• A Comprehensive Review of Pea (<em>Pisum sativum</em> L.): Chemical Composition, Processing, Health Benefits, and Food Applications
• A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness
• Bioinformatics and systems biology analysis revealed PMID26394986-Compound-10 as potential repurposable drug against covid-19
• CDK10/cyclin M is a protein kinase that controls ETS2 degradation and is deficient in STAR syndrome
• Clinical and genetic approach in the characterization of newborns with anorectal malformation
• Early Identification of Serum Biomarkers and Pathways of Sepsis Through GC-MS-Based Metabolomics Analysis
• Effect of Tan Tui combined with kinesio taping on the posture control of patients with PFPS: protocol for a randomized controlled trial
• Enhancing diversity of clinical trial populations in multiple sclerosis
• Functional activity of the caudate mediates the relation between early childhood microstructural variations and elevated metabolic syndrome scores
• Functional characterization of CDK10 and cyclin M truncated variants causing severe developmental disorders
• Further validation of craniosynostosis as a part of phenotypic spectrum of BCL11B-related BAFopathy
• Growth and Photosynthetic Efficiency of Microalgae and Plants with Different Levels of Complexity Exposed to a Simulated M-Dwarf Starlight
• High-dose ascorbic acid potentiates immune modulation through STAT1 phosphorylation inhibition and negative regulation of PD-L1 in experimental sepsis
• In skeletal muscle and neural crest cells, SMCHD1 regulates biological pathways relevant for Bosma syndrome and facioscapulohumeral dystrophy phenotype
• Lily's Story: STAR Syndrome
• Mediterranean diet and female reproductive health over lifespan: a systematic review and meta-analysis
• Metabolism-related brain morphology accelerates aging and predicts neurodegenerative diseases and stroke: a UK Biobank study
• Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype
• Multimodal imaging of retinal findings in syndactyly, telecanthus, anogenital, and renal malformations (STAR) syndrome
• Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
• Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndrome
• Oral follicle stimulating hormone (FSH) receptor agonist affects granulosa cells differently than recombinant human FSH
• Protocol for measuring BRAF autoinhibition in live cells using a proximity-based NanoBRET assay
• Relationships between self-perceived and clinical expression of pain and function differ based on the underlying pathology of the human hip
• Retinitis pigmentosa associated with the EYS C2139Y variant: an important cause of blindness in East Asian populations
• Sea star wasting syndrome reaches the high Antarctic: Two recent outbreaks in McMurdo Sound
• Simultaneous determination of three curative flavonoids and neurotoxic anisatin in star anise fruits by ultra-high performance liquid chromatography-tandem mass spectrometry
• STAR syndrome is part of the differential diagnosis of females with anorectal malformations
• STAR syndrome plus: The first description of a female patient with the lethal form
• STAR syndrome-associated CDK10/Cyclin M regulates actin network architecture and ciliogenesis
• STAR syndrome: a further case and the first report of maternal mosaicism
• The awakening of the CDK10/Cyclin M protein kinase
• The identification of a novel CCNQ gene tail extension variant contributing to syndactyly, telecanthus and anogenital and renal malformations syndrome