Cytoskeletal Integrators: The Spectrin Superfamily.
R. Liem
semanticscholar +1 more source
Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the <i>SPTB</i> gene that causes hereditary spherocytosis with hemolytic anemia. [PDF]
Cao K +6 more
europepmc +1 more source
A novel Homozygous Mutation in SPTBN4 (Spectrin beta chain, non-erythrocytic 4) with syndromic neurodevelopmental phenotype in a consanguineous family of Saudi Origin. [PDF]
Raja Hussain Ali, Muhammad Umair
openalex +1 more source
Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review. [PDF]
Vives-Corrons JL, Krishnevskaya E.
europepmc +1 more source
Calpain and spectrin breakdown products as potential biomarkers in tuberculous pleural effusion [PDF]
Ji Young Hong +4 more
openalex +1 more source
NMNAT3 is protective against the effects of neonatal cerebral hypoxia-ischemia [PDF]
Araki, Toshiyuki +6 more
core +2 more sources
Running on the edge: hematological responses to a non-stop ultramarathon with a focus on nitric oxide-mediated red blood cell deformability. [PDF]
Grau M +8 more
europepmc +1 more source
Endothelial βII Spectrin Deletion Exacerbates Inflammation and Impairs Tissue Regeneration in Ischemic-Diabetic Skin Wound Healing. [PDF]
Gupta R +8 more
europepmc +1 more source

