| scholarly article | Q13442814 |
| P50 | author | Thomas M. Maynard | Q37369807 |
| Andrea Streit | Q38803999 | ||
| Sally A Moody | Q43142574 | ||
| Ramya Ranganathan | Q57741877 | ||
| P2093 | author name string | Bo Yan | |
| Karen M Neilson | |||
| P2860 | cites work | Combined Whole-Mount in Situ Hybridization and Immunohistochemistry in Avian Embryos | Q59971442 |
| Molecular cloning and embryonic expression of Xenopus Six homeobox genes | Q73568844 | ||
| Thymus, kidney and craniofacial abnormalities in Six 1 deficient mice | Q73593261 | ||
| Branchio-oto-renal syndrome | Q75210297 | ||
| Competence of cranial ectoderm to respond to Fgf signaling suggests a two-step model of otic placode induction | Q82444181 | ||
| Identification of a novel EYA1 mutation presenting in a newborn with laryngomalacia, glossoptosis, retrognathia, and pectus excavatum | Q83324749 | ||
| How old genes make a new head: redeployment of Six and Eya genes during the evolution of vertebrate cranial placodes | Q84359707 | ||
| SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes | Q24292967 | ||
| Biochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutations | Q24317065 | ||
| A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family | Q24318377 | ||
| Structure, function and expression of a murine homeobox protein AREC3, a homologue of Drosophila sine oculis gene product, and implication in development | Q24545877 | ||
| Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya | Q24554423 | ||
| The Six1 homeoprotein stimulates tumorigenesis by reactivation of cyclin A1 | Q24564859 | ||
| Abrogation of the G2 cell cycle checkpoint associated with overexpression of HSIX1: a possible mechanism of breast carcinogenesis | Q24644884 | ||
| The origin and evolution of the ectodermal placodes | Q27012962 | ||
| Identification of early requirements for preplacodal ectoderm and sensory organ development | Q27345912 | ||
| Structure-function analyses of the human SIX1–EYA2 complex reveal insights into metastasis and BOR syndrome | Q27676610 | ||
| Primer3 on the WWW for general users and for biologist programmers | Q27861030 | ||
| Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing | Q28143175 | ||
| The role of Six1 in mammalian auditory system development | Q28188638 | ||
| Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins | Q28214522 | ||
| Six and Eya expression during human somitogenesis and MyoD gene family activation | Q28219080 | ||
| SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with branchio-oto syndrome | Q28237702 | ||
| Catweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome | Q28506861 | ||
| Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodes | Q28508554 | ||
| Six1 is required for the early organogenesis of mammalian kidney | Q28510085 | ||
| Initiation of olfactory placode development and neurogenesis is blocked in mice lacking both Six1 and Six4 | Q28585270 | ||
| Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1 | Q28586633 | ||
| Six1 controls patterning of the mouse otic vesicle | Q28589213 | ||
| A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis | Q28589314 | ||
| Expression of myogenin during embryogenesis is controlled by Six/sine oculis homeoproteins through a conserved MEF3 binding site | Q28589912 | ||
| Neuropilin 1 and 2 control cranial gangliogenesis and axon guidance through neural crest cells | Q28590138 | ||
| Six1 and Six4 promote survival of sensory neurons during early trigeminal gangliogenesis | Q28592504 | ||
| Six1 and Six4 homeoproteins are required for Pax3 and Mrf expression during myogenesis in the mouse embryo | Q28593548 | ||
| Balancing cell numbers during organogenesis: Six1a differentially affects neurons and sensory hair cells in the inner ear. | Q30425138 | ||
| Isthmin is a novel secreted protein expressed as part of the Fgf-8 synexpression group in the Xenopus midbrain-hindbrain organizer | Q30705224 | ||
| Xpbx1b and Xmeis1b play a collaborative role in hindbrain and neural crest gene expression in Xenopus embryos | Q31048761 | ||
| Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays | Q33202352 | ||
| Early development of the central and peripheral nervous systems is coordinated by Wnt and BMP signals | Q33320527 | ||
| Remembrance of things PAS: regulation of development by bHLH-PAS proteins | Q33745070 | ||
| Six1 is a key regulator of the developmental and evolutionary architecture of sensory neurons in craniates | Q33855467 | ||
| Xenopus NF-Y pre-sets chromatin to potentiate p300 and acetylation-responsive transcription from the Xenopus hsp70 promoter in vivo | Q33889834 | ||
| Six family genes--structure and function as transcription factors and their roles in development | Q33957333 | ||
| Vertebrate GLD2 poly(A) polymerases in the germline and the brain | Q34366483 | ||
| Six1 promotes proliferation of pancreatic cancer cells via upregulation of cyclin D1 expression | Q34634833 | ||
| Regulation of Drosophila eye development by the transcription factor Sine oculis. | Q35107917 | ||
| Dual transcriptional activities of SIX proteins define their roles in normal and ectopic eye development | Q35741929 | ||
| The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border | Q35810702 | ||
| Early development of the cranial sensory nervous system: from a common field to individual placodes | Q35942303 | ||
| Induction and specification of the vertebrate ectodermal placodes: precursors of the cranial sensory organs | Q36100723 | ||
| Sensory organs: making and breaking the pre-placodal region | Q36431499 | ||
| The preplacodal region: an ectodermal domain with multipotential progenitors that contribute to sense organs and cranial sensory ganglia. | Q36950092 | ||
| Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus | Q37021446 | ||
| From shared lineage to distinct functions: the development of the inner ear and epibranchial placodes. | Q37749102 | ||
| Making senses development of vertebrate cranial placodes | Q37783809 | ||
| The peripheral sensory nervous system in the vertebrate head: a gene regulatory perspective | Q38025839 | ||
| The aryl hydrocarbon receptor nuclear translocator (ARNT) family of proteins: transcriptional modifiers with multi-functional protein interfaces | Q38056974 | ||
| Human HOX gene disorders. | Q38163195 | ||
| Establishing the pre-placodal region and breaking it into placodes with distinct identities | Q38191727 | ||
| Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion | Q38289851 | ||
| Activation of Six1 target genes is required for sensory placode formation | Q39944176 | ||
| A balance of FGF, BMP and WNT signalling positions the future placode territory in the head | Q40398079 | ||
| Cell lineage analysis in Xenopus embryos | Q40882843 | ||
| Tissue and developmental distribution of Six family gene products. | Q41049478 | ||
| Xema, a foxi-class gene expressed in the gastrula stage Xenopus ectoderm, is required for the suppression of mesendoderm. | Q41868105 | ||
| Xiro, a Xenopus homolog of the Drosophila Iroquois complex genes, controls development at the neural plate | Q41976395 | ||
| Six1 is indispensable for production of functional progenitor cells during olfactory epithelial development | Q42483671 | ||
| Six1 is essential for early neurogenesis in the development of olfactory epithelium | Q42519074 | ||
| Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network | Q42690246 | ||
| dlx3b/4b are required for the formation of the preplacodal region and otic placode through local modulation of BMP activity | Q43138530 | ||
| foxD5 plays a critical upstream role in regulating neural ectodermal fate and the onset of neural differentiation | Q43142498 | ||
| Zebrafish fgf3 and fgf8 encode redundant functions required for otic placode induction | Q43661877 | ||
| Retinoic acid perturbs the expression of Xhox.lab genes and alters mesodermal determination in Xenopus laevis | Q43719396 | ||
| Tumorhead, a Xenopus gene product that inhibits neural differentiation through regulation of proliferation | Q43730350 | ||
| Fgf3 and Fgf8 are required together for formation of the otic placode and vesicle | Q43963574 | ||
| Fgf8 and Fgf3 are required for zebrafish ear placode induction, maintenance and inner ear patterning | Q44183757 | ||
| Regulation of Six1 expression by evolutionarily conserved enhancers in tetrapods | Q45098841 | ||
| SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR. | Q45219645 | ||
| Essential role for PDGF signaling in ophthalmic trigeminal placode induction. | Q45931416 | ||
| The transcription factor six1 inhibits neuronal and promotes hair cell fate in the developing zebrafish (Danio rerio) inner ear. | Q46113804 | ||
| A novel dominant mutation in SIX1, affecting a highly conserved residue, result in only auditory defects in humans | Q46350444 | ||
| The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system | Q46456013 | ||
| Fgf3 and Fgf8 dependent and independent transcription factors are required for otic placode specification | Q47073913 | ||
| Combinatorial activity of Six1-2-4 genes in cephalic neural crest cells controls craniofacial and brain development | Q47717338 | ||
| Xenopus Six1 gene is expressed in neurogenic cranial placodes and maintained in the differentiating lateral lines | Q47834355 | ||
| Six3, a murine homologue of the sine oculis gene, demarcates the most anterior border of the developing neural plate and is expressed during eye development. | Q48068853 | ||
| Molecular cloning and embryonic expression of the Xenopus Arnt gene | Q48340804 | ||
| Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm | Q48668204 | ||
| Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis | Q48705949 | ||
| Semaphorin and neuropilin expression during early morphogenesis of Xenopus laevis | Q48846064 | ||
| Xotx genes in the developing brain of Xenopus laevis | Q49019903 | ||
| Audiovestibular findings in a branchio-oto syndrome patient with a SIX1 mutation | Q50435298 | ||
| Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses | Q50456642 | ||
| Wnt-regulated temporal control of BMP exposure directs the choice between neural plate border and epidermal fate. | Q51945248 | ||
| Lens specification is the ground state of all sensory placodes, from which FGF promotes olfactory identity. | Q52005744 | ||
| An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation. | Q52042524 | ||
| Expression of Xenopus suppressor of cytokine signaling 3 (xSOCS3) is induced by epithelial wounding. | Q52049293 | ||
| Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor. | Q52085976 | ||
| Genetic determination of nephrogenesis: the Pax/Eya/Six gene network. | Q52096291 | ||
| Developmental changes in nerve growth factor (NGF) binding and NGF receptor proteins trkA and p75 in the facial nerve. | Q52215842 | ||
| Expression of zebrafish six1 during sensory organ development and myogenesis. | Q52649463 | ||
| Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR. | Q53323989 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 181-210 | |
| P577 | publication date | 2014-12-16 | |
| P1433 | published in | Developmental Dynamics | Q59752 |
| P1476 | title | Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development | |
| P478 | volume | 244 |
| Q46523851 | A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates |
| Q37684715 | An optimized method for cryogenic storage of Xenopus sperm to maximise the effectiveness of research using genetically altered frogs. |
| Q37280146 | Dissecting the pre-placodal transcriptome to reveal presumptive direct targets of Six1 and Eya1 in cranial placodes. |
| Q64062735 | Modeling congenital kidney diseases in |
| Q90356966 | Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation |
| Q92930977 | Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development |
| Q28081644 | Transcriptional regulation of cranial sensory placode development |
| Q28607001 | Using Xenopus to discover new genes involved in branchiootorenal spectrum disorders |
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