نتایج جستجو برای: ژن clcn1

تعداد نتایج: 15916  

2016
Guiying Chen Akio Masuda Hiroyuki Konishi Bisei Ohkawara Mikako Ito Masanobu Kinoshita Hiroshi Kiyama Tohru Matsuura Kinji Ohno

Myotonic dystrophy type 1 (DM1) is caused by abnormal expansion of CTG repeats in the 3' untranslated region of the DMPK gene. Expanded CTG repeats are transcribed into RNA and make an aggregate with a splicing regulator, MBNL1, in the nucleus, which is called the nuclear foci. The nuclear foci sequestrates and downregulates availability of MBNL1. Symptomatic treatments are available for DM1, b...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
C Fahlke C L Beck A L George

Autosomal dominant myotonia congenita is an inherited disorder of skeletal muscle caused by mutations in a voltage-gated Cl- channel gene (CLCN1, 7q35). Here, we report that a mutation predicting the substitution of Gly 230 by glutamic acid (G230E) between segments D3 and D4 dramatically alters the pore properties of a recombinant human muscle Cl- channel (hCIC-1) expressed in a mammalian cell ...

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 ...

2016
Inna Inashkina Eriks Jankevics Janis Stavusis Inta Vasiljeva Kristine Viksne Ieva Micule Jurgis Strautmanis Maruta S. Naudina Loreta Cimbalistiene Vaidutis Kucinskas Astrida Krumina Algirdas Utkus Birute Burnyte Ausra Matuleviciene Baiba Lace

BACKGROUND Limb-girdle muscular dystrophies are characterized by predominant involvement of the shoulder and pelvic girdle and trunk muscle groups. Currently, there are 31 genes implicated in the different forms of limb-girdle muscular dystrophies, which exhibit similar phenotypes and clinical overlap; therefore, advanced molecular techniques are required to achieve differential diagnosis. ME...

2011
Erik van Lunteren Michelle Moyer Jessica Cooperrider Jennifer Pollarine

BACKGROUND Genetic deficiency of the muscle CLC-1 chloride channel leads to myotonia, which is manifested most prominently by slowing of muscle relaxation. Humans experience this as muscle stiffness upon initiation of contraction, although this can be overcome with repeated efforts (the "warm-up" phenomenon). The extent to which CLC-1 deficiency impairs exercise activity is controversial. We hy...

2013
Jean-François Desaphy Gianluca Gramegna Concetta Altamura Maria Maddalena Dinardo Paola Imbrici Alfred L. George Anna Modoni Mauro LoMonaco Diana Conte Camerino

Myotonia congenita (MC) is caused by loss-of-function mutations of the muscle ClC-1 chloride channel. Clinical manifestations include the variable association of myotonia and transitory weakness. We recently described a cohort of recessive MC patients showing, at a low rate repetitive nerves stimulation protocol, different values of compound muscle action potential (CMAP) transitory depression,...

2015
Katharina Ronstedt Damien Sternberg Silvia Detro-Dassen Thomas Gramkow Birgit Begemann Toni Becher Petra Kilian Matthias Grieschat Jan-Philipp Machtens Günther Schmalzing Martin Fischer Christoph Fahlke

Mutations in the muscle chloride channel gene (CLCN1) cause myotonia congenita, an inherited condition characterized by muscle stiffness upon sudden forceful movement. We here studied the functional consequences of four disease-causing mutations that predict amino acid substitutions Q43R, S70L, Y137D and Q160H. Wild-type (WT) and mutant hClC-1 channels were heterologously expressed as YFP or CF...

Journal: :The Journal of clinical investigation 2002
Hai Wu Eric N Olson

Becker syndrome, a recessive nondystrophic myotonia caused by mutations in the chloride channel 1 gene (CLCN1), is characterized by delayed muscle relaxation after contraction. The ADR (arrested development of righting response) mouse is an animal model for Becker syndrome. Skeletal muscles from ADR myotonic animals show an increased number of oxidative fibers with a lack of glycolytic fibers a...

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