-
2
-
-
0029028701
-
Cancer: The rise of the genetic paradigm
-
Bishop JM: Cancer: The rise of the genetic paradigm. Genes Dev 9:1309-1315, 1995.
-
(1995)
Genes Dev
, vol.9
, pp. 1309-1315
-
-
Bishop, J.M.1
-
3
-
-
0027254069
-
How many mutations are required for tumorigenesis? Implications from human cancer data
-
Renan MJ: How many mutations are required for tumorigenesis? Implications from human cancer data. Mol Carcinog 7:139-146, 1993
-
(1993)
Mol Carcinog
, vol.7
, pp. 139-146
-
-
Renan, M.J.1
-
4
-
-
0020518746
-
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
-
Cavenee WK, Dryja TP, Phillips RA, et al.: Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature 305:779-784, 1983.
-
(1983)
Nature
, vol.305
, pp. 779-784
-
-
Cavenee, W.K.1
Dryja, T.P.2
Phillips, R.A.3
-
5
-
-
0029955159
-
The genetic attributable risk of breast and ovarian cancer
-
Claus EB, Schildkraut JM, Thompson WD, et al.: The genetic attributable risk of breast and ovarian cancer. Cancer 77:2318-2324, 1996.
-
(1996)
Cancer
, vol.77
, pp. 2318-2324
-
-
Claus, E.B.1
Schildkraut, J.M.2
Thompson, W.D.3
-
6
-
-
0028885339
-
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families
-
Narod SA, Ford D, Devilee P, et al.: An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Am J Hum Genet 56:254-264, 1995.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 254-264
-
-
Narod, S.A.1
Ford, D.2
Devilee, P.3
-
7
-
-
0029100049
-
Genetic heterogeneity of breast-ovarian cancer revisited
-
Narod S, Ford D, Devilee P, et al.: Genetic heterogeneity of breast-ovarian cancer revisited. Am J Hum Genet 57:957-958, 1995.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 957-958
-
-
Narod, S.1
Ford, D.2
Devilee, P.3
-
8
-
-
0027248156
-
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer
-
Lynch HT, Smyrk TC, Watson P, et al.: Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer. Gastroenterology 104:1535-1549, 1993.
-
(1993)
Gastroenterology
, vol.104
, pp. 1535-1549
-
-
Lynch, H.T.1
Smyrk, T.C.2
Watson, P.3
-
9
-
-
0027467494
-
Extracolonic cancer in hereditary nonpolyposis colorectal cancer
-
Watson P, Lynch HT: Extracolonic cancer in hereditary nonpolyposis colorectal cancer. Cancer 71:677-85, 1993.
-
(1993)
Cancer
, vol.71
, pp. 677-685
-
-
Watson, P.1
Lynch, H.T.2
-
10
-
-
0026663495
-
Hereditary ovarian cancer. A chincopathological study
-
Bewtra C, Watson P, Conway T, et al.: Hereditary ovarian cancer. A chincopathological study. Int J Gynecol Pathol 11:180-187, 1992.
-
(1992)
Int J Gynecol Pathol
, vol.11
, pp. 180-187
-
-
Bewtra, C.1
Watson, P.2
Conway, T.3
-
11
-
-
0028108802
-
Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage
-
Nystrom-Lahti M, Parsons R, Sistonen P, et al. Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage. Am J Hum Genet 55:659-665, 1994.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 659-665
-
-
Nystrom-Lahti, M.1
Parsons, R.2
Sistonen, P.3
-
12
-
-
0027933070
-
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
-
Nicolaides NC, Papadopoulos N, Liu B, et al.: Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature 371:75-80, 1994.
-
(1994)
Nature
, vol.371
, pp. 75-80
-
-
Nicolaides, N.C.1
Papadopoulos, N.2
Liu, B.3
-
13
-
-
0027433563
-
Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families: the Breast Cancer Linkage Consortium
-
Easton DF., Bishop DT, Ford D, et al.: Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families: The Breast Cancer Linkage Consortium. Am J Hum Genet 52:678-701, 1993.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 678-701
-
-
Easton, D.F.1
Bishop, D.T.2
Ford, D.3
-
14
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Edens D, et al.: A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266:66-71, 1994.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Edens, D.3
-
15
-
-
0029987651
-
BRCA1 is a 220-kDa nuclear phosphoprotein that is expressed and phosphorylated in a cell cycle-dependent manner
-
Chen Y, Farmer AA, Chen C-F, et al.: BRCA1 is a 220-kDa nuclear phosphoprotein that is expressed and phosphorylated in a cell cycle-dependent manner. Cancer Res 56:3168-3172, 1996
-
(1996)
Cancer Res
, vol.56
, pp. 3168-3172
-
-
Chen, Y.1
Farmer, A.A.2
Chen, C.-F.3
-
17
-
-
0029830051
-
Transcriptional activation by BRCA1
-
Chapman MS, Verma IM: Transcriptional activation by BRCA1. Nature 382:678-679, 1996.
-
(1996)
Nature
, vol.382
, pp. 678-679
-
-
Chapman, M.S.1
Verma, I.M.2
-
18
-
-
0030474170
-
Evidence for a transcnptional activation function for BRCA1 C-terminal region
-
Monteiro ANA, August A, Hanafusa H: Evidence for a transcnptional activation function for BRCA1 C-terminal region. Proc Natl Acad Sci USA 93:13595-13599, 1996.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13595-13599
-
-
Monteiro, A.N.A.1
August, A.2
Hanafusa, H.3
-
19
-
-
0030965157
-
BRCA1 is a component of the UNA polymerase II holoenzyme
-
Scully R, Anderson SF, Chao DM. et al: BRCA1 is a component of the UNA polymerase II holoenzyme. Proc Natl Acad Sci USA 94:5605-5610, 1997.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 5605-5610
-
-
Scully, R.1
Anderson, S.F.2
Chao, D.M.3
-
20
-
-
0029115660
-
The developmental pattern of BRCA1 expression implies a role in differentiation of breast and other tissues
-
Marquis ST, Rajan JV, Wynshaw-Boris A, et al.: The developmental pattern of BRCA1 expression implies a role in differentiation of breast and other tissues. Nature Genet 11:17-26, 1995.
-
(1995)
Nature Genet
, vol.11
, pp. 17-26
-
-
Marquis, S.T.1
Rajan, J.V.2
Wynshaw-Boris, A.3
-
21
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and metotic cells
-
Scully R, Chen J, Plug A, et al.: Association of BRCA1 with Rad51 in mitotic and metotic cells. Cell 88:265-275, 1997
-
(1997)
Cell
, vol.88
, pp. 265-275
-
-
Scully, R.1
Chen, J.2
Plug, A.3
-
22
-
-
11744381890
-
-
Breast Cancer information Core. NHGRI Web Site
-
Breast Cancer information Core. NHGRI Web Site (http://wwvv.nhgri.nih.gov/ Intramural_research/Lab_transfer/Bic), 1997.
-
(1997)
-
-
-
23
-
-
0029794992
-
Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
-
Roa BB, Boyd AA, Volcik K. et al: Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2. Nature Genet 14:185-187, 1996.
-
(1996)
Nature Genet
, vol.14
, pp. 185-187
-
-
Roa, B.B.1
Boyd, A.A.2
Volcik, K.3
-
24
-
-
0029083814
-
The carrier frequency of the BRCA1 185delAG mutation is approximately 1% in Ashkenazi Jewish individuals
-
Struewing JP, Abeliovich D, Peretz T, et al.: The carrier frequency of the BRCA1 185delAG mutation is approximately 1% in Ashkenazi Jewish individuals. Nature Genet 11:198-200, 1995
-
(1995)
Nature Genet
, vol.11
, pp. 198-200
-
-
Struewing, J.P.1
Abeliovich, D.2
Peretz, T.3
-
25
-
-
0029009749
-
Mutation analysis of the BRCA1 gene in ovarian cancers
-
Takahashi H, Behbakht K, McGovern PE, et al.: Mutation analysis of the BRCA1 gene in ovarian cancers. Cancer Res 55:2998-3002, 1995.
-
(1995)
Cancer Res
, vol.55
, pp. 2998-3002
-
-
Takahashi, H.1
Behbakht, K.2
McGovern, P.E.3
-
26
-
-
0028865866
-
Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients: Four germ-line mutations, but no evidence of somatic mutation
-
Matsushima M. Kobayashi K. Emi M. et al. Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients: Four germ-line mutations, but no evidence of somatic mutation. Hum Mol Genet 4:1953-1956, 1995.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1953-1956
-
-
Matsushima, M.1
Kobayashi, K.2
Emi, M.3
-
27
-
-
0031003498
-
Contribution of BRCA1 mutations to ovarian cancer
-
Stratton JF, Gayther SA, Russell P, et al.: Contribution of BRCA1 mutations to ovarian cancer. N Engl J Med 336:1125-1130, 1997.
-
(1997)
N Engl J Med
, vol.336
, pp. 1125-1130
-
-
Stratton, J.F.1
Gayther, S.A.2
Russell, P.3
-
28
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R, Bignell G, Lancaster J. 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
Bignell, G.2
Lancaster, J.3
-
29
-
-
13344269668
-
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
-
Tavtigian SV, Simard J, Rommens J, et al.: The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nature Genet 12:333-337, 1996.
-
(1996)
Nature Genet
, vol.12
, pp. 333-337
-
-
Tavtigian, S.V.1
Simard, J.2
Rommens, J.3
-
30
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
Thorlacius S, Olafsdottir G, Tryggvadottir L, et al.: A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nature Genet 13:117-119, 1996.
-
(1996)
Nature Genet
, vol.13
, pp. 117-119
-
-
Thorlacius, S.1
Olafsdottir, G.2
Tryggvadottir, L.3
-
31
-
-
9344244079
-
Mutations of the BRCA2 gene in ovarian carcinomas
-
Takahashi H, Chiu H-C, Bandera CA, et al.: Mutations of the BRCA2 gene in ovarian carcinomas. Cancer Res 56:2738-2741, 1996.
-
(1996)
Cancer Res
, vol.56
, pp. 2738-2741
-
-
Takahashi, H.1
Chiu, H.-C.2
Bandera, C.A.3
-
32
-
-
9444222467
-
Somatic and germline mutations of the BRCA2 gene in sporadic ovarian cancer
-
Foster KA, Harrington P. Kerr J, et al.: Somatic and germline mutations of the BRCA2 gene in sporadic ovarian cancer. Cancer Res 56:3622-3625, 1996.
-
(1996)
Cancer Res
, vol.56
, pp. 3622-3625
-
-
Foster, K.A.1
Harrington, P.2
Kerr, J.3
-
33
-
-
0030919135
-
Changes in BRCA2 expression during progression of the cell cycle
-
Wang SC, Lin SH, Su LK. et al: Changes in BRCA2 expression during progression of the cell cycle. Biochem Biophys Res Comm 234:247-251, 1997.
-
(1997)
Biochem Biophys Res Comm
, vol.234
, pp. 247-251
-
-
Wang, S.C.1
Lin, S.H.2
Su, L.K.3
-
34
-
-
0029997175
-
BRCA1 and BRCA2 mRNA levels are coordinately elevated in human breast cancer cells in response to estrogen
-
Spillman MA, Bowcock AM: BRCA1 and BRCA2 mRNA levels are coordinately elevated in human breast cancer cells in response to estrogen. Oncogene 13:1639-1645, 1996.
-
(1996)
Oncogene
, vol.13
, pp. 1639-1645
-
-
Spillman, M.A.1
Bowcock, A.M.2
-
35
-
-
0031040731
-
Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene
-
Conner F, Smith A, Wooster R, et al.: Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene. Hum Mol Genet 6:291-300, 1997.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 291-300
-
-
Conner, F.1
Smith, A.2
Wooster, R.3
-
36
-
-
0031569873
-
Developmental expression of Brca2 colocalizes with Brca1 and is associated with proliferation and differentiation in multiple tissues
-
Rajan JV, Marquis ST, Gardner HP, et al.: Developmental expression of Brca2 colocalizes with Brca1 and is associated with proliferation and differentiation in multiple tissues. Dev Biol 184:385-401, 1997.
-
(1997)
Dev Biol
, vol.184
, pp. 385-401
-
-
Rajan, J.V.1
Marquis, S.T.2
Gardner, H.P.3
-
37
-
-
0030933762
-
Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2
-
Sharan SK, Morimatsu M, Albrecht U, et al.: Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2. Nature 386:804-810, 1997.
-
(1997)
Nature
, vol.386
, pp. 804-810
-
-
Sharan, S.K.1
Morimatsu, M.2
Albrecht, U.3
-
38
-
-
0030892642
-
Transcnptional activation functions in BRCA2
-
Milner J, Ponder B, Hughes-Davies L, et ah Transcnptional activation functions in BRCA2. Nature 386:772-773, 1997.
-
(1997)
Nature
, vol.386
, pp. 772-773
-
-
Milner, J.1
Ponder, B.2
Hughes-Davies, L.3
-
39
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Askenazi Jewish individuals is approximately 1%
-
Oddoux C, Struewing JP, Clayton CM, et al.: The carrier frequency of the BRCA2 6174delT mutation among Askenazi Jewish individuals is approximately 1%. Nature Genet 14:188-190, 1996.
-
(1996)
Nature Genet
, vol.14
, pp. 188-190
-
-
Oddoux, C.1
Struewing, J.P.2
Clayton, C.M.3
-
40
-
-
0031035359
-
The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Askenazi women
-
Abeliovich D, Kaduri L, Lerer L et al: The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Askenazi women. Am J Hum Genet 60:505-514, 1997.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 505-514
-
-
Abeliovich, D.1
Kaduri, L.2
Lerer, L.3
-
41
-
-
0029089259
-
Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspectives
-
Marra G, Boland CR: Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspectives J Natl Cancer Inst 87:1114-1125, 1995.
-
(1995)
J Natl Cancer Inst
, vol.87
, pp. 1114-1125
-
-
Marra, G.1
Boland, C.R.2
-
42
-
-
0029042130
-
Identification of mismatch repair genes and their role in the development of cancer
-
Fishel R, Kolodner R. Identification of mismatch repair genes and their role in the development of cancer. Curr Opin Genet Dev 5:382-395, 1995.
-
(1995)
Curr Opin Genet Dev
, vol.5
, pp. 382-395
-
-
Fishel, R.1
Kolodner, R.2
-
43
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu B, Parsons R, Papadopoulos N, et al.: Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nature Med 2:169-174, 1996.
-
(1996)
Nature Med
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.2
Papadopoulos, N.3
-
44
-
-
0028867842
-
Mismatch repair: Mechanisms and relationship to cancer susceptibility
-
Kolodner RD: Mismatch repair: Mechanisms and relationship to cancer susceptibility. Trends Biochem Sci 20:397-401, 1995.
-
(1995)
Trends Biochem Sci
, vol.20
, pp. 397-401
-
-
Kolodner, R.D.1
-
45
-
-
0031017268
-
Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines
-
Kane MF, Loda M, Gaida GM, et al.: Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines. Cancer Res 57:808-811, 1997.
-
(1997)
Cancer Res
, vol.57
, pp. 808-811
-
-
Kane, M.F.1
Loda, M.2
Gaida, G.M.3
-
46
-
-
0029101616
-
Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer
-
de Wind N, Dekker M, Berns A, et al.: Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer. Cell 82:321-330, 1995.
-
(1995)
Cell
, vol.82
, pp. 321-330
-
-
De Wind, N.1
Dekker, M.2
Berns, A.3
-
47
-
-
0029099989
-
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis
-
Baker SM, Bronner CE, Zhang L, et al.: Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell 82:309-320, 1995.
-
(1995)
Cell
, vol.82
, pp. 309-320
-
-
Baker, S.M.1
Bronner, C.E.2
Zhang, L.3
-
48
-
-
8944232867
-
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
-
Baker SM, Plug AW, Prolla TA, et al.: Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nature Genet 13:336-342, 1996.
-
(1996)
Nature Genet
, vol.13
, pp. 336-342
-
-
Baker, S.M.1
Plug, A.W.2
Prolla, T.A.3
-
49
-
-
0028785603
-
Micro-satellite instability and mutations of the transforming growth factor b type II receptor gene in colorectal cancer
-
Parsons R, Myeroff L, Liu B, et al.: Micro-satellite instability and mutations of the transforming growth factor b type II receptor gene in colorectal cancer. Cancer Res 55:5548-5550, 1995.
-
(1995)
Cancer Res
, vol.55
, pp. 5548-5550
-
-
Parsons, R.1
Myeroff, L.2
Liu, B.3
-
50
-
-
0031018674
-
Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype
-
Rampino N, Yamamoto H, Ionov Y, et al.: Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype. Science 275:967-969, 1997.
-
(1997)
Science
, vol.275
, pp. 967-969
-
-
Rampino, N.1
Yamamoto, H.2
Ionov, Y.3
-
52
-
-
0028844202
-
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation
-
Gayther SA, Warren W, Mazoyer S, et al.: Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation. Nature Genet 11:428-433, 1995.
-
(1995)
Nature Genet
, vol.11
, pp. 428-433
-
-
Gayther, S.A.1
Warren, W.2
Mazoyer, S.3
-
53
-
-
0031012305
-
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
-
Gayther SA, Mangion J, Russell P, et al.: Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene Nature Genet 15:103-105, 1997.
-
(1997)
Nature Genet
, vol.15
, pp. 103-105
-
-
Gayther, S.A.1
Mangion, J.2
Russell, P.3
-
54
-
-
13344268996
-
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus
-
Phelan CM, Rebbeck TR, Weber BL, et al.: Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus. Nature Genet 12:309-311, 1996.
-
(1996)
Nature Genet
, vol.12
, pp. 309-311
-
-
Phelan, C.M.1
Rebbeck, T.R.2
Weber, B.L.3
-
55
-
-
0028843102
-
Breast and ovarian cancer incidence in BRCA1-mutation carriers
-
Easton DF, Ford D, Bishop DT, et al.: Breast and ovarian cancer incidence in BRCA1-mutation carriers. Am J Hum Genet 56:265-271, 1995.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 265-271
-
-
Easton, D.F.1
Ford, D.2
Bishop, D.T.3
-
56
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster R, Neuhausen SL, Mangion J, 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
Neuhausen, S.L.2
Mangion, J.3
-
57
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
Struewing JP, Hartge P, Wacholder S, et al.: The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews. N Engl J Med 336:1401-1408, 1997.
-
(1997)
N Engl J Med
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hartge, P.2
Wacholder, S.3
-
58
-
-
16944363862
-
Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: Frequency and differential penetrance in ovarian cancer and in breastovarian cancer families
-
Levy-Lahad E, Catane R, Eisenberg S, et al.: Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: Frequency and differential penetrance in ovarian cancer and in breastovarian cancer families. Am J Hum Genet 60:1059-1067, 1997.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1059-1067
-
-
Levy-Lahad, E.1
Catane, R.2
Eisenberg, S.3
-
59
-
-
10544220023
-
Clinical and pathologic features of ovarian cancer in women with germ-line mutations of BRCA1
-
Rubin SC, Benjamin I, Behbakht K, et al.: Clinical and pathologic features of ovarian cancer in women with germ-line mutations of BRCA1. N Engl J Med 335:1413-1416, 1996.
-
(1996)
N Engl J Med
, vol.335
, pp. 1413-1416
-
-
Rubin, S.C.1
Benjamin, I.2
Behbakht, K.3
-
60
-
-
13344262707
-
Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage
-
Marcus JN, Watson P, Page DL, et al.: Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage. Cancer 77:697-709, 1996.
-
(1996)
Cancer
, vol.77
, pp. 697-709
-
-
Marcus, J.N.1
Watson, P.2
Page, D.L.3
-
61
-
-
0342940785
-
Pathology of familial breast cancer: Differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases
-
Breast Cancer Linkage Consortium: Pathology of familial breast cancer: Differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Lancet 349:1505-1510, 1997.
-
(1997)
Lancet
, vol.349
, pp. 1505-1510
-
-
-
62
-
-
0030894785
-
Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations
-
Tirkkonen M, Johannsson O, Agnarsson BA, et al.: Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations. Cancer Res 57:1222-1227, 1997.
-
(1997)
Cancer Res
, vol.57
, pp. 1222-1227
-
-
Tirkkonen, M.1
Johannsson, O.2
Agnarsson, B.A.3
-
63
-
-
0031081108
-
Hereditary ovarian cancer: Molecular genetics and clinical implications
-
Boyd J, Rubin SC: Hereditary ovarian cancer: Molecular genetics and clinical implications Gynecol Oncol 64:196-206, 1997.
-
(1997)
Gynecol Oncol
, vol.64
, pp. 196-206
-
-
Boyd, J.1
Rubin, S.C.2
-
64
-
-
0029864134
-
Genetic testing for cancer susceptibility
-
Statement of the American Society of Clinical Oncology: Genetic testing for cancer susceptibility. J Clin Oncol 14:1730-1736, 1996.
-
(1996)
J Clin Oncol
, vol.14
, pp. 1730-1736
-
-
-
65
-
-
8044220285
-
Recommendations for follow-up care of individuals with an inherited predisposition to cancer: 1. Hereditary nonpolyposis colon cancer: Cancer Genetics Studies Consortium
-
Burke W, Petersen G, Lynch P, et al.: Recommendations for follow-up care of individuals with an inherited predisposition to cancer: 1. Hereditary nonpolyposis colon cancer: Cancer Genetics Studies Consortium. JAMA 277:915-919, 1997.
-
(1997)
JAMA
, vol.277
, pp. 915-919
-
-
Burke, W.1
Petersen, G.2
Lynch, P.3
-
66
-
-
0030893779
-
Recommendations for follow-up care of individuals with an inherited predisposition to cancer: II. BRCA1 and BRCA2: Cancer Genetics Studies Consortium
-
Burke W, Daly M, Garber J, et al.: Recommendations for follow-up care of individuals with an inherited predisposition to cancer: II. BRCA1 and BRCA2: Cancer Genetics Studies Consortium. JAMA 277:997-1003, 1997.
-
(1997)
JAMA
, vol.277
, pp. 997-1003
-
-
Burke, W.1
Daly, M.2
Garber, J.3
-
67
-
-
0008195461
-
A descriptive study of BRCA1 testing and reactions to disclosure of test results
-
Lynch HT, Lemon SJ, Durham C, et al.: A descriptive study of BRCA1 testing and reactions to disclosure of test results. Cancer 79:2219-2228, 1997.
-
(1997)
Cancer
, vol.79
, pp. 2219-2228
-
-
Lynch, H.T.1
Lemon, S.J.2
Durham, C.3
-
68
-
-
0030567718
-
A model protocol for evaluating the behavioral and psychosocial effects of BRCA1 testing
-
Botkin JR, Croyle RT, Smith KR, et al.: A model protocol for evaluating the behavioral and psychosocial effects of BRCA1 testing. J Natl Cancer Inst 88:872-882, 1996.
-
(1996)
J Natl Cancer Inst
, vol.88
, pp. 872-882
-
-
Botkin, J.R.1
Croyle, R.T.2
Smith, K.R.3
|