Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Irina Nucă"'
Autor:
Elena-Roxana Avădănei, Irina-Draga Căruntu, Irina Nucă, Raluca Balan, Ludmila Lozneanu, Simona-Eliza Giusca, Cornelia Amalinei
Publikováno v:
Medicina, Vol 60, Iss 3, p 351 (2024)
Background and Objectives: The most common mutation in malignant melanoma (MM) is the single-point mutation of v-raf murine sarcoma viral oncogene homolog B1 (BRAF) oncogene. Our study aims to evaluate BRAF V600E mutation, highlighting its frequency
Externí odkaz:
https://doaj.org/article/3b1d47c3078f4fc9af223ad2a30af0e8
Autor:
Eva-Cristiana Gavril, Irina Nucă, Monica-Cristina Pânzaru, Anca Viorica Ivanov, Cosmin-Teodor Mihai, Lucian-Mihai Antoci, Cristian-Gabriel Ciobanu, Cristina Rusu, Roxana Popescu
Publikováno v:
Genes
Volume 14
Issue 2
Pages: 465
Volume 14
Issue 2
Pages: 465
2q37 microdeletion/deletion syndrome (2q37DS) is one of the most common subtelomeric deletion disorders, caused by a 2q37 deletion of variable size. The syndrome is characterized by a broad and diverse spectrum of clinical findings: characteristic fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457f49c938b266752e5c01e8971afcfe
https://doi.org/10.3390/genes14020465
https://doi.org/10.3390/genes14020465
Autor:
Eva-Cristiana Gavril, Roxana Popescu, Irina Nucă, Cristian-Gabriel Ciobanu, Lăcrămioara Ionela Butnariu, Cristina Rusu, Monica-Cristina Pânzaru
Publikováno v:
Genes; Volume 13; Issue 11; Pages: 2083
The most frequent microdeletion, 22q11.2 deletion syndrome (22q11.2DS), has a wide and variable phenotype that causes difficulties in diagnosis. 22q11.2DS is a contiguous gene syndrome, but due to the existence of several low-copy-number repeat seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2dbfdf8868d5636956bb2251732e5e2
https://doi.org/10.3390/genes13112083
https://doi.org/10.3390/genes13112083