(Q24319094)

GOA release 2020-03-11

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C Charlier

2

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author name string

N A Singh

1

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D Stauffer

3

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B R DuPont

4

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R J Leach

5

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R Melis

6

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G M Ronen

7

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I Bjerre

8

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T Quattlebaum

9

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J V Murphy

10

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M L McHarg

11

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D Gagnon

12

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T O Rosales

13

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A Peiffer

14

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V E Anderson

15

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M Leppert

https://scigraph.springernature.com/pub.10.1038/ng0198-25

16

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language of work or name

English

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publication date

January 1998

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published in

Nature Genetics

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volume

18

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page(s)

25-9

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issue

1

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exact match

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cites work

Seizure characteristics in chromosome 20 benign familial neonatal convulsions

1 reference

7 January 2021

The epidemiology of epilepsy in Rochester, Minnesota, 1935 through 1967

1 reference

7 January 2021

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

1 reference

7 January 2021

Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity

1 reference

7 January 2021

Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.

1 reference

7 January 2021

D20S19, linked to low voltage EEG, benign neonatal convulsions, and Fanconi anaemia, maps to a region of enhanced recombination and is localized between CpG islands

1 reference

7 January 2021

Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q

1 reference

7 January 2021

Searching for human epilepsy genes: a progress report.

1 reference

7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

7 January 2021

Basic local alignment search tool

1 reference

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

7 January 2021

At least six nucleotides preceding the AUG initiator codon enhance translation in mammalian cells

1 reference

7 January 2021

Identification and cloning of neuroblastoma-specific and nerve tissue-specific genes through compiled expression profiles

1 reference

7 January 2021

Eight potassium channel families revealed by the C. elegans genome project.

1 reference

7 January 2021

Pathophysiology of ion channel mutations

1 reference

7 January 2021

Neurotransmission in epilepsy.

1 reference

7 January 2021

Cellular and molecular basis of epilepsy.

1 reference

7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

7 January 2021

A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation

1 reference

7 January 2021

Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2

1 reference

7 January 2021

KVLQT1 mutations in three families with familial or sporadic long QT syndrome

1 reference

7 January 2021

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

1 reference

7 January 2021

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

1 reference

7 January 2021

Cloned potassium channels from eukaryotes and prokaryotes

1 reference

7 January 2021

Evidence that the S6 segment of the Shaker voltage-gated K+ channel comprises part of the pore.

1 reference

7 January 2021

Mutations in the P-region of a mammalian potassium channel (RCK1): a comparison with the Shaker potassium channel.

1 reference

7 January 2021

Determination of key structural requirements of a K+ channel pore.

1 reference

7 January 2021

Mutations in the K+ channel signature sequence

1 reference

7 January 2021

Revealing the architecture of a K+ channel pore through mutant cycles with a peptide inhibitor.

1 reference

7 January 2021

Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q

1 reference

7 January 2021

Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system

1 reference

7 January 2021

Potassium channelopathies

1 reference

7 January 2021