-
1
-
-
0022417192
-
Symbiosis as a mechanism of evolution: Status of cell symbiosis theory
-
Margulis, L. and Bermudes, D. (1985) Symbiosis as a mechanism of evolution: status of cell symbiosis theory. Symbiosis, 1, 101-124.
-
(1985)
Symbiosis
, vol.1
, pp. 101-124
-
-
Margulis, L.1
Bermudes, D.2
-
2
-
-
0036208071
-
The phagotrophic origin of eukaryotes and phylogenetic classification of Protozoa
-
Cavalier-Smith, T. (2002) The phagotrophic origin of eukaryotes and phylogenetic classification of Protozoa. Int. J. Syst. Evol. Microbiol., 52, 297-354.
-
(2002)
Int. J. Syst. Evol. Microbiol.
, vol.52
, pp. 297-354
-
-
Cavalier-Smith, T.1
-
3
-
-
0037025197
-
Rooting the eukaryote tree by using a derived gene fusion
-
Stechmann, A. and Cavalier-Smith, T. (2002) Rooting the eukaryote tree by using a derived gene fusion. Science, 297, 89-91.
-
(2002)
Science
, vol.297
, pp. 89-91
-
-
Stechmann, A.1
Cavalier-Smith, T.2
-
4
-
-
0012599154
-
Two-dimensional analysis of flagellar proteins from wild-type and paralyzed mutants of Chlamydomonas reinhardtii
-
Piperno, G., Huang, B. and Luck, D.J. (1977) Two-dimensional analysis of flagellar proteins from wild-type and paralyzed mutants of Chlamydomonas reinhardtii. Proc. Natl Acad. Sci. USA, 74, 1600-1604.
-
(1977)
Proc. Natl. Acad. Sci. USA
, vol.74
, pp. 1600-1604
-
-
Piperno, G.1
Huang, B.2
Luck, D.J.3
-
5
-
-
0021360693
-
Genetic and biochemical dissection of the eucaryotic flagellum
-
Luck, D.J. (1984) Genetic and biochemical dissection of the eucaryotic flagellum. J. Cell Biol., 98, 789-794.
-
(1984)
J. Cell Biol.
, vol.98
, pp. 789-794
-
-
Luck, D.J.1
-
6
-
-
0036618084
-
A proteomic analysis of human cilia: Identification of novel components
-
Ostrowski, L.E, Blackburn, K., Radde, K.M., Moyer, M.B., Schlatzer, D.M., Moseley, A. and Boucher R.C. (2002) A proteomic analysis of human cilia: identification of novel components. Mol. Cell Proteomics, 1, 451-465.
-
(2002)
Mol. Cell Proteomics
, vol.1
, pp. 451-465
-
-
Ostrowski, L.E.1
Blackburn, K.2
Radde, K.M.3
Moyer, M.B.4
Schlatzer, D.M.5
Moseley, A.6
Boucher, R.C.7
-
8
-
-
0035745123
-
A study of helical and planar waves on sea urchin sperm flagella, with a theory of how they are generated
-
Woolley, D.M. and Vernon, G.G. (2001) A study of helical and planar waves on sea urchin sperm flagella, with a theory of how they are generated. J. Exp. Biol., 204, 1333-1345.
-
(2001)
J. Exp. Biol.
, vol.204
, pp. 1333-1345
-
-
Woolley, D.M.1
Vernon, G.G.2
-
9
-
-
0024193261
-
Development and functions of the cytoskeleton during ciliogenesis in metazoa
-
Lemullois, M., Boisvieux-Ulrich, E., Laine, M.C., Chailley, B. and Sandoz, D. (1988) Development and functions of the cytoskeleton during ciliogenesis in metazoa. Biol. Cell, 63, 195-208.
-
(1988)
Biol. Cell
, vol.63
, pp. 195-208
-
-
Lemullois, M.1
Boisvieux-Ulrich, E.2
Laine, M.C.3
Chailley, B.4
Sandoz, D.5
-
10
-
-
0029956112
-
Structural diversity of the ordinary and specialized lateral line organs
-
Cernuda-Cernuda, R. and Garcia-Fernandez, J.M. (1996) Structural diversity of the ordinary and specialized lateral line organs. Microsc. Res. Tech., 34, 302-312.
-
(1996)
Microsc. Res. Tech.
, vol.34
, pp. 302-312
-
-
Cernuda-Cernuda, R.1
Garcia-Fernandez, J.M.2
-
11
-
-
85047681474
-
Assembly and motility of eukaryotic cilia and flagella. Lessons from Chlamydomonas reinhardtii
-
Silflow, C.D. and Lefebvre, P.A. (2001) Assembly and motility of eukaryotic cilia and flagella. Lessons from Chlamydomonas reinhardtii. Plant Physiol., 127, 1500-1507.
-
(2001)
Plant Physiol.
, vol.127
, pp. 1500-1507
-
-
Silflow, C.D.1
Lefebvre, P.A.2
-
12
-
-
0028170819
-
Dyneins: Molecular structure and cellular function
-
Holzbaur, E. L. and Vallee, R.B. (1994) Dyneins: molecular structure and cellular function. A. Rev. Cell Biol., 10, 339-372.
-
(1994)
A. Rev. Cell Biol.
, vol.10
, pp. 339-372
-
-
Holzbaur, E.L.1
Vallee, R.B.2
-
13
-
-
0034677929
-
The dynein microtubule motor
-
1496
-
King, S.M. (2000) The dynein microtubule motor. Biochim. Biophys. Acta., 1496, 60-75.
-
(2000)
Biochim. Biophys. Acta
, pp. 60-75
-
-
King, S.M.1
-
14
-
-
0034722338
-
The 9+2 axoneme anchors multiple inner arm dyneins and a network of kinases and phosphatases that control motility
-
Porter, M.E. and Sale, W.S. (2000) The 9+2 axoneme anchors multiple inner arm dyneins and a network of kinases and phosphatases that control motility. J. Cell Biol., 151, 37-42.
-
(2000)
J. Cell Biol.
, vol.151
, pp. 37-42
-
-
Porter, M.E.1
Sale, W.S.2
-
15
-
-
0035995284
-
Functional diversity of axonemal dyneins as studied in Chlamydomonas mutants
-
Kamiya, R. (2002) Functional diversity of axonemal dyneins as studied in Chlamydomonas mutants. Int. Rev. Cytol., 219, 115-155.
-
(2002)
Int. Rev. Cytol.
, vol.219
, pp. 115-155
-
-
Kamiya, R.1
-
16
-
-
0029923060
-
Expression of primary cilia in mammalian cells
-
Wheatley, D.N., Wang, A.M. and Strugnell, G.E. (1996) Expression of primary cilia in mammalian cells. Cell Biol. Int., 20, 73-81.
-
(1996)
Cell Biol. Int.
, vol.20
, pp. 73-81
-
-
Wheatley, D.N.1
Wang, A.M.2
Strugnell, G.E.3
-
17
-
-
0036245322
-
Regulation of flagellar dynein by the axonemal central apparatus
-
Smith, E.F. (2002) Regulation of flagellar dynein by the axonemal central apparatus. Cell Motil. Cytoskeleton, 52, 33-42.
-
(2002)
Cell Motil. Cytoskeleton
, vol.52
, pp. 33-42
-
-
Smith, E.F.1
-
18
-
-
0033748135
-
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene
-
Omran, H., Sasmaz, G., Haffner, K., Volz, A., Olbrich, H., Melkaoui, R., Otto, E., Wienker, T.F., Korinthenberg, R., Brandis, M. et al. (2000) Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene. Am. J. Resp. Cell Mol. Biol., 23, 669-702.
-
(2000)
Am. J. Resp. Cell Mol. Biol.
, vol.23
, pp. 669-702
-
-
Omran, H.1
Sasmaz, G.2
Haffner, K.3
Volz, A.4
Olbrich, H.5
Melkaoui, R.6
Otto, E.7
Wienker, T.F.8
Korinthenberg, R.9
Brandis, M.10
-
19
-
-
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., 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 reinhardtii 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
-
20
-
-
0036199035
-
The outer dynein arm-docking complex: Composition and characterization of a subunit (Oda1) necessary for outer arm assembly
-
Takada, S., Wilkerson, C.G., Wakabayashi, K., Kamiya, R. and Witman, G.B. (2002) The outer dynein arm-docking complex: composition and characterization of a subunit (Oda1) necessary for outer arm assembly. Mol. Biol. Cell., 13, 1015-1029.
-
(2002)
Mol. Biol. Cell.
, vol.13
, pp. 1015-1029
-
-
Takada, S.1
Wilkerson, C.G.2
Wakabayashi, K.3
Kamiya, R.4
Witman, G.B.5
-
21
-
-
0031593475
-
The Mr 140,000 intermediate chain of Chlamydomonas flagellar inner arm dynein is a WD-repeat protein implicated in dynein arm anchoring
-
Yang, P. and Sale, W.S. (1998) The Mr 140,000 intermediate chain of Chlamydomonas flagellar inner arm dynein is a WD-repeat protein implicated in dynein arm anchoring. Mol. Biol. Cell., 9, 3335-3349.
-
(1998)
Mol. Biol. Cell.
, vol.9
, pp. 3335-3349
-
-
Yang, P.1
Sale, W.S.2
-
22
-
-
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
-
23
-
-
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
-
24
-
-
0031689323
-
Two rights make a wrong: Human left-right malformations
-
Casey, B. (1998) Two rights make a wrong: human left-right malformations. Hum. Mol. Genet., 7, 1565-1571.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1565-1571
-
-
Casey, B.1
-
25
-
-
0032521459
-
The compulsion of chirality: Toward an understanding of left-right asymmetry
-
Levin, M. and Mercola, M. (1998) The compulsion of chirality: toward an understanding of left-right asymmetry. Genes Dev., 12, 763-769.
-
(1998)
Genes Dev.
, vol.12
, pp. 763-769
-
-
Levin, M.1
Mercola, M.2
-
26
-
-
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
-
27
-
-
0034737302
-
Mechanisms of left-right determination in vertebrates
-
Capdevila, J., Vogan, K.J., Tabin, C.J. and Izpisua 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
Izpisua Belmonte, J.C.4
-
28
-
-
0035178866
-
Left-right asymmetry determination in vertebrates
-
Mercola, M. and Levin, M. (2001) Left-right asymmetry determination in vertebrates. A. Rev. Cell Dev. Biol., 17, 779-805.
-
(2001)
A. Rev. Cell Dev. Biol.
, vol.17
, pp. 779-805
-
-
Mercola, M.1
Levin, M.2
-
29
-
-
0036086113
-
Formation and malformation of the vertebrate left-right axis
-
Hackett, B.P. (2002) Formation and malformation of the vertebrate left-right axis. Curr. Mol. Med., 2, 39-66.
-
(2002)
Curr. Mol. Med.
, vol.2
, pp. 39-66
-
-
Hackett, B.P.1
-
30
-
-
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
-
31
-
-
0036250574
-
Establishment of vertebrate left-right asymmetry
-
Hamada, H., Meno, C., Watanabe, D. and Saijoh, Y. (2002) Establishment of vertebrate left-right asymmetry. Nat. Rev. Genet., 3, 103-113.
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 103-113
-
-
Hamada, H.1
Meno, C.2
Watanabe, D.3
Saijoh, Y.4
-
32
-
-
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
-
33
-
-
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
-
34
-
-
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
-
35
-
-
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
-
36
-
-
15844385078
-
PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein
-
Mochizuki, T., Wu, G., Hayashi, T., Xenophontos, S.L., Veldhuisen, B., Saris, J.J., Reynolds, D.M., Cai, Y., Gabow, P.A., Pierides, A. et al. (1996) PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein. Science, 272, 1339-1342
-
(1996)
Science
, vol.272
, pp. 1339-1342
-
-
Mochizuki, T.1
Wu, G.2
Hayashi, T.3
Xenophontos, S.L.4
Veldhuisen, B.5
Saris, J.J.6
Reynolds, D.M.7
Cai, Y.8
Gabow, P.A.9
Pierides, A.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
-
-
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
-
39
-
-
0037087624
-
Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus
-
Ibañez-Tallon, I., Gorokhova, S. and Heintz, N. (2002) Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus. Hum. Mol. Genet., 11, 715-721.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 715-721
-
-
Ibañez-Tallon, I.1
Gorokhova, S.2
Heintz, N.3
-
40
-
-
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
-
42
-
-
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
-
43
-
-
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. USA, 96, 5043-5048.
-
(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
-
44
-
-
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 Woychik, 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
Woychik, R.P.6
-
45
-
-
0032530312
-
Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry
-
Chen, J., Knowles, H.J., Hebert, J.L. and Hackett, B.P. Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry. J. Clin. Invest., 102, 1077-1082.
-
J. Clin. Invest.
, vol.102
, pp. 1077-1082
-
-
Chen, J.1
Knowles, H.J.2
Hebert, J.L.3
Hackett, B.P.4
-
46
-
-
0033901391
-
Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice
-
Brody, S.L., Yan, X.H., Wuerffel, M.K., Song, S.K. and Shapiro, S.D. (2000) Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice. Am. J. Respir Cell Mol. Biol., 23, 45-51.
-
(2000)
Am. J. Respir. Cell Mol. Biol.
, vol.23
, pp. 45-51
-
-
Brody, S.L.1
Yan, X.H.2
Wuerffel, M.K.3
Song, S.K.4
Shapiro, S.D.5
-
47
-
-
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
-
48
-
-
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
-
49
-
-
0019459120
-
Immotile cilia syndrome: A new cause of neonatal respiratory distress
-
Whitelaw, A., Evans, A. and Corrin, B. (1981) Immotile cilia syndrome: a new cause of neonatal respiratory distress. Arch. Dis. Child., 56, 432-435.
-
(1981)
Arch. Dis. Child.
, vol.56
, pp. 432-435
-
-
Whitelaw, A.1
Evans, A.2
Corrin, B.3
-
50
-
-
0020620860
-
Male and female infertility problems in the immotile cilia syndrome
-
Afzelius, B.A. and Eliasson, R. (1983) Male and female infertility problems in the immotile cilia syndrome. Eur. J. Resp. Dis., 64, 144-147.
-
(1983)
Eur. J. Resp. Dis.
, vol.64
, pp. 144-147
-
-
Afzelius, B.A.1
Eliasson, R.2
-
51
-
-
0028246542
-
Fertility in males with primary ciliary dyskinesia presenting with respiratory infection
-
Munro, N.C., Currie, D.C., Lindsay, K.S., Ryder, T.A., Rutman, A., Dewar, A., Greenstone, M.A., Hendry, W.F. and Cole, P.J. (1994) Fertility in males with primary ciliary dyskinesia presenting with respiratory infection. Thorax, 49, 684-687.
-
(1994)
Thorax
, vol.49
, pp. 684-687
-
-
Munro, N.C.1
Currie, D.C.2
Lindsay, K.S.3
Ryder, T.A.4
Rutman, A.5
Dewar, A.6
Greenstone, M.A.7
Hendry, W.F.8
Cole, P.J.9
-
52
-
-
0001668367
-
Immotile cilia syndrome (primary ciliary dyskinesia) including Kartagener Syndrome
-
Scriver, C.R., Beaudet, A.L. and Sly, W.S. (eds.), McGraw-Hill, New York
-
Afzelius, B.A. and Mossberg, B. (1995) Immotile cilia syndrome (primary ciliary dyskinesia) including Kartagener Syndrome. In Scriver, C.R., Beaudet, A.L. and Sly, W.S. (eds.), The Metabolic and Molecular Bases of Inherited Disease. McGraw-Hill, New York, pp. 3943-3954.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease
, pp. 3943-3954
-
-
Afzelius, B.A.1
Mossberg, B.2
-
53
-
-
0034571937
-
Ultrastructural expression of primary ciliary dyskinesia after ciliogenesis in culture
-
Jorissen, M., Willems, T., van der Schueren, B., Verbeken, E. and de Boeck, K. (2000) Ultrastructural expression of primary ciliary dyskinesia after ciliogenesis in culture. Acta oto-rhino-laryngol. Belg., 54, 343-356.
-
(2000)
Acta Oto-rhino-laryngol. Belg.
, vol.54
, pp. 343-356
-
-
Jorissen, M.1
Willems, T.2
van der Schueren, B.3
Verbeken, E.4
de Boeck, K.5
-
54
-
-
0028359813
-
Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome)
-
Narayan, D., Krishnan, S.N., Upender, M., Ravikumar, T. S., Mahoney, M. J., Dolan, T.F.J., Teebi, A.S. and Haddad, G.G. (1994) Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome). J. Med. Genet., 31, 493-496.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 493-496
-
-
Narayan, D.1
Krishnan, S.N.2
Upender, M.3
Ravikumar, T.S.4
Mahoney, M.J.5
Dolan, T.F.J.6
Teebi, A.S.7
Haddad, G.G.8
-
55
-
-
0034019801
-
Primary ciliary dyskinesia: A genome-wide linkage analysis reveals extensive locus heterogeneity
-
Blouin, J.L., Meeks, M., Radhakrishna, U., Sainsbury, A., Gehring, C., Sail, G.D., Bartoloni, L., Dombi, V., O'Rawe, A., Walne, A. et al. (2000) Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity. Eur. J. Hum. Genet., 8, 109-118.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 109-118
-
-
Blouin, J.L.1
Meeks, M.2
Radhakrishna, U.3
Sainsbury, A.4
Gehring, C.5
Sail, G.D.6
Bartoloni, L.7
Dombi, V.8
O'Rawe, A.9
Walne, A.10
-
56
-
-
0035068576
-
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener 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 (Kartagener 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
-
57
-
-
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, 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. USA, 99, 10282-10286.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 10282-10286
-
-
Bartoloni, L.1
Blouin, 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
-
58
-
-
0034532068
-
The human dynein intermediate chain 2 gene (DNAI2): Cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia
-
Pennarun, G., Chapelin, C., Escudier, E., Bridoux, A.-M., Dastot, F., Cacheux, V., Goossens, M., Amselem, S. and Duriez, B. (2000) The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia. Hum. Genet., 107, 642-649.
-
(2000)
Hum. Genet.
, vol.107
, pp. 642-649
-
-
Pennarun, G.1
Chapelin, C.2
Escudier, E.3
Bridoux, A.-M.4
Dastot, F.5
Cacheux, V.6
Goossens, M.7
Amselem, S.8
Duriez, B.9
-
59
-
-
0035865027
-
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia
-
Bartoloni, L., Blouin, J.L., Maiti, A.K., Sainsbury, A., Rossier, C., Gehrig, C., She, J.X., Marron, M.P., Lander, E.S., Meeks, M. et al. (2001) Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia. Genomics, 72, 21-33.
-
(2001)
Genomics
, vol.72
, pp. 21-33
-
-
Bartoloni, L.1
Blouin, J.L.2
Maiti, A.K.3
Sainsbury, A.4
Rossier, C.5
Gehrig, C.6
She, J.X.7
Marron, M.P.8
Lander, E.S.9
Meeks, M.10
-
60
-
-
0036988980
-
Identification of the human ortholog of the t-complex-encoded protein TCTEX2 and evaluation as a candidate gene for primary ciliary dyskinesia
-
(in press)
-
Neesen, J., Drenkhahn, J., Tiede, S., Burfeind, P., Grzmil, P., Konietzko, J., Dixkens, C., Kreutzberger, J., Laccone, F., Engel, W. et al. (2002) Identification of the human ortholog of the t-complex-encoded protein TCTEX2 and evaluation as a candidate gene for primary ciliary dyskinesia. Cytogenet. Genome Res. (in press).
-
(2002)
Cytogenet. Genome Res.
-
-
Neesen, J.1
Drenkhahn, J.2
Tiede, S.3
Burfeind, P.4
Grzmil, P.5
Konietzko, J.6
Dixkens, C.7
Kreutzberger, J.8
Laccone, F.9
Engel, W.10
-
61
-
-
0018305742
-
Kartagener's syndrome and the syndrome of immotile cilia
-
Rott, H.D. (1979) Kartagener's syndrome and the syndrome of immotile cilia. Hum. Genet., 46, 249-261.
-
(1979)
Hum. Genet.
, vol.46
, pp. 249-261
-
-
Rott, H.D.1
-
62
-
-
0021270023
-
Hydrocephalus and primary ciliary dyskinesia
-
Greenstone, M.A., Jones, R.W., Dewar, A., Neville, B.G. and Cole, P.J. (1984) Hydrocephalus and primary ciliary dyskinesia. Arch. Dis. Child., 59, 481-482.
-
(1984)
Arch. Dis. Child.
, vol.59
, pp. 481-482
-
-
Greenstone, M.A.1
Jones, R.W.2
Dewar, A.3
Neville, B.G.4
Cole, P.J.5
-
63
-
-
0022541080
-
Hydrocephalus in Kartagener's syndrome
-
Jabourian, Z., Lublin, F.D., Adler, A., Gonzales, C., Northrup, B. and Zwillenberg, D. (1986) Hydrocephalus in Kartagener's syndrome. Ear Nose Throat J., 65, 468-472.
-
(1986)
Ear Nose Throat J.
, vol.65
, pp. 468-472
-
-
Jabourian, Z.1
Lublin, F.D.2
Adler, A.3
Gonzales, C.4
Northrup, B.5
Zwillenberg, D.6
-
64
-
-
0025268397
-
Hydrocephalus, bronchiectasis, and ciliary aplasia
-
De Santi, M.M., Magni, A., Valetta, E.A., Gardi, C. and Lungarella, G. (1990) Hydrocephalus, bronchiectasis, and ciliary aplasia. Arch Dis. Child., 65, 543-544.
-
(1990)
Arch. Dis. Child.
, vol.65
, pp. 543-544
-
-
De Santi, M.M.1
Magni, A.2
Valetta, E.A.3
Gardi, C.4
Lungarella, G.5
-
65
-
-
0027772235
-
Immotile cilia syndrome associated with hydrocephalus and precocious puberty: A case report
-
Picco, P., Leveratto, L., Cama, A., Vigliarolo, M.A., Levato, G.L,, Gattorno, M., Zammarchi, E. and Donati, M.A. (1993) Immotile cilia syndrome associated with hydrocephalus and precocious puberty: a case report. Eur. J. Pediatr Surg., 3, 20-21.
-
(1993)
Eur. J. Pediatr. Surg.
, vol.3
, pp. 20-21
-
-
Picco, P.1
Leveratto, L.2
Cama, A.3
Vigliarolo, M.A.4
Levato, G.L.5
Gattorno, M.6
Zammarchi, E.7
Donati, M.A.8
-
66
-
-
0027532248
-
Unusual presentation of primary ciliary dyskinesia in two children
-
Zammarchi, E., Calzolari, C., Pignotti, M.S., Pezzati, P., Lignana, E. and Cama, A. (1993) Unusual presentation of primary ciliary dyskinesia in two children. Acta Paediatr, 82, 312-313.
-
(1993)
Acta Paediatr.
, vol.82
, pp. 312-313
-
-
Zammarchi, E.1
Calzolari, C.2
Pignotti, M.S.3
Pezzati, P.4
Lignana, E.5
Cama, A.6
-
67
-
-
0035212041
-
Ciliary dyskinesia associated with hydrocephalus and mental retardation in a Jordanian family
-
Al-Shroof, M., Karnik, A.M., Karnik, A.A., Longshore, J., Sliman, N.A. and Khan, F.A. (2001) Ciliary dyskinesia associated with hydrocephalus and mental retardation in a Jordanian family. Mayo Clin. Proc., 76, 1219-1224.
-
(2001)
Mayo Clin. Proc.
, vol.76
, pp. 1219-1224
-
-
Al-Shroof, M.1
Karnik, A.M.2
Karnik, A.A.3
Longshore, J.4
Sliman, N.A.5
Khan, F.A.6
-
69
-
-
84985427925
-
Immotile cilia syndrome in two Old English Sheepdog litter mates
-
Randolph, J.F. and Castleman, W.L. (1984) Immotile cilia syndrome in two Old English Sheepdog litter mates. J. Small Anim. Pract., 25, 679-686.
-
(1984)
J. Small Anim. Pract.
, vol.25
, pp. 679-686
-
-
Randolph, J.F.1
Castleman, W.L.2
-
70
-
-
0024441940
-
Familial immotile-cilia syndrome in English springer spaniel dogs
-
Edwards, D.F., Kennedy, J.R., Patton, C.S., Toal, R.L., Daniel, G.B. and Lothrop, C.D. (1989) Familial immotile-cilia syndrome in English springer spaniel dogs. Am. J. Med. Genet., 33, 290-298.
-
(1989)
Am. J. Med. Genet.
, vol.33
, pp. 290-298
-
-
Edwards, D.F.1
Kennedy, J.R.2
Patton, C.S.3
Toal, R.L.4
Daniel, G.B.5
Lothrop, C.D.6
-
71
-
-
0025973393
-
Ultrastructure of respiratory cilia of WIC-Hyd male rats: An animal model for human immotile cilia syndrome
-
Torikata, C., Kijimoto, C. and Koto, M. (1991) Ultrastructure of respiratory cilia of WIC-Hyd male rats: an animal model for human immotile cilia syndrome. Am. J. Pathol., 138, 341-347.
-
(1991)
Am. J. Pathol.
, vol.138
, pp. 341-347
-
-
Torikata, C.1
Kijimoto, C.2
Koto, M.3
-
72
-
-
0032706344
-
Respiratory and brain ependymal ciliary function
-
O'Callaghan, C., Sikand, K. and Rutman, A. (1999) Respiratory and brain ependymal ciliary function. Pediatr Res., 46, 704-707.
-
(1999)
Pediatr. Res.
, vol.46
, pp. 704-707
-
-
O'Callaghan, C.1
Sikand, K.2
Rutman, A.3
-
73
-
-
0035159015
-
Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia
-
Taulman, P.D., Haycraft, C.J., Balkovetz, D.F. and Yoder, B.K. (2001) Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia. Mol. Biol. Cell., 12, 589-599.
-
(2001)
Mol. Biol. Cell.
, vol.12
, pp. 589-599
-
-
Taulman, P.D.1
Haycraft, C.J.2
Balkovetz, D.F.3
Yoder, B.K.4
-
74
-
-
0022457502
-
Flowing cerebrospinal fluid in normal and hydrocephalic states: Appearance on MR images
-
Bradley, W.G., Kortman, K.E. and Burgoyne, B. (1986) Flowing cerebrospinal fluid in normal and hydrocephalic states: appearance on MR images. Radiology, 159, 611-616.
-
(1986)
Radiology
, vol.159
, pp. 611-616
-
-
Bradley, W.G.1
Kortman, K.E.2
Burgoyne, B.3
-
75
-
-
0019473406
-
Immotile-cilia syndrome and the cilia of the eye
-
Svedbergh, B., Johnsson, V. and Afzelius, B.A. (1981) Immotile-cilia syndrome and the cilia of the eye. Graefes Arch. Klin. Exp. Ophthalmol., 215, 265.
-
(1981)
Graefes Arch. Klin. Exp. Ophthalmol.
, vol.215
, pp. 265
-
-
Svedbergh, B.1
Johnsson, V.2
Afzelius, B.A.3
-
76
-
-
0027409796
-
Usher syndrome type-1 associated with bronchiectasis and immotile nasal cilia in two brothers
-
Bonneau, D., Raymond, F., Kremer, C., Klossek, J.M., Kaplan, J. and Patte, F. (1993) Usher syndrome type-1 associated with bronchiectasis and immotile nasal cilia in two brothers. J. Med. Genet., 30, 253-254.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 253-254
-
-
Bonneau, D.1
Raymond, F.2
Kremer, C.3
Klossek, J.M.4
Kaplan, J.5
Patte, F.6
-
77
-
-
1642431004
-
Kartagener's syndrome with familial eye changes
-
Segal, P., Kikiela, M., Mrzyglod, B. and Zeromska-Zbierska, I. (1963) Kartagener's syndrome with familial eye changes. Am. J. Ophthal., 55, 1043-1049.
-
(1963)
Am. J. Ophthal.
, vol.55
, pp. 1043-1049
-
-
Segal, P.1
Kikiela, M.2
Mrzyglod, B.3
Zeromska-Zbierska, I.4
-
78
-
-
1642472095
-
A case of immotile cilia syndrome accompanied by retinitis pigmentosa
-
Ohga, H., Suzuki, T., Fujiwara, H., Furutani, A. and Koga H. (1991) A case of immotile cilia syndrome accompanied by retinitis pigmentosa. Acta Soc. Ophthal. Jpn., 89, 795.
-
(1991)
Acta Soc. Ophthal. Jpn.
, vol.89
, pp. 795
-
-
Ohga, H.1
Suzuki, T.2
Fujiwara, H.3
Furutani, A.4
Koga, H.5
-
79
-
-
0002763351
-
The photoreceptor connecting cilium. A model for the transition zone
-
Bloodgood, R.A. (ed.) Plenum, New York
-
Besharse, J.C. and C.J. Horst. (1990) The photoreceptor connecting cilium. A model for the transition zone. In Bloodgood, R.A. (ed.) Ciliary and Flagellar Membranes. Plenum, New York, pp. 389-417.
-
(1990)
Ciliary and Flagellar Membranes
, pp. 389-417
-
-
Besharse, J.C.1
Horst, C.J.2
-
80
-
-
0033535057
-
Intraflagellar transport: The eyes have it
-
Rosenbaum, J.L., Cole, D.G. and Diener, D.R. (1999) Intraflagellar transport: the eyes have it. J. Cell Biol., 144, 385-388.
-
(1999)
J. Cell Biol.
, vol.144
, pp. 385-388
-
-
Rosenbaum, J.L.1
Cole, D.G.2
Diener, D.R.3
-
81
-
-
0036544554
-
The intraflagellar transport protein, IFT98, is essential for vertebrate photoreceptor assembly and maintenance
-
Pazour, G.J., Baker, S.A., Deane, J.A., Cole, D.G., Dickert, B.L., Rosenbaum, J.L., Witman, G.B. and Besharse, J.C. (2002) The intraflagellar transport protein, IFT98, is essential for vertebrate photoreceptor assembly and maintenance. J. Cell Biol., 157, 103-113.
-
(2002)
J. Cell Biol.
, vol.157
, pp. 103-113
-
-
Pazour, G.J.1
Baker, S.A.2
Deane, J.A.3
Cole, D.G.4
Dickert, B.L.5
Rosenbaum, J.L.6
Witman, G.B.7
Besharse, J.C.8
-
83
-
-
0025613559
-
Nephronophthisis with bronchiectasis
-
Bagga, A., Vasudev, A., Kabra, S.K., Mukhopadhyay, S., Bhuyan, U.N. and Srivastava, R. (1990) Nephronophthisis with bronchiectasis. Child Nephrol. Urol., 10, 211-213.
-
(1990)
Child Nephrol. Urol.
, vol.10
, pp. 211-213
-
-
Bagga, A.1
Vasudev, A.2
Kabra, S.K.3
Mukhopadhyay, S.4
Bhuyan, U.N.5
Srivastava, R.6
-
84
-
-
0033555463
-
Sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts: A new syndrome?
-
Balci, S., Bostanoglu, S., Altinok, G. and Ozaltin, F. (1999) Sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts: a new syndrome? Am. J. Med. Genet., 82, 166-169.
-
(1999)
Am. J. Med. Genet.
, vol.82
, pp. 166-169
-
-
Balci, S.1
Bostanoglu, S.2
Altinok, G.3
Ozaltin, F.4
-
85
-
-
0034737050
-
Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts
-
Balci, S., Bostanoglu, S., Altinok, G. and Ozaltin, F. (2000) Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts. Am. J. Med. Genet., 90, 185-187.
-
(2000)
Am. J. Med. Genet.
, vol.90
, pp. 185-187
-
-
Balci, S.1
Bostanoglu, S.2
Altinok, G.3
Ozaltin, F.4
-
86
-
-
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, 378-380.
-
(2002)
Curr. Biol.
, vol.12
, pp. 378-380
-
-
Pazour, G.J.1
San Agustin, J.T.2
Follit, J.A.3
Rosenbaum, J.L.4
Witman, G.B.5
-
87
-
-
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. Alephrol., 13, 2508-2516.
-
(2002)
J. Am. Soc. Alephrol.
, vol.13
, pp. 2508-2516
-
-
Yoder, B.K.1
Hou, X.2
Guay-Woodford, L.M.3
-
88
-
-
0028322016
-
Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice
-
Moyer, J.H., Lee-Tischler, M.J., Kwon, H.Y., Schrick, J.J., Avner, E.D., Sweeney, W.E., Godfrey, V.L., Cacheiro, N.L., Wilkinson, J.E. and Woychik, R.P. (1994) Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. Science, 27, 1329-1333.
-
(1994)
Science
, vol.27
, pp. 1329-1333
-
-
Moyer, J.H.1
Lee-Tischler, M.J.2
Kwon, H.Y.3
Schrick, J.J.4
Avner, E.D.5
Sweeney, W.E.6
Godfrey, V.L.7
Cacheiro, N.L.8
Wilkinson, J.E.9
Woychik, R.P.10
-
89
-
-
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 Woychik, 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
Woychik, R.P.6
-
90
-
-
0034735526
-
Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella
-
Pazour, G.J., Dickert, B.L., Vucica, Y., Seeley, E.S., Rosenbaum, J.L., Witman, G.B. and Cole, D.G. (2000) Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J. Cell Biol., 151, 709-718.
-
(2000)
J. Cell Biol.
, vol.151
, pp. 709-718
-
-
Pazour, G.J.1
Dickert, B.L.2
Vucica, Y.3
Seeley, E.S.4
Rosenbaum, J.L.5
Witman, G.B.6
Cole, D.G.7
-
91
-
-
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, 533-540.
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 533-540
-
-
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
-
92
-
-
0030586902
-
Multiple mouse chromosomal loci for dynein-based motility
-
Vaughan, K.T., Mikami, A., Paschal, B.M., Holzbaur, E.L., Hughes, S.M., Echeverri, C.J., Moore, K.J., Gilbert, D.J., Copeland, N.G., Jenkins, N.A. et al. (1996) Multiple mouse chromosomal loci for dynein-based motility. Genomics, 36, 29 38.
-
(1996)
Genomics
, vol.36
, pp. 29-38
-
-
Vaughan, K.T.1
Mikami, A.2
Paschal, B.M.3
Holzbaur, E.L.4
Hughes, S.M.5
Echeverri, C.J.6
Moore, K.J.7
Gilbert, D.J.8
Copeland, N.G.9
Jenkins, N.A.10
-
93
-
-
0030731609
-
Identification of dynein heavy chain genes expressed in human and mouse testis: Chromosomal localization of an axonemal dynein gene
-
Neesen, J., Koehler, M.R., Kirschner, R., Steinlein, C., Kreutzberger, J., Engel, W. and Schmid, M. (1997) Identification of dynein heavy chain genes expressed in human and mouse testis: chromosomal localization of an axonemal dynein gene. Gene, 200, 193 202.
-
(1997)
Gene
, vol.200
, pp. 193-202
-
-
Neesen, J.1
Koehler, M.R.2
Kirschner, R.3
Steinlein, C.4
Kreutzberger, J.5
Engel, W.6
Schmid, M.7
-
94
-
-
0030860532
-
Isolation of several human axonemal dynein heavy chain genes: Genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment
-
Chapelin, C., Duriez, B., Magnino, F., Goossens, M., Escudier, E. and Amselem, S. (1997) Isolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment. FEBS Lett., 412, 325-330.
-
(1997)
FEBS Lett.
, vol.412
, pp. 325-330
-
-
Chapelin, C.1
Duriez, B.2
Magnino, F.3
Goossens, M.4
Escudier, E.5
Amselem, S.6
-
95
-
-
0034516340
-
Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes
-
Maiti, A.K., Mattei, M.G., Jorissen, M., Volz, A., Zeigler, A. and Bouvagnet, P. (2000) Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes. Eur J. Hum. Genet., 8, 923-932.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 923-932
-
-
Maiti, A.K.1
Mattei, M.G.2
Jorissen, M.3
Volz, A.4
Zeigler, A.5
Bouvagnet, P.6
-
96
-
-
14344274965
-
Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency
-
Neesen, J., Kirschner, R., Ochs, M., Schmiedl, A., Habermann, B., Mueller, C., Holstein, A.F., Nuesslein T, Adham, I. and Engel, W. (2001) Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency. Hum. Mol. Genet., 10, 1117-1128.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1117-1128
-
-
Neesen, J.1
Kirschner, R.2
Ochs, M.3
Schmiedl, A.4
Habermann, B.5
Mueller, C.6
Holstein, A.F.7
Nuesslein, T.8
Adham, I.9
Engel, W.10
-
97
-
-
0037124060
-
Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia
-
Zhang, Y.J., O'Neal, W.K., Randell, S.H., Blackburn, K., Moyer, M.B., Boucher, R.C. and Ostrowski, L.E. (2002) Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia. J. Biol. Chem., 277, 17906-17915.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 17906-17915
-
-
Zhang, Y.J.1
O'Neal, W.K.2
Randell, S.H.3
Blackburn, K.4
Moyer, M.B.5
Boucher, R.C.6
Ostrowski, L.E.7
-
98
-
-
0029905303
-
Mammalian cells express three distinct dynein heavy chains that are localized to different cytoplasmic organelles
-
Vaisberg, E.A., Grissom, P.M. and McIntosh, J.R. (1996) Mammalian cells express three distinct dynein heavy chains that are localized to different cytoplasmic organelles. J. Cell Biol., 133, 831-842.
-
(1996)
J. Cell Biol.
, vol.133
, pp. 831-842
-
-
Vaisberg, E.A.1
Grissom, P.M.2
McIntosh, J.R.3
-
99
-
-
0033118291
-
An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci
-
Kalikin, L.M., George, R.A., Keller, M.P., Bort, S., Bowler, N.S., Law, D.J., Chance, P.F. and Petty, E.M. (1999) An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci. Genomics, 57, 36-42.
-
(1999)
Genomics
, vol.57
, pp. 36-42
-
-
Kalikin, L.M.1
George, R.A.2
Keller, M.P.3
Bort, S.4
Bowler, N.S.5
Law, D.J.6
Chance, P.F.7
Petty, E.M.8
|