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 91 - 100 of 141 Stock Publications
Pubmed ID Authors Title Journal
10572034 Chapouton P The role of Pax6 in restricting cell migration between developing cortex and basal ganglia. Development (1 999) 126:5569-79
10409504 Engelkamp D Role of Pax6 in development of the cerebellar system. Development (1 999) 126:3585-96
19505513 Haba H Subtype-specific reduction of olfactory bulb interneurons in Pax6 heterozygous mutant mice. Neurosci Res (2 009) 65:116-21
7559133 Kaufman MH Craniofacial abnormalities in homozygous Small eye (Sey/Sey) embryos and newborn mice. J Anat (1 995) 186 ( Pt 3):607-17
11739261 Muzio L Emx2 and Pax6 control regionalization of the pre-neuronogenic cortical primordium. Cereb Cortex (2 002) 12:129-39
18448636 Sakurai K The neurogenesis-controlling factor, Pax6, inhibits proliferation and promotes maturation in murine astrocytes. J Neurosci (2 008) 28:4604-12
11050125 Stoykova A Pax6 modulates the dorsoventral patterning of the mammalian telencephalon. J Neurosci (2 000) 20:8042-50
16476661 Waclaw RR The zinc finger transcription factor Sp8 regulates the generation and diversity of olfactory bulb interneurons. Neuron (2 006) 49:503-16
16979618 Quinn JC Pax6 controls cerebral cortical cell number by regulating exit from the cell cycle and specifies cortical cell identity by a cell autonomous mechanism. Dev Biol (2 007) 302:50-65
4972360 Clayton RM Small eye, a mutant in the house mouse apparently affecting the synthesis of extracellular membranes. J Physiol (1 968) 198:74passim-75p

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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