Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Anikó, Ujfalusi"'
Autor:
Nour Kurdi, Attila Mokánszki, Ingrid Balogh, Anikó Ujfalusi, Sándor Szabó, Gábor Méhes, Judit Bedekovics
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Extraneural metastasis of central nervous system tumors is generally rare and most often reported in glioblastomas and medulloblastomas, whereas oligodendrogliomas seem to have the lowest risk of extracranial metastasis. Given its
Externí odkaz:
https://doaj.org/article/ded374cc97b443489a46631fc9f00b4a
Akademický článek
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Autor:
Borbála Péterffy, Szilvia Krizsán, Bálint Egyed, Gábor Bedics, Anna Bekő, Dániel János Erdélyi, Judit Müller, Tibor Nagy, Lajos László Hegyi, Zsuzsanna Jakab, György Péter, Marianna Zombori, Krisztina Csanádi, Gábor Ottóffy, Katalin Csernus, Ágnes Vojcek, Lilla Györgyi Tiszlavicz, Krisztina Míta Gábor, Ágnes Kelemen, Péter Hauser, Krisztián Kállay, Gabriella Kertész, Zsuzsanna Gaál, István Szegedi, Ágnes Márk, Irén Haltrich, Zsuzsanna Hevessy, Anikó Ujfalusi, Béla Kajtár, Csongor Kiss, Gergely Kriván, András Matolcsy, Gábor Kovács, Csaba Bödör, Donát Alpár
Publikováno v:
HemaSphere, Vol 7, p e5932101 (2023)
Externí odkaz:
https://doaj.org/article/a68dee60f4b748d49f9ff83211db0f8a
Autor:
Kristóf Madarász, János András Mótyán, Judit Bedekovics, Zsófia Miltényi, Anikó Ujfalusi, Gábor Méhes, Attila Mokánszki
Publikováno v:
Cells, Vol 11, Iss 21, p 3475 (2022)
Background: Mutation of the TP53 gene is one of the major drivers of myelodysplastic neoplasias (MDS) and acute myeloid leukemia with myelodysplasia-related changes (AML-MR). TP53 mutations present in these hematopoietic malignancies form a distinct
Externí odkaz:
https://doaj.org/article/8d8e37cd792a44bdba2281df5cb07242
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Pathogenic variants of FOXP2 gene were identified first as a monogenic cause of childhood apraxia of speech (CAS), a complex disease that is associated with an impairment of the precision and consistency of movements underlying speech, due to deficit
Externí odkaz:
https://doaj.org/article/41edc5e334cc4e0681fa9622464c896b
Autor:
Gloria Kafui Esi Zodanu, Mónika Oszlánczi, Kálmán Havasi, Anita Kalapos, Gergely Rácz, Márta Katona, Anikó Ujfalusi, Orsolya Nagy, Márta Széll, Dóra Nagy
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Congenital heart defects (CHD) are the most common developmental abnormalities, affecting approximately 0.9% of livebirths. Genetic factors, including copy number variations (CNVs), play an important role in their development. The most common CNVs ar
Externí odkaz:
https://doaj.org/article/4f1e7a1d50c74cb0a782585c82c728d2
Publikováno v:
Journal of Human Reproductive Sciences, Vol 11, Iss 4, Pp 329-336 (2018)
Purpose: The aim of this study was to establish the Y chromosome microdeletion and partial AZFc microdeletion/duplication frequency firstly in East Hungarian population and to gain information about the molecular mechanism of the heterogeneous phenot
Externí odkaz:
https://doaj.org/article/8286ab01aedc41c09371b07843e7d65f
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Autor:
Katalin Gyurina, Bettina Kárai, Anikó Ujfalusi, Zsuzsanna Hevessy, Gábor Barna, Pál Jáksó, Gyöngyi Pálfi-Mészáros, Szilárd Póliska, Beáta Scholtz, János Kappelmayer, Gábor Zahuczky, Csongor Kiss
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
Background: Leukemic B-cell precursor (BCP) lymphoblasts were identified as a novel expression site for coagulation factor XIII subunit A (FXIII-A). Flow cytometry (FC) revealed three distinct expression patterns, i.e., FXIII-A negative, FXIII-A dim,
Externí odkaz:
https://doaj.org/article/308e8e85d76444048dc496658031754e
Autor:
Mokánszki, Kristóf Madarász, János András Mótyán, Judit Bedekovics, Zsófia Miltényi, Anikó Ujfalusi, Gábor Méhes, Attila
Publikováno v:
Cells; Volume 11; Issue 21; Pages: 3475
Background: Mutation of the TP53 gene is one of the major drivers of myelodysplastic neoplasias (MDS) and acute myeloid leukemia with myelodysplasia-related changes (AML-MR). TP53 mutations present in these hematopoietic malignancies form a distinct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::f82dd84cf14ceebe33a20755e03bddb3