Results 41 to 50 of about 369,616 (163)

A transgenic bacterial artificial chromosome approach to identify regulatory regions that direct Amhr2 and Osterix expression in Müllerian duct mesenchyme [PDF]

open access: yes, 2022
International audienceA transgenic mouse approach using bacterial artificial chromosomes (BAC) was used to identify regulatory regions that direct Müllerian duct expression for Amhr2 and Osterix (Osx, also known as Sp7).
Behringer, Richard, R   +11 more
core   +1 more source

A Uterus‐Preserving Laparoscopic Technique for Cervicovaginal Agenesis With Functional Uterine Remnants

open access: yesBJOG: An International Journal of Obstetrics &Gynaecology, EarlyView.
ABSTRACT Background Cervicovaginal agenesis with functional uterine remnants is a rare Müllerian anomaly that may cause obstructed menstrual flow, pelvic pain, haematometra, haematosalpinx and endometriosis. Uterus‐preserving reconstruction is challenging because it requires both neovaginal creation and durable uterine drainage.
Kiper Aslan   +3 more
wiley   +1 more source

Endometriosis and adenomyosis in a Mullerian agenesis patient: A delayed presentation

open access: yesAsian Journal of Medical Sciences
Mullerian duct anomalies are developmental anomalies resulting from failure in organogenesis, fusion, or the reabsorption of the paired Mullerian ducts. Endometriosis and Mullerian anomalies have a high coincidence rate. Obstructive uterine malformations
Monika Gautam   +5 more
doaj   +1 more source

Double Cervix with Normal Uterus and Vagina - An Unclassified Müllerian Anomaly [PDF]

open access: yesInternational Journal of Fertility and Sterility, 2019
Müllerian anomalies are very common, and a frequent cause of infertility. The most used classification system until now, proposed by the American Society for Reproductive Medicine in 1988, categorizes comprehensively uterine anomalies but fails to ...
Isabel Lobo Antunes   +5 more
doaj   +1 more source

Müllerian Duct Aplasia in a Girl With SMARCB1‐Related Coffin–Siris Syndrome: A Rare Co‐Occurring Anomaly

open access: yesClinical Genetics, EarlyView.
Genetic causes of Müllerian aplasia remain largely unknown. We report the first molecularly confirmed case of Coffin–Siris syndrome 3 caused by a de novo SMARCB1 variant presenting with Müllerian aplasia, supporting a potential association between BAF complex dysfunction and abnormal Müllerian duct development. Created in BioRender. Herlin, M. K. (2026)
Anneli C. S. Bolund   +5 more
wiley   +1 more source

Diagnostic Discordance in Recurrent Pregnancy Loss: Hysteroscopy Resolves Ultrasound–MRI Disagreement in Septate Uterus, but Concurrent Ovulation Induction Precludes Causal Attribution of the Reproductive Outcome

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Congenital uterine anomalies are an important and potentially treatable contributor to recurrent pregnancy loss (RPL). The septate uterus is the commonest Müllerian anomaly linked to first‐trimester loss, and its differentiation from the benign arcuate uterus is essential for management, yet imaging modalities may disagree.
Iftekhar Ahmed Sakib   +2 more
wiley   +1 more source

Standardized hysteroscopic management of complete septate uterus with duplicated cervices and longitudinal vaginal septum: A single‐center experience

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 175, Issue 1, Page 292-299, October 2026.
Abstract Objective To study perioperative and postoperative complications of a standardized ultrasound‐guided hysteroscopic treatment for complete septate uterus with duplicated cervices and non‐obstructive longitudinal vaginal septum, and to evaluate operative time, symptom changes, and reproductive outcomes. Methods Between January 2021 and May 2025,
Ursula Catena   +6 more
wiley   +1 more source

Morphology of the patent arterial duct : features relevant to treatment [PDF]

open access: yes, 2008
Patent ductus arteriosus (PDA), one of the most common congenital heart defects, is an abnormal persistence of a patent lumen in the arterial duct due to an arrest of the natural process of closure after it has served its function as a vital channel ...
Ho, Siew Yen   +2 more
core  

Septate uterus with double cervix and longitudinal vaginal septum – A report of two cases of rare uterine anomaly

open access: yesJournal of Medical Sciences and Health, 2020
Background: Embryological maldevelopment of the Mullerian or paramesonephric duct results in congenital uterine anomalies. A rare developmental anomaly is a septate uterus with cervical duplication and a longitudinal vaginal septum.
R Praveen   +3 more
doaj   +1 more source

Iron and Other Metal Ions in Human Health and Disease

open access: yesMedComm, Volume 7, Issue 10, October 2026.
Iron, copper, zinc, and calcium orchestrate cellular function through distinct yet cooperative mechanisms: redox‐active iron and copper cycle between oxidation states to act as Fenton catalysts and electron carriers in oxidative phosphorylation (OXPHOS); redox‐inert zinc serves as a structural component of zinc‐finger proteins and a catalytic cofactor ...
Xiaofeng Dai, Jitian Li
wiley   +1 more source

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