X-linked intellectual disability gene CASK regulates postnatal brain growth in a non-cell autonomous manner (Q27317003)

26 June 2017

title

X-linked intellectual disability gene CASK regulates postnatal brain growth in a non-cell autonomous manner (English)

1 reference

X-linked intellectual disability

26 June 2017

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disability affecting intellectual abilities

1 reference

Sarika Srivastava

1

1 reference

26 June 2017

Ryan McMillan

2

1 reference

26 June 2017

Jeffery Willis

3

1 reference

26 June 2017

Helen Clark

4

1 reference

26 June 2017

Vrushali Chavan

5

1 reference

26 June 2017

Chen Liang

6

1 reference

26 June 2017

Haiyan Zhang

7

1 reference

26 June 2017

Matthew Hulver

8

1 reference

26 June 2017

Konark Mukherjee

9

1 reference

26 June 2017

publication date

31 March 2016

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Acta Neuropathologica Communications

26 June 2017

published in

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26 June 2017

volume

4

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26 June 2017

issue

1

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page(s)

30

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Neuron-specific protein interactions of Drosophila CASK-β are revealed by mass spectrometry

26 June 2017

cites work

1 reference

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Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient

21 March 2017

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Evolution of CASK into a Mg2+-sensitive kinase

21 March 2017

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PGC-1alpha/beta upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutations

21 March 2017

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Deletion of CASK in mice is lethal and impairs synaptic function

21 March 2017

1 reference

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Direct interaction of CASK/LIN-2 and syndecan heparan sulfate proteoglycan and their overlapping distribution in neuronal synapses

21 March 2017

1 reference

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Eukaryotic proteins expressed in Escherichia coli: An improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase

21 March 2017

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CASK: a novel dlg/PSD95 homolog with an N-terminal calmodulin-dependent protein kinase domain identified by interaction with neurexins

21 March 2017

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Math5 determines the competence state of retinal ganglion cell progenitors

21 March 2017

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Ablation of NF1 function in neurons induces abnormal development of cerebral cortex and reactive gliosis in the brain

21 March 2017

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Central presynaptic terminals are enriched in ATP but the majority lack mitochondria

21 March 2017

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Calcium/calmodulin-dependent serine protein kinase is involved in exendin-4-induced insulin secretion in INS-1 cells

21 March 2017

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Cdk5 promotes synaptogenesis by regulating the subcellular distribution of the MAGUK family member CASK

21 March 2017

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Genetic analysis of Mint/X11 proteins: essential presynaptic functions of a neuronal adaptor protein family

21 March 2017

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A role for Sec8 in oligodendrocyte morphological differentiation

21 March 2017

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Nuclear translocation and transcription regulation by the membrane-associated guanylate kinase CASK/LIN-2

21 March 2017

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Phase separation of integral membrane proteins in Triton X-114 solution

21 March 2017

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7 April 2017

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7 April 2017

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28 September 2017

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Selective overexpression of Toll-like receptor-4 in skeletal muscle impairs metabolic adaptation to high-fat feeding

28 September 2017

1 reference

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Phenotypic and molecular insights into CASK-related disorders in males

28 September 2017

1 reference

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A Critical Role of GIT1 in Vertebrate and Invertebrate Brain Development

28 September 2017

1 reference

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Late-onset epileptic spasms in a female patient with a CASK mutation

28 September 2017

1 reference

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High expression of CASK correlates with progression and poor prognosis of colorectal cancer

28 September 2017

1 reference

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Structural constraints and functional divergences in CASK evolution.

28 September 2017

1 reference

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Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targets

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

CASK (LIN2) interacts with Cx43 in wounded skin and their coexpression affects cell migration

28 September 2017

1 reference

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Nestin reporter transgene labels multiple central nervous system precursor cells

28 September 2017

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The mitochondrial connection in auditory neuropathy

28 September 2017

1 reference

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The Respiratory Exchange Ratio is Associated with Fitness Indicators Both in Trained and Untrained Men: A Possible Application for People with Reduced Exercise Tolerance.

28 September 2017

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Central regulation of locomotor behavior of Drosophila melanogaster depends on a CASK isoform containing CaMK-like and L27 domains

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders.

28 September 2017

1 reference

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A missense mutation in CASK causes FG syndrome in an Italian family

28 September 2017

1 reference

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Respiratory chain complex I deficiency in an infant with Ohtahara syndrome.

28 September 2017

1 reference

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

The role of the MAGUK protein CASK in neural development and synaptic function.

28 September 2017

1 reference

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Intermediate filament protein nestin is expressed in developing kidney and heart and might be regulated by the Wilms' tumor suppressor Wt1.

28 September 2017

1 reference

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Proteomic analysis reveals novel molecules involved in insulin signaling pathway

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

X linked mental retardation: a clinical guide

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

Mapping and expression analysis of the human CASK gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

Cerebellar hypoplasia in respiratory chain dysfunction

28 September 2017

1 reference

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Neuron-specific gene expression of synapsin I. Major role of a negative regulatory mechanism

28 September 2017

1 reference

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Isolation of integral membrane proteins by phase partitioning with Triton X-114.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

Isolation and genetic characterization of cell-lineage mutants of the nematode Caenorhabditis elegans

28 September 2017

1 reference

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Vulnerable periods of brain development. In: lipids, malnutrition & the developing brain

28 September 2017

1 reference

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Identification and characterization of 22 genes that affect the vulval cell lineages of the nematode Caenorhabditis elegans

28 September 2017

1 reference

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CASK aberrations in male patients with Ohtahara syndrome and cerebellar hypoplasia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

Phenotypic spectrum associated with CASK loss-of-function mutations

31 May 2018

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A simple composite phenotype scoring system for evaluating mouse models of cerebellar ataxia.

31 May 2018

1 reference

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

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

Endocrine status in patients with optic nerve hypoplasia: relationship to midline central nervous system abnormalities and appearance of the hypothalamic-pituitary axis on magnetic resonance imaging.

31 May 2018

1 reference

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Cre recombinase expression in cerebellar Purkinje cells.

31 May 2018

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Isolated lissencephaly sequence and double-cortex syndrome in a German family with a novel doublecortin mutation.

31 May 2018

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31 May 2018

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31 May 2018

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The C. elegans vulval induction gene lin-2 encodes a member of the MAGUK family of cell junction proteins

31 May 2018

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Vulnerability of Developing Brain: Relative Effects of Growth Restriction during the Fetal and Suckling Periods on Behavior and Brain Composition of Adult Rats

31 May 2018

1 reference

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Tightly coupled respiration in rat brain homogenates

31 May 2018

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Impaired energy metabolism in a Drosophila model of mitochondrial aconitase deficiency.

31 May 2018

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Mitochondrial disease and epilepsy.

21 January 2018

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Evidence for SNARE zippering during Ca2+-triggered exocytosis in PC12 cells

21 January 2018

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Regulation of mitochondrial protein import by cytosolic kinases.

21 January 2018

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A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.

21 January 2018

1 reference

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N-terminal palmitoylation of PSD-95 regulates association with cell membranes and interaction with K+ channel Kv1.4.

21 January 2018

1 reference

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Mutations of TSEN and CASK genes are prevalent in pontocerebellar hypoplasias type 2 and 4

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-016-0295-6

The genetic landscape of infantile spasms

21 January 2018

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https://api.crossref.org/works/10.1186%2FS40478-016-0295-6

DAF-9, a cytochrome P450 regulating C. elegans larval development and adult longevity

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4818453

A de novo CASK mutation in pontocerebellar hypoplasia type 3 with early myoclonic epilepsy and tetralogy of Fallot

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27036546

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A case of Ohtahara syndrome with cytochrome oxidase deficiency

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27036546

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S40478-016-0295-6

1 reference

OpenCitations bibliographic resource ID

26 June 2017

4974494

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4974494

1 reference