Results 191 to 200 of about 1,687,286 (315)

VAV Family Gene [PDF]

, 2020
openaire   +1 more source

dUTPase is essential in zebrafish development and possesses several single‐nucleotide variants with pronounced structural and functional consequences

FEBS Open Bio, EarlyView.
dUTPases are involved in balancing the appropriate nucleotide pools. We showed that dUTPase is essential for normal development in zebrafish. The different zebrafish genomes contain several single‐nucleotide variations (SNPs) of the dut gene. One of the dUTPase variants displayed drastically lower protein stability and catalytic efficiency as compared ...
Viktória Perey‐Simon, Angéla Békesi, Latifa Kazzazy, Jázmin Mihály, Máté Varga, Beáta G. Vértessy, Kinga Nyíri   +6 more
wiley   +1 more source

Comprehensive Updated Genome-Wide Identification and Expression Patterns of the <i>TaGeBP</i> Gene Family in Wheat. [PDF]

Int J Mol Sci
Zhang S, Ding J, Li T, Zhao Y, Xu D, Zeng J, Liu W, Qu M, Ma W, Dai X.   +9 more
europepmc   +1 more source

The role of lipid metabolism in neuronal senescence

FEBS Open Bio, EarlyView.
Disrupted lipid metabolism, through alterations in lipid species or lipid droplet accumulation, can drive neuronal senescence. However, lipid dyshomeostasis can also occur alongside neuronal senescence, further amplifying tissue damage. Delineating how lipid‐induced senescence emerges in neurons and glial cells, and how it contributes to ageing and ...
Dikaia Tsagkari, Eleftheria Panagiotidou, Nektarios Tavernarakis   +2 more
wiley   +1 more source

Functional divergence and characterization of the HOTHEAD gene family in rice. [PDF]

BMC Genomics
Liu J, Ye Q, Shen Y, Wu Z, Jiang W, Guo D, Hu X, Wang X, Zhang Z, Hu L.   +9 more
europepmc   +1 more source

Tracking Motor Progression and Device‐Aided Therapy Eligibility in Parkinson's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterise the progression of motor symptoms and identify eligibility for device‐aided therapies in Parkinson's disease, using both the 5‐2‐1 criteria and a refined clinical definition, while examining differences across genetic subgroups.
David Ledingham, Sahana Sathyanarayana, Charlotte B. Stewart, Robyn Iredale, Victoria Foster, Debra Galley, Mark Baker, Nicola Pavese   +7 more
wiley   +1 more source

The roles of the small nucleolar RNA host gene family in ovarian cancer. [PDF]

Cancer Biol Ther
Zhang T, Wu D, Li Z, Han W, Shi J, Chen A, Zhu W.   +6 more
europepmc   +1 more source

Identification of a Novel Non-Stop Mutation in PDE6C Gene in an Iranian Family With Con-Rod Dystrophy

, 2020
Shahram Nasiri, Farah Talebi, Javad Mohammadi‐Asl, Farideh Ghanbari Mardasi   +3 more
openalex   +1 more source

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini, Emanuela Martinuzzi, Sandra Dhifallah, Abderhmane Slioui, Angela Puma, Luisa Villa, Michele Cavalli, Andra Ezaru, Jérémy Garcia, Manuela Gambella, Federico Torre, Luca Jacopo Pavan, Nicolas Glaichenhaus, Sabrina Sacconi   +13 more
wiley   +1 more source

Genome-wide analysis of the cellulose synthase gene family in autopolyploid sugarcane (<i>Saccharum spontaneum</i>). [PDF]

Front Plant Sci
Wei X, Wei Z, Yang M, Chen Q, Wang J, Zhao L, Zhang X, Wang L, Hu L.   +8 more
europepmc   +1 more source