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The Italian National Centre for Rare Diseases: where research and public health translate into action.
- Published in:
- Blood Transfusion (17232007), 2014, v. 12, p. s591, doi. 10.2450/2014.0040-14s
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- Article
Spectrin involvement in a 40°C structural transition of the red blood cell membrane.
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- Journal of Cellular Biochemistry, 1986, v. 30, n. 4, p. 361, doi. 10.1002/jcb.240300409
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- Article
Role of membrane thermotropic properties on hypotonic hemolysis and hypertonic cryohemolysis of human red blood cells.
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- Journal of Cellular Biochemistry, 1984, v. 25, n. 2, p. 61, doi. 10.1002/jcb.240250202
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- Article
Characterization of thermotropic structural transitions of the erythrocyte membrane: A biochemical and electron-paramagnetic resonance approach.
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- Journal of Cellular Biochemistry, 1984, v. 25, n. 2, p. 73, doi. 10.1002/jcb.240250203
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- Article
Protein-dependent lipid lateral phase separation as a mechanism of human erythrocyte ghost resealing.
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- Journal of Cellular Biochemistry, 1982, v. 19, n. 1, p. 59, doi. 10.1002/jcb.240190106
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- Article
Phosphorylation on threonine 11 of β-dystrobrevin alters its interaction with kinesin heavy chain.
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- FEBS Journal, 2012, v. 279, n. 22, p. 4131, doi. 10.1111/febs.12006
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- Article
Peroxynitrite induces tyrosine residue modifications in synaptophysin C-terminal domain, affecting its interaction with src.
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- Journal of Neurochemistry, 2009, v. 111, n. 3, p. 859, doi. 10.1111/j.1471-4159.2009.06378.x
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- Article
RIPK4 regulates cell–cell adhesion in epidermal development and homeostasis.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 15, p. 2535, doi. 10.1093/hmg/ddac046
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- Article
Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation.
- Published in:
- PLoS ONE, 2016, v. 11, n. 5, p. 1, doi. 10.1371/journal.pone.0156325
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- Article
The CaMKII/MLC1 Axis Confers Ca 2+ -Dependence to Volume-Regulated Anion Channels (VRAC) in Astrocytes.
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- Cells (2073-4409), 2022, v. 11, n. 17, p. 2656, doi. 10.3390/cells11172656
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- Article
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes.
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- Human Molecular Genetics, 2008, v. 17, n. 13, p. 2018, doi. 10.1093/hmg/ddn099
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- Article