Related Experiment Video

Updated: Jun 20, 2026

A Rat Tibial Growth Plate Injury Model to Characterize Repair Mechanisms and Evaluate Growth Plate Regeneration Strategies
06:53

A Rat Tibial Growth Plate Injury Model to Characterize Repair Mechanisms and Evaluate Growth Plate Regeneration Strategies

Published on: July 4, 2017

Five patients in a Chinese family with multiple epiphyseal dysplasia

Feng-xia Liu1, Meng-xue Yu, Yong-zhe Li

  • 1Department of Rheumatology, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100730, China.

Chinese Medical Journal
|September 29, 2009
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification
07:23

Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification

Published on: December 3, 2016

Tricolor Transgenic Murine Model for Studying Growth Plate Injury
07:58

Tricolor Transgenic Murine Model for Studying Growth Plate Injury

Published on: September 6, 2024

Related Experiment Videos

Last Updated: Jun 20, 2026

A Rat Tibial Growth Plate Injury Model to Characterize Repair Mechanisms and Evaluate Growth Plate Regeneration Strategies
06:53

A Rat Tibial Growth Plate Injury Model to Characterize Repair Mechanisms and Evaluate Growth Plate Regeneration Strategies

Published on: July 4, 2017

Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification
07:23

Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification

Published on: December 3, 2016

Tricolor Transgenic Murine Model for Studying Growth Plate Injury
07:58

Tricolor Transgenic Murine Model for Studying Growth Plate Injury

Published on: September 6, 2024

Related Concept Videos

Pleiotropy01:33

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
Sex-linked Disorders01:43

Sex-linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.

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

Topological Amorphization of VO2 via Chemical Locking for Durable Aqueous Zinc-Ion Storage.

Advanced materials (Deerfield Beach, Fla.)·2026

Neoadjuvant versus perioperative immunotherapy in resectable NSCLC: A PD-L1-stratified Bayesian network meta-analysis.

Frontiers in oncology·2026

Dysplasia epiphysealis hemimelic in the knee: a case report.

Frontiers in pediatrics·2026

Macrogenomic analysis showcases the diversity of tick RNA viruses in Mentougou, Beijing, China.

New microbes and new infections·2026

Global mortality of glaucoma: a systematic review and meta-analysis of prospective studies.

International ophthalmology·2026

Longitudinal surveillance of respiratory pathogens among acute respiratory infection patients in Changshu, Jiangsu, China, 2021-2024.

Journal of infection and public health·2026

Bacteriophages in humans: From discovery and mechanisms to therapeutic promise in combating disease.

Chinese medical journal·2026

Advancements and future directions in transforming therapies of prostate cancer.

Chinese medical journal·2026

IL-11 drives Treg cell differentiation by activating the MBD3/APOH-mediated fatty acid oxidation axis to promote hepatocellular carcinoma.

Chinese medical journal·2026

Sublethal heat stress-induced HSF4 upregulation via GRSF1 in an m6A-dependent manner in hepatocellular carcinoma.

Chinese medical journal·2026

E2F7 promotes lung adenocarcinoma progression by affecting phosphorylation and stabilization of β-catenin.

Chinese medical journal·2026

Improved diagnostic capability, rather than biologics, reduces surgical rates in Chinese Crohn's disease patients: A multicenter study.

Chinese medical journal·2026

Ultrasound-based transient elastography combined with metabolic biomarkers enhances the diagnostic efficacy for pediatric MASLD.

Medicine·2026

Association between cardiometabolic index and lung function in US adolescents: A cross-sectional study from the 2007 to 2012 NHANES.

Medicine·2026

Prevalence and associated family and lifestyle factors of precocious puberty in children: A retrospective observational study.

Medicine·2026

Ultrasound assessment of diaphragm thickness and related determinants in healthy female adolescents: a retrospective study.

BMC pulmonary medicine·2026

The role of the transdiagnostic sleep and circadian intervention in adolescent bedtime and sleep quality: a pilot study.

Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine·2026

Child with genetically confirmed Prader-Willi syndrome.

BMJ case reports·2026
See all related articles
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
Jove
Visualize
Contact Us