution of erythroid β-spectrin structure, and function in red cell morphogenesis and membrane stabilitySemantic proximity Read ↗

Protein 4.1R–deficient mice are viable but have erythroid membrane skeleton abnormalitiesSemantic proximity Read ↗

Using the Zebrafish as a Genetic Model to Study ErythropoiesisSemantic proximity Read ↗

Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1.Semantic proximity Read ↗

An update on the pathogenesis and diagnosis of Diamond–Blackfan anemiaSemantic proximity Read ↗

Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells.Semantic proximity Read ↗

Hereditary elliptocytosis: spectrin and protein 4.1R.Semantic proximity Read ↗

Establishment of a Diamond-Blackfan anemia like model in zebrafish.Semantic proximity Read ↗

Yippee like 4 (Ypel4) is essential for normal mouse red blood cell membrane integritySemantic proximity Read ↗

Modeling Diamond Blackfan anemia in the zebrafish.Semantic proximity Read ↗

Characterization of mutations affecting embryonic hematopoiesis in the medaka, Oryzias latipes.Semantic proximity Read ↗

Zebrafish erythropoiesis and the utility of fish as models of anemiaSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.