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- 2013
-
Mark
Molecular Mechanisms in Amyloid Disorders. Novel Treatment Options in Hereditary Cystatin C Amyloid Angiopathy.
(
- Thesis › Doctoral thesis (compilation)
- 2009
-
Mark
UK Myeloma Forum (UKMF) and Nordic Myeloma Study Group (NMSG): guidelines for the investigation of newly detected M-proteins and the management of monoclonal gammopathy of undetermined significance (MGUS)
(
- Contribution to journal › Article
- 2007
-
Mark
Domain swapping as a molecular mechanism in amyloidosis
(
- Thesis › Doctoral thesis (compilation)
- 2006
-
Mark
Checking the conformational stability of cystatin C and its L68Q variant by molecular dynamics studies: Why is the L68Q variant amyloidogenic?
(
- Contribution to journal › Article
- 2000
-
Mark
L68Q cystatin C. Expression, cellular transport and turnover of the cystatin C variant forming amyloid in patients with Hereditary Cystatin C Amyloid Angiopathy (HCCAA)
2000)(
- Thesis › Doctoral thesis (compilation)
- 1998
-
Mark
Cystatin C functions in vitro and in vivo. Studies on target enzyme inhibition by cystatin C variants and cystatin C deficient mice.
1998)(
- Thesis › Doctoral thesis (compilation)
- 1997
-
Mark
NMR structural studies of human cystatin C dimers and monomers
(
- Contribution to journal › Article
-
Mark
Endogenous proteins as markers of glomerular function and dysfunction
1997)(
- Thesis › Doctoral thesis (compilation)
- 1996
-
Mark
Mouse and rat cystatin C: Escherichia coli production, characterization and tissue distribution
1996) In Comparative Biochemistry and Physiology - Part B: Biochemistry & Molecular Biology 114(3). p.303-311(
- Contribution to journal › Article
- 1990
-
Mark
The aminoterminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated. Direct sequence analysis from agarose gel electropherograms
(
- Contribution to journal › Article