Barhl1 regulates migration and survival of cerebellar granule cells by controlling expression of the neurotrophin-3 gene (Q28512449)

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26 December 2019

title

Barhl1 regulates migration and survival of cerebellar granule cells by controlling expression of the neurotrophin-3 gene (English)

2 references

25 January 2017

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26 December 2019

0 references

1 reference

GOA release 2020-03-11

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Shengguo Li

1

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26 December 2019

Feng Qiu

2

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26 December 2019

Anlong Xu

3

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26 December 2019

Mengqing Xiang

5

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26 December 2019

Sandy M Price

4

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26 December 2019

language of work or name

English

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publication date

1 March 2004

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26 December 2019

published in

Journal of Neuroscience

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volume

24

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issue

12

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26 December 2019

page(s)

3104-3114

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Specification of distinct dopaminergic neural pathways: roles of the Eph family receptor EphB1 and ligand ephrin-B2.

26 December 2019

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Neurotrophin-3 is required for proper cerebellar development

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NeuroD is required for differentiation of the granule cells in the cerebellum and hippocampus

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Autoregulation and multiple enhancers control Math1 expression in the developing nervous system

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Netrin 1 acts as an attractive or as a repulsive cue for distinct migrating neurons during the development of the cerebellar system

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Increased cell death and delayed development in the cerebellum of mice lacking the rev-erbA(alpha) orphan receptor.

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Neurotrophin-3 controls proliferation of granular precursors as well as survival of mature granule neurons in the developing rat cerebellum.

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Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNS.

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Granule cells and cerebellar boundaries: analysis of Unc5h3 mutant chimeras

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The rhombic lip and early cerebellar development

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Ephrin-B reverse signaling is mediated by a novel PDZ-RGS protein and selectively inhibits G protein-coupled chemoattraction

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Overexpression of MATH1 disrupts the coordination of neural differentiation in cerebellum development.

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Proprioceptor pathway development is dependent on Math1.

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Sequential actions of BMP receptors control neural precursor cell production and fate

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Pax6 regulates granule cell polarization during parallel fiber formation in the developing cerebellum

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BDNF stimulates migration of cerebellar granule cells.

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Hearing loss caused by progressive degeneration of cochlear hair cells in mice deficient for the Barhl1 homeobox gene

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New directions in neuronal migration

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Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

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Regional expression of p75NTR contributes to neurotrophin regulation of cerebellar patterning.

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Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency

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Characterization of a neurotrophin signaling mechanism that mediates neuron survival in a temporally specific pattern.

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12 December 2020

Dual Bar homeo box genes of Drosophila required in two photoreceptor cells, R1 and R6, and primary pigment cells for normal eye development

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12 December 2020

Subtype determination of Drosophila embryonic external sensory organs by redundant homeo box genes BarH1 and BarH2.

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Ontogeny of afferents to the fetal rat cerebellum

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Role of the Barhl2 homeobox gene in the specification of glycinergic amacrine cells

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Identification of a different-type homeobox gene, BarH1, possibly causing Bar (B) and Om(1D) mutations in Drosophila.

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Development of the precerebellar nuclei in the rat: I. The precerebellar neuroepithelium of the rhombencephalon

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Development of the precerebellar nuclei in the rat: II. The intramural olivary migratory stream and the neurogenetic organization of the inferior olive

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Development of the precerebellar nuclei in the rat: III. The posterior precerebellar extramural migratory stream and the lateral reticular and external cuneate nuclei

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Development of the precerebellar nuclei in the rat: IV. The anterior precerebellar extramural migratory stream and the nucleus reticularis tegmenti pontis and the basal pontine gray

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Neurotrophin-3 is expressed in the posterior lobe of mouse cerebellum, but does not affect the cerebellar development

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The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons

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Brn-3b: a POU domain gene expressed in a subset of retinal ganglion cells

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A mammalian helix-loop-helix factor structurally related to the product of Drosophila proneural gene atonal is a positive transcriptional regulator expressed in the developing nervous system.

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Differential expression of brain-derived neurotrophic factor, neurotrophin-3, and low-affinity nerve growth factor receptor during the postnatal development of the rat cerebellar system.

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Neurotrophins promote the survival and development of neurons in the cerebellum of hypothyroid rats in vivo

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Deleted in Colorectal Cancer (DCC) encodes a netrin receptor

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12 December 2020

Evolutionary conservation of sequence and expression of the bHLH protein Atonal suggests a conserved role in neurogenesis

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12 December 2020

Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling

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12 December 2020

TrkB and TrkC neurotrophin receptors cooperate in promoting survival of hippocampal and cerebellar granule neurons.

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12 December 2020

Requirement for Brn-3.0 in differentiation and survival of sensory and motor neurons

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12 December 2020

Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system

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12 December 2020

Genes involved in cerebellar cell specification and differentiation

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Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene

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Vertebrate homologues of C. elegans UNC-5 are candidate netrin receptors

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Tissue-specific expression of murine Nkx3.1 in the male urogenital system

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Abnormal cerebellar development and foliation in BDNF-/- mice reveals a role for neurotrophins in CNS patterning.

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Math1 is essential for genesis of cerebellar granule neurons.

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12 December 2020

Embryonic phenotype of Unc5h3 mutant mice suggests chemorepulsion during the formation of the rostral cerebellar boundary

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12 December 2020

Progenitors of dorsal commissural interneurons are defined by MATH1 expression.

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12 December 2020

Mammalian BarH homologue is a potential regulator of neural bHLH genes

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12 December 2020

Truncation mutations in the transactivation region of PAX6 result in dominant-negative mutants

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Neurotrophin-3 promotes cerebellar granule cell exit from the EGL.

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12 December 2020

10.1523/JNEUROSCI.4444-03.2004

Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

741814

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