• <em>TBX3</em> and <em>EFNA4</em> Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis
• A de novo TBX3 mutation presenting as dorsalization of the little fingers: A forme fruste phenotype of ulnar-mammary syndrome
• A dominant repression domain in Tbx3 mediates transcriptional repression and cell immortalization: relevance to mutations in Tbx3 that cause ulnar-mammary syndrome
• A gene for ulnar-mammary syndrome maps to 12q23-q24.1
• Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63
• An essential interaction between T-box proteins and histone-modifying enzymes
• ATCUN-like metal-binding motifs in proteins: identification and characterization by crystal structure and sequence analysis
• Basal transcription of the human TBX3 gene, a key developmental regulator which is overexpressed in several cancers, requires functional NF-Y and Sp1 sites
• Clinical analysis of a large kindred with the Pallister ulnar-mammary syndrome
• Complex functional redundancy of Tbx2 and Tbx3 in mouse limb development
• Congenital palmar polyonychia with postaxial limb defects may be the same as the ulnar-mammary syndrome
• Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of Holt-Oram and ulnar-mammary syndromes
• Contiguous hemizygous deletion of TBX5, TBX3, and RBM19 resulting in a combined phenotype of Holt-Oram and ulnar-mammary syndromes
• Correspondence: Further studies on a kindred reported by Li 2009 as 'A new syndrome of ankyloglossia and ulnar ray defects in Newfoundland kindred'. From 'new syndrome' through EEC to ulnar mammary syndrome
• Development of a subset of forelimb muscles and their attachment sites requires the ulnar-mammary syndrome gene Tbx3
• Dichotomous roles of <em>TBX3</em> in the establishment of atrioventricular conduction pathways in the human heart
• Diverse functional networks of Tbx3 in development and disease
• Embryonic stem cells and mouse models of human syndromes: examples from the T-box gene family
• Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart-hand syndrome?
• Fatty hypertrophy cause obstructive sleep apnea after fat injection for velopharyngeal incompetence
• Genetic analysis of the TBX3 gene promoter in ventricular septal defects
• Genomic structure of TBX2 indicates conservation with distantly related T-box genes
• Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family
• Human Genetics of Ventricular Septal Defect
• Hypogonadotropic hypogonadism and pituitary hypoplasia as recurrent features in Ulnar-Mammary syndrome
• Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis
• Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19
• Interactions between FGF and Wnt signals and Tbx3 gene expression in mammary gland initiation in mouse embryos
• Isl1Cre reveals a common Bmp pathway in heart and limb development
• Isolation of a Drosophila T-box gene closely related to human TBX1
• Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis
• Life-threatening cardiac episode in a Polish patient carrying contiguous gene microdeletion of the <em>TBX5</em> and the <em>TBX3</em> genes
• Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27
• Literature review, report, and analysis of genotype and clinical phenotype of a rare case of ulnar-mammary syndrome
• Loss of Tbx3 in murine neural crest reduces enteric glia and causes cleft palate, but does not influence heart development or bowel transit
• Mammary gland, limb and yolk sac defects in mice lacking Tbx3, the gene mutated in human ulnar mammary syndrome
• Mechanical loading is required for initiation of extracellular matrix deposition at the developing murine myotendinous junction
• MicroRNA-17-92, a direct Ap-2α transcriptional target, modulates T-box factor activity in orofacial clefting
• Molecular interactions between Tbx3 and Bmp4 and a model for dorsoventral positioning of mammary gland development
• Mouse TBX3 mutants suggest novel molecular mechanisms for Ulnar-mammary syndrome
• Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
• Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex development
• Novel TBX3 mutation data in families with ulnar-mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects
• Novel TBX3 mutation in a family of Cypriot ancestry with ulnar-mammary syndrome
• Phenotype of a patient with contiguous deletion of TBX5 and TBX3: expanding the disease spectrum
• PMA-induced up-regulation of TBX3 is mediated by AP-1 and contributes to breast cancer cell migration
• Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome
• Postaxial polydactyly, ulnar ray dysgenesis, and renal cystic dysplasia in sibs
• Rare Case of Ulnar-Mammary-Like Syndrome With Left Ventricular Tachycardia and Lack of <em>TBX3</em> Mutation
• Regulation of Tbx3 expression by anteroposterior signalling in vertebrate limb development
• Short communication: Expression of T-box 2 and 3 in the bovine mammary gland
• Structure of the DNA-bound T-box domain of human TBX3, a transcription factor responsible for ulnar-mammary syndrome
• Studies of malformation syndromes of man XXXXIIB: mother and son affected with the ulnar-mammary syndrome type Pallister
• Synemin Redefined: Multiple Binding Partners Results in Multifunctionality
• T-box 3 is expressed in the adult mouse hypothalamus and medulla
• T-box genes in human disorders
• TBX-3, the gene mutated in Ulnar-Mammary Syndrome, is a negative regulator of p19ARF and inhibits senescence
• TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis
• TBX3 and its isoform TBX3+2a are functionally distinctive in inhibition of senescence and are overexpressed in a subset of breast cancer cell lines
• TBX3 and TBX5 duplication: A family with an atypical overlapping Holt-Oram/ulnar-mammary syndrome phenotype
• Tbx3 controls the fate of hepatic progenitor cells in liver development by suppressing p19ARF expression
• Tbx3 impinges on the p53 pathway to suppress apoptosis, facilitate cell transformation and block myogenic differentiation
• Tbx3 is a downstream target of the Wnt/beta-catenin pathway and a critical mediator of beta-catenin survival functions in liver cancer
• Tbx3 is required for outflow tract development
• TBX3 over-expression causes mammary gland hyperplasia and increases mammary stem-like cells in an inducible transgenic mouse model
• TBX3 promotes human embryonic stem cell proliferation and neuroepithelial differentiation in a differentiation stage-dependent manner
• TBX3 regulates splicing in vivo: a novel molecular mechanism for Ulnar-mammary syndrome
• Tbx3, a transcriptional factor, involves in proliferation and osteogenic differentiation of human adipose stromal cells
• TBX3, the gene mutated in ulnar-mammary syndrome, promotes growth of mammary epithelial cells via repression of p19ARF, independently of p53
• Tbx3, the ulnar-mammary syndrome gene, and Tbx2 interact in mammary gland development through a p19Arf/p53-independent pathway
• The face of Ulnar Mammary syndrome?
• The oncogenic TBX3 is a downstream target and mediator of the TGF-β1 signaling pathway
• The role of Tbx2 and Tbx3 in mammary development and tumorigenesis
• The roles and regulation of TBX3 in development and disease
• The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome
• The T-Box factor TBX3 is important in S-phase and is regulated by c-Myc and cyclin A-CDK2
• The T-box family
• The T-box repressors TBX2 and TBX3 specifically regulate the tumor suppressor gene p14ARF via a variant T-site in the initiator
• The T-Box transcription factor 3 in development and cancer
• The T-box transcription factors TBX2 and TBX3 in mammary gland development and breast cancer
• The ulnar-mammary syndrome gene, Tbx3, is a direct target of the retinoic acid signaling pathway, which regulates its expression during mouse limb development
• The ulnar-mammary syndrome: an autosomal dominant pleiotropic gene
• Transcription factor Tbx3 is required for the specification of the atrioventricular conduction system
• Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome
• Transcriptional repressor Tbx3 is required for the hormone-sensing cell lineage in mammary epithelium
• Ulnar aplasia, dysplastic radius and preaxial oligodactyly: Rare longitudinal limb defect in a sporadic male child
• Ulnar mammary syndrome
• Ulnar Mammary syndrome and TBX3: expanding the phenotype
• Ulnar-mammary syndrome
• Ulnar-Mammary syndrome with <em>TBX3</em> gene mutation in a Chinese family: A case report and literature review
• Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene
• Ulnar-Mammary syndrome with TBX3 gene mutation in a Chinese family: A case report and literature review
• Ulnar-mammary syndrome: clinical presentation, genetic underpinnings, diagnosis, and treatment
• Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome