• <em>Flavobacterium psychrophilum</em>: Response of Vaccinated Large Rainbow Trout to Different Strains
• <em>In Vitro</em> Evolution of Specific Phages Infecting the Fish Pathogen <em>Flavobacterium psychrophilum</em>
• A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning
• A novel missense mutation in TFAP2B associated with Char syndrome and central diabetes insipidus
• A study of familial Char syndrome involving the TFAP2B gene with a focus on facial shape characteristics
• AP-2β is a transcriptional regulator for determination of digit length in tetrapods
• Char Syndrome
• Char Syndrome
• Char Syndrome a novel mutation and new insights: A clinical report
• Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger
• Characterization of transcription factor AP-2 β mutations involved in familial isolated patent ductus arteriosus suggests haploinsufficiency
• Clinical characteristics and genetic analysis of a child with Char syndrome caused by TFAP2B gene variant
• Declining metabolic scaling parallels an ontogenetic change from elongate to deep-bodied shapes in juvenile Brown trout
• Evolution of pace-of-life syndrome under conditions of maternal PCB contamination and global warming in early life stages of cold stenothermic fish (Arctic char)
• First detection of Flavobacterium psychrophilum in juvenile Siberian sturgeons (Acipenser baerii) and description of the pathological findings
• Human Genetics of Ventricular Septal Defect
• Identification of a novel type II-C Cas9 from the fish pathogen <em>Flavobacterium psychrophilum</em>
• Immersion challenge model for Flavobacterium psychrophilum infection of Atlantic salmon (Salmo salar L.) fry
• Impact of coronavirus disease 2019 on pediatric intestinal intussusception in the United States
• Implementation of high-sensitivity troponin with a rapid diagnostic algorithm reduces emergency department length of stay for discharged patients
• KCTD1 mutants in scalp-ear-nipple syndrome and AP-2alpha P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/beta-catenin signaling
• KCTD1 mutants in scalp‑ear‑nipple syndrome and AP‑2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/β‑catenin signaling
• Maternal and Newborn Hospital Outcomes of Perinatal SARS-CoV-2 Infection: A National Registry
• Observations on Red Mark Syndrome in juvenile rainbow trout farmed in RAS system
• Red mark syndrome: Is the aquaculture water microbiome a keystone for understanding the disease aetiology?
• Research progress of genetic research on Char syndrome
• Sleep Architecture in Mice Is Shaped by the Transcription Factor AP-2β
• TfAP-2 is required for night sleep in Drosophila
• TFAP2 paralogs regulate midfacial development in part through a conserved <em>ALX</em> genetic pathway
• TFAP2 paralogs regulate midfacial development in part through a conserved ALX genetic pathway
• TFAP2B mutation and dental anomalies
• Tfap2b mutation in mice results in patent ductus arteriosus and renal malformation
• The AP-2 Transcription Factor APTF-2 Is Required for Neuroblast and Epidermal Morphogenesis in Caenorhabditis elegans Embryogenesis
• Time-course transcriptome analyses of spleen in rainbow trout (<em>Oncorhynchus mykiss</em>) post-<em>Flavobacterium psychrophilum</em> infection
• Transcription factor AP-2beta in development, differentiation and tumorigenesis
• Understanding the Pathogenesis of Red Mark Syndrome in Rainbow Trout (<em>Oncorhynchus mykiss</em>) through an Integrated Morphological and Molecular Approach
• Visual Acuity in Aniridia and WAGR Syndrome