Stock 129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

FESA Number

1589

Strain Name

129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

Mutation Strain Type

Attribution

Gene/Allele Information

Allele Name Allele MGI ID Gene Name Gene MGI ID Chromosome
Pax6<Sey> MGI:1856155 Pax6 MGI:97490 2
Tg(Hbb-b1)83Clo MGI:2655271 3

Phenotypic Description

Reiterated transgene is detectable by DNA in situ hybridisation.

Publications

Displaying 121 - 130 of 141 Stock Publications
Pubmed ID Authors Title Journal
25936505 Kong JH Notch activity modulates the responsiveness of neural progenitors to sonic hedgehog signaling. Dev Cell (2 015) 33:373-87
18371392 Nikoletopoulou V Neurotrophin receptor-mediated death of misspecified neurons generated from embryonic stem cells lacking Pax6. Cell Stem Cell (2 007) 1:529-40
11502253 Scardigli R Crossregulation between Neurogenin2 and pathways specifying neuronal identity in the spinal cord. Neuron (2 001) 31:203-17
21625468 Szabó NE Interaction between axons and specific populations of surrounding cells is indispensable for collateral formation in the mammillary system. PLoS One (2 011) 6:e20315
9108373 Warren N Roles of Pax-6 in murine diencephalic development. Development (1 997) 124:1573-82
12648492 Collinson JM The roles of Pax6 in the cornea, retina, and olfactory epithelium of the developing mouse embryo. Dev Biol (2 003) 255:303-12
18165280 Faedo A COUP-TFI coordinates cortical patterning, neurogenesis, and laminar fate and modulates MAPK/ERK, AKT, and beta-catenin signaling. Cereb Cortex (2 008) 18:2117-31
11896398 Heins N Glial cells generate neurons: the role of the transcription factor Pax6. Nat Neurosci (2 002) 5:308-15
15878992 Kroll TT Ventralized dorsal telencephalic progenitors in Pax6 mutant mice generate GABA interneurons of a lateral ganglionic eminence fate. Proc Natl Acad Sci U S A (2 005) 102:7374-9
20844123 Panayi H Sox1 is required for the specification of a novel p2-derived interneuron subtype in the mouse ventral spinal cord. J Neurosci (2 010) 30:12274-80

Pages

Orphanet Categories

Rare developmental defect during embryogenesis
Rare urogenital disease
Rare renal disease
Rare eye disease
Rare endocrine disease
Rare oncologic disease
Rare gynecologic or obstetric disease
Rare neurologic disease

EMMA ID

EM:01891

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