Results 221 to 230 of about 171,193 (280)

Large deletions in the DNA primase large subunit PRIM2 are associated with NADP‐malate dehydrogenase activity in a porcine F2 cross

open access: yesAnimal Genetics, Volume 57, Issue 1, February 2026.
Abstract Large porcine F2 crosses are a valuable resource for discovering QTL and genetic variants for relevant traits. Past studies have been largely limited to SNPs and short insertions and deletions. Structural variants (SVs) are becoming a major area of interest in this respect.
Clemens Falker‐Gieske   +6 more
wiley   +1 more source

The Lrs14-Like AbfR1 Homolog From Metallosphaera sedula Is a Nucleoid-Organizing Protein. [PDF]

open access: yesMicrobiologyopen
De Kock V   +5 more
europepmc   +1 more source

DNA Methylation Episignature as a Novel Diagnostic Tool for Diamond‐Blackfan Anemia Syndrome

open access: yesAmerican Journal of Hematology, Volume 101, Issue 2, Page 228-241, February 2026.
Diamond‐Blackfan Anemia Syndrome (DBAS) is a congenital bone marrow failure disorder characterized by defective erythropoiesis and a spectrum of congenital anomalies, including craniofacial malformations, limb abnormalities, and cardiac and renal defects.
Paola Quarello   +29 more
wiley   +1 more source

Multiomic single nuclei profiling the mouse hippocampus reveals that ACSS2 confers neuronal resilience to tauopathy

open access: yesAlzheimer's &Dementia, Volume 22, Issue 2, February 2026.
Abstract INTRODUCTION Epigenomic dysregulation contributes to Alzheimer's disease (AD) and related tauopathies. Acetyl‐CoA synthetase 2 (ACSS2), a nuclear‐localized metabolic enzyme in neurons, supports histone acetylation and learning‐related gene expression.
Gabor Egervari   +10 more
wiley   +1 more source

Graded Calorie Restriction Causes Graded Slowing of Epigenetic Ageing in Mice. [PDF]

open access: yesAging Cell
Moulds TP   +6 more
europepmc   +1 more source

Indian‐enriched genetic variants are associated with cognitive function

open access: yesAlzheimer's &Dementia, Volume 22, Issue 2, February 2026.
Abstract INTRODUCTION Little is known about genetic risk factors for dementia in South Asians. Examining genetic variants that occur at higher frequency in India compared to other ancestries (i.e., Indian enriched variants) may identify genetic associations with cognitive function that are potentially unique to the Indian population.
Hasan Abu‐Amara   +12 more
wiley   +1 more source

Uncovering the poisonous aconitine containing plants in homemade herbal liquor using a convergent approach. [PDF]

open access: yesSci Rep
Intharuksa A   +7 more
europepmc   +1 more source

Comparative Analysis of HEK293 Genomic Variability

open access: yesBiotechnology and Bioengineering, Volume 123, Issue 2, Page 436-448, February 2026.
An investigation of how HEK293‐derived cell lines adapt genetically to different culture conditions and environmental pressures: despite distinct phenotypes and cultivation histories, comparative whole‐genome analyses of established HEK293 variants as well as newly suspension‐adapted cells revealed a shared, common set of mutations linked to cell ...
Georg Smesnik   +4 more
wiley   +1 more source

Characterization of the transposable element landscape shaping the Ectocarpus genome. [PDF]

open access: yesGenome Biol
Dinatale E   +4 more
europepmc   +1 more source

Hypothalamic–Pituitary–Thyroid and Adrenal Axis Modulation in Response to Fetal Porcine Reproductive and Respiratory Virus Infection

open access: yesComprehensive Physiology, Volume 16, Issue 1, February 2026.
This study investigates the impact of fetal porcine reproductive and respiratory virus (PRRSV) infection on the Hypothalamic–Pituitary‐Thyroid/Adrenal axes. We report that infection‐induced nonthyroidal illness syndrome is associated with multitissue dysregulation of key genes involved in the control of endocrine function, providing insights into ...
Alyssa A. Smith   +4 more
wiley   +1 more source

Home - About - Disclaimer - Privacy