-
1
-
-
0004265596
-
-
John Wiley & Sons, New York
-
Ausubcl FM, Brenl R, Kingston RE, Moore DD, Seid-man JG, Smith JA, Struhl K: Current Protocols in Molecular Biologs (John Wiley & Sons, New York 1994).
-
(1994)
Current Protocols in Molecular Biologs
-
-
Ausubcl, F.M.1
Brenl, R.2
Kingston, R.E.3
Moore, D.D.4
Seid-Man, J.G.5
Smith, J.A.6
Struhl, K.7
-
2
-
-
0028814128
-
Integration of physical, breakpoint and genetic maps of chromosome 22: Localization of 587 yeast artificial chromosomes with 238 mapped markers
-
Bell CJ, Budarf ML, Nieuwenhuijsen BW, Bamoski BL, Buetow KM, Campbell K, Colbert AM, Collins J, Daly M, Desjardins PR, De Zwaan T, Eckman B, Foote S, Hart K, Hiester K, Van het Hoog J, Hopper E, Kaufman A, McDermid JE, Overton GC, Reeve MP, Searls DB, Stein L, Valmiki VH, Watson E, Williams S, Winston R, Nussbaum RL, Lander ES, Fischbeck KH, Emanuel BS, Hudson TJ: Integration of physical, breakpoint and genetic maps of chromosome 22: localization of 587 yeast artificial chromosomes with 238 mapped markers, Hum molec Genet 4:59-69 (1995).
-
(1995)
Hum Molec Genet
, vol.4
, pp. 59-69
-
-
Bell, C.J.1
Budarf, M.L.2
Nieuwenhuijsen, B.W.3
Bamoski, B.L.4
Buetow, K.M.5
Campbell, K.6
Colbert, A.M.7
Collins, J.8
Daly, M.9
Desjardins, P.R.10
De Zwaan, T.11
Eckman, B.12
Foote, S.13
Hart, K.14
Hiester, K.15
Van Het Hoog, J.16
Hopper, E.17
Kaufman, A.18
McDermid, J.E.19
Overton, G.C.20
Reeve, M.P.21
Searls, D.B.22
Stein, L.23
Valmiki, V.H.24
Watson, E.25
Williams, S.26
Winston, R.27
Nussbaum, R.L.28
Lander, E.S.29
Fischbeck, K.H.30
Emanuel, B.S.31
Hudson, T.J.32
more..
-
3
-
-
0029957733
-
Frequent type 2 neurofibromatosis gene transcript mutations in sporadic iniramedullarv spinal cord ependymomas
-
Birch BD, Johnson JP, Parsa A, Desai RD, Yoon JT, Lycette A, Li YM, Bruce JN: Frequent type 2 neurofibromatosis gene transcript mutations in sporadic iniramedullarv spinal cord ependymomas, Neurosurgery 39:135-140 (1996).
-
(1996)
Neurosurgery
, vol.39
, pp. 135-140
-
-
Birch, B.D.1
Johnson, J.P.2
Parsa, A.3
Desai, R.D.4
Yoon, J.T.5
Lycette, A.6
Li, Y.M.7
Bruce, J.N.8
-
4
-
-
8544234633
-
Microsalel-lite analysis of childhwd brain tumors
-
Blacker H, Rasheed BKA, McLendon RE, Friedman HS, Batra SK, Fuchs HD, Bigncr SH: Microsalel-lite analysis of childhwd brain tumors, Genes Chrom Cancer 15:54-63 (1996).
-
(1996)
Genes Chrom Cancer
, vol.15
, pp. 54-63
-
-
Blacker, H.1
Rasheed, B.2
McLendon, R.E.3
Friedman, H.S.4
Batra, S.K.5
Fuchs, H.D.6
Bigncr, S.H.7
-
5
-
-
0029988255
-
A metric map of humans: 23,500 loci in 850 bands
-
Collins A, Frézal J, Morton NE: A metric map of humans: 23,500 loci in 850 bands, Proc natl Acad Sci, USA 93:14771-14775 (1996).
-
(1996)
Proc Natl Acad Sci, USA
, vol.93
, pp. 14771-14775
-
-
Collins, A.1
Frézal, J.2
Morton, N.E.3
-
6
-
-
0030950736
-
Dunham 1: The organization of the y-glutamyl transferase genes and other low copy repeats in human chromosome 22q 11
-
Collins J, Mungali A, Badcock K, Fay J, Dunham 1: The organization of the y-glutamyl transferase genes and other low copy repeats in human chromosome 22q 11, Genome Res 7:522-531 (1997).
-
(1997)
Genome Res
, vol.7
, pp. 522-531
-
-
Collins, J.1
Mungali, A.2
Badcock, K.3
Fay, J.4
-
7
-
-
0024309572
-
Physical mapping of a translocation breakpoint in neurofibromatosis
-
Fountain JS, Wallace MR, Bruce MA, Seizinger BR, Menon AG, Gusclla JF, Michels VV, Schmidt MA, Dewald GW, Collins FS: Physical mapping of a translocation breakpoint in neurofibromatosis, Science 244:1085-1087 (1989).
-
(1989)
Science
, vol.244
, pp. 1085-1087
-
-
Fountain, J.S.1
Wallace, M.R.2
Bruce, M.A.3
Seizinger, B.R.4
Menon, A.G.5
Gusclla, J.F.6
Michels, V.V.7
Schmidt, M.A.8
Dewald, G.W.9
Collins, F.S.10
-
8
-
-
0017189899
-
Retinoblastoma and chromosome 13
-
Francke U: Retinoblastoma and chromosome 13, Cyto-genet Cell Genet 16:131-134 (1976).
-
(1976)
Cyto-Genet Cell Genet
, vol.16
, pp. 131-134
-
-
Francke, U.1
-
9
-
-
0026694294
-
Chromosome abnormalities in low-grade central nervous system tumors
-
Griffin CA, Long PP, Carson BS, Brem H: Chromosome abnormalities in low-grade central nervous system tumors, Cancer Genet Cylogcnet 60:67-73 (1992).
-
(1992)
Cancer Genet Cylogcnet
, vol.60
, pp. 67-73
-
-
Griffin, C.A.1
Long, P.P.2
Carson, B.S.3
Brem, H.4
-
10
-
-
0030999539
-
The molecular biology of ependymomas
-
Hamilton RL, Pollack IF: The molecular biology of ependymomas, Brain Pathol 7:807-822 (1997).
-
(1997)
Brain Pathol
, vol.7
, pp. 807-822
-
-
Hamilton, R.L.1
Pollack, I.F.2
-
11
-
-
0022810104
-
Gardner syndrome in a man with an interstitial deletion of 5q
-
Herrera L, Kakati S, Givas L, Pietrzak E, Sandberg AA: Gardner syndrome in a man with an interstitial deletion of 5q, Am J med Genet 25:473-476 (1986).
-
(1986)
Am J Med Genet
, vol.25
, pp. 473-476
-
-
Herrera, L.1
Kakati, S.2
Givas, L.3
Pietrzak, E.4
Sandberg, A.A.5
-
12
-
-
0025311299
-
An abundant transcript induced in differentiating human endothelial cells encodes a polypeptide with structural similarities to G-pro-tein-coupled receptors
-
Hla T, Maciag T: An abundant transcript induced in differentiating human endothelial cells encodes a polypeptide with structural similarities to G-pro-tein-coupled receptors, J biol Chem 265:9308-9313 (1990).
-
(1990)
J Biol Chem
, vol.265
, pp. 9308-9313
-
-
Hla, T.1
Maciag, T.2
-
13
-
-
0025143557
-
Loss of genetic information in central nervous system tumors common to children and young adults
-
James CD, He J, Carlbom E, Mikkelsen T, Ridderheim PA, Cavenee WK, Collins VP: Loss of genetic information in central nervous system tumors common to children and young adults, Genes Chrom Cancer 2:94-102 (1990).
-
(1990)
Genes Chrom Cancer
, vol.2
, pp. 94-102
-
-
James, C.D.1
He, J.2
Carlbom, E.3
Mikkelsen, T.4
Ridderheim, P.A.5
Cavenee, W.K.6
Collins, V.P.7
-
14
-
-
0028853347
-
Identification of the chromosome 12 translocation breakpoint region of a pleomorphic salivary gland adenoma with l (1; 12) (p22:Q 15) as the sole cytogenetic abnormality
-
Kools PF, Wanschura S, Schoenmakers EF, Geurts JM, Mols R, Kazmicrczak B, Bullerdick J, Van den Berghe H, Van de Vcn JM: Identification of the chromosome 12 translocation breakpoint region of a pleomorphic salivary gland adenoma with l (1; 12) (p22:q 15) as the sole cytogenetic abnormality, Cancer Genet Cytogcnct 79:1-7 (1995).
-
(1995)
Cancer Genet Cytogcnct
, vol.79
, pp. 1-7
-
-
Kools, P.F.1
Wanschura, S.2
Schoenmakers, E.F.3
Geurts, J.M.4
Mols, R.5
Kazmicrczak, B.6
Bullerdick, J.7
Van Den Berghe, H.8
Van De Vcn, J.M.9
-
15
-
-
0028109495
-
Cloning of the rat edg-l immediate-early gene expression pattern suggests diverse functions
-
Lado DC, Browe CS, Gaskin AA, Borden JM, MacLen-nan AJ: Cloning of the rat edg-l immediate-early gene expression pattern suggests diverse functions, Gene 149:331-336 (1994).
-
(1994)
Gene
, vol.149
, pp. 331-336
-
-
Lado, D.C.1
Browe, C.S.2
Gaskin, A.A.3
Borden, J.M.4
Maclen-Nan, A.J.5
-
16
-
-
0029977136
-
HlaT: The inducibleG protein-coupled receptor edg-l signals via the G (i)/mitogen-activated protein kinase palhwav
-
Lee MJ, Evans M, HlaT: The inducibleG protein-coupled receptor edg-l signals via the G (i)/mitogen-activated protein kinase palhwav, J biol Chem 271:11272-11279 (1996).
-
(1996)
J Biol Chem
, vol.271
, pp. 11272-11279
-
-
Lee, M.J.1
Evans, M.2
-
17
-
-
0026725180
-
Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification
-
Lcngaucr C, Green ED, Cremer T: Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification, Genomics 13:826-828 (1992).
-
(1992)
Genomics
, vol.13
, pp. 826-828
-
-
Lcngaucr, C.1
Green, E.D.2
Cremer, T.3
-
18
-
-
0029153013
-
Molecular characterization of a (1;10) (p22;q21) constitutional translocation from a patient with neuroblastoma
-
Mead RS, Cowell JK: Molecular characterization of a (1;10) (p22;q21) constitutional translocation from a patient with neuroblastoma, Cancer Genet Cytogcnct 81:151-157 (1995).
-
(1995)
Cancer Genet Cytogcnct
, vol.81
, pp. 151-157
-
-
Mead, R.S.1
Cowell, J.K.2
-
19
-
-
0030999555
-
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
-
Mitelman F, Mertens F, Johansson B: A breakpoint map of recurrent chromosomal rearrangements in human neoplasia, Nature Genet 15:417-474 (1997).
-
(1997)
Nature Genet
, vol.15
, pp. 417-474
-
-
Mitelman, F.1
Mertens, F.2
Johansson, B.3
-
20
-
-
0024396040
-
Two NF1 translocations map within a 600-kilobase segment of 17q 11.2
-
O’Connell P, Leach R, Cawthon RM, Culver M, Stevens J, Viskochil D, Fournier REK, Rich DC, Ledbetter DH, White R: Two NF1 translocations map within a 600-kilobase segment of 17q 11.2, Science 244:1087-1088 (1989).
-
(1989)
Science
, vol.244
, pp. 1087-1088
-
-
O’connell, P.1
Leach, R.2
Cawthon, R.M.3
Culver, M.4
Stevens, J.5
Viskochil, D.6
Fournier, R.7
Rich, D.C.8
Ledbetter, D.H.9
White, R.10
-
21
-
-
0029865075
-
Constitutional de novo t (1;22-p22;q11.2) and ependymoma
-
Park JP, Chaffee S, Noll WW, Rhodes CH: Constitutional de novo t (1;22-p22;q11.2) and ependymoma, Cancer Genet Cytogenet 86:150-152 (1996).
-
(1996)
Cancer Genet Cytogenet
, vol.86
, pp. 150-152
-
-
Park, J.P.1
Chaffee, S.2
Noll, W.W.3
Rhodes, C.H.4
-
22
-
-
0027944927
-
Brain tumors in children
-
Pollack IF: Brain tumors in children, New Engl J Med 331:1500-1507 (1994).
-
(1994)
New Engl J Med
, vol.331
, pp. 1500-1507
-
-
Pollack, I.F.1
-
23
-
-
0026676710
-
Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas
-
Ransom D, Ritland SR, Kimmel DW, Moertel CA, Dahl RJ, Scheithauer BW, Kelly PJ, Jenkins RB: Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas, Genes Chrom Cancer 5:348-356 (1992).
-
(1992)
Genes Chrom Cancer
, vol.5
, pp. 348-356
-
-
Ransom, D.1
Ritland, S.R.2
Kimmel, D.W.3
Moertel, C.A.4
Dahl, R.J.5
Scheithauer, B.W.6
Kelly, P.J.7
Jenkins, R.B.8
-
24
-
-
0019138365
-
The aniridia-Wilms" association: The clinical role of chromosome band 11 pi 3
-
Riccardi VM, Hitter HM, Franke U, Yunis JJ, Ledbetter D, Borges W: The aniridia-Wilms" association: the clinical role of chromosome band 11 pi 3, Cancer Genet Cytogenet 2:131 (1980).
-
(1980)
Cancer Genet Cytogenet
, vol.2
, pp. 131
-
-
Riccardi, V.M.1
Hitter, H.M.2
Franke, U.3
Yunis, J.J.4
Ledbetter, D.5
Borges, W.6
-
25
-
-
0030902113
-
Cloning of the human Gfi-1 gene and its mapping to chromosome region lp22
-
Roberts T, Cowell J: Cloning of the human Gfi-1 gene and its mapping to chromosome region lp22, Oncogene 14:1003-1005 (1997).
-
(1997)
Oncogene
, vol.14
, pp. 1003-1005
-
-
Roberts, T.1
Cowell, J.2
-
26
-
-
0030248551
-
Regional localization of 192 genic markers on human chromosome 1
-
Roberts TAC, Cowell J: Regional localization of 192 genic markers on human chromosome 1, Genomics 36:337-340 (1996).
-
(1996)
Genomics
, vol.36
, pp. 337-340
-
-
Roberts, T.1
Cowell, J.2
-
27
-
-
0027489653
-
Chromosomes in the genesis and progression of ependvmomas
-
Rogatto SR, Casartelli C, Rainho CA, Barbieri NJ: Chromosomes in the genesis and progression of ependvmomas, Cancer Genet Cytogenet 69 (2): 146-52 (1993).
-
(1993)
Cancer Genet Cytogenet
, vol.69
, Issue.2
, pp. 146-152
-
-
Rogatto, S.R.1
Casartelli, C.2
Rainho, C.A.3
Barbieri, N.J.4
-
28
-
-
0028144439
-
Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas
-
Rubio MP, Correa KM, Ramesh V, MacCollin MM, Jacoby LB, von Deimling A, Gusella JF, Louis DN: Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas, Cancer Res 54:45-47 (1994).
-
(1994)
Cancer Res
, vol.54
, pp. 45-47
-
-
Rubio, M.P.1
Correa, K.M.2
Ramesh, V.3
Maccollin, M.M.4
Jacoby, L.B.5
Von Deimling, A.6
Gusella, J.F.7
Louis, D.N.8
-
29
-
-
0029088063
-
Recurrent rearrangements in the high mobility group protein gene, HMG1-C, in benign mesenchymal tumours
-
Schoenmakers EF, Wanschura S, Mols R, Bullerdiek J, Van den Bcrgltc J, Van de Ven WJM: Recurrent rearrangements in the high mobility group protein gene, HMG1-C, in benign mesenchymal tumours, Nature Genet 10:436-444 (1995).
-
(1995)
Nature Genet
, vol.10
, pp. 436-444
-
-
Schoenmakers, E.F.1
Wanschura, S.2
Mols, R.3
Bullerdiek, J.4
Van Den Bcrgltc, J.5
Van De Ven, W.6
-
30
-
-
0031128131
-
Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial svndrome
-
Sirotkin H, O'Donnell H, Das Gupta R, Halford S, St Jore B, Puech A, Parimoo S, Morrow B, Skoultchi A, Weissman S, Scrambler P, Kucherlapati R: Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial svndrome, Genomics 41:75-83 (1997).
-
(1997)
Genomics
, vol.41
, pp. 75-83
-
-
Sirotkin, H.1
O'donnell, H.2
Das Gupta, R.3
Halford, S.4
St Jore, B.5
Puech, A.6
Parimoo, S.7
Morrow, B.8
Skoultchi, A.9
Weissman, S.10
Scrambler, P.11
Kucherlapati, R.12
-
31
-
-
0029123934
-
Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas
-
Slave I, MacCollin MM, Dunn M, Jones S, Sutton L, Gusella JF, Biegel JA: Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas. Int J Cancer 64 (41):243-247 (1995).
-
(1995)
Int J Cancer
, vol.64
, Issue.41
, pp. 243-247
-
-
Slave, I.1
Maccollin, M.M.2
Dunn, M.3
Jones, S.4
Sutton, L.5
Gusella, J.F.6
Biegel, J.A.7
-
32
-
-
0026544721
-
Karyotypes in 90 human gliomas
-
Thiel G, Losanowa T, Kintzel D, Nisch G, Martin H, Vorpahl K, Witkowski R: Karyotypes in 90 human gliomas, Cancer Genet Cytogenet 58:109-120 (1992).
-
(1992)
Cancer Genet Cytogenet
, vol.58
, pp. 109-120
-
-
Thiel, G.1
Losanowa, T.2
Kintzel, D.3
Nisch, G.4
Martin, H.5
Vorpahl, K.6
Witkowski, R.7
-
33
-
-
85025545206
-
Cytogenetic studies in 45 pediatric brain tumors (Published erratum appears in Pediatr Hc-matol Oncol 10:117 (1993)]
-
Vagner CA, Gentct JC, Gambarelli D, Pellissier JF, Gouzien M, Lena G, Genitori L, Choux M, Ray-baud C: Cytogenetic studies in 45 pediatric brain tumors published erratum appears in Pediatr Hc-matol Oncol 10:117 (1993)], Pediatr Hematol Oncol 9:223-35 (1992).
-
(1992)
Pediatr Hematol Oncol
, vol.9
, pp. 223-235
-
-
Vagner, C.A.1
Gentct, J.C.2
Gambarelli, D.3
Pellissier, J.F.4
Gouzien, M.5
Lena, G.6
Genitori, L.7
Choux, M.8
Ray-Baud, C.9
-
34
-
-
0026689599
-
Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma
-
Wercntowicz S, Kupsky WJ, Morton CC, Fletcher JA: Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma, Cancer Genet Cytogenet 61:193-196 (1992).
-
(1992)
Cancer Genet Cytogenet
, vol.61
, pp. 193-196
-
-
Wercntowicz, S.1
Kupsky, W.J.2
Morton, C.C.3
Fletcher, J.A.4
-
35
-
-
0024540966
-
Assignment of autosomal dominant spinocerebellar ataxia (SCAI) ccntro-meric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis
-
Zoghbi H, Sandkuyl L, Ott J, Daiger S, Pollack M, O'Brien W, Beaudet A: Assignment of autosomal dominant spinocerebellar ataxia (SCAI) ccntro-meric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis, Am J hum Genet 44:255-263 (1989).
-
(1989)
Am J Hum Genet
, vol.44
, pp. 255-263
-
-
Zoghbi, H.1
Sandkuyl, L.2
Ott, J.3
Daiger, S.4
Pollack, M.5
O'brien, W.6
Beaudet, A.7
|