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Novel mechanisms of early upper and lower urinary tract patterning regulated by RetY1015 docking tyrosine in mice

Mutations in the receptor tyrosine kinase RET are associated with congenital anomalies of kidneys or urinary tract (CAKUT). RET tyrosine Y1015 is the docking site for PLCγ, a major regulator of RET signaling. Abrogating signaling via Y1015 causes CAKUT that are markedly different than renal agenesis...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Hoshi, Masato, Batourina, Ekatherina, Mendelsohn, Cathy, Jain, Sanjay
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Company of Biologists 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3367447/
https://ncbi.nlm.nih.gov/pubmed/22627285
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.078667
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