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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Bibliografiska uppgifter
I publikationen:Exp Biol Med (Maywood)
Huvudupphovsmän: Byun, Yong-Sub, Kim, Eun-Kyoung, Araki, Kimi, Yamamura, Ken-ichi, Lee, Kihoon, Yoon, Won-Kee, Won, Young-Suk, Kim, Hyoung-Chin, Choi, Kyung-Chul, Nam, Ki-Hoan
Materialtyp: Artigo
Språk:Inglês
Publicerad: SAGE Publications 2018
Ämnen:
Original Research
Länkar: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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