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Fryl deficiency is associated with defective kidney development and function in mice
FRY like transcription coactivator (Fryl) gene located on chromosome 5 is a paralog of FRY microtubule binding protein (Fry) in vertebrates. It encodes a protein with unknown functions. Fryl gene is conserved in various species ranging from eukaryotes to human. Although there are several reports on...
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| Publicado no: | Exp Biol Med (Maywood) |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5882029/ https://ncbi.nlm.nih.gov/pubmed/29409347 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1535370218758249 |
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