15 Articoli
Original Article
Accesso libero | 26 ago 2020
Effect of exogenous transcription factors integration sites on safety and pluripotency of induced pluripotent stem cells
, , , , , , e
Accesso libero | 26 ago 2020
Relationship between chromosomal aberrations and gene expressions in the p53 pathway in chronic lymphocytic leukemia
, , , , , , , , e
Accesso libero | 26 ago 2020
The expression levels of microRNAs associated with T and B cell differentiation/stimulation in ankylosing spondylitis
, , e
Accesso libero | 26 ago 2020
The effects of O6-methyl guanine DNA-methyl transferase promotor methylation and CpG1, CpG2, CpG3 and CpG4 methylation on treatment response and their prognostic significance in patients with glioblastoma
, , , , , , e
Accesso libero | 26 ago 2020
β-Elemene inhibits the proliferation and migration of human glioblastoma cell lines via suppressing ring finger protein 135
, , , , e
Accesso libero | 26 ago 2020
RANKL is a new epigenetic biomarker for the vasomotor symptom during Menopause
, e
Accesso libero | 26 ago 2020
The interaction of female age and active male smoking has negative influence on success rates of the in vitro fertilization treatments
Accesso libero | 26 ago 2020
An investigation of the COMT gene Val158Met polymorphism in patients admitted to the emergency department because of synthetic cannabinoid use
, , , , e
Accesso libero | 26 ago 2020
Implication of VDR rs7975232 and FCGR2A rs1801274 gene polymorphisms in the risk and the prognosis of
autoimmune thyroid diseases in the Tunisian population
, , e
Accesso libero | 26 ago 2020
Association of the brain-derived neurotrophic factor Val66Met polymorphism with body mass index, fasting glucose levels and lipid status in adolescents
, , , , , , , , e
Case Report
Accesso libero | 26 ago 2020
De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly
, , e
Accesso libero | 26 ago 2020
A new splice-site mutation of SPINK5 gene in the Netherton syndrome with different clinical features: A case report
, e
Accesso libero | 26 ago 2020
Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene
, , , e
Accesso libero | 26 ago 2020
Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report
, , , e
Cerca
Tutti i volumi ed i numeri in questa rivista
Volume 26 (2023)
Volume 25 (2022)
Volume 24 (2021)
Volume 23 (2020)
Volume 22 (2019)
Volume 21 (2018)
Volume 20 (2017)
Volume 19 (2016)
Volume 18 (2015)
Volume 17 (2014)
Volume 16 (2013)
Volume 14 (2011)
Volume 13 (2010)
Volume 12 (2009)
Volume 11 (2008)
Volume 10 (2007)