(Q36358136)

13 August 2017

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title

Neuronal survival in epilepsy: to die or not to die? (English)

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13 August 2017

Subramaniam Ganesh

1

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13 August 2017

Shweta Singh

series ordinal

2

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13 August 2017

publication date

1 December 2005

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13 August 2017

published in

Journal of Biosciences

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13 August 2017

volume

30

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13 August 2017

issue

5

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13 August 2017

page(s)

561-566

1 reference

https://scigraph.springernature.com/pub.10.1007/bf02703553

13 August 2017

exact match

0 references

cites work

Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF02703553

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

21 January 2018

1 reference

12 December 2020

Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis.

1 reference

12 December 2020

BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy

1 reference

12 December 2020

LGI1, a putative tumor metastasis suppressor gene, controls in vitro invasiveness and expression of matrix metalloproteinases in glioma cells through the ERK1/2 pathway

1 reference

12 December 2020

A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors

1 reference

12 December 2020

Causes of epilepsy: contributions of the Rochester epidemiology project.

1 reference

12 December 2020

Advances in the genetics of progressive myoclonus epilepsy

1 reference

12 December 2020

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

1 reference

12 December 2020

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

1 reference

12 December 2020

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

1 reference

12 December 2020

Expanding roles of programmed cell death in mammalian neurodevelopment

1 reference

12 December 2020

Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice

1 reference

12 December 2020

Abnormal cerebral structure in juvenile myoclonic epilepsy demonstrated with voxel-based analysis of MRI

1 reference

12 December 2020

The CLN3 gene is a novel molecular target for cancer drug discovery.

1 reference

12 December 2020

Cystatin B-deficient mice have increased expression of apoptosis and glial activation genes

1 reference

12 December 2020

To die or not to die for neurons in ischemia, traumatic brain injury and epilepsy: a review on the stress-activated signaling pathways and apoptotic pathways

1 reference

12 December 2020

Nuclear localization of a non-caspase truncation product of atrophin-1, with an expanded polyglutamine repeat, increases cellular toxicity

1 reference

12 December 2020

Activation-induced nuclear translocation of RING3

1 reference

12 December 2020

Recent developments in the quest for myoclonic epilepsy genes.

1 reference

12 December 2020

Flupirtine blocks apoptosis in batten patient lymphoblasts and in human postmitotic CLN3- and CLN2-deficient neurons

1 reference

12 December 2020

Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice

1 reference

12 December 2020

Change in nuclear-cytoplasmic localization of a double-bromodomain protein during proliferation and differentiation of mouse spinal cord and dorsal root ganglia

1 reference

12 December 2020

Epilepsy's role in the historical differentiation of religion, magic, and science

1 reference

12 December 2020

The channelopathies: novel insights into molecular and genetic mechanisms of human disease

1 reference

12 December 2020

Mutations in EFHC1 cause juvenile myoclonic epilepsy

1 reference

12 December 2020

Channelopathies as a genetic cause of epilepsy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02703553

1 reference

release_a7ooslt2kjbv5kqgcxc7jvjujm

13 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/a7ooslt2kjbv5kqgcxc7jvjujm

24 November 2022

mapped directly with Wikidata item

1 reference