Animal Models for Understanding Human Skeletal Defects.


Journal

Advances in experimental medicine and biology
ISSN: 0065-2598
Titre abrégé: Adv Exp Med Biol
Pays: United States
ID NLM: 0121103

Informations de publication

Date de publication:
2020
Historique:
entrez: 19 4 2020
pubmed: 19 4 2020
medline: 24 4 2020
Statut: ppublish

Résumé

Skeletal defects, such as cleft palate, scoliosis, and shortening of the limb bones are common in the human population. Animal models have been essential for characterizing the molecular and cellular mechanisms that underlie these and other skeletal disorders. This chapter will explore the cellular origins of the vertebrate skeleton and introduce a selection of animal models for human disorders of the skull and facial bones, spinal column, and limbs. The common genetic pathways that build the skeleton of various vertebrate species and how these similarities facilitate the study of human developmental processes in laboratory animals will be a focus of discussion. This chapter will also highlight how current genome editing technologies can be applied to model various perturbations of human chromatin structure in laboratory animals.

Identifiants

pubmed: 32304073
doi: 10.1007/978-981-15-2389-2_7
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

157-188

Auteurs

Isabella Skuplik (I)

Department of Biological Sciences, University of Calgary, Calgary, AB, Canada.

John Cobb (J)

Department of Biological Sciences, University of Calgary, Calgary, AB, Canada. jacobb@ucalgary.ca.

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Classifications MeSH