The genetic basis of the development and malformations of teeth and craniofacial tissues University of Helsinki Institute of Dentistry More details FINLAND Finland HELSINKI Genetic basis in mouse models of the development of teeth and other ectodermal appendages and pathogenesis of their congenital defects University of Helsinki Developmental Biology More details FINLAND Finland HELSINKI SkinDev: In vitro and in vivo models of congenital rare skin diseases for molecular characterization and drug screening (coordination) Universität zu Köln Abteilung Dermatogenetik More details GERMANY Nordrhein-Westfalen KÖLN Molecular and functional study of p63 mutant proteins occurring in EEC, AEC and other human hereditary ectodermal syndromes Università degli Studi Federico II Laboratorio di Genetica Molecolare More details ITALY CAMPANIA NAPOLI Function of p63 in normal skin and in ectodermal dysplasia syndromes Azienda Ospedaliera Universitaria Policlinico di Tor Vergata Laboratorio di Trasduzione del Segnale More details ITALY LAZIO ROMA Translating current and new knowledge on the developmental functions of p63 into restoring normal development in models of organ culture and in vivo Università degli Studi di Roma Tor Vergata Dipartimento di Biologia More details ITALY LAZIO ROMA Towrds an innovative therapy of ectrodactyly ectodermal dysplasia clefting syndrome using allele specific RNA silencing Fondazione Banca degli Occhi del Veneto Onlus Dipartimento di Medicina Molecolare More details ITALY VENETO ZELARINO Diagnosis and management of ectodermal dysplasia in neonates and infants Medizinische Universität Innsbruck Stoffwechsellabor der Universitätsklinik für Kinder- und Jugendheilkunde More details AUSTRIA TIROL INNSBRUCK Ectodermal dysplasia and incontinentia pigmenti: clinic and genetic stripping; physiopathologic mechanisms study CHU Paris - Hôpital Necker-Enfants Malades MAGEC - Service de dermatologie More details FRANCE ILE-DE-FRANCE PARIS Detection and simulation of femoroacetabular impingement University of Ottawa School of Electrical Engineering and Computer Science (EECS) More details CANADA Ontario OTTAWA, ONTARIO SKELNET - Skeletal Dysplasia Network (coordination) Universitätsklinikum Freiburg Geschäftsstelle SKELNET e.V. More details Istraživački centri u Evropi za EEC GERMANY Baden-Württemberg FREIBURG SKELNET : Chondrocyte specific genes as part of the signaling regulation of chondrocyte differentiation Universität Duisburg-Essen Abteilung Entwicklungsbiologie More details GERMANY Nordrhein-Westfalen ESSEN GENESKIN: European network on rare genetic skin diseases (coordination) Istituto Dermopatico dellImmacolata - IRCCS Laboratorio di Biologia Molecolare e Cellulare More details ITALY LAZIO ROMA The Deciphering Developmental Disorders (the DDD study) Wellcome Trust Sanger Institute DECIPHER More details UNITED KINGDOM Cambridgeshire HINXTON Exploring the Genetics of Renal Developmental Disease Royal Devon and Exeter Hospital Department of Urology More details UNITED KINGDOM Devon EXETER Natural history and management in Skeletal Dysplasias Great Ormond Street Hospital for Children NHS Foundation Trust Clinical Genetics More details UNITED KINGDOM Greater London LONDON ESDN: European Skeletal Dysplasia Network (coordination) International Centre for Life Institute of Genetic Medicine More details UNITED KINGDOM Tyne & Wear NEWCASTLE UPON TYNE NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics Wellcome Trust/MRC Building Cambridge Institute for Medical Research More details UNITED KINGDOM Cambridgeshire CAMBRIDGE NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund) Birmingham Womens NHS Foundation Trust Regional Genetics Unit More details
Posted on: Fri, 28 Mar 2014 16:26:12 +0000
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