Cranial Neural Crest Specific Deletion of <i>Alpl</i> (TNAP) via P0-Cre Causes Abnormal Chondrocyte Maturation and Deficient Cranial Base Growth
Bone growth plate abnormalities and skull shape defects are seen in hypophosphatasia, a heritable disorder in humans that occurs due to the deficiency of tissue nonspecific alkaline phosphatase (TNAP, <i>Alpl</i>) enzyme activity. The abnormal development of the cranial base growth plate...
Main Authors: | Naoto Ohkura, Hwa Kyung Nam, Fei Liu, Nan Hatch |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-10-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/24/20/15401 |
Similar Items
-
Cranial Base Synchondrosis: Chondrocytes at the Hub
by: Shawn A. Hallett, et al.
Published: (2022-07-01) -
New Insights Into Cranial Synchondrosis Development: A Mini Review
by: Noriko Funato, et al.
Published: (2020-08-01) -
Case Report of Lethal Perinatal Hypophosphatasia with Seizure and Respiratory Failure Diagnosed by ALPL Gene Mutation
by: Seung Jae Lee, et al.
Published: (2020-02-01) -
Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review
by: Xiaojian Mao, et al.
Published: (2019-11-01) -
Clinical application experience of asfotase alfa for a young patient with childhood hypophosphatasia
by: Nataliya Y. Kalinchenko, et al.
Published: (2019-11-01)