Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.

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Identification of a Novel ENU-Induced Mutation in Mouse Tbx1 Linked to Human DiGeorge Syndrome.Screening for Mutations in the TBX1 Gene on Chromosome 22q11.2 in Schizophrenia.

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Q37571750-D4F07CAA-AA3F-41D8-8CA2-65DAB6C57575 Q39159190-DB6B9C15-DCC0-4ADE-A6C9-5972AB49D59C

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Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.

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2016 nî lūn-bûn

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2016年の論文

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Cortical Development Requires ...... in 22q11.2 Deletion Syndrome.

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Cortical Development Requires ...... in 22q11.2 Deletion Syndrome.

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Cortical Development Requires ...... in 22q11.2 Deletion Syndrome.

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Cortical Development Requires ...... in 22q11.2 Deletion Syndrome.

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Cortical Development Requires ...... in 22q11.2 Deletion Syndrome.

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Cortical Development Requires ...... in 22q11.2 Deletion Syndrome.

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Cortical Development Requires ...... in 22q11.2 Deletion Syndrome.

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Elizabeth Illingworth

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Gemma Flore

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Marchesa Bilio

http://www.w3.org/2001/XMLSchema#string

Sara Cioffi

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P2860

Role of TBX1 in human del22q11.2 syndrome

T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex

Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis.

Expression of the antiproliferative gene TIS21 at the onset of neurogenesis identifies single neuroepithelial cells that switch from proliferative to neuron-generating division

Live imaging at the onset of cortical neurogenesis reveals differential appearance of the neuronal phenotype in apical versus basal progenitor progeny

Tbx1 regulates the BMP-Smad1 pathway in a transcription independent manner.

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

Human studies of prepulse inhibition of startle: normal subjects, patient groups, and pharmacological studies

Oscillations in notch signaling regulate maintenance of neural progenitors

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2210-2225

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scholarly article

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10.1093/CERCOR/BHW076

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2016-03-21T00:00:00Z

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27005988

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haploinsufficiency

Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.

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P2860

P2860

Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.

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P577

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P577

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