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 Experiment Videos

Branching morphogenesis and kidney disease.

Mita M Shah1, Rosemary V Sampogna, Hiroyuki Sakurai

  • 1Department of Pediatrics, University of California, San Diego, CA 92093-0693, USA.

Development (Cambridge, England)
|March 17, 2004
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Japanese Consensus Document on NexoBrid<sup>®</sup>, a Burn Eschar Removal Agent.

European burn journal·2026
Same author

Lanreotide acetate subcutaneous injection-induced granulomatous inflammation after surgery for neuroendocrine tumor of unknown primary origin.

International cancer conference journal·2026
Same author

Investigation of the Relationship Between Adrenal Gland Signal Intensity and Age in Whole-body MRI/DWIBS.

In vivo (Athens, Greece)·2026
Same author

[Invasive Mucinous Adenocarcinoma Diagnosed During the Follow-up of Atelectasis:Report of a Case].

Kyobu geka. The Japanese journal of thoracic surgery·2025
Same author

Eyelid Symmetry and Cosmetic Results Following Lateral Paracanthal Incision in the Transconjunctival Approach for Facial Fractures.

The Journal of craniofacial surgery·2025
Same author

Discovery of a Selective Inhibitor of ZIP14 with Therapeutic Potential for Cancer-associated Cachexia.

bioRxiv : the preprint server for biology·2025
Same journal

Dissecting planar and vertical organiser signals in early chick neural development.

Development (Cambridge, England)·2026
Same journal

Real-time transcriptomic profiling of hPSC-derived cartilage during development identifies a key role for the extracellular matrix in homeostasis and protection.

Development (Cambridge, England)·2026
Same journal

In preprints - housekeeping the housekeeping genes.

Development (Cambridge, England)·2026
Same journal

In preprints - light, cluster, friction: a cell dance on the gastrulation stage.

Development (Cambridge, England)·2026
Same journal

PBX-dependent and -independent Hox programs establish and maintain motor neuron terminal identity.

Development (Cambridge, England)·2026
Same journal

NUDT21 regulates 3'UTR dynamics in epididymal principal cells to preserve sperm integrity.

Development (Cambridge, England)·2026
See all related articles

Kidney branching morphogenesis is crucial for development. Disruptions can cause kidney diseases, and understanding molecular interactions offers insights into these disorders.

Area of Science:

  • Developmental Biology
  • Nephrology
  • Molecular Biology

Background:

  • Branching morphogenesis is a complex, regulated process essential for kidney development.
  • Disruptions in this process are linked to various kidney diseases, including hereditary syndromes, hypertension, and chronic kidney failure.

Purpose of the Study:

  • To synthesize current data on kidney branching morphogenesis from rodent studies.
  • To apply these findings to understand human kidney diseases related to aberrant branching.
  • To explore the role of molecular interactions in kidney development and disease.

Main Methods:

  • Review of in vitro and in vivo rodent studies on kidney development.
  • Synthesis of data on molecular interactions governing branching morphogenesis.

Related Experiment Videos

  • Application of findings to human kidney disease contexts.
  • Main Results:

    • Established a framework for understanding kidney development through molecular interactions.
    • Highlighted the link between aberrant branching and kidney pathologies.
    • Provided insights into potential mechanisms underlying kidney disorders.

    Conclusions:

    • Understanding the molecular organization of kidney development is key to deciphering branching disorders.
    • Rodent models offer valuable insights applicable to human kidney diseases.
    • This review provides a mechanistic framework for studying kidney developmental abnormalities.