News

Updated acknowledgement of CCP in research outputs

19. 02. 2024 Information News

The Czech Centre for Phenogenomics receives funding from public providers, which allows CCP to offer state-of-the-art services and technologies to its users. Therefore, all the work performed at CCP should be acknowledged by users in their outputs (publications, presentations etc.). This acknowledgement provides an evidence of the impact of CCP on quality of research and…

ASGENT continues supporting CCP research on Angelman syndrome in 2024

16. 02. 2024 Information News

On the occasion of the International Angelman Syndrome Day, Radislav Sedlacek, director of the Czech Centre fo Phenogenomics, received yesterday a cheque in the amount of CZK 1 million for the continuation of Angelman syndrome research using mouse models from the Association of Gene Therapy (ASGENT), which has long supported this research.At the same time,…

Rare Disease Day 2024

15. 02. 2024 Event

29 February 2024 / Raising awareness and generating change for the 300 million people worldwide living with a rare disease, their families and carers. https://www.rarediseaseday.org/ Informace o aktivitách v České republice na webu České asociace pro vzácná onemocnění.

12th European Conference on Rare Diseases and Orphan Products

15. 02. 2024 Event

15 – 16 May 2024, hybrid event / The ECRD is the largest, patient-led, rare disease policy-shaping event held in Europe. By bringing together people with rare diseases and patient advocates, policy makers, healthcare industry representatives, clinicians, regulators and Member State representatives, EURORDIS harnesses the power of this extensive network to shape goal-driven rare disease…

International Day of Angelman Syndrome

09. 02. 2024 Event

15 February 2023, Praha / Join us on 15 February to light up the Czech Republic in blue.

Discussion “Can a rare disease concern me or my loved ones?”

25. 01. 2024 Event Lecture

26 February 2023, Hradec Králové / Come and join the debate on the topic “Can a rare disease affect me or my loved ones?” Why are so few rare diseases curable? Gene and cell therapy – when science fiction became reality. Leading Czech scientists and physicians will discuss current and future prevention and treatment options.…

A link between autoimmune disorders and tooth enamel defects revealed

07. 12. 2023 News Publication

In a groundbreaking study published in Nature, an international team of researchers has discovered a crucial link between autoimmune disorders and defects in tooth enamel development. This study sheds light on the poorly understood conditions of Amelogenesis Imperfecta in patients with Autoimmune Polyglandular Syndrome Type-1 (APS-1) and Celiac Disease. Ameloblasts, the cells responsible for tooth…

Virtuální charitativní běh Doba genová v pohybu

04. 12. 2023 Uncategorized

Máme zde první ročník virtuálního běhu! Nejen vaše vědomosti, ale nyní i pohyb může zahýbat českou vědou. Všem, kdo chtějí pomoci pohybem, nabízíme nenáročnou a neomezenou možnost, ať už chůzí nebo během, na kole, koloběžce, bruslích a nebo i lyžích. Máte chuť pomoci? Je jedno kdy, kde a kolik toho svým pohybem zvládneš, protože každý…

Radislav Sedláček in Press Club of Frekvence 1 Radio about genes and human diseases

15. 11. 2023 News PR

The guest of the Press Club was our leading expert on genetically modified organisms Radislav Sedláček from the Czech Centre for Phenogenomics. The presenter Bára Nesvadbová also came across a possible leak of the SARS-CoV-2 virus from the laboratory. You can listen to the whole interview here (in Czech).

Meet the new deputy director of the Czech Centre for Phenogenomics

Interview with Jan Procházka Jan Procházka, PhD has been appointed as the new deputy director of the Czech Centre for Phenogenomics (CCP). Jan leads the Phenotyping Module aiming at standardized, systematic characterization of mouse models as well as preclinical research and development. During his three-year postdoctoral fellowship at University of California Jan worked on tissue…