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Search results 901 to 944 out of 944 for Pde6b

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Type Details Score
Publication
- | J:144087
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
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Publication
20940301 | -
First Author: Muradov H
Year: 2010
Journal: J Biol Chem
Title: Rod phosphodiesterase-6 PDE6A and PDE6B subunits are enzymatically equivalent.
Volume: 285
Issue: 51
Pages: 39828-34
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HT Experiment
GSE183117 | Multi-omics analyses reveal early metabolic imbalance and mitochondrial stress in neonatal photoreceptors leading to cell death in Pde6b rd1/rd1 mouse model of retinal degeneration
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
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Allele
Pde6b<tm1Eye> | MGI:5544444
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; targeted mutation 1, Stephen H Tsang
Allele Type: Targeted
Attribute String: Conditional ready
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Allele
Pde6b<atrd1> | MGI:2178311
 
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; atypical retinal degeneration 1
Allele Type: Chemically induced (ENU)
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Allele
Pde6b<atrd2> | MGI:2178315
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; atypical retinal degeneration 2
Allele Type: Chemically induced (ENU)
Attribute String: Hypomorph
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Allele
Pde6b<atrd3> | MGI:2178316
 
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; atypical retinal degeneration 3
Allele Type: Chemically induced (ENU)
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Allele
Pde6b<rd1-3H> | MGI:2178319
 
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 3 Harwell
Allele Type: Chemically induced (ENU)
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Allele
Pde6b<rd1-4H> | MGI:2178320
 
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 4 Harwell
Allele Type: Chemically induced (ENU)
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Allele
Pde6b<rd1-2J> | MGI:2665102
 
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 2 Jackson
Allele Type: Chemically induced (ENU)
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: C3H/HeJ
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b Gt(ROSA)26Sor/Gt(ROSA)26Sor<+>
Background: involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J
Zygosity: cn
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: C3H
Zygosity: hm
Has Mutant Allele: true
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DO Term
DOID:0110375 | retinitis pigmentosa 40
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: C57BL/6J-Pde6b/J
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: involves: BALB/cAnN * C3H/HeN
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: Not Specified
Zygosity: hm
Has Mutant Allele: true
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DO Term
DOID:0110863 | congenital stationary night blindness autosomal dominant 2
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Allele
Pde6b<rd1> | MGI:1856373
 
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1
Allele Type: Spontaneous
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Allele
Pde6b<rd10> | MGI:2388259
 
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 10
Allele Type: Spontaneous
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Strain
MGI:2173852 | B6.CXB1-Pde6b<rd10>/J
Attribute String: congenic, mutant strain, spontaneous mutation
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Genotype
Genotype
Symbol: Pde6b/Pde6b
Background: B6.CXB1-Pde6b/J
Zygosity: hm
Has Mutant Allele: true
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Publication
20503361 | J:160592
First Author: Blazek JD
Year: 2010
Journal: Dev Dyn
Title: Embryonic and not maternal trisomy causes developmental attenuation in the Ts65Dn mouse model for Down syndrome.
Volume: 239
Issue: 6
Pages: 1645-53
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Publication
31709889 | J:292843
First Author: George AK
Year: 2019
Journal: Physiol Genomics
Title: Effect of MMP-9 gene knockout on retinal vascular form and function.
Volume: 51
Issue: 12
Pages: 613-622
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Publication
22247471 | J:196773
First Author: Collin GB
Year: 2012
Journal: Invest Ophthalmol Vis Sci
Title: Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis.
Volume: 53
Issue: 2
Pages: 967-74
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Publication
8661727 | J:33168
First Author: Lord EA
Year: 1996
Journal: Mamm Genome
Title: The linkage map of sheep Chromosome 6 compared with orthologous regions in other species.
Volume: 7
Issue: 5
Pages: 373-6
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Publication
9716380 | J:49380
First Author: Yanaka N
Year: 1998
Journal: Eur J Biochem
Title: Expression, structure and chromosomal localization of the human cGMP-binding cGMP-specific phosphodiesterase PDE5A gene.
Volume: 255
Issue: 2
Pages: 391-9
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Publication
27186975 | J:253182
First Author: Yao L
Year: 2016
Journal: PLoS One
Title: The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome.
Volume: 11
Issue: 5
Pages: e0155619
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Publication
9770645 | J:49969
First Author: Mohamed MK
Year: 1998
Journal: J Mol Neurosci
Title: Structure and upstream region characterization of the human gene encoding rod photoreceptor cGMP phosphodiesterase alpha-subunit.
Volume: 10
Issue: 3
Pages: 235-50
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Publication
14744904 | J:109741
First Author: Dalke C
Year: 2004
Journal: Invest Ophthalmol Vis Sci
Title: Electroretinography as a screening method for mutations causing retinal dysfunction in mice.
Volume: 45
Issue: 2
Pages: 601-9
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Publication
26091175 | J:233801
First Author: Yang J
Year: 2015
Journal: PLoS One
Title: Destructive Changes in the Neuronal Structure of the FVB/N Mouse Retina.
Volume: 10
Issue: 6
Pages: e0129719
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Publication
15489334 | -
First Author: Gerhard DS
Year: 2004
Journal: Genome Res
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Volume: 14
Issue: 10B
Pages: 2121-7
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