-
1
-
-
0027482019
-
All in the (cancer) family
-
Knudson, A.G. All in the (cancer) family. Nature Genet. 5, 103-104 (1993).
-
(1993)
Nature Genet.
, vol.5
, pp. 103-104
-
-
Knudson, A.G.1
-
2
-
-
0028073794
-
BRCA1 mutations in primary breast and ovarian carcinomas
-
Futreal, P. A. et al. BRCA1 mutations in primary breast and ovarian carcinomas. Science 266, 120-122 (1994).
-
(1994)
Science
, vol.266
, pp. 120-122
-
-
Futreal, P.A.1
-
3
-
-
0029283880
-
A somatic BRCA1 mutation in an ovarian tumor
-
Hosking, L et al. A somatic BRCA1 mutation in an ovarian tumor. Nature Genet. 9, 343-344 (1995).
-
(1995)
Nature Genet.
, vol.9
, pp. 343-344
-
-
Hosking, L.1
-
4
-
-
0028960025
-
Somatic mutations in the BRCA1 gene in sporadic ovarian tumor
-
Merajver, S. D. et al. Somatic mutations in the BRCA1 gene in sporadic ovarian tumor Nature Genet. 9, 439-443 (1995).
-
(1995)
Nature Genet.
, vol.9
, pp. 439-443
-
-
Merajver, S.D.1
-
5
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster, R. et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 265, 2088-2090 (1994).
-
(1994)
Science
, vol.265
, pp. 2088-2090
-
-
Wooster, R.1
-
6
-
-
0029160005
-
Linkage to BRCA2 region in hereditary male breast cancer
-
Thoriacius, S. et al. Linkage to BRCA2 region in hereditary male breast cancer. Lancet 346, 544-545 (1995).
-
(1995)
Lancet
, vol.346
, pp. 544-545
-
-
Thoriacius, S.1
-
7
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster, R. et al. Identification of the breast cancer susceptibility gene BRCA2. Nature 378, 789-792 (1995).
-
(1995)
Nature
, vol.378
, pp. 789-792
-
-
Wooster, R.1
-
8
-
-
13344269668
-
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
-
Tavtigian, S. V. et al. The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nature Genet. 12, 1-6 (1996).
-
(1996)
Nature Genet.
, vol.12
, pp. 1-6
-
-
Tavtigian, S.V.1
-
9
-
-
0029007696
-
Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13
-
Collins, N. et al. Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13. Oncogene 10, 1673-1675 (1995).
-
(1995)
Oncogene
, vol.10
, pp. 1673-1675
-
-
Collins, N.1
-
10
-
-
0029041032
-
Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region
-
Schutte, M. et al. Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region. Proc. Natl. Acad. Sci. USA 92, 5950-5954, (1995).
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 5950-5954
-
-
Schutte, M.1
-
11
-
-
0006153881
-
Response to Rates of p16 (MTS1) Mutations in Primary Tumors with 9p Loss. Cairns et al. 1995
-
Kamb, A. et al. Response to Rates of p16 (MTS1) Mutations in Primary Tumors with 9p Loss. Cairns et al. 1995 Science 265, 416-417 (1994).
-
(1994)
Science
, vol.265
, pp. 416-417
-
-
Kamb, A.1
-
12
-
-
0028866753
-
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13
-
Cleton-Jansen, A. M. et al. Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13. Br. J. Cancer 72, 1241-1244 (1995).
-
(1995)
Br. J. Cancer
, vol.72
, pp. 1241-1244
-
-
Cleton-Jansen, A.M.1
-
13
-
-
0030138354
-
Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer
-
Neuhausen, S. et al. Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer. Nature Genet. 13, 126-128 (1996).
-
(1996)
Nature Genet.
, vol.13
, pp. 126-128
-
-
Neuhausen, S.1
-
14
-
-
0028875205
-
Methylation of the 5′ CpG island of the P16/CDKN2 tumor suppressor gene in normal and a transformed human tissues correlates with gene silencing
-
Gonzalez-Zulueta, M. et al. Methylation of the 5′ CpG island of the P16/CDKN2 tumor suppressor gene in normal and a transformed human tissues correlates with gene silencing. Cancer Res. 55, 4531-4535 (1995).
-
(1995)
Cancer Res.
, vol.55
, pp. 4531-4535
-
-
Gonzalez-Zulueta, M.1
-
15
-
-
0029011539
-
5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers
-
Merlo, A. et al. 5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers. Nature Med. 1, 686-691 (1995).
-
(1995)
Nature Med.
, vol.1
, pp. 686-691
-
-
Merlo, A.1
-
16
-
-
0023775771
-
Altered expression of the retinoblastoma (RB) gene in small-cell carcinoma of the lung
-
Yokota, J. et al. Altered expression of the retinoblastoma (RB) gene in small-cell carcinoma of the lung. Oncogene 3, 471-475 (1988).
-
(1988)
Oncogene
, vol.3
, pp. 471-475
-
-
Yokota, J.1
-
17
-
-
0025311341
-
Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer
-
Hensel, C. H. et al. Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer. Cancer Res. 50, 3067-3072 (1990).
-
(1990)
Cancer Res.
, vol.50
, pp. 3067-3072
-
-
Hensel, C.H.1
-
18
-
-
0024514647
-
Allelotype of colorectal carcinomas
-
Vogelstein, B. et al. Allelotype of colorectal carcinomas. Science 244, 207-211 (1989).
-
(1989)
Science
, vol.244
, pp. 207-211
-
-
Vogelstein, B.1
-
19
-
-
0028901842
-
CDKN2 (MTS1) tumor suppressor gene mutations in human tumor cell lines
-
Liu, Q. et al. CDKN2 (MTS1) tumor suppressor gene mutations in human tumor cell lines. Oncogene 10, 1061-1067 (1995).
-
(1995)
Oncogene
, vol.10
, pp. 1061-1067
-
-
Liu, Q.1
-
20
-
-
0027366136
-
A novel metalloprotease/disintegrin-like gene at 17q21.3 is somatically rearranged in two primary breast cancers
-
Emi, M. et al. A novel metalloprotease/disintegrin-like gene at 17q21.3 is somatically rearranged in two primary breast cancers, Nature Genet. 5, 151-157 (1993).
-
(1993)
Nature Genet.
, vol.5
, pp. 151-157
-
-
Emi, M.1
-
21
-
-
0029339936
-
How neutral are synonymous codon mutations?
-
Richard, I. & Beckmann, J. S. How neutral are synonymous codon mutations? Nature Genet. 10, 259 (1995).
-
(1995)
Nature Genet.
, vol.10
, pp. 259
-
-
Richard, I.1
Beckmann, J.S.2
|