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Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene.

Open access
Karaplis, A C, Luz, A, Glowacki, J, Bronson, R T, Tybulewicz, V L, Kronenberg, H M, Mulligan, R C·1994·Genes & Development

Abstract

The parathyroid hormone-related peptide (PTHrP) gene was disrupted in murine embryonic stem cells by homologous recombination, and the null allele was introduced into the mouse germ line. Mice homozygous for the PTHrP null mutation died postnatally, probably from asphyxia, and exhibited widespread abnormalities of endochondral bone development. Histological examination revealed a diminution of chondrocyte proliferation, associated with premature maturation of chondrocytes and accelerated bone formation. Analysis of earlier developmental stages revealed that disturbance in cartilage growth preceded abnormal endochondral bone formation. There were no morphological abnormalities apparent in other tissues. These results provide direct evidence implicating PTHrP in normal skeletal development and serve to emphasize its potential involvement in human osteochondrodysplasias.

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Metadata

Authors
Karaplis, A. C., Luz, A., Glowacki, J., Bronson, R. T., Tybulewicz, V. L., Kronenberg, H. M., & Mulligan, R. C.
Venue
Genes & Development
Published
1994-02-01
Volume
8
Issue
3
Pages
277-289
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2163047938
Cited by
1,153
References
0
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene. https://app.cochat.ai/papers/10.1101/gad.8.3.277
The paper
Karaplis, A. C., Luz, A., Glowacki, J., Bronson, R. T., Tybulewicz, V. L., Kronenberg, H. M., & Mulligan, R. C. (1994). Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene. Genes & Development. https://doi.org/10.1101/gad.8.3.277

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