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Search results 1 to 100 out of 197 for Eya1

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Category: Publication
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Type Details Score
Publication
10072433 | J:54408
First Author: Johnson KR
Year: 1999
Journal: Hum Mol Genet
Title: Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome.
Volume: 8
Issue: 4
Pages: 645-53
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Publication
24489909 | J:212689
First Author: Musharraf A
Year: 2014
Journal: PLoS One
Title: BOR-syndrome-associated Eya1 mutations lead to enhanced proteasomal degradation of Eya1 protein.
Volume: 9
Issue: 1
Pages: e87407
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Publication
17098221 | J:119948
First Author: Grifone R
Year: 2007
Journal: Dev Biol
Title: Eya1 and Eya2 proteins are required for hypaxial somitic myogenesis in the mouse embryo.
Volume: 302
Issue: 2
Pages: 602-16
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Publication
25816987 | J:239288
First Author: Eisner A
Year: 2015
Journal: Dev Cell
Title: The Eya1 phosphatase promotes Shh signaling during hindbrain development and oncogenesis.
Volume: 33
Issue: 1
Pages: 22-35
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Publication
14517553 | J:86371
First Author: Floyd JA
Year: 2003
Journal: Nat Genet
Title: A natural allele of Nxf1 suppresses retrovirus insertional mutations.
Volume: 35
Issue: 3
Pages: 221-8
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Publication
12070080 | J:79848
First Author: Xu PX
Year: 2002
Journal: Development
Title: Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid.
Volume: 129
Issue: 13
Pages: 3033-44
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Publication
15226428 | J:91574
First Author: Grifone R
Year: 2004
Journal: Mol Cell Biol
Title: Six1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotype.
Volume: 24
Issue: 14
Pages: 6253-67
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Publication
25458011 | J:250210
First Author: Xu J
Year: 2014
Journal: Dev Cell
Title: Eya1 interacts with Six2 and Myc to regulate expansion of the nephron progenitor pool during nephrogenesis.
Volume: 31
Issue: 4
Pages: 434-47
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Publication
24752894 | J:223694
First Author: Sun Y
Year: 2014
Journal: Mol Cell Biol
Title: The canonical wnt signal restricts the glycogen synthase kinase 3/fbw7-dependent ubiquitination and degradation of eya1 phosphatase.
Volume: 34
Issue: 13
Pages: 2409-17
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Publication
11734542 | J:124751
First Author: Buller C
Year: 2001
Journal: Hum Mol Genet
Title: Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome.
Volume: 10
Issue: 24
Pages: 2775-81
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Publication
16024294 | J:103131
First Author: Purcell P
Year: 2005
Journal: Gene Expr Patterns
Title: Pax6-dependence of Six3, Eya1 and Dach1 expression during lens and nasal placode induction.
Volume: 6
Issue: 1
Pages: 110-8
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Publication
22685326 | J:198889
First Author: El-Hashash AH
Year: 2012
Journal: J Cell Sci
Title: Eya1 protein phosphatase regulates tight junction formation in lung distal epithelium.
Volume: 125
Issue: Pt 17
Pages: 4036-48
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Publication
18678597 | J:140027
First Author: Zou D
Year: 2008
Journal: Hum Mol Genet
Title: Eya1 gene dosage critically affects the development of sensory epithelia in the mammalian inner ear.
Volume: 17
Issue: 21
Pages: 3340-56
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Publication
21968101 | J:178455
First Author: Wang C
Year: 2011
Journal: Dev Biol
Title: Six1 and Eya1 are critical regulators of peri-cloacal mesenchymal progenitors during genitourinary tract development.
Volume: 360
Issue: 1
Pages: 186-94
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Publication
34716243 | J:330416
First Author: Li J
Year: 2021
Journal: J Am Soc Nephrol
Title: Chromatin Remodelers Interact with Eya1 and Six2 to Target Enhancers to Control Nephron Progenitor Cell Maintenance.
Volume: 32
Issue: 11
Pages: 2815-2833
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Publication
18836772 | J:148630
First Author: Niu H
Year: 2008
Journal: Mamm Genome
Title: Mapping of genetic modifiers of Eya1 ( bor/bor ) in CAST/EiJ and BALB/cJ that suppress cochlear aplasia and associated deafness.
Volume: 19
Issue: 9
Pages: 634-9
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Publication
15817220 | J:98114
First Author: Friedman RA
Year: 2005
Journal: Mech Dev
Title: Eya1 acts upstream of Tbx1, Neurogenin 1, NeuroD and the neurotrophins BDNF and NT-3 during inner ear development.
Volume: 122
Issue: 5
Pages: 625-34
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Publication
15496442 | J:94396
First Author: Zou D
Year: 2004
Journal: Development
Title: Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodes.
Volume: 131
Issue: 22
Pages: 5561-72
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Publication
9853969 | J:51285
First Author: Kalatzis V
Year: 1998
Journal: Dev Dyn
Title: Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome.
Volume: 213
Issue: 4
Pages: 486-99
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Publication
37181748 | J:335760
 
First Author: Zhang T
Year: 2023
Journal: Front Cell Dev Biol
Title: The role of Eya1 and Eya2 in the taste system of mice from embryonic stage to adulthood.
Volume: 11
Pages: 1126968
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Publication
21385765 | J:171504
First Author: El-Hashash AH
Year: 2011
Journal: Development
Title: Eya1 controls cell polarity, spindle orientation, cell fate and Notch signaling in distal embryonic lung epithelium.
Volume: 138
Issue: 7
Pages: 1395-407
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Publication
36130284 | J:330216
First Author: Li J
Year: 2022
Journal: Nucleic Acids Res
Title: The transcriptional coactivator Eya1 exerts transcriptional repressive activity by interacting with REST corepressors and REST-binding sequences to maintain nephron progenitor identity.
Volume: 50
Issue: 18
Pages: 10343-10359
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Publication
22513373 | J:184001
First Author: Ahmed M
Year: 2012
Journal: Development
Title: EYA1 and SIX1 drive the neuronal developmental program in cooperation with the SWI/SNF chromatin-remodeling complex and SOX2 in the mammalian inner ear.
Volume: 139
Issue: 11
Pages: 1965-77
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Publication
16916509 | J:119574
First Author: Zou D
Year: 2006
Journal: Dev Biol
Title: Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear.
Volume: 298
Issue: 2
Pages: 430-41
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Publication
9020840 | J:38771
First Author: Abdelhak S
Year: 1997
Journal: Nat Genet
Title: A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.
Volume: 15
Issue: 2
Pages: 157-64
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Publication
16488112 | J:114904
First Author: Niu H
Year: 2006
Journal: Genomics
Title: Identification of two major loci that suppress hearing loss and cochlear dysmorphogenesis in Eya1bor/bor mice.
Volume: 88
Issue: 3
Pages: 302-8
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17785448 | J:129070
First Author: Gong KQ
Year: 2007
Journal: Mol Cell Biol
Title: A Hox-Eya-Pax complex regulates early kidney developmental gene expression.
Volume: 27
Issue: 21
Pages: 7661-8
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Publication
22340499 | J:181471
First Author: Ahmed M
Year: 2012
Journal: Dev Cell
Title: Eya1-Six1 interaction is sufficient to induce hair cell fate in the cochlea by activating Atoh1 expression in cooperation with Sox2.
Volume: 22
Issue: 2
Pages: 377-90
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Publication
9342347 | J:43703
First Author: Xu PX
Year: 1997
Journal: Proc Natl Acad Sci U S A
Title: Mouse Eya genes are expressed during limb tendon development and encode a transcriptional activation function.
Volume: 94
Issue: 22
Pages: 11974-9
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Publication
21364285 | J:172023
First Author: Guo C
Year: 2011
Journal: J Clin Invest
Title: A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis.
Volume: 121
Issue: 4
Pages: 1585-95
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Publication
20503367 | J:160589
First Author: Freyer L
Year: 2010
Journal: Dev Dyn
Title: Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle.
Volume: 239
Issue: 6
Pages: 1708-22
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Publication
29140246 | J:254919
   
First Author: Zhang H
Year: 2017
Journal: Elife
Title: An Eya1-Notch axis specifies bipotential epibranchial differentiation in mammalian craniofacial morphogenesis.
Volume: 6
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11804780 | J:74492
First Author: Heanue TA
Year: 2002
Journal: Mech Dev
Title: Dach1, a vertebrate homologue of Drosophila dachshund, is expressed in the developing eye and ear of both chick and mouse and is regulated independently of Pax and Eya genes.
Volume: 111
Issue: 1-2
Pages: 75-87
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Publication
19234442 | J:147286
First Author: Cook PJ
Year: 2009
Journal: Nature
Title: Tyrosine dephosphorylation of H2AX modulates apoptosis and survival decisions.
Volume: 458
Issue: 7238
Pages: 591-6
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20956555 | J:187563
First Author: Landgraf K
Year: 2010
Journal: Mol Cell Biol
Title: Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development.
Volume: 30
Issue: 24
Pages: 5764-75
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Publication
35178390 | J:320689
 
First Author: Xu J
Year: 2022
Journal: Front Cell Dev Biol
Title: Six1 and Six2 of the Sine Oculis Homeobox Subfamily are Not Functionally Interchangeable in Mouse Nephron Formation.
Volume: 10
Pages: 815249
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Publication
9887327 | J:52368
First Author: Borsani G
Year: 1999
Journal: Hum Mol Genet
Title: EYA4, a novel vertebrate gene related to Drosophila eyes absent.
Volume: 8
Issue: 1
Pages: 11-23
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Publication
10471511 | J:57313
First Author: Xu PX
Year: 1999
Journal: Nat Genet
Title: Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia.
Volume: 23
Issue: 1
Pages: 113-7
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Publication
12050119 | J:88686
First Author: Wellik DM
Year: 2002
Journal: Genes Dev
Title: Hox11 paralogous genes are essential for metanephric kidney induction.
Volume: 16
Issue: 11
Pages: 1423-32
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30561639 | J:274580
First Author: Bademci G
Year: 2019
Journal: Hum Mol Genet
Title: FOXF2 is required for cochlear development in humans and mice.
Volume: 28
Issue: 8
Pages: 1286-1297
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16442091 | J:107078
First Author: Poladia DP
Year: 2006
Journal: Dev Biol
Title: Role of fibroblast growth factor receptors 1 and 2 in the metanephric mesenchyme.
Volume: 291
Issue: 2
Pages: 325-39
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Publication
20110314 | J:157941
First Author: Nie X
Year: 2010
Journal: Development
Title: SIX1 acts synergistically with TBX18 in mediating ureteral smooth muscle formation.
Volume: 137
Issue: 5
Pages: 755-65
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Publication
23895934 | J:202226
First Author: Lu K
Year: 2013
Journal: Dev Biol
Title: Abrogation of Eya1/Six1 disrupts the saccular phase of lung morphogenesis and causes remodeling.
Volume: 382
Issue: 1
Pages: 110-23
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Publication
9006082 | J:38379
First Author: Xu PX
Year: 1997
Journal: Development
Title: Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode.
Volume: 124
Issue: 1
Pages: 219-31
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Publication
12783782 | J:83432
First Author: Xu PX
Year: 2003
Journal: Development
Title: Six1 is required for the early organogenesis of mammalian kidney.
Volume: 130
Issue: 14
Pages: 3085-94
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Publication
14628042 | J:86619
First Author: Li X
Year: 2003
Journal: Nature
Title: Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis.
Volume: 426
Issue: 6964
Pages: 247-54
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Publication
16530750 | J:108725
First Author: Zou D
Year: 2006
Journal: Dev Biol
Title: Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1.
Volume: 293
Issue: 2
Pages: 499-512
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Publication
21129374 | J:170236
First Author: El-Hashash AH
Year: 2011
Journal: Dev Biol
Title: Eyes absent 1 (Eya1) is a critical coordinator of epithelial, mesenchymal and vascular morphogenesis in the mammalian lung.
Volume: 350
Issue: 1
Pages: 112-26
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Publication
23614009 | J:200106
First Author: Duncan JS
Year: 2013
Journal: PLoS One
Title: Continued expression of GATA3 is necessary for cochlear neurosensory development.
Volume: 8
Issue: 4
Pages: e62046
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Publication
12874121 | J:84974
First Author: Zheng W
Year: 2003
Journal: Development
Title: The role of Six1 in mammalian auditory system development.
Volume: 130
Issue: 17
Pages: 3989-4000
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Publication
16990542 | J:112841
First Author: Alkuraya FS
Year: 2006
Journal: Science
Title: SUMO1 haploinsufficiency leads to cleft lip and palate.
Volume: 313
Issue: 5794
Pages: 1751
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Publication
14628052 | J:86608
First Author: Rayapureddi JP
Year: 2003
Journal: Nature
Title: Eyes absent represents a class of protein tyrosine phosphatases.
Volume: 426
Issue: 6964
Pages: 295-8
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Publication
15141091 | J:90664
First Author: Ruf RG
Year: 2004
Journal: Proc Natl Acad Sci U S A
Title: SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
Volume: 101
Issue: 21
Pages: 8090-5
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Publication
32988586 | J:304751
First Author: Fédou C
Year: 2020
Journal: Biochem Biophys Res Commun
Title: The low affinity p75 neurotrophin receptor is down-regulated in congenital anomalies of the kidney and the urinary tract: Possible involvement in early nephrogenesis.
Volume: 533
Issue: 4
Pages: 786-791
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10370123 | J:56122
First Author: Sahly I
Year: 1999
Journal: Dev Genes Evol
Title: The zebrafish eya1 gene and its expression pattern during embryogenesis.
Volume: 209
Issue: 7
Pages: 399-410
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10490620 | J:113793
First Author: Ohto H
Year: 1999
Journal: Mol Cell Biol
Title: Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya.
Volume: 19
Issue: 10
Pages: 6815-24
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9915577 | J:51920
First Author: Caubit X
Year: 1999
Journal: Dev Dyn
Title: Mouse Dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud.
Volume: 214
Issue: 1
Pages: 66-80
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Publication
28892484 | J:264213
First Author: Zhang T
Year: 2017
Journal: PLoS Genet
Title: Six1 is essential for differentiation and patterning of the mammalian auditory sensory epithelium.
Volume: 13
Issue: 9
Pages: e1006967
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Publication
- | J:79402
     
First Author: The Jackson Laboratory Office of Genetic Resources
Year: 1983
Journal: MGI Direct Data Submission
Title: Registry of Remutation at The Jackson Laboratory, 1983-1984
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28492243 | J:249581
 
First Author: Xu J
Year: 2017
Journal: Nat Commun
Title: Identification of mouse cochlear progenitors that develop hair and supporting cells in the organ of Corti.
Volume: 8
Pages: 15046
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18219393 | J:131873
First Author: Depreux FF
Year: 2008
Journal: J Clin Invest
Title: Eya4-deficient mice are a model for heritable otitis media.
Volume: 118
Issue: 2
Pages: 651-8
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11700312 | J:74329
First Author: Clark SW
Year: 2002
Journal: J Biol Chem
Title: Misexpression of the eyes absent family triggers the apoptotic program.
Volume: 277
Issue: 5
Pages: 3560-7
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14973294 | J:88584
First Author: Tucker AS
Year: 2004
Journal: Development
Title: Bapx1 regulates patterning in the middle ear: altered regulatory role in the transition from the proximal jaw during vertebrate evolution.
Volume: 131
Issue: 6
Pages: 1235-45
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Publication
9195991 | J:41373
First Author: Duncan MK
Year: 1997
Journal: Mamm Genome
Title: Eyes absent: a gene family found in several metazoan phyla.
Volume: 8
Issue: 7
Pages: 479-85
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19716816 | J:154470
First Author: Yallowitz AR
Year: 2009
Journal: Dev Biol
Title: Non-homeodomain regions of Hox proteins mediate activation versus repression of Six2 via a single enhancer site in vivo.
Volume: 335
Issue: 1
Pages: 156-65
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Publication
16790474 | J:117734
First Author: James RG
Year: 2006
Journal: Development
Title: Odd-skipped related 1 is required for development of the metanephric kidney and regulates formation and differentiation of kidney precursor cells.
Volume: 133
Issue: 15
Pages: 2995-3004
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Publication
25903664 | J:223331
First Author: Xu J
Year: 2015
Journal: Dev Dyn
Title: Eya-six are necessary for survival of nephrogenic cord progenitors and inducing nephric duct development before ureteric bud formation.
Volume: 244
Issue: 7
Pages: 866-73
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Publication
15130495 | J:90324
First Author: Grieshammer U
Year: 2004
Journal: Dev Cell
Title: SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site.
Volume: 6
Issue: 5
Pages: 709-17
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Publication
31956913 | J:291604
First Author: Li J
Year: 2020
Journal: Nucleic Acids Res
Title: Dynamic changes in cis-regulatory occupancy by Six1 and its cooperative interactions with distinct cofactors drive lineage-specific gene expression programs during progressive differentiation of the auditory sensory epithelium.
Volume: 48
Issue: 6
Pages: 2880-2896
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21936910 | J:177132
 
First Author: Rapicavoli NA
Year: 2011
Journal: Neural Dev
Title: The long noncoding RNA Six3OS acts in trans to regulate retinal development by modulating Six3 activity.
Volume: 6
Pages: 32
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20589882 | J:163648
First Author: Fairbridge NA
Year: 2010
Journal: Birth Defects Res A Clin Mol Teratol
Title: Cecr2 mutations causing exencephaly trigger misregulation of mesenchymal/ectodermal transcription factors.
Volume: 88
Issue: 8
Pages: 619-25
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Publication
30635573 | J:270550
First Author: Yermalovich AV
Year: 2019
Journal: Nat Commun
Title: Lin28 and let-7 regulate the timing of cessation of murine nephrogenesis.
Volume: 10
Issue: 1
Pages: 168
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Publication
21128305 | J:167305
First Author: Sims-Lucas S
Year: 2011
Journal: Dev Dyn
Title: Fgfr1 and the IIIc isoform of Fgfr2 play critical roles in the metanephric mesenchyme mediating early inductive events in kidney development.
Volume: 240
Issue: 1
Pages: 240-9
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Publication
36205075 | J:331052
 
First Author: Sharma A
Year: 2022
Journal: Development
Title: FGF8 induces chemokinesis and regulates condensation of mouse nephron progenitor cells.
Volume: 149
Issue: 21
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15499560 | J:93820
First Author: Lilleväli K
Year: 2004
Journal: Dev Dyn
Title: Partially overlapping expression of Gata2 and Gata3 during inner ear development.
Volume: 231
Issue: 4
Pages: 775-81
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Publication
24067355 | J:204605
First Author: Minoux M
Year: 2013
Journal: Development
Title: Mouse Hoxa2 mutations provide a model for microtia and auricle duplication.
Volume: 140
Issue: 21
Pages: 4386-97
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Publication
20727173 | J:163537
 
First Author: Bouchard M
Year: 2010
Journal: BMC Dev Biol
Title: Pax2 and Pax8 cooperate in mouse inner ear morphogenesis and innervation.
Volume: 10
Pages: 89
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Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
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Publication
11688560 | J:71242
First Author: Nishinakamura R
Year: 2001
Journal: Development
Title: Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development.
Volume: 128
Issue: 16
Pages: 3105-15
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Publication
24598167 | J:208647
First Author: Xu J
Year: 2014
Journal: Development
Title: Osr1 acts downstream of and interacts synergistically with Six2 to maintain nephron progenitor cells during kidney organogenesis.
Volume: 141
Issue: 7
Pages: 1442-52
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Publication
12642503 | J:82307
First Author: Hulander M
Year: 2003
Journal: Development
Title: Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice.
Volume: 130
Issue: 9
Pages: 2013-25
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Publication
33723076 | J:304643
 
First Author: Xu J
Year: 2021
Journal: Proc Natl Acad Sci U S A
Title: Chromatin remodelers and lineage-specific factors interact to target enhancers to establish proneurosensory fate within otic ectoderm.
Volume: 118
Issue: 12
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Publication
16018995 | J:100569
First Author: Sajithlal G
Year: 2005
Journal: Dev Biol
Title: Eya 1 acts as a critical regulator for specifying the metanephric mesenchyme.
Volume: 284
Issue: 2
Pages: 323-36
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Publication
18485340 | J:137524
First Author: Mugford JW
Year: 2008
Journal: Dev Biol
Title: Hoxd11 specifies a program of metanephric kidney development within the intermediate mesoderm of the mouse embryo.
Volume: 319
Issue: 2
Pages: 396-405
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Publication
20736290 | J:164582
First Author: Hurd EA
Year: 2010
Journal: Development
Title: The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner ear.
Volume: 137
Issue: 18
Pages: 3139-50
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Publication
34861428 | J:316185
 
First Author: Cesario J
Year: 2021
Journal: Gene Expr Patterns
Title: Candidate positive targets of LHX6 and LHX8 transcription factors in the developing upper jaw.
Volume: 43
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