Evidence map›Paper›PMID 22173492›Full record

ArticleJournal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban2011

Electrophysiological study of V535M hERG mutation of LQT2.

Chunyan Shao, Yan Lu, Mohan Liu, Qi Chen, Yunfeng Lan, Yan Liu, Min Lin, Yang Li

Abstract read
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In one paragraph

Article in Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 91% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Chunyan ShaoInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China.
Yan LuInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China.
Mohan LiuInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China.
Qi ChenInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China.
Yunfeng LanInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China.
Yan LiuInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China.
Min LinInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China.
Yang LiInstitute of Geriatric Cardiology of Chinese PLA General Hospital, Beijing, 100853, China. liyangbsh@163.com.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study examined the current changes of human ether-a-go-go-related gene (hERG) mutation derived from a LQT2 Chinese family with a highly penetrating phenotype. Mutation was identified and site-directed mutagenesis was performed to induce the mutation in wild-type (WT) hERG. WT hERG and mutated V535M were cloned and transiently expressed in HEK293 cells. At the 48th and 72nd h after transfection, membrane currents were recorded using whole cell patch-clamp procedures. An A>G transition at 1605 resulting in replacement of V535M was identified. Compared to WT, V535M mutation significantly decreased tail currents of hERG. At test potential of -40 mV after depolarizing at +50 mV, tail current densities were 83.35±7.06 pA/pF in WT and 50.38±7.74 pA/pF in V535M respectively (n=20, P<0.01). Gating kinetics of hERG revealed that V (1/2) of steady-state inactivation shifted to negative potential in the mutant (V (1/2,V535M): -61.81±1.7 mV vs. V (1/2, WT): -43.1±0.71 mV). The time constant of recovery from inactivation was markedly prolonged in the mutant compared to WT among test potentials. V535M hERG mutation demonstrated markedly decreased tail current densities, which suggests that V535M is a new loss-of-function mutation of hERG channel responsible for LQT2.

Indexed as

MutationAdolescentElectrocardiographyERG1 Potassium ChannelEther-A-Go-Go Potassium ChannelsHEK293 CellsHumansLong QT SyndromeMaleMembrane PotentialsMutagenesis, Site-DirectedPedigreeSyncopeTransfectionERG1 Potassium ChannelEther-A-Go-Go Potassium ChannelsKCNH2 protein, human

Identifiers

PMID22173492
OpenAlexW1988973836

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.