-
1
-
-
0032837927
-
Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat
-
Alwazzan M., Newman E., Hamshere M.G., Brook J.D. Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat. Hum. Mol. Genet. 8:1999;1491-1497
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1491-1497
-
-
Alwazzan, M.1
Newman, E.2
Hamshere, M.G.3
Brook, J.D.4
-
2
-
-
0028818586
-
A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat
-
Boucher C.A., King S.K., Carey N., Krahe R., Winchester C.L., Rahman S., Creavin T., Meghji P., Bailey M.E., Chartier F.L., et al. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat. Hum. Mol. Genet. 4:1995;1919-1925
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1919-1925
-
-
Boucher, C.A.1
King, S.K.2
Carey, N.3
Krahe, R.4
Winchester, C.L.5
Rahman, S.6
Creavin, T.7
Meghji, P.8
Bailey, M.E.9
Chartier, F.L.10
-
3
-
-
0016063911
-
The genetics of Caenorhabditis elegans
-
Brenner S. The genetics of Caenorhabditis elegans. Genetics. 77:1974;71-94
-
(1974)
Genetics
, vol.77
, pp. 71-94
-
-
Brenner, S.1
-
4
-
-
0027122152
-
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
-
Brook J.D., McCurrach M.E., Harley H.G., Buckler A.J., Church D., Aburatani H., Hunter K., Stanton V.P., Thirion J.P., Hudson T., et al. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell. 69:1992;385
-
(1992)
Cell
, vol.69
, pp. 385
-
-
Brook, J.D.1
McCurrach, M.E.2
Harley, H.G.3
Buckler, A.J.4
Church, D.5
Aburatani, H.6
Hunter, K.7
Stanton, V.P.8
Thirion, J.P.9
Hudson, T.10
-
5
-
-
0027372107
-
Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy
-
Carango P., Noble J.E., Marks H.G., Funanage V.L. Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy. Genomics. 18:1993;340-348
-
(1993)
Genomics
, vol.18
, pp. 340-348
-
-
Carango, P.1
Noble, J.E.2
Marks, H.G.3
Funanage, V.L.4
-
6
-
-
0028244770
-
The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system
-
Cheyette B.N., Green P.J., Martin K., Garren H., Hartenstein V., Zipursky S.L. The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system. Neuron. 12:1994;977-996
-
(1994)
Neuron
, vol.12
, pp. 977-996
-
-
Cheyette, B.N.1
Green, P.J.2
Martin, K.3
Garren, H.4
Hartenstein, V.5
Zipursky, S.L.6
-
7
-
-
0031930963
-
Analysis of osm-6, a gene that affects sensory cilium structure and sensory neuron function in Caenorhabditis elegans
-
Collet J., Spike C.A., Lundquist E.A., Shaw J.E., Herman R.K. Analysis of osm-6, a gene that affects sensory cilium structure and sensory neuron function in Caenorhabditis elegans. Genetics. 148:1998;187-200
-
(1998)
Genetics
, vol.148
, pp. 187-200
-
-
Collet, J.1
Spike, C.A.2
Lundquist, E.A.3
Shaw, J.E.4
Herman, R.K.5
-
8
-
-
0035881212
-
The Caenorhabditis elegans Six/sine oculis class homeobox gene ceh-32 is required for head morphogenesis
-
Dozier C., Kagoshima H., Niklaus G., Cassata G., Bürglin T.R. The Caenorhabditis elegans Six/sine oculis class homeobox gene ceh-32 is required for head morphogenesis. Dev. Biol. 236:2001;289-303
-
(2001)
Dev. Biol.
, vol.236
, pp. 289-303
-
-
Dozier, C.1
Kagoshima, H.2
Niklaus, G.3
Cassata, G.4
Bürglin, T.R.5
-
9
-
-
0022497852
-
Genetic control of programmed cell death in the nematode C. elegans
-
Ellis H.M., Horvitz H.R. Genetic control of programmed cell death in the nematode C. elegans. Cell. 44:1986;817-829
-
(1986)
Cell
, vol.44
, pp. 817-829
-
-
Ellis, H.M.1
Horvitz, H.R.2
-
10
-
-
0034935016
-
CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus
-
Filippova G.N., Thienes C.P., Penn B.H., Cho D.H., Hu Y.J., Moore J.M., Klesert T.R., Lobanenkov V.V., Tapscott S.J. CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus. Nat. Genet. 28:2001;335-343
-
(2001)
Nat. Genet.
, vol.28
, pp. 335-343
-
-
Filippova, G.N.1
Thienes, C.P.2
Penn, B.H.3
Cho, D.H.4
Hu, Y.J.5
Moore, J.M.6
Klesert, T.R.7
Lobanenkov, V.V.8
Tapscott, S.J.9
-
11
-
-
0032545933
-
Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans
-
Fire A., Xu S.-Q., Montgomery M.K., Kostas S.A., Driver S.E., Mello C.C. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature. 391:1998;806-811
-
(1998)
Nature
, vol.391
, pp. 806-811
-
-
Fire, A.1
Xu, S.-Q.2
Montgomery, M.K.3
Kostas, S.A.4
Driver, S.E.5
Mello, C.C.6
-
12
-
-
0031883750
-
Identification of Caenorhabditis elegans genes required for neuronal differentiation and migration
-
Forrester W.C., Perens E., Zallen J.A., Garriga G. Identification of Caenorhabditis elegans genes required for neuronal differentiation and migration. Genetics. 148:1998;151-165
-
(1998)
Genetics
, vol.148
, pp. 151-165
-
-
Forrester, W.C.1
Perens, E.2
Zallen, J.A.3
Garriga, G.4
-
13
-
-
0027246344
-
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy
-
Fu Y.H., Friedman D.L., Richards S., Pearlman J.A., Gibbs R.A., Pizzuti A., Ashizawa T., Perryman M.B., Scarlato G., Fenwick R.G. Jr., et al. Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy. Science. 260:1993;235-238
-
(1993)
Science
, vol.260
, pp. 235-238
-
-
Fu, Y.H.1
Friedman, D.L.2
Richards, S.3
Pearlman, J.A.4
Gibbs, R.A.5
Pizzuti, A.6
Ashizawa, T.7
Perryman, M.B.8
Scarlato, G.9
Fenwick Jr., R.G.10
-
14
-
-
0032826288
-
Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies
-
Gallardo M.E., Lopez-Rios J., Fernaud-Espinosa I., Granadino B., Sanz R., Ramos C., Ayuso C., Seller M.J., Brunner H.G., Bovolenta P., Rodríguez de Córdoba S. Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies. Genomics. 61:1999;82-91
-
(1999)
Genomics
, vol.61
, pp. 82-91
-
-
Gallardo, M.E.1
Lopez-Rios, J.2
Fernaud-Espinosa, I.3
Granadino, B.4
Sanz, R.5
Ramos, C.6
Ayuso, C.7
Seller, M.J.8
Brunner, H.G.9
Bovolenta, P.10
Rodríguez De Córdoba, S.11
-
15
-
-
0031927040
-
MyoD and the specification of muscle and non-muscle fates during postembryonic development of the C. elegans mesoderm
-
Harfe B.D., Branda C.S., Krause M., Stern M.J., Fire A. MyoD and the specification of muscle and non-muscle fates during postembryonic development of the C. elegans mesoderm. Development. 125:1998;2479-2488
-
(1998)
Development
, vol.125
, pp. 2479-2488
-
-
Harfe, B.D.1
Branda, C.S.2
Krause, M.3
Stern, M.J.4
Fire, A.5
-
16
-
-
3543032767
-
Analysis of a Caenorhabditis elegans Twist homolog identifies conserved and divergent aspects of mesodermal patterning
-
Harfe B.D., Vas Gomez A., Kenyon C., Liu J., Krause M., Fire A. Analysis of a Caenorhabditis elegans Twist homolog identifies conserved and divergent aspects of mesodermal patterning. Genes Dev. 12:1998;2623-2635
-
(1998)
Genes Dev.
, vol.12
, pp. 2623-2635
-
-
Harfe, B.D.1
Vas Gomez, A.2
Kenyon, C.3
Liu, J.4
Krause, M.5
Fire, A.6
-
17
-
-
0026523591
-
Unstable DNA sequence in myotonic dystrophy
-
Harley H.G., Rundle S.A., Reardon W., Myring J., Crow S., Brook J.D., Harper P.S., Shaw D.J. Unstable DNA sequence in myotonic dystrophy. Lancet. 339:1992;1125-1128
-
(1992)
Lancet
, vol.339
, pp. 1125-1128
-
-
Harley, H.G.1
Rundle, S.A.2
Reardon, W.3
Myring, J.4
Crow, S.5
Brook, J.D.6
Harper, P.S.7
Shaw, D.J.8
-
18
-
-
3342993362
-
Third ed.
-
London: Saunders
-
Harper P.S. third ed. Myotonic Dystrophy. vol. 37:2001;Saunders, London
-
(2001)
Myotonic Dystrophy
, vol.37
-
-
Harper, P.S.1
-
19
-
-
0033573003
-
Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation
-
Heanue T.A., Reshef R., Davis R.J., Mardon G., Oliver G., Tomarev S., Lassar A.B., Tabin C.J. Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation. Genes Dev. 13:1999;3231-3243
-
(1999)
Genes Dev.
, vol.13
, pp. 3231-3243
-
-
Heanue, T.A.1
Reshef, R.2
Davis, R.J.3
Mardon, G.4
Oliver, G.5
Tomarev, S.6
Lassar, A.B.7
Tabin, C.J.8
-
21
-
-
0034141791
-
Functions of LIM-homeobox genes
-
Hobert O., Westphal H. Functions of LIM-homeobox genes. Trends Genet. 16:2000;75-83
-
(2000)
Trends Genet.
, vol.16
, pp. 75-83
-
-
Hobert, O.1
Westphal, H.2
-
22
-
-
0033924215
-
Six family genes - Structure and function as transcription factors and their roles in development
-
Kawakami K., Sato S., Ozaki H., Ikeda K. Six family genes - Structure and function as transcription factors and their roles in development. BioEssays. 22:2000;616-626
-
(2000)
BioEssays
, vol.22
, pp. 616-626
-
-
Kawakami, K.1
Sato, S.2
Ozaki, H.3
Ikeda, K.4
-
23
-
-
0018725140
-
The postembryonic cell lineages of the hermaphrodite and male gonads in Caenorhabditis elegans
-
Kimble J., Hirsh D. The postembryonic cell lineages of the hermaphrodite and male gonads in Caenorhabditis elegans. Dev. Biol. 70:1979;396-417
-
(1979)
Dev. Biol.
, vol.70
, pp. 396-417
-
-
Kimble, J.1
Hirsh, D.2
-
24
-
-
0035838315
-
Drosophila homolog of the myotonic dystrophy-associated gene, SIX5, is required for muscle and gonad development
-
Kirby R.J., Hamilton G.M., Finnegan D.J., Johnson K.J., Jarman A.P. Drosophila homolog of the myotonic dystrophy-associated gene, SIX5, is required for muscle and gonad development. Curr. Biol. 11:2001;1044-1049
-
(2001)
Curr. Biol.
, vol.11
, pp. 1044-1049
-
-
Kirby, R.J.1
Hamilton, G.M.2
Finnegan, D.J.3
Johnson, K.J.4
Jarman, A.P.5
-
25
-
-
0030845879
-
Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP
-
Klesert T.R., Otten A.D., Bird T.D., Tapscott S.J. Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP. Nat. Genet. 16:1997;402-406
-
(1997)
Nat. Genet.
, vol.16
, pp. 402-406
-
-
Klesert, T.R.1
Otten, A.D.2
Bird, T.D.3
Tapscott, S.J.4
-
26
-
-
0034019306
-
Mice deficient in Six5 develop cataracts: Implications for myotonic dystrophy
-
Klesert T.R., Cho D.H., Clark J.I., Maylie J., Adelman J., Snider L., Yuen E.C., Soriano P., Tapscott S.J. Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy. Nat. Genet. 25:2000;105-109
-
(2000)
Nat. Genet.
, vol.25
, pp. 105-109
-
-
Klesert, T.R.1
Cho, D.H.2
Clark, J.I.3
Maylie, J.4
Adelman, J.5
Snider, L.6
Yuen, E.C.7
Soriano, P.8
Tapscott, S.J.9
-
27
-
-
0031691193
-
Overexpression of the forebrain-specific homeobox gene six3 induces rostral forebrain enlargement in zebrafish
-
Kobayashi M., Toyama R., Takeda H., Dawid I.B., Kawakami K. Overexpression of the forebrain-specific homeobox gene six3 induces rostral forebrain enlargement in zebrafish. Development. 125:1998;2973-2982
-
(1998)
Development
, vol.125
, pp. 2973-2982
-
-
Kobayashi, M.1
Toyama, R.2
Takeda, H.3
Dawid, I.B.4
Kawakami, K.5
-
28
-
-
0037080871
-
The T-box factor MLS-1 acts as a molecular switch during the specification of nonstriated muscle in C. elegans
-
Kostas S.A., Fire A. The T-box factor MLS-1 acts as a molecular switch during the specification of nonstriated muscle in C. elegans. Genes Dev. 16:2002;257-269
-
(2002)
Genes Dev.
, vol.16
, pp. 257-269
-
-
Kostas, S.A.1
Fire, A.2
-
29
-
-
0037561930
-
Altered myogenesis in Six1-deficient mice
-
Laclef C., Hamard G., Demignon J., Souil E., Houbron C., Maire P. Altered myogenesis in Six1-deficient mice. Development. 130:2003;2239-2252
-
(2003)
Development
, vol.130
, pp. 2239-2252
-
-
Laclef, C.1
Hamard, G.2
Demignon, J.3
Souil, E.4
Houbron, C.5
Maire, P.6
-
30
-
-
0034956322
-
Six3 promotes the formation of ectopic optic vesicle-like structures in mouse embryos
-
Lagutin O., Zhu C.C., Furuta Y., Rowitch D.H., McMahon A.P., Oliver G. Six3 promotes the formation of ectopic optic vesicle-like structures in mouse embryos. Dev. Dyn. 221:2001;342-349
-
(2001)
Dev. Dyn.
, vol.221
, pp. 342-349
-
-
Lagutin, O.1
Zhu, C.C.2
Furuta, Y.3
Rowitch, D.H.4
McMahon, A.P.5
Oliver, G.6
-
31
-
-
0035195553
-
Three C. elegans Rac proteins and several alternative Rac regulators control axon guidance, cell migration and apoptotic cell phagocytosis
-
Lundquist E.A., Reddien P.W., Hartwieg E., Horvitz H.R., Bargmann C.I. Three C. elegans Rac proteins and several alternative Rac regulators control axon guidance, cell migration and apoptotic cell phagocytosis. Development. 128:2001;4475-4488
-
(2001)
Development
, vol.128
, pp. 4475-4488
-
-
Lundquist, E.A.1
Reddien, P.W.2
Hartwieg, E.3
Horvitz, H.R.4
Bargmann, C.I.5
-
32
-
-
0025332945
-
Mutations affecting embryonic cell migrations in Caenorhabditis elegans
-
Manser J., Wood W.B. Mutations affecting embryonic cell migrations in Caenorhabditis elegans. Dev. Genet. 11:1990;49-64
-
(1990)
Dev. Genet.
, vol.11
, pp. 49-64
-
-
Manser, J.1
Wood, W.B.2
-
33
-
-
0028837546
-
Mechanosensory signalling in C. elegans mediated by the GLR-1 glutamate receptor
-
Maricq A.V., Peckol E., Driscoll M., Bargmann C.I. Mechanosensory signalling in C. elegans mediated by the GLR-1 glutamate receptor. Nature. 378:1995;78-81
-
(1995)
Nature
, vol.378
, pp. 78-81
-
-
Maricq, A.V.1
Peckol, E.2
Driscoll, M.3
Bargmann, C.I.4
-
35
-
-
0034703395
-
Skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase
-
Mounsey J.P., Mistry D.J., Ai C.W., Reddy S., Moorman J.R. Skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase. Hum. Mol. Genet. 9:2000;2313-2320
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2313-2320
-
-
Mounsey, J.P.1
Mistry, D.J.2
Ai, C.W.3
Reddy, S.4
Moorman, J.R.5
-
36
-
-
0029059218
-
Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure
-
Otten A.D., Tapscott S.J. Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure. Proc. Natl. Acad. Sci. U. S. A. 92:1995;5465-5469
-
(1995)
Proc. Natl. Acad. Sci. U. S. A.
, vol.92
, pp. 5465-5469
-
-
Otten, A.D.1
Tapscott, S.J.2
-
37
-
-
0033773030
-
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly
-
Pasquier L., Dubourg C., Blayau M., Lazaro L., Le Marec B., David V., Odent S. A new mutation in the six-domain of SIX3 gene causes holoprosencephaly. Eur. J. Hum. Genet. 8:2000;797-800
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 797-800
-
-
Pasquier, L.1
Dubourg, C.2
Blayau, M.3
Lazaro, L.4
Le Marec, B.5
David, V.6
Odent, S.7
-
38
-
-
0032076126
-
Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy
-
Philips A.V., Timchenko L.T., Cooper T.A. Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy. Science. 280:1998;737-741
-
(1998)
Science
, vol.280
, pp. 737-741
-
-
Philips, A.V.1
Timchenko, L.T.2
Cooper, T.A.3
-
39
-
-
0034103010
-
Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts
-
Sarkar P.S., Appukuttan B., Han J., Ito Y., Ai C., Tsai W., Chai Y., Stout J.T., Reddy S. Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts. Nat. Genet. 25:2000;110-114
-
(2000)
Nat. Genet.
, vol.25
, pp. 110-114
-
-
Sarkar, P.S.1
Appukuttan, B.2
Han, J.3
Ito, Y.4
Ai, C.5
Tsai, W.6
Chai, Y.7
Stout, J.T.8
Reddy, S.9
-
40
-
-
0034023675
-
The Drosophila homeobox gene optix is capable of inducing ectopic eyes by an eyeless-independent mechanism
-
Seimiya M., Gehring W.J. The Drosophila homeobox gene optix is capable of inducing ectopic eyes by an eyeless-independent mechanism. Development. 127:2000;1879-1886
-
(2000)
Development
, vol.127
, pp. 1879-1886
-
-
Seimiya, M.1
Gehring, W.J.2
-
41
-
-
0028019609
-
Sine oculis is a homeobox gene required for Drosophila visual system development
-
Serikaku M.A., O'Tousa J.E. Sine oculis is a homeobox gene required for Drosophila visual system development. Genetics. 138:1994;1137-1150
-
(1994)
Genetics
, vol.138
, pp. 1137-1150
-
-
Serikaku, M.A.1
O'Tousa, J.E.2
-
42
-
-
0032564423
-
Expression of myogenin during embryogenesis is controlled by Six/sine oculis homeoproteins through a conserved MEF3 binding site
-
Spitz F., Demignon J., Porteu A., Kahn A., Concordet J.P., Daegelen D., Maire P. Expression of myogenin during embryogenesis is controlled by Six/sine oculis homeoproteins through a conserved MEF3 binding site. Proc. Natl. Acad. Sci. U. S. A. 95:1998;14220-14225
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 14220-14225
-
-
Spitz, F.1
Demignon, J.2
Porteu, A.3
Kahn, A.4
Concordet, J.P.5
Daegelen, D.6
Maire, P.7
-
43
-
-
0017618537
-
Post-embryonic cell lineages of the nematode, Caenorhabditis elegans
-
Sulston J.E., Horvitz H.R. Post-embryonic cell lineages of the nematode, Caenorhabditis elegans. Dev. Biol. 56:1977;110-156
-
(1977)
Dev. Biol.
, vol.56
, pp. 110-156
-
-
Sulston, J.E.1
Horvitz, H.R.2
-
45
-
-
0030861573
-
Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene
-
Thornton C.A., Wymer J.P., Simmons Z., McClain C., Moxley R.T. III Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene. Nat. Genet. 16:1997;407-409
-
(1997)
Nat. Genet.
, vol.16
, pp. 407-409
-
-
Thornton, C.A.1
Wymer, J.P.2
Simmons, Z.3
McClain, C.4
Moxley III, R.T.5
-
46
-
-
0036817811
-
Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene
-
Wakimoto H., Maguire C.T., Sherwood M.C., Vargas M.M., Sarkar P.S., Han J., Reddy S., Berul C.I. Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene. J. Interv. Card Electrophysiol. 7:2002;127-135
-
(2002)
J. Interv. Card Electrophysiol.
, vol.7
, pp. 127-135
-
-
Wakimoto, H.1
Maguire, C.T.2
Sherwood, M.C.3
Vargas, M.M.4
Sarkar, P.S.5
Han, J.6
Reddy, S.7
Berul, C.I.8
-
47
-
-
0033064156
-
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
-
Wallis D.E., Roessler E., Hehr U., Nanni L., Wiltshire T., Richieri-Costa A., Gillessen-Kaesbach G., Zackai E.H., Rommens J., Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nat. Genet. 22:1999;196-198
-
(1999)
Nat. Genet.
, vol.22
, pp. 196-198
-
-
Wallis, D.E.1
Roessler, E.2
Hehr, U.3
Nanni, L.4
Wiltshire, T.5
Richieri-Costa, A.6
Gillessen-Kaesbach, G.7
Zackai, E.H.8
Rommens, J.9
Muenke, M.10
-
49
-
-
0032977087
-
Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy
-
Winchester C.L., Ferrier R.K., Sermoni A., Clark B.J., Johnson K.J. Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy. Hum. Mol. Genet. 8:1999;481-492
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 481-492
-
-
Winchester, C.L.1
Ferrier, R.K.2
Sermoni, A.3
Clark, B.J.4
Johnson, K.J.5
|