نتایج جستجو برای: scn4a

تعداد نتایج: 166  

Journal: :Brain : a journal of neurology 2016
Fenfen Wu Wentao Mi Yu Fu Arie Struyk Stephen C Cannon

Over 60 mutations of SCN4A encoding the NaV1.4 sodium channel of skeletal muscle have been identified in patients with myotonia, periodic paralysis, myasthenia, or congenital myopathy. Most mutations are missense with gain-of-function defects that cause susceptibility to myotonia or periodic paralysis. Loss-of-function from enhanced inactivation or null alleles is rare and has been associated w...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
K Jurkat-Rott N Mitrovic C Hang A Kouzmekine P Iaizzo J Herzog H Lerche S Nicole J Vale-Santos D Chauveau B Fontaine F Lehmann-Horn

The pathomechanism of familial hypokalemic periodic paralysis (HypoPP) is a mystery, despite knowledge of the underlying dominant point mutations in the dihydropyridine receptor (DHPR) voltage sensor. In five HypoPP families without DHPR gene defects, we identified two mutations, Arg-672-->His and -->Gly, in the voltage sensor of domain 2 of a different protein: the skeletal muscle sodium chann...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2009
J Trip G Drost H B Ginjaar F H M Nieman A J van der Kooi M de Visser B G M van Engelen C G Faber

OBJECTIVE To redefine phenotypical characteristics for both chloride (ClCh) and sodium channelopathies (NaCh) in non-dystrophic myotonic syndromes (NDM). METHODS In a cross-sectional, nationwide study, standardised interviews and clinical bedside tests were performed in 62 genetically confirmed NDM patients, 32 ClCh and 30 NaCh. RESULTS Standardised interviews revealed that ClCh reported a ...

Journal: :Molecular and cellular biology 2005
Mikko J Frilander Xiaojuan Meng

U12 snRNA is required for branch point recognition in the U12-dependent spliceosome. Using site-specific cross-linking, we have captured an unexpected interaction between the 5' end of the U12 snRNA and the -2 position upstream of the 5' splice site of P120 and SCN4a splicing substrates. The U12 snRNA nucleotides that contact the 5' exon are the same ones that form the catalytically important h...

Journal: :Human molecular genetics 1995
F Lehmann-Horn V Mailänder R Heine A L George

The group of dominant non-dystrophic myotonias, comprising disorders characterized by clinically similar forms of myogenic muscle stiffness, is genetically inhomogeneous. Dominant myotonia congenita (Thomsen's disease) is linked to CLCN1, the gene encoding the major muscle chloride channel, localized on chromosome 7q35. In contrast, dominant myotonias sensitive to potassium are caused by point ...

2018
Emma Matthews Christoph Neuwirth Fatima Jaffer Renata S. Scalco Doreen Fialho Matt Parton Dipa Raja Rayan Karen Suetterlin Richa Sud Roland Spiegel Rachel Mein Henry Houlden Andrew Schaefer Estelle Healy Jacqueline Palace Ros Quinlivan Susan Treves Janice L. Holton Heinz Jungbluth Michael G. Hanna

OBJECTIVE To characterize the phenotype of patients with symptoms of periodic paralysis (PP) and ryanodine receptor (RYR1) gene mutations. METHODS Cases with a possible diagnosis of PP but additional clinicopathologic findings previously associated with RYR1-related disorders were referred for a tertiary neuromuscular clinical assessment in which they underwent detailed clinical evaluation, i...

Journal: :Human molecular genetics 2018
Silvia Corrochano Gonzalo Blanco Debbie Williams Jessica Wettstein Michelle Simon Saumya Kumar Lee Moir Thomas Agnew Michelle Stewart Allison Landman Vassilios N Kotiadis Michael R Duchen Henning Wackerhage David C Rubinsztein Steve D M Brown Abraham Acevedo-Arozena

Polyglutamine expansions in the huntingtin gene cause Huntington's disease (HD). Huntingtin is ubiquitously expressed, leading to pathological alterations also in peripheral organs. Variations in the length of the polyglutamine tract explain up to 70% of the age-at-onset variance, with the rest of the variance attributed to genetic and environmental modifiers. To identify novel disease modifier...

Journal: :Genetics 2008
Helen A Lindsay Richard Baines Richard ffrench-Constant Kathryn Lilley Howard T Jacobs Kevin M C O'Dell

Here we report the molecular characterization of Out-cold (Ocd) mutants of Drosophila melanogaster, which produce a dominant, X-linked, cold-sensitive paralytic phenotype. From its initial 1.5-Mb cytological location within 13F1-16A2, P-element and SNP mapping reduced the Ocd critical region to <100 kb and to six candidate genes: hangover, CG9947, CG4420, eIF2a, Rbp2, and paralytic (para). Comp...

2014
Marlyn Zapata Ilda S. Kunii Rolf M. Paninka Denise M. N. Simões Víctor A. Castillo Archivaldo Reche Rui M. B. Maciel Magnus R. Dias da Silva

Neck ventroflexion in cats has different causes; however, the most common is the hypokalemia associated with flaccid paralysis secondary to chronic renal failure. In humans, the most common causes of acute flaccid paralysis are hypokalemia precipitated by thyrotoxicosis and familial forms linked to mutations in sodium, potassium, and calcium channel genes. Here, we describe the sequencing and a...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2008
Jean-Philippe Lengelé Hendrica Belge Olivier Devuyst

In 1865, Claude Bernard wrote that ‘the constancy of the internal milieu is the essential condition to a free and independent life’ [1]. It would be hard to find a more illustrative paradigm for that statement than for the case of hyperkalaemic periodic paralysis (HyperPP) reported by Grgic et al. in this issue [2]. A 14-year-old male was admitted for a sudden ascending paralysis involving the ...

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