-
2
-
-
0028661210
-
Karyotypic changes in phyllodes tumors of the breast
-
Dietrich C.U., Pandis N., Bardi G., Teixeira M.R., Soukhikh T., Petersson C., Andersen J.A., and Heim S. Karyotypic changes in phyllodes tumors of the breast. Cancer Genet Cytogenet 78 (1994) 200-206
-
(1994)
Cancer Genet Cytogenet
, vol.78
, pp. 200-206
-
-
Dietrich, C.U.1
Pandis, N.2
Bardi, G.3
Teixeira, M.R.4
Soukhikh, T.5
Petersson, C.6
Andersen, J.A.7
Heim, S.8
-
3
-
-
5144221371
-
Cytogenetic findings in phyllodes tumor and fibroadenomas of the breast
-
Barbosa M.L., Ribeiro E.M., Silva G.F., Maciel M.E., Lima R.S., Cavalli L.R., and Cavalli I.J. Cytogenetic findings in phyllodes tumor and fibroadenomas of the breast. Cancer Genet Cytogenet 154 (2004) 156-159
-
(2004)
Cancer Genet Cytogenet
, vol.154
, pp. 156-159
-
-
Barbosa, M.L.1
Ribeiro, E.M.2
Silva, G.F.3
Maciel, M.E.4
Lima, R.S.5
Cavalli, L.R.6
Cavalli, I.J.7
-
4
-
-
13144261762
-
Cytogenetic findings in phyllodes tumors of the breast: karyotypic complexity differentiates between benign and malignant tumors
-
Dietrich C.U., Pandis N., Rizou H., Petersson C., Bardi G., Qvist H., Apostolikas N., Bøhler P.J., Andersen J.A., Idvall I., Mitelman F., and Heim S. Cytogenetic findings in phyllodes tumors of the breast: karyotypic complexity differentiates between benign and malignant tumors. Hum Pathol 28 (1997) 1379-1382
-
(1997)
Hum Pathol
, vol.28
, pp. 1379-1382
-
-
Dietrich, C.U.1
Pandis, N.2
Rizou, H.3
Petersson, C.4
Bardi, G.5
Qvist, H.6
Apostolikas, N.7
Bøhler, P.J.8
Andersen, J.A.9
Idvall, I.10
Mitelman, F.11
Heim, S.12
-
5
-
-
33947607981
-
Phyllodes tumors of the breast segregate in two groups according to genetic criteria
-
Laé M., Vincent-Salomon A., Savignoni A., Huon I., Fréneaux P., Sigal-Zafrani B., Aurias A., Sastre-Garau X., and Couturier J. Phyllodes tumors of the breast segregate in two groups according to genetic criteria. Mod Pathol 20 (2007) 435-444
-
(2007)
Mod Pathol
, vol.20
, pp. 435-444
-
-
Laé, M.1
Vincent-Salomon, A.2
Savignoni, A.3
Huon, I.4
Fréneaux, P.5
Sigal-Zafrani, B.6
Aurias, A.7
Sastre-Garau, X.8
Couturier, J.9
-
6
-
-
41649118931
-
Phyllodes Tumour Consortium. A comprehensive genetic profile of phyllodes tumours of the breast detects important mutations, intra-tumoral genetic heterogeneity and new genetic changes on recurrence
-
Jones A.M., Mitter R., Springall R., Graham T., Winter E., Gillett C., Hanby A.M., Tomlinson I.P., and Sawyer E.J. Phyllodes Tumour Consortium. A comprehensive genetic profile of phyllodes tumours of the breast detects important mutations, intra-tumoral genetic heterogeneity and new genetic changes on recurrence. J Pathol 214 (2008) 533-544
-
(2008)
J Pathol
, vol.214
, pp. 533-544
-
-
Jones, A.M.1
Mitter, R.2
Springall, R.3
Graham, T.4
Winter, E.5
Gillett, C.6
Hanby, A.M.7
Tomlinson, I.P.8
Sawyer, E.J.9
-
7
-
-
0035143677
-
Diagnosis of aneuploidy in archival, paraffin-embedded pregnancy-loss tissues by comparative genomic hybridization
-
Bell K.A., Van Deerlin P.G., Feinberg R.F., du Manoir S., and Haddad B.R. Diagnosis of aneuploidy in archival, paraffin-embedded pregnancy-loss tissues by comparative genomic hybridization. Fertil Steril 75 (2001) 374-379
-
(2001)
Fertil Steril
, vol.75
, pp. 374-379
-
-
Bell, K.A.1
Van Deerlin, P.G.2
Feinberg, R.F.3
du Manoir, S.4
Haddad, B.R.5
-
8
-
-
40149104979
-
Recent advances in the genetics of phaeochromocytoma and functional paraganglioma
-
Gimenez-Roqueplo A.P., Burnichon N., Amar L., Favier J., Jeunemaitre X., and Plouin P.F. Recent advances in the genetics of phaeochromocytoma and functional paraganglioma. Clin Exp Pharmacol Physiol 35 (2008) 376-379
-
(2008)
Clin Exp Pharmacol Physiol
, vol.35
, pp. 376-379
-
-
Gimenez-Roqueplo, A.P.1
Burnichon, N.2
Amar, L.3
Favier, J.4
Jeunemaitre, X.5
Plouin, P.F.6
-
9
-
-
32544439562
-
Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?
-
Cascón A., Montero-Conde C., Ruiz-Llorente S., Mercadillo F., Letón R., Rodríguez-Antona C., Martínez-Delgado B., Delgado M., Díez A., Rovira A., Díaz J.A., and Robledo M. Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?. Genes Chromosomes Cancer 45 (2006) 213-219
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 213-219
-
-
Cascón, A.1
Montero-Conde, C.2
Ruiz-Llorente, S.3
Mercadillo, F.4
Letón, R.5
Rodríguez-Antona, C.6
Martínez-Delgado, B.7
Delgado, M.8
Díez, A.9
Rovira, A.10
Díaz, J.A.11
Robledo, M.12
-
10
-
-
37349074531
-
Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD
-
Pasini B., McWhinney S.R., Bei T., Matyakhina L., Stergiopoulos S., Muchow M., Boikos S.A., Ferrando B., Pacak K., Assie G., Baudin E., Chompret A., Ellison J.W., Briere J.J., Rustin P., Gimenez-Roqueplo A.P., Eng C., Carney J.A., and Stratakis C.A. Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. Eur J Hum Genet 16 (2008) 79-88
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 79-88
-
-
Pasini, B.1
McWhinney, S.R.2
Bei, T.3
Matyakhina, L.4
Stergiopoulos, S.5
Muchow, M.6
Boikos, S.A.7
Ferrando, B.8
Pacak, K.9
Assie, G.10
Baudin, E.11
Chompret, A.12
Ellison, J.W.13
Briere, J.J.14
Rustin, P.15
Gimenez-Roqueplo, A.P.16
Eng, C.17
Carney, J.A.18
Stratakis, C.A.19
-
11
-
-
34548386693
-
Familial gastrointestinal stromal tumors and germ-line mutations
-
International Carney Triad and Carney-Stratakis Syndrome Consortium
-
McWhinney S.R., Pasini B., Stratakis C.A., and International Carney Triad and Carney-Stratakis Syndrome Consortium. Familial gastrointestinal stromal tumors and germ-line mutations. N Engl J Med 357 (2007) 1054-1056
-
(2007)
N Engl J Med
, vol.357
, pp. 1054-1056
-
-
McWhinney, S.R.1
Pasini, B.2
Stratakis, C.A.3
-
12
-
-
34447562827
-
Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screening
-
Sharif S., Moran A., Huson S.M., Iddenden R., Shenton A., Howard E., and Evans D.G. Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screening. J Med Genet 44 (2007) 481-484
-
(2007)
J Med Genet
, vol.44
, pp. 481-484
-
-
Sharif, S.1
Moran, A.2
Huson, S.M.3
Iddenden, R.4
Shenton, A.5
Howard, E.6
Evans, D.G.7
-
13
-
-
0033757791
-
Allelic loss at the neurofibromatosis type 1 (NF1) gene locus is frequent in desmoplastic neurotropic melanoma
-
Gutzmer R., Herbst R.A., Mommert S., Kiehl P., Matiaske F., Rütten A., Kapp A., and Weiss J. Allelic loss at the neurofibromatosis type 1 (NF1) gene locus is frequent in desmoplastic neurotropic melanoma. Hum Genet 107 (2000) 357-361
-
(2000)
Hum Genet
, vol.107
, pp. 357-361
-
-
Gutzmer, R.1
Herbst, R.A.2
Mommert, S.3
Kiehl, P.4
Matiaske, F.5
Rütten, A.6
Kapp, A.7
Weiss, J.8
-
14
-
-
22644446003
-
NF1 gene loss of heterozygosity and expression analysis in sporadic colon cancer
-
Cacev T., Radosević S., Spaventi R., Pavelić K., and Kapitanović S. NF1 gene loss of heterozygosity and expression analysis in sporadic colon cancer. Gut 54 (2005) 1129-1135
-
(2005)
Gut
, vol.54
, pp. 1129-1135
-
-
Cacev, T.1
Radosević, S.2
Spaventi, R.3
Pavelić, K.4
Kapitanović, S.5
-
15
-
-
33846924623
-
Mitotic recombination as evidence of alternative pathogenesis of gastrointestinal stromal tumours in neurofibromatosis type 1
-
Stewart D.R., Corless C.L., Rubin B.P., Heinrich M.C., Messiaen L.M., Kessler L.J., Zhang P.J., and Brooks D.G. Mitotic recombination as evidence of alternative pathogenesis of gastrointestinal stromal tumours in neurofibromatosis type 1. J Med Genet 44 (2007) e61
-
(2007)
J Med Genet
, vol.44
-
-
Stewart, D.R.1
Corless, C.L.2
Rubin, B.P.3
Heinrich, M.C.4
Messiaen, L.M.5
Kessler, L.J.6
Zhang, P.J.7
Brooks, D.G.8
-
16
-
-
0031895154
-
DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies
-
Knuutila S., Björkqvist A.M., Autio K., Tarkkanen M., Wolf M., Monni O., Szymanska J., Larramendy M.L., Tapper J., Pere H., El-Rifai W., Hemmer S., Wasenius V.M., Vidgren V., and Zhu Y. DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies. Am J Pathol 152 (1998) 1107-1123
-
(1998)
Am J Pathol
, vol.152
, pp. 1107-1123
-
-
Knuutila, S.1
Björkqvist, A.M.2
Autio, K.3
Tarkkanen, M.4
Wolf, M.5
Monni, O.6
Szymanska, J.7
Larramendy, M.L.8
Tapper, J.9
Pere, H.10
El-Rifai, W.11
Hemmer, S.12
Wasenius, V.M.13
Vidgren, V.14
Zhu, Y.15
-
17
-
-
12844259590
-
High-resolution chromosome arm 5p array CGH analysis of small cell lung carcinoma cell lines
-
Coe B.P., Henderson L.J., Garnis C., Tsao M.S., Gazdar A.F., Minna J., Lam S., Macaulay C., and Lam W.L. High-resolution chromosome arm 5p array CGH analysis of small cell lung carcinoma cell lines. Genes Chromosomes Cancer 42 (2005) 308-313
-
(2005)
Genes Chromosomes Cancer
, vol.42
, pp. 308-313
-
-
Coe, B.P.1
Henderson, L.J.2
Garnis, C.3
Tsao, M.S.4
Gazdar, A.F.5
Minna, J.6
Lam, S.7
Macaulay, C.8
Lam, W.L.9
-
18
-
-
33847663898
-
Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer
-
Kloth J.N., Oosting J., van Wezel T., Szuhai K., Knijnenburg J., Gorter A., Kenter G.G., Fleuren G.J., and Jordanova E.S. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer. BMC Genomics 8 (2007) 53
-
(2007)
BMC Genomics
, vol.8
, pp. 53
-
-
Kloth, J.N.1
Oosting, J.2
van Wezel, T.3
Szuhai, K.4
Knijnenburg, J.5
Gorter, A.6
Kenter, G.G.7
Fleuren, G.J.8
Jordanova, E.S.9
-
19
-
-
0032567513
-
Distinct cytogenetic alterations in squamous intraepithelial lesions of the cervix revealed by laser-assisted microdissection and comparative genomic hybridization
-
Aubele M., Zitzelsberger H., Schenck U., Walch A., Höfler H., and Werner M. Distinct cytogenetic alterations in squamous intraepithelial lesions of the cervix revealed by laser-assisted microdissection and comparative genomic hybridization. Cancer 84 (1998) 375-379
-
(1998)
Cancer
, vol.84
, pp. 375-379
-
-
Aubele, M.1
Zitzelsberger, H.2
Schenck, U.3
Walch, A.4
Höfler, H.5
Werner, M.6
-
20
-
-
0033571112
-
Chromosomal imbalances are associated with a high risk of progression in early invasive (pT1) urinary bladder cancer
-
Richter J., Wagner U., Schraml P., Maurer R., Alund G., Knönagel H., Moch H., Mihatsch M.J., Gasser T.C., and Sauter G. Chromosomal imbalances are associated with a high risk of progression in early invasive (pT1) urinary bladder cancer. Cancer Res 59 (1999) 5687-5691
-
(1999)
Cancer Res
, vol.59
, pp. 5687-5691
-
-
Richter, J.1
Wagner, U.2
Schraml, P.3
Maurer, R.4
Alund, G.5
Knönagel, H.6
Moch, H.7
Mihatsch, M.J.8
Gasser, T.C.9
Sauter, G.10
-
21
-
-
0038369153
-
Amplification of chromosome 5p correlates with increased expression of Skp2 in HPV-immortalized keratinocytes
-
Dowen S.E., Neutze D.M., Pett M.R., Cottage A., Stern P., Coleman N., and Stanley M.A. Amplification of chromosome 5p correlates with increased expression of Skp2 in HPV-immortalized keratinocytes. Oncogene 22 (2003) 2531-2540
-
(2003)
Oncogene
, vol.22
, pp. 2531-2540
-
-
Dowen, S.E.1
Neutze, D.M.2
Pett, M.R.3
Cottage, A.4
Stern, P.5
Coleman, N.6
Stanley, M.A.7
|