Associated Papers
Understanding the Mechanisms of Diminished Ovarian Reserve: Insights from Genetic Variants and Regulatory Factors.
Zhu Q et al.
Reproductive Sciences (thousand Oaks, Calif.), 2024
Ovarian insufficiency and secondary amenorrhea in a patient with a novel variant within GDF9 gene.
Marinakis NM et al.
Menopause (new York, N.y.), 2022
Premature Ovarian Insufficiency: Phenotypic Characterization Within Different Etiologies.
Jiao X et al.
The Journal of Clinical Endocrinology and Metabolism, 2017
Single nucleotide polymorphisms in premature ovarian failure-associated genes in a Chinese Hui population.
Ma L et al.
Molecular Medicine Reports, 2015
Aberrant GDF9 expression and activation are associated with common human ovarian disorders.
Simpson CM et al.
The Journal of Clinical Endocrinology and Metabolism, 2014
Genes involved in human premature ovarian failure.
Persani L et al.
Journal of Molecular Endocrinology, 2010
Identification of novel missense mutations of GDF9 in Chinese women with polycystic ovary syndrome.
Wang B et al.
Reproductive Biomedicine Online, 2010
Two distinct regions of latency-associated peptide coordinate stability of the latent transforming growth factor-beta1 complex.
Walton KL et al.
The Journal of Biological Chemistry, 2010
Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure.
Zhao H et al.
Fertility and Sterility, 2007
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