-
1
-
-
0029653613
-
Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence
-
Adams, M. D., Kerlavage, A. R., Fleischmann, R. D., Fuldner, R. A., Bult, C. J., Lee, N. H., Kirkness, E. F., Weinstock, K. G., Gocayne, J. D., White, O., Sutton, G., Blake, J. A., Brandon, R. C, Chui, M.-W., Clayton, R. A., Cline, R. T., Cotton, M. D., Earle-Hughes, J., Fine, L. D., FitzGerald, L. M., FitzHugh, W. M., Fritchman, J. L., Geoghagen, N. S. M, Glodek, A., Gnehm, C. L., Hanna, M. C, Hedblom, E., Hinkle, P. S. Jr., Kelley, J. M., Klimek, K. M., Kelley, J. C, Liu, L.-L, Marmaros, S. M., Merrick, J. M., Moreno-Palanques, R. F., McDonald, L. A., Nguyen, D. T., Pellegrino, S. M., Phillips, C. A., Ryder, S. E., Scott, J. L., Saudek, D. M., Shirley, R., Small, K. V., Spriggs, T. A' Utterback, T. R., Weidman, J. F., Li, Y' Barthlow, R., Bednarik, D. P., Cao, L., Cepeda, M. A., Coleman, T. A., Collins, E.-J., Dimke, D., Feng, P., Ferrie, A., Fischer, C, Hastings, G. A., He, W.-W., Hu, J.-S., Huddleston, K. A., Greene, J. M., Gruber, J., Hudson, P., Kim, A., Kozak, D. L., Kunsch, C, Ji, H., Li, H., Meissner, P. S., Olsen, H., Raymond, L., Wei, Y.-F., Wing, J., Xu, C, Yu, G.-L., Ruben, S. M., Dillon, P. J., Fannon, M. R., Rosen, C. A., Haseltine, W. A., Fields, C, Fraser, C. and Venter, J. C. (1995) "Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence", Nature, 377, 3-174.
-
(1995)
Nature
, vol.377
, pp. 3-174
-
-
Adams, M.D.1
Kerlavage, A.R.2
Fleischmann, R.D.3
Fuldner, R.A.4
Bult, C.J.5
Lee, N.H.6
Kirkness, E.F.7
Weinstock, K.G.8
Gocayne, J.D.9
White, O.10
Sutton, G.11
Blake, J.A.12
Brandon, R.C.13
Chui, M.-W.14
Clayton, R.A.15
Cline, R.T.16
Cotton, M.D.17
Earle-Hughes, J.18
Fine, L.D.19
Fitzgerald, L.M.20
Fitzhugh, W.M.21
Fritchman, J.L.22
Geoghagen, N.S.M.23
Glodek, A.24
Gnehm, C.L.25
Hanna, M.C.26
Hedblom, E.27
Hinkle Jr., P.S.28
Kelley, J.M.29
Klimek, K.M.30
Kelley, J.C.31
Liu, L.-L.32
Marmaros, S.M.33
Merrick, J.M.34
Moreno-Palanques, R.F.35
McDonald, L.A.36
Nguyen, D.T.37
Pellegrino, S.M.38
Phillips, C.A.39
Ryder, S.E.40
Scott, J.L.41
Saudek, D.M.42
Shirley, R.43
Small, K.V.44
Spriggs, T.A.45
Utterback, T.R.46
Weidman, J.F.47
Li, Y.48
Barthlow, R.49
Bednarik, D.P.50
Cao, L.51
Cepeda, M.A.52
Coleman, T.A.53
Collins, E.-J.54
Dimke, D.55
Feng, P.56
Ferrie, A.57
Fischer, C.58
Hastings, G.A.59
He, W.-W.60
Hu, J.-S.61
Huddleston, K.A.62
Greene, J.M.63
Gruber, J.64
Hudson, P.65
Kim, A.66
Kozak, D.L.67
Kunsch Ji C, H.68
Li, H.69
Meissner, P.S.70
Olsen, H.71
Raymond, L.72
Wei, Y.-F.73
Wing, J.74
Xu Yu C, G.-L.75
Ruben, S.M.76
Dillon, P.J.77
Fannon, M.R.78
Rosen, C.A.79
Haseltine, W.A.80
Fields Fraser C, C.81
Venter, J.C.82
more..
-
2
-
-
0025882349
-
PROSITE: A dictionary of sites and patterns in proteins
-
Bairoch, A. (1991) "PROSITE: a dictionary of sites and patterns in proteins", Nucleic Acid Res., 19 (Suppl.), 2241-2245.
-
(1991)
Nucleic Acid Res.
, vol.19
, Issue.SUPPL.
, pp. 2241-2245
-
-
Bairoch, A.1
-
3
-
-
0028023078
-
Molecular cloning of a protein serine/threonine phosphatase containing a putative regulatory tetratricopeptide repeat domain
-
Becker, W., Kentrup, H., Klumpp, S., Schultz, J. E. and Joost, H. G. (1994) "Molecular cloning of a protein serineJthreonine phosphatase containing a putative regulatory tetratri-copepfide repeat domain", J. Biol. Chem., 269,22586-22592. (Pubitemid 24273364)
-
(1994)
Journal of Biological Chemistry
, vol.269
, Issue.36
, pp. 22586-22592
-
-
Becker, W.1
Kentrup, H.2
Klumpp, S.3
Schultz, J.E.4
Joost, H.G.5
-
4
-
-
0028949226
-
+Jmyo-inositol cotransporter gene (SLC5A3): Molecular cloning and localization of chromosome 21
-
+Jmyo-inositol cotransporter gene (SLC5A3): molecular cloning and localization of chromosome 21", Genomics, 25,507-513.
-
(1995)
Genomics
, vol.25
, pp. 507-513
-
-
Berry, G.T.1
Mallee, J.I.2
Kwon, H.M.3
Rim, J.S.4
Mulla, W.R.5
Muenke, M.6
Spinner, N.B.7
-
5
-
-
0028886136
-
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
Bonne, G., Carrier, L., Bercovici, J., Cruaud, C, Richard, P., Hainque, B., Gautel, M., Labeit, S., James, M., Beckmann, J., Weissenbach, J., Vosberg, H.-P., Fiszman, M., Komajda, M. and Schwartz, K. (1995) "Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy", Nature Genet, 11,438-440.
-
(1995)
Nature Genet
, vol.11
, pp. 438-440
-
-
Bonne, G.1
Carrier, L.2
Bercovici, J.3
Cruaud, C.4
Richard, P.5
Hainque, B.6
Gautel, M.7
Labeit, S.8
James, M.9
Beckmann, J.10
Weissenbach, J.11
Vosberg, H.-P.12
Fiszman, M.13
Komajda, M.14
Schwartz, K.15
-
6
-
-
0029302628
-
Single-minded and Down syndrome?
-
Chen, H., Chrast, R., Rossier, C, Gos, A., Antonarakis, S., Kudoh, J., Yamaki, A., Shindoh, N., Maeda, H., Minoshima, S. and Shimizu, N. (1995a) "Single-minded and Down syndrome?", Nature Genet., 10,9-10.
-
(1995)
Nature Genet.
, vol.10
, pp. 9-10
-
-
Chen, H.1
Chrast, R.2
Rossier, C.3
Gos, A.4
Antonarakis, S.5
Kudoh, J.6
Yamaki, A.7
Shindoh, N.8
Maeda, H.9
Minoshima, S.10
Shimizu, N.11
-
7
-
-
0029135016
-
Cloning of the cDNA for the human ATP synthase OSCP subunit (ATP50) by exon trapping and mapping to chromosome 2lq22.1-q22.2
-
Chen, H., Morris, M. A., Rossier, C, Blouin, J. L. and Antonarakis, S. E. (1995b) "Cloning of the cDNA for the human ATP synthase OSCP subunit (ATP50) by exon trapping and mapping to chromosome 2lq22.1-q22.2", Genomics, 28, 470-476.
-
(1995)
Genomics
, vol.28
, pp. 470-476
-
-
Chen, H.1
Morris, M.A.2
Rossier, C.3
Blouin, J.L.4
Antonarakis, S.E.5
-
8
-
-
0002758687
-
Marathon™ cDNA amplification: A new method for cloning full-length cDNAs
-
Chenchik, A., Moqadam, F. and Siebert, P. D. (1995) "Marathon™ cDNA amplification: a new method for cloning full-length cDNAs", CLONTECHniques, X, 5-8.
-
(1995)
CLONTECHniques
, vol.10
, pp. 5-8
-
-
Chenchik, A.1
Moqadam, F.2
Siebert, P.D.3
-
9
-
-
0028117770
-
Targeting of a distinctive protein-serine phosphatase to the protein kinase-like domain of the strial natriuretic peptide receptor
-
Clunkers, M. (1994) "Targeting of a distinctive protein-serine phosphatase to the protein kinase-like domain of the strial natriuretic peptide receptor", Proc. Natl. Acad. Sci. USA, 91, 11075-11079.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 11075-11079
-
-
Clunkers, M.1
-
10
-
-
0023835990
-
The single-minded gene of Drosophila is required for the expression of genes important for the development of CNS midline cells
-
Crews, S. T., Thomas, J. B. and Goodman, C. S. (1988) "The single-minded gene of Drosophila is required for the expression of genes important for the development of CNS midline cells", Cell, 52,143-151.
-
(1988)
Cell
, vol.52
, pp. 143-151
-
-
Crews, S.T.1
Thomas, J.B.2
Goodman, C.S.3
-
11
-
-
0029025925
-
Down syndrome-critical region contains a gene homologous to Drosophila sim expressed during rat and human central nervous system development
-
Dahmane, N., Charron, G., Lopes, C, Yaspo, M.-L., Maunoury, C, Decorte, L., Sinet, P.-M., Bloch, B. and Delabar, J.-M. (1995) "Down syndrome-critical region contains a gene homologous to Drosophila sim expressed during rat and human central nervous system development", Proc. Natl. Acad. Sci. USA, 92,9191-9195.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 9191-9195
-
-
Dahmane, N.1
Charron, G.2
Lopes, C.3
Yaspo, M.-L.4
Maunoury, C.5
Decorte, L.6
Sinet, P.-M.7
Bloch, B.8
Delabar, J.-M.9
-
12
-
-
0028344760
-
3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21
-
Dufrensne-Zacharia, M.-C, Dahmane, N., Theophile, D., Orti, R' Chettouh, Z., Sinet, P.-M. and Delabar, J.-M. (1994) "3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21", Genomics, 19,462-169.
-
(1994)
Genomics
, vol.19
, pp. 462-169
-
-
Dufrensne-Zacharia, M.-C.1
Dahmane, N.2
Theophile, D.3
Orti, R.4
Chettouh, Z.5
Sinet, P.-M.6
Delabar, J.-M.7
-
13
-
-
0030038105
-
1.8-Mb megabases fine physical map encompassing IFNAR and AML1 loci on human chromosome 21q22.1
-
Eki, T., Abe, M., Furuya, K., Fujishima, N., Kishida, H., Shiratori, A., Yokoyama, K., Le Paslier, D., Cohen, D. and Murakami, Y. (1996) "1.8-Mb megabases fine physical map encompassing IFNAR and AML1 loci on human chromosome 21q22.1", DNA Sequence, 6, 95-108.
-
(1996)
DNA Sequence
, vol.6
, pp. 95-108
-
-
Eki, T.1
Abe, M.2
Furuya, K.3
Fujishima, N.4
Kishida, H.5
Shiratori, A.6
Yokoyama, K.7
Le Paslier, D.8
Cohen, D.9
Murakami, Y.10
-
14
-
-
0028856422
-
A new human gene from the Down's syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart
-
Fuentes, J. J., Pritchard, M. A., Planas, A. M, Bosch, A., Ferrer, I. and Estivill, X. (1995) "A new human gene from the Down's syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart", Human Mol. Genet., 4,1935-1944.
-
(1995)
Human Mol. Genet.
, vol.4
, pp. 1935-1944
-
-
Fuentes, J.J.1
Pritchard, M.A.2
Planas, A.M.3
Bosch, A.4
Ferrer, I.5
Estivill, X.6
-
15
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A beta cardiac myosin heavy chain gene mis-sense mutation
-
Geisterfer-Lowrance, A. A., Kass, S., Tanigawa, G., Vosberg, H. P., McKenna, W., Seidman, C. E. and Seidman, J. G. (1990) "A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene mis-sense mutation", Cell, 62, 999-1006.
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.P.4
McKenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
16
-
-
0029240247
-
A high-resolution map of 1.6 Mb in the Down syndrome region: A new map between D21S55 and ETS2
-
Gosset, P., Crete, N., Ait Ghezala, G., Theophile, D., Van Broeckhoven, C, Vayssettes, C, Sinet, P. M. and Creau, N. (1995) "A high-resolution map of 1.6 Mb in the Down syndrome region: a new map between D21S55 and ETS2", Mammalian Genome, 6, 127-130.
-
(1995)
Mammalian Genome
, vol.6
, pp. 127-130
-
-
Gosset, P.1
Crete, N.2
Ait Ghezala, G.3
Theophile, D.4
Van Broeckhoven, C.5
Vayssettes, C.6
Sinet, P.M.7
Creau, N.8
-
17
-
-
0025018004
-
Structure and function of profilin
-
Haarer, B. K. and Brown, S. S. (1990) "Structure and function of profilin", Cell Motil Cytoskeleton, 17, 71-74. (Pubitemid 20372174)
-
(1990)
Cell Motility and the Cytoskeleton
, vol.17
, Issue.2
, pp. 71-74
-
-
Haarer, B.K.1
Brown, S.S.2
-
18
-
-
0000207681
-
TMBASE-A database of membrane spanning protein segments
-
Hofmann, K. and Stoffel, W. (1993) "TMBASE-A database of membrane spanning protein segments", Biol. Chem. Hoppe-Seyler, 374,166.
-
(1993)
Biol. Chem. Hoppe-Seyler
, vol.374
, pp. 166
-
-
Hofmann, K.1
Stoffel, W.2
-
19
-
-
0025891138
-
Homology of a 150K cytoplasmic dynein-associated polypeptide with the Drosophila gene Glued
-
Holzbaur, E. L., Hammarback, J. A., Paschal, B. M., Kravit, N. G., Pfister, K. K. and Vallee, R. B. (1991) "Homology of a 150K cytoplasmic dynein-associated polypeptide with the Drosophila gene Glued", Nature, 351, 579-583. (Pubitemid 21896645)
-
(1991)
Nature
, vol.351
, Issue.6327
, pp. 579-583
-
-
Holzbaur, E.L.F.1
Hammarback, J.A.2
Paschal, B.M.3
Kravrt, N.G.4
Pfister, K.K.5
Vallee, R.B.6
-
20
-
-
0027184311
-
A NotI restriction map of the entire long arm of human chromosome 21
-
DOI 10.1038/ng0893-361
-
Ichikawa, H, Hosoda, F., Arai, Y., Shimizu, K., Ohira, M. and Ohki, M. (1993) "A Not I restriction map of the entire long arm of human chromosome 21", Nature Genet, 4, 361-366. (Pubitemid 23231484)
-
(1993)
Nature Genetics
, vol.4
, Issue.4
, pp. 361-366
-
-
Ichikawa, H.1
Hosoda, F.2
Arai, Y.3
Shimizu, K.4
Ohira, M.5
Ohki, M.6
-
21
-
-
0025259313
-
Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes
-
Karlin, S. and Altschul, S. F. (1990) "Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes", Proc. Natl. Acad. Sci. USA, 87, 2264-2268.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 2264-2268
-
-
Karlin, S.1
Altschul, S.F.2
-
22
-
-
0028341315
-
Down syndrome phenotypes: The consequences of chromosomal imbalance
-
DOI 10.1073/pnas.91.11.4997
-
Korenberg, J. R., Chen, X.-N., Schipper, R., Sun, Z., Gonsky, R., Gerwehr, S., Carpenter, N., Daumer, C, Dignan, P., Disteche, C, Grahm, J. M. Jr., Hugdins, L., McGillivay, B., Miyazaki, K., Ogasawara, N., Park, J. P., Pagon, R., Pueshel, S., Sack, G., Say, B., Schuffenhauer, S., Soukup, S. and Yamanaka, T. (1994) "Down syndrome phenotypes: The consequences of chromosomal imbalance", Proc. Natl. Acad. Sci. USA, 91,4997-5001. (Pubitemid 24177778)
-
(1994)
Proceedings of the National Academy of Sciences of the United States of America
, vol.91
, Issue.11
, pp. 4997-5001
-
-
Korenberg, J.R.1
Chen, X.-N.2
Schipper, R.3
Sun, Z.4
Gonsky, R.5
Gerwehr, S.6
Carpenter, N.7
Daumer, C.8
Dignan, P.9
Disteche, C.10
Graham Jr., J.M.11
Hugdins, L.12
Mcgillivray, B.13
Miyazaki, K.14
Ogasawara, N.15
Park, J.P.16
Pagon, R.17
Pueschel, S.18
Sack, G.19
Say, B.20
Schuffenhauer, S.21
Soukup, S.22
Yamanaka, T.23
more..
-
23
-
-
0020475449
-
A simple method for displaying the hydropathic character of a protein
-
Kyte, J. and Doolittle, R. F. (1982) "A simple method for displaying the hydropathic character of a protein", J. Mol. Biol, 157,105-132.
-
(1982)
J. Mol. Biol
, vol.157
, pp. 105-132
-
-
Kyte, J.1
Doolittle, R.F.2
-
24
-
-
0028787577
-
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 impor-tantfor Down syndrome
-
Muenke, M., Bone, L. J., Mitchell, H. F., Hart, I., Walton, K., Hall-Johnson, K., Ippel, E. F., Dietz-Band,J., Kvaloy, K, Fan, C.-M., Tessier-Lavigne, M. and Patterson, D. (1995) "Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 impor-tantfor Down syndrome", Am. J. Human Genet., 57,1074-1079.
-
(1995)
Am. J. Human Genet.
, vol.57
, pp. 1074-1079
-
-
Muenke, M.1
Bone, L.J.2
Mitchell, H.F.3
Hart, I.4
Walton, K.5
Hall-Johnson, K.6
Ippel, E.F.7
Dietz-Band, J.8
Kvaloy, K.9
Fan, C.-M.10
Tessier-Lavigne, M.11
Patterson, D.12
-
25
-
-
0029016299
-
Analysis of the nucleotide sequence of chromosome VI from Saccharomyces cerevisiae
-
Murakami, Y., Naitou, M., Hagiwara, H, Shibata, T., Ozawa, M., Sasanuma, S., Sasanuma, M., Tsuchiya, Y., Soeda, E., Yokoyama, K., Yamazaki, M., Tashiro, H. and Eki, T. (1995) "Analysis of the nucleotide sequence of chromosome VI from Saccharomyces cerevisiae", Nature Genet., 10,261-268.
-
(1995)
Nature Genet.
, vol.10
, pp. 261-268
-
-
Murakami, Y.1
Naitou, M.2
Hagiwara, H.3
Shibata, T.4
Ozawa, M.5
Sasanuma, S.6
Sasanuma, M.7
Tsuchiya, Y.8
Soeda, E.9
Yokoyama, K.10
Yamazaki, M.11
Tashiro, H.12
Eki, T.13
-
26
-
-
17644430449
-
A 1.6-Mb P1-based physical map of the Down syndrome region on chromosome 21
-
DOI 10.1006/geno.1996.0160
-
Ohira, M., Ichikawa, H., Suzuki, E., Iwaki, M., Suzuki, K., Saito-Ohara, F., Ikeuchi, T., Chumakov, I., Tanahashi, H, Tashiro, K., Sakaki, Y. and Ohki, M. (1996a) "A 1.6-Mb Pl-based physical map of the Down syndrome region on chromosome 21", Genomics, 33, 65-74. (Pubitemid 26119396)
-
(1996)
Genomics
, vol.33
, Issue.1
, pp. 65-74
-
-
Ohira, M.1
Ichikawa, H.2
Suzuki, E.3
Iwaki, M.4
Suzuki, K.5
Saito-Ohara, F.6
Ikeuchi, T.7
Chumakov, I.8
Tanahashi, H.9
Tashiro, K.10
Sakaki, Y.11
Ohki, M.12
-
27
-
-
0030605426
-
Identification of a novel human gene containing the tetratricopeptide repeat domain from the Down syndrome region of chromosome 21
-
Ohira, M., Ootsuyama, A., Suzuki, E., Ichikawa, H., Seki, N., Nagase, T., Nomura, N. and Ohki, M. (1996b) "Identification of a novel human gene containing the tetratricopeptide repeat domain from the Down syndrome region of chromosome 21", DNA Res., 3,9-16. (Pubitemid 126682807)
-
(1996)
DNA Research
, vol.3
, Issue.1
, pp. 9-16
-
-
Ohira, M.1
Ootsuyama, A.2
Suzuki, E.3
Ichikawa, H.4
Seki, N.5
Nagase, T.6
Nomura, N.7
Ohki, M.8
-
28
-
-
0028076769
-
A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21
-
Patil, N., Peterson, A., Rothman, A., de Jong, P. J., Myers, R. M. and Cox, D. R. (1994) "A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21", Human Mol. Genet., 3,1811-1817. (Pubitemid 24310476)
-
(1994)
Human Molecular Genetics
, vol.3
, Issue.10
, pp. 1811-1817
-
-
Patil, N.1
Peterson, A.2
Rothman, A.3
De Jong, P.J.4
Myers, R.M.5
Cox, D.R.6
-
29
-
-
0028839912
-
Thymic abnormalities and enhanced apoptosis of thymocytes and bone marrow cells in transgenic mice over-expressing CuJZn-superoxide dismutase: Implications of Down syndrome
-
Peled-Kamar, M., Lotem, J., Okon, E., Sachs, L. and Groner, Y. (1995) "Thymic abnormalities and enhanced apoptosis of thymocytes and bone marrow cells in transgenic mice over-expressing CuJZn-superoxide dismutase: implications of Down syndrome", EMBO J., 14, 4985-4993.
-
(1995)
EMBO J.
, vol.14
, pp. 4985-4993
-
-
Peled-Kamar, M.1
Lotem, J.2
Okon, E.3
Sachs, L.4
Groner, Y.5
-
30
-
-
0028147991
-
A transcript map of the Down syndrome critical region on chromosome 21
-
Peterson, A., Patil, N., Robbins, C, Wang, L., Cox, D. R. and Myers, R. M. (1994) "A transcript map of the Down Syndrome critical region on chromosome 21", Human Mol Genet, 3, 1735-1742. (Pubitemid 24310464)
-
(1994)
Human Molecular Genetics
, vol.3
, Issue.10
, pp. 1735-1742
-
-
Peterson, A.1
Patil, N.2
Robbins, C.3
Wang, L.4
Cox, D.R.5
Myers, R.M.6
-
31
-
-
0012083187
-
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
-
Rahmani, Z., Blouin, J. L., Creau-Goldberg, N., Watkins, P. C, Mattei, J. F., Poissonnier, M., Prieur, M., Chettouh, Z., Nicole, A' Aurias, A., Sinet, P. M. and Delabar, J. M. (1989) "Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome", Proc. Natl. Acad. Sci. USA, 86,5958-5962. (Pubitemid 19217567)
-
(1989)
Proceedings of the National Academy of Sciences of the United States of America
, vol.86
, Issue.15
, pp. 5958-5962
-
-
Rahmani, Z.1
Blouin, J.-L.2
Creau-Goldberg, N.3
Watkins, P.C.4
Mattei, J.-F.5
Poissonnier, M.6
Prieur, M.7
Chettouh, Z.8
Nicole, A.9
Aurias, A.10
Sinet, P.-M.11
Delabar, J.-M.12
-
32
-
-
0029114706
-
A mouse model for Down syndrome exhibits learning and behaviour deficits
-
Reeves, R. H., Irving, N. G., Moran, T. H' Wohn, A., Kitt, C, Sinsodia, S. S., Schmidt, C, Bronson, R. T. and Davisson, M. T. (1995) "A mouse model for Down syndrome exhibits learning and behaviour deficits", Nature Genet., 11, 177-184.
-
(1995)
Nature Genet.
, vol.11
, pp. 177-184
-
-
Reeves, R.H.1
Irving, N.G.2
Moran, T.H.3
Wohn, A.4
Kitt, C.5
Sinsodia, S.S.6
Schmidt, C.7
Bronson, R.T.8
Davisson, M.T.9
-
33
-
-
0004136246
-
-
2nd ed., (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY)
-
Sambrook, J., Fritsch, E. F. and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual, 2nd ed., (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY).
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
34
-
-
0020082091
-
Down's syndrome as a model disease
-
DOI 10.1001/archinte.142.3.462
-
Scoggin, C. H. and Patterson, D. (1982) "Down's syndrome as a model disease", Arch. Int. Med., 142, 462-464. (Pubitemid 12190732)
-
(1982)
Archives of Internal Medicine
, vol.142
, Issue.3
, pp. 462-464
-
-
Scoggin, C.H.1
Patterson, D.2
-
35
-
-
0028814298
-
Report of the fifth international workshop on human chromosome 21 mapping 1994
-
Shimizu, N., Antonarakis, S. E., Van Brockhoven, C, Patterson, D., Gardiner, K., Nizetic, D., Creau, N., Delabar, J.-M., Korenberg, J., Reeves, R., Doering, J., Chakravarti, A., Minoshirna, S., Ritter, O. and Cuticchia, J. (1995) "Report of the fifth international workshop on human chromosome 21 mapping 1994", Cytogenet. Cell Genet., 70,147-182.
-
(1995)
Cytogenet. Cell Genet.
, vol.70
, pp. 147-182
-
-
Shimizu, N.1
Antonarakis, S.E.2
Van Brockhoven, C.3
Patterson, D.4
Gardiner, K.5
Nizetic, D.6
Creau, N.7
Delabar, J.-M.8
Korenberg, J.9
Reeves, R.10
Doering, J.11
Chakravarti, A.12
Minoshirna, S.13
Ritter, O.14
Cuticchia, J.15
-
36
-
-
0029587531
-
An infrared fluorescent dATP for labeling DNA
-
Steffens, D. L., Jang, G. Y., Sutter, S. L., Brumbaugh, J. A., Middendorf, L. R., Muhlegger, K., Mardis, E. R., Weinstock, L. A. and Wilson, R. K. (1995) "An infrared fluorescent dATP for labeling DNA", Genome Res., 5, 393-399. (Pubitemid 26016745)
-
(1995)
Genome Research
, vol.5
, Issue.4
, pp. 393-399
-
-
Steffens, D.L.1
Jang, G.Y.2
Sutter, S.L.3
Brumbaugh, J.A.4
Middendorf, L.R.5
Muhlegger, K.6
Mardis, E.R.7
Weinstock, L.A.8
Wilson, R.K.9
-
37
-
-
0025164036
-
A molecular basis for familial hypertrophic cardiomyopathy: An alpha Jbeta cardiac nyosin heavy chain hybrid gene
-
Tanigawa, G., Jarcho, J. A., Kass, S., Solomon, S. D., Vosberg, H. P., Seidman, J. G. and Seidman, C. E. (1990) "A molecular basis for familial hypertrophic cardiomyopathy: an alpha Jbeta cardiac nyosin heavy chain hybrid gene", Cell, 62,991-998.
-
(1990)
Cell
, vol.62
, pp. 991-998
-
-
Tanigawa, G.1
Jarcho, J.A.2
Kass, S.3
Solomon, S.D.4
Vosberg, H.P.5
Seidman, J.G.6
Seidman, C.E.7
-
38
-
-
0026351408
-
Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach
-
Uberbacher, E. C. and Mural, R. J. (1991) "Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach", Proc. Natl. Acad. Sci. USA, 88, 11261-11265. (Pubitemid 21916020)
-
(1991)
Proceedings of the National Academy of Sciences of the United States of America
, vol.88
, Issue.24
, pp. 11261-11265
-
-
Uberbacher, E.C.1
Mural, R.J.2
-
39
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins, H., Conner, D., Thierfelder, L., Jarcho, J. A., MacRae, C, McKenna, W. J., Maron, B. J., Seidman, J. G. and Seidman, C. E. (1995) "Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy", Nature Genet., 11, 434-437.
-
(1995)
Nature Genet.
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
Jarcho, J.A.4
MacRae, C.5
McKenna, W.J.6
Maron, B.J.7
Seidman, J.G.8
Seidman, C.E.9
-
40
-
-
0028835212
-
BEAUTY: An enhanced BL AST-based search tool that integrates multiple biological information resources into sequence similarity search results
-
Worley, K. C, Wiese, B. A. and Smith, R. F. (1995) "BEAUTY: An enhanced BL AST-based search tool that integrates multiple biological information resources into sequence similarity search results", Genome Res., 5,173-184.
-
(1995)
Genome Res.
, vol.5
, pp. 173-184
-
-
Worley, K.C.1
Wiese, B.A.2
Smith, R.F.3
-
41
-
-
0026767624
-
CENP-E is a putative kinetochore motor that accumulates just before mitosis
-
Yen, T. J., Li, G., Schaar, B. T., Szilak, I. and Cleveland, D. W. (1992) "CENP-E is a putative kinetochore motor that accumulates just before mitosis", Nature, 359, 536-539.
-
(1992)
Nature
, vol.359
, pp. 536-539
-
-
Yen, T.J.1
Li, G.2
Schaar, B.T.3
Szilak, I.4
Cleveland, D.W.5
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