The fifth HEROES auction for the benefit of Institut Imagine reaches €10 million Read more about The fifth HEROES auction for the benefit of Institut Imagine reaches €10 million
The first inherited TNF deficiency in human underlies susceptibility to tuberculosis Read more about The first inherited TNF deficiency in human underlies susceptibility to tuberculosis
Innov4-ePiK: Innovative diagnostic and therapeutic approaches in potassium channel developmental and epileptic encephalopathies (K-DEEs) using 4P for medicine. Read more about Innov4-ePiK: Innovative diagnostic and therapeutic approaches in potassium channel developmental and epileptic encephalopathies (K-DEEs) using 4P for medicine.
The role of dendritic cells in papillomavirus infections: from the FLT3LG gene to therapeutic perspectives Read more about The role of dendritic cells in papillomavirus infections: from the FLT3LG gene to therapeutic perspectives
From the probability of being born left-handed to Rare Diseases: The Mysteries of Tubulin Beta 4B Variations (TUBB4B) Read more about From the probability of being born left-handed to Rare Diseases: The Mysteries of Tubulin Beta 4B Variations (TUBB4B)
Identification of a new key player in the immune control of Epstein-Barr virus infection Read more about Identification of a new key player in the immune control of Epstein-Barr virus infection
Discovery of a frequent genetic cause of autoimmunity From rare to frequent variants: the case of pre-TCRα deficiency Read more about Discovery of a frequent genetic cause of autoimmunity From rare to frequent variants: the case of pre-TCRα deficiency
A new mutation implicated in autoimmune lymphoproliferative syndrome Read more about A new mutation implicated in autoimmune lymphoproliferative syndrome
CENTOGENE and the Laboratory of Human Genetics of Infectious Diseases at Institut Imagine Announce Rare Disease Research Collaboration Read more about CENTOGENE and the Laboratory of Human Genetics of Infectious Diseases at Institut Imagine Announce Rare Disease Research Collaboration
Identification of a new genetic disease responsible for pulmonary alveolar proteinosis and mycobacterial infections Read more about Identification of a new genetic disease responsible for pulmonary alveolar proteinosis and mycobacterial infections
