Aberrant DNA methylation in the PAX2 promoter is associated with Müllerian duct anomalies

The diverse roles of DNA methylation in mammalian development and disease

(2019) Maxim V. C. Greenberg et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

DNA methylation alterations—potential cause of endometriosis pathogenesis or a reflection of tissue heterogeneity?†

(2018) Merli Saare et al.   BIOLOGY OF REPRODUCTION

The cell biology and molecular genetics of Müllerian duct development

(2018) Zahida Yesmin Roly et al.   Wiley Interdisciplinary Reviews-Developmental Biology

Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients

(2018) Thomas Eggermann et al.   Molecular Genetics & Genomic Medicine

Congenital anal atresia with rectovestibular fistula, scoliosis, unilateral renal agenesis, and finger defect (VACTERL association) in a patient with partial bicornuate uterus and distal vaginal atresia

(2018) Jia Kang et al.   MEDICINE

Three-dimensional scan of the uterine cavity of infertile women before assisted reproductive technology use

(2018) Liana Pleş et al.   MEDICINE

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females

(2016) Zuying Xu et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

HOXA10, EMX2 and TENM1 expression in the mid-secretory endometrium of infertile women with a Müllerian duct anomaly

(2016) Ying Zhu et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Evidence for intermediate mesoderm and kidney progenitor cell specification by Pax2 and PTIP dependent mechanisms

(2015) Egon J. Ranghini et al.   DEVELOPMENTAL BIOLOGY

Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete müllerian fusion

(2015) Shan Liu et al.   FERTILITY AND STERILITY

Müllerian duct anomalies diagnosed by saline contrast sonohysterography: prevalence in a general population

(2014) Eva Dreisler et al.   FERTILITY AND STERILITY

Regulation of endometrial receptivity by the highly expressed HOXA9, HOXA11 and HOXD10 HOX-class homeobox genes

(2014) B. Xu et al.   HUMAN REPRODUCTION

The ESHRE/ESGE consensus on the classification of female genital tract congenital anomalies

(2013) G. F. Grimbizis et al.   HUMAN REPRODUCTION

Accuracy of 3-Dimensional Sonography for Diagnosis and Classification of Congenital Uterine Anomalies

(2013) Ashraf Moini et al.   JOURNAL OF ULTRASOUND IN MEDICINE

Two novel EGFP insertion alleles reveal unique aspects of Pax2 function in embryonic and adult kidneys

(2012) Abdul Soofi et al.   DEVELOPMENTAL BIOLOGY

PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis

(2012) Peng Wang et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia

(2011) Maria Sandbacka et al.   FERTILITY AND STERILITY

A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients

(2011) Katharina Rall et al.   Orphanet Journal of Rare Diseases

SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome

(2010) Cristina Gervasini et al.   GENETICS IN MEDICINE

Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree ofH19Hypomethylation Associates with Phenotype Severity and Genital and Skeletal Anomalies

(2008) Sara Bruce et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM