-
1
-
-
0017162819
-
A human syndrome caused by immotile cilia
-
Afzelius, B.A. 1976. A human syndrome caused by immotile cilia. Science 193: 317-319.
-
(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, M.M. and Sternberg, P.W. 1999. A polycystic kidney-disease gene homologue required for male mating behaviour in C. elegans. Nature 401: 386-389.
-
(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, M.M., DeModena, J., Braun, D., Nguyen, C.Q., Hall, D.H., and Steinberg, P.W. 2001. The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway. Curr. Biol. 11: 1341-1346.
-
(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
Steinberg, 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., Bloiun, J.L., Pan, Y., Gehrig, C., Maiti, A.K., Scamuffa, N., Rossier, C., Jorissen, M., Armengot, M., Meeks, M., 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. 99:10282-10286.
-
(2002)
Proc. Natl. Acad. Sci.
, vol.99
, pp. 10282-10286
-
-
Bartoloni, L.1
Bloiun, J.L.2
Pan, Y.3
Gehrig, C.4
Maiti, A.K.5
Scamuffa, N.6
Rossier, C.7
Jorissen, M.8
Armengot, M.9
Meeks, M.10
-
5
-
-
0029873599
-
Cell proliferation in mammalian gastrulation: The ventral node and notochord are relatively quiescent
-
Bellomo, D., Lander, A., Harragan, I., and Brown, N.A. 1996. Cell proliferation in mammalian gastrulation: The ventral node and notochord are relatively quiescent. Dev. Dyn. 205: 471-485.
-
(1996)
Dev. Dyn.
, vol.205
, pp. 471-485
-
-
Bellomo, D.1
Lander, A.2
Harragan, I.3
Brown, N.A.4
-
6
-
-
0037106188
-
Nodal activity in the node governs left-right asymmetry
-
Brennan, J., Norris, D.P., and Robertson, E.J. 2002. Nodal activity in the node governs left-right asymmetry. Genes & Dev. 16: 2339-2344.
-
(2002)
Genes & Dev.
, vol.16
, pp. 2339-2344
-
-
Brennan, J.1
Norris, D.P.2
Robertson, E.J.3
-
7
-
-
0025364567
-
The development of handedness in left/right asymmetry
-
Brown, N.A. and Wolpert, L. 1990. The development of handedness in left/right asymmetry. Development 109: 1-9.
-
(1990)
Development
, vol.109
, pp. 1-9
-
-
Brown, N.A.1
Wolpert, L.2
-
8
-
-
0035879553
-
Cilia propel the embryo in the right direction
-
Brueckner, M. 2001. Cilia propel the embryo in the right direction. Am. J. Med. Genet. 101: 339-344.
-
(2001)
Am. J. Med. Genet.
, vol.101
, pp. 339-344
-
-
Brueckner, M.1
-
9
-
-
0034175652
-
Conserved and divergent mechanisms in left-right axis formation
-
Burdine, R.D. and Schier, A.F. 2000. Conserved and divergent mechanisms in left-right axis formation. Genes & Dev. 14: 763-776.
-
(2000)
Genes & Dev.
, vol.14
, pp. 763-776
-
-
Burdine, R.D.1
Schier, A.F.2
-
10
-
-
0034737302
-
Mechanisms of left-right determination in vertebrates
-
Capdevila, J., Vogan, K.J., Tabin, C.J., and Izpisúa Belmonte, J.C. 2000. Mechanisms of left-right determination in vertebrates. Cell 101: 9-21.
-
(2000)
Cell
, vol.101
, pp. 9-21
-
-
Capdevila, J.1
Vogan, K.J.2
Tabin, C.J.3
Izpisúa Belmonte, J.C.4
-
11
-
-
0029993646
-
Relationship between asymmetric nodal expression and the direction of embryonic turning
-
Collignon, J., Varlet, I., and Robertson, E.J. 1996. Relationship between asymmetric nodal expression and the direction of embryonic turning. Nature 381: 155-158.
-
(1996)
Nature
, vol.381
, pp. 155-158
-
-
Collignon, J.1
Varlet, I.2
Robertson, E.J.3
-
12
-
-
0037019298
-
Conserved function for embryonic nodal cilia
-
Essner, J.J., Vogan, K.J., Wagner, M.K., Tabin, C.J., Yost, H.J., and Brueckner, M. 2002. Conserved function for embryonic nodal cilia. Nature 418: 37-38.
-
(2002)
Nature
, vol.418
, pp. 37-38
-
-
Essner, J.J.1
Vogan, K.J.2
Wagner, M.K.3
Tabin, C.J.4
Yost, H.J.5
Brueckner, M.6
-
13
-
-
0035068576
-
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartegener syndrome)
-
Guichard, C., Harricane, M.C., Lafitte, J.J., Godard, P., Zaegel, M., Tack, V., Lalau, G., and Bouvagnet, P. 2001. Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartegener syndrome). Am. J. Hum. Genet. 68: 1030-1035.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1030-1035
-
-
Guichard, C.1
Harricane, M.C.2
Lafitte, J.J.3
Godard, P.4
Zaegel, M.5
Tack, V.6
Lalau, G.7
Bouvagnet, P.8
-
14
-
-
0034700483
-
Co-assembly of polycystin-1 and -2 produced unique cation-permeable currents
-
Hanaoka, K., Qian, F., Boletta, A., Bhunia, A.K., Piontek, K., Tsiokas, L., Sukhatme, V.P., Guggino, W.B., and Germino, G.G. 2000. Co-assembly of polycystin-1 and -2 produced unique cation-permeable currents. Nature 408: 990-994.
-
(2000)
Nature
, vol.408
, pp. 990-994
-
-
Hanaoka, K.1
Qian, F.2
Boletta, A.3
Bhunia, A.K.4
Piontek, K.5
Tsiokas, L.6
Sukhatme, V.P.7
Guggino, W.B.8
Germino, G.G.9
-
15
-
-
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, C.J., Swoboda, P., Taulman, P.D., Thomas, J.H., and Yoder, B.K. 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: 1493-1505.
-
(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
-
16
-
-
0036177603
-
Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease
-
Hou, X., Mrug, M., Yoder, B.K., Lefkowitz, E.J., Kremmidiotis, G., D'Eustachio, P., Beier, D.R., and Guay-Woodford, L.M. 2002. Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. J. Clin. Invest. 109: 553-540.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 553-540
-
-
Hou, X.1
Mrug, M.2
Yoder, B.K.3
Lefkowitz, E.J.4
Kremmidiotis, G.5
D'Eustachio, P.6
Beier, D.R.7
Guay-Woodford, L.M.8
-
17
-
-
0036707893
-
Genetics and pathogenesis of polycystic kidney disease
-
Igarashi, P. and Somlo, S. 2002. Genetics and pathogenesis of polycystic kidney disease. J. Am. Soc. Nephrol. 13: 2384-2398.
-
(2002)
J. Am. Soc. Nephrol.
, vol.13
, pp. 2384-2398
-
-
Igarashi, P.1
Somlo, S.2
-
18
-
-
0036122434
-
Polycystin-2 is an intracellular calcium release channel
-
Koulen, P., Cai, Y., Geng, L., Maeda, Y., Nishimura, S., Witzgall, R., Ehrlich, B.E., and Somlo, S. 2002. Polycystin-2 is an intracellular calcium release channel. Nat. Cell Biol. 4: 191-197.
-
(2002)
Nat. Cell Biol.
, vol.4
, pp. 191-197
-
-
Koulen, P.1
Cai, Y.2
Geng, L.3
Maeda, Y.4
Nishimura, S.5
Witzgall, R.6
Ehrlich, B.E.7
Somlo, S.8
-
19
-
-
0032212639
-
Gap junctions are involved in the early generation of left-right asymmetry
-
Levin, M. and Mercola, M. 1998. Gap junctions are involved in the early generation of left-right asymmetry. Dev. Biol. 203:90-105.
-
(1998)
Dev. Biol.
, vol.203
, pp. 90-105
-
-
Levin, M.1
Mercola, M.2
-
20
-
-
0032707182
-
Gap junction-mediated transfer of left-right patterning signals in the early chick blastoderm is upstream of Shh asymmetry in the node
-
-. 1999. Gap junction-mediated transfer of left-right patterning signals in the early chick blastoderm is upstream of Shh asymmetry in the node. Development 126: 4703-4714.
-
(1999)
Development
, vol.126
, pp. 4703-4714
-
-
-
21
-
-
0029089617
-
A molecular pathway determining left-right asymmetry in chick embryogenesis
-
Levin, M., Johnson, R.L., Stern, C.D., Kuehn, M., and Tabin, C. 1995. A molecular pathway determining left-right asymmetry in chick embryogenesis. Cell 82: 803-814.
-
(1995)
Cell
, vol.82
, pp. 803-814
-
-
Levin, M.1
Johnson, R.L.2
Stern, C.D.3
Kuehn, M.4
Tabin, C.5
-
23
-
-
0029913091
-
Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus
-
Lowe, L.A., Supp, D.M., Sampath, K., Yokoyama, T., Wright, C.V., Potter, S.S., Overbeek, P., and Kuehn, M.R. 1996. Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus. Nature 381: 158-161.
-
(1996)
Nature
, vol.381
, pp. 158-161
-
-
Lowe, L.A.1
Supp, D.M.2
Sampath, K.3
Yokoyama, T.4
Wright, C.V.5
Potter, S.S.6
Overbeek, P.7
Kuehn, M.R.8
-
24
-
-
0033609103
-
Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II
-
Marszalek, J.R., Ruiz-Lozano, P., Roberts, E., Chien, K.R., and Goldstein, L.S. 1999. Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II. Proc. Natl. Acad. Sci. 96: 5043-5048.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 5043-5048
-
-
Marszalek, J.R.1
Ruiz-Lozano, P.2
Roberts, E.3
Chien, K.R.4
Goldstein, L.S.5
-
25
-
-
0029932564
-
Left-right asymmetric gene expression of the TGFβ-family member lefty in mouse embryos
-
Meno, C., Saijoh, Y., Fujii, H., Ikeda, M., Yokoyama, T., Yokoyama, M., Toyoda, Y., and Hamada, H. 1996. Left-right asymmetric gene expression of the TGFβ-family member lefty in mouse embryos. Nature 381: 151-155.
-
(1996)
Nature
, vol.381
, pp. 151-155
-
-
Meno, C.1
Saijoh, Y.2
Fujii, H.3
Ikeda, M.4
Yokoyama, T.5
Yokoyama, M.6
Toyoda, Y.7
Hamada, H.8
-
26
-
-
0033575364
-
Differences in left-right axis pathways in mouse and chick: Functions of FGF8 and SHH
-
Meyers, E.N. and Martin, G.R. 1999. Differences in left-right axis pathways in mouse and chick: Functions of FGF8 and SHH. Science 285: 403-406.
-
(1999)
Science
, vol.285
, pp. 403-406
-
-
Meyers, E.N.1
Martin, G.R.2
-
27
-
-
0032504963
-
Cloning of inv, a gene that controls left/right asymmetry and kidney development
-
Mochizuki, T., Saijoh, Y., Tsuchiya, K., Shirayoshi, Y., Takai, S., Taya, C., Yonekawa, H., Yamada, K., Nihei, H., Nakatsuji, N., et al. 1998. Cloning of inv, a gene that controls left/right asymmetry and kidney development. Nature 395: 177-181
-
(1998)
Nature
, vol.395
, pp. 177-181
-
-
Mochizuki, T.1
Saijoh, Y.2
Tsuchiya, K.3
Shirayoshi, Y.4
Takai, S.5
Taya, C.6
Yonekawa, H.7
Yamada, K.8
Nihei, H.9
Nakatsuji, N.10
-
28
-
-
17344366038
-
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse
-
Morgan, D., Turnpenny, L., Goodship, J., Dai, W., Majumder, K., Matthews, L., Gardner, A., Schuster, G., Vien, L., Harrison, W., et al. 1998. Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse. Nat. Genet. 20: 149-156.
-
(1998)
Nat. Genet.
, vol.20
, pp. 149-156
-
-
Morgan, D.1
Turnpenny, L.2
Goodship, J.3
Dai, W.4
Majumder, K.5
Matthews, L.6
Gardner, A.7
Schuster, G.8
Vien, L.9
Harrison, W.10
-
29
-
-
0036556271
-
The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin
-
Morgan, D., Goodship, J., Essner, J.J., Vogan, K.J., Turnpenny, L., Yost, H.J., Tabin, C.J., and Strachan, T. 2002. The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin. Hum. Genet. 110: 377-384.
-
(2002)
Hum. Genet.
, vol.110
, pp. 377-384
-
-
Morgan, D.1
Goodship, J.2
Essner, J.J.3
Vogan, K.J.4
Turnpenny, L.5
Yost, H.J.6
Tabin, C.J.7
Strachan, T.8
-
30
-
-
0034042763
-
The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination
-
Murcia, N.S., Richards, W.G., Yoder, B.K., Mucenski, M.L., Dunlap, J.R., and Woychick, R.P. 2000. The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination. Development 127: 2347-2355.
-
(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
Woychick, R.P.6
-
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., Takeda, S., Harada, A., Kanai, Y., Kido, M.., and Hirokawa, N. 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: 829-837.
-
(1998)
Cell
, vol.95
, pp. 829-837
-
-
Nonaka, S.1
Tanaka, Y.2
Okada, Y.3
Takeda, S.4
Harada, A.5
Kanai, Y.6
Kido, M.7
Hirokawa, N.8
-
32
-
-
0037019287
-
Determination of left-right patterning of the mouse embryo by artificial nodal flow
-
Nonaka, S., Shiratori, H., Saijoh, Y., and Hamada, H. 2002. Determination of left-right patterning of the mouse embryo by artificial nodal flow. Nature 418: 96-99.,
-
(2002)
Nature
, vol.418
, pp. 96-99
-
-
Nonaka, S.1
Shiratori, H.2
Saijoh, Y.3
Hamada, H.4
-
33
-
-
0036479029
-
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry
-
Olbrich, H., Haffner, K., Kispert, A., Volkel, A., Volz, A., Sasmaz, G., Reinhardt, R., Hennig, S., Lehrach, H., Konietzko, N., et al. 2002. Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. Nat. Genet. 30: 143-144.
-
(2002)
Nat. Genet.
, vol.30
, pp. 143-144
-
-
Olbrich, H.1
Haffner, K.2
Kispert, A.3
Volkel, A.4
Volz, A.5
Sasmaz, G.6
Reinhardt, R.7
Hennig, S.8
Lehrach, H.9
Konietzko, N.10
-
34
-
-
0033212985
-
Abnormal nodal flow precedes situs inversus in iv and inv mice
-
Okada, Y., Nonaka, S., Tanaka, Y., Saijoh, Y., Hamada, H., and Hirokawa, N. 1999. Abnormal nodal flow precedes situs inversus in iv and inv mice. Mol. Cell 4: 459-468.
-
(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
-
35
-
-
0037019017
-
Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease
-
Pazour, G.J., San Agustin, J.T., Follit, J.A., Rosenbaum, J.L., and Witman, G.B. 2002. Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease. Curr. Biol. 12: R378-R380.
-
(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
-
36
-
-
0033365058
-
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardti dynein IC78 result in primary ciliary dyskinesia
-
Pennarun, G., Escudier, E., Chapelin, C., Bridoux, A.M., Cacheux, V., Roger, G., Clement, A., Goossens, M., Amselem, S., and Duriez, B. 1999. Loss-of-function mutations in a human gene related to Chlamydomonas reinhardti dynein IC78 result in primary ciliary dyskinesia. Am. J. Hum. Genet. 65:1508-1519.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1508-1519
-
-
Pennarun, G.1
Escudier, E.2
Chapelin, C.3
Bridoux, A.M.4
Cacheux, V.5
Roger, G.6
Clement, A.7
Goossens, M.8
Amselem, S.9
Duriez, B.10
-
37
-
-
0037018850
-
The ion channel polycystin-2 is required for left-right axis determination in mice
-
Pennekamp, P., Karcher, C., Fischer, A., Schweickert, A., Skryabin, B., Horst, J., Blum, M., and Dworniczak, B. 2002. The ion channel polycystin-2 is required for left-right axis determination in mice. Curr. Biol. 12:938-943.
-
(2002)
Curr. Biol.
, vol.12
, pp. 938-943
-
-
Pennekamp, P.1
Karcher, C.2
Fischer, A.3
Schweickert, A.4
Skryabin, B.5
Horst, J.6
Blum, M.7
Dworniczak, B.8
-
38
-
-
0035498717
-
Bending the MDCK primary cilium increases intracellular calcium
-
Praetorius, H.A. and Spring, K.R. 2001. Bending the MDCK primary cilium increases intracellular calcium. J. Membrane Biol. 184: 71-79.
-
(2001)
J. Membrane Biol.
, vol.184
, pp. 71-79
-
-
Praetorius, H.A.1
Spring, K.R.2
-
39
-
-
0030909957
-
PKD1 interacts with PKD2 through a probable coiled-coil domain
-
Qian, F., Germino, F.J., Cai, Y., Zhang, X., Somlo, S., and Germino, G.G. 1997. PKD1 interacts with PKD2 through a probable coiled-coil domain. Nat. Genet. 16: 179-183.
-
(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
-
40
-
-
0035916823
-
An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons
-
Qin, H., Rosenbaum, J.L., and Barr, M.M. 2001. An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons. Curr. Biol. 11: 457-461.
-
(2001)
Curr. Biol.
, vol.11
, pp. 457-461
-
-
Qin, H.1
Rosenbaum, J.L.2
Barr, M.M.3
-
41
-
-
0034050737
-
Regulation of left-right patterning in mice by growth/differentiation factor-1
-
Rankin, C.T., Bunton, T., Lawler, A.M., and Lee, S.-J. 2000. Regulation of left-right patterning in mice by growth/differentiation factor-1. Nat. Genet. 24: 262-265.
-
(2000)
Nat. Genet.
, vol.24
, pp. 262-265
-
-
Rankin, C.T.1
Bunton, T.2
Lawler, A.M.3
Lee, S.-J.4
-
42
-
-
0027985756
-
Morphogenesis of the murine node and notochordal plate
-
Sulik, K., Dehart, D.B., Inagaki, T., Carson, J.L., Vrablic, T., Gesteland, K., and Schoenwolf, G.C. 1994. Morphogenesis of the murine node and notochordal plate. Dev. Dyn. 201: 260-278.
-
(1994)
Dev. Dyn.
, vol.201
, pp. 260-278
-
-
Sulik, K.1
Dehart, D.B.2
Inagaki, T.3
Carson, J.L.4
Vrablic, T.5
Gesteland, K.6
Schoenwolf, G.C.7
-
43
-
-
0030656618
-
Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice
-
Supp, D.M., Witte, D.P., Potter, S.S., and Brueckner, M. 1997. Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice. Nature 389: 963-966.
-
(1997)
Nature
, vol.389
, pp. 963-966
-
-
Supp, D.M.1
Witte, D.P.2
Potter, S.S.3
Brueckner, M.4
-
44
-
-
0033377234
-
Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries
-
Supp, D.M., Brueckner, M., Kuehn, M.R., Witte, D.P., Lowe, L.A., McGrath, J., Corrales, J., and Potter, S.S. 1999. Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries. Development 126:5495-5504.
-
(1999)
Development
, vol.126
, pp. 5495-5504
-
-
Supp, D.M.1
Brueckner, M.2
Kuehn, M.R.3
Witte, D.P.4
Lowe, L.A.5
McGrath, J.6
Corrales, J.7
Potter, S.S.8
-
46
-
-
0033611462
-
A new spin on handed asymmetry
-
Vogan, K.J. and Tabin, C.J. 1999. A new spin on handed asymmetry. Nature 397:295-298.
-
(1999)
Nature
, vol.397
, pp. 295-298
-
-
Vogan, K.J.1
Tabin, C.J.2
-
47
-
-
0034708071
-
Left-right development: The roles of nodal cilia
-
Wagner, M.K. and Yost, H.J. 2000. Left-right development: The roles of nodal cilia. Curr. Biol. 10: R149-R151.
-
(2000)
Curr. Biol.
, vol.10
-
-
Wagner, M.K.1
Yost, H.J.2
-
48
-
-
0035172027
-
Calmodulin binds to inv protein: Implication for the regulation of inv function
-
Yasuhiko, Y., Imai, F., Ookubo, K., Takakuwa, Y., Shiokawa, K., and Yokoyama, T. 2001. Calmodulin binds to inv protein: Implication for the regulation of inv function. Develop. Growth Differ. 43: 671-681.
-
(2001)
Develop. 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
-
49
-
-
0036785149
-
The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia
-
Yoder, B.K., Hou, X., and Guay-Woodford, L.M. 2002. The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. J. Am. Soc. Nephrol. 13: 2508-2516.
-
(2002)
J. Am. Soc. Nephrol.
, vol.13
, pp. 2508-2516
-
-
Yoder, B.K.1
Hou, X.2
Guay-Woodford, L.M.3
-
50
-
-
0027158027
-
Reversal of left-right asymmetry: A situs inversus mutation
-
Yokoyama, T., Copeland, N.G., Jenkins, N.A., Montgomery, C.A., Bider, F.F.B., and Overbeek, P.A. 1993. Reversal of left-right asymmetry: A situs inversus mutation. Science 260: 679-682.
-
(1993)
Science
, vol.260
, pp. 679-682
-
-
Yokoyama, T.1
Copeland, N.G.2
Jenkins, N.A.3
Montgomery, C.A.4
Bider, F.F.B.5
Overbeek, P.A.6
|