Results 191 to 200 of about 42,373 (249)

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]

Front Genet
Cao K, Luo X, Liu L, Mao X, Liu R, Chen Y, Banerjee S.   +6 more
europepmc   +1 more source

Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review. [PDF]

Int J Mol Sci
Vives-Corrons JL, Krishnevskaya E.
europepmc   +1 more source

Main events and mechanism of human erythrocyte ageing. [PDF]

Expert Rev Mol Med
Huang YX.
europepmc   +1 more source

Endothelial βII Spectrin Deletion Exacerbates Inflammation and Impairs Tissue Regeneration in Ischemic-Diabetic Skin Wound Healing. [PDF]

Wound Repair Regen
Gupta R, Cooper PO, Chai W, Mulagura P, Lee SM, Theocharidis G, Sidawy AN, Shook BA, Nguyen BN.   +8 more
europepmc   +1 more source

Running on the edge: hematological responses to a non-stop ultramarathon with a focus on nitric oxide-mediated red blood cell deformability. [PDF]

Front Physiol
Grau M, Bruns J, Stücher M, John L, Munk M, Siebers M, Siebers C, Bloch W, Bizjak DA.   +8 more
europepmc   +1 more source

Correction: Dihedral angle measurements for structure determination by biomolecular solid-state NMR spectroscopy. [PDF]

Front Mol Biosci
van der Wel PCA.
europepmc   +1 more source

Functional characterization of the predicted SMC domain in Nesprin-2 [PDF]

, 2013
Xing, Xin
core  

Dystrophin-Deficient Cardiomyopathy Due to a Novel Hemizygous DMD Indel Variant. [PDF]

JACC Case Rep
Albrecht K, Averbuch T, Huculak C, Marcadier J, Oudit G, van Landeghem FKH, Adam B, Lyons KJ, Kiamanesh O.   +8 more
europepmc   +1 more source

Reviewer #3 (Public review): BetaII-Spectrin Gaps and Patches Emerge from the Patterned Assembly of the Actin/Spectrin Membrane Skeleton in Human Motor Neuron Axons

Nahir Guadalupe Gazal, Maria Jose Castellanos-Montiel, Guillermina Bruno, Anna Kristina Franco-Flores, Sarah Lépine, Lale Gursu, Ghazal Haghi, Gilles Maussion, Agustín Anastasía, Mariano Bisbal, Ezequiel Axel Gorostiza, Thomas M Durcan, Nicolás Unsain   +12 more
openalex   +1 more source

Hereditary Elliptocytosis Resulting From Heterozygosity for β Spectrin Tandil. [PDF]

Am J Hematol
Molina-Arrebola MA, Bain BJ.
europepmc   +1 more source