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Funded by an IRDiRC member =

    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: Molecular diagnosis and exome sequencing in ion channel diseases (project 7)
    • CeGaT GmbH
    • CeGaT GmbH und Praxis für Humangenetik
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: Regulation of surface expression and development of bio assays to improve the situation of patients harbouring a mutation leading to transporter defect in channelopathies (project 6)
    • Forschungsinstitut für Augenheilkunde
    • Molekulargenetisches Labor
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Genetics of familial and sporadic hemiplegic migraine (Investigations on CACNA1A, ATP1A2 und SCN1A genes)
    • Hertie-Institut für klinische Hirnforschung (HIH)
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Differential physiological and pathophysiological role of neuronal voltage gated Na+ channels Nav1.1 (SCN1A) and Nav1.2 (SCN2A)
    • Hertie-Institut für klinische Hirnforschung (HIH)
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: German Network on neurological and ophthalmological ion channel diseases: Coordination and management (project 1)
    • Hertie-Institut für klinische Hirnforschung (HIH)
    • Abteilung für Neurologie mit Schwerpunkt Epileptologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • IonNeurONet: German Network on neurological and ophthalmological ion channel diseases: Coordination and management (project 1)
    • Institut für Medizinische Genetik und angewandte Genomik Tübingen
    • Institut für Humangenetik
    • More details
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Excitation-contraction coupling in health and disease: Ion channel diseases - diagnosis, pathogenesis and therapy
    • Universität Ulm
    • Institut für Angewandte Physiologie
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Mutational analysis of CACNA1A, ATP1A2 and SCN1A genes (direct sequencing)
    • LMU Klinikum der Universität München - Campus Großhadern
    • Arbeitsgruppe Neurogenetik
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Functional characterization of ATP1A2 mutations associated with FHM by cell survival assays
    • LMU Klinikum der Universität München - Campus Großhadern
    • Arbeitsgruppe Neurogenetik
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Generation of a knock-in mouse model for FHM3
    • LMU Klinikum der Universität München - Campus Großhadern
    • Arbeitsgruppe Neurogenetik
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Genetics of familial and sporadic hemiplegic migraine (Investigations on CACNA1A, ATP1A2 und SCN1A genes)
    • LMU Klinikum der Universität München - Campus Großhadern
    • Arbeitsgruppe Neurogenetik
    • More details
    • GERMANY
    • Hamburg
    • HAMBURG
    • IonNeurONet: Gene identification and characterisation of hemiplegic migraine (project 4)
    • UKE - Universitätsklinikum Hamburg-Eppendorf
    • Institut für Humangenetik
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Genetic and micro-environmental factors regulate the role of atp as transmitter of pain in a migraine model
    • Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
    • Centro Grossi Paoletti
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Funded by an IRDiRC member
    • Studies of familial hemiplegic migraine transgenic mouse models and patients to investigate the crosstalk between sensory neurons and neuroinflammatory cells in trigeminal ganglia in relation to migraine pain.
    • Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
    • Centro Grossi Paoletti
    • More details
    • ITALY
    • VENETO
    • PADOVA
    • Functional consequences of mutations associated to familial hemiplegic migraine and migraine mechanisms
    • Università degli Studi di Padova- Polo A.Vallisneri
    • Dipartimento di Scienze Biomediche
    • More details
    • NETHERLANDS
    • Zuid-Holland
    • LEIDEN
    • Migraine genes and neurobiological pathways
    • LUMC - Leids Universitair Medisch Centrum
    • Afdeling Neurologie
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • CACNA1A gene involvement in cognition and synaptic function in calcium channel disease.
    • Instituto de Biologia Molecular e Celular
    • Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • Search for disease modifiers in spinocerebellar ataxias: human and animal-based approaches.
    • Instituto de Biologia Molecular e Celular
    • Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Funded by an IRDiRC member
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Genetic disorders of human brain development
    • Western General Hospital
    • MRC Human Genetics Unit
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details