15 Articles
Original Article
Open Access | Aug 26, 2020
Effect of exogenous transcription factors integration sites on safety and pluripotency of induced pluripotent stem cells
, , , , , , and
Open Access | Aug 26, 2020
Relationship between chromosomal aberrations and gene expressions in the p53 pathway in chronic lymphocytic leukemia
, , , , , , , , and
Open Access | Aug 26, 2020
The expression levels of microRNAs associated with T and B cell differentiation/stimulation in ankylosing spondylitis
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Open Access | Aug 26, 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
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Open Access | Aug 26, 2020
β-Elemene inhibits the proliferation and migration of human glioblastoma cell lines via suppressing ring finger protein 135
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Open Access | Aug 26, 2020
RANKL is a new epigenetic biomarker for the vasomotor symptom during Menopause
, and
Open Access | Aug 26, 2020
The interaction of female age and active male smoking has negative influence on success rates of the in vitro fertilization treatments
Open Access | Aug 26, 2020
An investigation of the COMT gene Val158Met polymorphism in patients admitted to the emergency department because of synthetic cannabinoid use
, , , , and
Open Access | Aug 26, 2020
Implication of VDR rs7975232 and FCGR2A rs1801274 gene polymorphisms in the risk and the prognosis of
autoimmune thyroid diseases in the Tunisian population
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Open Access | Aug 26, 2020
Association of the brain-derived neurotrophic factor Val66Met polymorphism with body mass index, fasting glucose levels and lipid status in adolescents
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Case Report
Open Access | Aug 26, 2020
De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly
, , and
Open Access | Aug 26, 2020
A new splice-site mutation of SPINK5 gene in the Netherton syndrome with different clinical features: A case report
, and
Open Access | Aug 26, 2020
Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene
, , , and
Open Access | Aug 26, 2020
Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report
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