Ciliopathies
Teams
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Laurence Legeai-Mallet and Valérie Cormier-Daire
>> Research Lab
Molecular and physiopathological bases of osteochondrodysplasia -
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Imagine's Offers
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in progress
Nephronophthisis (NPH)Genotype PhenotypeTargetsTherapeuticsClinical trials -
in progress
HeterotaxiaGenotype PhenotypeTargets-
In vivo models
Ift20 inactivation (KO & conditional KO mouse models)
Nodal inactivation (conditional KO mouse model)
TherapeuticsClinical trialsSitus invertusGenotype Phenotype-
Cohorts
Please contact us
TargetsTherapeuticsClinical trials -
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in progress
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in progress
Joubert syndrome (JS)Genotype PhenotypeTargetsTherapeuticsClinical trialsMeckel syndrome (MKS)Genotype PhenotypeTargetsTherapeuticsClinical trialsHydrolethalus syndrome (HLS)Genotype PhenotypeTargetsTherapeuticsClinical trialsCorpus Callosum malformationsGenotype PhenotypeTargetsTherapeuticsClinical trialsMalformations of cortical developmentGenotype PhenotypeTargetsTherapeuticsClinical trials -
in progress
Leber Congenital Amaurosis (LCA)Genotype PhenotypeTargetsTherapeuticsClinical trialsX-linked retinitis pigmentosa (XLRP)Genotype PhenotypeTargetsTherapeuticsClinical trials
Contacts
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Thibaut PERCHET
Business development manager
- thibaut.perchet@institutimagine.org
- +33 1 42 75 42 55
