Results 201 to 210 of about 3,873,512 (229)

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra   +17 more
wiley   +1 more source

JACMP 2015 – 2019

open access: yes
Journal of Applied Clinical Medical Physics, EarlyView.
Per. H. Halvorsen
wiley   +1 more source

Conception and Synthesis of Sequence-Coded Morpholinos. [PDF]

open access: yesChemistry
Pousse B   +4 more
europepmc   +1 more source

The Cambridge Centre for Ageing and Neuroscience (Cam-CAN) longitudinal study protocol: Phase 4 (“Enrichment”) and Phase 5 (“Rescan”)

open access: yes
Demetriou I   +17 more
europepmc   +1 more source

The Main Sequence

1990
We consider here a sequence of chemically homogeneous models in complete (mechanical and thermal) equilibrium with central hydrogen burning. All of them are composed of the same hydrogen-rich mixture, while the stellar mass M varies from model to model along the sequence.
Alfred Weigert, Rudolf Kippenhahn
openaire   +2 more sources

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