| P50 | author | Karen Steel | Q15109532 |
| | Martin Hrabě de Angelis | Q28606776 |
| P2093 | author name string | Helmut Fuchs | |
| | Erika A Bosman | |
| | Elizabeth Quint | |
| P2860 | cites work | SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes | Q24292967 |
| | A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family | Q24318377 |
| | Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome | Q24682920 |
| | The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear | Q25256767 |
| | The role of Six1 in mammalian auditory system development | Q28188638 |
| | A family with the branchio-oto-renal syndrome: clinical and genetic correlations | Q28198376 |
| | Mouse Serrate-1 (Jagged-1): expression in the developing tooth is regulated by epithelial-mesenchymal interactions and fibroblast growth factor-4. | Q52195580 |
| | Expression of zebrafish six1 during sensory organ development and myogenesis. | Q52649463 |
| | Standard atlas of the gross anatomy of the developing inner ear of the chicken. | Q53623285 |
| | The development of semicircular canals in the inner ear: role of FGFs in sensory cristae | Q61852088 |
| | Molecular cloning and embryonic expression of Xenopus Six homeobox genes | Q73568844 |
| | Thymus, kidney and craniofacial abnormalities in Six 1 deficient mice | Q73593261 |
| | Genetic heterogeneity associated with branchio-oto-renal syndrome | Q74650984 |
| | SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with branchio-oto syndrome | Q28237702 |
| | Distinct expression patterns of notch family receptors and ligands during development of the mammalian inner ear | Q28291907 |
| | Slc12a2 is a direct target of two closely related homeobox proteins, Six1 and Six4 | Q28507323 |
| | Six1 is required for the early organogenesis of mammalian kidney | Q28510085 |
| | Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear | Q28585081 |
| | Initiation of olfactory placode development and neurogenesis is blocked in mice lacking both Six1 and Six4 | Q28585270 |
| | Sox2 is required for sensory organ development in the mammalian inner ear | Q28585583 |
| | Multiple mutations in mouse Chd7 provide models for CHARGE syndrome | Q28587098 |
| | Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia | Q28587212 |
| | Six1 controls patterning of the mouse otic vesicle | Q28589213 |
| | Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome | Q28593604 |
| | The role of Pax2 in mouse inner ear development | Q28595027 |
| | Advances in hereditary deafness | Q30665416 |
| | The Notch ligand Jagged1 is required for inner ear sensory development. | Q35043790 |
| | Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion | Q38289851 |
| | Localization of calretinin mRNA in rat and guinea pig inner ear by in situ hybridization using radioactive and non-radioactive probes | Q38316605 |
| | A single amino acid can determine the DNA binding specificity of homeodomain proteins. | Q38343141 |
| | DAN directs endolymphatic sac and duct outgrowth in the avian inner ear. | Q38345462 |
| | The paintfill method as a tool for analyzing the three-dimensional structure of the inner ear. | Q38468893 |
| | Two contrasting roles for Notch activity in chick inner ear development: specification of prosensory patches and lateral inhibition of hair-cell differentiation. | Q40456713 |
| | Involvement of Bone Morphogenetic Protein-4 (BMP-4) and Vgr-1 in morphogenesis and neurogenesis in the mouse | Q41161285 |
| | Six1 is essential for early neurogenesis in the development of olfactory epithelium | Q42519074 |
| | Genome-wide, large-scale production of mutant mice by ENU mutagenesis. | Q43520565 |
| | The transcription factor six1 inhibits neuronal and promotes hair cell fate in the developing zebrafish (Danio rerio) inner ear. | Q46113804 |
| | Mutations affecting development of the zebrafish inner ear and lateral line. | Q47073141 |
| | Comparative morphology of rodent vestibular periphery. II. Cristae ampullares | Q47231004 |
| | Molecular anatomy of placode development in Xenopus laevis | Q47273875 |
| | Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome | Q48460077 |
| | In situ hybridization and reverse transcription--polymerase chain reaction studies on the expression of the GABA(C) receptor rho1- and rho2-subunit genes in avian and rat brain. | Q48535348 |
| | Incus and stapes necrosis associated with diabetes mellitus | Q50463406 |
| | A compendium of mouse knockouts with inner ear defects. | Q50486350 |
| | Familial branchio-oto-renal dysplasia: A new addition to the branchial arch syndromes | Q50628136 |
| | Temporal bone anomalies in the branchio-oto-renal syndrome: detailed computed tomographic and magnetic resonance imaging findings. | Q50760293 |
| | Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor. | Q52085976 |
| | Development of the mouse inner ear and origin of its sensory organs. | Q52188228 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Sine oculis-related homeobox 1 | Q21981883 |
| | Jagged 1 | Q21985075 |
| P304 | page(s) | 285-296 | |
| P577 | publication date | 2009-02-02 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | Catweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome | |
| P478 | volume | 328 | |