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Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome.
Ciobanu CG, Nucă I, Popescu R, Antoci LM, Caba L, Ivanov AV, Cojocaru KA, Rusu C, Mihai CT, Pânzaru MC. Ciobanu CG, et al. Among authors: rusu c. Int J Mol Sci. 2023 May 24;24(11):9206. doi: 10.3390/ijms24119206. Int J Mol Sci. 2023. PMID: 37298158 Free PMC article. Review.
Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variants.
Khan S, Focșa IO, Budișteanu M, Stoica C, Nedelea F, Bohîlțea L, Caba L, Butnariu L, Pânzaru M, Rusu C, Jurcă C, Chirita-Emandi A, Bănescu C, Abbas W, Sadeghpour A, Baig SM, Bălgrădean M, Davis EE. Khan S, et al. Among authors: rusu c. Am J Med Genet A. 2023 Sep;191(9):2376-2391. doi: 10.1002/ajmg.a.63322. Epub 2023 Jun 9. Am J Med Genet A. 2023. PMID: 37293956
Clinical, Pathological and Molecular Insights on KRAS, NRAS, BRAF, PIK3CA and TP53 Mutations in Metastatic Colorectal Cancer Patients from Northeastern Romania.
Afrăsânie VA, Marinca MV, Gafton B, Alexa-Stratulat T, Rusu A, Froicu EM, Sur D, Lungulescu CV, Popovici L, Lefter AV, Afrăsânie I, Ivanov AV, Miron L, Rusu C. Afrăsânie VA, et al. Among authors: rusu c. Int J Mol Sci. 2023 Aug 11;24(16):12679. doi: 10.3390/ijms241612679. Int J Mol Sci. 2023. PMID: 37628868 Free PMC article.
Combined flow cytometry natural killer immunophenotyping and KIR/HLA-C genotyping reveal remarkable differences in acute myeloid leukemia patients, but suggest an overall impairment of the natural killer response.
Cianga VA, Rusu C, Pavel-Tanasa M, Dascalescu A, Danaila C, Harnau S, Aanei CM, Cianga P. Cianga VA, et al. Among authors: rusu c. Front Med (Lausanne). 2023 Mar 7;10:1148748. doi: 10.3389/fmed.2023.1148748. eCollection 2023. Front Med (Lausanne). 2023. PMID: 36960339 Free PMC article.
155 results