-
1
-
-
0026322066
-
Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4
-
Altherr M. R., Bengtsson U., Elder F. F. B., Ledbetter D. H., Wasmuth J. J., McDonald M. E., Gusella J. F., Greenberg F. Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4. Am. J. Hum. Genet. 49:1991;1235-1242.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 1235-1242
-
-
Altherr, M.R.1
Bengtsson, U.2
Elder, F.F.B.3
Ledbetter, D.H.4
Wasmuth, J.J.5
McDonald, M.E.6
Gusella, J.F.7
Greenberg, F.8
-
2
-
-
0025183708
-
Basic local alignment search tool
-
Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J. Mol. Biol. 215:1990;403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
3
-
-
0028928132
-
IMAGE: Integrated molecular analysis of the human genome and its expression
-
Auffray C., Behar G., Bois F., Bouchier C., Dasilva C., Devignes M., Duprat S., Houlgatte R., Jumeau M., Lamy B., Lorenzo F., Mitchell H., Mariagesamson R., Pietu G., Pouliot Y., Sebastianikabaktchis C., Tessier A. IMAGE: Integrated molecular analysis of the human genome and its expression. C.R. Acad. Sci. III. 318:1995;263-272.
-
(1995)
C.R. Acad. Sci. III
, vol.318
, pp. 263-272
-
-
Auffray, C.1
Behar, G.2
Bois, F.3
Bouchier, C.4
Dasilva, C.5
Devignes, M.6
Duprat, S.7
Houlgatte, R.8
Jumeau, M.9
Lamy, B.10
Lorenzo, F.11
Mitchell, H.12
Mariagesamson, R.13
Pietu, G.14
Pouliot, Y.15
Sebastianikabaktchis, C.16
Tessier, A.17
-
4
-
-
0025896024
-
Defined physical limits of the Huntington disease gene candidate region
-
Bates G. P., MacDonald M. E., Baxendale S., Youngman S., Lin C., Whaley W. L., Wasmuth J. J., Gusella J. F., Lehrach H. Defined physical limits of the Huntington disease gene candidate region. Am. J. Hum. Genet. 49:1991;7-16.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 7-16
-
-
Bates, G.P.1
MacDonald, M.E.2
Baxendale, S.3
Youngman, S.4
Lin, C.5
Whaley, W.L.6
Wasmuth, J.J.7
Gusella, J.F.8
Lehrach, H.9
-
5
-
-
0027310529
-
A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene
-
Baxendale S., MacDonald M. E., Mott R., Francis F., Lin C., Kirby S. F., James M., Zehetner G., Hummerich H., Valdes J., Collins F. S., Deaven L. J., Gusella J. F., Lehrach H., Bates G. P. A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene. Nat. Genet. 4:1993;181-186.
-
(1993)
Nat. Genet.
, vol.4
, pp. 181-186
-
-
Baxendale, S.1
MacDonald, M.E.2
Mott, R.3
Francis, F.4
Lin, C.5
Kirby, S.F.6
James, M.7
Zehetner, G.8
Hummerich, H.9
Valdes, J.10
Collins, F.S.11
Deaven, L.J.12
Gusella, J.F.13
Lehrach, H.14
Bates, G.P.15
-
6
-
-
0005828441
-
4p microdeletion in a child with Pitt-Rogers-Danks syndrome
-
Clemens M., McPherson E. W., Surt U. 4p microdeletion in a child with Pitt-Rogers-Danks syndrome. Am. J. Hum. Genet. 57:1995;A85.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 85
-
-
Clemens, M.1
McPherson, E.W.2
Surt, U.3
-
7
-
-
0030784958
-
Mechanism and regulation of mRNA polyadenylation
-
Colgan D. F., Manley J. L. Mechanism and regulation of mRNA polyadenylation. Genes Dev. 11:1997;2755-2766.
-
(1997)
Genes Dev.
, vol.11
, pp. 2755-2766
-
-
Colgan, D.F.1
Manley, J.L.2
-
8
-
-
0028137737
-
Bone morphogenetic proteins and a signaling pathway that controls patterning in the the developing chick limb
-
Francis P. H., Richardson M. K., Brickell P. M., Tickle C. Bone morphogenetic proteins and a signaling pathway that controls patterning in the the developing chick limb. Development. 120:1994;209-218.
-
(1994)
Development
, vol.120
, pp. 209-218
-
-
Francis, P.H.1
Richardson, M.K.2
Brickell, P.M.3
Tickle, C.4
-
9
-
-
0029034805
-
Expression of genes encoding bone morphogenetic proteins and sonic hedgehog in Talpid (TA(3)) limb buds: Their relationships in the signaling cascade involved in limb patterning
-
FrancisWest P. H., Robertson K. E., Ede D. A., Rodriguez C., Izpisuabelmonte J. C., Houston B., Burt D. W., Gribbin C., Brickell P. M., Tickle C. Expression of genes encoding bone morphogenetic proteins and sonic hedgehog in Talpid (TA(3)) limb buds: Their relationships in the signaling cascade involved in limb patterning. Dev. Dyn. 203:1995;187-197.
-
(1995)
Dev. Dyn.
, vol.203
, pp. 187-197
-
-
Franciswest, P.H.1
Robertson, K.E.2
Ede, D.A.3
Rodriguez, C.4
Izpisuabelmonte, J.C.5
Houston, B.6
Burt, D.W.7
Gribbin, C.8
Brickell, P.M.9
Tickle, C.10
-
10
-
-
0013834960
-
Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion
-
Hirschhorn K., Cooper H. L., Firschein I. L. Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion. Humangenetik. 1:1965;479-482.
-
(1965)
Humangenetik
, vol.1
, pp. 479-482
-
-
Hirschhorn, K.1
Cooper, H.L.2
Firschein, I.L.3
-
11
-
-
0000207681
-
TMbase - A database of membrane spanning protein segments
-
Hofmann K., Stoffel W. TMbase - A database of membrane spanning protein segments. Biol. Chem. Hoppe-Seyler. 374:1993;166.
-
(1993)
Biol. Chem. Hoppe-Seyler
, vol.374
, pp. 166
-
-
Hofmann, K.1
Stoffel, W.2
-
12
-
-
0027965882
-
FISH detection of Wolf-Hirschhorn syndrome: Exclusion of D4F26 as critical site
-
Johnson W. P., Altherr M. R., Blake J. M., Keppen L. D. FISH detection of Wolf-Hirschhorn syndrome: Exclusion of D4F26 as critical site. Am. J. Med. Genet. 52:1994;70-74.
-
(1994)
Am. J. Med. Genet.
, vol.52
, pp. 70-74
-
-
Johnson, W.P.1
Altherr, M.R.2
Blake, J.M.3
Keppen, L.D.4
-
13
-
-
0030746880
-
Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3
-
Kant S. G., van Haeringen A., Bakker E., Stec I., Donnai D., Mollevanger P., Beverstock G. C., Lindeman-Kusse M. C., van Ommen G.-J. B. Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3. J. Med. Genet. 34:1997;569-572.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 569-572
-
-
Kant, S.G.1
Van Haeringen, A.2
Bakker, E.3
Stec, I.4
Donnai, D.5
Mollevanger, P.6
Beverstock, G.C.7
Lindeman-Kusse, M.C.8
Van Ommen, G.-J.B.9
-
14
-
-
0030213227
-
Interpreting cDNA sequences: Some insights from studies on translation
-
Kozak M. Interpreting cDNA sequences: Some insights from studies on translation. Mamm. Genome. 7:1996;563-574.
-
(1996)
Mamm. Genome
, vol.7
, pp. 563-574
-
-
Kozak, M.1
-
15
-
-
0020475449
-
A simple method for displaying the hydropathic character of a protein
-
Kyte J., Doolittle R. F. A simple method for displaying the hydropathic character of a protein. J. Mol. Biol. 157:1982;105-132.
-
(1982)
J. Mol. Biol.
, vol.157
, pp. 105-132
-
-
Kyte, J.1
Doolittle, R.F.2
-
16
-
-
0026356891
-
Predicting coiled coils from protein sequences
-
Lupas A., Van Dyke M., Stock J. Predicting coiled coils from protein sequences. Science. 252:1991;1162-1164.
-
(1991)
Science
, vol.252
, pp. 1162-1164
-
-
Lupas, A.1
Van Dyke, M.2
Stock, J.3
-
17
-
-
0018855606
-
The Wolf-Hirschhorn syndrome
-
Lurie I. W., Lazjuk G. I., Ussova Y. I., Presman E. B., Gurevich D. B. The Wolf-Hirschhorn syndrome. Clin. Genet. 17:1980;375-384.
-
(1980)
Clin. Genet.
, vol.17
, pp. 375-384
-
-
Lurie, I.W.1
Lazjuk, G.I.2
Ussova, Y.I.3
Presman, E.B.4
Gurevich, D.B.5
-
18
-
-
0027105007
-
A knowledge base for predicting protein localization sites in eukaryotic cells
-
Nakai K., Kanehisa M. A knowledge base for predicting protein localization sites in eukaryotic cells. Genomics. 14:1992;897-911.
-
(1992)
Genomics
, vol.14
, pp. 897-911
-
-
Nakai, K.1
Kanehisa, M.2
-
19
-
-
0021750136
-
Mental retardation, unusual face, and intrauterine growth retardation
-
Pitt D., Rogers J. G., Danks D. M. Mental retardation, unusual face, and intrauterine growth retardation. Am. J. Med. Genet. 19:1984;307-313.
-
(1984)
Am. J. Med. Genet.
, vol.19
, pp. 307-313
-
-
Pitt, D.1
Rogers, J.G.2
Danks, D.M.3
-
20
-
-
0003292415
-
Novel Neural Network Algorithms for improved eukaryotic Promoter Site Recognition
-
Hilton Head Island, SC
-
Reese, M. G, and, Eeckman, F. E. 1995, Novel Neural Network Algorithms for improved eukaryotic Promoter Site Recognition, Seventh International Genome Sequencing and Analysis Conference, Hilton Head Island, SC.
-
(1995)
Seventh International Genome Sequencing and Analysis Conference
-
-
Reese, M.G.1
Eeckman, F.E.2
-
21
-
-
0000744775
-
Confirmation of a suspected deletion of 4p16 by fluorescent in situ hybridization (FISH) with a cosmid probe
-
Roulston D., Altherr M., Wasmuth J. J., Christian C., Graham J., Schreck R. R. Confirmation of a suspected deletion of 4p16 by fluorescent in situ hybridization (FISH) with a cosmid probe. Am. J. Hum. Genet. 49:1991;274.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 274
-
-
Roulston, D.1
Altherr, M.2
Wasmuth, J.J.3
Christian, C.4
Graham, J.5
Schreck, R.R.6
-
22
-
-
0028940853
-
Genetic characterization and cloning of mothers against dpp, a gene required for decapentaplegic function in Drosophila melanogaster
-
Sekelsky J., Newfeld S. J., Raftery L., Chartoiff E., Gelbart W. Genetic characterization and cloning of mothers against dpp, a gene required for decapentaplegic function in Drosophila melanogaster. Genetics. 139:1995;1347-1358.
-
(1995)
Genetics
, vol.139
, pp. 1347-1358
-
-
Sekelsky, J.1
Newfeld, S.J.2
Raftery, L.3
Chartoiff, E.4
Gelbart, W.5
-
23
-
-
0031779421
-
WHSC1, a 90kb SET domain-containing gene, expessed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma
-
Stec I., Wright T. J., van Ommen G.-J. B., de Boer P. A. J., van Haeringen A., Moorman A. F. M., Altherr M. R., den Dunnen J. T. WHSC1, a 90kb SET domain-containing gene, expessed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma. Hum. Mol. Genet. 7:1998;1071-1082.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1071-1082
-
-
Stec, I.1
Wright, T.J.2
Van Ommen, G.-J.B.3
De Boer, P.A.J.4
Van Haeringen, A.5
Moorman, A.F.M.6
Altherr, M.R.7
Den Dunnen, J.T.8
-
24
-
-
0027076730
-
The Wolf-Hirschhorn syndrome in fetuses
-
Tachdijan G., Fondacci C., Tapia S., Huten Y., Blot P., Nessman C. The Wolf-Hirschhorn syndrome in fetuses. Clin. Genet. 42:1992;281-287.
-
(1992)
Clin. Genet.
, vol.42
, pp. 281-287
-
-
Tachdijan, G.1
Fondacci, C.2
Tapia, S.3
Huten, Y.4
Blot, P.5
Nessman, C.6
-
25
-
-
0031889595
-
Characterization of the MADH2/Smad2 gene, a human Mad homolog responsible for the transforming growth factor-β And activin signal transduction pathway
-
Takenoshita S., Mogi A., Nagashima M., Yang K., Yagi K., Hanyu A., Nagamachi Y., Miyazono K., Hagiwara K. Characterization of the MADH2/Smad2 gene, a human Mad homolog responsible for the transforming growth factor-β and activin signal transduction pathway. Genomics. 48:1998;1-11.
-
(1998)
Genomics
, vol.48
, pp. 1-11
-
-
Takenoshita, S.1
Mogi, A.2
Nagashima, M.3
Yang, K.4
Yagi, K.5
Hanyu, A.6
Nagamachi, Y.7
Miyazono, K.8
Hagiwara, K.9
-
26
-
-
0026351408
-
Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach
-
Uberbacher E. C., Mural R. J. Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach. Proc. Natl. Acad. Sci. USA. 88:1991;11261-11265.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 11261-11265
-
-
Uberbacher, E.C.1
Mural, R.J.2
-
27
-
-
0026635941
-
The biochemistry of 3′-end cleavage and polyadenylation of messenger RNA precursors
-
Wahle E., Keller W. The biochemistry of 3′-end cleavage and polyadenylation of messenger RNA precursors. Annu. Rev. Biochem. 61:1992;419-440.
-
(1992)
Annu. Rev. Biochem.
, vol.61
, pp. 419-440
-
-
Wahle, E.1
Keller, W.2
-
28
-
-
0019801687
-
Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del (4p)]
-
Wilson M. G., Towner J. W., Coffin G. S., Ebbin A. J., Siris E., Brager P. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del (4p)]. Hum. Genet. 59:1981;297-307.
-
(1981)
Hum. Genet.
, vol.59
, pp. 297-307
-
-
Wilson, M.G.1
Towner, J.W.2
Coffin, G.S.3
Ebbin, A.J.4
Siris, E.5
Brager, P.6
-
29
-
-
0013831101
-
Defizienz an den kurzen Armen eines Chromosoms nr. 4
-
Wolf U., Reinwein H., Porsch R., Schroter R., Baitsch H. Defizienz an den kurzen Armen eines Chromosoms nr. 4. Humangenetik. 1:1965;397-413.
-
(1965)
Humangenetik
, vol.1
, pp. 397-413
-
-
Wolf, U.1
Reinwein, H.2
Porsch, R.3
Schroter, R.4
Baitsch, H.5
-
30
-
-
0032477859
-
Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions
-
Wright T. J., Clemens M., Quarrell O., Altherr M. R. Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions. Am. J. Med. Genet. 75:1998;345-350.
-
(1998)
Am. J. Med. Genet.
, vol.75
, pp. 345-350
-
-
Wright, T.J.1
Clemens, M.2
Quarrell, O.3
Altherr, M.R.4
-
31
-
-
8044224043
-
A transcript map of the newly defined 165kb Wolf-Hirschhorn syndrome critical region
-
Wright T. J., Ricke D. O., Denison K., Abmayr S., Cotter P. D., Hirschhorn K., Keinanen M., McDonald-McGinn D., Somer M., Spinner N., Yang-Feng T., Zackai E., Altherr M. R. A transcript map of the newly defined 165kb Wolf-Hirschhorn syndrome critical region. Hum. Mol. Genet. 6:1997;317-324.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 317-324
-
-
Wright, T.J.1
Ricke, D.O.2
Denison, K.3
Abmayr, S.4
Cotter, P.D.5
Hirschhorn, K.6
Keinanen, M.7
McDonald-McGinn, D.8
Somer, M.9
Spinner, N.10
Yang-Feng, T.11
Zackai, E.12
Altherr, M.R.13
-
32
-
-
0027272951
-
Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of chromosome 4
-
Zuo J., Robbins C., Baharloo S., Cox D. R., Myers R. M. Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of chromosome 4. Hum. Mol. Genet. 2:1993;889-899.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 889-899
-
-
Zuo, J.1
Robbins, C.2
Baharloo, S.3
Cox, D.R.4
Myers, R.M.5
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