Evidence of emerging transcriptome mediators of Alzheimer's disease in canine cognitive dysfunction
Canine cognitive dysfunction (CCD) may be a promising model of Alzheimer's disease (AD). To assess AD‐related molecular signatures in CCD, we generated transcriptome data on dog cortex and plasma extracellular vesicles (EVs). CCD‐related transcriptome changes were similar to those in aging/AD humans and were detectable in EVs from the same animals ...
Shelby C. Osburn +7 more
wiley +1 more source
The frequency and severity of congenital heart disease vary extensively in individuals with 22q11.22–23 distal deletions. Reduced gene dosage particularly within the low copy repeat (LCR22) D–E region including MAPK1 and HIC2 conveys risk for these defects.
Tanner J. Nelson +22 more
wiley +1 more source
Some African Cyphostemma species evolved much larger genomes as they adapted to dry, rocky habitats. These expansions are linked to succulent traits and specialization on nutrient‐rich limestone outcrops. The findings show how climate‐driven aridification shaped plant evolution and highlight broader genome‐environment patterns across flowering plants ...
Rindra M. Ranaivoson +18 more
wiley +1 more source
A novel biallelic loss-of-function variant in DAND5 causes heterotaxy syndrome. [PDF]
Ganapathi M +9 more
europepmc +1 more source
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing [PDF]
Muhammad Tariq +4 more
core +1 more source
Incidental Heterotaxy Syndrome With Polysplenia and Inferior Vena Cava Agenesis Identified During Trauma Evaluation. [PDF]
Ahmed Z +4 more
europepmc +1 more source
Multisystem Phenotypic Spectrum in Pediatric Heterotaxy Syndrome: A Case Series. [PDF]
Mukherjee TG +2 more
europepmc +1 more source
Characterization of phenotypic spectrum of fetal heterotaxy syndrome by combining ultrasound and magnetic resonance imaging. [PDF]
Seidl-Mlczoch E +9 more
europepmc +1 more source
Preliminary experience with cardiovascular magnetic resonance in evaluation of fetal cardiovascular anomalies [PDF]
core +1 more source
Heterotaxy syndrome: a rare risk factor for a pulmonary embolism in a young person. [PDF]
Mathys L +4 more
europepmc +1 more source

