Skip to content
<title>Channels - Potential Rad54 separation of function mutation highlights unique roles during homologous recombination :: FRELIP Discovery
Channels Potential Rad54 separation of function mutation highlights unique roles during homologous recombination
Identification of a Novel DNAAF3 Variant in a 54-Year-Old Patient With Newly Diagnosed Primary Ciliary Dyskinesia (PCD)
Mechanism of single-strand annealing from native mass spectrometry and cryo-EM structures of RAD52 homolog Mgm101
Karyotype and reproductive traits of the unique symbiotic mealybug Orbuspedum machinator G.-Z. (Homoptera, Coccinea)
ssDNA-PLA, a proximity ligation assay to interrogate DNA damage response proteins involved in homologous recombination
Extracellular Vesicles in Pancreatic Cancer Function and Potential Clinical Applications
Craniometaphyseal dysplasia with severe maxillary hypoplasia due to gene mutation: A case report
Novel LAMA1 Mutations in a Pedigree With Poretti‐Boltshauser Syndrome: Implications for Hypomyelination
MCT8 Deficiency in Two Brothers With a Novel Deletion Mutation in SLC16A2
Development of molecular assays to detect the G143A point mutation responsible for group 11 fungicide insensitivity in
Separating selection from mutation in antibody language models
Highlighting chromosomal rearrangements of five species of Galliformes (Domestic fowl, Common and Japanese quail, Barbary and Chukar partridge) and the Houbara bustard, an endangered Otidiformes: banding cytogenetic is a powerful tool
Hypokalemic Periodic Paralysis Associated With a Rare CACNA1S Variant (p.Leu1243Val): Expanding the Mutational Spectrum
A Rare Case of Concurrent SNRPB Mutation and 22q11.2 Microduplication in a Child With Cerebro-Costo-Mandibular Syndrome
First Thai Case of Lethal Desbuquois Dysplasia Type I Caused by Novel Compound Heterozygous CANT1 Mutations: Expanding the Molecular Spectrum
Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature
"Characterization of Nigerian breast cancer reveals prevalent homologous recombination deficiency and aggressive molecular features"
Coxsackievirus A6 was the predominant pathogen of hand, foot, and mouth disease with frequent recombination and mutations in Shandong Province, 2023
Genomic and functional insights into pathogenicity of
Evaluation of the Mutagenic Potential of Glucocorticoids by Allium cepa
Expression and Function of Meflin in Human Endometrial Decidualization
Three Unrelated Children With Childhood Apraxia of Speech: Exome Sequencing and Functional Gene Analysis Imply a Role of Laminin-511 in Early Neurodevelopment
Correction to “Expression and Function of Meflin in Human Endometrial Decidualization”
Metabolic shift and signature metabolites unveiled during infection of
