Associated Papers
Primary ovarian insufficiency due to homozygous variants in the homeobox transcription factor NOBOX.
Zidoune H et al.
Molecular Biology Reports, 2025
Reclassifying NOBOX variants in primary ovarian insufficiency cases with a corrected gene model and a novel quantitative framework.
Veitia RA et al.
Human Reproduction (oxford, England), 2025
Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variants.
Van Der Kelen A et al.
Journal of Assisted Reproduction and Genetics, 2025
NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights.
Jordan P et al.
Journal of Assisted Reproduction and Genetics, 2024
Sumoylation regulates functional properties of the oocyte transcription factors SOHLH1 and NOBOX.
Patton BK et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2023
Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea.
Sassi A et al.
Molecular Genetics & Genomic Medicine, 2021
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing.
Laissue P
Molecular and Cellular Endocrinology, 2015
Genetics of premature ovarian failure.
Bilgin EM et al.
Current Opinion in Obstetrics & Gynecology, 2015
Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women.
Qin Y et al.
Maturitas, 2014
Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort.
Bouilly J et al.
Human Mutation, 2011
Genetics of Female Infertility: Molecular Study of Newborn Ovary Homeobox Gene in Poor Ovarian Responders.
Batiha O et al.
Journal of Human Reproductive Sciences, 0
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