-
1
-
-
0017162819
-
A human syndrome caused by immotile cilia
-
Afzelius BA (1976) A human syndrome caused by immotile cilia. Science 193, 317-19.
-
(1976)
Science
, vol.193
, pp. 317-319
-
-
Afzelius, B.A.1
-
2
-
-
0033598394
-
A polycystic kidney-disease gene homologue required for male mating behaviour in C. elegans
-
Barr MM, Sternberg PW (1999) A polycystic kidney-disease gene homologue required for male mating behaviour in C. elegans. Nature 401, 386-9.
-
(1999)
Nature
, vol.401
, pp. 386-389
-
-
Barr, M.M.1
Sternberg, P.W.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, Nguyen CQ, Hall DH, Sternberg PW (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
Nguyen, C.Q.4
Hall, D.H.5
Sternberg, P.W.6
-
4
-
-
0036678117
-
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia
-
Bartoloni L, Blouin JL, Pan Y et al. (2002) Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia. Proc Natl Acad Sci USA 99, 10 282-6.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
-
-
Bartoloni, L.1
Blouin, J.L.2
Pan, Y.3
-
5
-
-
0035834136
-
Cardiovascular, skeletal, and renal defects in mice with a targeted disruption of the Pkd 1 gene
-
Boulter C, Mulroy S, Webb S, Fleming S, Brindle K, Sandford R (2001) Cardiovascular, skeletal, and renal defects in mice with a targeted disruption of the Pkd 1 gene. Proc Natl Acad Sci USA 98, 12 174-9.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
-
-
Boulter, C.1
Mulroy, S.2
Webb, S.3
Fleming, S.4
Brindle, K.5
Sandford, R.6
-
6
-
-
0035068576
-
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)
-
Guichard C, Harricane MC, Lafitte JJ et al. (2001) Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome). Am J Hum Genet 68, 1030-5.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1030-1035
-
-
Guichard, C.1
Harricane, M.C.2
Lafitte, J.J.3
-
7
-
-
0034700483
-
Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents
-
Hanaoka K, Qian F, Boletta A et al. (2000) Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents. Nature 408, 990-4.
-
(2000)
Nature
, vol.408
, pp. 990-994
-
-
Hanaoka, K.1
Qian, F.2
Boletta, A.3
-
8
-
-
0036256982
-
Molecular basis of polycystic kidney disease: PKD1, PKD2 and PKHD1
-
Harris PC (2002) Molecular basis of polycystic kidney disease: PKD1, PKD2 and PKHD1. Curr Opin Nephrol Hypertens 11, 309-14.
-
(2002)
Curr. Opin. Nephrol. Hypertens.
, vol.11
, pp. 309-314
-
-
Harris, P.C.1
-
9
-
-
0034987372
-
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 (2001) 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. Development 128, 1493-505.
-
(2001)
Development
, vol.128
, pp. 1493-1505
-
-
Haycraft, C.J.1
Swoboda, P.2
Taulman, P.D.3
Thomas, J.H.4
Yoder, B.K.5
-
10
-
-
0030868540
-
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1
-
Hildebrandt F, Otto E, Rensing C et al. (1997) A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1. Nat Genet 17, 149-53.
-
(1997)
Nat. Genet.
, vol.17
, pp. 149-153
-
-
Hildebrandt, F.1
Otto, E.2
Rensing, C.3
-
11
-
-
0036177603
-
Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease
-
Hou X, Mrug M, Yoder BK et al. (2002) Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. J Clin Invest 109, 533-40.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 533-540
-
-
Hou, X.1
Mrug, M.2
Yoder, B.K.3
-
12
-
-
77957211015
-
Visceral inversion and associated anomalies in the mouse
-
Hummel K, Chapman DB (1959) Visceral inversion and associated anomalies in the mouse. J Hered 50, 9-13.
-
(1959)
J. Hered.
, vol.50
, pp. 9-13
-
-
Hummel, K.1
Chapman, D.B.2
-
13
-
-
0037087624
-
Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus
-
Ibanez-Tallon I, Gorokhova S, Heintz N (2002) Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus. Hum Mol Genet 11, 715-21.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 715-721
-
-
Ibanez-Tallon, I.1
Gorokhova, S.2
Heintz, N.3
-
14
-
-
1642564276
-
To beat or not to beat: Roles of cilia in development and disease
-
Ibanez-Tallon I, Heintz N, Omran H (2003) To beat or not to beat: Roles of cilia in development and disease. Hum Mol Genet 12, R27-35.
-
(2003)
Hum. Mol. Genet.
, vol.12
-
-
Ibanez-Tallon, I.1
Heintz, N.2
Omran, H.3
-
15
-
-
0000483282
-
Zur Pathogenese der Bronchiektasien. I. Mitteilung Bronchiektasien bei Situs viscerum inversus
-
Kartagener M (1933) Zur Pathogenese der Bronchiektasien. I. Mitteilung Bronchiektasien bei Situs viscerum inversus. Beitr Klin Tuberk 83, 498-501.
-
(1933)
Beitr. Klin. Tuberk.
, vol.83
, pp. 498-501
-
-
Kartagener, M.1
-
16
-
-
0017050268
-
Random determination of a developmental process: Reversal of normal visceral asymmetry in the mouse
-
Layton WM Jr (1976) Random determination of a developmental process: Reversal of normal visceral asymmetry in the mouse. J Hered 67, 336-8.
-
(1976)
J. Hered.
, vol.67
, pp. 336-338
-
-
Layton Jr., W.M.1
-
17
-
-
0029089617
-
A molecular pathway determining left-right asymmetry in chick embryogenesis
-
Levin M, Johnson RL, Stern CD, Kuehn M, Tabin C (1995) A molecular pathway determining left-right asymmetry in chick embryogenesis. Cell 82, 803-14.
-
(1995)
Cell
, vol.82
, pp. 803-814
-
-
Levin, M.1
Johnson, R.L.2
Stern, C.D.3
Kuehn, M.4
Tabin, C.5
-
18
-
-
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
-
19
-
-
0029913091
-
Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus
-
Lowe LA, Supp DM, Sampath K et al. (1996) Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus. Nature 381, 158-61.
-
(1996)
Nature
, vol.381
, pp. 158-161
-
-
Lowe, L.A.1
Supp, D.M.2
Sampath, K.3
-
20
-
-
0031252295
-
Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation
-
Lu W, Peissel B, Babakhanlou H et al. (1997) Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation. Nat Genet 17, 179-81.
-
(1997)
Nat. Genet.
, vol.17
, pp. 179-181
-
-
Lu, W.1
Peissel, B.2
Babakhanlou, H.3
-
21
-
-
0033609103
-
Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II
-
Marszalek JR, Ruiz-Lozano P, Roberts E, Chien KR, Goldstein LS (1999) Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II. Proc Natl Acad Sci USA 96, 5043-8.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5043-5048
-
-
Marszalek, J.R.1
Ruiz-Lozano, P.2
Roberts, E.3
Chien, K.R.4
Goldstein, L.S.5
-
22
-
-
0029932564
-
Left-right asymmetric expression of the TGF beta-family member lefty in mouse embryos
-
Meno C, Saijoh Y, Fujii H et al. (1996) Left-right asymmetric expression of the TGF beta-family member lefty in mouse embryos. Nature 381, 151-5.
-
(1996)
Nature
, vol.381
, pp. 151-155
-
-
Meno, C.1
Saijoh, Y.2
Fujii, H.3
-
23
-
-
0033575364
-
Differences in left-right axis pathways in mouse and chick: Functions of FGF8 and SHH
-
Meyers EN, Martin GR (1999) Differences in left-right axis pathways in mouse and chick: Functions of FGF8 and SHH. Science 285, 403-6.
-
(1999)
Science
, vol.285
, pp. 403-406
-
-
Meyers, E.N.1
Martin, G.R.2
-
24
-
-
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
-
25
-
-
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
-
26
-
-
18644368159
-
The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin
-
Mollet G, Salomon R, Gribouval O et al. (2002) The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin. Nat Genet 32, 300-5.
-
(2002)
Nat. Genet.
, vol.32
, pp. 300-305
-
-
Mollet, G.1
Salomon, R.2
Gribouval, O.3
-
27
-
-
0036556271
-
The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin
-
Morgan D, Goodship J, Essner JJ et al. (2002) The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin. Hum Genet 110, 377-84.
-
(2002)
Hum. Genet.
, vol.110
, pp. 377-384
-
-
Morgan, D.1
Goodship, J.2
Essner, J.J.3
-
28
-
-
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
-
29
-
-
0034042763
-
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 (2000) The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination. Development 127, 2347-55.
-
(2000)
Development
, vol.127
, pp. 2347-2355
-
-
Murcia, N.S.1
Richards, W.G.2
Yoder, B.K.3
Mucenski, M.L.4
Dunlap, J.R.5
Woychik, R.P.6
-
30
-
-
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
-
31
-
-
0032428685
-
Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein
-
Nonaka S, Tanaka Y, Okada Y et al. (1998) Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein. Cell 95, 829-37.
-
(1998)
Cell
, vol.95
, pp. 829-837
-
-
Nonaka, S.1
Tanaka, Y.2
Okada, Y.3
-
32
-
-
0037019287
-
Determination of left-right patterning of the mouse embryo by artificial nodal flow
-
Nonaka S, Shiratori H, Saijoh Y, Hamada H (2002) Determination of left-right patterning of the mouse embryo by artificial nodal flow. Nature 418, 96-9.
-
(2002)
Nature
, vol.418
, pp. 96-99
-
-
Nonaka, S.1
Shiratori, H.2
Saijoh, Y.3
Hamada, H.4
-
33
-
-
0033212985
-
Abnormal nodal flow precedes situs inversus in iv and inv mice
-
Okada Y, Nonaka S, Tanaka Y, Saijoh Y, Hamada H, Hirokawa N (1999) Abnormal nodal flow precedes situs inversus in iv and inv mice. Mol Cell 4, 459-68.
-
(1999)
Mol. Cell
, vol.4
, pp. 459-468
-
-
Okada, Y.1
Nonaka, S.2
Tanaka, Y.3
Saijoh, Y.4
Hamada, H.5
Hirokawa, N.6
-
34
-
-
0036479029
-
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry
-
Olbrich H, Haffner K, Kispert A et al. (2002) Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. Nat Genet 30, 143-4.
-
(2002)
Nat. Genet.
, vol.30
, pp. 143-144
-
-
Olbrich, H.1
Haffner, K.2
Kispert, A.3
-
35
-
-
0042093746
-
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapetoretinal degeneration and hepatic fibrosis
-
Olbrich H, Fliegauf M, Hoefele J et al. (2003) Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapetoretinal degeneration and hepatic fibrosis. Nat Genet 34, 455-9.
-
(2003)
Nat. Genet.
, vol.34
, pp. 455-459
-
-
Olbrich, H.1
Fliegauf, M.2
Hoefele, J.3
-
36
-
-
18344366124
-
PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats
-
Onuchic LF, Furu L, Nagasawa Y et al. (2002) PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. Am J Hum Genet 70, 1305-17.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 1305-1317
-
-
Onuchic, L.F.1
Furu, L.2
Nagasawa, Y.3
-
37
-
-
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
-
38
-
-
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
-
39
-
-
0037019017
-
Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease
-
Pazour GJ, San Agustin JT, Follit JA, Rosenbaum JL, Witman GB (2002) Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease. Curr Biol 12, R378-80.
-
(2002)
Curr. Biol.
, vol.12
-
-
Pazour, G.J.1
San Agustin, J.T.2
Follit, J.A.3
Rosenbaum, J.L.4
Witman, G.B.5
-
40
-
-
0033365058
-
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia
-
Pennarun G, Escudier E, Chapelin C et al. (1999) Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. Am J Hum Genet 65, 1508-19.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1508-1519
-
-
Pennarun, G.1
Escudier, E.2
Chapelin, C.3
-
41
-
-
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
-
42
-
-
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
-
43
-
-
0030909957
-
PKD1 interacts with PKD2 through a probable coiled-coil domain
-
Qian F, Germino FJ, Cai Y, Zhang X, Somlo S, Germino GG (1997) PKD1 interacts with PKD2 through a probable coiled-coil domain. Nat Genet 16, 179-83.
-
(1997)
Nat. Genet.
, vol.16
, pp. 179-183
-
-
Qian, F.1
Germino, F.J.2
Cai, Y.3
Zhang, X.4
Somlo, S.5
Germino, G.G.6
-
44
-
-
0036488027
-
Identification, genomic organization, chromosomal mapping and mutation analysis of the human INV gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresia
-
Schön P, Tsuchiya K, Lenoir D et al. (2002) Identification, genomic organization, chromosomal mapping and mutation analysis of the human INV gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresia. Hum Genet 110, 157-65.
-
(2002)
Hum. Genet.
, vol.110
, pp. 157-165
-
-
Schön, P.1
Tsuchiya, K.2
Lenoir, D.3
-
45
-
-
0030656618
-
Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice
-
Supp DM, Witte DP, Potter SS, Brueckner M (1997) Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice. Nature 389, 963-6.
-
(1997)
Nature
, vol.389
, pp. 963-966
-
-
Supp, D.M.1
Witte, D.P.2
Potter, S.S.3
Brueckner, M.4
-
46
-
-
0033577894
-
Left-right asymmetry and kinesin superfamily protein KIF3A: New insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis
-
Takeda S, Yonekawa Y, Tanaka Y, Okada Y, Nonaka S, Hirokawa N (1999) Left-right asymmetry and kinesin superfamily protein KIF3A: New insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis. J Cell Biol 145, 825-36.
-
(1999)
J. Cell Biol.
, vol.145
, pp. 825-836
-
-
Takeda, S.1
Yonekawa, Y.2
Tanaka, Y.3
Okada, Y.4
Nonaka, S.5
Hirokawa, N.6
-
47
-
-
0028278058
-
The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16
-
The European Polycystic Kidney Disease Consortium
-
The European Polycystic Kidney Disease Consortium (1994) The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16, Cell 77, 881-94.
-
(1994)
Cell
, vol.77
, pp. 881-894
-
-
-
48
-
-
0036509712
-
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein
-
Ward CJ, Hogan MC, Rossetti S et al. (2002) The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein. Nat Genet 30, 259-69.
-
(2002)
Nat. Genet.
, vol.30
, pp. 259-269
-
-
Ward, C.J.1
Hogan, M.C.2
Rossetti, S.3
-
49
-
-
0037959910
-
The left-right determinant Inversin is a component of node monocilia and other 9 + 0 cilia
-
Watanabe D, Saijoh Y, Nonaka S et al. (2003) The left-right determinant Inversin is a component of node monocilia and other 9 + 0 cilia. Development 130, 1725-34.
-
(2003)
Development
, vol.130
, pp. 1725-1734
-
-
Watanabe, D.1
Saijoh, Y.2
Nonaka, S.3
-
50
-
-
0032540226
-
Somatic inactivation of Pkd2 results in polycystic kidney disease
-
Wu G, D'Agati V, Cai Y et al. (1998) Somatic inactivation of Pkd2 results in polycystic kidney disease. Cell 93, 177-88.
-
(1998)
Cell
, vol.93
, pp. 177-188
-
-
Wu, G.1
D'Agati, V.2
Cai, Y.3
-
51
-
-
0035172027
-
Calmodulin binds to inv protein: Implication for the regulation of inv function
-
Yasuhiko Y, Imai F, Ookubo K, Takakuwa Y, Shiokawa K, Yokoyama T (2001) Calmodulin binds to inv protein: Implication for the regulation of inv function. Dev Growth Differ 43, 671-81.
-
(2001)
Dev. Growth Differ.
, vol.43
, pp. 671-681
-
-
Yasuhiko, Y.1
Imai, F.2
Ookubo, K.3
Takakuwa, Y.4
Shiokawa, K.5
Yokoyama, T.6
-
52
-
-
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 (2002a) 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
-
53
-
-
0036086844
-
Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium
-
Yoder BK, Tousson A, Millican L et al. (2002b) Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium. Am J Physiol Renal Physiol 282, F541-52.
-
(2002)
Am. J. Physiol. Renal. Physiol.
, vol.282
-
-
Yoder, B.K.1
Tousson, A.2
Millican, L.3
-
54
-
-
0033520394
-
Antagonistic signaling by Caronte, a novel Cerberus-related gene, establishes left-right asymmetric gene expression
-
Yokouchi Y, Vogan KJ, Pearse 2nd RV, Tabin CJ (1999) Antagonistic signaling by Caronte, a novel Cerberus-related gene, establishes left-right asymmetric gene expression. Cell 98, 573-83.
-
(1999)
Cell
, vol.98
, pp. 573-583
-
-
Yokouchi, Y.1
Vogan, K.J.2
Pearse II, R.V.3
Tabin, C.J.4
-
55
-
-
0027158027
-
Reversal of left-right asymmetry: A situs inversus mutation
-
Yokoyama T, Copeland NG, Jenkins NA, Montgomery CA, Elder FF, Overbeek PA (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
Montgomery, C.A.4
Elder, F.F.5
Overbeek, P.A.6
-
56
-
-
0032493866
-
Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry
-
Yoshioka H, Meno C, Koshiba K et al. (1998) Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry. Cell 94, 299-305.
-
(1998)
Cell
, vol.94
, pp. 299-305
-
-
Yoshioka, H.1
Meno, C.2
Koshiba, K.3
|