-
1
-
-
80051469652
-
Dopamine receptor type 5 in the primary cilia has dual chemo- and mechano-sensory roles
-
Abdul-Majeed S, Nauli SM. 2011. Dopamine receptor type 5 in the primary cilia has dual chemo- and mechano-sensory roles. Hypertension 58:325-31.
-
(2011)
Hypertension
, vol.58
, pp. 325-331
-
-
Abdul-Majeed, S.1
Nauli, S.M.2
-
2
-
-
84856360903
-
Stages of ciliogenesis and regulation of ciliary length
-
Avasthi P, Marshall WF. 2012. Stages of ciliogenesis and regulation of ciliary length. Differentiation 83:S30-42.
-
(2012)
Differentiation
, vol.83
-
-
Avasthi, P.1
Marshall, W.F.2
-
3
-
-
0035806961
-
The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway
-
Barr MM, DeModena J, Braun D, et al. 2001. The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway. Curr Biol 11:1341-6.
-
(2001)
Curr Biol
, vol.11
, pp. 1341-1346
-
-
Barr, M.M.1
DeModena, J.2
Braun, D.3
-
4
-
-
0033598394
-
A polycystic kidney-disease gene homologue required for male mating behaviour in C
-
Barr MM, Sternberg PW. 1999. A polycystic kidney-disease gene homologue required for male mating behaviour in C. elegans. Nature 401:386-9.
-
(1999)
elegans. Nature
, vol.401
, pp. 386-389
-
-
Barr, M.M.1
Sternberg, P.W.2
-
5
-
-
74449086803
-
Identification of signaling pathways regulating primary cilium length and flow-mediated adaptation
-
Besschetnova TY, Kolpakova-Hart E, Guan Y, et al. 2010. Identification of signaling pathways regulating primary cilium length and flow-mediated adaptation. Curr Biol 20:182-7.
-
(2010)
Curr Biol
, vol.20
, pp. 182-187
-
-
Besschetnova, T.Y.1
Kolpakova-Hart, E.2
Guan, Y.3
-
6
-
-
84883111223
-
Molecular basis of tubulin transport within the cilium by IFT74 and IFT81
-
Bhogaraju S, Cajanek L, Fort C, et al. 2013. Molecular basis of tubulin transport within the cilium by IFT74 and IFT81. Science 341:1009-12.
-
(2013)
Science
, vol.341
, pp. 1009-1012
-
-
Bhogaraju, S.1
Cajanek, L.2
Fort, C.3
-
7
-
-
27744436054
-
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, et al. 2005. Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis. Dev Biol 287:274-88.
-
(2005)
Dev Biol
, vol.287
, pp. 274-288
-
-
Bisgrove, B.W.1
Snarr, B.S.2
Emrazian, A.3
-
8
-
-
84885864917
-
IFT88 plays a Cilia- and PCP-independent role in controlling oriented cell divisions during vertebrate embryonic development
-
Borovina A, Ciruna B. 2013. IFT88 plays a Cilia- and PCP-independent role in controlling oriented cell divisions during vertebrate embryonic development. Cell Rep 5:37-43.
-
(2013)
Cell Rep
, vol.5
, pp. 37-43
-
-
Borovina, A.1
Ciruna, B.2
-
9
-
-
4243144134
-
Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization
-
Cano DA, Murcia NS, Pazour GJ, et al. 2004. Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization. Development 131:3457-67.
-
(2004)
Development
, vol.131
, pp. 3457-3467
-
-
Cano, D.A.1
Murcia, N.S.2
Pazour, G.J.3
-
10
-
-
48349109103
-
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
-
Cantagrel V, Silhavy JL, Bielas SL, et al. 2008. Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. Am J Hum Genet 83:170-9.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 170-179
-
-
Cantagrel, V.1
Silhavy, J.L.2
Bielas, S.L.3
-
11
-
-
84884303444
-
Cdc42 deficiency causes ciliary abnormalities and cystic kidneys
-
Choi SY, Chacon-Heszele MF, Huang L, et al. 2013. Cdc42 deficiency causes ciliary abnormalities and cystic kidneys. J Am Soc Nephrol 24:1435-50.
-
(2013)
J Am Soc Nephrol
, vol.24
, pp. 1435-1450
-
-
Choi, S.Y.1
Chacon-Heszele, M.F.2
Huang, L.3
-
12
-
-
84889094538
-
Compartmentalized calcium signaling in cilia regulates intraflagellar transport
-
Collingridge P, Brownlee C, Wheeler GL. 2013. Compartmentalized calcium signaling in cilia regulates intraflagellar transport. Curr Biol 23:2311-8.
-
(2013)
Curr Biol
, vol.23
, pp. 2311-2318
-
-
Collingridge, P.1
Brownlee, C.2
Wheeler, G.L.3
-
13
-
-
26644460824
-
Vertebrate smoothened functions at the primary cilium
-
Corbit KC, Aanstad P, Singla V, et al. 2005. Vertebrate smoothened functions at the primary cilium. Nature 437:1018-21.
-
(2005)
Nature
, vol.437
, pp. 1018-1021
-
-
Corbit, K.C.1
Aanstad, P.2
Singla, V.3
-
15
-
-
33846785192
-
Centriole/basal body morphogenesis and migration during ciliogenesis in animal cells
-
Dawe HR, Farr H, Gull K. 2007. Centriole/basal body morphogenesis and migration during ciliogenesis in animal cells. J Cell Sci 120(Pt 1):7-15.
-
(2007)
J Cell Sci
, vol.120
, Issue.PART 1
, pp. 7-15
-
-
Dawe, H.R.1
Farr, H.2
Gull, K.3
-
16
-
-
33846646986
-
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation
-
Dawe HR, Smith UM, Cullinane AR, et al. 2007. The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. Hum Mol Genet 16:173-86.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 173-186
-
-
Dawe, H.R.1
Smith, U.M.2
Cullinane, A.R.3
-
17
-
-
84862580595
-
Exome sequencing can improve diagnosis and alter patient management
-
138ra78
-
Dixon-Salazar TJ, Silhavy JL, Udpa N, et al. 2012. Exome sequencing can improve diagnosis and alter patient management. Sci Transl Med 4:138ra78.
-
(2012)
Sci Transl Med
, vol.4
-
-
Dixon-Salazar, T.J.1
Silhavy, J.L.2
Udpa, N.3
-
19
-
-
70450176073
-
Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion
-
Duldulao NA, Lee S, Sun Z. 2009. Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion. Development 136:4033-42.
-
(2009)
Development
, vol.136
, pp. 4033-4042
-
-
Duldulao, N.A.1
Lee, S.2
Sun, Z.3
-
20
-
-
76649133765
-
Molecular mechanisms of protein and lipid targeting to ciliary membranes
-
Emmer BT, Maric D, Engman DM. 2010. Molecular mechanisms of protein and lipid targeting to ciliary membranes. J Cell Sci 123(Pt 4):529-36.
-
(2010)
J Cell Sci
, vol.123
, Issue.PART 4
, pp. 529-536
-
-
Emmer, B.T.1
Maric, D.2
Engman, D.M.3
-
21
-
-
29444450890
-
Defective planar cell polarity in polycystic kidney disease
-
Fischer E, Legue E, Doyen A, et al. 2006. Defective planar cell polarity in polycystic kidney disease. Nat Genet 38:21-3.
-
(2006)
Nat Genet
, vol.38
, pp. 21-23
-
-
Fischer, E.1
Legue, E.2
Doyen, A.3
-
22
-
-
79955634491
-
The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes
-
Fogelgren B, Lin SY, Zuo X, et al. 2011. The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes. PLoS Genet 7:e1001361.
-
(2011)
PLoS Genet
, vol.7
-
-
Fogelgren, B.1
Lin, S.Y.2
Zuo, X.3
-
23
-
-
33748327050
-
The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly
-
Follit JA, Tuft RA, Fogarty KE, et al. 2006. The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly. Mol Biol Cell 17:3781-92.
-
(2006)
Mol Biol Cell
, vol.17
, pp. 3781-3792
-
-
Follit, J.A.1
Tuft, R.A.2
Fogarty, K.E.3
-
24
-
-
75749089291
-
The cytoplasmic tail of fibrocystin contains a ciliary targeting sequence
-
Follit JA, Li L, Vucica Y, et al. 2010. The cytoplasmic tail of fibrocystin contains a ciliary targeting sequence. J Cell Biol 188:21-8.
-
(2010)
J Cell Biol
, vol.188
, pp. 21-28
-
-
Follit, J.A.1
Li, L.2
Vucica, Y.3
-
25
-
-
84863992161
-
Scoring a backstage pass: mechanisms of ciliogenesis and ciliary access
-
Garcia-Gonzalo FR, Reiter JF. 2012. Scoring a backstage pass: mechanisms of ciliogenesis and ciliary access. J Cell Biol 197:697-709.
-
(2012)
J Cell Biol
, vol.197
, pp. 697-709
-
-
Garcia-Gonzalo, F.R.1
Reiter, J.F.2
-
27
-
-
77951101203
-
The primary cilium: a signalling centre during vertebrate development
-
Goetz SC, Anderson KV. 2010. The primary cilium: a signalling centre during vertebrate development. Nat Rev Genet 11:331-44.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 331-344
-
-
Goetz, S.C.1
Anderson, K.V.2
-
28
-
-
0034925405
-
Polycystic kidney disease: from the bedside to the gene and back
-
Grantham JJ. 2001. Polycystic kidney disease: from the bedside to the gene and back. Curr Opin Nephrol Hypertens 10:533-42.
-
(2001)
Curr Opin Nephrol Hypertens
, vol.10
, pp. 533-542
-
-
Grantham, J.J.1
-
29
-
-
0032577562
-
Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells
-
Grindstaff KK, Yeaman C, Anandasabapathy N, et al. 1998. Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells. Cell 93:731-40.
-
(1998)
Cell
, vol.93
, pp. 731-740
-
-
Grindstaff, K.K.1
Yeaman, C.2
Anandasabapathy, N.3
-
30
-
-
0033558093
-
The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis
-
Guo W, Roth D, Walch-Solimena C, et al. 1999. The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis. EMBO J 18:1071-80.
-
(1999)
EMBO J
, vol.18
, pp. 1071-1080
-
-
Guo, W.1
Roth, D.2
Walch-Solimena, C.3
-
31
-
-
40749144679
-
Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function
-
Haycraft CJ, Banizs B, Aydin-Son Y, et al. 2005. Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. PLoS Genet 1:e53.
-
(2005)
PLoS Genet
, vol.1
-
-
Haycraft, C.J.1
Banizs, B.2
Aydin-Son, Y.3
-
32
-
-
70949085969
-
Planar cell polarity effector gene Fuzzy regulates cilia formation and Hedgehog signal transduction in mouse
-
Heydeck W, Zeng H, Liu A. 2009. Planar cell polarity effector gene Fuzzy regulates cilia formation and Hedgehog signal transduction in mouse. Dev Dyn 238:3035-42.
-
(2009)
Dev Dyn
, vol.238
, pp. 3035-3042
-
-
Heydeck, W.1
Zeng, H.2
Liu, A.3
-
35
-
-
0030464563
-
The mammalian brain rsec6/8 complex
-
Hsu SC, Ting AE, Hazuka CD, et al. 1996. The mammalian brain rsec6/8 complex. Neuron 17:1209-19.
-
(1996)
Neuron
, vol.17
, pp. 1209-1219
-
-
Hsu, S.C.1
Ting, A.E.2
Hazuka, C.D.3
-
36
-
-
77954841928
-
A septin diffusion barrier at the base of the primary cilium maintains ciliary membrane protein distribution
-
Hu Q, Milenkovic L, Jin H, et al. 2010. A septin diffusion barrier at the base of the primary cilium maintains ciliary membrane protein distribution. Science 329:436-9.
-
(2010)
Science
, vol.329
, pp. 436-439
-
-
Hu, Q.1
Milenkovic, L.2
Jin, H.3
-
37
-
-
0023557377
-
Mapping of the Saccharomyces cerevisiae CDC3, CDC25, and CDC42 genes to chromosome XII by chromosome blotting and tetrad analysis
-
Johnson DI, Jacobs CW, Pringle JR, et al. 1987. Mapping of the Saccharomyces cerevisiae CDC3, CDC25, and CDC42 genes to chromosome XII by chromosome blotting and tetrad analysis. Yeast 3:243-53.
-
(1987)
Yeast
, vol.3
, pp. 243-253
-
-
Johnson, D.I.1
Jacobs, C.W.2
Pringle, J.R.3
-
38
-
-
0025363198
-
Molecular characterization of CDC42, a Saccharomyces cerevisiae gene involved in the development of cell polarity
-
Johnson DI, Pringle JR. 1990. Molecular characterization of CDC42, a Saccharomyces cerevisiae gene involved in the development of cell polarity. J Cell Biol 111:143-52.
-
(1990)
J Cell Biol
, vol.111
, pp. 143-152
-
-
Johnson, D.I.1
Pringle, J.R.2
-
39
-
-
56149097603
-
Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease
-
Jonassen JA, San Agustin J, Follit JA, et al. 2008. Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease. J Cell Biol 183:377-84.
-
(2008)
J Cell Biol
, vol.183
, pp. 377-384
-
-
Jonassen, J.A.1
San Agustin, J.2
Follit, J.A.3
-
40
-
-
37549052499
-
Ciliary proteins link basal body polarization to planar cell polarity regulation
-
Jones C, Roper VC, Foucher I, et al. 2008. Ciliary proteins link basal body polarization to planar cell polarity regulation. Nat Genet 40:69-77.
-
(2008)
Nat Genet
, vol.40
, pp. 69-77
-
-
Jones, C.1
Roper, V.C.2
Foucher, I.3
-
42
-
-
0036122434
-
Polycystin-2 is an intracellular calcium release channel
-
Koulen P, Cai Y, Geng L, et al. 2002. Polycystin-2 is an intracellular calcium release channel. Nat Cell Biol 4:191-7.
-
(2002)
Nat Cell Biol
, vol.4
, pp. 191-197
-
-
Koulen, P.1
Cai, Y.2
Geng, L.3
-
44
-
-
2342501364
-
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene
-
Li JB, Gerdes JM, Haycraft CJ, et al. 2004. Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. Cell 117:541-52.
-
(2004)
Cell
, vol.117
, pp. 541-552
-
-
Li, J.B.1
Gerdes, J.M.2
Haycraft, C.J.3
-
45
-
-
0037884961
-
Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease
-
Lin F, Hiesberger T, Cordes K, et al. 2003. Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease. Proc Natl Acad Sci USA 100:5286-91.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 5286-5291
-
-
Lin, F.1
Hiesberger, T.2
Cordes, K.3
-
46
-
-
0033638380
-
Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins
-
Lipschutz JH, Guo W, O'Brien LE, et al. 2000. Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins. Mol Biol Cell 11:4259-75.
-
(2000)
Mol Biol Cell
, vol.11
, pp. 4259-4275
-
-
Lipschutz, J.H.1
Guo, W.2
O'Brien, L.E.3
-
47
-
-
0037899298
-
The exocyst affects protein synthesis by acting on the translocation machinery of the endoplasmic reticulum
-
Lipschutz JH, Lingappa VR, Mostov KE. 2003. The exocyst affects protein synthesis by acting on the translocation machinery of the endoplasmic reticulum. J Biol Chem 278:20954-60.
-
(2003)
J Biol Chem
, vol.278
, pp. 20954-20960
-
-
Lipschutz, J.H.1
Lingappa, V.R.2
Mostov, K.E.3
-
48
-
-
0001647625
-
Exocytosis: the many masters of the exocyst
-
Lipschutz JH, Mostov KE. 2002. Exocytosis: the many masters of the exocyst. Curr Biol 12:R212-4.
-
(2002)
Curr Biol
, vol.12
-
-
Lipschutz, J.H.1
Mostov, K.E.2
-
49
-
-
0031941550
-
Molecular development of the kidney: a review of the results of gene disruption studies
-
Lipschutz JH. 1998. Molecular development of the kidney: a review of the results of gene disruption studies. Am J Kidney Dis 31:383-97.
-
(1998)
Am J Kidney Dis
, vol.31
, pp. 383-397
-
-
Lipschutz, J.H.1
-
50
-
-
34548429735
-
The proteome of the mouse photoreceptor sensory cilium complex
-
Liu Q, Tan G, Levenkova N, et al. 2007. The proteome of the mouse photoreceptor sensory cilium complex. Mol Cell Proteomics 6:1299-317.
-
(2007)
Mol Cell Proteomics
, vol.6
, pp. 1299-1317
-
-
Liu, Q.1
Tan, G.2
Levenkova, N.3
-
51
-
-
26844561983
-
Mechanoregulation of intracellular Ca2+ concentration is attenuated in collecting duct of monocilium-impaired orpk mice
-
Liu W, Murcia NS, Duan Y, et al. 2005. Mechanoregulation of intracellular Ca2+ concentration is attenuated in collecting duct of monocilium-impaired orpk mice. Am J Physiol Renal Physiol 289:F978-88.
-
(2005)
Am J Physiol Renal Physiol
, vol.289
-
-
Liu, W.1
Murcia, N.S.2
Duan, Y.3
-
52
-
-
57149087523
-
Cholangiocyte primary cilia are chemosensory organelles that detect biliary nucleotides via P2Y12 purinergic receptors
-
Masyuk AI, Gradilone SA, Banales JM, et al. 2008. Cholangiocyte primary cilia are chemosensory organelles that detect biliary nucleotides via P2Y12 purinergic receptors. Am J Physiol Gastrointest Liver Physiol 295:G725-34.
-
(2008)
Am J Physiol Gastrointest Liver Physiol
, vol.295
-
-
Masyuk, A.I.1
Gradilone, S.A.2
Banales, J.M.3
-
53
-
-
15844385078
-
PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein
-
Mochizuki T, Wu G, Hayashi T, et al. 1996. PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein. Science 272:1339-42.
-
(1996)
Science
, vol.272
, pp. 1339-1342
-
-
Mochizuki, T.1
Wu, G.2
Hayashi, T.3
-
54
-
-
0032504963
-
Cloning of inv, a gene that controls left/right asymmetry and kidney development
-
Mochizuki T, Saijoh Y, Tsuchiya K, et al. 1998. Cloning of inv, a gene that controls left/right asymmetry and kidney development. Nature 395:177-81.
-
(1998)
Nature
, vol.395
, pp. 177-181
-
-
Mochizuki, T.1
Saijoh, Y.2
Tsuchiya, K.3
-
55
-
-
34347400228
-
Differences in renal tubule primary cilia length in a mouse model of Bardet-Biedl syndrome
-
Mokrzan EM, Lewis JS, Mykytyn K. 2007. Differences in renal tubule primary cilia length in a mouse model of Bardet-Biedl syndrome. Nephron Exp Nephrol 106:e88-96.
-
(2007)
Nephron Exp Nephrol
, vol.106
-
-
Mokrzan, E.M.1
Lewis, J.S.2
Mykytyn, K.3
-
56
-
-
0037115494
-
Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle
-
Morgan D, Eley L, Sayer J, et al. 2002. Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle. Hum Mol Genet 11:3345-50.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 3345-3350
-
-
Morgan, D.1
Eley, L.2
Sayer, J.3
-
58
-
-
0028322016
-
Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice
-
Moyer JH, Lee-Tischler MJ, Kwon HY, et al. 1994. Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. Science 264:1329-33.
-
(1994)
Science
, vol.264
, pp. 1329-1333
-
-
Moyer, J.H.1
Lee-Tischler, M.J.2
Kwon, H.Y.3
-
59
-
-
34250012834
-
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
-
Nachury MV, Loktev AV, Zhang Q, et al. 2007. A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis. Cell 129:1201-13.
-
(2007)
Cell
, vol.129
, pp. 1201-1213
-
-
Nachury, M.V.1
Loktev, A.V.2
Zhang, Q.3
-
60
-
-
0037317302
-
Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
-
Nauli SM, Alenghat FJ, Luo Y, et al. 2003. Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells. Nat Genet 33:129-37.
-
(2003)
Nat Genet
, vol.33
, pp. 129-137
-
-
Nauli, S.M.1
Alenghat, F.J.2
Luo, Y.3
-
61
-
-
0018930046
-
Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway
-
Novick P, Field C, Schekman R. 1980. Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway. Cell 21:205-15.
-
(1980)
Cell
, vol.21
, pp. 205-215
-
-
Novick, P.1
Field, C.2
Schekman, R.3
-
62
-
-
0041592700
-
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
-
Otto EA, Schermer B, Obara T, et al. 2003. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination. Nat Genet 34:413-20.
-
(2003)
Nat Genet
, vol.34
, pp. 413-420
-
-
Otto, E.A.1
Schermer, B.2
Obara, T.3
-
63
-
-
33644624937
-
Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling
-
Park TJ, Haigo SL, Wallingford JB. 2006. Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling. Nat Genet 38:303-11.
-
(2006)
Nat Genet
, vol.38
, pp. 303-311
-
-
Park, T.J.1
Haigo, S.L.2
Wallingford, J.B.3
-
64
-
-
44349116202
-
Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia
-
Patel V, Li L, Cobo-Stark P, et al. 2008. Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia. Hum Mol Genet 17:1578-90.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 1578-1590
-
-
Patel, V.1
Li, L.2
Cobo-Stark, P.3
-
65
-
-
0034735526
-
Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella
-
Pazour GJ, Dickert BL, Vucica Y, et al. 2000. Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J Cell Biol 151:709-18.
-
(2000)
J Cell Biol
, vol.151
, pp. 709-718
-
-
Pazour, G.J.1
Dickert, B.L.2
Vucica, Y.3
-
67
-
-
0037018850
-
The ion channel polycystin-2 is required for left-right axis determination in mice
-
Pennekamp P, Karcher C, Fischer A, et al. 2002. The ion channel polycystin-2 is required for left-right axis determination in mice. Curr Biol 12:938-43.
-
(2002)
Curr Biol
, vol.12
, pp. 938-943
-
-
Pennekamp, P.1
Karcher, C.2
Fischer, A.3
-
68
-
-
0031453864
-
Confocal analysis of primary cilia structure and colocalization with the Golgi apparatus in chondrocytes and aortic smooth muscle cells
-
Poole CA, Jensen CG, Snyder JA, et al. 1997. Confocal analysis of primary cilia structure and colocalization with the Golgi apparatus in chondrocytes and aortic smooth muscle cells. Cell Biol Int 21:483-94.
-
(1997)
Cell Biol Int
, vol.21
, pp. 483-494
-
-
Poole, C.A.1
Jensen, C.G.2
Snyder, J.A.3
-
69
-
-
0035498717
-
Bending the MDCK cell primary cilium increases intracellular calcium
-
Praetorius HA, Spring KR. 2001. Bending the MDCK cell primary cilium increases intracellular calcium. J Membr Biol 184:71-9.
-
(2001)
J Membr Biol
, vol.184
, pp. 71-79
-
-
Praetorius, H.A.1
Spring, K.R.2
-
70
-
-
0037557518
-
Removal of the MDCK cell primary cilium abolishes flow sensing
-
Praetorius HA, Spring KR. 2003. Removal of the MDCK cell primary cilium abolishes flow sensing. J Membr Biol 191:69-76.
-
(2003)
J Membr Biol
, vol.191
, pp. 69-76
-
-
Praetorius, H.A.1
Spring, K.R.2
-
73
-
-
19044374304
-
Intraflagellar transport
-
Rosenbaum J. 2002. Intraflagellar transport. Curr Biol 12:R125.
-
(2002)
Curr Biol
, vol.12
-
-
Rosenbaum, J.1
-
74
-
-
48349125616
-
Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease
-
Saburi S, Hester I, Fischer E, et al. 2008. Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease. Nat Genet 40:1010-5.
-
(2008)
Nat Genet
, vol.40
, pp. 1010-1015
-
-
Saburi, S.1
Hester, I.2
Fischer, E.3
-
75
-
-
0023568404
-
Early organogenesis of the kidney
-
Saxen L, Sariola H. 1987. Early organogenesis of the kidney. Pediatr Nephrol 1:385-92.
-
(1987)
Pediatr Nephrol
, vol.1
, pp. 385-392
-
-
Saxen, L.1
Sariola, H.2
-
76
-
-
34248597580
-
Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw
-
Schottenfeld J, Sullivan-Brown J, Burdine RD. 2007. Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw. Development 134:1605-15.
-
(2007)
Development
, vol.134
, pp. 1605-1615
-
-
Schottenfeld, J.1
Sullivan-Brown, J.2
Burdine, R.D.3
-
77
-
-
77951895173
-
Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia
-
Shiba D, Manning DK, Koga H, et al. 2010. Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia. Cytoskeleton (Hoboken) 67:112-9.
-
(2010)
Cytoskeleton (Hoboken)
, vol.67
, pp. 112-119
-
-
Shiba, D.1
Manning, D.K.2
Koga, H.3
-
78
-
-
20944435539
-
Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways
-
Simons M, Gloy J, Ganner A, et al. 2005. Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways. Nat Genet 37:537-43.
-
(2005)
Nat Genet
, vol.37
, pp. 537-543
-
-
Simons, M.1
Gloy, J.2
Ganner, A.3
-
79
-
-
58149185543
-
Planar cell polarity signaling: from fly development to human disease
-
Simons M, Mlodzik M. 2008. Planar cell polarity signaling: from fly development to human disease. Annu Rev Genet 42:517-40.
-
(2008)
Annu Rev Genet
, vol.42
, pp. 517-540
-
-
Simons, M.1
Mlodzik, M.2
-
80
-
-
0001577217
-
Centrioles and the formation of rudimentary cilia by fibroblasts and smooth muscle cells
-
Sorokin S. 1962. Centrioles and the formation of rudimentary cilia by fibroblasts and smooth muscle cells. J Cell Biol 15:363-77.
-
(1962)
J Cell Biol
, vol.15
, pp. 363-377
-
-
Sorokin, S.1
-
81
-
-
0014291368
-
Reconstructions of centriole formation and ciliogenesis in mammalian lungs
-
Sorokin SP. 1968. Reconstructions of centriole formation and ciliogenesis in mammalian lungs. J Cell Sci 3:207-30.
-
(1968)
J Cell Sci
, vol.3
, pp. 207-230
-
-
Sorokin, S.P.1
-
82
-
-
4544383179
-
A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney
-
Sun Z, Amsterdam A, Pazour GJ, et al. 2004. A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney. Development 131:4085-93.
-
(2004)
Development
, vol.131
, pp. 4085-4093
-
-
Sun, Z.1
Amsterdam, A.2
Pazour, G.J.3
-
83
-
-
0035159015
-
Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia
-
Taulman PD, Haycraft CJ, Balkovetz DF, et al. 2001. Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia. Mol Biol Cell 12:589-99.
-
(2001)
Mol Biol Cell
, vol.12
, pp. 589-599
-
-
Taulman, P.D.1
Haycraft, C.J.2
Balkovetz, D.F.3
-
84
-
-
0029002967
-
Polycystic kidney disease: the complete structure of the PKD1 gene and its protein. The International Polycystic Kidney Disease Consortium
-
The International Polycystic Kidney Disease Consortium
-
The International Polycystic Kidney Disease Consortium. 1995. Polycystic kidney disease: the complete structure of the PKD1 gene and its protein. The International Polycystic Kidney Disease Consortium. Cell 81:289-98.
-
(1995)
Cell
, vol.81
, pp. 289-298
-
-
-
86
-
-
54049087300
-
Dishevelled links basal body docking and orientation in ciliated epithelial cells
-
Vladar EK, Axelrod JD. 2008. Dishevelled links basal body docking and orientation in ciliated epithelial cells. Trends Cell Biol 18:517-20.
-
(2008)
Trends Cell Biol
, vol.18
, pp. 517-520
-
-
Vladar, E.K.1
Axelrod, J.D.2
-
87
-
-
0016705067
-
Fine structure of mammalian renal cilia
-
Webber WA, Lee J. 1975. Fine structure of mammalian renal cilia. Anat Rec 182:339-43.
-
(1975)
Anat Rec
, vol.182
, pp. 339-343
-
-
Webber, W.A.1
Lee, J.2
-
88
-
-
76049118573
-
The Exo70 subunit of the exocyst is an effector for both Cdc42 and Rho3 function in polarized exocytosis
-
Wu H, Turner C, Gardner J, et al. 2010. The Exo70 subunit of the exocyst is an effector for both Cdc42 and Rho3 function in polarized exocytosis. Mol Biol Cell 21:430-42.
-
(2010)
Mol Biol Cell
, vol.21
, pp. 430-442
-
-
Wu, H.1
Turner, C.2
Gardner, J.3
-
89
-
-
27144456598
-
Sec15 interacts with Rab11 via a novel domain and affects Rab11 localization in vivo
-
Wu S, Mehta SQ, Pichaud F, et al. 2005. Sec15 interacts with Rab11 via a novel domain and affects Rab11 localization in vivo. Nat Struct Mol Biol 12:879-85.
-
(2005)
Nat Struct Mol Biol
, vol.12
, pp. 879-885
-
-
Wu, S.1
Mehta, S.Q.2
Pichaud, F.3
-
90
-
-
0036785149
-
The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia
-
Yoder BK, Hou X, Guay-Woodford LM. 2002. The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. J Am Soc Nephrol 13:2508-16.
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 2508-2516
-
-
Yoder, B.K.1
Hou, X.2
Guay-Woodford, L.M.3
-
91
-
-
0027158027
-
Reversal of left-right asymmetry: a situs inversus mutation
-
Yokoyama T, Copeland NG, Jenkins NA, et al. 1993. Reversal of left-right asymmetry: a situs inversus mutation. Science 260:679-82.
-
(1993)
Science
, vol.260
, pp. 679-682
-
-
Yokoyama, T.1
Copeland, N.G.2
Jenkins, N.A.3
-
92
-
-
0028282550
-
Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen
-
Zerres K, Mucher G, Bachner L, et al. 1994. Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen. Nat Genet 7:429-32.
-
(1994)
Nat Genet
, vol.7
, pp. 429-432
-
-
Zerres, K.1
Mucher, G.2
Bachner, L.3
-
93
-
-
5644261225
-
Sec15 is an effector for the Rab11 GTPase in mammalian cells
-
Zhang XM, Ellis S, Sriratana A, et al. 2004. Sec15 is an effector for the Rab11 GTPase in mammalian cells. J Biol Chem 279:43027-34.
-
(2004)
J Biol Chem
, vol.279
, pp. 43027-43034
-
-
Zhang, X.M.1
Ellis, S.2
Sriratana, A.3
-
94
-
-
84951612651
-
Beitrage Zur Kenntniss einiger Drusen und epithelien
-
Zimmermann K. 1898. Beitrage Zur Kenntniss einiger Drusen und epithelien. Arch Mikrosk Anat 52:552-706.
-
(1898)
Arch Mikrosk Anat
, vol.52
, pp. 552-706
-
-
Zimmermann, K.1
-
95
-
-
79959358443
-
The small GTPase Cdc42 is necessary for primary ciliogenesis in renal tubular epithelial cells
-
Zuo X, Fogelgren B, Lipschutz JH. 2011. The small GTPase Cdc42 is necessary for primary ciliogenesis in renal tubular epithelial cells. J Biol Chem 286:22469-77.
-
(2011)
J Biol Chem
, vol.286
, pp. 22469-22477
-
-
Zuo, X.1
Fogelgren, B.2
Lipschutz, J.H.3
-
96
-
-
66249115336
-
The exocyst protein Sec10 is necessary for primary ciliogenesis and cystogenesis in vitro
-
Zuo X, Guo W, Lipschutz JH. 2009. The exocyst protein Sec10 is necessary for primary ciliogenesis and cystogenesis in vitro. Mol Biol Cell 20:2522-9.
-
(2009)
Mol Biol Cell
, vol.20
, pp. 2522-2529
-
-
Zuo, X.1
Guo, W.2
Lipschutz, J.H.3
|