Craniometaphyseal dysplasia with increased bone turnover and secondary hyperparathyroidism: therapeutic effect of calcitonin.
about
The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor geneCraniometaphyseal dysplasia (CMD), autosomal dominant formMolecular, phenotypic aspects and therapeutic horizons of rare genetic bone disorders.A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)Progressive ankylosis protein (ANK) in osteoblasts and osteoclasts controls bone formation and bone remodeling.Bone marrow-derived osteoclast-like cells from a patient with craniometaphyseal dysplasia lack expression of osteoclast-reactive vacuolar proton pump.Introduction of a Phe377del mutation in ANK creates a mouse model for craniometaphyseal dysplasia.Cardiopulmonary arrest caused by craniometaphyseal dysplasia.Craniometaphyseal dysplasia.
P2860
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P2860
Craniometaphyseal dysplasia with increased bone turnover and secondary hyperparathyroidism: therapeutic effect of calcitonin.
description
1988 nî lūn-bûn
@nan
1988年の論文
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1988年学术文章
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1988年学术文章
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1988年学术文章
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1988年学术文章
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1988年学术文章
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1988年學術文章
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1988年學術文章
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name
Craniometaphyseal dysplasia wi ...... rapeutic effect of calcitonin.
@en
Craniometaphyseal dysplasia wi ...... rapeutic effect of calcitonin.
@nl
type
label
Craniometaphyseal dysplasia wi ...... rapeutic effect of calcitonin.
@en
Craniometaphyseal dysplasia wi ...... rapeutic effect of calcitonin.
@nl
prefLabel
Craniometaphyseal dysplasia wi ...... rapeutic effect of calcitonin.
@en
Craniometaphyseal dysplasia wi ...... rapeutic effect of calcitonin.
@nl
P2093
P1476
Craniometaphyseal dysplasia wi ...... rapeutic effect of calcitonin.
@en
P2093
Boltshauser E
Fischer JA
Landolt AM
P304
P356
10.1016/S0022-3476(88)80176-8
P407
P577
1988-04-01T00:00:00Z