(Q24793088)

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The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy

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scholarly article

1 reference

Europe PubMed Central

2 July 2017

The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy (English)

1 reference

Europe PubMed Central

2 July 2017

0 references

neuronal ceroid lipofuscinosis

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

3

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Anna-Elina Lehesjoki

7

object named as

Anna-Elina Lehesjoki

1 reference

Europe PubMed Central

2 July 2017

author name string

Liina Lonka

1

1 reference

Europe PubMed Central

2 July 2017

Antti Aalto

2

1 reference

Europe PubMed Central

2 July 2017

Mervi Kuronen

4

1 reference

Europe PubMed Central

2 July 2017

Zaal Kokaia

5

1 reference

Europe PubMed Central

2 July 2017

Mart Saarma

6

1 reference

Europe PubMed Central

2 July 2017

Outi Kopra

3

1 reference

Europe PubMed Central

2 July 2017

language of work or name

0 references

publication date

13 April 2005

1 reference

Europe PubMed Central

2 July 2017

BMC Neuroscience

1 reference

Europe PubMed Central

2 July 2017

6

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Europe PubMed Central

2 July 2017

1

0 references

27

1 reference

Europe PubMed Central

2 July 2017

https://scigraph.springernature.com/pub.10.1186/1471-2202-6-27

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-2202-6-27

Two novel mammalian Nogo receptor homologs differentially expressed in the central and peripheral nervous systems

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7 April 2017

Disruption of PPT1 or PPT2 causes neuronal ceroid lipofuscinosis in knockout mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

CLN3 protein is targeted to neuronal synapses but excluded from synaptic vesicles: new clues to Batten disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Palmitoyl protein thioesterase (PPT) localizes into synaptosomes and synaptic vesicles in neurons: implications for infantile neuronal ceroid lipofuscinosis (INCL)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Apparent loss and hypertrophy of interneurons in a mouse model of neuronal ceroid lipofuscinosis: evidence for partial response to insulin-like growth factor-1 treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Modification of seizure activity by electrical stimulation. II. Motor seizure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Status epilepticus induces changes in the expression and localization of endogenous palmitoyl-protein thioesterase 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Developmental expression of palmitoyl protein thioesterase in normal mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Palmitoyl-protein thioesterase, an enzyme implicated in neurodegeneration, is localized in neurons and is developmentally regulated in rat brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Spinal cord GLT-1 glutamate transporter and blood glutamic acid alterations in motor neuron degeneration (Mnd) mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Cytoplasmic inclusions in spinal neurons of the motor neuron degeneration (Mnd) mouse. I. Light microscopic analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Retinal degeneration in motor neuron degeneration (mnd) mutant mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Autosomal dominance in a late-onset motor neuron disease in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Neurofilament distribution is altered in the Mnd (motor neuron degeneration) mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

7 April 2017

Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

Regulation of the mitochondrial ATP-synthase in health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

Generalization of rapidly recurring seizures is suppressed in mice lacking glial cell line-derived neurotrophic factor family receptor alpha2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

Progress towards understanding the neurobiology of Batten disease or neuronal ceroid lipofuscinosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

The neuronal ceroid-lipofuscinoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

Development and persistence of kindling epilepsy are impaired in mice lacking glial cell line-derived neurotrophic factor family receptor alpha 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

GDNF family ligands and receptors are differentially regulated after brain insults in the rat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

A permanent change in brain function resulting from daily electrical stimulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

Neuronal ceroid-lipofuscinoses in childhood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 September 2017

Hippocampal lesions in the neuronal ceroid lipofuscinoses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

30 May 2018

Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 null mutant mouse model of infantile neuronal ceroid lipofuscinosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 November 2018

Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 November 2018

Evaluation of 36 patients from Turkey with neuronal ceroid lipofuscinosis: clinical, neurophysiological, neuroradiological and histopathologic studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 November 2018

Expression of glutamate receptor subtypes in the spinal cord of control and mnd mice, a model of motor neuron disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 November 2018

Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 November 2018

Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 November 2018

The expression of palmitoyl-protein thioesterase is developmentally regulated in neural tissues but not in nonneural tissues.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1087490

28 November 2018

Histopathology of the late-onset motor neuron degeneration (Mnd) mutant in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/15826318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accumulating autofluorescent material as a marker for early changes in the spinal cord of the Mnd mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/15826318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated cathepsin D expression in kainate-evoked rat brain neurodegeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/15826318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Persistence of kindling: effect of partial kindling, retention interval, kindling site, and stimulation parameters

1 reference

https://pubmed.ncbi.nlm.nih.gov/15826318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of mRNAs for neurotrophins and their receptors in developing rat heart

1 reference

https://pubmed.ncbi.nlm.nih.gov/15826318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth

1 reference

https://pubmed.ncbi.nlm.nih.gov/15826318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2202-6-27

1 reference

Europe PubMed Central

2 July 2017

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1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-2202-6-27

0 references

1 reference

Europe PubMed Central

2 July 2017

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