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Search results 1101 to 1200 out of 1412 for Des

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Type Details Score
Publication
20545945 | -
First Author: Kutach AK
Year: 2010
Journal: Chem Biol Drug Des
Title: Crystal structures of IL-2-inducible T cell kinase complexed with inhibitors: insights into rational drug design and activity regulation.
Volume: 76
Issue: 2
Pages: 154-63
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Publication
17085431 | -
First Author: Stam MR
Year: 2006
Journal: Protein Eng Des Sel
Title: Dividing the large glycoside hydrolase family 13 into subfamilies: towards improved functional annotations of alpha-amylase-related proteins.
Volume: 19
Issue: 12
Pages: 555-62
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Publication
- | J:13368
First Author: Dolle P
Year: 1992
Journal: C R Seances Soc Biol Fil
Title: Expression des homeogenes au cours du developpement embryonnaire de la Souris
Volume: 186
Issue: 3
Pages: 293-296
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Author
des Francs-Small CC
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Author
des Portes V
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Author
des Georges A
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Author
Des Rosiers C
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Author
deS Senanayake P
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Author
Bonnet des Claustres M
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Author
Buissant des Amorie J
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Author
des Bordes C
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Author
des Rieux A
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Author
Burin des Roziers C
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GXD Expression
GXD Expression
   
Assay Type: In situ reporter (knock in)
Annotation Date: 2023-02-28
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:2823928
Stage: TS28
Assay Id: MGI:7439177
Age: postnatal adult
Image: 2B Eltd1 middle
Note: Expression did not colocalize with Des in the mesangial cells.
Specimen Label: 2B Eltd1 middle
Detected: false
Specimen Num: 6
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Publication
- | J:14899
 
First Author: Kobozieff N
Year: 1962
Journal: Rec Med Vet
Title: Hemimelie chez la souris. II. Etude morphologique des homozygotes atteints de differentes anomalies du squelette. D. Squelette axial
Volume: 138
Pages: 671-86
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Publication
27090909 | -
First Author: Garrido-Arandia M
Year: 2016
Journal: J Comput Aided Mol Des
Title: Computational study of pH-dependent oligomerization and ligand binding in Alt a 1, a highly allergenic protein with a unique fold.
Volume: 30
Issue: 5
Pages: 365-79
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Publication
- | J:26410
 
First Author: von Krischke W
Year: 1962
Journal: Arch Geschwulstforsch
Title: Weitere versuche zur abhangigkeit der Wirkung des virus der myeloischen leukamie der Maus von versuchiedenen biologischen Bedingangen der infizierten tiere.
Volume: 20
Pages: 22-9
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Allele
Tg(Pbsn-IGF1*)5305Ng | MGI:3831172
Name: transgene insertion 5305, Norman M Greenberg
Allele Type: Transgenic
Attribute String: Humanized sequence, Inserted expressed sequence
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Allele
Meltf<tm1Drrn> | MGI:3691276
Name: melanotransferrin; targeted mutation 1, Des R Richardson
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Des<em1Smoc> | MGI:7289317
Name: desmin; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Transgene
MGI:3831170 | Tg(Pbsn-IGF1*)5305Ng
Type: transgene
Organism: mouse, laboratory
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Publication
12750377 | -
First Author: Tudzynski B
Year: 2003
Journal: J Biol Chem
Title: Characterization of the final two genes of the gibberellin biosynthesis gene cluster of Gibberella fujikuroi: des and P450-3 encode GA4 desaturase and the 13-hydroxylase, respectively.
Volume: 278
Issue: 31
Pages: 28635-43
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DO Term
DOID:0110431 | dilated cardiomyopathy 1I
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Allele
Tg(Otog-cre)1Ugds | MGI:2183511
Name: transgene insertion 1, Unite de Genetique des Deficits Sensoriels
Allele Type: Transgenic
Attribute String: Recombinase
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Allele
Otof<tm1Ugds> | MGI:3640614
Name: otoferlin; targeted mutation 1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Pjvk<tm1Ugds> | MGI:3654320
Name: pejvakin; targeted mutation 1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Humanized sequence
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Publication
17449903 | J:125816
First Author: Suryo Rahmanto Y
Year: 2007
Journal: Carcinogenesis
Title: Identification of distinct changes in gene expression after modulation of melanoma tumor antigen p97 (melanotransferrin) in multiple models in vitro and in vivo.
Volume: 28
Issue: 10
Pages: 2172-83
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Allele
Strc<tm1Ugds> | MGI:3818633
Name: stereocilin; targeted mutation 1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Pjvk<tm2Ugds> | MGI:5908027
Name: pejvakin; targeted mutation 2, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready
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Allele
Pjvk<tm2.1Ugds> | MGI:5908028
Name: pejvakin; targeted mutation 2.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Otogl<tm1.2Ugds> | MGI:6466540
Name: otogelin-like; targeted mutation 1.2, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Otogl<tm1.1Ugds> | MGI:6466541
Name: otogelin-like; targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready
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Allele
Otof<tm2Ugds> | MGI:6466542
Name: otoferlin; targeted mutation 2, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Modified isoform(s)
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Genotype
Genotype
Symbol: Meltf/Meltf
Background: involves: 129X1/SvJ * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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Strain
MGI:6354734 | C57BL/6JSmoc-Des<em1Smoc>/Smoc
Attribute String: coisogenic, mutant strain, endonuclease-mediated mutation
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Publication
30936319 | J:273835
First Author: Defourny J
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage.
Volume: 116
Issue: 16
Pages: 8010-8017
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Publication
18287496 | J:131715
First Author: Beurg M
Year: 2008
Journal: J Neurosci
Title: Calcium- and otoferlin-dependent exocytosis by immature outer hair cells.
Volume: 28
Issue: 8
Pages: 1798-803
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Allele
Gjb2<tm1Ugds> | MGI:2183509
Name: gap junction protein, beta 2; targeted mutation 1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready, No functional change
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Publication
25122888 | J:216182
First Author: Vincent PF
Year: 2014
Journal: J Neurosci
Title: Exocytotic machineries of vestibular type I and cochlear ribbon synapses display similar intrinsic otoferlin-dependent Ca2+ sensitivity but a different coupling to Ca2+ channels.
Volume: 34
Issue: 33
Pages: 10853-69
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Publication
26568308 | J:228056
   
First Author: Vincent PF
Year: 2015
Journal: Elife
Title: A synaptic F-actin network controls otoferlin-dependent exocytosis in auditory inner hair cells.
Volume: 4
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Publication
24862576 | J:215798
First Author: Revelo NH
Year: 2014
Journal: J Cell Biol
Title: A new probe for super-resolution imaging of membranes elucidates trafficking pathways.
Volume: 205
Issue: 4
Pages: 591-606
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Publication
30833506 | J:274660
First Author: Tertrais M
Year: 2019
Journal: J Neurosci
Title: Viral Transfer of Mini-Otoferlins Partially Restores the Fast Component of Exocytosis and Uncovers Ultrafast Endocytosis in Auditory Hair Cells of Otoferlin Knock-Out Mice.
Volume: 39
Issue: 18
Pages: 3394-3411
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Publication
19710301 | J:152316
First Author: Dulon D
Year: 2009
Journal: J Neurosci
Title: Otoferlin is critical for a highly sensitive and linear calcium-dependent exocytosis at vestibular hair cell ribbon synapses.
Volume: 29
Issue: 34
Pages: 10474-87
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Publication
28193694 | J:239813
First Author: Vincent PF
Year: 2017
Journal: J Neurosci
Title: Different CaV1.3 Channel Isoforms Control Distinct Components of the Synaptic Vesicle Cycle in Auditory Inner Hair Cells.
Volume: 37
Issue: 11
Pages: 2960-2975
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Publication
30566869 | J:270761
First Author: Vincent PFY
Year: 2018
Journal: Cell Rep
Title: Clustered Ca2+ Channels Are Blocked by Synaptic Vesicle Proton Release at Mammalian Auditory Ribbon Synapses.
Volume: 25
Issue: 12
Pages: 3451-3464.e3
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Publication
30782832 | J:273895
     
First Author: Akil O
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model.
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Allele
Ush1c<tm1.1Ugds> | MGI:3757683
Name: USH1 protein network component harmonin; targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Myo15a<tm1.1(cre)Ugds> | MGI:4361284
Name: myosin XVA; targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Recombinase
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Allele
Cdh23<tm1.1Ugds> | MGI:4361286
Name: cadherin related 23 (otocadherin); targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready, No functional change
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Allele
Ush1g<tm1.1Ugds> | MGI:4361359
Name: USH1 protein network component sans; targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready, No functional change
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Allele
Cdh23<tm1.2Ugds> | MGI:4441515
Name: cadherin related 23 (otocadherin); targeted mutation 1.2, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Ush1g<tm1.2Ugds> | MGI:4950014
Name: USH1 protein network component sans; targeted mutation 1.2, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Allele
Pcdh15<tm1.1Ugds> | MGI:5566900
Name: protocadherin 15; targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready
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Allele
Pcdh15<tm2.1Ugds> | MGI:6389238
Name: protocadherin 15; targeted mutation 2.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready, No functional change
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Allele
Pcdh15<tm3.1Ugds> | MGI:6389239
Name: protocadherin 15; targeted mutation 3.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready, No functional change
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Publication
29111973 | J:254993
   
First Author: Michalski N
Year: 2017
Journal: Elife
Title: Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses.
Volume: 6
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Publication
32059781 | J:340422
First Author: Kirst C
Year: 2020
Journal: Cell
Title: Mapping the Fine-Scale Organization and Plasticity of the Brain Vasculature.
Volume: 180
Issue: 4
Pages: 780-795.e25
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Allele
Myo3a<tm1Ugds> | MGI:7330351
Name: myosin IIIA; targeted mutation 1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Conditional ready, No functional change
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Allele
Myo3a<tm1.1Ugds> | MGI:7330352
Name: myosin IIIA; targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
Allele Type: Targeted
Attribute String: Null/knockout
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Genotype
Genotype
Symbol: Pjvk/Pjvk
Background: involves: 129S2/SvPas * BALB/c * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Otof/Otof
Background: involves: 129S2/SvPas * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Strc/Strc
Background: involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pjvk/Pjvk
Background: involves: 129S2/SvPas * C57BL/6J
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Otof/Otof
Background: involves: 129S2/SvPas
Zygosity: hm
Has Mutant Allele: true
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HT Experiment
E-MEXP-1853 | Transcription profiling of mouse fetal and early adult liver
 
Experiment Type: transcription profiling by array
Study Type: Baseline
Source: ArrayExpress
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Publication
17583724 | J:123076
First Author: Khairallah M
Year: 2007
Journal: J Mol Cell Cardiol
Title: Metabolic and signaling alterations in dystrophin-deficient hearts precede overt cardiomyopathy.
Volume: 43
Issue: 2
Pages: 119-29
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Publication
12777443 | J:83777
First Author: Kessler SP
Year: 2003
Journal: J Biol Chem
Title: Maintenance of normal blood pressure and renal functions are independent effects of angiotensin-converting enzyme.
Volume: 278
Issue: 23
Pages: 21105-12
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Publication
10094833 | J:115222
First Author: Haapajärvi T
Year: 1999
Journal: Exp Cell Res
Title: UV radiation is a transcriptional inducer of p21(Cip1/Waf1) cyclin-kinase inhibitor in a p53-independent manner.
Volume: 248
Issue: 1
Pages: 272-9
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Publication
18223187 | J:135352
First Author: Gélinas R
Year: 2008
Journal: Am J Physiol Heart Circ Physiol
Title: Alterations in carbohydrate metabolism and its regulation in PPARalpha null mouse hearts.
Volume: 294
Issue: 4
Pages: H1571-80
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Publication
26494228 | J:242389
First Author: Demers A
Year: 2015
Journal: Arterioscler Thromb Vasc Biol
Title: PCSK9 Induces CD36 Degradation and Affects Long-Chain Fatty Acid Uptake and Triglyceride Metabolism in Adipocytes and in Mouse Liver.
Volume: 35
Issue: 12
Pages: 2517-25
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Publication
32369418 | J:296834
First Author: Oppong AK
Year: 2020
Journal: Am J Physiol Endocrinol Metab
Title: Reducing 14-3-3ζ expression influences adipocyte maturity and impairs function.
Volume: 319
Issue: 1
Pages: E117-E132
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Publication
32169475 | J:297220
First Author: Gouin O
Year: 2020
Journal: J Invest Dermatol
Title: Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature.
Volume: 140
Issue: 6
Pages: 1184-1194
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Publication
13404364 | J:25332
First Author: RUDALI G
Year: 1956
Journal: Bull Assoc Fr Etud Cancer
Title: [Various characteristics of mice belonging to a new cancer strain: the Curie Foundation NLC strain].
Volume: 43
Issue: 3
Pages: 364-83
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Allele
Des<tm1Cap> | MGI:2178321
Name: desmin; targeted mutation 1, Yassemi Capetanaki
Allele Type: Targeted
Attribute String: Null/knockout
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Publication
23706745 | -
First Author: Hashem Y
Year: 2013
Journal: Cell
Title: Structure of the mammalian ribosomal 43S preinitiation complex bound to the scanning factor DHX29.
Volume: 153
Issue: 5
Pages: 1108-19
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Publication
20682769 | -
First Author: Koprivova A
Year: 2010
Journal: J Biol Chem
Title: Identification of a pentatricopeptide repeat protein implicated in splicing of intron 1 of mitochondrial nad7 transcripts.
Volume: 285
Issue: 42
Pages: 32192-9
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Publication
18474859 | J:134880
First Author: Khairallah M
Year: 2008
Journal: Proc Natl Acad Sci U S A
Title: Sildenafil and cardiomyocyte-specific cGMP signaling prevent cardiomyopathic changes associated with dystrophin deficiency.
Volume: 105
Issue: 19
Pages: 7028-33
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Publication
20971771 | J:166227
First Author: Ascah A
Year: 2011
Journal: Am J Physiol Heart Circ Physiol
Title: Stress-induced opening of the permeability transition pore in the dystrophin-deficient heart is attenuated by acute treatment with sildenafil.
Volume: 300
Issue: 1
Pages: H144-53
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Publication
21926346 | J:178785
First Author: Bolduc V
Year: 2011
Journal: Am J Physiol Heart Circ Physiol
Title: Heart rate-associated mechanical stress impairs carotid but not cerebral artery compliance in dyslipidemic atherosclerotic mice.
Volume: 301
Issue: 5
Pages: H2081-92
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Publication
35617965 | J:347567
First Author: Parsa R
Year: 2022
Journal: Immunity
Title: Newly recruited intraepithelial Ly6A(+)CCR9(+)CD4(+) T cells protect against enteric viral infection.
Volume: 55
Issue: 7
Pages: 1234-1249.e6
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Publication
26083030 | J:237806
First Author: Labrie M
Year: 2015
Journal: PLoS One
Title: Apolipoprotein D Transgenic Mice Develop Hepatic Steatosis through Activation of PPARγ and Fatty Acid Uptake.
Volume: 10
Issue: 6
Pages: e0130230
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Publication
18590915 | J:139240
First Author: Khairallah RJ
Year: 2008
Journal: J Mol Cell Cardiol
Title: Cyclic GMP signaling in cardiomyocytes modulates fatty acid trafficking and prevents triglyceride accumulation.
Volume: 45
Issue: 2
Pages: 230-9
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Publication
24186097 | J:274169
First Author: Vaillant F
Year: 2014
Journal: Am J Physiol Heart Circ Physiol
Title: Mouse strain differences in metabolic fluxes and function of ex vivo working hearts.
Volume: 306
Issue: 1
Pages: H78-87
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Publication
34195596 | J:349010
 
First Author: Nandadasa S
Year: 2021
Journal: Matrix Biol Plus
Title: A new mouse mutant with cleavage-resistant versican and isoform-specific versican mutants demonstrate that proteolysis at the Glu(441)-Ala(442) peptide bond in the V1 isoform is essential for interdigital web regression.
Volume: 10
Pages: 100064
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Publication
5213409 | J:280834
First Author: Krischke W
Year: 1963
Journal: Arch Geschwulstforsch
Title: [Additional experiments on the dependence of the action of the myelocytic leukemia virus of the mouse on different biological conditions of the infected animals].
Volume: 20
Issue: 1
Pages: 22-9
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Publication
17055430 | J:116097
First Author: Roux I
Year: 2006
Journal: Cell
Title: Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.
Volume: 127
Issue: 2
Pages: 277-89
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Publication
16704991 | J:114955
First Author: Dunn LL
Year: 2006
Journal: Carcinogenesis
Title: The function of melanotransferrin: a role in melanoma cell proliferation and tumorigenesis.
Volume: 27
Issue: 11
Pages: 2157-69
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Publication
16291590 | J:115256
First Author: Sekyere EO
Year: 2006
Journal: Blood
Title: Role of melanotransferrin in iron metabolism: studies using targeted gene disruption in vivo.
Volume: 107
Issue: 7
Pages: 2599-601
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Strain
MGI:3716470 | B6;129P2-Gjb2<tm1Ugds>/Cnrm
Attribute String: mutant stock, targeted mutation
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Publication
32958814 | J:346709
First Author: van de Wiel J
Year: 2020
Journal: Commun Biol
Title: Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata.
Volume: 3
Issue: 1
Pages: 521
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Publication
37459544 | J:354679
First Author: Calhoun G
Year: 2023
Journal: Proc Natl Acad Sci U S A
Title: Bilateral widefield calcium imaging reveals circuit asymmetries and lateralized functional activation of the mouse auditory cortex.
Volume: 120
Issue: 30
Pages: e2219340120
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Publication
25253474 | J:269136
First Author: Wright S
Year: 2014
Journal: J Neurophysiol
Title: Synaptic transmission between end bulbs of Held and bushy cells in the cochlear nucleus of mice with a mutation in Otoferlin.
Volume: 112
Issue: 12
Pages: 3173-88
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Publication
34849612 | J:354675
First Author: Mukherjee D
Year: 2022
Journal: Cereb Cortex
Title: Impaired Hearing and Altered Subplate Circuits During the First and Second Postnatal Weeks of Otoferlin-Deficient Mice.
Volume: 32
Issue: 13
Pages: 2816-2830
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Publication
28835534 | J:251690
First Author: Emptoz A
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G.
Volume: 114
Issue: 36
Pages: 9695-9700
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Publication
31637240 | J:311093
 
First Author: Sorusch N
Year: 2019
Journal: Front Cell Dev Biol
Title: SANS (USH1G) Molecularly Links the Human Usher Syndrome Protein Network to the Intraflagellar Transport Module by Direct Binding to IFT-B Proteins.
Volume: 7
Pages: 216
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Genotype
Genotype
Symbol: Ush1c/Ush1c
Background: involves: 129S2/SvPas
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Cdh23/Cdh23
Background: involves: 129S1/SvImJ * BALB/c * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Cdh23/Cdh23
Background: involves: 129S1/SvImJ * C57BL/6
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Ush1g/Ush1g
Background: involves: 129S1/SvImJ * BALB/c * C57BL/6 * C57BL/6J
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Cdh23/Cdh23
Background: involves: 129S1/SvImJ
Zygosity: hm
Has Mutant Allele: true
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