Novel WEE2 compound heterozygous mutations identified in patients with fertilization failure or poor fertilization

Clinical exome sequencing identifies novel compound heterozygous mutations of the WEE2 gene in primary infertile women with fertilization failure

(2021) Ancong Wang et al.   GYNECOLOGICAL ENDOCRINOLOGY

Genetic factors as potential molecular markers of human oocyte and embryo quality

(2021) Qing Sang et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Calcium Oscillatory Patterns and Oocyte Activation During Fertilization: a Possible Mechanism for Total Fertilization Failure (TFF) in Human In Vitro Fertilization?

(2020) Bei Sun et al.   Reproductive Sciences

Novel mutations in WEE2 : expanding the spectrum of mutations responsible for human fertilization failure

(2019) Zhihua Zhang et al.   CLINICAL GENETICS

Homozygous missense mutation Arg207Cys in the WEE2 gene causes female infertility and fertilization failure

(2019) Xiaoyu Yang et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation

(2019) Zhou Zhou et al.   HUMAN GENETICS

New biallelic mutations in WEE2: expanding the spectrum of mutations that cause fertilization failure or poor fertilization

(2019) Jing Dai et al.   FERTILITY AND STERILITY

Novel WEE2 gene variants identified in patients with fertilization failure and female infertility

(2019) Shuai Zhao et al.   FERTILITY AND STERILITY

Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure

(2019) Xiaopei Zhou et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility

(2018) Qing Sang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Segregating Chromosomes in the Mammalian Oocyte

(2018) Aleksandar I. Mihajlović et al.   CURRENT BIOLOGY

Calcium Signaling in Mammalian Eggs at Fertilization

(2016) Hideki Shirakawa et al.   CURRENT TOPICS IN MEDICINAL CHEMISTRY

Novel mutations and structural deletions in TUBB8 : expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development

(2016) Biaobang Chen et al.   HUMAN REPRODUCTION

Oocyte activation deficiency: a role for an oocyte contribution?

(2015) Marc Yeste et al.   HUMAN REPRODUCTION UPDATE

Protein Tyrosine Kinase Wee1B Is Essential for Metaphase II Exit in Mouse Oocytes

(2011) J. S. Oh et al.   SCIENCE

Wee1B, Myt1, and Cdc25 function in distinct compartments of the mouse oocyte to control meiotic resumption

(2010) Jeong Su Oh et al.   JOURNAL OF CELL BIOLOGY