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Experimental Dermatology|July 18, 2006
The expression of keratinocyte growth factor receptor (FGFR2-IIIb) correlates with the high proliferative rate of HaCaT keratinocytesNikoletta Nagy, Zsuzsanna Bata-Csörgo, Norbert Kopasz, et al.
Wound Repair and Regeneration : Official Publication of the Wound Healing Society [And] the European Tissue Repair Society|July 22, 2008
The altered expression of syndecan 4 in the uninvolved skin of venous leg ulcer patients may predispose to venous leg ulcerNikoletta Nagy, István Balázs Németh, Gábor Szabad, et al.
Experimental Dermatology|November 23, 2012
A novel missense mutation of the CYLD gene identified in a Hungarian family with Brooke-Spiegler syndromeNikoletta Nagy, Katalin Farkas, Agnes Kinyo, et al.
The Journal of Investigative Dermatology|March 18, 2011
MiR-125b, a microRNA downregulated in psoriasis, modulates keratinocyte proliferation by targeting FGFR2Ning Xu, Petter Brodin, Tianling Wei, et al.
Pathology Oncology Research : POR|April 23, 2025
Timely recognition of a probably life-threatening genodermatosis: familial case report of hereditary leiomyomatosis and renal cell cancerJudit Kárteszi, Nikoletta Nagy, Márta Széll, et al.
BMC Pediatrics|January 15, 2024
A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorderNikoletta Nagy, Margit Pál, Dóra Nagy, et al.
Archives of Dermatological Research|September 18, 2015
Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutationEdina Nemes, Katalin Farkas, Barbara Kocsis-Deák, et al.
Archives of Dermatological Research|August 31, 2013
A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ-Siemens-Touraine syndromeAgnes Kinyó, Péter Vályi, Katalin Farkas, et al.
International Journal of Environmental Research and Public Health|September 10, 2021
Physiological and Psychological Responses to a Maximal Swimming Exercise Test in Adolescent Elite AthletesGábor Almási, Edit Bosnyák, Ákos Móra, et al.
Brain and Behavior|April 18, 2017
High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosisKornélia Tripolszki, Dóra Török, David Goudenège, et al.
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