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

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...

You might also read

Related Articles

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

Sort by
Same author

Occlusal function and masticatory efficiency of sagittal malocclusions: a cross-sectional cohort study of orthognathic therapy.

Head & face medicine·2026
Same author

Learning MRI with ImmeRgaMe: Exploring the pedagogical potential of an innovative serious game for radiographer training.

Radiography (London, England : 1995)·2025
Same author

Assessment of bystander coronary artery disease in transcatheter aortic valve replacement (TAVR) patients using noncoronary-dedicated planning computed tomography angiography (CTA): diagnostic accuracy in a retrospective real-world cohort.

Clinical radiology·2025
Same author

tRNA-derived fragments are altered in diabetes.

Diabetic medicine : a journal of the British Diabetic Association·2023
Same author

A census of general surgery consultants in England and Wales: implications for the current and future surgical workforce.

Annals of the Royal College of Surgeons of England·2023
Same author

Identification, validation and biological characterisation of novel glioblastoma tumour microenvironment subtypes: implications for precision immunotherapy.

Annals of oncology : official journal of the European Society for Medical Oncology·2022

Related Experiment Video

Updated: May 11, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
09:06

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method

Published on: October 7, 2025

Identification of circulating microRNAs in HNF1A-MODY carriers.

C Bonner1, K C Nyhan, S Bacon

  • 1Department of Physiology and Medical Physics, Royal College of Surgeons, Dublin, Ireland.

Diabetologia
|May 16, 2013
PubMed
Summary

Hepatocyte Nuclear Factor 1-alpha Monogenic Diabetes of Youth (HNF1A-MODY) is linked to elevated serum microRNAs (miRNAs), specifically miR-103 and miR-224. These miRNAs can be detected in carriers, aiding in HNF1A-MODY diagnosis.

More Related Videos

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
08:12

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer

Published on: March 14, 2019

Genome-wide Analysis of HDAC Inhibitor-mediated Modulation of microRNAs and mRNAs in B Cells Induced to Undergo Class-switch DNA Recombination and Plasma Cell Differentiation
11:06

Genome-wide Analysis of HDAC Inhibitor-mediated Modulation of microRNAs and mRNAs in B Cells Induced to Undergo Class-switch DNA Recombination and Plasma Cell Differentiation

Published on: September 20, 2017

Related Experiment Videos

Last Updated: May 11, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
09:06

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method

Published on: October 7, 2025

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
08:12

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer

Published on: March 14, 2019

Genome-wide Analysis of HDAC Inhibitor-mediated Modulation of microRNAs and mRNAs in B Cells Induced to Undergo Class-switch DNA Recombination and Plasma Cell Differentiation
11:06

Genome-wide Analysis of HDAC Inhibitor-mediated Modulation of microRNAs and mRNAs in B Cells Induced to Undergo Class-switch DNA Recombination and Plasma Cell Differentiation

Published on: September 20, 2017

Area of Science:

  • Endocrinology
  • Molecular Biology
  • Genetics

Background:

  • Hepatocyte Nuclear Factor 1-alpha Monogenic Diabetes of Youth (HNF1A-MODY) is a genetic form of diabetes.
  • Identifying biomarkers for HNF1A-MODY is crucial for early diagnosis and management.

Purpose of the Study:

  • To identify specific microRNAs (miRNAs) associated with HNF1A-MODY.
  • To determine if these miRNAs are detectable in the serum of HNF1A-MODY carriers.

Main Methods:

  • An miRNA array was performed on rat INS-1 insulinoma cells expressing a common HNF1A mutation.
  • Differentially expressed miRNAs were validated using quantitative real-time PCR.
  • Serum miRNA levels were quantified in HNF1A-MODY carriers, MODY-negative controls, and individuals with type 2 diabetes mellitus.

Main Results:

  • Expression of the HNF1A mutation upregulated miR-103, miR-224, and miR-292-3p in cell lines.
  • miR-103 and miR-224 showed significantly elevated levels in the serum of HNF1A-MODY carriers.
  • Serum miR-103 levels could differentiate HNF1A-MODY carriers from individuals with type 2 diabetes mellitus.

Conclusions:

  • The pathophysiology of HNF1A-MODY involves the overexpression of miR-103 and miR-224.
  • These specific miRNAs are detectable in the serum, offering potential as diagnostic biomarkers for HNF1A-MODY.