Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Éva Czemmel"'
Autor:
Pálma Anker, Norbert Kiss, István Kocsis, Éva Czemmel, Krisztina Becker, Sára Zakariás, Dóra Plázár, Klára Farkas, Balázs Mayer, Nikoletta Nagy, Márta Széll, Nándor Ács, Zsuzsanna Szalai, Márta Medvecz
Publikováno v:
Life, Vol 11, Iss 7, p 624 (2021)
Collodion baby is a congenital, transient phenotype encountered in approximately 70–90% of autosomal recessive congenital ichthyosis and is an important entity of neonatal erythroderma. The clinical outcome after this severe condition is variable.
Externí odkaz:
https://doaj.org/article/bcc1326cb5a44ea7b20651ae08bfd1f6
Autor:
Balogh, Zsuzsanna Szűcs, Réka Fitala, Ágnes Renáta Nyuzó, Krisztina Fodor, Éva Czemmel, Nóra Vrancsik, Mónika Bessenyei, Tamás Szabó, Katalin Szakszon, István
Publikováno v:
Genes; Volume 12; Issue 9; Pages: 1331
Ufmylation is a relatively newly discovered type of post-translational modification when the ubiquitin-fold modifier 1 (UFM1) protein is covalently attached to its target proteins in a three-step enzymatic reaction involving an E1 activating enzyme (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::ed206485189d0830c882ea95cdd40a37
Autor:
Zsuzsanna Szűcs, Réka Fitala, Ágnes Renáta Nyuzó, Krisztina Fodor, Éva Czemmel, Nóra Vrancsik, Mónika Bessenyei, Tamás Szabó, Katalin Szakszon, István Balogh
Publikováno v:
Genes, Vol 12, Iss 1331, p 1331 (2021)
Ufmylation is a relatively newly discovered type of post-translational modification when the ubiquitin-fold modifier 1 (UFM1) protein is covalently attached to its target proteins in a three-step enzymatic reaction involving an E1 activating enzyme (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::0f8a8743a46e4ed4e6537d99aebfb930
https://www.mdpi.com/2073-4425/12/9/1331
https://www.mdpi.com/2073-4425/12/9/1331
Autor:
Éva Czemmel, Balázs Mayer, Zsuzsanna Szalai, Márta Medvecz, Sara Zakarias, Nikoletta Nagy, Pálma Anker, K. Farkas, Márta Széll, Dóra Plázár, Nándor Ács, István Kocsis, Norbert Kiss, Krisztina Becker
Publikováno v:
Life, Vol 11, Iss 624, p 624 (2021)
Life
Life
Collodion baby is a congenital, transient phenotype encountered in approximately 70–90% of autosomal recessive congenital ichthyosis and is an important entity of neonatal erythroderma. The clinical outcome after this severe condition is variable.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0350ecb3f4b8a3be93c40be7d2027c99
https://doi.org/10.3390/life11070624
https://doi.org/10.3390/life11070624