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Search results 1201 to 1300 out of 1412 for Des

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Hits by Strain

Type Details Score
Genotype
Genotype
Symbol: Ush1g/Ush1g
Background: involves: 129S1/SvImJ
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Otof/Otof<+>
Background: involves: 129S2/SvPas
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Des/Des
Background: involves: 129S7/SvEvBrd * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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DO Term
DOID:0111551 | neurogenic scapuloperoneal syndrome Kaeser type
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Publication
27496881 | J:236619
First Author: Vaillant F
Year: 2016
Journal: Am J Physiol Heart Circ Physiol
Title: Ivabradine and metoprolol differentially affect cardiac glucose metabolism despite similar heart rate reduction in a mouse model of dyslipidemia.
Volume: 311
Issue: 4
Pages: H991-H1003
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Publication
37902616 | J:355496
First Author: Liu Y
Year: 2023
Journal: FASEB J
Title: Perturbations in lipid metabolism and gut microbiota composition precede cardiac dysfunction in a mouse model of thalassemia.
Volume: 37
Issue: 12
Pages: e23257
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Publication
31341105 | J:332678
 
First Author: Ruiz M
Year: 2019
Journal: JCI Insight
Title: Lipidomics unveils lipid dyshomeostasis and low circulating plasmalogens as biomarkers in a monogenic mitochondrial disorder.
Volume: 4
Issue: 14
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Publication
34413467 | J:314249
First Author: Cuillerier A
Year: 2021
Journal: Commun Biol
Title: Adaptive optimization of the OXPHOS assembly line partially compensates lrpprc-dependent mitochondrial translation defects in mice.
Volume: 4
Issue: 1
Pages: 989
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Publication
28575497 | J:243637
First Author: Cuillerier A
Year: 2017
Journal: Hum Mol Genet
Title: Loss of hepatic LRPPRC alters mitochondrial bioenergetics, regulation of permeability transition and trans-membrane ROS diffusion.
Volume: 26
Issue: 16
Pages: 3186-3201
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Publication
26558681 | J:250461
First Author: Ruiz M
Year: 2016
Journal: Diabetes
Title: MK2 Deletion in Mice Prevents Diabetes-Induced Perturbations in Lipid Metabolism and Cardiac Dysfunction.
Volume: 65
Issue: 2
Pages: 381-92
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Publication
21685264 | J:176919
First Author: Gélinas R
Year: 2011
Journal: Am J Physiol Heart Circ Physiol
Title: Prolonged QT interval and lipid alterations beyond β-oxidation in very long-chain acyl-CoA dehydrogenase null mouse hearts.
Volume: 301
Issue: 3
Pages: H813-23
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Publication
21960686 | J:194713
First Author: Galvao TF
Year: 2012
Journal: Cardiovasc Res
Title: High intake of saturated fat, but not polyunsaturated fat, improves survival in heart failure despite persistent mitochondrial defects.
Volume: 93
Issue: 1
Pages: 24-32
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Publication
24988191 | J:218935
First Author: Stewart MK
Year: 2014
Journal: PLoS One
Title: Mammary gland specific knockdown of the physiological surge in Cx26 during lactation retains normal mammary gland development and function.
Volume: 9
Issue: 7
Pages: e101546
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Publication
26439696 | J:303036
First Author: Stewart MK
Year: 2015
Journal: Oncotarget
Title: Cx26 knockout predisposes the mammary gland to primary mammary tumors in a DMBA-induced mouse model of breast cancer.
Volume: 6
Issue: 35
Pages: 37185-99
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Publication
21714813 | J:177941
First Author: Nagy JI
Year: 2011
Journal: Eur J Neurosci
Title: Connexin26 expression in brain parenchymal cells demonstrated by targeted connexin ablation in transgenic mice.
Volume: 34
Issue: 2
Pages: 263-71
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Publication
18308698 | J:135639
First Author: Marx-Stoelting P
Year: 2008
Journal: Toxicol Sci
Title: Tumor promotion in liver of mice with a conditional Cx26 knockout.
Volume: 103
Issue: 2
Pages: 260-7
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Publication
16740338 | J:115078
First Author: Ott T
Year: 2006
Journal: Eur J Cell Biol
Title: Ablation of gap junctional communication in hepatocytes of transgenic mice does not lead to disrupted cellular homeostasis or increased spontaneous tumourigenesis.
Volume: 85
Issue: 8
Pages: 717-28
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Publication
30801007 | J:288364
First Author: Cartagena-Rivera AX
Year: 2019
Journal: Sci Adv
Title: Cochlear outer hair cell horizontal top connectors mediate mature stereocilia bundle mechanics.
Volume: 5
Issue: 2
Pages: eaat9934
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Strain
MGI:6423874 | B6N.Cg-Gjb2<tm1Ugds> Tg(Sox10-cre)1Wdr/Cnrm
Attribute String: mutant strain, congenic, targeted mutation, transgenic
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Publication
22975134 | J:189014
First Author: Liang C
Year: 2012
Journal: Neurosci Lett
Title: Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.
Volume: 528
Issue: 1
Pages: 36-41
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Publication
24333301 | J:206835
 
First Author: Takada Y
Year: 2014
Journal: Hear Res
Title: Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy.
Volume: 309
Pages: 124-35
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Publication
30199819 | J:267859
 
First Author: Fetoni AR
Year: 2018
Journal: Redox Biol
Title: Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway.
Volume: 19
Pages: 301-317
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Publication
21876744 | J:176346
First Author: Crispino G
Year: 2011
Journal: PLoS One
Title: BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice.
Volume: 6
Issue: 8
Pages: e23279
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Publication
24431429 | J:205573
First Author: Neef J
Year: 2014
Journal: J Neurosci
Title: Modes and regulation of endocytic membrane retrieval in mouse auditory hair cells.
Volume: 34
Issue: 3
Pages: 705-16
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Genotype
Genotype
Symbol: Gsdme/Gsdme Pjvk/Pjvk
Background: involves: 129P2/OlaHsd * 129S2/SvPas * BALB/c * C57BL/6 * CBA/Ca
Zygosity: cx
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Gjb2/Gjb2 Tg(Sox10-cre)1Wdr/?
Background: involves: 129S2/SvPasCrl * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Gjb2/Gjb2 Tg(Sox10-cre)1Wdr/?
Background: involves: 129P2/OlaHsd * C57BL/6 * CBA
Zygosity: cn
Has Mutant Allele: true
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DO Term
DOID:0050997 | cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome
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Publication
22526732 | J:231131
First Author: Cox BC
Year: 2012
Journal: J Assoc Res Otolaryngol
Title: Conditional gene expression in the mouse inner ear using Cre-loxP.
Volume: 13
Issue: 3
Pages: 295-322
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Publication
16804542 | J:111260
First Author: Delmaghani S
Year: 2006
Journal: Nat Genet
Title: Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy.
Volume: 38
Issue: 7
Pages: 770-8
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Publication
24940003 | J:244761
First Author: Pepermans E
Year: 2014
Journal: EMBO Mol Med
Title: The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells.
Volume: 6
Issue: 7
Pages: 984-92
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Publication
25251605 | J:218449
 
First Author: Chang Q
Year: 2015
Journal: Neurobiol Dis
Title: Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing.
Volume: 73
Pages: 418-27
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Strain
MGI:6334972 | STOCK Gt(ROSA)26Sor<tm1(cre/ERT)Brn> Gjb2<tm1Ugds>/Cnrm
Attribute String: mutant stock, targeted mutation
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Publication
19047647 | J:142084
First Author: Ortolano S
Year: 2008
Journal: Proc Natl Acad Sci U S A
Title: Coordinated control of connexin 26 and connexin 30 at the regulatory and functional level in the inner ear.
Volume: 105
Issue: 48
Pages: 18776-81
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Publication
33505961 | J:341879
 
First Author: Xu K
Year: 2020
Journal: Front Cell Dev Biol
Title: Local Macrophage-Related Immune Response Is Involved in Cochlear Epithelial Damage in Distinct Gjb2-Related Hereditary Deafness Models.
Volume: 8
Pages: 597769
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Publication
26965868 | J:269202
 
First Author: Green KL
Year: 2016
Journal: Sci Rep
Title: ACEMg Diet Supplement Modifies Progression of Hereditary Deafness.
Volume: 6
Pages: 22690
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Publication
30518746 | J:315629
First Author: Chen S
Year: 2018
Journal: Cell Death Dis
Title: The spatial distribution pattern of Connexin26 expression in supporting cells and its role in outer hair cell survival.
Volume: 9
Issue: 12
Pages: 1180
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Publication
23653198 | J:207255
 
First Author: Zhu Y
Year: 2013
Journal: Nat Commun
Title: Active cochlear amplification is dependent on supporting cell gap junctions.
Volume: 4
Pages: 1786
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Publication
28701711 | J:257242
First Author: Lukashkina VA
Year: 2017
Journal: Sci Rep
Title: Amplification mode differs along the length of the mouse cochlea as revealed by connexin 26 deletion from specific gap junctions.
Volume: 7
Issue: 1
Pages: 5185
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Publication
27959894 | J:256797
First Author: Chan DK
Year: 2016
Journal: PLoS One
Title: Sound-Induced Intracellular Ca2+ Dynamics in the Adult Hearing Cochlea.
Volume: 11
Issue: 12
Pages: e0167850
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Publication
34907797 | J:339492
First Author: Zhao HB
Year: 2022
Journal: J Neurophysiol
Title: Efferent neurons control hearing sensitivity and protect hearing from noise through the regulation of gap junctions between cochlear supporting cells.
Volume: 127
Issue: 1
Pages: 313-327
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Publication
28779115 | J:288216
First Author: Crispino G
Year: 2017
Journal: Sci Rep
Title: In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors.
Volume: 7
Issue: 1
Pages: 6567
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Publication
25451287 | J:221450
 
First Author: Zhu Y
Year: 2015
Journal: Neuroscience
Title: Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss.
Volume: 284
Pages: 719-29
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Publication
35308122 | J:338593
 
First Author: Sun L
Year: 2022
Journal: Front Cell Neurosci
Title: Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca(2+) Signaling in Kölliker's Organ.
Volume: 16
Pages: 816079
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Publication
24491564 | J:218582
First Author: Chen S
Year: 2014
Journal: Biochem Biophys Res Commun
Title: Down regulated connexin26 at different postnatal stage displayed different types of cellular degeneration and formation of organ of Corti.
Volume: 445
Issue: 1
Pages: 71-7
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Publication
28552523 | J:251476
First Author: Zong L
Year: 2017
Journal: Biochem Biophys Res Commun
Title: Progressive age-dependence and frequency difference in the effect of gap junctions on active cochlear amplification and hearing.
Volume: 489
Issue: 2
Pages: 223-227
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Publication
31034913 | J:289715
 
First Author: Xie L
Year: 2019
Journal: Neurochem Int
Title: Reduced postnatal expression of cochlear Connexin26 induces hearing loss and affects the developmental status of pillar cells in a dose-dependent manner.
Volume: 128
Pages: 196-205
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Publication
26927086 | J:290005
First Author: Zhou XX
Year: 2016
Journal: Int J Mol Sci
Title: Reduced Connexin26 in the Mature Cochlea Increases Susceptibility to Noise-Induced Hearing Lossin Mice.
Volume: 17
Issue: 3
Pages: 301
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Publication
35345836 | J:322799
 
First Author: Liu XZ
Year: 2021
Journal: Front Mol Neurosci
Title: F-Actin Dysplasia Involved in Organ of Corti Deformity in Gjb2 Knockdown Mouse Model.
Volume: 14
Pages: 808553
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Publication
- | J:209275
     
First Author: Petit C
Year: 2014
Journal: MGI Direct Data Submission
Title: Direct Data Submission for Pcdh15 floxed allele from Ugds
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Publication
29386551 | J:264491
First Author: Trouillet A
Year: 2018
Journal: Sci Rep
Title: Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments.
Volume: 8
Issue: 1
Pages: 1968
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Publication
37694145 | J:341110
First Author: Cortada M
Year: 2023
Journal: iScience
Title: mTORC2 regulates auditory hair cell structure and function.
Volume: 26
Issue: 9
Pages: 107687
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Genotype
Genotype
Symbol: Gjb2/Gjb2 Tg(Otog-cre)1Ugds/?
Background: involves: 129P2/OlaHsd * C57BL/6
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Cdh23/Cdh23 Myo15a/Myo15a<+>
Background: involves: 129S1/SvImJ * C57BL/6J
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pcdh15/Pcdh15 Myo15a/Myo15a<+>
Background: involves: 129S1/SvImJ * C57BL/6J
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Myo15a/Myo15a<+> Myo7a/Myo7a
Background: involves: 129S1/SvImJ * C57BL/6N
Zygosity: cn
Has Mutant Allele: true
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Publication
15162322 | -
First Author: Freude K
Year: 2004
Journal: Am J Hum Genet
Title: Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation.
Volume: 75
Issue: 2
Pages: 305-9
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Publication
36603072 | J:334424
First Author: Hata M
Year: 2023
Journal: Science
Title: Past history of obesity triggers persistent epigenetic changes in innate immunity and exacerbates neuroinflammation.
Volume: 379
Issue: 6627
Pages: 45-62
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Publication
31182869 | J:281489
First Author: Lloyd AF
Year: 2019
Journal: Nat Neurosci
Title: Central nervous system regeneration is driven by microglia necroptosis and repopulation.
Volume: 22
Issue: 7
Pages: 1046-1052
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Publication
29635338 | J:329798
First Author: van Weeghel M
Year: 2018
Journal: Cardiovasc Res
Title: Increased cardiac fatty acid oxidation in a mouse model with decreased malonyl-CoA sensitivity of CPT1B.
Volume: 114
Issue: 10
Pages: 1324-1334
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Publication
29674152 | -
 
First Author: Lebar MD
Year: 2018
Journal: Fungal Genet Biol
Title: Identification and functional analysis of the aspergillic acid gene cluster in Aspergillus flavus.
Volume: 116
Pages: 14-23
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Publication
28708398 | -
First Author: Wollenberg RD
Year: 2017
Journal: J Nat Prod
Title: Chrysogine Biosynthesis Is Mediated by a Two-Module Nonribosomal Peptide Synthetase.
Volume: 80
Issue: 7
Pages: 2131-2135
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Publication
27056201 | -
First Author: Bonsch B
Year: 2016
Journal: Chem Commun (Camb)
Title: Identification of genes encoding squalestatin S1 biosynthesis and in vitro production of new squalestatin analogues.
Volume: 52
Issue: 41
Pages: 6777-80
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Publication
28370936 | -
First Author: Bai J
Year: 2017
Journal: Angew Chem Int Ed Engl
Title: A Cascade of Redox Reactions Generates Complexity in the Biosynthesis of the Protein Phosphatase-2 Inhibitor Rubratoxin A.
Volume: 56
Issue: 17
Pages: 4782-4786
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Protein Domain
IPR044053 | AsaB-like
Type: Family
Description: This entry includes a group of oxidoreductases, including AsaB from Aspergillus flavus [], Oxidoreductase R1/R2 from Phoma sp., DES from Gibberella fujikuroi, and Chry3 from Gibberella zeae. AsaB is involved in secondary metabolite biosynthesis. It converts aspergillic acid to hydroxyaspergillic acid []. R1/R2 is part of the gene cluster that mediates the biosynthesis of squalestatin S1 []. Chry3 is part of the gene cluster that mediates the biosynthesis of the yellow pigment chrysogine []. DES is part of the gene cluster that mediates the biosynthesis of gibberellins (GAs), diterpenoids that may provide a selective advantage during infection of the preferred host plant, rice [, , , , ].Proteins in this entry are related to RbtB and RbtG from Penicillium dangeardii. RbtB and RbtG are alpha-ketoglutarate-dependent dioxygenases involved in rubratoxin biosynthesis [].
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Publication
26754646 | J:230827
First Author: Lelli A
Year: 2016
Journal: J Cell Biol
Title: Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.
Volume: 212
Issue: 2
Pages: 231-44
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Publication
26544938 | J:228036
First Author: Delmaghani S
Year: 2015
Journal: Cell
Title: Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes.
Volume: 163
Issue: 4
Pages: 894-906
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Publication
18339676 | J:135991
First Author: Lefèvre G
Year: 2008
Journal: Development
Title: A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
Volume: 135
Issue: 8
Pages: 1427-37
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Publication
19197295 | J:158065
First Author: Decrock E
Year: 2009
Journal: Cell Death Differ
Title: Connexin-related signaling in cell death: to live or let die?
Volume: 16
Issue: 4
Pages: 524-36
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Publication
20926654 | J:165099
First Author: Beurg M
Year: 2010
Journal: J Neurosci
Title: Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells.
Volume: 30
Issue: 40
Pages: 13281-90
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Publication
15013803 | J:88743
First Author: Bry C
Year: 2004
Journal: Dev Biol
Title: Loss of connexin 26 in mammary epithelium during early but not during late pregnancy results in unscheduled apoptosis and impaired development.
Volume: 267
Issue: 2
Pages: 418-29
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Publication
36753545 | J:339757
First Author: Liu LM
Year: 2023
Journal: Sci Adv
Title: Cx26 heterozygous mutations cause hyperacusis-like hearing oversensitivity and increase susceptibility to noise.
Volume: 9
Issue: 6
Pages: eadf4144
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Publication
19433060 | J:150588
First Author: Wang Y
Year: 2009
Journal: Biochem Biophys Res Commun
Title: Targeted connexin26 ablation arrests postnatal development of the organ of Corti.
Volume: 385
Issue: 1
Pages: 33-7
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Publication
18849963 | J:141421
First Author: Verpy E
Year: 2008
Journal: Nature
Title: Stereocilin-deficient mice reveal the origin of cochlear waveform distortions.
Volume: 456
Issue: 7219
Pages: 255-8
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Publication
29361521 | J:257514
 
First Author: Chen S
Year: 2018
Journal: Dis Model Mech
Title: Developmental abnormalities in supporting cell phalangeal processes and cytoskeleton in the Gjb2 knockdown mouse model.
Volume: 11
Issue: 2
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Publication
28077706 | J:238404
First Author: Johnson SL
Year: 2017
Journal: J Neurosci
Title: Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea.
Volume: 37
Issue: 2
Pages: 258-268
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Publication
28823936 | J:259579
 
First Author: Mei L
Year: 2017
Journal: Neurobiol Dis
Title: A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.
Volume: 108
Pages: 195-203
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Publication
24732355 | J:219459
First Author: Chen J
Year: 2014
Journal: Biochem Biophys Res Commun
Title: Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders.
Volume: 448
Issue: 1
Pages: 28-32
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Publication
19673007 | J:187353
First Author: Sun Y
Year: 2009
Journal: J Comp Neurol
Title: Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea.
Volume: 516
Issue: 6
Pages: 569-79
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Publication
26490746 | J:239951
 
First Author: Zhu Y
Year: 2015
Journal: Sci Rep
Title: Connexin26 gap junction mediates miRNA intercellular genetic communication in the cochlea and is required for inner ear development.
Volume: 5
Pages: 15647
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Publication
39324853 | J:355459
First Author: Conrad LJ
Year: 2024
Journal: J Physiol
Title: The upregulation of K(+) and HCN channels in developing spiral ganglion neurons is mediated by cochlear inner hair cells.
Volume: 602
Issue: 20
Pages: 5329-5351
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Publication
36483015 | J:333049
First Author: Calvet C
Year: 2022
Journal: iScience
Title: The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses.
Volume: 25
Issue: 12
Pages: 105628
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Genotype
Genotype
Symbol: Myo15a/Myo15a<+> Ush1g/Ush1g
Background: involves: 129S1/SvImJ * C57BL/6J
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Clrn1/Clrn1 Myo15a/Myo15a<+>
Background: involves: 129S1/SvImJ * C57BL/6N
Zygosity: cn
Has Mutant Allele: true
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Publication
28420746 | -
First Author: Blomme J
Year: 2017
Journal: Plant Cell
Title: The Mitochondrial DNA-Associated Protein SWIB5 Influences mtDNA Architecture and Homologous Recombination.
Volume: 29
Issue: 5
Pages: 1137-1156
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Publication
29371602 | J:259944
First Author: Gélinas R
Year: 2018
Journal: Nat Commun
Title: AMPK activation counteracts cardiac hypertrophy by reducing O-GlcNAcylation.
Volume: 9
Issue: 1
Pages: 374
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Publication
10655063 | J:60135
First Author: Zemni R
Year: 2000
Journal: Nat Genet
Title: A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation.
Volume: 24
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Pages: 167-70
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HT Experiment
E-TABM-295 | Transcription profiling of liver from wild type and tumor suppressor Apc knock-out mice
 
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: ArrayExpress
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HT Experiment
GSE123360 | Esrrb function in the extraembryonic ectoderm is required for proper primordial germ cell specification [microarray]
 
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: GEO
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Publication
23825955 | -
First Author: Wiemann P
Year: 2013
Journal: PLoS Pathog
Title: Deciphering the cryptic genome: genome-wide analyses of the rice pathogen Fusarium fujikuroi reveal complex regulation of secondary metabolism and novel metabolites.
Volume: 9
Issue: 6
Pages: e1003475
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Publication
9917370 | -
First Author: Tudzynski B
Year: 1998
Journal: Fungal Genet Biol
Title: Gibberellin biosynthetic pathway in Gibberella fujikuroi: evidence for a gene cluster.
Volume: 25
Issue: 3
Pages: 157-70
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Publication
10347043 | -
First Author: Linnemannstöns P
Year: 1999
Journal: Appl Environ Microbiol
Title: Deletions in the gibberellin biosynthesis gene cluster of Gibberella fujikuroi by restriction enzyme-mediated integration and conventional transformation-mediated mutagenesis.
Volume: 65
Issue: 6
Pages: 2558-64
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15925394 | -
First Author: Malonek S
Year: 2005
Journal: Phytochemistry
Title: Distribution of gibberellin biosynthetic genes and gibberellin production in the Gibberella fujikuroi species complex.
Volume: 66
Issue: 11
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Publication
21165971 | J:186025
First Author: Verpy E
Year: 2011
Journal: J Comp Neurol
Title: Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane.
Volume: 519
Issue: 2
Pages: 194-210
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Publication
33009420 | J:299425
First Author: Michel V
Year: 2020
Journal: Sci Rep
Title: Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells.
Volume: 10
Issue: 1
Pages: 16430
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Publication
28705869 | J:244775
First Author: Libé-Philippot B
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction.
Volume: 114
Issue: 30
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Publication
20332152 | J:158897
First Author: Etournay R
Year: 2010
Journal: Development
Title: Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape.
Volume: 137
Issue: 8
Pages: 1373-83
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Publication
26035172 | J:233555
 
First Author: Chen J
Year: 2015
Journal: Sci Rep
Title: Pannexin1 channels dominate ATP release in the cochlea ensuring endocochlear potential and auditory receptor potential generation and hearing.
Volume: 5
Pages: 10762
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Publication
29985171 | J:265318
First Author: Dulon D
Year: 2018
Journal: J Clin Invest
Title: Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome.
Volume: 128
Issue: 8
Pages: 3382-3401
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Publication
39746042 | J:360306
First Author: Underhill A
Year: 2025
Journal: Proc Natl Acad Sci U S A
Title: MYO7A is required for the functional integrity of the mechanoelectrical transduction complex in hair cells of the adult cochlea.
Volume: 122
Issue: 1
Pages: e2414707122
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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