Results 261 to 270 of about 188,115 (331)

The C-terminal ZZ domain of the Drosophila ORB2 RNA-binding protein is required for spermatid individualization. [PDF]

G3 (Bethesda)
Low TCH, Falk BL, Brill JA, Lipshitz HD.
europepmc   +1 more source

Causal Effect of Dietary Patterns on Cerebral Small Vessel Disease: A Mendelian Randomization Study

Food Science &Nutrition, Volume 14, Issue 2, February 2026.
This Mendelian randomization (MR) study reveals causal links between dietary factors and cerebral small vessel disease (CSVD) neuroimaging markers. Genetically predicted higher polyunsaturated fatty acid (PUFA) levels reduce white matter hyperintensity volume, while monounsaturated fatty acid (MUFA) intake lowers lobar brain microbleeds (BMB) risk.
Yong Zeng, Ziqian Zhao, Hongyan Liu, Yijun Zeng, Song Xu, Shanjing Nie   +5 more
wiley   +1 more source

Ultra-Conserved Poison Exons Enable Rapid and Safe Splicing Factor Gene Expression Switches: A Hypothesis. [PDF]

Bioessays
Dalgliesh C, Ghorbani F, Wollman AJM, Elliott DJ.   +3 more
europepmc   +1 more source

Identifying Causal Genotype–Phenotype Relationships for Population‐Sampled Parent–Child Trios

Genetic Epidemiology, Volume 50, Issue 1, February 2026.
ABSTRACT The process by which genes are transmitted from parent to child provides a source of randomization preceding all other factors that may causally influence any particular child phenotype. Because of this, it is natural to consider genetic transmission as a source of experimental randomization.
Yushi Tang, Irineo Cabreros, John D. Storey   +2 more
wiley   +1 more source

Accumulation of ph1 (zip4-5B) and ph2 (msh7-3D) mutations fails to boost homoeologous recombination in hexaploid wheat. [PDF]

Front Plant Sci
Haquet C, Nadaud I, Martin AC, Rey MD, Ben Bouslah A, John-Bejai C, Moore G, Sourdille P.   +7 more
europepmc   +1 more source

Extending the Use of Mendelian Randomisation With Non‐Inherited Variants to Assess Socially Transmitted Parental Exposures Under Assortative Mating

Genetic Epidemiology, Volume 50, Issue 1, February 2026.
ABSTRACT A longstanding aim of developmental psychology and epidemiology is to understand the causal effects of parental phenotypes on offspring outcomes. Traditional approaches often fail to account for confounding and reverse causation. We evaluate the use of Mendelian randomisation with non‐inherited variants (MR‐NIV) to address these limitations ...
Benjamin Woolf, Amy Mason, Chin Yang Shapland, Hyunseung Kang, Hannah M. Sallis, Stephen Burgess, Marcus R. Munafò   +6 more
wiley   +1 more source

Histone H3 N-Terminal Tail Residues Important for Meiosis in <i>Saccharomyces cerevisiae</i>. [PDF]

Biomolecules
Prichard A, Johansson M, Kirkpatrick DT, Clarke DJ.   +3 more
europepmc   +1 more source

Testicular Morphology and Spermatogenesis in Potamotrygon motoro: Insights Into Reproduction of Freshwater Stingrays

Journal of Morphology, Volume 287, Issue 2, February 2026.
Electron microscopy of Potamotrygon motoro spermatozoa. a – Illustration of a schematic sperm cell depicting the helical head, intermediate piece (midpiece), and flagellum. b ‐ Helical heads (Hh) of spermatozoa inserted into the cytoplasm of Sertoli cells (S) through openings in the plasma membrane. Scales: 10 μm.
Maria Luiza Ribeiro Delgado, Patricia Postingel Quirino, Luciane Gomes‐Silva, Viktoriya Dzyuba, Borys Dzyuba, Alexandre Ninhaus‐Silveira, Rosicleire Veríssimo‐Silveira   +6 more
wiley   +1 more source

Meiotic Sex Chromosome Inactivation: Conservation across the Drosophila genus. [PDF]

PLoS Genet
Avelino CC, Mendonca CA, Goldstein G, Bruno HB, Carvalho AB, Vibranovski MD.   +5 more
europepmc   +1 more source

Identification of a Novel Missense Homozygous Variant in LINS1 in Two Distinct Iranian Families With Consanguineous Marriage

Molecular Genetics &Genomic Medicine, Volume 14, Issue 2, February 2026.
A novel homozygous missense variant in LINS1 (c.1354G>C; p.Ala452Pro) was identified in two consanguineous families with autosomal recessive intellectual disability, supporting the gene's role in neurodevelopment and its relevance in genetic diagnosis and counseling of ARID. Reported pathogenic LINS1 variants.
Elham Alimoradi, Parham Nejati, Arash Salmaninejad, Nafiseh Falsafi, Fatemeh Molavi, Mohamad Javad Alibakhshi, Filippo Pinto e Vairo, Eric W. Klee, Reza Alibakhshi   +8 more
wiley   +1 more source