channel mutation Latest Research Papers

In vivo functional validation of the V402L voltage gated sodium channel mutation in the malaria vector An. gambiae

Pest Management Science ◽

10.1002/ps.6731 ◽

2021 ◽

Author(s):

Jessica Williams ◽

Ruth Cowlishaw ◽

Antoine Sanou ◽

Hilary Ranson ◽

Linda Grigoraki

Keyword(s):

Sodium Channel ◽

Malaria Vector ◽

Functional Validation ◽

Voltage Gated Sodium Channel ◽

Voltage Gated ◽

Channel Mutation ◽

Sodium Channel Mutation

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Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family

eJHaem ◽

10.1002/jha2.267 ◽

2021 ◽

Author(s):

Sasha Waldstein ◽

Sarah Arnold‐Croop ◽

Laura Carrel ◽

M. Elaine Eyster

Keyword(s):

Gardos Channel ◽

Channel Mutation

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Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy

Acta Neurologica Belgica ◽

10.1007/s13760-021-01645-x ◽

2021 ◽

Author(s):

Rohan R. Mahale ◽

Ravindu Tiwari ◽

Gautham Arunachal ◽

Hansashree Padmanabha ◽

Pooja Mailankody

Keyword(s):

Potassium Channel ◽

Myoclonic Epilepsy ◽

Myoclonus Epilepsy ◽

Progressive Myoclonic Epilepsy ◽

Channel Mutation

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Uncoupling sodium channel dimers restores the phenotype of a pain‐linked Na v 1.7 channel mutation

British Journal of Pharmacology ◽

10.1111/bph.15196 ◽

2020 ◽

Vol 177 (19) ◽

pp. 4481-4496 ◽

Cited By ~ 1

Author(s):

Annika H. Rühlmann ◽

Jannis Körner ◽

Ralf Hausmann ◽

Nikolay Bebrivenski ◽

Christian Neuhof ◽

...

Keyword(s):

Sodium Channel ◽

Channel Mutation

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Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype

Pediatric Diabetes ◽

10.1111/pedi.13041 ◽

2020 ◽

Vol 21 (6) ◽

pp. 932-941 ◽

Cited By ~ 2

Author(s):

Laure Garcin ◽

Veronica Mericq ◽

Anne‐Laure Fauret‐Amsellem ◽

Helene Cave ◽

Michel Polak ◽

...

Keyword(s):

Potassium Channel ◽

Neonatal Diabetes ◽

Channel Mutation

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A cardiac sodium channel mutation associated with epinephrine‐induced marked QT‐prolongation

Journal of Cardiovascular Electrophysiology ◽

10.1111/jce.14572 ◽

2020 ◽

Vol 31 (8) ◽

pp. 2116-2117

Author(s):

Mohamad N. El Moheb ◽

Marwan M. Refaat

Keyword(s):

Sodium Channel ◽

Qt Prolongation ◽

Cardiac Sodium Channel ◽

Channel Mutation ◽

Sodium Channel Mutation

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A Cardiac Sodium Channel Mutation Associated with Epinephrine-Induced Marked QT-Prolongation

10.22541/au.158981254.49747549 ◽

2020 ◽

Author(s):

Mohamad El Moheb ◽

Marwan Refaat

Keyword(s):

Sodium Channel ◽

Qt Prolongation ◽

Cardiac Sodium Channel ◽

Channel Mutation ◽

Sodium Channel Mutation

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Decision letter for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

10.1111/pedi.13041/v4/decision1 ◽

2020 ◽

Keyword(s):

Potassium Channel ◽

Neonatal Diabetes ◽

Channel Mutation

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Review for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

10.1111/pedi.13041/v4/review1 ◽

2020 ◽

Author(s):

Tohru Yorifuji

Keyword(s):

Potassium Channel ◽

Neonatal Diabetes ◽

Channel Mutation

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Decision letter for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

10.1111/pedi.13041/v3/decision1 ◽

2020 ◽

Keyword(s):

Potassium Channel ◽

Neonatal Diabetes ◽

Channel Mutation

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channel mutation
Recently Published Documents

TOTAL DOCUMENTS

H-INDEX

In vivo functional validation of the V402L voltage gated sodium channel mutation in the malaria vector An. gambiae

Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family

Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy

Uncoupling sodium channel dimers restores the phenotype of a pain‐linked Na v 1.7 channel mutation

Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype

A cardiac sodium channel mutation associated with epinephrine‐induced marked QT‐prolongation

A Cardiac Sodium Channel Mutation Associated with Epinephrine-Induced Marked QT-Prolongation

Decision letter for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

Review for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

Decision letter for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

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channel mutationRecently Published Documents

TOTAL DOCUMENTS

H-INDEX

In vivo functional validation of the V402L voltage gated sodium channel mutation in the malaria vector An. gambiae

Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family

Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy

Uncoupling sodium channel dimers restores the phenotype of a pain‐linked Na v 1.7 channel mutation

Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype

A cardiac sodium channel mutation associated with epinephrine‐induced marked QT‐prolongation

A Cardiac Sodium Channel Mutation Associated with Epinephrine-Induced Marked QT-Prolongation

Decision letter for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

Review for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

Decision letter for "Neonatal diabetes due to potassium channel mutation: response to sulfonylurea according to the genotype"

channel mutation
Recently Published Documents