Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis.
about
Atlantic salmon (Salmo salar L.) skin contains a novel kininogen and another cysteine proteinase inhibitor.Decreased metastatic spread in mice homozygous for a null allele of the cystatin C protease inhibitor geneA drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries.Role of salivary and candidal proteins in denture stomatitis: an exploratory proteomic analysis.High throughput testing of drug library substances and monoclonal antibodies for capacity to reduce formation of cystatin C dimers to identify candidates for treatment of hereditary cystatin C amyloid angiopathy.EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. Second of two parts.Increased body temperature accelerates aggregation of the Leu-68-->Gln mutant cystatin C, the amyloid-forming protein in hereditary cystatin C amyloid angiopathy.Energetic Calculations to Decipher pH-Dependent Oligomerization and Domain Swapping of Proteins.The role of cystatins in cells of the immune system.Salivary proteome and its genetic polymorphisms.Intracellular accumulation of the amyloidogenic L68Q variant of human cystatin C in NIH/3T3 cells.Disulfide bonds in amyloidogenesis diseases related proteins.Cystatin C is a disease-associated protein subject to multiple regulation.Human cystatin C monomer, dimer, oligomer, and amyloid structures are related to health and disease.The molecular pathology of hereditary cystatin C amyloid angiopathy causing brain hemorrhage.Recurrent cerebral haemorrhage in a 65 year old man: advanced clinical neurology course, Edinburgh, 1997.Hereditary cystatin C amyloid angiopathy: monitoring the presence of the Leu-68-->Gln cystatin C variant in cerebrospinal fluids and monocyte cultures by MS.Identification and characterization of antibodies elicited by human cystatin C fragment.Distinct structural changes in wild-type and amyloidogenic chicken cystatin caused by disruption of C95-C115 disulfide bond.
P2860
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P2860
Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis.
description
1992 nî lūn-bûn
@nan
1992 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@ast
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@en
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@nl
type
label
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@ast
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@en
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@nl
prefLabel
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@ast
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@en
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@nl
P2093
P356
P1433
P1476
Hereditary cystatin C amyloid ...... chain reaction based analysis.
@en
P2093
Abrahamson M
Jonsdottir S
Olafsson I
P2888
P304
P356
10.1007/BF00194306
P577
1992-06-01T00:00:00Z
P6179
1004586657