The beta proteins in amyloid deposits of Alzheimer's disease have been found to be racemized
and/or isomerized at their Asp residues (Roher, AE, Lowenson, JD, Clarke, S., Wolkow, C…

To investigate the pathomechanism of amyloid β protein (Aβ) deposition in brains with
Alzheimer's disease (AD), cerebrospinal fluid (CSF) levels of Aβ species (CSF-Aβ) with different …

Chiral bis-phosphoric acid 1 was designed to identify a new class of structural features in
chiral Brønsted acid catalysts. X-ray diffraction analysis revealed the single atropisomer 1, …

BACKGROUND AND PURPOSE Features of tumefactive demyelinating lesion (TDL) on
magnetic resonance imaging (MRI) can facilitate the differential diagnosis of TDL and neoplastic …

Triple A syndrome is an autosomal recessive neuroendocrinological disease caused by
mutations in a gene that encodes 546 amino acid residues. The encoded protein is the …

… Correlation of two ELISAs PAb of anti-ht2 (x-axis) and MAb of F-F11 (y-axis) were used as
… seen (r = 0.967) except the slope of the regression li~e is 0.624 and the y intereept is 0.084. …

Objective Early‐onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH)/ataxia
with oculomotor apraxia type 1 (AOA1) is an autosomal recessive form of cerebellar ataxia. …

Humanin (HN) was originally identified as an endogenous peptide that protects neuronal
cells from apoptosis induced by various types of Alzheimer’s disease-related insults. We have …

OBJECTIVES: Sleep attacks (SAs) in Parkinson's disease (PD) are rare, but clinically important
because they significantly impair the daily lives of patients. Causes of SAs include long-…

Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant disease caused by
mutations in the gene encoding protein kinase Cγ (PKCγ). We report an SCA14 family with a …