Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Aneurysm I: Introduction01:30

Aneurysm I: Introduction

41
An aortic aneurysm is a localized outpouching or dilation at a weak point in the artery wall. It may involve different parts of the aorta, such as the abdominal aorta, aortic arch, or thoracic aorta.Etiological factorsSeveral disorders are associated with aortic aneurysms.Congenital causes, such as primary connective tissue disorders like Marfan syndrome, impact the integrity and strength of connective tissues, notably affecting the aorta. Marfan syndrome is a genetic disorder that specifically...
41
Smooth Endoplasmic Reticulum01:21

Smooth Endoplasmic Reticulum

6.6K
Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
6.6K
Nondisjunction01:21

Nondisjunction

4.2K
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers.  Nondisjunction is common during anaphase I or anaphase II of meiosis.  Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold...
4.2K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Ovarian reserve testing in long-term hormonal contraceptive users - proceed with caution.

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC·2026
Same author

Physician Management of Non-Cavity Distorting Intramural Fibroids and Infertility: A Survey of REI Providers.

International journal of women's health·2026
Same author

Emerging Topics in Neurogenomics: Summary From Inaugural Child Neurology Society Genetics Summit.

Pediatric neurology·2026
Same author

Transabdominal retrieval of oocytes when transvaginal access is not an option: mastering an egg-cellent technique.

Fertility and sterility·2026
Same author

Augmenting Medical Education Scholarship Using Artificial Intelligence and Glassick's Criteria.

Academic pediatrics·2026
Same author

Let's Talk Tech: The Role of Technology in Neurology Education.

Seminars in neurology·2026

Related Experiment Video

Updated: Oct 13, 2025

Laparoscopic Oocyte Retrieval and Cryopreservation during Vaginoplasty for Treatment of Mayer-Rokitansky-Kuster-Hauser Syndrome
11:53

Laparoscopic Oocyte Retrieval and Cryopreservation during Vaginoplasty for Treatment of Mayer-Rokitansky-Kuster-Hauser Syndrome

Published on: May 10, 2022

3.7K

ASRM müllerian anomalies classification 2021.

Samantha M Pfeifer, Marjan Attaran, Jessica Goldstein

    Fertility and Sterility
    |November 10, 2021
    PubMed
    Summary
    This summary is machine-generated.

    The new American Society for Reproductive Medicine (ASRM) Müllerian Anomalies Classification 2021 updates the 1988 AFS system. It provides a more comprehensive and clear classification for a wider range of müllerian anomalies.

    More Related Videos

    Arterial Pouch Microsurgical Bifurcation Aneurysm Model in the Rabbit
    06:11

    Arterial Pouch Microsurgical Bifurcation Aneurysm Model in the Rabbit

    Published on: May 14, 2020

    2.5K
    Microsatellite DNA Genotyping and Flow Cytometry Ploidy Analyses of Formalin-fixed Paraffin-embedded Hydatidiform Molar Tissues
    11:54

    Microsatellite DNA Genotyping and Flow Cytometry Ploidy Analyses of Formalin-fixed Paraffin-embedded Hydatidiform Molar Tissues

    Published on: October 20, 2019

    9.3K

    Related Experiment Videos

    Last Updated: Oct 13, 2025

    Laparoscopic Oocyte Retrieval and Cryopreservation during Vaginoplasty for Treatment of Mayer-Rokitansky-Kuster-Hauser Syndrome
    11:53

    Laparoscopic Oocyte Retrieval and Cryopreservation during Vaginoplasty for Treatment of Mayer-Rokitansky-Kuster-Hauser Syndrome

    Published on: May 10, 2022

    3.7K
    Arterial Pouch Microsurgical Bifurcation Aneurysm Model in the Rabbit
    06:11

    Arterial Pouch Microsurgical Bifurcation Aneurysm Model in the Rabbit

    Published on: May 14, 2020

    2.5K
    Microsatellite DNA Genotyping and Flow Cytometry Ploidy Analyses of Formalin-fixed Paraffin-embedded Hydatidiform Molar Tissues
    11:54

    Microsatellite DNA Genotyping and Flow Cytometry Ploidy Analyses of Formalin-fixed Paraffin-embedded Hydatidiform Molar Tissues

    Published on: October 20, 2019

    9.3K

    Area of Science:

    • Reproductive Medicine
    • Gynecology
    • Embryology

    Background:

    • Müllerian anomalies are diverse and often misdiagnosed due to limitations in existing classification systems.
    • The 1988 American Fertility Society (AFS) Classification, while widely used, has shortcomings including exclusion of cervical and vaginal anomalies and lack of clear diagnostic criteria.
    • These limitations can lead to delayed diagnosis, inadequate treatment, and adverse reproductive outcomes.

    Purpose of the Study:

    • To introduce the new American Society for Reproductive Medicine (ASRM) Müllerian Anomalies Classification 2021.
    • To address the limitations of previous classifications by providing a more comprehensive and updated system.
    • To improve the understanding, diagnosis, and management of müllerian anomalies.

    Main Methods:

    • Development of a new classification system by the ASRM Task Force on Müllerian Anomalies Classification.
    • Building upon the foundational AFS Classification from 1988, incorporating improvements for broader applicability.
    • Focus on clarity, comprehensiveness, and clinical utility.

    Main Results:

    • The ASRM Müllerian Anomalies Classification 2021 offers an expanded framework for categorizing müllerian duct anomalies.
    • It aims to provide clearer diagnostic criteria and encompass anomalies of the uterus, cervix, and vagina.
    • The classification is designed to facilitate better clinical decision-making and patient care.

    Conclusions:

    • The ASRM Müllerian Anomalies Classification 2021 represents a significant advancement in the field.
    • This updated system is expected to enhance provider education, patient advocacy, and the overall management of müllerian anomalies.
    • It provides a unified and more precise approach to understanding these congenital conditions.