Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Denisa Ilenčíková"'
Autor:
Gabriela Hrčková, Eszter Hegyi, Katarína Skalická, Iveta Čierna, Tomáš Dallos, Denisa Ilenčíková
Publikováno v:
Nefrología, Vol 40, Iss 3, Pp 351-355 (2020)
Introduction: In children, chronic pancreatitis (CP) is usually associated with anatomical anomalies of the pancreas and biliary tract or is genetically determined. Autosomal dominant polycystic kidney disease (ADPKD) may present with extrarenal cyst
Externí odkaz:
https://doaj.org/article/5ecd34398be94e8daf8864b6439e205b
Autor:
Denisa Ilenčíková
Publikováno v:
Human Reproduction & Genetic Ethics. 11:49-54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d8109199538ad374cbe43ea3eea7725
https://doi.org/10.1179/hrge.11.2.e24512750t180w2q
https://doi.org/10.1179/hrge.11.2.e24512750t180w2q
Publikováno v:
Medical oncology (Northwood, London, England). 29(2)
Follicular lymphoma (FL) is one of the most common Non-Hodgkin lymphoma (NHL) subtype. Only small number of studies concerning NHL and DNA reparation gene polymorphisms has been performed so far. Hence, we have assessed the effect of 4 selected polym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f257cdca26389264e9f12bccc749890
https://pubmed.ncbi.nlm.nih.gov/21476145
https://pubmed.ncbi.nlm.nih.gov/21476145
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Myhre syndrome is a rare condition caused by a mutation in the SMAD4 gene, which leads to a defective TGF-β/BMP signaling, resulting in the proliferation of abnormal fibrous tissues. Clinically, patients with Myhre syndrome manifest with defects of
Externí odkaz:
https://doaj.org/article/2dbf8beed8654308a5e3fc342b5068b4
Autor:
Victoria K. Tesch, Hanna IJspeert, Andrea Raicht, Daniel Rueda, Nerea Dominguez-Pinilla, Luis M. Allende, Chrystelle Colas, Thorsten Rosenbaum, Denisa Ilencikova, Hagit N. Baris, Michaela H. M. Nathrath, Manon Suerink, Danuta Januszkiewicz-Lewandowska, Iman Ragab, Amedeo A. Azizi, Soeren S. Wenzel, Johannes Zschocke, Wolfgang Schwinger, Matthias Kloor, Claudia Blattmann, Laurence Brugieres, Mirjam van der Burg, Katharina Wimmer, Markus G. Seidel
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Immunoglobulin class-switch recombination (CSR) and somatic hypermutations (SHMs) are prerequisites for antibody and immunoglobulin receptor maturation and adaptive immune diversity. The mismatch repair (MMR) machinery, consisting of homologs of MutS
Externí odkaz:
https://doaj.org/article/34b5e5ca683a46b5b6319eb07943d6d2