|
rs267607161
|
|
|
0.870 |
GeneticVariation |
BEFREE |
Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser.
|
31521469 |
2020 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
BEFREE |
This study confirmed the structural modulation effect of tafamidis on A97S-TTR and implied the potential therapeutic benefit of tafamidis for A97S TTR-FAP.
|
31502419 |
2019 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
BEFREE |
This is the first FAP family with a proven missense mutation c.349G>T in Mainland China, as well as the first FAP case with chronic paroxysmal dry cough.
|
30361054 |
2019 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
BEFREE |
These results demonstrate that the hTTR<sup>A97S</sup> mouse model develops sensory nerve pathology and corresponding physiology mimicking A97S-FAP and provides a platform to develop new therapies for the early stage of A97S-FAP.
|
29423915 |
2018 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
BEFREE |
Herein, we demonstrate genetic confirmation of the ATTR Ala97Ser mutation, the most common endemic mutation in Taiwan.
|
29939164 |
2018 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Hereditary Transthyretin Amyloidosis in Eight Chinese Families.
|
26521788 |
2015 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis.
|
23713495 |
2013 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Direct tissue evaluation via immunofluorescence: in the diagnosis of hereditary transthyretin cardiac amyloidosis.
|
22412233 |
2012 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Our study included 8 cases of acquired monoclonal immunoglobulin light chain amyloidosis, 11 cases of transthyretin amyloidosis (3 with the Val30Met mutation, 2 with the Val32Ala mutation, 2 with the Thr60Ala mutation, 1 with the Ala109Ser mutation, 1 with the Phe64Leu mutation, 1 with the Ala97Ser mutation, and 1 not sequenced), and 2 cases of gelsolin amyloidosis (1 with the Asp187Asn mutation and 1 not sequenced).
|
20937937 |
2011 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
BEFREE |
This study investigated skin innervation and its clinical significance in genetically defined FAP due to a hot-spot Ala97Ser TTR mutation (Ala97Ser).
|
20697105 |
2010 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Liver transplantation and combined liver-heart transplantation in patients with familial amyloid polyneuropathy: a single-center experience.
|
20209591 |
2010 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
This study investigated skin innervation and its clinical significance in genetically defined FAP due to a hot-spot Ala97Ser TTR mutation (Ala97Ser).
|
20697105 |
2010 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Pathology and functional diagnosis of small-fiber painful neuropathy.
|
20714957 |
2010 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
These five FAP patients shared an identical missense mutation, Ala97Ser, in the TTR gene.
|
18022643 |
2008 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
UNIPROT |
Genetic microheterogeneity of human transthyretin detected by IEF.
|
17503405 |
2007 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
UNIPROT |
A new transthyretin variant (Glu61Gly) associated with cardiomyopathy.
|
17453626 |
2007 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
UNIPROT |
Cys114-linked dimers of transthyretin are compatible with amyloid formation.
|
16185074 |
2005 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
UNIPROT |
A severe form of amyloidotic polyneuropathy in a Costa Rican family with a rare transthyretin mutation (Glu54Lys).
|
15214015 |
2004 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Clinical and pathological studies of cardiac amyloidosis in transthyretin type familial amyloid polyneuropathy.
|
14986482 |
2003 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Tabulation of human transthyretin (TTR) variants, 2003.
|
14640030 |
2003 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
The hereditary amyloidoses.
|
15123043 |
2003 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
UNIPROT |
Disulfide-bond formation in the transthyretin mutant Y114C prevents amyloid fibril formation in vivo and in vitro.
|
12403615 |
2002 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
UNIPROT |
Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.
|
12050338 |
2002 |
|
rs267607161
|
|
T |
0.870 |
CausalMutation |
CLINVAR |
Transthyretin mutations in hyperthyroxinemia and amyloid diseases.
|
11385707 |
2001 |
|
rs267607161
|
|
|
0.870 |
GeneticVariation |
UNIPROT |
Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu).
|
11445644 |
2001 |