Results 1 - 19 of 19 results
GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base. , Jang DG, Kwon KY, Kweon YC, Kim BG, Myung K, Lee HS , Young Park C, Kwon T , Park TJ., Elife. August 25, 2022; 11
The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus. , Beckers A, Fuhl F, Ott T, Boldt K, Brislinger MM, Walentek P , Schuster-Gossler K, Hegermann J, Alten L, Kremmer E, Przykopanski A, Serth K, Ueffing M, Blum M , Gossler A., Sci Rep. June 25, 2021; 11 (1): 13333.
Aquatic models of human ciliary diseases. , Corkins ME, Krneta-Stankic V, Kloc M , Miller RK ., Genesis. February 1, 2021; 59 (1-2): e23410.
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): e0221698.
Stabilization of speckle-type POZ protein ( Spop) by Daz interacting protein 1 ( Dzip1) is essential for Gli turnover and the proper output of Hedgehog signaling. , Schwend T , Jin Z, Jiang K, Mitchell BJ , Jia J, Yang J ., J Biol Chem. November 8, 2013; 288 (45): 32809-32820.
Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry. , Kim S, Zaghloul NA , Bubenshchikova E, Oh EC, Rankin S , Katsanis N, Obara T, Tsiokas L., Nat Cell Biol. April 1, 2011; 13 (4): 351-60.
Rare copy number variations in congenital heart disease patients identify unique genes in left- right patterning. , Fakhro KA, Choi M, Ware SM , Belmont JW, Towbin JA, Lifton RP, Khokha MK , Brueckner M ., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.
The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation. , Dammermann A, Pemble H, Mitchell BJ , McLeod I, Yates JR, Kintner C , Desai AB, Oegema K., Genes Dev. September 1, 2009; 23 (17): 2046-59.
FGF signalling during embryo development regulates cilia length in diverse epithelia. , Neugebauer JM, Amack JD, Peterson AG, Bisgrove BW, Yost HJ ., Nature. April 2, 2009; 458 (7238): 651-4.
Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros. , Tran U , Pickney LM, Ozpolat BD , Wessely O ., Dev Biol. July 1, 2007; 307 (1): 152-64.
Xenopus cDNA microarray identification of genes with endodermal organ expression. , Park EC , Hayata T, Cho KW , Han JK ., Dev Dyn. June 1, 2007; 236 (6): 1633-49.
Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer''s vesicle are required for specification of the zebrafish left- right axis. , Bisgrove BW, Snarr BS, Emrazian A, Yost HJ ., Dev Biol. November 15, 2005; 287 (2): 274-88.
Localization and loss-of-function implicates ciliary proteins in early, cytoplasmic roles in left- right asymmetry. , Qiu D, Cheng SM, Wozniak L, McSweeney M, Perrone E, Levin M ., Dev Dyn. September 1, 2005; 234 (1): 176-89.
Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization. , Cano DA, Murcia NS, Pazour GJ, Hebrok M., Development. July 1, 2004; 131 (14): 3457-67.
The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms. , Haycraft CJ, Swoboda P, Taulman PD, Thomas JH, Yoder BK., Development. May 1, 2001; 128 (9): 1493-505.
An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons. , Qin H, Rosenbaum JL, Barr MM., Curr Biol. March 20, 2001; 11 (6): 457-61.
Expression of the orpk disease gene during kidney development and maturation. , Nakanishi K, Sweeney WE, Avner ED, Murcia NS., Pediatr Nephrol. March 1, 2001; 16 (3): 219-26.
Polaris, a protein involved in left- right axis patterning, localizes to basal bodies and cilia. , Taulman PD, Haycraft CJ, Balkovetz DF, Yoder BK., Mol Biol Cell. March 1, 2001; 12 (3): 589-99.
The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left- right axis determination. , Murcia NS, Richards WG, Yoder BK, Mucenski ML, Dunlap JR, Woychik RP., Development. June 1, 2000; 127 (11): 2347-55.