(Q24337176)

presynaptic membrane organization

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Alexis Brice

14

0 references

Renzo Guerrini

16

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Davide Mei

13

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Alexander Zimprich

19

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Eva Reinthaler

2

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Salwa Eltawil

Salwa Eltawil

3

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Sherif Edris

Sherif Edris

9

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Fritz Zimprich

Friedrich Zimprich

17

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Suzanne Lesage

15

Suzanne Lesage

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author name string

Elisabeth Stogmann

1

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Mohammed A El Etribi

4

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Mahmoud Hemeda

5

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Nevine El Nahhas

6

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Ahmed M Gaber

7

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Amal Fouad

8

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Anna Benet-Pages

10

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Sebastian H Eck

11

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Ekaterina Pataraia

12

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Tim M Strom

Seizures and reduced life span in mice lacking the potassium channel subunit Kv1.2, but hypoexcitability and enlarged Kv1 currents in auditory neurons

18

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language of work or name

English

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publication date

April 2013

0 references

published in

Brain

0 references

volume

136

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issue

Pt 4

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page(s)

1155-60

0 references

cites work

1 reference

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Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus

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Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWT068

TAG-1-deficient mice have marked elevation of adenosine A1 receptors in the hippocampus

21 January 2018

1 reference

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Abnormal corticomuscular and intermuscular coupling in high-frequency rhythmic myoclonus

21 January 2018

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1 reference

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Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2.

21 January 2018

1 reference

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Multiple molecular interactions determine the clustering of Caspr2 and Kv1 channels in myelinated axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWT068

Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.

21 January 2018

1 reference

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Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.

21 January 2018

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Exome sequencing identifies the cause of a mendelian disorder

21 January 2018

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The local differentiation of myelinated axons at nodes of Ranvier

21 January 2018

1 reference

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Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

21 January 2018

1 reference

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Impairment of learning and memory in TAG-1 deficient mice associated with shorter CNS internodes and disrupted juxtaparanodes

21 January 2018

1 reference

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Deletion of the K(V)1.1 potassium channel causes epilepsy in mice

21 January 2018

1 reference

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Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

21 January 2018

1 reference

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Familial cortical tremor and epilepsy: a well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification.

21 January 2018

1 reference

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Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers

21 January 2018

1 reference

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Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features

21 January 2018

1 reference

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A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

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Tropomyosins in skeletal muscle diseases.

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