Novel approaches to studying the genetic basis of cerebellar development (Q33553583)

28 July 2017

1 reference

title

Novel approaches to studying the genetic basis of cerebellar development (English)

1 reference

28 July 2017

Kathleen J Millen

3

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author name string

Samin A Sajan

series ordinal

1

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28 July 2017

Kathryn E Waimey

series ordinal

2

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28 July 2017

publication date

1 September 2010

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28 July 2017

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28 July 2017

volume

9

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28 July 2017

issue

3

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28 July 2017

page(s)

272-283

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A developmental and genetic classification for midbrain-hindbrain malformations

28 July 2017

cites work

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Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation

21 June 2018

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Anatomy of zebrafish cerebellum and screen for mutations affecting its development

21 June 2018

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Malformations of the midbrain and hindbrain: a retrospective study and review of the literature

21 June 2018

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Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum

21 June 2018

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Identification of a transient subpial neurogenic zone in the developing dentate gyrus and its regulation by Cxcl12 and reelin signaling

21 June 2018

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CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290

21 June 2018

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The cerebellum, cerebellar disorders, and cerebellar research--two centuries of discoveries

21 June 2018

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The balance of reproducibility, sensitivity, and specificity of lists of differentially expressed genes in microarray studies

21 June 2018

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tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

21 June 2018

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Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome

21 June 2018

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The MAGUK-family protein CASK is targeted to nuclei of the basal epidermis and controls keratinocyte proliferation

21 June 2018

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Cerebellar development and disease

21 June 2018

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Hh and Wnt signaling regulate formation of olig2+ neurons in the zebrafish cerebellum

21 June 2018

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CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa

21 June 2018

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Annotating genes of known and unknown function by large-scale coexpression analysis

21 June 2018

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Primary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool

21 June 2018

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Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

21 June 2018

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Neurogenesis in the cerebellum

21 June 2018

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Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia

21 June 2018

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Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development

21 June 2018

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The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

21 June 2018

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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

21 June 2018

1 reference

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Morphology, molecular codes, and circuitry produce the three-dimensional complexity of the cerebellum

21 June 2018

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Conditional gene targeting in the mouse nervous system: Insights into brain function and diseases.

21 June 2018

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Decreased GAD67 mRNA levels in cerebellar Purkinje cells in autism: pathophysiological implications

21 June 2018

1 reference

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The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome

21 June 2018

1 reference

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Cerebellar 'transcriptome' reveals cell-type and stage-specific expression during postnatal development and tumorigenesis

21 June 2018

1 reference

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The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

21 June 2018

1 reference

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Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome

21 June 2018

1 reference

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Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum

21 June 2018

1 reference

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Proteomic analysis of a eukaryotic cilium

21 June 2018

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The ZIC gene family in development and disease.

21 June 2018

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Mutations in PTF1A cause pancreatic and cerebellar agenesis

21 June 2018

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Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness.

21 June 2018

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Autism and abnormal development of brain connectivity.

21 June 2018

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Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria

21 June 2018

1 reference

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Deletion of the neuron-specific protein delta-catenin leads to severe cognitive and synaptic dysfunction

21 June 2018

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Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation

21 June 2018

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Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome

21 June 2018

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Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)

21 June 2018

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Dandy-Walker malformation: a review of 78 cases diagnosed by prenatal sonography

21 June 2018

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The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome

21 June 2018

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Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene

21 June 2018

1 reference

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RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathways

21 June 2018

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Development and malformations of the cerebellum in mice

21 June 2018

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Human malformations of the midbrain and hindbrain: review and proposed classification scheme

21 June 2018

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Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4

21 June 2018

1 reference

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Staggerer, a new mutation in the mouse affecting the cerebellum

21 June 2018

1 reference

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Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

21 June 2018

1 reference

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Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

21 June 2018

1 reference

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Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia

21 June 2018

1 reference

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Efficient recombination in diverse tissues by a tamoxifen-inducible form of Cre: a tool for temporally regulated gene activation/inactivation in the mouse

21 June 2018

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Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations

21 June 2018

1 reference

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

21 June 2018

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The isthmic organizer and brain regionalization

21 June 2018

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Neural plate patterning: upstream and downstream of the isthmic organizer

21 June 2018

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Otx2, Gbx2 and Fgf8 interact to position and maintain a mid-hindbrain organizer

21 June 2018

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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

21 June 2018

1 reference

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Granule cells and cerebellar boundaries: analysis of Unc5h3 mutant chimeras

21 June 2018

1 reference

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Hemizygosity of delta-catenin (CTNND2) is associated with severe mental retardation in cri-du-chat syndrome

21 June 2018

1 reference

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Role of Pax6 in development of the cerebellar system

21 June 2018

1 reference

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Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog

21 June 2018

1 reference

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The bHLH protein PTF1-p48 is essential for the formation of the exocrine and the correct spatial organization of the endocrine pancreas

21 June 2018

1 reference

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Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner

21 June 2018

1 reference

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Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin.

21 June 2018

1 reference

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Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice

21 June 2018

1 reference

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Neuropathology of the cerebellum in schizophrenia--an update: 1996 and future directions

21 June 2018

1 reference

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The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein

21 June 2018

1 reference

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Ataxia and altered dendritic calcium signaling in mice carrying a targeted null mutation of the calbindin D28k gene

21 June 2018

1 reference

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Absence epilepsy in tottering mutant mice is associated with calcium channel defects

21 June 2018

1 reference

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Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration

21 June 2018

1 reference

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Deficits in memory and hippocampal long-term potentiation in mice with reduced calbindin D28K expression.

21 June 2018

1 reference

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Developmental changes in expression and distribution of the glutamate receptor channel delta 2 subunit according to the Purkinje cell maturation.

21 June 2018

1 reference

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Disruption of the nuclear hormone receptor RORalpha in staggerer mice

21 June 2018

1 reference

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The brain in infantile autism: posterior fossa structures are abnormal

21 June 2018

1 reference

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Motor deficit and impairment of synaptic plasticity in mice lacking mGluR1.

21 June 2018

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21 June 2018

1 reference

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A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Architectonic and hodological organization of the cerebellum in reeler mutant mice

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Numerical matching between granule and Purkinje cells in lurcher chimeric mice: a hypothesis for the trophic rescue of granule cells from target-related cell death

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Anatomical, Physiological and biochemical studies of the cerebellum fromreelermutant mouse

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Microstructural organization of cerebellar tracts in schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Stem cells in the adult zebrafish cerebellum: initiation and maintenance of a novel stem cell niche.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Altered expression of genes involved in GABAergic transmission and neuromodulation of granule cell activity in the cerebellum of schizophrenia patients

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Immunohistochemical localization of GABA, GAD65, and the receptor subunits GABAAalpha1 and GABAB1 in the zebrafish cerebellum

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Forkhead transcription factor FoxM1 regulates mitotic entry and prevents spindle defects in cerebellar granule neuron precursors.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Pax6 is required for delta-catenin/neurojugin expression during retinal, cerebellar and cortical development in mice

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

The roof plate regulates cerebellar cell-type specification and proliferation

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Highly restricted expression of Cre recombinase in cerebellar Purkinje cells

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Altered neuronal excitability in cerebellar granule cells of mice lacking calretinin.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Molecular analysis of gene expression in the developing pontocerebellar projection system

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Impairment of motor coordination, Purkinje cell synapse formation, and cerebellar long-term depression in GluR delta 2 mutant mice

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Cerebellar cell degeneration in the leaner mutant mouse

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2921561

Staggerer chimeras: Intrinsic nature of purkinje cell defects and implications for normal cerebellar development

31 October 2018

1 reference

12 December 2020

Multiple innervation of cerebellar Purkinje cells by climbing fibres in staggerer mutant mouse

1 reference

12 December 2020

Role of the Staggerer gene in determining Purkinje cell number in the cerebellar cortex of mouse chimeras

1 reference

12 December 2020

Isthmus organizer for midbrain and hindbrain development

1 reference

12 December 2020

Cilia Proteins Control Cerebellar Morphogenesis by Promoting Expansion of the Granule Progenitor Pool

1 reference

12 December 2020

10.1007/S12311-010-0169-6

Identifiers

DOI

1 reference

Dimensions Publication ID

28 July 2017

0 references

1 reference

28 July 2017

1 reference