Conditional heterozygous loss of Kit receptor tyrosine kinase in neural crest cell lineage is associated with midline cleft lip and bifid nose deformity

pubmed: wnt1 2024-12-21

Summary:

CONCLUSION: Conditional heterozygous loss of Kit in Wnt1-Cre; Kit^(2lox/+) embryos is associated with craniofacial dysplasia and exhibit defective NC development in vitro and in vivo.

Link:

https://pubmed.ncbi.nlm.nih.gov/39426597/?utm_source=Other&utm_medium=rss&utm_campaign=None&utm_content=16uwQpOeqFYN8R4TKOtwPy2utpqy9ex2oldalD2yF_fQHv2caq&fc=None&ff=20241221043555&v=2.18.0.post9+e462414

From feeds:

Exome ยป pubmed: wnt1

Tags:

Authors:

Hitomi Aoki, Hiroyuki Tomita, Akira Hara, Takahiro Kunisada

Date tagged:

12/21/2024, 04:36

Date published:

10/19/2024, 06:00