AxD (Alexander disease) is a rare disorder caused by heterozygous mutations in GFAP (glial
fibrillary acidic protein) resulting in accumulation of the GFAP protein and elevation of Gfap …

Alexander disease is a rare, progressive, and generally fatal neurological disorder that
results from dominant mutations affecting the coding region of GFAP, the gene encoding glial …

… 19 (current study and unpublished observations, JX Connor, PL Jany). Comparison of
GFAP concentration in CSF or blood and age revealed significant linear positive correlation in …

… This was directly proven by our PL measurements, which showed less intensity of PL at
the boundary compared to the bulk TiO 2 (Fig. 4e). Such behavior is also reflected in the …

… The total amount of toxin in the assay was determined by adding 20 pl digestive fluid to the
… (#g/pl) per the total amount of toxin added to the digested fluid (pg) and has the units pl -~. …

The food enzyme considered in this opinion is a pullulanase (pullulan 6‐α‐glucanohydrolase;
EC 3.2.1.41) produced with a non‐genetically modified Pullulanibacillus naganoensis (…

… This study shows that a UC is not mandatory, since a UC left in place ≤24 h does not
reduce the risk of acute urinary retention, nor does it increase the risk of urinary tract infection. …

… Nasal place assimilation … No nasal place assimilation Nasal place assimilation does
not occur with the bilabial nasal /m/ …

… The eluate obtained was concentrated in a vacuum evaporator to 500 pL.Twenty pL of the
samples analyzed by HPLC (high pressure liquid chromatography) ion-pair chromatography …

… Above 50 K at high temperatures, the PL emissions are dominated by carriers on delocalized
states and the dependence of PL peak energy follows Varshni’s expression. The full width …