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on page 1 showing 20 out of 1,705 results

Cite this (MGI Cat# 5000268, RRID:MGI:5000268)

Source Database: MGI, catalog # 5000268
Genetic Background: C57BL/6J-Ticam1
Affected Genes: Ticam1
Genomic Alteration: Lps2
Availability: Availability unknown check source stock center
Reference: PMID:19825364, PMID:18209032, PMID:18981228, PMID:18713975, PMID:20855887
Notes: decreased susceptibility to induced colitis, nervous system phenotype, abnormal enterocyte physiology, abnormal postnatal growth/weight/body size, decreased interleukin-6 secretion, abnormal cytokine secretion, abnormal retinal progenitor cell morphology, abnormal circulating tumor necrosis factor level, decreased susceptibility to hepatic steatosis, immune system phenotype Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3759808, RRID:MGI:3759808)

Source Database: MGI, catalog # 3759808
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Affected Genes: Mapk1
Genomic Alteration: tm1Kuta
Availability: Availability unknown check source stock center
Reference: PMID:17913910
Notes: abnormal contextual conditioning behavior, abnormal cued conditioning behavior, abnormal spatial learning, behavior/neurological phenotype, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3802986, RRID:MGI:3802986)

Source Database: MGI, catalog # 3802986
Genetic Background: B6.Cg-Adcy1 Adcy1 Tg(Emx1-cre)3Ito
Affected Genes: Adcy1
Genomic Alteration: Tg(Emx1-cre)3Ito; tm1.1Ito; tm1Ito
Availability: Availability unknown check source stock center
Reference: PMID:18524897
Notes: nervous system phenotype, reduced long term potentiation, abnormal miniature excitatory postsynaptic currents, abnormal barrel cortex morphology Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 4833965, RRID:MGI:4833965)

Source Database: MGI, catalog # 4833965
Genetic Background: involves: C57BL/6 * C57BL/6J * DBA/2
Affected Genes: Tnfrsf1a
Genomic Alteration: tm1Imx; Tg(Thy1-APP)3Somm
Availability: Availability unknown check source stock center
Reference: PMID:17724122
Notes: behavior/neurological phenotype, nervous system phenotype, cerebral amyloid angiopathy, microgliosis, amyloid beta deposits Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 4818570, RRID:MGI:4818570)

Source Database: MGI, catalog # 4818570
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: En1, Gata2
Genomic Alteration: tm1Msal; tm2(cre)Wrst
Availability: Availability unknown check source stock center
Reference: PMID:19088086
Notes: nervous system phenotype, abnormal serotonergic neuron morphology, abnormal neuron differentiation, abnormal GABAergic neuron morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3760750, RRID:MGI:3760750)

Source Database: MGI, catalog # 3760750
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Affected Genes: Gucy2d, Sema3c
Genomic Alteration: tm1.1Jra; tm1Mom
Availability: Availability unknown check source stock center
Reference: PMID:17942483
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3613509, RRID:MGI:3613509)

Source Database: MGI, catalog # 3613509
Genetic Background: involves: 129S1/SvImJ * C57BL/6J
Affected Genes: Mobp
Genomic Alteration: tm1Irg
Availability: Availability unknown check source stock center
Reference: PMID:12203392
Notes: nervous system phenotype, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3798665, RRID:MGI:3798665)

Source Database: MGI, catalog # 3798665
Genetic Background: involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m musculus
Affected Genes: Dmd, Utrn
Genomic Alteration: tm1Ked; mdx-3Cv
Availability: Availability unknown check source stock center
Reference: PMID:10204788
Notes: nervous system phenotype, abnormal skeletal muscle morphology, renal/urinary system phenotype, respiratory system phenotype, liver/biliary system phenotype, reproductive system phenotype Allele Detail: Chemically induced (ENU), Targeted

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Cite this (MGI Cat# 3720209, RRID:MGI:3720209)

Source Database: MGI, catalog # 3720209
Genetic Background: involves: FVB
Affected Genes:
Genomic Alteration: Tg(Thy1-MAPT)1Vln
Availability: Availability unknown check source stock center
Reference: PMID:11007782, PMID:10595944
Notes: skeletal muscle fiber atrophy, decreased skeletal muscle mass, abnormal axon morphology, abnormal postural reflex, limb grasping, abnormal locomotor activation, impaired coordination, tau protein deposits, abnormal axon morphology, muscle weakness, abnormal cell cytoskeleton morphology, abnormal neuron morphology, muscular atrophy, nervous system phenotype, decreased body weight, astrocytosis, impaired coordination, impaired righting response, axon degeneration, muscular atrophy Allele Detail: Transgenic

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Cite this (MGI Cat# 4867727, RRID:MGI:4867727)

Source Database: MGI, catalog # 4867727
Genetic Background: 129S/SvEv-Mapk8ip2
Affected Genes: Mapk8ip2
Genomic Alteration: tm1.1Gol
Availability: Availability unknown check source stock center
Reference: PMID:21048139
Notes: impaired coordination, vision/eye phenotype, thin cerebellar molecular layer, enhanced NMDA-mediated synaptic currents, abnormal Purkinje cell morphology, decreased synaptic glutamate release, nervous system phenotype, reduced AMPA-mediated synaptic currents, taste/olfaction phenotype, decreased grip strength, reduced fertility, decreased exploration in new environment, abnormal Purkinje cell dendrite morphology, decreased anxiety-related response, behavior/neurological phenotype, abnormal social investigation, abnormal miniature excitatory postsynaptic currents, abnormal excitatory postsynaptic currents Allele Detail: Targeted

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Cite this (MGI Cat# 5824114, RRID:MGI:5824114)

Source Database: MGI, catalog # 5824114
Genetic Background: involves: 129S/SvEv * C3H * C57BL/6 * C57BL/6N
Affected Genes: Ndor1, Fus
Genomic Alteration: Tg(UBC-cre/ERT2)1Ejb; tm1c(EUCOMM)Wtsi; tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:26842965
Notes: nervous system phenotype Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5527535, RRID:MGI:5527535)

Source Database: MGI, catalog # 5527535
Genetic Background: involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * FVB/N * SJL
Affected Genes: Dmrta2
Genomic Alteration: tm1.2Fuma
Availability: Availability unknown check source stock center
Reference: PMID:23056351
Notes: abnormal cerebral cortex morphology, decreased neuron number, nervous system phenotype, absent hippocampus, small olfactory bulb, abnormal neuronal precursor proliferation, telencephalon hypoplasia, decreased neuronal precursor cell number Allele Detail: Targeted

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Cite this (MGI Cat# 4836986, RRID:MGI:4836986)

Source Database: MGI, catalog # 4836986
Genetic Background: involves: 129S/SvEv * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
Affected Genes: Smn1
Genomic Alteration: tm1.1Dscd; tm1Msd
Availability: Availability unknown check source stock center
Reference: PMID:20705738
Notes: nervous system phenotype, decreased vertical activity, hypoactivity, decreased grip strength Allele Detail: Targeted

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Cite this (MGI Cat# 3720601, RRID:MGI:3720601)

Source Database: MGI, catalog # 3720601
Genetic Background: involves: BALB/c
Affected Genes: Reln
Genomic Alteration: rl
Availability: Availability unknown check source stock center
Reference: PMID:10876649
Notes: decreased Purkinje cell number, small cerebellum, Purkinje cell degeneration, nervous system phenotype Allele Detail: Spontaneous

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Cite this (MGI Cat# 5432789, RRID:MGI:5432789)

Source Database: MGI, catalog # 5432789
Genetic Background: involves: 129S6/SvEvTac * C57BL/6NTac
Affected Genes: Cntf
Genomic Alteration: tm1Vlcg
Availability: Availability unknown check source stock center
Reference: PMID:18305256
Notes: decreased neuronal precursor cell number, nervous system phenotype, abnormal neuron proliferation Allele Detail: Targeted

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Cite this (MGI Cat# 3713514, RRID:MGI:3713514)

Source Database: MGI, catalog # 3713514
Genetic Background: B6.Cg-Tyr Sept5
Affected Genes: Sept5
Genomic Alteration: tm1Bld
Availability: Availability unknown check source stock center
Reference: PMID:16684884
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 4420999, RRID:MGI:4420999)

Source Database: MGI, catalog # 4420999
Genetic Background: involves: C57BL/6
Affected Genes: Tg(Camk2a-tTA)1Mmay
Genomic Alteration: Tg(tetO-LRRK2*G2019S)E3Cai; Tg(Camk2a-tTA)1Mmay
Availability: Availability unknown check source stock center
Reference: PMID:20064389
Notes: decreased body weight, abnormal nervous system physiology, abnormal neuron morphology, abnormal locomotor activation, hyperactivity, nervous system phenotype, behavior/neurological phenotype Allele Detail: Transgenic

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Cite this (MGI Cat# 3764503, RRID:MGI:3764503)

Source Database: MGI, catalog # 3764503
Genetic Background: involves: 129P2/OlaHsd * BALB/c
Affected Genes: Camk2a
Genomic Alteration: tm1Sva
Availability: Availability unknown check source stock center
Reference: PMID:1378648
Notes: decreased anxiety-related response, decreased paired-pulse facilitation, nervous system phenotype, reduced long term potentiation Allele Detail: Targeted

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Cite this (MGI Cat# 2450119, RRID:MGI:2450119)

Source Database: MGI, catalog # 2450119
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ugt8a
Genomic Alteration: tm1Pop
Availability: Availability unknown check source stock center
Reference: PMID:8706126, PMID:9464989, PMID:10601330
Notes: abnormal lipid level, ataxia, decreased body weight, abnormal head movements, premature death, tremors, hindlimb paralysis, abnormal myelination, abnormal nerve conduction, nervous system phenotype, immune system phenotype, abnormal nerve conduction Allele Detail: Targeted

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Cite this (MGI Cat# 3718910, RRID:MGI:3718910)

Source Database: MGI, catalog # 3718910
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: App
Genomic Alteration: tm1Umu
Availability: Availability unknown check source stock center
Reference: PMID:17634375
Notes: nervous system phenotype, growth/size/body region phenotype, behavior/neurological phenotype Allele Detail: Targeted

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