Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome (Q36342477)

13 August 2017

Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome (English)

1 reference

13 August 2017

Alice Meunier

2

0 references

Nathalie Spassky

object named as

Nathalie Spassky

8

0 references

Andrea Aguilar

object named as

Andrea Aguilar

1

0 references

Tania Attié-Bitach

object named as

Tania Attie-Bitach

6

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author name string

Laetitia Strehl

3

1 reference

13 August 2017

Jelena Martinovic

4

1 reference

13 August 2017

Maryse Bonniere

5

1 reference

13 August 2017

Féréchté Encha-Razavi

7

1 reference

13 August 2017

language of work or name

English

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publication date

1 October 2012

1 reference

Proceedings of the National Academy of Sciences of the United States of America

13 August 2017

1 reference

13 August 2017

109

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13 August 2017

42

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13 August 2017

16951-16956

1 reference

describes a project that uses

13 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3479472/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

1 reference

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Modeling human disease in humans: the ciliopathies

30 September 2017

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A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition

30 September 2017

1 reference

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Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome

30 September 2017

1 reference

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Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

30 September 2017

1 reference

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KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes

30 September 2017

1 reference

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Cilia in the nervous system: linking cilia function and neurodevelopmental disorders

30 September 2017

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Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1.

30 September 2017

1 reference

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Ciliopathies: an expanding disease spectrum

30 September 2017

1 reference

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Joubert Syndrome and related disorders

30 September 2017

1 reference

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The ciliary pocket: an endocytic membrane domain at the base of primary and motile cilia

30 September 2017

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Transventricular delivery of Sonic hedgehog is essential to cerebellar ventricular zone development

30 September 2017

1 reference

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The primary cilium: a signalling centre during vertebrate development

30 September 2017

1 reference

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The primary cilium as a Hedgehog signal transduction machine

30 September 2017

1 reference

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Dual and opposing roles of primary cilia in medulloblastoma development

30 September 2017

1 reference

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The nonmotile ciliopathies

30 September 2017

1 reference

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A mouse model for Meckel syndrome type 3.

30 September 2017

1 reference

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CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

30 September 2017

1 reference

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CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease

30 September 2017

1 reference

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Cep164, a novel centriole appendage protein required for primary cilium formation

30 September 2017

1 reference

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A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

30 September 2017

1 reference

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

30 September 2017

1 reference

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Genetic basis of Joubert syndrome and related disorders of cerebellar development

30 September 2017

1 reference

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Spatial pattern of sonic hedgehog signaling through Gli genes during cerebellum development

30 September 2017

1 reference

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Sonic hedgehog signaling is required for expansion of granule neuron precursors and patterning of the mouse cerebellum

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Cerebellar vermis hypoplasia in a patient with Bardet-Biedl syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Wnt/beta-catenin/Tcf signaling induces the transcription of Axin2, a negative regulator of the signaling pathway

30 September 2017

1 reference

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Sonic hedgehog regulates the growth and patterning of the cerebellum

30 September 2017

1 reference

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Purkinje-cell-derived Sonic hedgehog regulates granule neuron precursor cell proliferation in the developing mouse cerebellum

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Modulation of transcriptional regulation by LEF-1 in response to Wnt-1 signaling and association with beta-catenin

30 September 2017

1 reference

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Nucleokinesis in tangentially migrating neurons comprises two alternating phases: forward migration of the Golgi/centrosome associated with centrosome splitting and myosin contraction at the rear.

30 September 2017

1 reference

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Expression of Sonic hedgehog during cell proliferation in the human cerebellum

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

Induction of a beta-catenin-LEF-1 complex by wnt-1 and transforming mutants of beta-catenin

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479472

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

22 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23027964

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.1201408109

1 reference

13 August 2017

0 references

1 reference

13 August 2017

PubMed publication ID

23027964

1 reference