Objectives Many adenocarcinomas have the ability to capture from an extracellular matrix
the oligonucleotides and nanoparticles by pinocytosis, when the non-cancerous cells are not …

We assessed the geographical distribution of C9orf72 G 4 C 2 expansions in a pan‐ E
uropean frontotemporal lobar degeneration ( FTLD ) cohort (n = 1,205), ascertained by the E …

Background Many adenocarcinomas have the ability to capture from an extracellular matrix
the oligonucleotides and nanoparticles by pinocytosis, when the non-cancerous cells are not …

… In the analysis of AACT we used Southern blot hybridization of StuI digested DNA with a o.-*P
labelled 1.5 … For each amplification one of the primers was end-labelled with o."PusingT4 …

… Tissue peroxidase was blocked with 5 % H 2 O 2 in methanol for 16 min followed by a brief
rinse with deionized water. Sections were settled in PBS with 0.05 % Brij35. Blocking was …

Background Frontotemporal dementia (FTD) is a complex disorder characterised by a broad
range of clinical manifestations, differential pathological signatures, and genetic variability. …

Frontotemporal dementia (FTD) is the second most frequent type of neurodegenerative
dementias. Mutations in the progranulin gene (GRN, PGRN) were recently identified in FTDU‐17, …

Pathological expansion of a G 4 C 2 repeat, located in the 5'regulatory region of C9orf72, is
the most common genetic cause of frontotemporal lobar degeneration (FTLD) and …

… The most recent study validating in the context of the Nurses Health study18 produced an
E/O ratio of 0.94 (0.89–0.99) compared with our screening population results, which were …

… and B o and 2 o are constant. Due to the condition that the extracellular current ie(y )
must have a finite value, B o = 0. The constants Vo and 2o can be found using the following …