Knut Sletten

University of Oslo — Norway

Biochemistry, Genetics and Molecular Biology · Life Sciences

57h-index11.9kcitations244works0.02yr avg
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Research Topics

Amyloidosis: Diagnosis, Treatment, Outcomes(112), Alzheimer's disease research and treatments(45), Glycosylation and Glycoproteins Research(37), Drug Transport and Resistance Mechanisms(18), Trace Elements in Health(18)

Publications244 total

Fibril protein fragmentation pattern in systemic AL‐amyloidosis
The Journal of Pathology·2009· 72 cited
AL-amyloid fibrils contain small constant region fragments that form amyloid-like fibrils in vitro
2009
Cyclic Peptides from <i>Oldenlandia affinis</i> DC. Molecular and Biological Properties
Chemistry & Biodiversity·2008· 68 cited
Germ Line Origin and Somatic Mutations Determine the Target Tissues in Systemic AL-Amyloidosis
PLoS ONE·2007· 48 citedOpen Access
Ageing and Amyloid Fibrillogenesis: Lessons from Apolipoprotein Al, Transthyretin and Islet Amyloid Polypeptide
Novartis Foundation symposium·2007· 14 cited
Unwinding fibril formation of medin, the peptide of the most common form of human amyloid
Biochemical and Biophysical Research Communications·2007· 43 cited
Glycan analysis of monoclonal antibodies secreted in deposition disorders indicates that subsets of plasma cells differentially process IgG glycans
Arthritis & Rheumatism·2006· 55 cited
The amino acid sequence of an AL-protein, AL-KH, isolated from the heart of a patient with Waldenstroms macroglobulinemia and amyloidosis
Amyloid·2006· 1 cited
Lactadherin binds to elastin – a starting point for medin amyloid formation?
Amyloid·2006· 57 cited
Amyloid deposits in transthyretin‐derived amyloidosis: cleaved transthyretin is associated with distinct amyloid morphology
The Journal of Pathology·2005· 241 cited
Serum Amyloid P Component in Mink *
2004
Serum Amyloid P Component in Mink
2004
Glycosylation Studies of Monoclonal Immunoglobulin Deposition Disorders
2004
Artefacts formed by addition of urea to <i>N</i> ‐linked glycans released with peptide‐ <i>N</i> ‐glycosidase F for analysis by mass spectrometry
Rapid Communications in Mass Spectrometry·2004· 14 cited
Serum amyloid A protein forms a complex with a fragment of Apolipoprotein A-I in the domestic blue fox: a protective mechanism against AA amyloidosis?
Amyloid·2004· 3 cited
Serum amyloid P component in mink, a non-glycosylated protein with affinity for phosphorylethanolamine and phosphorylcholine
Amyloid·2004· 7 cited
The amino acid sequence of a glycosylated AL-chain from a patient with primary amyloidosis
Amyloid·2004· 2 cited
Two different types of amyloid deposits—apolipoprotein A-IV and transthyretin—in a patient with systemic amyloidosis
Laboratory Investigation·2004· 88 citedOpen Access
Cleavage of AL amyloid proteins and AL amyloid deposits by cathepsins B, K, and L
The Journal of Pathology·2004· 66 cited
Articular, monoclonal γ3 heavy‐chain deposition disease: Characterization of a partially deleted heavy‐chain gene and its protein product synthesized in vivo and in vitro
Arthritis & Rheumatism·2003· 4 citedOpen Access
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Frequent Co-authors

Per Westermark(14), Gunnar Husby(11), Ingolf F. Nes(7), J. B. Natvig(7), Sarah Rioton(5), Charles L. Murphy(5), Alan Solomon(5), Deborah Weiss(4), Helge Holo(3), Joakim Bergström(3), Lorents Gran(3), Gibbons G. Cornwell(2), Jessie Juul(2), Ulf Hellman(2), Bo Häggqvist(2), Gunilla T. Westermark(2), G Mucchiano(2), Gudmund Marhaug(2), Stefan Stevanović(2), Manfred Eulitz(2)