| scholarly article | Q13442814 |
| P356 | DOI | 10.1242/DEV.125.16.3063 |
| P953 | full work available online at | http://dev.biologists.org/cgi/content/abstract/125/16/3063 |
| https://journals.biologists.com/dev/article-pdf/125/16/3063/3139252/develop_125_16_3063.pdf | ||
| P698 | PubMed publication ID | 9671580 |
| P2093 | author name string | M. Brand | |
| M. Busslinger | |||
| T. Gerster | |||
| P. L. Pfeffer | |||
| K. Lun | |||
| P2860 | cites work | Alternative splicing of Pax-8 gene transcripts is developmentally regulated and generates isoforms with different transactivation properties | Q24318806 |
| Deregulation of PAX-5 by translocation of the Emu enhancer of the IgH locus adjacent to two alternative PAX-5 promoters in a diffuse large-cell lymphoma | Q24606757 | ||
| Stages of embryonic development of the zebrafish | Q27860947 | ||
| Two-color whole-mount in situ hybridization to vertebrate and Drosophila embryos | Q28239551 | ||
| Follicular cells of the thyroid gland require Pax8 gene function | Q28271054 | ||
| Pax8, a murine paired box gene expressed in the developing excretory system and thyroid gland | Q28587076 | ||
| Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. | Q34314263 | ||
| The Pax2 homolog sparkling is required for development of cone and pigment cells in theDrosophila eye | Q35188802 | ||
| The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney | Q35934032 | ||
| Cooperation of Pax2 and Pax5 in midbrain and cerebellum development | Q36156319 | ||
| Conserved biological function between Pax-2 and Pax-5 in midbrain and cerebellum development: evidence from targeted mutations | Q36823395 | ||
| Zebrafishwnt8andwnt8bshare a common activity but are involved in distinct developmental pathways | Q38531729 | ||
| Involvement of Wnt1 and Pax2 in the formation of the midbrain‐hindbrain boundary in the zebrafish gastrula | Q38532050 | ||
| Mammalian Pax genes | Q40613979 | ||
| C-terminal activating and inhibitory domains determine the transactivation potential of BSAP (Pax-5), Pax-2 and Pax-8. | Q41064693 | ||
| Early mesencephalon/metencephalon patterning and development of the cerebellum | Q41724283 | ||
| Zebrafish pax[b] is involved in the formation of the midbrain-hindbrain boundary | Q44725306 | ||
| The paired domain-containing nuclear factor pax[b] is expressed in specific commissural interneurons in zebrafish embryos | Q47073782 | ||
| The characterization of novel Pax genes of the sea urchin and Drosophila reveal an ancient evolutionary origin of the Pax2/5/8 subfamily | Q47775692 | ||
| Comparative analysis of Pax-2 protein distributions during neurulation in mice and zebrafish | Q48435638 | ||
| Essential functions of Pax5 (BSAP) in pro-B cell development: difference between fetal and adult B lymphopoiesis and reduced V-to-DJ recombination at the IgH locus | Q52196159 | ||
| DNA sequence recognition by Pax proteins: bipartite structure of the paired domain and its binding site | Q52222420 | ||
| Vertebrate Palaeontology | Q56919375 | ||
| Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP | Q58326934 | ||
| Vertebrate genome evolution and the zebrafish gene map | Q74428368 | ||
| Coordinate embryonic expression of three zebrafish engrailed genes | Q112778217 | ||
| P433 | issue | 16 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Danio rerio | Q169444 |
| Paired box 2a | Q29822086 | ||
| P1104 | number of pages | 12 | |
| P304 | page(s) | 3063-3074 | |
| P577 | publication date | 1998-08-01 | |
| P1433 | published in | Development | Q3025404 |
| P1476 | title | Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 expression on the Pax2.1 (noi) function | |
| P478 | volume | 125 |
| Q21283806 | A symphony of inner ear developmental control genes |
| Q45204036 | Abundant corneal gelsolin in Zebrafish and the 'four-eyed' fish, Anableps anableps: possible analogy with multifunctional lens crystallins |
| Q30842196 | Ancestral and novel roles of Pax family genes in mollusks |
| Q30276371 | BMP and retinoic acid regulate anterior-posterior patterning of the non-axial mesoderm across the dorsal-ventral axis |
| Q28481285 | Characterization of Pax2 expression in the goldfish optic nerve head during retina regeneration |
| Q35850331 | Comparative genomics using Fugu reveals insights into regulatory subfunctionalization |
| Q42944450 | Conditions that influence the response to Fgf during otic placode induction |
| Q30666987 | Cooperative and independent functions of FGF and Wnt signaling during early inner ear development |
| Q33901600 | Correct anteroposterior patterning of the zebrafish neurectoderm in the absence of the early dorsal organizer. |
| Q35022221 | Dissecting teleost B cell differentiation using transcription factors |
| Q41663178 | Dlx3b/4b is required for early-born but not later-forming sensory hair cells during zebrafish inner ear development |
| Q33699382 | Duplicate dmbx1genes regulate progenitor cell cycle and differentiation during zebrafish midbrain and retinal development |
| Q57814132 | EF-hand domain containing 2 (Efhc2) is crucial for distal segmentation of pronephros in zebrafish |
| Q33518467 | Early evolution of conserved regulatory sequences associated with development in vertebrates |
| Q38365010 | Early steps in inner ear development: induction and morphogenesis of the otic placode |
| Q89055216 | Embryonic Stem Cell-Derived Peripheral Auditory Neurons Form Neural Connections with Mouse Central Auditory Neurons In Vitro via the α2δ1 Receptor |
| Q33362560 | Evolution of developmental roles of Pax2/5/8 paralogs after independent duplication in urochordate and vertebrate lineages |
| Q38557953 | Evx1 and Evx2 specify excitatory neurotransmitter fates and suppress inhibitory fates through a Pax2-independent mechanism. |
| Q28585081 | Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear |
| Q33269857 | Fgf-dependent otic induction requires competence provided by Foxi1 and Dlx3b |
| Q30521484 | Formation of the spinal network in zebrafish determined by domain-specific pax genes. |
| Q73597573 | Functional evolution in the ancestral lineage of vertebrates or when genomic complexity was wagging its morphological tail |
| Q38150656 | Gene regulatory network of renal primordium development |
| Q30451387 | Graded levels of Pax2a and Pax8 regulate cell differentiation during sensory placode formation |
| Q30415639 | HNF1β is essential for nephron segmentation during nephrogenesis |
| Q36527064 | Histone deacetylase 1 is required for the development of the zebrafish inner ear. |
| Q38159948 | Hnf1beta and nephron segmentation. |
| Q34059245 | Identification of B cells as a major site for cyprinid herpesvirus 3 latency |
| Q90480873 | Impaired intermediate formation in mouse embryos expressing reduced levels of Tbx6 |
| Q26765261 | Insights into kidney stem cell development and regeneration using zebrafish |
| Q28312182 | Isolation and expression analysis of foxj1 and foxj1.2 in zebrafish embryos |
| Q27694725 | Kidney organogenesis in the zebrafish: insights into vertebrate nephrogenesis and regeneration |
| Q28660316 | Localization of BDNF expression in the developing brain of zebrafish |
| Q33632027 | Maternal thyroid hormones are essential for neural development in zebrafish |
| Q34734332 | MicroRNA-183 family conservation and ciliated neurosensory organ expression |
| Q34558026 | Minor change, major difference: divergent functions of highly conserved cis-regulatory elements subsequent to whole genome duplication events |
| Q28654292 | Molecular analysis of neurogenic placode development in a basal ray-finned fish |
| Q39962950 | Molecular and cellular analysis of B-cell populations in the rainbow trout using Pax5 and immunoglobulin markers |
| Q28659308 | Molecular evolution of the vertebrate mechanosensory cell and ear |
| Q28585002 | Nephric lineage specification by Pax2 and Pax8 |
| Q26785918 | Nephron Patterning: Lessons from Xenopus, Zebrafish, and Mouse Studies |
| Q41646445 | Nephron proximal tubule patterning and corpuscles of Stannius formation are regulated by the sim1a transcription factor and retinoic acid in zebrafish |
| Q30369088 | Neurosensory Differentiation and Innervation Patterning in the Human Fetal Vestibular End Organs between the Gestational Weeks 8-12. |
| Q41876790 | Nkcc1 (Slc12a2) is required for the regulation of endolymph volume in the otic vesicle and swim bladder volume in the zebrafish larva |
| Q37468603 | Non-homeodomain regions of Hox proteins mediate activation versus repression of Six2 via a single enhancer site in vivo |
| Q28361877 | Origins of anteroposterior patterning and Hox gene regulation during chordate evolution |
| Q34186659 | PAX8 promotes tumor cell growth by transcriptionally regulating E2F1 and stabilizing RB protein |
| Q48174449 | Patterns of gene divergence and VL promoter activity in immunoglobulin light chain clusters of the channel catfish. |
| Q35684950 | Pax gene diversity in the basal cnidarian Acropora millepora (Cnidaria, Anthozoa): implications for the evolution of the Pax gene family |
| Q28512751 | Pax2 and Pax8 cooperate in mouse inner ear morphogenesis and innervation |
| Q41481970 | Pax2 and Pea3 synergize to activate a novel regulatory enhancer for spalt4 in the developing ear. |
| Q42418162 | Pax2 coordinates epithelial morphogenesis and cell fate in the inner ear. |
| Q35808758 | Pax2/5/8 and Pax6 alternative splicing events in basal chordates and vertebrates: a focus on paired box domain |
| Q39886410 | Pax2/8 act redundantly to specify glycinergic and GABAergic fates of multiple spinal interneurons |
| Q30469933 | Pax2/8 proteins coordinate sequential induction of otic and epibranchial placodes through differential regulation of foxi1, sox3 and fgf24 |
| Q38760594 | Pronephric tubule formation in zebrafish: morphogenesis and migration. |
| Q64078128 | Prostaglandin signaling regulates renal multiciliated cell specification and maturation |
| Q92063390 | Pseudolaric acid B inhibits PAX2 expression through Wnt signaling and induces BAX expression, therefore promoting apoptosis in HeLa cervical cancer cells |
| Q41978654 | Rapid identification of PAX2/5/8 direct downstream targets in the otic vesicle by combinatorial use of bioinformatics tools |
| Q41665931 | Rbms3 functions in craniofacial development by posttranscriptionally modulating TGF-β signaling |
| Q34426067 | Regionalisation and acquisition of polarity in the optic tectum |
| Q38979241 | Roles of Hedgehog pathway components and retinoic acid signalling in specifying zebrafish ventral spinal cord neurons |
| Q45179815 | Scratch2 prevents cell cycle re-entry by repressing miR-25 in postmitotic primary neurons. |
| Q28299254 | Semicircular canal morphogenesis in the zebrafish inner ear requires the function of gpr126 (lauscher), an adhesion class G protein-coupled receptor gene |
| Q28741138 | Shaping sound in space: the regulation of inner ear patterning |
| Q41048052 | Temporal and spatial requirements for Nodal-induced anterior mesendoderm and mesoderm in anterior neurulation |
| Q24596814 | The homeodomain protein vax1 is required for axon guidance and major tract formation in the developing forebrain |
| Q36660562 | The molecular basis of neurosensory cell formation in ear development: a blueprint for hair cell and sensory neuron regeneration? |
| Q30440464 | The myc road to hearing restoration |
| Q42905527 | The paired-box homeodomain transcription factor Pax6 binds to the upstream region of the TRAP gene promoter and suppresses receptor activator of NF-κB ligand (RANKL)-induced osteoclast differentiation. |
| Q28188638 | The role of Six1 in mammalian auditory system development |
| Q30401498 | The role of foxi family transcription factors in the development of the ear and jaw. |
| Q46113804 | The transcription factor six1 inhibits neuronal and promotes hair cell fate in the developing zebrafish (Danio rerio) inner ear. |
| Q44902326 | The zebrafish buttonhead-like factor Bts1 is an early regulator ofpax2.1expression during mid-hindbrain development |
| Q42860533 | TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency |
| Q24594237 | Transcriptional repression by Pax5 (BSAP) through interaction with corepressors of the Groucho family |
| Q27027305 | Where hearing starts: the development of the mammalian cochlea |
| Q38594630 | Wt1a, Foxc1a, and the Notch mediator Rbpj physically interact and regulate the formation of podocytes in zebrafish |
| Q34337070 | Zebrafish Lmx1b.1 and Lmx1b.2 are required for maintenance of the isthmic organizer |
| Q41940759 | Zebrafish Tbx16 regulates intermediate mesoderm cell fate by attenuating Fgf activity |
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| Q30527836 | Zebrafish larvae exposed to ginkgotoxin exhibit seizure-like behavior that is relieved by pyridoxal-5'-phosphate, GABA and anti-epileptic drugs |
| Q41943633 | Zebrafish nephrogenesis is regulated by interactions between retinoic acid, mecom, and Notch signaling |
| Q42590691 | Zebrafish zic2a patterns the forebrain through modulation of Hedgehog-activated gene expression |
| Q33637124 | spiel ohne grenzen/pou2 is required during establishment of the zebrafish midbrain-hindbrain boundary organizer |
| Q39930689 | vox homeobox gene: a novel regulator of midbrain-hindbrain boundary development in medaka fish? |
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