SELDI-TOF mass spectrometry evaluation of variant transthyretins for diagnosis and pathogenesis of familial amyloidotic polyneuropathy.
about
Proteomics in molecular diagnosis: typing of amyloidosisChallenges for biomarker discovery in body fluids using SELDI-TOF-MS.Biomarker discovery and clinical proteomics.Age-dependent increase in thiol conjugated forms of transthyretin (TTR) in the elderly: quantitative analyses by the surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS) protein chip system.The relative amounts of plasma transthyretin forms in familial transthyretin amyloidosis: a quantitative analysis by Fourier transform ion-cyclotron resonance mass spectrometry.Ovine serum biomarkers of early and late phase scrapie.Allele specific expression of the transthyretin gene in swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles.Recent advances in transthyretin amyloidosis therapyDerivatization strategies for CE-LIF analysis of biomarkers: Toward a clinical diagnostic of familial transthyretin amyloidosis.Rapid detection of wild-type and mutated transthyretins.Mass spectrometric immunoassay for quantitative determination of transthyretin and its variants.Transthyretin-related familial amyloidotic polyneuropathy-Progress in Kumamoto, Japan (1967-2010)-.Clinical proteomics for diagnosis and typing of systemic amyloidoses.Diagnosis of familial amyloid polyneuropathy: wide-ranged clinicopathological features.Identification of CXCL5/ENA-78 as a factor involved in the interaction between cholangiocarcinoma cells and cancer-associated fibroblasts.Pathological, biochemical, and biophysical characteristics of the transthyretin variant Y114H (p.Y134H) explain its very mild clinical phenotype.Aged vervet monkeys developing transthyretin amyloidosis with the human disease-causing Ile122 allele: a valid pathological model of the human disease.Genetic and clinical characteristics of hereditary transthyretin amyloidosis in endemic and non-endemic areas: experience from a single-referral center in Japan.Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm.Dominant cardiac type of familial amyloidotic polyneuropathy associated with a novel transthyretin variant Thr59Arg.Clinicopathological features of senile systemic amyloidosis: an ante- and post-mortem study.Systemic amyloidoses and proteomics: The state of the art.AbstractsHow proteomic ApoE serotyping could impact Alzheimer’s disease risk assessment: genetic testing by proteomicsTransthyretin-derived amyloidosis in musculoskeletal systemsKnee osteoarthritis associated with different kinds of amyloid deposits and the impact of aging on type of amyloidTwo brothers homozygous for the TTR V30M both presenting with a phenotype dominated by central nervous complicationsSpinal multifocal amyloidosis derived from wild-type transthyretin
P2860
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P2860
SELDI-TOF mass spectrometry evaluation of variant transthyretins for diagnosis and pathogenesis of familial amyloidotic polyneuropathy.
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
SELDI-TOF mass spectrometry ev ...... al amyloidotic polyneuropathy.
@ast
SELDI-TOF mass spectrometry ev ...... al amyloidotic polyneuropathy.
@en
type
label
SELDI-TOF mass spectrometry ev ...... al amyloidotic polyneuropathy.
@ast
SELDI-TOF mass spectrometry ev ...... al amyloidotic polyneuropathy.
@en
prefLabel
SELDI-TOF mass spectrometry ev ...... al amyloidotic polyneuropathy.
@ast
SELDI-TOF mass spectrometry ev ...... al amyloidotic polyneuropathy.
@en
P2093
P1433
P1476
SELDI-TOF mass spectrometry ev ...... ial amyloidotic polyneuropathy
@en
P2093
Hirofumi Jono
Kazutoshi Ota
Masaaki Nakamura
Mineyuki Mizuguchi
Mitsuharu Ueda
Satoru Shinriki
Shu-ichi Ikeda
Taro Yamashita
Yohei Misumi
Yoshiki Sekijima
P304
P356
10.1373/CLINCHEM.2008.118505
P407
P50
P577
2009-04-16T00:00:00Z