Antimüllerian hormone varies according to the stage of the menstrual cycle, and the day of blood collection may alter the clinical classification of ovarian response in women seeking fertility therapy.
Overweight and obese women with polycystic ovary syndrome who increased their serum 25-hydroxyvitamin D levels more during lifestyle intervention achieved greater improvement in waist circumference and cholesterol.
In a study on tubo-ovarian dysplasia, rats exposed to ovulation stimulation protocols exhibited tubal and ovarian histopathologic and immunohistochemical abnormalities with a dose effect different from those of genetic origin.
CpG-driven innate immune activation can cause activation and amplification of macrophages followed by their migration to the fetomaternal microenvironment, up-regulated tumor necrosis factor-a production, and consequent adverse outcomes of pregnancy.
Junctional proteins regulate vascular permeability in the human corpus luteum. We demonstrate that vascular endothelial cadherin, nectin 2, and claudin 5 are involved in this regulation in a mutually interacting manner.
A missense mutation of KAL1, c.1828G>A, led to pVal610Ile substitution in two brothers with Kallmann syndrome; their mother is heterozygous for this missense mutation encoded by the single-nucleotide polymorphism rs2229013.
We demonstrate the significance of macrophages in the development of endometriosis and the involvement of signal transducer and activator of transcription-3 in interactions between endometrial stromal cells and macrophages.
Intrauterine exposure to acceptable levels of diesel exhaust diminishes ovarian reserve of sexually mature mice. The authors recommend more careful examination of the environmental guidelines in humans.
Spermatozoa of normozoospermic men in idiopathic recurrrent spontaneous miscarriage do not reveal aberrations in DNA methylation at intergenic differentially methylated regions, MEST, ZAC, and LINE-1 CpG islands.
Azoospermia factor region microdeletions were not detected in Slovenian men with IRSA. Our comparisons with previous studies show that Y chromosome microdeletions are most likely not associated with IRSA.
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