Articles with "follicle syndrome" as a keyword



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A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation

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Published in 2020 at "Journal of Assisted Reproduction and Genetics"

DOI: 10.1007/s10815-020-01995-0

Abstract: Purpose To identify disease-causing genes involved in female infertility. Methods Whole-exome sequencing and Sanger DNA sequencing were used to identify the mutations in disease-causing genes. We performed subcellular protein localization, western immunoblotting analysis, and co-immunoprecipitation… read more here.

Keywords: follicle syndrome; novel mutation; zp3; female infertility ... See more keywords
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Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development.

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Published in 2018 at "Human reproduction"

DOI: 10.1093/humrep/dey215

Abstract: Empty follicle syndrome (EFS) is a disorder associated with female infertility and presents as a complete failure to retrieve oocytes during ART cycles despite normal follicle development and careful aspiration. To date, only two EFS… read more here.

Keywords: novel homozygous; follicle syndrome; follicle; disorder sex ... See more keywords
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Empty follicle syndrome: Frequency and probable causes in Pakistani Population.

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Published in 2020 at "JPMA. The Journal of the Pakistan Medical Association"

DOI: 10.5455/jpma.18623

Abstract: OBJECTIVE To determine the frequency of empty follicle syndrome in in-vitro fertilization-stimulated cycles and to evaluate the causes associated with this phenomenon. METHODS The retrospective study was conducted at the Baqai Institute of Reproduction and… read more here.

Keywords: follicle syndrome; frequency probable; follicle; syndrome frequency ... See more keywords