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Literature for DOID 0050777: Joubert syndrome
Xenbase Articles
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The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1.,
Ott T,Kaufmann L,Granzow M,Hinderhofer K,Bartram CR,Theiß S,Seitz A,Paramasivam N,Schulz A,Moog U,Blum M,Evers CM,
Front Physiol. January 1, 2019; 10:1664-042X.
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Divergent roles of the Wnt/PCP Formin Daam1 in renal ciliogenesis.,
Corkins ME,Krneta-Stankic V,Kloc M,McCrea PD,Gladden AB,Miller RK,
PLoS One. August 30, 2019; 14(8):1932-6203.
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| Editorial: Xenopus Models of Organogenesis and Disease., Griffin JN,Liu KJ,Liu KJ,Sempou E, Front Physiol. January 1, 2020; 11:1664-042X. |
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Aquatic models of human ciliary diseases.,
Corkins ME,Krneta-Stankic V,Kloc M,Miller RK,
Genesis. February 1, 2021; 59(1-2):1526-968X.
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Cerebellar granular neuron progenitors exit their germinative niche via BarH-like1 activity mediated partly by inhibition of T-cell factor.,
Bou-Rouphael J,Doulazmi M,Eschstruth A,Abdou A,Durand BC,
Development. July 1, 2024; 151(13):1477-9129.
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