(Q35237718)

English

Finding the most appropriate mouse model of juvenile CLN3 (Batten) disease for therapeutic studies: the importance of genetic background and gender

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Finding the most appropriate mouse model of juvenile CLN3 (Batten) disease for therapeutic studies: the importance of genetic background and gender (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

Attila D Kovács

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

David A Pearce

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

publication date

1 April 2015

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Disease Models & Mechanisms

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

351-361

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Location- and sex-specific differences in weight and motor coordination in two commonly used mouse strains

1 reference

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NCL diseases - clinical perspectives

1 reference

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Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses.

1 reference

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New nomenclature and classification scheme for the neuronal ceroid lipofuscinoses

1 reference

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Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system

1 reference

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Age-dependent therapeutic effect of memantine in a mouse model of juvenile Batten disease

1 reference

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Interplay between DISC1 and GABA signaling regulates neurogenesis in mice and risk for schizophrenia

1 reference

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N-acetylcysteine prevents loss of dopaminergic neurons in the EAAC1-/- mouse

1 reference

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Altered sensitivity of cerebellar granule cells to glutamate receptor overactivation in the Cln3(Δex7/8)-knock-in mouse model of juvenile neuronal ceroid lipofuscinosis

1 reference

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Temporary inhibition of AMPA receptors induces a prolonged improvement of motor performance in a mouse model of juvenile Batten disease

1 reference

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27 July 2018

Immunosuppression alters disease severity in juvenile Batten disease mice

1 reference

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27 July 2018

Altered sensitivity to excitotoxic cell death and glutamate receptor expression between two commonly studied mouse strains

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Involvement of NMDAR2A tyrosine phosphorylation in depression-related behaviour

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Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis.

1 reference

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Sex-specific genetic architecture of human disease

1 reference

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27 July 2018

Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models

1 reference

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27 July 2018

Attenuation of AMPA receptor activity improves motor skills in a mouse model of juvenile Batten disease

1 reference

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Alterations in striatal dopamine catabolism precede loss of substantia nigra neurons in a mouse model of juvenile neuronal ceroid lipofuscinosis

1 reference

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Mouse strain differences in autonomic responses to stress

1 reference

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27 July 2018

Selectively increased sensitivity of cerebellar granule cells to AMPA receptor-mediated excitotoxicity in a mouse model of Batten disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381334

27 July 2018

Visual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons

1 reference

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27 July 2018

High resolution 1H NMR-based metabolomics indicates a neurotransmitter cycling deficit in cerebral tissue from a mouse model of Batten disease

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The tail suspension test as a model for assessing antidepressant activity: review of pharmacological and genetic studies in mice

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Genetic vulnerability to diet-induced obesity in the C57BL/6J mouse: physiological and molecular characteristics

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Current state of clinical and morphological features in human NCL.

1 reference

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Motor dysfunction in type 5 adenylyl cyclase-null mice

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Transgenic studies of pain and analgesia: mutation or background genotype?

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27 July 2018

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

1 reference

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Behavioral organization is independent of locomotor activity in 129 and C57 mouse strains

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Reversal of diet-induced obesity and diabetes in C57BL/6J mice.

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Isolation of a novel gene underlying Batten disease, CLN3. The International Batten Disease Consortium

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1 reference

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1 reference

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A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis.

1 reference

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1 reference

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1 reference

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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/26035843

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inferred from PubMed ID database lookup

Genetic modifiers interact with maternal determinants in vascular development of Tgfb1(-/-) mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/26035843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of Nicotinamide Nucleotide Transhydrogenase: A New Quantitive Trait Locus Accounting for Glucose Intolerance in C57BL/6J Mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/26035843

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based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/26035843

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Identifiers

10.1242/DMM.018804

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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