Identification of Novel SHOX Target Genes in the Developing Limb Using a Transgenic Mouse Model

Deficiency of the human short stature homeobox-containing gene (SHOX) has been identified in several disorders characterized by reduced height and skeletal anomalies such as Turner syndrome, Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia as well as isolated short stature. SHOX acts as a...

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Detaylı Bibliyografya
Asıl Yazarlar: Beiser, Katja U., Glaser, Anne, Kleinschmidt, Kerstin, Scholl, Isabell, Röth, Ralph, Li, Li, Gretz, Norbert, Mechtersheimer, Gunhild, Karperien, Marcel, Marchini, Antonio, Richter, Wiltrud, Rappold, Gudrun A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2014
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4041798/
https://ncbi.nlm.nih.gov/pubmed/24887312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0098543
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