-
1
-
-
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. Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. Cell 2004; 117: 541-552
-
(2004)
Cell
, vol.117
, pp. 541-552
-
-
Li, J.B.1
Gerdes, J.M.2
Haycraft, C.J.3
-
2
-
-
2342657884
-
Decoding cilia function: Defining specialized genes required for compartmentalized cilia biogenesis
-
Avidor-Reiss T, Maer AM, Koundakjian E et al. Decoding cilia function: defining specialized genes required for compartmentalized cilia biogenesis. Cell 2004; 117: 27-39
-
(2004)
Cell
, vol.117
, pp. 27-39
-
-
Avidor-Reiss, T.1
Maer, A.M.2
Koundakjian, E.3
-
3
-
-
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. Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J Cell Biol 2000; 151: 709-718
-
(2000)
J Cell Biol
, vol.151
, pp. 709-718
-
-
Pazour, G.J.1
Dickert, B.L.2
Vucica, Y.3
-
4
-
-
0034042763
-
The Oak Ridge polycystic kidney (orpk) disease gene is required for left-right axis determination
-
Murcia NS, Richards WG, Yoder BK et al. The Oak Ridge polycystic kidney (orpk) disease gene is required for left-right axis determination. Development 2000; 27: 2347-2355
-
(2000)
Development
, vol.27
, pp. 2347-2355
-
-
Murcia, N.S.1
Richards, W.G.2
Yoder, B.K.3
-
5
-
-
0037334326
-
Polycystic kidney disease-the ciliary connection
-
Ong AC, Wheatley DN. Polycystic kidney disease-the ciliary connection. Lancet 2003; 361: 774-776
-
(2003)
Lancet
, vol.361
, pp. 774-776
-
-
Ong, A.C.1
Wheatley, D.N.2
-
8
-
-
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. The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. J Am Soc Nephrol 2002; 13: 2508-2516
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 2508-2516
-
-
Yoder, B.K.1
Hou, X.2
Guay-Woodford, L.M.3
-
9
-
-
0033598394
-
A polycystic kidney-disease gene homologue required for male mating behaviour in C
-
Barr MM, Sternberg PW. A polycystic kidney-disease gene homologue required for male mating behaviour in C. elegans. Nature 1999; 401: 386-389
-
(1999)
Elegans. Nature
, vol.401
, pp. 386-389
-
-
Barr, M.M.1
Sternberg, P.W.2
-
10
-
-
0037317302
-
Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
-
Nauli SM, Alenghat FJ, Luo Y et al. Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells. Nat Genet 2003; 33: 129-137
-
(2003)
Nat Genet
, vol.33
, pp. 129-137
-
-
Nauli, S.M.1
Alenghat, F.J.2
Luo, Y.3
-
11
-
-
0037018850
-
The ion channel polycystin-2 is required for left-right axis determination in mice
-
Pennekamp P, Karcher C, Fischer A et al. The ion channel polycystin-2 is required for left-right axis determination in mice. Curr Biol 2002; 12: 938-943
-
(2002)
Curr Biol
, vol.12
, pp. 938-943
-
-
Pennekamp, P.1
Karcher, C.2
Fischer, A.3
-
12
-
-
28844460656
-
Cilia and centrosomes: A unifying pathogenic concept for cystic kidney disease?
-
Hildebrandt F, Otto E. Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease?. Nat Rev Genet 2005; 6: 928-940
-
(2005)
Nat Rev Genet
, vol.6
, pp. 928-940
-
-
Hildebrandt, F.1
Otto, E.2
-
13
-
-
84870448608
-
Cystic kidney diseases: Many ways to form a cyst
-
Loftus H, Ong AC. Cystic kidney diseases: many ways to form a cyst. Pediatr Nephrol 2013; 28: 33-49
-
(2013)
Pediatr Nephrol
, vol.28
, pp. 33-49
-
-
Loftus, H.1
Ong, A.C.2
-
14
-
-
36849037019
-
A critical developmental switch defines the kinetics of kidney cyst formation after loss of Pkd1
-
Piontek K, Menezes LF, Garcia-Gonzalez MA et al. A critical developmental switch defines the kinetics of kidney cyst formation after loss of Pkd1. Nat Med 2007; 13: 1490-1495
-
(2007)
Nat Med
, vol.13
, pp. 1490-1495
-
-
Piontek, K.1
Menezes, L.F.2
Garcia-Gonzalez, M.A.3
-
15
-
-
34548490748
-
Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney disease
-
Davenport JR, Watts AJ, Roper VC et al. Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney disease. Curr Biol : CB 2007; 17: 1586-1594
-
(2007)
Curr Biol : CB
, vol.17
, pp. 1586-1594
-
-
Davenport, J.R.1
Watts, A.J.2
Roper, V.C.3
-
16
-
-
20944435539
-
Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch betweenWnt signaling pathways
-
Simons M, Gloy J, Ganner A et al. Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch betweenWnt signaling pathways. Nat Genet 2005; 37: 537-543
-
(2005)
Nat Genet
, vol.37
, pp. 537-543
-
-
Simons, M.1
Gloy, J.2
Ganner, A.3
-
17
-
-
84866360631
-
Dishevelled stabilization by the ciliopathy protein Rpgrip1 l is essential for planar cell polarity
-
Mahuzier A, Gaude HM, Grampa V et al. Dishevelled stabilization by the ciliopathy protein Rpgrip1 l is essential for planar cell polarity. J Cell Biol 2012; 198: 927-940
-
(2012)
J Cell Biol
, vol.198
, pp. 927-940
-
-
Mahuzier, A.1
Gaude, H.M.2
Grampa, V.3
-
18
-
-
34250758641
-
HEF1-dependent Aurora A activation induces disassembly of the primary cilium
-
Pugacheva EN, Jablonski SA, Hartman TR et al. HEF1-dependent Aurora A activation induces disassembly of the primary cilium. Cell 2007; 129: 1351-1363
-
(2007)
Cell
, vol.129
, pp. 1351-1363
-
-
Pugacheva, E.N.1
Jablonski, S.A.2
Hartman, T.R.3
-
19
-
-
80051733318
-
Cilia and cell cycle re-entry: More than a coincidence
-
Kim S, Tsiokas L. Cilia and cell cycle re-entry: more than a coincidence. Cell Cycle 2011; 10: 2683-2690
-
(2011)
Cell Cycle
, vol.10
, pp. 2683-2690
-
-
Kim, S.1
Tsiokas, L.2
-
20
-
-
3042618920
-
Renal cysts of inv/inv mice resemble early infantile nephronophthisis
-
Phillips CL, Miller KJ, Filson AJ et al. Renal cysts of inv/inv mice resemble early infantile nephronophthisis. J Am Soc Nephrol 2004; 15: 1744-1755
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 1744-1755
-
-
Phillips, C.L.1
Miller, K.J.2
Filson, A.J.3
-
21
-
-
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. Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia. Cytoskeleton 2010; 67: 112-119
-
(2010)
Cytoskeleton
, vol.67
, pp. 112-119
-
-
Shiba, D.1
Manning, D.K.2
Koga, H.3
-
22
-
-
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. 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 2002; 11: 3345-3350
-
(2002)
Hum Mol Genet
, vol.11
, pp. 3345-3350
-
-
Morgan, D.1
Eley, L.2
Sayer, J.3
-
23
-
-
0036732917
-
Inversin forms a complex with catenins and N-cadherin in polarized epithelial cells
-
Nurnberger J, Bacallao RL, Phillips CL. Inversin forms a complex with catenins and N-cadherin in polarized epithelial cells. Mol Biol Cell 2002; 13: 3096-3106
-
(2002)
Mol Biol Cell
, vol.13
, pp. 3096-3106
-
-
Nurnberger, J.1
Bacallao, R.L.2
Phillips, C.L.3
-
24
-
-
79959410384
-
Aurora A kinase activity influences calcium signaling in kidney cells
-
Plotnikova OV, Pugacheva EN, Golemis EA. Aurora A kinase activity influences calcium signaling in kidney cells. J Cell Biol 2011; 193: 1021-1032
-
(2011)
J Cell Biol
, vol.193
, pp. 1021-1032
-
-
Plotnikova, O.V.1
Pugacheva, E.N.2
Golemis, E.A.3
-
25
-
-
84877056647
-
Hyperphosphorylation of polycystin-2 at a critical residue in disease reveals an essential role for polycystin-1-regulated dephosphorylation
-
Streets AJ, Wessely O, Peters DJ et al. Hyperphosphorylation of polycystin-2 at a critical residue in disease reveals an essential role for polycystin-1-regulated dephosphorylation. Hum Mol Genet 2013; 22: 1924-1939
-
(2013)
Hum Mol Genet
, vol.22
, pp. 1924-1939
-
-
Streets, A.J.1
Wessely, O.2
Peters, D.J.3
-
26
-
-
41549092173
-
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia
-
Bergmann C, Fliegauf M, Bruchle NO et al. Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. Am J Hum Genet 2008; 82: 959-970
-
(2008)
Am J Hum Genet
, vol.82
, pp. 959-970
-
-
Bergmann, C.1
Fliegauf, M.2
Bruchle, N.O.3
-
27
-
-
33749235323
-
Development of polycystic kidney disease in juvenile cystic kidney mice: Insights into pathogenesis, ciliary abnormalities, and common features with human disease
-
Smith LA, Bukanov NO, Husson H et al. Development of polycystic kidney disease in juvenile cystic kidney mice: insights into pathogenesis, ciliary abnormalities, and common features with human disease. J Am Soc Nephrol 2006; 17: 2821-2831
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 2821-2831
-
-
Smith, L.A.1
Bukanov, N.O.2
Husson, H.3
-
28
-
-
84868613964
-
Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity
-
Hopp K, Ward CJ, Hommerding CJ et al. Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity. J Clin Invest 2012; 122: 4257-4273
-
(2012)
J Clin Invest
, vol.122
, pp. 4257-4273
-
-
Hopp, K.1
Ward, C.J.2
Hommerding, C.J.3
-
29
-
-
70349918229
-
Renal primary cilia lengthen after acute tubular necrosis
-
Verghese E, Ricardo SD, Weidenfeld R et al. Renal primary cilia lengthen after acute tubular necrosis. J Am Soc Nephrol 2009; 20: 2147-2153
-
(2009)
J Am Soc Nephrol
, vol.20
, pp. 2147-2153
-
-
Verghese, E.1
Ricardo, S.D.2
Weidenfeld, R.3
-
30
-
-
72049098241
-
Pkd1 haploinsufficiency increases renal damage and induces microcyst formation following ischemia/reperfusion
-
Bastos AP, Piontek K, Silva AM et al. Pkd1 haploinsufficiency increases renal damage and induces microcyst formation following ischemia/reperfusion. J Am0: 2389-2402
-
J Am0
, pp. 2389-2402
-
-
Bastos, A.P.1
Piontek, K.2
Silva, A.M.3
-
31
-
-
73549122173
-
Pkd2 dosage influences cellular repair responses following ischemia-reperfusion injury
-
Prasad S, McDaid JP, Tam FW et al. Pkd2 dosage influences cellular repair responses following ischemia-reperfusion injury. Am J Pathol 2009; 175: 1493-1503
-
(2009)
Am J Pathol
, vol.175
, pp. 1493-1503
-
-
Prasad, S.1
McDaid, J.P.2
Tam, F.W.3
|