Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Brigitta, Orlik"'
Autor:
Mohammad Walid Al-Smadi, Laszlo Adam Fazekas, Siran Aslan, Brigitta Bernat, Anas Beqain, Mustafa Qais Muhsin Al-Khafaji, Daniel Priksz, Brigitta Orlik, Norbert Nemeth
Publikováno v:
Biomedicines, Vol 11, Iss 11, p 2970 (2023)
Arteriovenous malformation (AVM) is an anomaly of blood vessel formation. Numerous models have been established to understand the nature of AVM. These models have limitations in terms of the diameter of the vessels used and the impact on the circulat
Externí odkaz:
https://doaj.org/article/ce0dc1b3b8c04a11b013e86160d8a430
Autor:
Vince Szegeczki, László Fazekas, Máté Kulcsár, Dora Reglodi, Péter Török, Brigitta Orlik, Antonio Simone Laganà, Attila Jakab, Tamas Juhasz
Publikováno v:
Diagnostics, Vol 12, Iss 4, p 970 (2022)
Endometriosis is a chronic gynecological disease that causes numerous severe symptoms in affected women. Revealing alterations of the molecular processes in ectopic endometrial tissue is the current policy for understanding the pathomechanisms and di
Externí odkaz:
https://doaj.org/article/a979ab281d80468fa14b67708b9d2a33
Autor:
Juhasz, Vince Szegeczki, László Fazekas, Máté Kulcsár, Dora Reglodi, Péter Török, Brigitta Orlik, Antonio Simone Laganà, Attila Jakab, Tamas
Publikováno v:
Diagnostics; Volume 12; Issue 4; Pages: 970
Endometriosis is a chronic gynecological disease that causes numerous severe symptoms in affected women. Revealing alterations of the molecular processes in ectopic endometrial tissue is the current policy for understanding the pathomechanisms and di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::082733fe7f76a432eab2ae342db581c3
Autor:
David A, Parry, Lukas, Tamayo-Orrego, Paula, Carroll, Joseph A, Marsh, Philip, Greene, Olga, Murina, Carolina, Uggenti, Andrea, Leitch, Rita, Káposzta, Gabriella, Merő, Andrea, Nagy, Brigitta, Orlik, Balázs, Kovács-Pászthy, Alan J, Quigley, Magdolna, Riszter, Julia, Rankin, Martin A M, Reijns, Katalin, Szakszon, Andrew P, Jackson, Nicola, Williams
Publikováno v:
Genes & Development
Parry, D A, Tamayo Orrego, L, Carroll, P, Marsh, J A, Greene, P, Murina, O, Uggenti, C, Leitch, A, Káposzta, R, Merő, G, Nagy, A, Orlik, B, Kovács-Pászthy, B, Quigley, A J, Riszter, M, Rankin, J, Reijns, M A M & Szakszon, K & Jackson, A P 2020, ' PRIM1 Deficiency Causes a Distinctive Primordial Dwarfism Syndrome ', Genes & Development, vol. 34, pp. 1520-1533 . https://doi.org/10.1101/gad.340190.120
Genes Dev
Parry, D A, Tamayo Orrego, L, Carroll, P, Marsh, J A, Greene, P, Murina, O, Uggenti, C, Leitch, A, Káposzta, R, Merő, G, Nagy, A, Orlik, B, Kovács-Pászthy, B, Quigley, A J, Riszter, M, Rankin, J, Reijns, M A M & Szakszon, K & Jackson, A P 2020, ' PRIM1 Deficiency Causes a Distinctive Primordial Dwarfism Syndrome ', Genes & Development, vol. 34, pp. 1520-1533 . https://doi.org/10.1101/gad.340190.120
Genes Dev
DNA replication is fundamental for cell proliferation in all organisms. Nonetheless, components of the replisome have been implicated in human disease, and here we report PRIM1 encoding the catalytic subunit of DNA primase as a novel disease gene. Us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26ce4b6b78f912bb32057b749c26ef71