4 Einträge gefunden

1. Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy

   1. Warnecke, Nele Annika
   2. Ulmer, Bärbel M
   3. Laufer, Sandra D
   4. Shibamiya, Aya
   5. Krämer, Elisabeth
   6. Neuber, Christiane
   7. Hanke, Sophia

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
2. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular non-compaction phenotype

   1. Kolokotronis, Konstantinos
   2. Kühnisch, Jirko
   3. Klopocki, Eva
   4. Dartsch, Josephine
   5. Rost, Simone
   6. Huculak, Cathleen
   7. Mearini, Giulia

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
3. Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3

   1. Kühnisch, Jirko
   2. Herbst, Christopher
   3. Al-Wakeel-Marquard, Nadya
   4. Dartsch, Josephine
   5. Holtgrewe, Manuel
   6. Baban, Anwar
   7. Mearini, Giulia

   2019 - Forschungsinformationssystem des UKE
4. MIA is a potential biomarker for tumour load in neurofibromatosis type 1.

   1. Kolanczyk, Mateusz
   2. Mautner, Viktor Felix
   3. Kossler, Nadine
   4. Nguyen, Rosa
   5. Kühnisch, Jirko
   6. Zemojtel, Tomasz
   7. Jamsheer, Aleksander

   2011 - Forschungsinformationssystem des UKE - frei zugänglich