-
1
-
-
85030287029
-
-
Atlanta, American Cancer Society, 1996
-
1. Cancer Facts and Figures - 1996, Atlanta, American Cancer Society, 1996
-
(1996)
-
-
-
2
-
-
0002034756
-
Epithelial ovarian cancer
-
Hoskins WJ, Perez CA, Young RC (eds): Philadelphia, JB Lippincott
-
2. Ozols RF, et al.: Epithelial ovarian cancer, in Hoskins WJ, Perez CA, Young RC (eds): Principles and Practice of Gynecologic Oncology, Philadelphia, JB Lippincott, 1992, pp 731-781
-
(1992)
Principles and Practice of Gynecologic Oncology
, pp. 731-781
-
-
Ozols, R.F.1
-
3
-
-
0018761410
-
Incessant ovulation" and ovarian cancer
-
3. Casagrande JT, et al: "Incessant ovulation" and ovarian cancer. Lancet 2:170-172, 1979
-
(1979)
Lancet
, vol.2
, pp. 170-172
-
-
Casagrande, J.T.1
-
4
-
-
0026410941
-
The epidemiology of ovarian cancer
-
4. Parazzini F, et al: The epidemiology of ovarian cancer. Gynecol Oncol 43:9-23, 1991
-
(1991)
Gynecol Oncol
, vol.43
, pp. 9-23
-
-
Parazzini, F.1
-
5
-
-
0026010995
-
Molecular themes in oncogenesis
-
5. Bishop JM: Molecular themes in oncogenesis. Cell 64:235-248, 1991
-
(1991)
Cell
, vol.64
, pp. 235-248
-
-
Bishop, J.M.1
-
6
-
-
0024399684
-
Oncogenes, antioncogenes, and the molecular basis of multistep carcinogenesis
-
6. Weinberg RA: Oncogenes, antioncogenes, and the molecular basis of multistep carcinogenesis. Cancer Res 49:3713-3721, 1989
-
(1989)
Cancer Res
, vol.49
, pp. 3713-3721
-
-
Weinberg, R.A.1
-
7
-
-
0025303739
-
Genetic and cellular basis of multistep carcinogenesis
-
7. Boyd J, Barrett JC: Genetic and cellular basis of multistep carcinogenesis. Pharmacol Ther 46:469-486, 1990
-
(1990)
Pharmacol Ther
, vol.46
, pp. 469-486
-
-
Boyd, J.1
Barrett, J.C.2
-
8
-
-
0027254069
-
How many mutations are required for tumorigenesis? implications from human cancer data
-
8. 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
-
9
-
-
0027413895
-
Mutation of K-ras protooncogene in human ovarian epithelial tumors of borderline malignancy
-
9. Mok SC, et al: Mutation of K-ras protooncogene in human ovarian epithelial tumors of borderline malignancy. Cancer Res 53:1489-1492, 1993
-
(1993)
Cancer Res
, vol.53
, pp. 1489-1492
-
-
Mok, S.C.1
-
10
-
-
0027182705
-
p53 and Ki-ras gene mutations in epithelial ovarian neoplasms
-
10. Teneriello MG, et al: p53 and Ki-ras gene mutations in epithelial ovarian neoplasms. Cancer Res 53:3103-3108, 1993
-
(1993)
Cancer Res
, vol.53
, pp. 3103-3108
-
-
Teneriello, M.G.1
-
11
-
-
0028115872
-
Mutation of K-ras protooncogene is associated with histological subtypes in human mucinous ovarian tumors
-
11. Ichikawa Y, et al.: Mutation of K-ras protooncogene is associated with histological subtypes in human mucinous ovarian tumors. Cancer Res 54:33-35, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 33-35
-
-
Ichikawa, Y.1
-
12
-
-
0024337144
-
Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer
-
12. Slamon DJ, et al.: Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer. Science 244:707-712, 1989
-
(1989)
Science
, vol.244
, pp. 707-712
-
-
Slamon, D.J.1
-
13
-
-
0025281906
-
Overexpression of HER-2/neu is associated with poor survival in advanced epithelial ovarian cancer
-
13. Berchuck A, et al: Overexpression of HER-2/neu is associated with poor survival in advanced epithelial ovarian cancer. Cancer Res 50:4087-4091, 1990
-
(1990)
Cancer Res
, vol.50
, pp. 4087-4091
-
-
Berchuck, A.1
-
14
-
-
0027407511
-
Prognostic significance of HER-2/neu expression in advanced epithelial ovarian cancer: A multivariate analysis
-
14. Rubin SC, et al.: Prognostic significance of HER-2/neu expression in advanced epithelial ovarian cancer: A multivariate analysis. Am J Obstet Gynecol 168:162-169, 1993
-
(1993)
Am J Obstet Gynecol
, vol.168
, pp. 162-169
-
-
Rubin, S.C.1
-
15
-
-
0028927113
-
Overexpression of c-erbB-2 in epithelial ovarian cancer: Prognostic value and relationship with response to therapy
-
15. Felip E, et al.: Overexpression of c-erbB-2 in epithelial ovarian cancer: Prognostic value and relationship with response to therapy. Cancer 75:2147-2152, 1995
-
(1995)
Cancer
, vol.75
, pp. 2147-2152
-
-
Felip, E.1
-
16
-
-
0028265741
-
The p53 tumor suppressor gene frequently is altered in gynecologic cancers
-
16. Berchuck A, et al: The p53 tumor suppressor gene frequently is altered in gynecologic cancers. Am J Obstet Gynecol 170:246-252, 1994
-
(1994)
Am J Obstet Gynecol
, vol.170
, pp. 246-252
-
-
Berchuck, A.1
-
17
-
-
0028177368
-
p53 expression in epithelial ovarian neoplasms: Relationship to clinical and pathological parameters, Ki-67 expression and flow cytometry
-
17. Henriksen R, et al.: p53 expression in epithelial ovarian neoplasms: Relationship to clinical and pathological parameters, Ki-67 expression and flow cytometry. Gynecol Oncol 53:301-306, 1994
-
(1994)
Gynecol Oncol
, vol.53
, pp. 301-306
-
-
Henriksen, R.1
-
18
-
-
0028898748
-
Mutant p53 protein overexpression is associated with poor outcome in patients with well or moderately differentiated ovarian carcinoma
-
18. Levesque MA, et al: Mutant p53 protein overexpression is associated with poor outcome in patients with well or moderately differentiated ovarian carcinoma. Cancer 75:1327-1338, 1995
-
(1995)
Cancer
, vol.75
, pp. 1327-1338
-
-
Levesque, M.A.1
-
19
-
-
0025321563
-
Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas
-
19. Lee JH, et al: Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas. Cancer Res 50:2724-2728, 1990
-
(1990)
Cancer Res
, vol.50
, pp. 2724-2728
-
-
Lee, J.H.1
-
20
-
-
0025941543
-
Allelotype of human ovarian cancer
-
20. Sato T, et al: Allelotype of human ovarian cancer. Cancer Res 51:5118-5122, 1991
-
(1991)
Cancer Res
, vol.51
, pp. 5118-5122
-
-
Sato, T.1
-
21
-
-
0026727299
-
Molecular genetic changes in human epithelial ovarian malignancies
-
21. Gallion HH, et al: Molecular genetic changes in human epithelial ovarian malignancies. Gynecol Oncol 47:137-142, 1992
-
(1992)
Gynecol Oncol
, vol.47
, pp. 137-142
-
-
Gallion, H.H.1
-
22
-
-
0027269573
-
Human epithelial ovarian cancer allelotype
-
22. Cliby W, et al: Human epithelial ovarian cancer allelotype. Cancer Res 53:2393-2398, 1993
-
(1993)
Cancer Res
, vol.53
, pp. 2393-2398
-
-
Cliby, W.1
-
23
-
-
0027269846
-
Allelic loss in ovarian cancer
-
23. Yang-Feng TL, et al.: Allelic loss in ovarian cancer. Int. J. Cancer 54:546-551, 1993
-
(1993)
Int. J. Cancer
, vol.54
, pp. 546-551
-
-
Yang-Feng, T.L.1
-
24
-
-
0027942717
-
Molecular genetic changes associated with ovarian cancer
-
24. Weitzel JN, et al. : Molecular genetic changes associated with ovarian cancer. Gynecol Oncol 55:245-252, 1994
-
(1994)
Gynecol Oncol
, vol.55
, pp. 245-252
-
-
Weitzel, J.N.1
-
25
-
-
0023721922
-
Familial ovarian cancer: A population-based case - Control study
-
25. Schildkraut JM, Thompson WD: Familial ovarian cancer: A population-based case - control study. Am J Epidemiol 128:456-466, 1988
-
(1988)
Am J Epidemiol
, vol.128
, pp. 456-466
-
-
Schildkraut, J.M.1
Thompson, W.D.2
-
26
-
-
0026739411
-
Age at onset for familial epithelial ovarian cancer
-
26. Amos CI, et al: Age at onset for familial epithelial ovarian cancer. JAMA 268:1896-1899, 1992
-
(1992)
JAMA
, vol.268
, pp. 1896-1899
-
-
Amos, C.I.1
-
27
-
-
0027404252
-
Genetic epidemiology of epithelial ovarian cancer
-
27. Amos, CI, Struewing JP: Genetic epidemiology of epithelial ovarian cancer. Cancer 71:566-572, 1993
-
(1993)
Cancer
, vol.71
, pp. 566-572
-
-
Amos, C.I.1
Struewing, J.P.2
-
28
-
-
0025641069
-
Analysis of 138 consecutive ovarian cancer patients: Incidence and characteristics of familial cases
-
28. Greggi S, et al: Analysis of 138 consecutive ovarian cancer patients: Incidence and characteristics of familial cases. Gynecol Oncol 39:300-304, 1990
-
(1990)
Gynecol Oncol
, vol.39
, pp. 300-304
-
-
Greggi, S.1
-
29
-
-
0026326424
-
Genetic epidemiology of ovarian cancer: Segregation analysis
-
29. Houlston RS, et al: Genetic epidemiology of ovarian cancer: Segregation analysis. Ann Hum Genet 55:291-299, 1991
-
(1991)
Ann Hum Genet
, vol.55
, pp. 291-299
-
-
Houlston, R.S.1
-
30
-
-
0028089706
-
Hereditary and familial ovarian cancer in southern ontario
-
30. Narod SA, et al.: Hereditary and familial ovarian cancer in southern Ontario. Cancer 74:2341-2346, 1994
-
(1994)
Cancer
, vol.74
, pp. 2341-2346
-
-
Narod, S.A.1
-
31
-
-
0020618874
-
Genetic epidemiology of breast cancer and associated cancers in high risk families
-
31. Go RCP, et al.: Genetic epidemiology of breast cancer and associated cancers in high risk families. I. Segregation analysis. J Natl Cancer Inst 71:455-461, 1983
-
(1983)
I. Segregation Analysis. J Natl Cancer Inst
, vol.71
, pp. 455-461
-
-
Go, R.C.P.1
-
32
-
-
0027466018
-
Familial ovarian cancer: A report of 658 families from the Gilda Radner Familial Ovarian Cancer Registry 1981-1991
-
32. Piver MS, et al.: Familial ovarian cancer: A report of 658 families from the Gilda Radner Familial Ovarian Cancer Registry 1981-1991. Cancer 71:582-588, 1993
-
(1993)
Cancer
, vol.71
, pp. 582-588
-
-
Piver, M.S.1
-
33
-
-
0026032613
-
Hereditary ovarian cancer: Heterogeneity at age of diagnosis
-
33. Lynch HT, et al.: Hereditary ovarian cancer: Heterogeneity at age of diagnosis. Cancer 67:1460-1466, 1991
-
(1991)
Cancer
, vol.67
, pp. 1460-1466
-
-
Lynch, H.T.1
-
34
-
-
0026663495
-
Hereditary ovarian cancer: A clinicopathological study
-
34. Bewtra C, et al.: Hereditary ovarian cancer: A clinicopathological study. Int J Gynecol Pathol 11:180-187, 1992
-
(1992)
Int J Gynecol Pathol
, vol.11
, pp. 180-187
-
-
Bewtra, C.1
-
35
-
-
0024436296
-
Evaluating genetic association among ovarian, breast, and endometrial cancer: Evidence for a breast/ovarian cancer relationship
-
35. Schildkraut JM, Risch N, Thompson WD: Evaluating genetic association among ovarian, breast, and endometrial cancer: Evidence for a breast/ovarian cancer relationship. Am J Hum Genet 45:521-529, 1989
-
(1989)
Am J Hum Genet
, vol.45
, pp. 521-529
-
-
Schildkraut, J.M.1
Risch, N.2
Thompson, W.D.3
-
36
-
-
0025814797
-
Hereditary ovarian cancer: Pedigree studies, part II
-
36. Lynch HT, Conway T, Lynch J: Hereditary ovarian cancer: Pedigree studies, part II. Cancer Genet Cytogenet 52:161-183, 1991
-
(1991)
Cancer Genet Cytogenet
, vol.52
, pp. 161-183
-
-
Lynch, H.T.1
Conway, T.2
Lynch, J.3
-
37
-
-
0027467494
-
Extracolonic cancer in hereditary nonpolyposis colorectal cancer
-
37. Watson P, Lynch HT: Extracolonic cancer in hereditary nonpolyposis colorectal cancer. Cancer 71:677-685, 1993
-
(1993)
Cancer
, vol.71
, pp. 677-685
-
-
Watson, P.1
Lynch, H.T.2
-
38
-
-
0028073532
-
Familial site-specific ovarian cancer is linked to BRCA1 on 17q12-21
-
38. Steichen-Gersdorf E, et al.: Familial site-specific ovarian cancer is linked to BRCA1 on 17q12-21. Am J Hum Genet 55:870-875, 1994
-
(1994)
Am J Hum Genet
, vol.55
, pp. 870-875
-
-
Steichen-Gersdorf, E.1
-
39
-
-
0017845567
-
Familial association of breast/ovarian carcinoma
-
39. Lynch HT, et al.: Familial association of breast/ovarian carcinoma. Cancer 41:1543-1548, 1978
-
(1978)
Cancer
, vol.41
, pp. 1543-1548
-
-
Lynch, H.T.1
-
40
-
-
0027433563
-
Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families. The Breast Cancer Linkage Consortium
-
40. Easton DF, 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
-
41
-
-
0028885339
-
An evaluation of genetic heterogeneity in 145 breast - Ovarian cancer families
-
41. Narod SA, 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
-
42
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
42. Hall JM, et al: Linkage of early-onset familial breast cancer to chromosome 17q21. Science 250:1684-1689, 1990
-
(1990)
Science
, vol.250
, pp. 1684-1689
-
-
Hall, J.M.1
-
43
-
-
42449107062
-
Familial breast - Ovarian cancer locus on chromosome 17q12-q23
-
43. Narod SA, et al.: Familial breast - ovarian cancer locus on chromosome 17q12-q23. Lancet 338:82-83, 1991
-
(1991)
Lancet
, vol.338
, pp. 82-83
-
-
Narod, S.A.1
-
44
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
44. 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
-
45
-
-
0029100049
-
Genetic heterogeneity of breast - Ovarian cancer revisited
-
45. Narod S, 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
-
46
-
-
0027248156
-
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer
-
46. Lynch HT, 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
-
47
-
-
0027263363
-
Genetic mapping of a locus predisposing to human colorectal cancer
-
47. Peltomäki P, et al: Genetic mapping of a locus predisposing to human colorectal cancer. Science 260:810-812, 1993
-
(1993)
Science
, vol.260
, pp. 810-812
-
-
Peltomäki, P.1
-
48
-
-
0027485551
-
Genetic mapping of a second locus predisposing to hereditary nonpolyposis colon cancer
-
48. Lindblom A, et al: Genetic mapping of a second locus predisposing to hereditary nonpolyposis colon cancer. Nature Genet 5:279-282, 1993
-
(1993)
Nature Genet
, vol.5
, pp. 279-282
-
-
Lindblom, A.1
-
49
-
-
0028108802
-
Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage
-
49. Nystrom-Lahti M, 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
-
50
-
-
0027933070
-
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
-
50. Nicolaides NC, 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
-
51
-
-
0028011973
-
Histology of BRCA1-associated ovarian tumours
-
51. Narod S, et al.: Histology of BRCA1-associated ovarian tumours. Lancet 343:236, 1994
-
(1994)
Lancet
, vol.343
, pp. 236
-
-
Narod, S.1
-
52
-
-
10544220023
-
Clinicopathologic characteristics of ovarian cancers occurring in women with germline mutations of BRCA1
-
52. Rubin SC, et al: Clinicopathologic characteristics of ovarian cancers occurring in women with germline 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
-
53
-
-
0026885264
-
Anticipation legetimized: Unstable DNA to the rescue
-
53. Sutherland GR, Richards RI: Anticipation legetimized: Unstable DNA to the rescue. Am J Hum Genet 51:7-9, 1992
-
(1992)
Am J Hum Genet
, vol.51
, pp. 7-9
-
-
Sutherland, G.R.1
Richards, R.I.2
-
54
-
-
0028034348
-
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families
-
54. Friedman LS, et al.: Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nature Genet 8:399-404, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 399-404
-
-
Friedman, L.S.1
-
55
-
-
0028981764
-
Detection of eight BRCA1 mutations in 10 breast/ ovarian cancer families, including one family with male breast cancer
-
55. Struewing JP, et al: Detection of eight BRCA1 mutations in 10 breast/ ovarian cancer families, including one family with male breast cancer. Am J Hum Genet 57:1-7, 1995
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1-7
-
-
Struewing, J.P.1
-
56
-
-
0030007136
-
Frequency of the BRCA1 185delAG mutation among Jewish women with ovarian cancer and matched population controls
-
56. Muto MG, et al.: Frequency of the BRCA1 185delAG mutation among Jewish women with ovarian cancer and matched population controls. Cancer Res 56:1250-1252, 1996
-
(1996)
Cancer Res
, vol.56
, pp. 1250-1252
-
-
Muto, M.G.1
-
57
-
-
19144364122
-
Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden
-
57. Johannsson O, et al.: Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden. Am J Hum Genet 58:441-450, 1996
-
(1996)
Am J Hum Genet
, vol.58
, pp. 441-450
-
-
Johannsson, O.1
-
58
-
-
0027749127
-
Familial ovarian cancer
-
58. Buller RE, et al.: Familial ovarian cancer. Gynecol Oncol 51:160-166, 1993
-
(1993)
Gynecol Oncol
, vol.51
, pp. 160-166
-
-
Buller, R.E.1
-
59
-
-
0027980751
-
Breast cancer incidence, penetrance and survival in probable carriers of BRCA1 gene mutation in families linked to BRCA1 on chromosome 17q12-21
-
59. Porter DE, et al.: Breast cancer incidence, penetrance and survival in probable carriers of BRCA1 gene mutation in families linked to BRCA1 on chromosome 17q12-21. Br J Surg 81:1512-1515, 1994
-
(1994)
Br J Surg
, vol.81
, pp. 1512-1515
-
-
Porter, D.E.1
-
60
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
60. Miki Y, 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
-
61
-
-
0028148889
-
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer
-
61. Castilla LH, et al.: Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer. Nature Genet 8:387-391, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 387-391
-
-
Castilla, L.H.1
-
62
-
-
0027939506
-
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families
-
62. Simard J, et al. : Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families. Nature Genet 8:392-398, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 392-398
-
-
Simard, J.1
-
63
-
-
0028073794
-
BRCA1 mutations in primary breast and ovarian cancers
-
63. Futreal PA, et al: BRCA1 mutations in primary breast and ovarian cancers. Science 266:120-122, 1994
-
(1994)
Science
, vol.266
, pp. 120-122
-
-
Futreal, P.A.1
-
64
-
-
0028834145
-
A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene
-
64. Shattuck-Eidens D, et al.: A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. JAMA 273:535-541, 1995
-
(1995)
JAMA
, vol.273
, pp. 535-541
-
-
Shattuck-Eidens, D.1
-
65
-
-
0029009749
-
Mutation analysis of the BRCA1 gene in ovarian cancers
-
65. Takahashi H, 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
-
66
-
-
0029115660
-
The developmental pattern of BRCA1 expression implies a role in differentiation of breast and other tissues
-
66. Marquis ST, 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
-
67
-
-
13344249759
-
BRCA1 is secreted and exhibits properties of a granin
-
67. Jensen RA, et al.: BRCA1 is secreted and exhibits properties of a granin. Nature Genet 12:303-308, 1996
-
(1996)
Nature Genet
, vol.12
, pp. 303-308
-
-
Jensen, R.A.1
-
68
-
-
0028783773
-
Aberrant subcellular localization of BRCA1 in breast cancer
-
68. Chen Y, et al: Aberrant subcellular localization of BRCA1 in breast cancer. Science 270:789-791, 1995
-
(1995)
Science
, vol.270
, pp. 789-791
-
-
Chen, Y.1
-
69
-
-
0030570004
-
Location of BRCA1 in human breast and ovarian cancer cells
-
69. Scully R, et al.: Location of BRCA1 in human breast and ovarian cancer cells. Science 272:123-126, 1996
-
(1996)
Science
, vol.272
, pp. 123-126
-
-
Scully, R.1
-
70
-
-
0029925529
-
Growth retardation and tumour inhibition by BRCA1
-
70. Holt JT, et al.: Growth retardation and tumour inhibition by BRCA1. Nature Genet 12:298-302, 1996
-
(1996)
Nature Genet
, vol.12
, pp. 298-302
-
-
Holt, J.T.1
-
71
-
-
0026935108
-
Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome
-
71. Smith SA, et al.: Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome. Nature Genet 2:128-131, 1992
-
(1992)
Nature Genet
, vol.2
, pp. 128-131
-
-
Smith, S.A.1
-
72
-
-
0029068315
-
Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early-onset breast and ovarian cancer
-
72. Merajver SD, et al.: Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early-onset breast and ovarian cancer. Clin Cancer Res 1:539-544, 1995
-
(1995)
Clin Cancer Res
, vol.1
, pp. 539-544
-
-
Merajver, S.D.1
-
73
-
-
0028844202
-
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype - Phenotype correlation
-
73. Gayther SA, 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
-
74
-
-
13344268996
-
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus
-
74. Phelan CM, 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
-
75
-
-
0025087287
-
Allele loss from chromosome 17 in ovarian cancer
-
75. Russell SEH, et al. : Allele loss from chromosome 17 in ovarian cancer. Oncogene 5:1581-1583, 1990
-
(1990)
Oncogene
, vol.5
, pp. 1581-1583
-
-
Russell, S.E.H.1
-
76
-
-
0025783622
-
Allele loss on chromosome 17q in sporadic ovarian cancer
-
76. Foulkes W, et al.: Allele loss on chromosome 17q in sporadic ovarian cancer. Lancet 338:444-445, 1991
-
(1991)
Lancet
, vol.338
, pp. 444-445
-
-
Foulkes, W.1
-
77
-
-
0026667781
-
Early loss of heterozygosity on 17q in ovarian cancer
-
77. Eccles DM, et al.: Early loss of heterozygosity on 17q in ovarian cancer. Oncogene 7:2069-2072, 1992
-
(1992)
Oncogene
, vol.7
, pp. 2069-2072
-
-
Eccles, D.M.1
-
78
-
-
0028960025
-
Somatic mutations in the BRCA1 gene in sporadic ovarian tumours
-
78. Merajver SD, et al.: Somatic mutations in the BRCA1 gene in sporadic ovarian tumours. Nature Genet 9:439-443, 1995
-
(1995)
Nature Genet
, vol.9
, pp. 439-443
-
-
Merajver, S.D.1
-
79
-
-
0029283880
-
A somatic BRCA1 mutation in an ovarian tumor
-
79. 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
-
80
-
-
0028865866
-
Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients: Four germline mutations, but no evidence of somatic mutation
-
80. Matsushima M, et al: Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients: Four germline 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
-
81
-
-
0027408639
-
A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus
-
81. Jacobs IJ, et al: A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus. Cancer Res 53:1218-1221, 1993
-
(1993)
Cancer Res
, vol.53
, pp. 1218-1221
-
-
Jacobs, I.J.1
-
82
-
-
0027217756
-
Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors
-
82. Saito H, et al.: Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM region on 17q21.3 often and commonly deleted in tumors. Cancer Res 53:3382-3385, 1993
-
(1993)
Cancer Res
, vol.53
, pp. 3382-3385
-
-
Saito, H.1
-
83
-
-
0028050103
-
A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1
-
83. Godwin AK, et al.: A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1. Am J Hum Genet 55:666-677, 1994
-
(1994)
Am J Hum Genet
, vol.55
, pp. 666-677
-
-
Godwin, A.K.1
-
84
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
84. 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
-
85
-
-
13344269668
-
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
-
85. Tavtigian SV, 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
-
86
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
86. Thorlacius S, 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
-
87
-
-
0030137718
-
Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families
-
87. Phelan CM, et al.: Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families. Nature Genet 13:120-122, 1996
-
(1996)
Nature Genet
, vol.13
, pp. 120-122
-
-
Phelan, C.M.1
-
88
-
-
0030139524
-
BRCA2 germline mutations in male breast cancer cases and breast cancer families
-
88. Couch FJ, et al: BRCA2 germline mutations in male breast cancer cases and breast cancer families. Nature Genet 13:123-125, 1996
-
(1996)
Nature Genet
, vol.13
, pp. 123-125
-
-
Couch, F.J.1
-
89
-
-
0029917946
-
Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype
-
89. Gudmundsson J, et al: Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype. Am J Hum Genet 58:749-756, 1996
-
(1996)
Am J Hum Genet
, vol.58
, pp. 749-756
-
-
Gudmundsson, J.1
-
90
-
-
9344244079
-
Mutations of the BRCA2 gene in ovarian carcinomas
-
90. Takahashi H, et al.: Mutations of the BRCA2 gene in ovarian carcinomas. Cancer Res 56:2738-2341, 1996
-
(1996)
Cancer Res
, vol.56
, pp. 2738-12341
-
-
Takahashi, H.1
-
91
-
-
0029007696
-
Consistent loss of the wild-type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13
-
91. 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
-
92
-
-
0028819984
-
Different tumor types from BRCA2 mutation carriers show wild-type chromosome deletions on 13q12-q13
-
92. Gudmundsson J, et al.: Different tumor types from BRCA2 mutation carriers show wild-type chromosome deletions on 13q12-q13. Cancer Res 55:4830-4832, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 4830-4832
-
-
Gudmundsson, J.1
-
93
-
-
0028595722
-
Binding of mismatched microsatellite DNA sequences by the human MSH2 protein
-
93. Fishel R, et al.: Binding of mismatched microsatellite DNA sequences by the human MSH2 protein. Science 266:1403-1405, 1994
-
(1994)
Science
, vol.266
, pp. 1403-1405
-
-
Fishel, R.1
-
94
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
94. Leach FS, et al.: Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell 75:1215-1225, 1993
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
-
95
-
-
0028221943
-
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
-
95. Bronner CE, et al.: Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature 368:258-261, 1994
-
(1994)
Nature
, vol.368
, pp. 258-261
-
-
Bronner, C.E.1
-
96
-
-
0028350601
-
-
96. Papadopoulos N, et al: Mutation of a mutL homolog in hereditary colon cancer. Science 263:1625-1629, 1994
-
(1994)
Science
, vol.263
, pp. 1625-1629
-
-
Papadopoulos, N.1
-
97
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancer
-
97. Aaltonen LA, et al.: Clues to the pathogenesis of familial colorectal cancer. Science 260:812-816, 1993
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
-
98
-
-
0027366916
-
Genetic instability of microsatellites in endometrial carcinoma
-
98. Risinger JI, et al: Genetic instability of microsatellites in endometrial carcinoma. Cancer Res 53:5100-5103, 1993
-
(1993)
Cancer Res
, vol.53
, pp. 5100-5103
-
-
Risinger, J.I.1
-
99
-
-
0028226295
-
Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients
-
99. Aaltonen LA, et al.: Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients. Cancer Res 54:1645-1648, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 1645-1648
-
-
Aaltonen, L.A.1
-
100
-
-
0027137935
-
+ tumor cells
-
+ tumor cells. Cell 75:1227-1236, 1993
-
(1993)
Cell
, vol.75
, pp. 1227-1236
-
-
Parsons, R.1
-
101
-
-
0028301255
-
Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability
-
101. Umar A, et al: Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability. J Biol Chem 269:14367-14370, 1994
-
(1994)
J Biol Chem
, vol.269
, pp. 14367-14370
-
-
Umar, A.1
-
102
-
-
0029096730
-
A hPMS2 mutant cell line is defective in strand-specific mismatch repair
-
102. Risinger JI, et al.: A hPMS2 mutant cell line is defective in strand-specific mismatch repair. J Biol Chem 270:18183-18186, 1995
-
(1995)
J Biol Chem
, vol.270
, pp. 18183-18186
-
-
Risinger, J.I.1
-
103
-
-
0028877162
-
Microsatellite instability in gynecological sarcomas and in hMSH2 mutant uterine sarcoma cell lines defective in mismatch repair activity
-
103. Risinger JI, et al.: Microsatellite instability in gynecological sarcomas and in hMSH2 mutant uterine sarcoma cell lines defective in mismatch repair activity. Cancer Res 55:5664-5669, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 5664-5669
-
-
Risinger, J.I.1
-
104
-
-
0028941627
-
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human mutl homologs
-
104. Li G-M, Modrich P: Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs. Proc Natl Acad Sci USA 92:1950-1954, 1995
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 1950-1954
-
-
Li, G.-M.1
Modrich, P.2
-
105
-
-
0027936057
-
Human chromosome 3 corrects mismatch repair deficiency and microsatellite instability and reduces N-methyl-N′-nitro-N-nitrosoguanidine tolerance in colon tumor cells with homozygous hMLH1 mutation
-
105. Koi M, et al.: Human chromosome 3 corrects mismatch repair deficiency and microsatellite instability and reduces N-methyl-N′-nitro-N-nitrosoguanidine tolerance in colon tumor cells with homozygous hMLH1 mutation. Cancer Res 54:4308-4312, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 4308-4312
-
-
Koi, M.1
-
106
-
-
0028152314
-
Loss of the wild-type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer
-
106. Hemminki A, et al.: Loss of the wild-type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer. Nature Genet 8:405-410, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 405-410
-
-
Hemminki, A.1
-
107
-
-
0028859671
-
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability
-
107. Liu B, et al.: Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability. Nature Genet 9:48-55, 1995
-
(1995)
Nature Genet
, vol.9
, pp. 48-55
-
-
Liu, B.1
-
108
-
-
0028019398
-
Microsatellite instability: Marker of a mutator phenotype in cancer
-
108. Loeb LA: Microsatellite instability: Marker of a mutator phenotype in cancer. Cancer Res 54:5059-5063, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 5059-5063
-
-
Loeb, L.A.1
-
109
-
-
0028564949
-
Mismatch repair, genetic stability, and cancer
-
109. Modrich P: Mismatch repair, genetic stability, and cancer. Science 266:1959-1960, 1994
-
(1994)
Science
, vol.266
, pp. 1959-1960
-
-
Modrich, P.1
-
110
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
110. Fishel R, et al.: The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell 75:1027-1038, 1993
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.1
-
111
-
-
0028585821
-
Structure of the human MSH2 locus and analysis of two Muir - Torre kindreds for msh2 mutations
-
111. Kolodner RD, et al.: Structure of the human MSH2 locus and analysis of two Muir - Torre kindreds for msh2 mutations. Genomics 24:516-526, 1994
-
(1994)
Genomics
, vol.24
, pp. 516-526
-
-
Kolodner, R.D.1
-
112
-
-
0028106776
-
hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds
-
112. Liu B, et al.: hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. Cancer Res 54:4590-4594, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 4590-4594
-
-
Liu, B.1
-
113
-
-
0028833856
-
Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal cancer kindred for mlh1 mutations
-
113. Kolodner RD, et al: Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal cancer kindred for mlh1 mutations. Cancer Res 55:242-248, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 242-248
-
-
Kolodner, R.D.1
-
114
-
-
0028955451
-
Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis
-
114. Wijnen J, et al.: Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. Am J Hum Genet 56:1060-1066, 1995
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1060-1066
-
-
Wijnen, J.1
-
115
-
-
0028883556
-
Mutations in DNA mismatch repair genes are not responsible for microsatellite instability in most sporadic endometrial carcinomas
-
115. Katabuchi H, et al: Mutations in DNA mismatch repair genes are not responsible for microsatellite instability in most sporadic endometrial carcinomas. Cancer Res 55:5556-5560, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 5556-5560
-
-
Katabuchi, H.1
-
116
-
-
0029066689
-
Inactivation of the type II TGF-β receptor in colon cancer cells with microsatellite instability
-
116. Markowitz S, et al.: Inactivation of the type II TGF-β receptor in colon cancer cells with microsatellite instability. Science 268:1336-1338, 1995
-
(1995)
Science
, vol.268
, pp. 1336-1338
-
-
Markowitz, S.1
-
117
-
-
0028785603
-
Microsatellite instability and mutations of the transforming growth factor β type II receptor gene in colorectal cancer
-
117. Parsons R, et al.: Microsatellite instability and mutations of the transforming growth factor β type II receptor gene in colorectal cancer. Cancer Res 55:5548-5550, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 5548-5550
-
-
Parsons, R.1
-
118
-
-
0026327775
-
Nuclear structure and the three-dimensional organization of DNA
-
118. Getzenberg RH, et al: Nuclear structure and the three-dimensional organization of DNA. J Cell Biochem 47:289-299, 1991
-
(1991)
J Cell Biochem
, vol.47
, pp. 289-299
-
-
Getzenberg, R.H.1
-
119
-
-
0027491391
-
Multitude of inverted repeats characterizes a class of anchorage sites of chromatin loops to the nuclear matrix
-
119. Boulikas T, Kong CF: Multitude of inverted repeats characterizes a class of anchorage sites of chromatin loops to the nuclear matrix. J Cell Biochem 53:1-12, 1993
-
(1993)
J Cell Biochem
, vol.53
, pp. 1-12
-
-
Boulikas, T.1
Kong, C.F.2
-
120
-
-
0028148836
-
Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition
-
120. Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition. Am J Hum Genet 55:i-iv, 1994
-
(1994)
Am J Hum Genet
, vol.55
-
-
-
121
-
-
23444445336
-
Statement on use of DNA testing for presymptomatic identification of cancer risk
-
121. Statement on use of DNA testing for presymptomatic identification of cancer risk. JAMA 271:785, 1994
-
(1994)
JAMA
, vol.271
, pp. 785
-
-
-
122
-
-
0029864134
-
Statement of the American Society of Clinical Oncology: Genetic testing for cancer susceptibility
-
122. 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
-
-
-
123
-
-
0030049353
-
BRCA1-lots of mutations, lots of dilemmas
-
123. Collins FS: BRCA1-lots of mutations, lots of dilemmas. N Engl J Med 334:186-188, 1996
-
(1996)
N Engl J Med
, vol.334
, pp. 186-188
-
-
Collins, F.S.1
-
124
-
-
0029679636
-
Are we ready to screen for inherited susceptibility to cancer?
-
124. Holtzman NA: Are we ready to screen for inherited susceptibility to cancer? Oncology 10:57-64, 1996
-
(1996)
Oncology
, vol.10
, pp. 57-64
-
-
Holtzman, N.A.1
-
125
-
-
0029681496
-
Genetic counseling for hereditary cancer
-
125. Lynch HT, Lynch J: Genetic counseling for hereditary cancer. Oncology 10:27-34, 1996
-
(1996)
Oncology
, vol.10
, pp. 27-34
-
-
Lynch, H.T.1
Lynch, J.2
-
126
-
-
0029679712
-
Genetic counseling in hereditary nonpolyposis colorectal cancer
-
126. Menko FH, et al.: Genetic counseling in hereditary nonpolyposis colorectal cancer. Oncology 10:71-76, 1996
-
(1996)
Oncology
, vol.10
, pp. 71-76
-
-
Menko, F.H.1
-
127
-
-
0027465404
-
Genetic counseling for families with inherited susceptibility to breast and ovarian cancer
-
127. Biesecker BB, et al.: Genetic counseling for families with inherited susceptibility to breast and ovarian cancer. JAMA 269:1970-1974, 1993
-
(1993)
JAMA
, vol.269
, pp. 1970-1974
-
-
Biesecker, B.B.1
-
128
-
-
0028814530
-
Assessment and counseling for women with a family history of breast cancer
-
128. Hoskins KF, et al.: Assessment and counseling for women with a family history of breast cancer. JAMA 273:577-585, 1995
-
(1995)
JAMA
, vol.273
, pp. 577-585
-
-
Hoskins, K.F.1
-
129
-
-
15844404355
-
BRCA1 testing in families with hereditary breast -ovarian cancer: A prospective study of patient decision making and outcomes
-
129. Lerman C, et al: BRCA1 testing in families with hereditary breast -ovarian cancer: A prospective study of patient decision making and outcomes. JAMA 275:1885-1892, 1996
-
(1996)
JAMA
, vol.275
, pp. 1885-1892
-
-
Lerman, C.1
-
130
-
-
0030567718
-
A model protocol for evaluating the behavioral and psychosocial effects of BRCA1 testing
-
130. Botkin JR, 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
-
131
-
-
0028872836
-
American Society of Human Genetics Board of Directors and American College of Medical Genetics Board of Directors: Points to consider: Ethical, legal, and psychosocial implications of genetic testing in children and adolescents
-
131. American Society of Human Genetics Board of Directors and American College of Medical Genetics Board of Directors: Points to consider: Ethical, legal, and psychosocial implications of genetic testing in children and adolescents. Am J Hum Genet 57:1233-1241, 1995
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1233-1241
-
-
-
132
-
-
0028813762
-
Ad Hoc Committee on Genetic Testing/Insurance Issues: Background statement: Genetic testing and insurance
-
132. Ad Hoc Committee on Genetic Testing/Insurance Issues: Background statement: Genetic testing and insurance. Am J Hum Genet 56:327-331, 1995
-
(1995)
Am J Hum Genet
, vol.56
, pp. 327-331
-
-
-
133
-
-
0028843102
-
Breast and ovarian cancer incidence in BRCA1-mutation carriers
-
133. Eastern DF, 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
-
-
Eastern, D.F.1
-
134
-
-
0028826709
-
Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence
-
134. Ford D, Easton DF, Peto J: Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence. Am J Hum Genet 57:1457-1462, 1995
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1457-1462
-
-
Ford, D.1
Easton, D.F.2
Peto, J.3
-
135
-
-
0029083814
-
The carrier frequency of the BRCA1 185delAG mutation is approximately 1% in Ashkenazi Jewish individuals
-
135. Struewing JP, 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
-
136
-
-
13344260688
-
Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer
-
136. Fitzgerald MG, et al.: Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer. N Engl J Med 334:143-149, 1996
-
(1996)
N Engl J Med
, vol.334
, pp. 143-149
-
-
Fitzgerald, M.G.1
-
137
-
-
0030138354
-
Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer
-
137. 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
-
138
-
-
0029794992
-
Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
-
138. Roa BB, 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
-
139
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
139. Oddoux C, et al: The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nature Genet 14:188-190, 1996
-
(1996)
Nature Genet
, vol.14
, pp. 188-190
-
-
Oddoux, C.1
-
140
-
-
0029089259
-
Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspectives
-
140. 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
-
141
-
-
0028845693
-
Founding mutations and Alu-mediated recombination in hereditary colon cancer
-
141. Nystrom-Lahti M, et al: Founding mutations and Alu-mediated recombination in hereditary colon cancer. Nature Med 1:1203-1206, 1995
-
(1995)
Nature Med
, vol.1
, pp. 1203-1206
-
-
Nystrom-Lahti, M.1
-
142
-
-
0019960002
-
Intraabdominal carcinomatosis after prophylactic oophorectomy in ovarian cancer prone families
-
142. Tobacman JK, et al: Intraabdominal carcinomatosis after prophylactic oophorectomy in ovarian cancer prone families. Lancet 2:795-797, 1982
-
(1982)
Lancet
, vol.2
, pp. 795-797
-
-
Tobacman, J.K.1
-
143
-
-
0022965596
-
Familial ovarian cancer: Clinical nuances
-
143. Lynch HT, Bewtra C, Lynch JF: Familial ovarian cancer: Clinical nuances. Am J Med 81:1073-1076, 1986
-
(1986)
Am J Med
, vol.81
, pp. 1073-1076
-
-
Lynch, H.T.1
Bewtra, C.2
Lynch, J.F.3
-
144
-
-
0027483251
-
Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian cancer: A report of the Gilda Radner Familial Ovarian Cancer Registry
-
144. Piver MS, et al: Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian cancer: A report of the Gilda Radner Familial Ovarian Cancer Registry. Cancer 71:2751-2755, 1993
-
(1993)
Cancer
, vol.71
, pp. 2751-2755
-
-
Piver, M.S.1
-
145
-
-
0022386154
-
Peritoneal carcinomatosis after prophylactic oophorectomy in familial ovarian cancer syndrome
-
145. Chen KTK, Schooley JF, Flam MS: Peritoneal carcinomatosis after prophylactic oophorectomy in familial ovarian cancer syndrome. Obstet Gynecol 66:93S-94S, 1985
-
(1985)
Obstet Gynecol
, vol.66
-
-
Chen, K.T.K.1
Schooley, J.F.2
Flam, M.S.3
-
146
-
-
0026078502
-
Familial ovarian cancer in Israeli Jewish women
-
146. Menczer J, Ben-Baruch G: Familial ovarian cancer in Israeli Jewish women. Obstet Gynecol 77:276-277, 1991
-
(1991)
Obstet Gynecol
, vol.77
, pp. 276-277
-
-
Menczer, J.1
Ben-Baruch, G.2
-
147
-
-
0002491160
-
Hereditary ovarian cancer
-
Sharp F, Mason WP, Leake RE (eds): New York, WW Norton
-
147. Lynch HT, Conway T, Lynch J: Hereditary ovarian cancer, in Sharp F, Mason WP, Leake RE (eds): Ovarian Cancer: Biological and Therapeutic Challenges, New York, WW Norton, 1990, pp 7-19
-
(1990)
Ovarian Cancer: Biological and Therapeutic Challenges
, pp. 7-19
-
-
Lynch, H.T.1
Conway, T.2
Lynch, J.3
-
148
-
-
0024348044
-
Prevention of ovarian cancer: A survey of the practice of prophylactic oophorectomy by fellows and members of the Royal College of Obstetricians and Gynaecologists
-
148. Jacobs I, Oram D: Prevention of ovarian cancer: A survey of the practice of prophylactic oophorectomy by fellows and members of the Royal College of Obstetricians and Gynaecologists. Br J Obstet Gynaecol 96:510-515, 1989
-
(1989)
Br J Obstet Gynaecol
, vol.96
, pp. 510-515
-
-
Jacobs, I.1
Oram, D.2
-
149
-
-
0024313994
-
Transabdominal ultrasound screening for early ovarian cancer
-
149. Campbell S, et al: Transabdominal ultrasound screening for early ovarian cancer. Br Med J 299:1363-1367, 1989
-
(1989)
Br Med J
, vol.299
, pp. 1363-1367
-
-
Campbell, S.1
-
150
-
-
0025021127
-
Transvaginal sonography as a screening method for ovarian cancer
-
150. Van Nagell JR, et al: Transvaginal sonography as a screening method for ovarian cancer. Cancer 65:573-577, 1990
-
(1990)
Cancer
, vol.65
, pp. 573-577
-
-
Van Nagell, J.R.1
-
151
-
-
0023144402
-
Serum CA 125 levels in a group of nonhospitalized women: Relevance for the early detection of ovarian cancer
-
151. Zurawski VR, et al: Serum CA 125 levels in a group of nonhospitalized women: Relevance for the early detection of ovarian cancer. Obstet Gynecol 69:606-611, 1987
-
(1987)
Obstet Gynecol
, vol.69
, pp. 606-611
-
-
Zurawski, V.R.1
|