Results 151 to 160 of about 4,489 (232)

Evidence of emerging transcriptome mediators of Alzheimer's disease in canine cognitive dysfunction

open access: yesBrain Pathology, Volume 36, Issue 3, May 2026.
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

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

open access: yesClinical Genetics, Volume 109, Issue 5, Page 859-868, May 2026.
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

Plastid and nuclear phylogenomics of Cyphostemma (Vitaceae) provide new insights into genome size evolution across sub‐Saharan Africa

open access: yesJournal of Integrative Plant Biology, Volume 68, Issue 5, Page 1399-1420, May 2026.
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]

open access: yesCold Spring Harb Mol Case Stud, 2022
Ganapathi M   +9 more
europepmc   +1 more source

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing [PDF]

open access: yes, 2011
Muhammad Tariq   +4 more
core   +1 more source

Characterization of phenotypic spectrum of fetal heterotaxy syndrome by combining ultrasound and magnetic resonance imaging. [PDF]

open access: yesUltrasound Obstet Gynecol, 2021
Seidl-Mlczoch E   +9 more
europepmc   +1 more source

Heterotaxy syndrome: a rare risk factor for a pulmonary embolism in a young person. [PDF]

open access: yesProc (Bayl Univ Med Cent)
Mathys L   +4 more
europepmc   +1 more source

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