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Sökning: WFRF:(Ibrahim J) > (2010-2014) > Nerve conduction ve...

Nerve conduction velocity is regulated by the inositol polyphosphate-4-phosphatase II gene

Lemcke, S. (författare)
University of Lübeck, Lübeck, Germany
Müller, S. (författare)
University of Lübeck, Lübeck, Germany
Möller, S. (författare)
University of Lübeck, Lübeck, Germany
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Schillert, A. (författare)
University of Lübeck, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany
Ziegler, A. (författare)
University of Lübeck, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany
Cepok-Kauffeld, S. (författare)
University Hospital, Technical University of Munich, Munich, Germany
Comabella, M. (författare)
University Hospital Vall d’Hebron, Barcelona, Spain
Montalban, X. (författare)
University Hospital Vall d’Hebron, Barcelona, Spain
Rülicke, T. (författare)
University of Veterinary Medicine, Vienna, Austria
Nandakumar, Kutty Selva, 1965- (författare)
Karolinska Institutet,Karolinska Institute, Stockholm, Sweden
Hemmer, B. (författare)
University Hospital, Technical University of Munich, Munich, Germany
Holmdahl, R. (författare)
Karolinska Institutet,Karolinska Institute, Stockholm, Sweden
Pahnke, J. (författare)
University of Magdeburg, Magdeburg, Germany; German Center for Neurodegenerative Diseases Magdeburg, Magdeburg, Germany; Leibniz Institute for Neurobiology, Magdeburg, Germany
Ibrahim, S. M. (författare)
University of Lübeck, Lübeck, Germany
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 (creator_code:org_t)
Elsevier BV, 2014
2014
Engelska.
Ingår i: American Journal of Pathology. - : Elsevier BV. - 0002-9440 .- 1525-2191. ; 184:9, s. 2420-2429
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Impairment of nerve conduction is common in neurodegenerative and neuroinflammatory diseases such as multiple sclerosis (MS), and measurement of evoked potentials (visual, motor, or sensory) has been widely used for diagnosis and recently also as a prognostic marker for MS. We used a classical genetic approach to identify novel genes controlling nerve conduction. First, we used quantitative trait mapping in F2 progeny of B10/SJL mice to identify EAE31, a locus controlling latency of motor evoked potentials (MEPs) and clinical onset of experimental autoimmune encephalomyelitis. Then, by combining congenic mapping, in silico haplotype analyses, and comparative genomics we identified inositol polyphosphate-4-phosphatase, type II (Inpp4b) as the quantitative trait gene for EAE31. Sequence variants of Inpp4b (C/A, exon 13; A/C, exon 14) were identified as differing among multiple mouse strains and correlated with individual cortical MEP latency differences. To evaluate the functional relevance of the amino acid exchanges at positions S474R and H548P, we generated transgenic mice carrying the longer-latency allele (Inpp4b(474R/548P)) in the C57BL/6J background. Inpp4b(474R/548P) mice exhibited significantly longer cortical MEP latencies (4.5 +/- 0.22 ms versus 3.7 +/- 0.13 ms; P = 1.04 x 10(-9)), indicating that INPP4B regulates nerve conduction velocity. An association of an INPP4B polymorphism (rs13102150) with MS was observed in German and Spanish MS cohorts (3676 controls and 911 cases) (P = 8.8 x 10(-3)).

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Genetik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Genetics (hsv//eng)

Nyckelord

Amino Acid Sequence
Animals
Encephalomyelitis
Autoimmune
Experimental
Evoked Potentials
Motor/*genetics
Genotype
Humans
Mice
Mice
Inbred C57BL
Mice
Transgenic
Molecular Sequence Data
Multiple Sclerosis/*genetics
Neural Conduction/*genetics
Phosphoric Monoester Hydrolases/*genetics
Quantitative Trait Loci
Reverse Transcriptase Polymerase Chain Reaction

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