-
6
-
-
0030941038
-
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma
-
(1997)
Oncogene
, vol.14
, pp. 1503-1510
-
-
Casola, S.1
Pedone, P.V.2
Cavazzana, A.O.3
Basso, G.4
Luksch, R.5
D'Amore, E.S.6
Carli, M.7
Bruni, C.B.8
Riccio, A.9
-
7
-
-
0030220849
-
Chromosomal 11 alterations in non-small-cell lung carcinomas in Hong Kong
-
(1996)
Lung Cancer
, vol.15
, pp. 51-65
-
-
Chan, A.S.1
Lam, W.K.2
Wong, M.P.3
Fu, K.H.4
Lee, J.5
Yew, W.W.6
Chiu, S.W.7
Lung, M.L.8
-
8
-
-
0030787915
-
Deletion of chromosome 11p15, p12, q22, q23-24 loci in human prostate cancer
-
(1997)
Int J Cancer
, vol.72
, pp. 283-288
-
-
Dahiya, R.1
McCarville, J.2
Lee, C.3
Hu, W.4
Kaur, G.5
Carroll, P.6
Deng, G.7
-
9
-
-
0031940675
-
Risk of cancer during the first four years of life in children from the Beckwith-Wiedemann syndrome registry
-
(1998)
J Pediatr
, vol.132
, pp. 398-400
-
-
DeBaun, M.R.1
Tucker, M.A.2
-
11
-
-
0028293639
-
Hamartomas of the chest wall in infants
-
(1994)
Ann Thorac Surg
, vol.57
, pp. 868-875
-
-
Dounies, R.1
Chwals, W.J.2
Lally, K.P.3
Isaacs, H.4
Senac, M.O.5
Hanson, B.A.6
Hossein Mahour, G.7
Sherman, N.J.8
-
15
-
-
0030840738
-
Structural and functional abnormalities at 11p15 are associated with the malignant phenotype in sporadic adrenocortical tumors: Study on a series of 82 tumors
-
(1997)
J Clin Endocrinol Metabol
, vol.82
, pp. 2559-2565
-
-
Gicquel, C.1
Raffin-Sanson, M.L.2
Gaston, V.3
Bertagna, X.4
Plouin, P.F.5
Schlumberger, M.6
Louvel, A.7
Luton, J.P.8
Le Bouc, Y.9
-
17
-
-
0029896367
-
KIP2 and its reduced expression in Wilms' tumors
-
(1996)
Hum Mol Genet
, vol.5
, pp. 783-788
-
-
Hatada, I.1
Inzawa, J.2
Abe, T.3
Nakayama, M.4
Kaneko, Y.5
Jinno, Y.6
Niikawa, N.7
Ohashi, H.8
Fukushima, Y.9
Iida, K.10
Yutani, C.11
Takahashi, S.12
Chiba, Y.13
Ohishi, S.14
Mukai, T.15
-
18
-
-
16044364516
-
KIP2 is mutated in Beckwith-Wiedemann syndrome
-
(1996)
Nature Genet
, vol.14
, pp. 171-173
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
Okada, A.7
Ohishi, S.8
Nabetani, A.9
Morisaki, H.10
Nakayama, M.11
Niikawa, N.12
Mukai, T.13
-
19
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 12456-12460
-
-
Hoovers, J.M.N.1
Kalikin, L.M.2
Johnson, L.A.3
Alders, M.4
Redeker, B.5
Law, D.J.6
Bliek, J.7
Steenman, M.8
Benedict, M.9
Wiegant, J.10
Lengauer, C.11
Taillon-Miller, P.12
Schlessinger, D.13
Edwards, M.C.14
Elledge, S.J.15
Ivens, A.16
Westerveld, A.17
Little, P.18
Mannens, M.19
Feinberg, A.P.20
more..
-
20
-
-
0027369355
-
Pulmonary carcinoma associated with hamartoma in an 11-year-old boy
-
(1993)
Am J Pediatr Hematol Oncol
, vol.15
, pp. 439-442
-
-
Kojima, R.1
Mizuguchi, M.2
Bessho, F.3
Oka, T.4
Watanabe, H.5
Yonezawa, M.6
Asano, N.7
Iwanaka, T.8
-
21
-
-
0029869293
-
KIP2 gene at 11p15.5
-
(1996)
Oncogene
, vol.12
, pp. 1365-1368
-
-
Kondo, M.1
Matsuoka, S.2
Uchida, K.3
Osada, H.4
Nagatake, M.5
Takagi, K.6
Harper, J.W.7
Takahashi, T.8
Elledge, S.J.9
Tsakahashi, T.10
-
22
-
-
0024517062
-
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5
-
(1989)
Am J Med Genet
, vol.44
, pp. 711-719
-
-
Koufos, A.1
Grundy, P.2
Morgan, K.3
Aleck, K.A.4
Hadro, T.5
Lampkin, B.C.6
Kalbakji, A.7
Cavenee, W.8
-
23
-
-
0025017191
-
The phakomatoses as paracrine growth disorders (paracrinopathies)
-
(1990)
Clin Genet
, vol.37
, pp. 97-105
-
-
Kousseff, B.G.1
-
27
-
-
0029978017
-
KIP2, on chromosome 11p15
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 3026-3030
-
-
Matsuoka, S.1
Thompson, J.S.2
Edwards, M.C.3
Barletta, J.M.4
Grundy, P.5
Kalikin, L.M.6
Wade Harper, J.7
Elledge, S.J.8
Feinberg, A.P.9
-
30
-
-
0027285258
-
Relaxation on insulin-like growth factor II gene imprinting implicated in Wilms' tumour
-
(1993)
Nature
, vol.362
, pp. 749-751
-
-
Ogawa, O.1
Eccles, M.R.2
Szeto, J.3
McNoe, L.A.4
Yun, K.5
Maw, M.A.6
Smith, P.J.7
Reeve, A.E.8
-
34
-
-
13144257678
-
Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3873-3878
-
-
Schwienbacher, C.1
Sabbioni, S.2
Campi, M.3
Veronese, A.4
Bernardi, G.5
Memegatti, A.6
Hatada, I.7
Mukai, T.8
Ohashi, H.9
Barbanti-Brodano, G.10
Croce, C.M.11
Negrini, M.12
-
35
-
-
0020638763
-
Beckwith-Wiedemann syndrome: Role of ultrasound in its management
-
(1983)
Clin Radiol
, vol.34
, pp. 313-319
-
-
Shah, K.J.1
-
37
-
-
0029066736
-
Loss of heterozygosity at 11p15 in malignant glioma
-
(1995)
Cancer Res
, vol.55
, pp. 2166-2168
-
-
Sonoda, Y.1
Iizuka, M.2
Yasuda, J.3
Makino, R.4
Ono, T.5
Kayama, T.6
Yoshimoto, T.7
Sekiya, T.8
-
40
-
-
9244257359
-
Allelic-expression imbalance of the insulin-like growth factor 2 gene in hepatocellular carcinoma and underlying disease
-
(1996)
Oncogene
, vol.12
, pp. 1589-1592
-
-
Takeda, S.1
Kondo, M.2
Kumada, T.3
Koshikawa, T.4
Ueda, R.5
Nishio, M.6
Osada, H.7
Suzuki, H.8
Nagatake, M.9
Washimi, O.10
Takagi, K.11
Takahashi, T.12
Nakao, A.13
Takahashi, T.14
-
45
-
-
0029055009
-
Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis
-
(1995)
Cancer Res
, vol.55
, pp. 2660-2664
-
-
Winqvist, R.1
Hampton, G.M.2
Mannermaa, A.3
Blanco, G.4
Alavaikko, M.5
Kiviniemi, H.6
Taskinen, P.J.7
Evans, G.A.8
Wright, F.A.9
Newsham, I.10
Cavenee, W.K.11
-
48
-
-
1842335753
-
Altered cell differentiation and proliferation in mice lacking p57(KIP2) indicates a role in Beckwith-Wiedemann syndrome
-
(1997)
Nature
, vol.387
, pp. 151-158
-
-
Zhang, P.1
Leigeois, N.J.2
Wong, C.3
Finegold, M.4
Hou, H.5
Thompson, J.C.6
Silverman, A.7
Harper, J.W.8
DePinho, R.A.9
Elledge, S.J.10
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