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Short-limbed dwarfism: slw is a new allele of Npr2 causing chondrodysplasia

The Journal of Heredity

Aug 31, 2007

Chizuru SogawaTetsuo Kunieda

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Abstract

Short-limbed dwarfism (SLW) is a new mutant mouse characterized by a dwarf phenotype with markedly short body, limbs, and tail. In the present study, we investigated the skeletal phenotypes of the SLW mouse and determined the chromosomal localization to identify the gene responsible for...read more

Mentioned in this Paper

Establishment and Maintenance of Localization
Chondrodysplasia
Endochondral Ossification
Npr2 protein, rat
Chondrocyte Proliferation
Hereditary Multiple Exostoses
Hypertrophic Cardiomyopathy
Chondrodysplasia Punctata
Hypertrophy
Chondrocyte
Paper Details
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Short-limbed dwarfism: slw is a new allele of Npr2 causing chondrodysplasia

The Journal of Heredity

Aug 31, 2007

Chizuru SogawaTetsuo Kunieda

PMID: 17728275

DOI: 10.1093/jhered/esm065

Abstract

Short-limbed dwarfism (SLW) is a new mutant mouse characterized by a dwarf phenotype with markedly short body, limbs, and tail. In the present study, we investigated the skeletal phenotypes of the SLW mouse and determined the chromosomal localization to identify the gene responsible for...read more

Mentioned in this Paper

Establishment and Maintenance of Localization
Chondrodysplasia
Endochondral Ossification
Npr2 protein, rat
Chondrocyte Proliferation
Hereditary Multiple Exostoses
Hypertrophic Cardiomyopathy
Chondrodysplasia Punctata
Hypertrophy
Chondrocyte

Feeds With Similar Papers

Cardiomyopathy

Cardiomyopathy is a disease of the heart muscle, that can lead to muscular or electrical dysfunction of the heart. It is often an irreversible disease that is associated with a poor prognosis. There are different causes and classifications of cardiomyopathies. Here are the latest discoveries pertaining to this disease.

sGC Modulators

Soluble guanylate cyclase (sGC) stimulators and activators have been developed to treat patients with pulmonary hypertension and heart failure, respectively. Recently these sGC modulators have been explored for the treatment of fibrosis. Discover the latest research on sGC modulators here.

Related Papers

Biochemical and Biophysical Research Communications

Hypomorphic mutation in mouse Nppc gene causes retarded bone growth due to impaired endochondral ossification

Biochemical and Biophysical Research CommunicationsSeptember 9, 2008
Takehito TsujiTetsuo Kunieda
Paper Details
References
  • References
  • Citations15
  • finger pointing at paper

    References currently unavailable

    We're still populating references for this paper, please check back later.
  • References
  • Citations15
12

Download from

Publisher
PubMed
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