Understanding how BMP signaling affects craniofacial development

Characterizing the cranial neural crest response to BMP signaling through gastrulation and neurulation

['FUNDING_OTHER'] · JOHNS HOPKINS UNIVERSITY · NIH-11052488

This study is looking at how certain signals in the body help shape the cells that form our face, with the hope of finding new ways to prevent or treat birth defects like Treacher Collins syndrome and cleft palate.

Quick facts

Phase['FUNDING_OTHER']
Study typeNih_funding
SexAll
SponsorJOHNS HOPKINS UNIVERSITY (nih funded)
Locations1 site (BALTIMORE, UNITED STATES)
Trial IDNIH-11052488 on ClinicalTrials.gov

What this research studies

This research investigates the role of BMP signaling in the development of cranial neural crest cells, which are crucial for forming facial structures such as bones and cartilage. By examining how BMP gradients influence the specification and differentiation of these cells during early development, the research aims to uncover mechanisms that could lead to new treatments for craniofacial birth defects. The study employs both live imaging and quantitative analysis to track BMP signaling throughout key developmental stages. Patients may benefit from insights gained that could inform preventative and therapeutic strategies for conditions like Treacher Collins syndrome and cleft palate.

Who could benefit from this research

Good fit: Ideal candidates for this research are individuals affected by craniofacial birth defects, such as those with 22q11 deletion syndrome or Treacher Collins syndrome.

Not a fit: Patients with craniofacial conditions not related to BMP signaling may not benefit from this research.

Why it matters

Potential benefit: If successful, this research could lead to novel treatments and preventative measures for various craniofacial birth defects.

How similar studies have performed: Previous research has shown promising results in understanding BMP signaling in craniofacial development, indicating that this approach has potential for success.

Where this research is happening

BALTIMORE, UNITED STATES

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.

View on NIH RePORTER →

Conditions: 22q11 Chromosomal Microdeletion Syndrome, 22q11 Deletion Syndrome, 22q11.2 deletion syndrome, Autosomal dominant Opitz G/BBB syndrome, Berry syndrome

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.