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on page 1 showing 20 out of 1,332 results from 1 sources

Cite this (MGI Cat# 3663441, RRID:MGI:3663441)

Source Database: MGI, catalog # 3663441
Genetic Background: 129S6.Cg-Htr2a Htr2a Emx1
Affected Genes: Emx1, Htr2a
Genomic Alteration: tm1(cre)Ito; tm2Grch; tm1Grch
Availability: Availability unknown check source stock center
Reference: PMID:16873667
Notes: behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5908184, RRID:MGI:5908184)

Source Database: MGI, catalog # 5908184
Genetic Background: B6(Cg)-Kcnt2
Affected Genes: Kcnt2
Genomic Alteration: tm1.2Clin
Availability: Availability unknown check source stock center
Reference: PMID:26559620
Notes: behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5518626, RRID:MGI:5518626)

Source Database: MGI, catalog # 5518626
Genetic Background: involves: FVB/N
Affected Genes:
Genomic Alteration: Tg(Pcp2-ATXN1*30Q)2Horr
Availability: Availability unknown check source stock center
Reference: PMID:7553854
Notes: behavior/neurological phenotype Allele Detail: Transgenic

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Cite this (MGI Cat# 5818669, RRID:MGI:5818669)

Source Database: MGI, catalog # 5818669
Genetic Background: C3Fe.C3-Pcnx2 Gria4
Affected Genes: Gria4, Pcnx2
Genomic Alteration: spkw1; em4Frk
Availability: Availability unknown check source stock center
Reference: PMID:25010494
Notes: behavior/neurological phenotype Allele Detail: QTL, Endonuclease-mediated

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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# 3603413, RRID:MGI:3603413)

Source Database: MGI, catalog # 3603413
Genetic Background: involves: 129S/SvEv * C57BL/6
Affected Genes: Oxt
Genomic Alteration: tm1Wsy
Availability: Availability unknown check source stock center
Reference: PMID:9181490
Notes: behavior/neurological phenotype, abnormal defecation Allele Detail: Targeted

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Cite this (MGI Cat# 5298867, RRID:MGI:5298867)

Source Database: MGI, catalog # 5298867
Genetic Background: involves: C57BL/6 * DBA/2
Affected Genes:
Genomic Alteration: Tg(Avil-cre)1Phep
Availability: Availability unknown check source stock center
Reference: PMID:21906401
Notes: behavior/neurological phenotype Allele Detail: Transgenic

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Cite this (MGI Cat# 2684657, RRID:MGI:2684657)

Source Database: MGI, catalog # 2684657
Genetic Background: involves: FVB/N
Affected Genes: Psen1
Genomic Alteration: Tg(Thy1-cre)1Vln; tm1Vln
Availability: Availability unknown check source stock center
Reference: PMID:11978821
Notes: behavior/neurological phenotype, abnormal long term potentiation, nervous system phenotype, amyloid beta deposits Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 3722689, RRID:MGI:3722689)

Source Database: MGI, catalog # 3722689
Genetic Background: involves: 129S6/SvEvTac * C57BL/6NCr * C57BL/6NTac
Affected Genes: Nmur1
Genomic Alteration: tm1Rtor
Availability: Availability unknown check source stock center
Reference: PMID:17379411
Notes: behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3849318, RRID:MGI:3849318)

Source Database: MGI, catalog # 3849318
Genetic Background: involves: 129P2/OlaHsd
Affected Genes: B3gat1
Genomic Alteration: tm1Tkaw
Availability: Availability unknown check source stock center
Reference: PMID:19265195
Notes: behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 4438371, RRID:MGI:4438371)

Source Database: MGI, catalog # 4438371
Genetic Background: involves: 129S4/SvJae
Affected Genes: Bdnf
Genomic Alteration: tm3Jae
Availability: Availability unknown check source stock center
Reference: PMID:20133801
Notes: impaired cued conditioning behavior, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5297805, RRID:MGI:5297805)

Source Database: MGI, catalog # 5297805
Genetic Background: B6.129P2-Cic
Affected Genes: Cic
Genomic Alteration: Gt(XE565)Byg
Availability: Availability unknown check source stock center
Reference: PMID:22053053
Notes: behavior/neurological phenotype, mortality/aging Allele Detail: Gene trapped

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Cite this (MGI Cat# 4417866, RRID:MGI:4417866)

Source Database: MGI, catalog # 4417866
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J
Affected Genes: Dnajc3, Sil1
Genomic Alteration: tm8663Wcl; Gt(RST462)Byg
Availability: Availability unknown check source stock center
Reference: PMID:19801575
Notes: behavior/neurological phenotype, Purkinje cell degeneration Allele Detail: Gene trapped, Targeted

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Cite this (MGI Cat# 3620241, RRID:MGI:3620241)

Source Database: MGI, catalog # 3620241
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Plp1
Genomic Alteration: tm1Kan
Availability: Availability unknown check source stock center
Reference: PMID:9010205
Notes: behavior/neurological phenotype, abnormal myelin sheath morphology, axonal spheroids Allele Detail: Targeted

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Cite this (MGI Cat# 5487808, RRID:MGI:5487808)

Source Database: MGI, catalog # 5487808
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Gpm6b
Genomic Alteration: tm1Kan
Availability: Availability unknown check source stock center
Reference: PMID:23322581
Notes: behavior/neurological phenotype, abnormal axon morphology, abnormal myelin sheath morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3810360, RRID:MGI:3810360)

Source Database: MGI, catalog # 3810360
Genetic Background: involves: 129 * 129S/SvEv
Affected Genes: Hprt
Genomic Alteration: b-m1
Availability: Availability unknown check source stock center
Reference: PMID:3221240
Notes: decreased vertical activity, behavior/neurological phenotype, decreased dopamine level, abnormal motor coordination/balance Allele Detail: Transgenic

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Cite this (MGI Cat# 6159389, RRID:MGI:6159389)

Source Database: MGI, catalog # 6159389
Genetic Background: involves: C3H * C57BL/6J * C57BL/6N * FVB/N
Affected Genes: Brpf3
Genomic Alteration: tm1d(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:26677226
Notes: behavior/neurological phenotype, homeostasis/metabolism phenotype, reproductive system phenotype, mortality/aging, hematopoietic system phenotype, cellular phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 6158942, RRID:MGI:6158942)

Source Database: MGI, catalog # 6158942
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6
Affected Genes: Scg3
Genomic Alteration: Gt(VICTR20)13Lex
Availability: Availability unknown check source stock center
Reference: PMID:29281094
Notes: abnormal pancreas physiology, reproductive system phenotype, increased susceptibility to diet-induced obesity, abnormal pituitary gland physiology, behavior/neurological phenotype, decreased circulating insulin level, homeostasis/metabolism phenotype, mortality/aging, impaired glucose tolerance Allele Detail: Gene trapped

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Cite this (MGI Cat# 6159715, RRID:MGI:6159715)

Source Database: MGI, catalog # 6159715
Genetic Background: C57BL/6J-Arid1b
Affected Genes: Arid1b
Genomic Alteration: em1Hzhu
Availability: Availability unknown check source stock center
Reference: PMID:28695822
Notes: decreased heart weight, small kidney, abnormal insulin-like growth factor I level, decreased body size, increased grooming behavior, increased anxiety-related response, decreased circulating insulin-like growth factor I level, decreased neuron number, abnormal hypothalamus physiology, hydroencephaly, abnormal response to social novelty, abnormal vocalization, behavior/neurological phenotype, decreased corpus callosum size, decreased dentate gyrus size, decreased grip strength, decreased cerebral cortex cell number, thin cerebral cortex, abnormal dentate gyrus morphology, decreased body length, decreased body weight, postnatal growth retardation, decreased kidney weight, small heart, muscle weakness, abnormal homeostasis Allele Detail: Endonuclease-mediated

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Cite this (MGI Cat# 3819777, RRID:MGI:3819777)

Source Database: MGI, catalog # 3819777
Genetic Background: involves: C3H/HeRos * C57BL/10Ros
Affected Genes: ckr
Genomic Alteration: ckr
Availability: Availability unknown check source stock center
Reference: PMID:14709346
Notes: behavior/neurological phenotype, dilated lateral ventricles Allele Detail: Transgenic

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