Pages that link to "Q24312711"

The following pages link to Inactivation of IL11 signaling causes craniosynostosis, delayed tooth eruption, and supernumerary teeth (Q24312711):

Displaying 50 items.

• Interleukin 11 receptor subunit alpha (Q21130438) ‎ (← links)
• A Genetic-Pathophysiological Framework for Craniosynostosis (Q26784240) ‎ (← links)
• STAT3 and the Hyper-IgE syndrome: Clinical presentation, genetic origin, pathogenesis, novel findings and remaining uncertainties (Q26829298) ‎ (← links)
• Hyper-IgE syndrome update (Q26994673) ‎ (← links)
• An update on the hyper-IgE syndromes (Q27021598) ‎ (← links)
• Continuous dental replacement in a hyper-chisel tooth digging rodent (Q28743619) ‎ (← links)
• Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children (Q33707712) ‎ (← links)
• Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism (Q33921719) ‎ (← links)
• Assessing the association of taurodontism with numeric dentition anomalies in an adult central Indian population (Q34002941) ‎ (← links)
• Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis (Q34086690) ‎ (← links)
• Odontomas and supernumerary teeth: is there a common origin? (Q34550421) ‎ (← links)
• Identification of putative target genes of the transcription factor RUNX2. (Q35070834) ‎ (← links)
• Signaling pathways in osteogenesis and osteoclastogenesis: Lessons from cranial sutures and applications to regenerative medicine. (Q35587493) ‎ (← links)
• Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses. (Q35809894) ‎ (← links)
• Inborn errors of human JAKs and STATs (Q35908479) ‎ (← links)
• Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection (Q36547873) ‎ (← links)
• Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis (Q36629781) ‎ (← links)
• Sox2 marks epithelial competence to generate teeth in mammals and reptiles (Q36682930) ‎ (← links)
• Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey (Q36923083) ‎ (← links)
• Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosis (Q37398115) ‎ (← links)
• A Novel Large Deletion Encompassing the Whole of the Galactose-1-Phosphate Uridyltransferase (GALT) Gene and Extending into the Adjacent Interleukin 11 Receptor Alpha (IL11RA) Gene Causes Classic Galactosemia Associated with Additional Phenotypic Ab (Q37500702) ‎ (← links)
• Diagnostic value of exome and whole genome sequencing in craniosynostosis (Q37720856) ‎ (← links)
• Signaling networks regulating tooth organogenesis and regeneration, and the specification of dental mesenchymal and epithelial cell lineages (Q37993428) ‎ (← links)
• The role of vertebrate models in understanding craniosynostosis (Q38032780) ‎ (← links)
• The cup runneth over: lessons from the ever-expanding pool of primary immunodeficiency diseases (Q38124223) ‎ (← links)
• Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition (Q38134658) ‎ (← links)
• Primary Immunodeficiencies with Elevated IgE. (Q38477275) ‎ (← links)
• A novel mutation of adenomatous polyposis coli (APC) gene results in the formation of supernumerary teeth (Q38646198) ‎ (← links)
• The epidemiology of supernumerary teeth and the associated molecular mechanism (Q38672910) ‎ (← links)
• A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis (Q40118329) ‎ (← links)
• IL-11/IL11RA receptor mediated signaling: a web accessible knowledgebase (Q43798406) ‎ (← links)
• Transcription analysis of the interaction between chicken thymus and recombinant avian leukosis virus isolate FJ15HT0. (Q45324474) ‎ (← links)
• IL-11 is a crucial determinant of cardiovascular fibrosis. (Q46257233) ‎ (← links)
• Clinical genetics of craniosynostosis (Q47796796) ‎ (← links)
• The Biology Underlying Abnormalities of Tooth Number in Humans (Q47983362) ‎ (← links)
• Altered transcription of inflammation-related genes in dental pulp of coeliac children (Q48123853) ‎ (← links)
• Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice. (Q50701179) ‎ (← links)
• Genetic advances in craniosynostosis. (Q52795305) ‎ (← links)
• Syndromes with supernumerary teeth. (Q53782947) ‎ (← links)
• STAT3-Mediated Transcriptional Regulation of Osteopontin in STAT3 Loss-of-Function Related Hyper IgE Syndrome. (Q54942168) ‎ (← links)
• craniosynostosis and dental anomalies (Q55784239) ‎ (← links)
• Gene links skull and teeth abnormalities (Q56329338) ‎ (← links)
• Selective loss of function variants in IL6ST cause Hyper-IgE Syndrome with distinct impairments of T cell phenotype and function (Q57475968) ‎ (← links)
• Human hyper-IgE syndrome: singular or plural? (Q61632990) ‎ (← links)
• Signaling Mechanisms Underlying Genetic Pathophysiology of Craniosynostosis (Q61809349) ‎ (← links)
• A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity (Q62658170) ‎ (← links)
• IL-11 in cardiac and renal fibrosis: Late to the party but a central player (Q89542063) ‎ (← links)
• [The role of interleukin-11 in osteosarcoma] (Q89802560) ‎ (← links)
• IgE Glycosylation in Health and Disease (Q92027568) ‎ (← links)
• Differences in Shedding of the Interleukin-11 Receptor by the Proteases ADAM9, ADAM10, ADAM17, Meprin α, Meprin β and MT1-MMP (Q92257614) ‎ (← links)