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Funded by an IRDiRC member =

Research projects

FINLAND

Finland
TURKU

FRANCE

OCCITANIE
TOULOUSE

Structure-function relationship of the TSH receptor and of the related receptors
CHU de Toulouse - Hôpital Rangueil
Institut des Maladies Métaboliques et Cardiovasculaires

FRANCE

PAYS DE LA LOIRE
ANGERS

ITALY

LIGURIA
GENOVA

New technologies and new strategies for neonatal screening
IRCCS Istituto G. Gaslini - Ospedale Pediatrico
Laboratorio per lo Studio degli Errori Congeniti del Metabolismo

NETHERLANDS

Noord-Holland
AMSTERDAM

Causes of X-linked Hypothyroidism
Amsterdam UMC, locatie AMC
Kinderpolikliniek Klinische Genetica

SWEDEN

Västra Götalandsregionen
GÖTEBORG

Novel mechanisms of impaired thyroid development and function implicated in congenital hypothyroidism
Göteborg University
Department of Medical Biochemistry and Cell Biology

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberIodine status and congenital hypothyroidism in the usa
Institution: Information not provided - US

CANADA

Ontario
TORONTO

Funded by an IRDiRC memberDeciphering the Role of UBR1 E3 Ubiquitin Ligase using a C. elegans Model
Mount Sinai Hospital
Lunenfeld-Tanenbaum Research Institute

GERMANY

Berlin
BERLIN

SPP 1629: THYROID TRANS ACT - Development of T3-peptide ligands to treat MCT8 deficiency via a Trojan horse like mechanism
Charité - Universitätsmedizin Berlin (CVK)
Institut für Experimentelle Pädiatrische Endokrinologie

GERMANY

Berlin
BERLIN

SPP 1629: THYROID TRANS ACT - Cell type-specific inactivation of Mct8 in brain cells: Gene expression, metabolism, morphology
Charité - Universitätsmedizin Berlin (CVK)
Institut für experimentelle Endokrinologie

GERMANY

Nordrhein-Westfalen
BONN

SPP 1629: THYROID TRANS ACT - Structure and function of the thyroid hormone transporter MCT8
Medizinische Fakultät der Universität Bonn
Institut für Biochemie und Molekularbiologie

SWITZERLAND

Suisse Alémanique
AARAU

Hereditary Hearing Loss: linkage analysis, mapping of genes
Kantonsspital Aarau
Interdisziplinäre Spezialsprechstunde für hereditäre ORL-Erkrankungen

UNITED STATES

South Dakota
SIOUX FALLS

CANADA

Québec
MONTRÉAL

Abnormal Thyroid Development: a Model Disorder for Congenital Malformations and Neurocognitive Development
Centre hospitalier universitaire Sainte-Justine
CHU Ste-Justine-Centre de recherche - Service d'Endocrinologie

FRANCE

ILE-DE-FRANCE
PARIS

Funded by an IRDiRC memberSTaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196

FRANCE

PAYS DE LA LOIRE
NANTES

Funded by an IRDiRC memberFROGH : FRench Regional Origins in Genetics for Health - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291

ITALY

CAMPANIA
NAPOLI

Funded by an IRDiRC memberTelethon Undiagnosed Disease Program - Revised Proposal
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

JAPAN

JAPAN
ADDRESS : NOT PROVIDED - JP

JAPAN

JAPAN
TOKYO

Funded by an IRDiRC memberFormation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute

Multicentric Research projects