Hereditary amyloidogenic transthyretin (TTR)(ATTR) amyloidosis is an autosomal dominant
form of fatal hereditary amyloidosis. Owing to progress in biochemical and molecular genetic …

Hereditary amyloidogenic transthyretin (ATTRv) amyloidosis is a rare autosomal dominantly
inherited disorder caused by mutations in the transthyretin (TTR) gene. The pathogenetic …

What is known and objective Transthyretin (TTR) is a representative amyloidogenic protein
in humans. Rate‐limiting tetramer dissociation and rapid monomer misfolding and …

Transthyretin (ATTR) amyloidosis is a life-threatening, gain-of-toxic-function disease
characterised by extracellular deposition of amyloid fibrils composed of transthyretin (TTR) …

Transthyretin (TTR), which is one of the major amyloidogenic proteins in systemic
amyloidosis, forms extracellular amyloid deposits in the systemic organs such as nerves …

Transthyretin (TTR) is a transport protein for thyroid hormones and vitamin A and might have
an important role in the nervous system. However, TTR can undergo a conformational …

Transthyretin (TTR) amyloidosis is caused by systemic deposition of wild-type or variant
amyloidogenic TTR (ATTRwt and ATTRv, respectively). ATTRwt amyloidosis has …

Transthyretin (TTR) amyloidosis (ATTR amyloidosis) is an underdiagnosed and important
type of cardiomyopathy and/or polyneuropathy that requires increased awareness within the …

Amyloidoses represent a group of diseases characterized by the pathological accumulation
in the extracellular area of insoluble misfolded protein material called “amyloid”. The …

Amyloidosis is a group of conditions characterized by the accumulation of amyloid deposits
in various tissues. Among these disorders, ATTR amyloidosis occurs either with or without a …