Add to ORKGEtude du mécanisme moléculaire de la formation de fibres amyloïdes à l'aide de fragments d'anticorps à chaînes lourdes comme protéines modèle
Formation of large fibers and plaques by amyloid proteins is recognized as the molecular hallmark of...
Six variants of human lysozyme (single-point mutatants I56T, F57I, W64R, D67H and double mutants F57...
Human lysozyme variants form amyloid fibrils in individuals suffering from a familial non-neuropath...
To understand the mechanism of amyloid fibril formation of a protein, we examined wild-type and thre...
Amyloid deposits regress when the supply of fibril precursor proteins is sufficiently reduced, indic...
Etude du mécanisme moléculaire de la formation de fibres amyloïdes à l'aide de fragments d'anticorps...
The aggregation of amyloid fibrils can lead to various diseases including Alzheimer’s, Parkinson’s d...
Human lysozyme variants form amyloid fibrils in individuals suffering from a familial non-neuropathi...
Amyloid-β is an intrinsically disordered protein that forms fibrils in the brains of patients with A...
The amyloidoses constitute a large group of diseases caused by an alteration in the conformation and...
Fibrillar protein aggregation is a hallmark of a variety of human diseases. Examples include the dep...
Tissue deposition of soluble proteins as amyloid fibrils underlies a range of fatal diseases. The tw...
Etude du mécanisme moléculaire de la formation de fibres amyloïdes à l'aide de fragments d'anticorps...
In this thesis I have used electrospray mass spectrometry (ESI-MS) to investigate various aspects of...
Six variants of human lysozyme (I56T, F57I, W64R, D67H, F57I/T70N and W112R/T70N) are associated wit...
Formation of large fibers and plaques by amyloid proteins is recognized as the molecular hallmark of...
Six variants of human lysozyme (single-point mutatants I56T, F57I, W64R, D67H and double mutants F57...
Human lysozyme variants form amyloid fibrils in individuals suffering from a familial non-neuropath...
To understand the mechanism of amyloid fibril formation of a protein, we examined wild-type and thre...
Amyloid deposits regress when the supply of fibril precursor proteins is sufficiently reduced, indic...
Etude du mécanisme moléculaire de la formation de fibres amyloïdes à l'aide de fragments d'anticorps...
The aggregation of amyloid fibrils can lead to various diseases including Alzheimer’s, Parkinson’s d...
Human lysozyme variants form amyloid fibrils in individuals suffering from a familial non-neuropathi...
Amyloid-β is an intrinsically disordered protein that forms fibrils in the brains of patients with A...
The amyloidoses constitute a large group of diseases caused by an alteration in the conformation and...
Fibrillar protein aggregation is a hallmark of a variety of human diseases. Examples include the dep...
Tissue deposition of soluble proteins as amyloid fibrils underlies a range of fatal diseases. The tw...
Etude du mécanisme moléculaire de la formation de fibres amyloïdes à l'aide de fragments d'anticorps...
In this thesis I have used electrospray mass spectrometry (ESI-MS) to investigate various aspects of...
Six variants of human lysozyme (I56T, F57I, W64R, D67H, F57I/T70N and W112R/T70N) are associated wit...
Formation of large fibers and plaques by amyloid proteins is recognized as the molecular hallmark of...
Six variants of human lysozyme (single-point mutatants I56T, F57I, W64R, D67H and double mutants F57...
Human lysozyme variants form amyloid fibrils in individuals suffering from a familial non-neuropath...