2018
DOI: 10.4066/biomedicalresearch.29-18-849
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An experimental model: intrauterine adhesion versus subendometrial fibrosis

Abstract: Background: Intrauterine adhesions (IUA) remain a major cause of infertility. The prevalence of IUA varies geographically and keeps increasing over the last few decades due to increased hysteroscopic surgeries. Therefore, IUA management has received considerable attention. However, the management of IUAs still presents a big challenge: the recurrence rate could be up to 62.5% in severe IUAs. Intrauterine adhesion (IUA) occurs as a result of endometrial destruction by surgical interventions or infection causing… Show more

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Cited by 16 publications
(12 citation statements)
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References 13 publications
(16 reference statements)
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“…The sequences of the specific primers used are listed in Table 1 . The following thermal cycling conditions were applied: 50 °C for 2 min, then 95 °C for10 min followed by 40 cycles of 95 °C for 30 s, 60 °C for 30 s, and 72 °C for 30 s. Changes in the expression of each target mRNAs were normalized relative to the mean critical threshold values of GAPDH mRNA(internal reference) using the ΔΔCt method [ 25 ].…”
Section: Methodsmentioning
confidence: 99%
“…The sequences of the specific primers used are listed in Table 1 . The following thermal cycling conditions were applied: 50 °C for 2 min, then 95 °C for10 min followed by 40 cycles of 95 °C for 30 s, 60 °C for 30 s, and 72 °C for 30 s. Changes in the expression of each target mRNAs were normalized relative to the mean critical threshold values of GAPDH mRNA(internal reference) using the ΔΔCt method [ 25 ].…”
Section: Methodsmentioning
confidence: 99%
“…The PCR run was performed on a Rotor Gene Real-Time PCR System (Qiagen). Normalization for variation in the expression of each target gene was performed referring to the mean critical threshold (CT) values of ß-actin housekeeping gene expression by the ΔΔCt method [18]. Primers sequence for all studied genes was listed as following in Table 1.…”
Section: Real-time Quantitative Polymerase Chain Reaction (Qpcr)mentioning
confidence: 99%
“…To remove any possible genomic DNA contamination, the total RNA samples were pre-treated using DNA-free™ DNase treatment and removal of reagents kit (Ambion, Austin, TX, USA) following the manufacturer's protocol and were recovered in 100 μl molecular biology grade water and stored at -20°C. The RNA concentration and purity were determined by Nanodrop Spectrophotometer absorption (Thermo Scientific, USA) at 260 nm 16 .…”
Section: Chromosomal Aberration Assay In Bone Marrow and Mouse Spermamentioning
confidence: 99%