Early changes in gene expression in two models of Batten disease. (Q48366315)

11 February 2018

title

Early changes in gene expression in two models of Batten disease. (English)

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11 February 2018

author name string

Yasser Elshatory

1

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11 February 2018

Andrew I Brooks

2

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11 February 2018

Subrata Chattopadhyay

3

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11 February 2018

Timothy M Curran

4

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11 February 2018

Praveena Gupta

5

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11 February 2018

Vijay Ramalingam

6

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11 February 2018

Sandra L Hofmann

7

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11 February 2018

David A Pearce

8

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11 February 2018

language of work or name

English

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publication date

1 March 2003

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11 February 2018

published in

FEBS Letters

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11 February 2018

volume

538

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11 February 2018

issue

1-3

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11 February 2018

page(s)

207-212

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11 February 2018

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Neuronal ceroid lipofuscinoses caused by defects in soluble lysosomal enzymes (CLN1 and CLN2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Biochemistry of neuronal ceroid lipofuscinoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Batten disease and the ATP synthase subunit c turnover pathway: raising antibodies to subunit c.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Batten disease: evaluation of CLN3 mutations on protein localization and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Protection against oxidative stress-induced cell death by intracellular platelet-activating factor-acetylhydrolase II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Lipid thioesters derived from acylated proteins accumulate in infantile neuronal ceroid lipofuscinosis: correction of the defect in lymphoblasts by recombinant palmitoyl-protein thioesterase

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

A new K+ channel beta subunit to specifically enhance Kv2.2 (CDRK) expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Calsyntenin-1, a proteolytically processed postsynaptic membrane protein with a cytoplasmic calcium-binding domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

An autoantibody inhibitory to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Positron emission tomography shows reduced striatal dopamine D1 but not D2 receptors in juvenile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

[18F]fluorodopa PET shows striatal dopaminergic dysfunction in juvenile neuronal ceroid lipofuscinosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Specific delay of degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis (Batten disease)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Specific storage of subunit c of mitochondrial ATP synthase in lysosomes of neuronal ceroid lipofuscinosis (Batten's disease)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

Classification of gas5 as a multi-small-nucleolar-RNA (snoRNA) host gene and a member of the 5'-terminal oligopyrimidine gene family reveals common features of snoRNA host genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900162-5

10.1016/S0014-5793(03)00162-5

7 January 2021

Identifiers

DOI

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11 February 2018

PubMed ID

12633880

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11 February 2018