Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida

Novel mutation in the ZP1 gene and clinical implications

(2019) Ping Yuan 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

Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters

(2019) Ling Sun et al.   HUMAN MUTATION

Molecular basis of egg coat cross-linking sheds light on ZP1-associated female infertility

(2019) Kaoru Nishimura et al.   Nature Communications

ZP2 pathogenic variants cause in vitro fertilization failure and female infertility

(2018) Can Dai et al.   GENETICS IN MEDICINE

Mutant ZP1 in Familial Infertility

(2014) Hua-Lin Huang et al.   NEW ENGLAND JOURNAL OF MEDICINE

Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome

(2011) Kemal O. Yariz et al.   FERTILITY AND STERILITY

In humans, zona pellucida glycoprotein-1 binds to spermatozoa and induces acrosomal exocytosis

(2010) Anasua Ganguly et al.   HUMAN REPRODUCTION

Native human zona pellucida glycoproteins: purification and binding properties

(2008) P. C.N. Chiu et al.   HUMAN REPRODUCTION