-
1
-
-
0028023142
-
Structure, promoter analysis and chromosomal assignment of the human APEX gene
-
Akiyama K., Seki S., Oshida T., Yoshida M. C. Structure, promoter analysis and chromosomal assignment of the human APEX gene. Biochim. Biophys. Acta. 1219:1994;15-25.
-
(1994)
Biochim. Biophys. Acta
, vol.1219
, pp. 15-25
-
-
Akiyama, K.1
Seki, S.2
Oshida, T.3
Yoshida, M.C.4
-
2
-
-
0033555945
-
A 1.4-Mb high-resolution physical map and contig of chromosome segment 11p15.5 and genes in the LOH11A metastasis suppressor region
-
Bepler G., O'Briant K. C., Kim Y. C., Schreiber G., Pitterle D. M. A 1.4-Mb high-resolution physical map and contig of chromosome segment 11p15.5 and genes in the LOH11A metastasis suppressor region. Genomics. 55:1999;164-175.
-
(1999)
Genomics
, vol.55
, pp. 164-175
-
-
Bepler, G.1
O'Briant, K.C.2
Kim, Y.C.3
Schreiber, G.4
Pitterle, D.M.5
-
3
-
-
0031974484
-
Comparison of DNA copy number changes in malignant mesothelioma, adenocarcinoma and large-cell anaplastic carcinoma of the lung
-
Bjorkqvist A. M., Tammilehto L., Nordling S., Nurminen M., Anttila S., Mattson K., Knuutila S. Comparison of DNA copy number changes in malignant mesothelioma, adenocarcinoma and large-cell anaplastic carcinoma of the lung. Br. J. Cancer. 77:1998;260-269.
-
(1998)
Br. J. Cancer
, vol.77
, pp. 260-269
-
-
Bjorkqvist, A.M.1
Tammilehto, L.2
Nordling, S.3
Nurminen, M.4
Anttila, S.5
Mattson, K.6
Knuutila, S.7
-
4
-
-
0032520906
-
Construction of a 1.5-Mb bacterial artificial chromosome contig in Xp11.23, a region of high gene content
-
Boycott K. M., Zahorchak R. J., Summer C. G., Boycott N. P., Kotak V., Russell C. G., Bech-Hansen N. T. Construction of a 1.5-Mb bacterial artificial chromosome contig in Xp11.23, a region of high gene content. Genomics. 48:1998;369-372.
-
(1998)
Genomics
, vol.48
, pp. 369-372
-
-
Boycott, K.M.1
Zahorchak, R.J.2
Summer, C.G.3
Boycott, N.P.4
Kotak, V.5
Russell, C.G.6
Bech-Hansen, N.T.7
-
5
-
-
0030991656
-
Cytogenetic studies in prostate cancer: Are we making progress
-
Brothman A. R. Cytogenetic studies in prostate cancer: Are we making progress. Cancer Genet. Cytogenet. 95:1997;116-121.
-
(1997)
Cancer Genet. Cytogenet.
, vol.95
, pp. 116-121
-
-
Brothman, A.R.1
-
6
-
-
0022397926
-
The complex of myxomas, spotty pigmentation, and endocrine overactivity
-
Carney J. A., Gordon H., Carpenter P. C., Shenoy B. V., Go V. L. The complex of myxomas, spotty pigmentation, and endocrine overactivity. Medicine. 64:1985;270-283.
-
(1985)
Medicine
, vol.64
, pp. 270-283
-
-
Carney, J.A.1
Gordon, H.2
Carpenter, P.C.3
Shenoy, B.V.4
Go, V.L.5
-
7
-
-
0032231398
-
From amplification to gene in thyroid cancer: A high-resolution mapped bacterial-artificial-chromosome resource for cancer chromosome aberrations guides gene discovery after comparative genome hybridization
-
Chen X., Knauf J. A., Gonsky R., Wang M., Lai E. H., Chissoe S., Fagin J. A., Korenberg J. R. From amplification to gene in thyroid cancer: A high-resolution mapped bacterial-artificial-chromosome resource for cancer chromosome aberrations guides gene discovery after comparative genome hybridization. Am. J. Hum. Genet. 63:1998;625-637.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 625-637
-
-
Chen, X.1
Knauf, J.A.2
Gonsky, R.3
Wang, M.4
Lai, E.H.5
Chissoe, S.6
Fagin, J.A.7
Korenberg, J.R.8
-
8
-
-
0031017322
-
A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2
-
Comuzzie A. G., Hixson J. E., Almasy L., Mitchell B. D., Mahaney M. C., Dyer T. D., Stern M. P., MacCluer J. W., Blangero J. A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2. Nat. Genet. 15:1997;273-276.
-
(1997)
Nat. Genet.
, vol.15
, pp. 273-276
-
-
Comuzzie, A.G.1
Hixson, J.E.2
Almasy, L.3
Mitchell, B.D.4
Mahaney, M.C.5
Dyer, T.D.6
Stern, M.P.7
MacCluer, J.W.8
Blangero, J.9
-
9
-
-
0030012657
-
Human/mouse homology relationships
-
DeBry R. W., Seldin M. F. Human/mouse homology relationships. Genomics. 33:1996;337-351.
-
(1996)
Genomics
, vol.33
, pp. 337-351
-
-
Debry, R.W.1
Seldin, M.F.2
-
10
-
-
0032561502
-
A physical map of 30,000 human genes
-
Deloukas P., Schuler G. D., Gyapay G., Beasley E. M., Soderlund C., Rodriguez-Tome P., Hui L., Matise T. C., McKusick K. B., Beckmann J. S., Bentolila S., Bihoreau M., Birren B. B., Browne J., Butler A., Castle A. B., Chiannilkulchai N., Clee C., Day P. J., Dehejia A., Dibling T., Drouot N., Duprat S., Fizames C., Bentley D. R. A physical map of 30,000 human genes. Science. 282:1998;744-746.
-
(1998)
Science
, vol.282
, pp. 744-746
-
-
Deloukas, P.1
Schuler, G.D.2
Gyapay, G.3
Beasley, E.M.4
Soderlund, C.5
Rodriguez-Tome, P.6
Hui, L.7
Matise, T.C.8
McKusick, K.B.9
Beckmann, J.S.10
Bentolila, S.11
Bihoreau, M.12
Birren, B.B.13
Browne, J.14
Butler, A.15
Castle, A.B.16
Chiannilkulchai, N.17
Clee, C.18
Day, P.J.19
Dehejia, A.20
Dibling, T.21
Drouot, N.22
Duprat, S.23
Fizames, C.24
Bentley, D.R.25
more..
-
11
-
-
0032167968
-
Malattia leventinese: Refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusen
-
Edwards A. O., Klein M. L., Berselli C. B., Hejtmancik J. F., Rust K., Wirtz M. K., G. W. R., Acott T. S. Malattia leventinese: Refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusen. Am. J. Opthalmol. 126:1998;417-424.
-
(1998)
Am. J. Opthalmol.
, vol.126
, pp. 417-424
-
-
Edwards, A.O.1
Klein, M.L.2
Berselli, C.B.3
Hejtmancik, J.F.4
Rust, K.5
Wirtz, M.K.6
G., W.R.7
Acott, T.S.8
-
12
-
-
0345524288
-
A new gene (DYX3) for dyslexia is located on chromosome 2
-
Fagerheim T., Raeymaekers P., Toennessen F. E., Pedersen M., Tranebjaerg L., Lubs H. A. A new gene (DYX3) for dyslexia is located on chromosome 2. Am. J. Hum. Genet. 63:1998;A288.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 288
-
-
Fagerheim, T.1
Raeymaekers, P.2
Toennessen, F.E.3
Pedersen, M.4
Tranebjaerg, L.5
Lubs, H.A.6
-
13
-
-
0032054912
-
Clinical relevance of chromosome abnormalities in non-small cell lung cancer
-
Feder M., Siegfried J. M., Balshem A., Litwin S., Keller S. M., Liu Z., Testa J. R. Clinical relevance of chromosome abnormalities in non-small cell lung cancer. Cancer Genet. Cytogenet. 102:1998;25-31.
-
(1998)
Cancer Genet. Cytogenet.
, vol.102
, pp. 25-31
-
-
Feder, M.1
Siegfried, J.M.2
Balshem, A.3
Litwin, S.4
Keller, S.M.5
Liu, Z.6
Testa, J.R.7
-
14
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
Fishel R., Lescoe M. K., Rao M. R., Copeland N. G., Jenkins N. A., Garber J., Kane M., Kolodner R. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell. 75:1993;1027-1038.
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.1
Lescoe, M.K.2
Rao, M.R.3
Copeland, N.G.4
Jenkins, N.A.5
Garber, J.6
Kane, M.7
Kolodner, R.8
-
15
-
-
0030035986
-
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16
-
Gregory C. Y., Evans K., Wijesuriya S. D., Kermani S., Jay M. R., Plant C., Cox N., Bird A. C., Bhattacharya S. S. The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16. Hum. Mol. Genet. 5:1996;1055-1059.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1055-1059
-
-
Gregory, C.Y.1
Evans, K.2
Wijesuriya, S.D.3
Kermani, S.4
Jay, M.R.5
Plant, C.6
Cox, N.7
Bird, A.C.8
Bhattacharya, S.S.9
-
16
-
-
9044240048
-
A radiation hybrid map of the human genome
-
Gyapay G., Schmitt K., Fizames C., Jones H., Vega-Czarny N., Spillett D., Muselet D., Prud'Homme J. F., Dib C., Auffray C., Morissette J., Weissenbach J., Goodfellow P. N. A radiation hybrid map of the human genome. Hum. Mol. Genet. 5:1996;339-346.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 339-346
-
-
Gyapay, G.1
Schmitt, K.2
Fizames, C.3
Jones, H.4
Vega-Czarny, N.5
Spillett, D.6
Muselet, D.7
Prud'Homme, J.F.8
Dib, C.9
Auffray, C.10
Morissette, J.11
Weissenbach, J.12
Goodfellow, P.N.13
-
17
-
-
0028205148
-
High resolution ordering of YAC contigs using extended chromatin and chromosomes
-
Haaf T., Ward D. C. High resolution ordering of YAC contigs using extended chromatin and chromosomes. Hum. Mol. Genet. 3:1994;629-633.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 629-633
-
-
Haaf, T.1
Ward, D.C.2
-
18
-
-
17344371519
-
A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10
-
Hager J., Dina C., Francke S., Dubois S., Houari M., Vatin V., Vaillant E., Lorentz N., Basdevant A., Clement K., Guy-Grand B., Froguel P. A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10. Nat. Genet. 20:1998;304-308.
-
(1998)
Nat. Genet.
, vol.20
, pp. 304-308
-
-
Hager, J.1
Dina, C.2
Francke, S.3
Dubois, S.4
Houari, M.5
Vatin, V.6
Vaillant, E.7
Lorentz, N.8
Basdevant, A.9
Clement, K.10
Guy-Grand, B.11
Froguel, P.12
-
19
-
-
9044250844
-
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21
-
Heon E., Piguet B., Munier F., Sneed S. R., Morgan C. M., Forni S., Pescia G., Schorderet D., Taylor C. M., Streb L. M., Wiles C. D., Nishimura D. Y., Sheffield V. C., Stone E. M. Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21. Arch. Ophthalmol. 114:1996;193-198.
-
(1996)
Arch. Ophthalmol.
, vol.114
, pp. 193-198
-
-
Heon, E.1
Piguet, B.2
Munier, F.3
Sneed, S.R.4
Morgan, C.M.5
Forni, S.6
Pescia, G.7
Schorderet, D.8
Taylor, C.M.9
Streb, L.M.10
Wiles, C.D.11
Nishimura, D.Y.12
Sheffield, V.C.13
Stone, E.M.14
-
20
-
-
0028201842
-
A method for simultaneous detection of fluorescent G-bands and in situ hybridization signals
-
Hirai M., Suto Y., Kanoh M. A method for simultaneous detection of fluorescent G-bands and in situ hybridization signals. Cytogenet. Cell Genet. 66:1994;149-151.
-
(1994)
Cytogenet. Cell Genet.
, vol.66
, pp. 149-151
-
-
Hirai, M.1
Suto, Y.2
Kanoh, M.3
-
21
-
-
0033009635
-
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)
-
Kermani S., Gregory-Evans K., Tarttelin E. E., Bellingham J., Plant C., Bird A. C., Fox M., Bhattacharya S. S., Gregory-Evans C. Y. Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD). Hum. Genet. 104:1999;77-82.
-
(1999)
Hum. Genet.
, vol.104
, pp. 77-82
-
-
Kermani, S.1
Gregory-Evans, K.2
Tarttelin, E.E.3
Bellingham, J.4
Plant, C.5
Bird, A.C.6
Fox, M.7
Bhattacharya, S.S.8
Gregory-Evans, C.Y.9
-
22
-
-
0033030196
-
Large scale preparation of sequence-ready BAC DNA using Qiagen columns
-
Kirschner L. S., Stratakis C. A. Large scale preparation of sequence-ready BAC DNA using Qiagen columns. BioTechniques. 27:1999;72-74.
-
(1999)
BioTechniques
, vol.27
, pp. 72-74
-
-
Kirschner, L.S.1
Stratakis, C.A.2
-
23
-
-
0032979047
-
Genotyping of adrenocortical tumors: Very frequent deletions of the MEN1 locus in 11q13 and of a 1-centimorgan region in 2p16
-
Kjellman M., Roshani L., Teh B. T., Kallioniemi O. P., Hoog A., Gray S., Farnebo L. O., Holst M., Backdahl M., Larsson C. Genotyping of adrenocortical tumors: Very frequent deletions of the MEN1 locus in 11q13 and of a 1-centimorgan region in 2p16. J. Clin. Endocrinol. Metab. 84:1999;730-735.
-
(1999)
J. Clin. Endocrinol. Metab.
, vol.84
, pp. 730-735
-
-
Kjellman, M.1
Roshani, L.2
Teh, B.T.3
Kallioniemi, O.P.4
Hoog, A.5
Gray, S.6
Farnebo, L.O.7
Holst, M.8
Backdahl, M.9
Larsson, C.10
-
24
-
-
10544251842
-
Detection of chromosomal DNA gains and losses in testicular germ cell tumors by comparative genomic hybridization
-
Korn W. M., Oide Weghuis D. E., Suijkerbuijk R. F., Schmidt U., Otto T., du Manoir S., Geurts van Kessel A., Harstrick A., Seeber S., Becher R. Detection of chromosomal DNA gains and losses in testicular germ cell tumors by comparative genomic hybridization. Genes Chromosomes Cancer. 17:1996;78-87.
-
(1996)
Genes Chromosomes Cancer
, vol.17
, pp. 78-87
-
-
Korn, W.M.1
Oide Weghuis, D.E.2
Suijkerbuijk, R.F.3
Schmidt, U.4
Otto, T.5
Du Manoir, S.6
Geurts Van Kessel, A.7
Harstrick, A.8
Seeber, S.9
Becher, R.10
-
25
-
-
0028835899
-
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene
-
Kremer H., Kraaij R., Toledo S. P., Post M., Fridman J. B., Hayashida C. Y., van Reen M., Milgrom E., Ropers H. H., Mariman E. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nat. Genet. 9:1995;160-164.
-
(1995)
Nat. Genet.
, vol.9
, pp. 160-164
-
-
Kremer, H.1
Kraaij, R.2
Toledo, S.P.3
Post, M.4
Fridman, J.B.5
Hayashida, C.Y.6
Van Reen, M.7
Milgrom, E.8
Ropers, H.H.9
Mariman, E.10
-
26
-
-
0029156762
-
A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia
-
Laue L., Wu S. M., Kudo M., Hsueh A. J., Cutler G. B. Jr., Griffin J. E., Wilson J. D., Brain C., Berry A. C., Grant D. B. A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia. Hum. Mol. Genet. 4:1995;1429-1433.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1429-1433
-
-
Laue, L.1
Wu, S.M.2
Kudo, M.3
Hsueh, A.J.4
Cutler G.B., Jr.5
Griffin, J.E.6
Wilson, J.D.7
Brain, C.8
Berry, A.C.9
Grant, D.B.10
-
27
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
Leach F. S., Nicolaides N. C., Papadopoulos N., Liu B., Jen J., Parsons R., Peltomaki P., Sistonen P., Aaltonen L. A., Nystrom-Lahti M. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell. 75:1993;1215-1225.
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.C.2
Papadopoulos, N.3
Liu, B.4
Jen, J.5
Parsons, R.6
Peltomaki, P.7
Sistonen, P.8
Aaltonen, L.A.9
Nystrom-Lahti, M.10
-
28
-
-
0031278322
-
Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer
-
Miyaki M., Konishi M., Tanaka K., Kikuchi-Yanoshita R., Muraoka M., Yasuno M., Igari T., Koike M., Chiba M., Mori T. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. Nat. Genet. 17:1997;271-272.
-
(1997)
Nat. Genet.
, vol.17
, pp. 271-272
-
-
Miyaki, M.1
Konishi, M.2
Tanaka, K.3
Kikuchi-Yanoshita, R.4
Muraoka, M.5
Yasuno, M.6
Igari, T.7
Koike, M.8
Chiba, M.9
Mori, T.10
-
29
-
-
0032490119
-
Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci
-
O'Connell P., Pekkel V., Fuqua S. A., Osborne C. K., Clark G. M., Allred D. C. Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci. J. Natl. Cancer Inst. 90:1998;697-703.
-
(1998)
J. Natl. Cancer Inst.
, vol.90
, pp. 697-703
-
-
O'Connell, P.1
Pekkel, V.2
Fuqua, S.A.3
Osborne, C.K.4
Clark, G.M.5
Allred, D.C.6
-
30
-
-
0029684555
-
End rescue from YACs using the vectorette
-
Ogilvie D. J., James L. A. End rescue from YACs using the vectorette. Methods Mol. Biol. 54:1996;131-138.
-
(1996)
Methods Mol. Biol.
, vol.54
, pp. 131-138
-
-
Ogilvie, D.J.1
James, L.A.2
-
31
-
-
0029069972
-
Mutations of GTBP in genetically unstable cells
-
Papadopoulos N., Nicolaides N. C., Liu B., Parsons R., Lengauer C., Palombo F., D'Arrigo A., Markowitz S., Willson J. K., Kinzler K. W. Mutations of GTBP in genetically unstable cells. Science. 268:1995;1915-1917.
-
(1995)
Science
, vol.268
, pp. 1915-1917
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Liu, B.3
Parsons, R.4
Lengauer, C.5
Palombo, F.6
D'Arrigo, A.7
Markowitz, S.8
Willson, J.K.9
Kinzler, K.W.10
-
32
-
-
0343319476
-
Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy 21 and translocations of chromosome 4
-
Pinkel D., Landegent J., Collins C., Fuscoe J., Segraves R., Lucas J., Gray J. Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy 21 and translocations of chromosome 4. Proc. Natl. Acad. Sci. USA. 85:1988;9138-9142.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 9138-9142
-
-
Pinkel, D.1
Landegent, J.2
Collins, C.3
Fuscoe, J.4
Segraves, R.5
Lucas, J.6
Gray, J.7
-
33
-
-
0025936119
-
Isolation of cDNA clones encoding a human apurinic/apyrimidinic endonuclease that corrects DNA repair and mutagenesis defects in E. coli xth (exonuclease III) mutants
-
Robson C. N., Hickson I. D. Isolation of cDNA clones encoding a human apurinic/apyrimidinic endonuclease that corrects DNA repair and mutagenesis defects in E. coli xth (exonuclease III) mutants. Nucleic Acids Res. 19:1991;5519-5523.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 5519-5523
-
-
Robson, C.N.1
Hickson, I.D.2
-
34
-
-
0026744908
-
Structure of the human DNA repair gene HAP1 and its localisation to chromosome 14q 11.2-12
-
Robson C. N., Hochhauser D., Craig R., Rack K., Buckle V. J., Hickson I. D. Structure of the human DNA repair gene HAP1 and its localisation to chromosome 14q 11.2-12. Nucleic Acids Res. 20:1992;4417-4421.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 4417-4421
-
-
Robson, C.N.1
Hochhauser, D.2
Craig, R.3
Rack, K.4
Buckle, V.J.5
Hickson, I.D.6
-
35
-
-
0025244014
-
Localization of the human luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chromosome 2p21
-
Rousseau-Merck M. F., Misrahi M., Atger M., Loosfelt H., Milgrom E., Berger R. Localization of the human luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chromosome 2p21. Cytogenet. Cell Genet. 54:1990;77-79.
-
(1990)
Cytogenet. Cell Genet.
, vol.54
, pp. 77-79
-
-
Rousseau-Merck, M.F.1
Misrahi, M.2
Atger, M.3
Loosfelt, H.4
Milgrom, E.5
Berger, R.6
-
36
-
-
0032533496
-
Refined chromosomal localization of the mismatch repair and hereditary nonpolyposis colorectal cancer genes hMSH2 and hMSH6
-
Schmutte C., Marinescu R. C., Copeland N. G., Jenkins N. A., Overhauser J., Fishel R. Refined chromosomal localization of the mismatch repair and hereditary nonpolyposis colorectal cancer genes hMSH2 and hMSH6. Cancer Res. 58:1998;5023-5026.
-
(1998)
Cancer Res.
, vol.58
, pp. 5023-5026
-
-
Schmutte, C.1
Marinescu, R.C.2
Copeland, N.G.3
Jenkins, N.A.4
Overhauser, J.5
Fishel, R.6
-
37
-
-
10244230901
-
A gene map of the human genome
-
Schuler G. D., Boguski M. S., Stewart E. A., Stein L. D., Gyapay G., Rice K., White R. E., Rodriguez-Tome P., Aggarwal A., Bajorek E., Bentolila S., Birren B. B., Butler A., Castle A. B., Chiannilkulchai N., Chu A., Clee C., Cowles S., Day P. J., Dibling T., Drouot N., Dunham I., Duprat S., East C., Hudson T. J. A gene map of the human genome. Science. 274:1996;540-546.
-
(1996)
Science
, vol.274
, pp. 540-546
-
-
Schuler, G.D.1
Boguski, M.S.2
Stewart, E.A.3
Stein, L.D.4
Gyapay, G.5
Rice, K.6
White, R.E.7
Rodriguez-Tome, P.8
Aggarwal, A.9
Bajorek, E.10
Bentolila, S.11
Birren, B.B.12
Butler, A.13
Castle, A.B.14
Chiannilkulchai, N.15
Chu, A.16
Clee, C.17
Cowles, S.18
Day, P.J.19
Dibling, T.20
Drouot, N.21
Dunham, I.22
Duprat, S.23
East, C.24
Hudson, T.J.25
more..
-
38
-
-
0029890634
-
Allelic losses at chromosomes 1p, 2p, 6p, 10p, 13q, 17p, and 21q significantly correlate with the chromophobe subtype of renal cell carcinoma
-
Schwerdtle R. F., Storkel S., Neuhaus C., Brauch H., Weidt E., Brenner W., Hohenfellner R., Huber C., Decker H. J. Allelic losses at chromosomes 1p, 2p, 6p, 10p, 13q, 17p, and 21q significantly correlate with the chromophobe subtype of renal cell carcinoma. Cancer Res. 56:1996;2927-2930.
-
(1996)
Cancer Res.
, vol.56
, pp. 2927-2930
-
-
Schwerdtle, R.F.1
Storkel, S.2
Neuhaus, C.3
Brauch, H.4
Weidt, E.5
Brenner, W.6
Hohenfellner, R.7
Huber, C.8
Decker, H.J.9
-
39
-
-
15444353331
-
Polymerase chain reaction-based microsatellite polymorphism analysis of follicular and Hurthle cell neoplasms of the thyroid
-
Segev D. L., Saji M., Phillips G. S., Westra W. H., Takiyama Y., Piantadosi S., Smallridge R. C., Nishiyama R. H., Udelsman R., Zeiger M. A. Polymerase chain reaction-based microsatellite polymorphism analysis of follicular and Hurthle cell neoplasms of the thyroid. J. Clin. Endocrinol. Metab. 83:1998;2036-2042.
-
(1998)
J. Clin. Endocrinol. Metab.
, vol.83
, pp. 2036-2042
-
-
Segev, D.L.1
Saji, M.2
Phillips, G.S.3
Westra, W.H.4
Takiyama, Y.5
Piantadosi, S.6
Smallridge, R.C.7
Nishiyama, R.H.8
Udelsman, R.9
Zeiger, M.A.10
-
40
-
-
0027372340
-
A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty
-
Shenker A., Laue L., Kosugi S., Merendino J. J. Jr., Minegishi T., Cutler G. B. Jr. A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty. Nature. 365:1993;652-654.
-
(1993)
Nature
, vol.365
, pp. 652-654
-
-
Shenker, A.1
Laue, L.2
Kosugi, S.3
Merendino J.J., Jr.4
Minegishi, T.5
Cutler G.B., Jr.6
-
41
-
-
0031055329
-
Multiple mechanisms of N-phosphonacetyl-l-aspartate resistance in human cell lines: Carbamyl-P synthetase/aspartate transcarbamylase/dihydro-orotase gene amplification is frequent only when chromosome 2 is rearranged
-
Smith K. A., Chernova O. B., Groves R. P., Stark M. B., Martinez J. L., Davidson J. N., Trent J. M., Patterson T. E., Agarwal A., Duncan P., Agarwal M. L., Stark G. R. Multiple mechanisms of N-phosphonacetyl-l-aspartate resistance in human cell lines: Carbamyl-P synthetase/aspartate transcarbamylase/dihydro-orotase gene amplification is frequent only when chromosome 2 is rearranged. Proc. Natl. Acad. Sci. USA. 94:1997;1816-1821.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 1816-1821
-
-
Smith, K.A.1
Chernova, O.B.2
Groves, R.P.3
Stark, M.B.4
Martinez, J.L.5
Davidson, J.N.6
Trent, J.M.7
Patterson, T.E.8
Agarwal, A.9
Duncan, P.10
Agarwal, M.L.11
Stark, G.R.12
-
42
-
-
0029940485
-
Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996
-
Spur N. K., Bashir R., Bushby K., Cox A., Cox S., Hilde Brandt F., Hill N., Kao F. T., Krols L., Marzella R., Miller N., Nothwang H. G., Rocchi M., Sarfarazi M., Stratakis C. A., Wallgren-Petterson C., Naylor S. Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996. Cytogenet. Cell Genet. 73:1996;255-273.
-
(1996)
Cytogenet. Cell Genet.
, vol.73
, pp. 255-273
-
-
Spur, N.K.1
Bashir, R.2
Bushby, K.3
Cox, A.4
Cox, S.5
Hilde Brandt, F.6
Hill, N.7
Kao, F.T.8
Krols, L.9
Marzella, R.10
Miller, N.11
Nothwang, H.G.12
Rocchi, M.13
Sarfarazi, M.14
Stratakis, C.A.15
Wallgren-Petterson, C.16
Naylor, S.17
-
43
-
-
15144342084
-
An STS-based radiation hybrid map of the human genome
-
Stewart E. A., McKusick K. B., Aggarwal A., Bajorek E., Brady S., Chu A., Fang N., Hadley D., Harris M., Hussain S., Lee R., Maratukulam A., O'Connor K., Perkins S., Piercy M., Qin F., Reif T., Sanders C., She X., Sun W. L., Tabar P., Voyticky S., Cowles S., Fan J. B., Cox D. R. An STS-based radiation hybrid map of the human genome. Genome Res. 7:1997;422-433.
-
(1997)
Genome Res.
, vol.7
, pp. 422-433
-
-
Stewart, E.A.1
McKusick, K.B.2
Aggarwal, A.3
Bajorek, E.4
Brady, S.5
Chu, A.6
Fang, N.7
Hadley, D.8
Harris, M.9
Hussain, S.10
Lee, R.11
Maratukulam, A.12
O'Connor, K.13
Perkins, S.14
Piercy, M.15
Qin, F.16
Reif, T.17
Sanders, C.18
She, X.19
Sun, W.L.20
Tabar, P.21
Voyticky, S.22
Cowles, S.23
Fan, J.B.24
Cox, D.R.25
more..
-
44
-
-
0033027071
-
A single EFEMP1 mutation associated with both malattia leventinese and Doyne honeycomb retinal dystrophy
-
Stone E. M., Lotery A. J., Munier F. L., Héon E., Piguet B., Guymer R. H., Vandenburgh K., Cousin P., Nishimura D., Swiderski R. E., Silvestri G., Mackey D. A., Hageman G. S., Bird A. C., Sheffield V. C., Schorderet D. F. A single EFEMP1 mutation associated with both malattia leventinese and Doyne honeycomb retinal dystrophy. Nat. Genet. 22:1999;199-202.
-
(1999)
Nat. Genet.
, vol.22
, pp. 199-202
-
-
Stone, E.M.1
Lotery, A.J.2
Munier, F.L.3
Héon, E.4
Piguet, B.5
Guymer, R.H.6
Vandenburgh, K.7
Cousin, P.8
Nishimura, D.9
Swiderski, R.E.10
Silvestri, G.11
Mackey, D.A.12
Hageman, G.S.13
Bird, A.C.14
Sheffield, V.C.15
Schorderet, D.F.16
-
45
-
-
0030049026
-
Carney complex, a familial multiple neoplasia and lentiginosis syndrome: Analysis of 11 kindreds and linkage to the short arm of chromosome 2
-
Stratakis C. A., Carney J. A., Lin J. P., Papanicolaou D. A., Karl M., Kastner D. L., Pras E., Chrousos G. P. Carney complex, a familial multiple neoplasia and lentiginosis syndrome: Analysis of 11 kindreds and linkage to the short arm of chromosome 2. J. Clin. Invest. 97:1996;699-705.
-
(1996)
J. Clin. Invest.
, vol.97
, pp. 699-705
-
-
Stratakis, C.A.1
Carney, J.A.2
Lin, J.P.3
Papanicolaou, D.A.4
Karl, M.5
Kastner, D.L.6
Pras, E.7
Chrousos, G.P.8
-
46
-
-
0030969847
-
Evidence for divergence of DNA copy number changes in serous, mucinous and endometrioid ovarian carcinomas
-
Tapper J., Butzow R., Wahlstrom T., Seppala M., Knuutila S. Evidence for divergence of DNA copy number changes in serous, mucinous and endometrioid ovarian carcinomas. Br. J. Cancer. 75:1997;1782-1787.
-
(1997)
Br. J. Cancer
, vol.75
, pp. 1782-1787
-
-
Tapper, J.1
Butzow, R.2
Wahlstrom, T.3
Seppala, M.4
Knuutila, S.5
-
47
-
-
0033558977
-
Radiation hybrid mapping of chromosomal region 2p15-p16: Integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne's honeycomb retinal dystrophy (DHRD) loci
-
Taymans S. E., Kirschner L. S., Giatzakis C., Stratakis C. A. Radiation hybrid mapping of chromosomal region 2p15-p16: Integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne's honeycomb retinal dystrophy (DHRD) loci. Genomics. 56:1999;344-349.
-
(1999)
Genomics
, vol.56
, pp. 344-349
-
-
Taymans, S.E.1
Kirschner, L.S.2
Giatzakis, C.3
Stratakis, C.A.4
-
48
-
-
0031733012
-
Human CYP11B2 (aldosterone synthase) maps to chromosome 8q24.3
-
Taymans S. E., Pack S., Pak E., Torpy D. J., Zhuang Z., Stratakis C. A. Human CYP11B2 (aldosterone synthase) maps to chromosome 8q24.3. J. Clin. Endocrinol. Metab. 83:1998;1033-1036.
-
(1998)
J. Clin. Endocrinol. Metab.
, vol.83
, pp. 1033-1036
-
-
Taymans, S.E.1
Pack, S.2
Pak, E.3
Torpy, D.J.4
Zhuang, Z.5
Stratakis, C.A.6
-
50
-
-
0031686514
-
A panel of partial chromosome paints and YAC probes specific for human chromosome 2
-
Viggiano L., Marzella R., Ricco A. S., Storlazzi T. C., Fratello A., Varella-Garcia M., Archidiacono N., Rocchi M. A panel of partial chromosome paints and YAC probes specific for human chromosome 2. Somat. Cell Mol. Genet. 24:1998;13-21.
-
(1998)
Somat. Cell Mol. Genet.
, vol.24
, pp. 13-21
-
-
Viggiano, L.1
Marzella, R.2
Ricco, A.S.3
Storlazzi, T.C.4
Fratello, A.5
Varella-Garcia, M.6
Archidiacono, N.7
Rocchi, M.8
-
51
-
-
0032968828
-
"kARIBIN," an information resource for obtaining genomic information in a cytogenetic band
-
Zhang J., Shen-Ong G., Ostell J. "KARIBIN," an information resource for obtaining genomic information in a cytogenetic band. Genome Res. 9:1999;91-98.
-
(1999)
Genome Res.
, vol.9
, pp. 91-98
-
-
Zhang, J.1
Shen-Ong, G.2
Ostell, J.3
|