-
1
-
-
0033516320
-
Colorectal cancer: Molecules and populations
-
Potter, J. D. Colorectal cancer: molecules and populations. J. Natl Cancer Inst. 91, 916-932 (1999). A comprehensive review of the molecular population-genetics aspects of colorectal cancer.
-
(1999)
J. Natl Cancer Inst.
, vol.91
, pp. 916-932
-
-
Potter, J.D.1
-
2
-
-
0003571561
-
-
(eds Braunwals, E. et al.) (McGraw-Hill, New York)
-
th Edition (eds Braunwals, E. et al.) 581-588 (McGraw-Hill, New York, 2001).
-
(2001)
th Edition
, pp. 581-588
-
-
Mayer, R.J.1
-
3
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon, E. R. & Vogelstein, B. A genetic model for colorectal tumorigenesis. Cell 61, 759-767 (1990). A comprehensive early review of the molecular basis of colorectal cancer.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
4
-
-
0030592517
-
Lessons from hereditary colorectal cancer
-
Kinzler, K. W. & Vogelstein, B. Lessons from hereditary colorectal cancer. Cell 87, 159-170 (1996).
-
(1996)
Cell
, vol.87
, pp. 159-170
-
-
Kinzler, K.W.1
Vogelstein, B.2
-
5
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer
-
Salovaara, R. et al. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J. Clin. Oncol. 18, 2193-2200 (2000).
-
(2000)
J. Clin. Oncol.
, vol.18
, pp. 2193-2200
-
-
Salovaara, R.1
-
6
-
-
0141996493
-
Family history of colorectal cancer in a Swedish county
-
Olsson, L. & Lindblom, A. Family history of colorectal cancer in a Swedish county. Familial Cancer 2, 87-93 (2003).
-
(2003)
Familial Cancer
, vol.2
, pp. 87-93
-
-
Olsson, L.1
Lindblom, A.2
-
7
-
-
0027267282
-
Cancer risk in relatives of patients with common colorectal cancer
-
St. John, D. J. B. et al. Cancer risk in relatives of patients with common colorectal cancer. Ann. Int. Med. 118, 785-790 (1993).
-
(1993)
Ann. Int. Med.
, vol.118
, pp. 785-790
-
-
St. John, D.J.B.1
-
8
-
-
0034793635
-
A systematic review and meta-analysis of familial colorectal cancer risk
-
Johns, L. E. & Houlston, R. S. A systematic review and meta-analysis of familial colorectal cancer risk. Am. J. Gastroenterol. 96, 2992-3003 (2001).
-
(2001)
Am. J. Gastroenterol.
, vol.96
, pp. 2992-3003
-
-
Johns, L.E.1
Houlston, R.S.2
-
9
-
-
0037062434
-
Attenuated APC alleles produce functional protein from internal translation initiation
-
Goss, K. H., Trzepacz, C., Tuohy, T. M. F. & Groden, J. Attenuated APC alleles produce functional protein from internal translation initiation. Proc. Natl Acad. Sci. 99, 8161-8166 (2002). The explanation of the paradox that truncating mutations in the most proximal part of the APC gene cause a milder 'attenuated' form of familial adenomatous polyposis.
-
(2002)
Proc. Natl Acad. Sci.
, vol.99
, pp. 8161-8166
-
-
Goss, K.H.1
Trzepacz, C.2
Tuohy, T.M.F.3
Groden, J.4
-
10
-
-
0036334007
-
Small changes in expression affect predisposition to tumorigenesis
-
Yan, H. et al. Small changes in expression affect predisposition to tumorigenesis. Nature Genet. 30, 25-26 (2002). First evidence that allele-specific reduction in APC expression is heritable and causes predisposition to familial adenomatous polyposis.
-
(2002)
Nature Genet.
, vol.30
, pp. 25-26
-
-
Yan, H.1
-
11
-
-
0017737651
-
Familial cancer syndromes: A survey
-
Lynch, H. T., Guirgis, H. A., Lynch, P. M., Lynch, J. F. & Harris, R. E. Familial cancer syndromes: a survey. Cancer (Suppl) 39, 1867-1881 (1977).
-
(1977)
Cancer (Suppl)
, vol.39
, pp. 1867-1881
-
-
Lynch, H.T.1
Guirgis, H.A.2
Lynch, P.M.3
Lynch, J.F.4
Harris, R.E.5
-
12
-
-
0015077284
-
Cancer family 'G' revisited: 1895-1970
-
Lynch, H. T. & Krush, A. J. Cancer family 'G' revisited: 1895-1970. Cancer 27, 1505-1511 (1971). An early reminder from Henry Lynch that predisposition to non-polyposis colorectal and other cancers can be inherited as a dominant trait.
-
(1971)
Cancer
, vol.27
, pp. 1505-1511
-
-
Lynch, H.T.1
Krush, A.J.2
-
13
-
-
1042290354
-
Testing guidelines for hereditary non-polyposis colorectal cancer
-
Umar, A., Risinger, J. I., Hawk, E. T. & Barrett, J. C. Testing guidelines for hereditary non-polyposis colorectal cancer. Nature Rev. Cancer 4, 153-158 (2004).
-
(2004)
Nature Rev. Cancer
, vol.4
, pp. 153-158
-
-
Umar, A.1
Risinger, J.I.2
Hawk, E.T.3
Barrett, J.C.4
-
14
-
-
0037422027
-
Genomic medicine: Hereditary colon cancer
-
Lynch, H. T. & de la Chapelle, A. Genomic medicine: hereditary colon cancer. N. Engl. J. Med. 348, 919-932 (2003).
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 919-932
-
-
Lynch, H.T.1
De La Chapelle, A.2
-
15
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
Aaltonen, L. A. et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N. Engl. J. Med. 338, 1481-1487 (1998).
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 1481-1487
-
-
Aaltonen, L.A.1
-
16
-
-
0034827025
-
The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas
-
Cunningham, J. M. et al. The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas. Am. J. Hum. Genet. 69, 780-790 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 780-790
-
-
Cunningham, J.M.1
-
17
-
-
0035478506
-
Molecular screening for hereditary nonpolyposis colorectal cancer: A prospective, population-based study
-
Percesepe, A. et al. Molecular screening for hereditary nonpolyposis colorectal cancer: a prospective, population-based study. J. Clin. Oncol. 19, 2944-3950 (2001).
-
(2001)
J. Clin. Oncol.
, vol.19
, pp. 2944-3950
-
-
Percesepe, A.1
-
18
-
-
0034799747
-
The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer
-
Samowitz, W. S. et al. The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer. Gastroenterology 121, 830-838 (2001).
-
(2001)
Gastroenterology
, vol.121
, pp. 830-838
-
-
Samowitz, W.S.1
-
19
-
-
0033916953
-
Incidence of germline hMLH1 and hMSH2 mutations (HNPCC patients) among newly diagnosed colorectal cancers in a Slovenian population
-
Ravnik-Glavac, M., Potocnik, U. & Glavac, D. Incidence of germline hMLH1 and hMSH2 mutations (HNPCC patients) among newly diagnosed colorectal cancers in a Slovenian population. J. Med. Genet. 37, 533-536 (2000).
-
(2000)
J. Med. Genet.
, vol.37
, pp. 533-536
-
-
Ravnik-Glavac, M.1
Potocnik, U.2
Glavac, D.3
-
20
-
-
0027137935
-
Hypermutability and mismatch repair deficiency in RER+ tumor cells
-
Parsons, R. et al. Hypermutability and mismatch repair deficiency in RER+ tumor cells. Cell 75, 1227-1236 (1993).
-
(1993)
Cell
, vol.75
, pp. 1227-1236
-
-
Parsons, R.1
-
21
-
-
0028152314
-
Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer
-
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
-
22
-
-
0028106776
-
hMSH2 mutations in hereditary non-polyposis colorectal cancer kindreds
-
Liu, B. et al. hMSH2 mutations in hereditary non-polyposis colorectal cancer kindreds. Cancer Res. 54, 4590-4594 (1994).
-
(1994)
Cancer Res.
, vol.54
, pp. 4590-4594
-
-
Liu, B.1
-
23
-
-
0028859671
-
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability
-
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
-
24
-
-
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, M. F. 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
-
25
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancer
-
Aaltonen, L. A. et al. Clues to the pathogenesis of familial colorectal cancer. Science 260, 812-816 (1993). The first demonstration that microsatellite instability is a hallmark of Lynch syndrome.
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
-
26
-
-
0028226295
-
Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients
-
Aaltonen, L. A. 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
-
27
-
-
0032534069
-
A National Cancer Institute Workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
-
Boland, C. R. et al. A National Cancer Institute Workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res. 58, 5248-5257 (1998).
-
(1998)
Cancer Res.
, vol.58
, pp. 5248-5257
-
-
Boland, C.R.1
-
28
-
-
0030054532
-
Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer
-
Konishi, M. et al. Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer. Gastroenterology 111, 307-317 (1996).
-
(1996)
Gastroenterology
, vol.111
, pp. 307-317
-
-
Konishi, M.1
-
29
-
-
0029066689
-
Inactivation of the type II TGF-β receptor in colon cancer cells with microsatellite instability
-
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
-
30
-
-
0030882381
-
Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study
-
The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer
-
Peltomäki, P. & Vasen, H. F. Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer. Gastroenterology 113, 1146-1158 (1997). An early, comprehensive summary of the mutational spectrum in Lynch syndrome.
-
(1997)
Gastroenterology
, vol.113
, pp. 1146-1158
-
-
Peltomäki, P.1
Vasen, H.F.2
-
31
-
-
0141973793
-
Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancer
-
Renkonen, E. et al. Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancer. J. Clin. Oncol. 21, 3629-3637 (2003).
-
(2003)
J. Clin. Oncol.
, vol.21
, pp. 3629-3637
-
-
Renkonen, E.1
-
32
-
-
0031278322
-
Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer
-
Miyaki, M. et al. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. Nature Genet. 17, 271-272 (1997).
-
(1997)
Nature Genet.
, vol.17
, pp. 271-272
-
-
Miyaki, M.1
-
33
-
-
0027933070
-
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
-
Nicolaides, N. C. 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
-
34
-
-
0028849441
-
Genomic organization of the human PMS2 gene family
-
Nicolaides, N. C. et al. Genomic organization of the human PMS2 gene family. Genomics 30, 195-206 (1995).
-
(1995)
Genomics
, vol.30
, pp. 195-206
-
-
Nicolaides, N.C.1
-
35
-
-
0031910118
-
A natural occurring hPMS2 mutation can confer a dominant negative phenotype
-
Nicolaides, N. C., Littman, S., Modrich, P., Kinzler, K. W. & Vogelstein, B. A natural occurring hPMS2 mutation can confer a dominant negative phenotype. Mol. Cell. Biol. 18, 1635-1641 (1998).
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 1635-1641
-
-
Nicolaides, N.C.1
Littman, S.2
Modrich, P.3
Kinzler, K.W.4
Vogelstein, B.5
-
36
-
-
3142748325
-
Mismatch repair gene PMS2: Disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein but paralogous genes obscure mutation detection and interpretation
-
Nakagawa, H. et al. Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein but paralogous genes obscure mutation detection and interpretation. Cancer Res. 64, 4721-4727 (2004).
-
(2004)
Cancer Res.
, vol.64
, pp. 4721-4727
-
-
Nakagawa, H.1
-
37
-
-
2342506542
-
Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome
-
De Vos, M. et al. Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome. Am. J. Hum. Genet. 74, 954-964 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 954-964
-
-
De Vos, M.1
-
38
-
-
0034795933
-
A role for MLH3 in hereditary nonpolyposis colorectal cancer
-
Wu, Y. et al. A role for MLH3 in hereditary nonpolyposis colorectal cancer. Nature Genet. 29, 137-138 (2001).
-
(2001)
Nature Genet.
, vol.29
, pp. 137-138
-
-
Wu, Y.1
-
39
-
-
2342613578
-
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer
-
Lammi, L. et al. Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. Am. J. Hum. Genet. 74, 1043-1050 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 1043-1050
-
-
Lammi, L.1
-
40
-
-
0032065913
-
HNPCC associated with germline mutation in the TGF-β type II receptor gene
-
Lu, S.-L. et al. HNPCC associated with germline mutation in the TGF-β type II receptor gene. Nature Genet 19, 17-18 (1998).
-
(1998)
Nature Genet.
, vol.19
, pp. 17-18
-
-
Lu, S.-L.1
-
41
-
-
0028859670
-
Polymerase δ variants in RER colorectal tumours
-
da Costa, L. T. et al. Polymerase δ variants in RER colorectal tumours. Nature Genet. 9, 10-11 (1995).
-
(1995)
Nature Genet.
, vol.9
, pp. 10-11
-
-
Da Costa, L.T.1
-
42
-
-
0033039550
-
A common MSH2 mutation in English and North American HNPCC families: Origin, phenotypic expression, and sex specific differences in colorectal cancer
-
Froggatt, N. J. et al. A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer. J. Med. Genet. 36, 97-102 (1999).
-
(1999)
J. Med. Genet.
, vol.36
, pp. 97-102
-
-
Froggatt, N.J.1
-
43
-
-
0033828829
-
Recurrent germline mutation in MSH2 arises frequently de novo
-
Desai, D. C. et al. Recurrent germline mutation in MSH2 arises frequently de novo. J. Med. Genet. 37, 646-662 (2000).
-
(2000)
J. Med. Genet.
, vol.37
, pp. 646-662
-
-
Desai, D.C.1
-
44
-
-
0035942495
-
A novel germline 1.8-kb deletion of hMLH1 mimicking altemative splicing: A founder mutation in the Chinese population
-
Chan, T. L. et al. A novel germline 1.8-kb deletion of hMLH1 mimicking altemative splicing: a founder mutation in the Chinese population. Oncogens 20, 2976-2981 (2001).
-
(2001)
Oncogens
, vol.20
, pp. 2976-2981
-
-
Chan, T.L.1
-
45
-
-
0030747145
-
Reduced frequency of extracolonic cancers in hereditary nonpolylposis colorectal cancer families with monoallelic hMLH1 expression
-
Jaeger, A. C. et al. Reduced frequency of extracolonic cancers in hereditary nonpolylposis colorectal cancer families with monoallelic hMLH1 expression. Am. J. Hum. Genet. 61, 129-138 (1997).
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 129-138
-
-
Jaeger, A.C.1
-
46
-
-
0035476883
-
A nonsense mutation in MLH1 causes exon skipping in three unrelated HNPCC families
-
Stella, A. et al. A nonsense mutation in MLH1 causes exon skipping in three unrelated HNPCC families. Cancer Res. 61, 7020-7024 (2001).
-
(2001)
Cancer Res.
, vol.61
, pp. 7020-7024
-
-
Stella, A.1
-
47
-
-
2942575173
-
A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability
-
Caluseriu, O. et al. A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability. J. Med. Genet. 41, e34 (2004).
-
(2004)
J. Med. Genet.
, vol.41
-
-
Caluseriu, O.1
-
48
-
-
2342464930
-
MSH2 c. 1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese populations
-
Chan, T. L. et al. MSH2 c. 1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese populations. Am. J. Hum. Genet. 74, 1035-1042 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 1035-1042
-
-
Chan, T.L.1
-
49
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
Hemminki, A. et al. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 39, 184-187 (1998).
-
(1998)
Nature
, vol.39
, pp. 184-187
-
-
Hemminki, A.1
-
50
-
-
0042622241
-
Further observations of LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome
-
Lim, W. et al. Further observations of LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. Br. J. Cancer 89, 308-313 (2003).
-
(2003)
Br. J. Cancer
, vol.89
, pp. 308-313
-
-
Lim, W.1
-
51
-
-
0032524069
-
Mutations in the SMAD4/DPC4 gene in juvenile polyposis
-
Howe, J. R. et al. Mutations in the SMAD4/DPC4 gene in juvenile polyposis. Science 280, 1086-1088 (1998).
-
(1998)
Science
, vol.280
, pp. 1086-1088
-
-
Howe, J.R.1
-
52
-
-
0034972978
-
Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis
-
Howe, J. R. et al. Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis. Nature Genet. 28, 184-187 (2001).
-
(2001)
Nature Genet.
, vol.28
, pp. 184-187
-
-
Howe, J.R.1
-
53
-
-
7844251203
-
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases
-
Houlston, R. et al. Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases. Hum. Mol. Genet. 7, 1907-1912 (1998).
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1907-1912
-
-
Houlston, R.1
-
54
-
-
0036842005
-
Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis
-
Sayed, M. G. et al. Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis. Ann. Surg. Oncol. 9, 901-906 (2002).
-
(2002)
Ann. Surg. Oncol.
, vol.9
, pp. 901-906
-
-
Sayed, M.G.1
-
55
-
-
0036478899
-
Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors
-
Al-Tassan, N. et al. Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors. Nature Genet. 30, 227-232 (2002). The first demonstration of a gene that causes a high level of predisposition to colorectal cancer when both alleles are mutated, and therefore shows typical recessive inheritance.
-
(2002)
Nature Genet.
, vol.30
, pp. 227-232
-
-
Al-Tassan, N.1
-
56
-
-
0036848267
-
Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C→T:A mutations
-
Jones, S. et al. Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C→T:A mutations. Hum. Mol. Genet. 11, 2961-2967 (2002).
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2961-2967
-
-
Jones, S.1
-
57
-
-
0037468517
-
Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH
-
Sieber, O. M. et al. Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH. N. Engl. J. Med. 348, 791-799 (2003).
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 791-799
-
-
Sieber, O.M.1
-
58
-
-
12144289614
-
Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas
-
Gismondi, V. et al. Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas. Int. J. Cancer 109, 680 (2004).
-
(2004)
Int. J. Cancer
, vol.109
, pp. 680
-
-
Gismondi, V.1
-
59
-
-
0041423452
-
Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients
-
Enholm, S. et al. Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients. Am. J. Pathol. 163, 827-832 (2003).
-
(2003)
Am. J. Pathol.
, vol.163
, pp. 827-832
-
-
Enholm, S.1
-
60
-
-
1542719919
-
Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer
-
Fleischmann, C. et al. Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer. Int. J. Cancer 109, 554-558 (2004).
-
(2004)
Int. J. Cancer
, vol.109
, pp. 554-558
-
-
Fleischmann, C.1
-
61
-
-
0242363139
-
A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22. 2-31. 2
-
Wiesner, G. L. et al. A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22. 2-31. 2. Proc. Natl Acad. Sci. USA 100, 12961-12965 (2003).
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 12961-12965
-
-
Wiesner, G.L.1
-
62
-
-
0033067274
-
Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22
-
Tomlinson, I. et al. Inherited susceptibility to colorectal adenomas and carcinomas: evidence for a new predisposition gene on 15q14-q22. Gastroenterology 116, 789-795 (1999).
-
(1999)
Gastroenterology
, vol.116
, pp. 789-795
-
-
Tomlinson, I.1
-
63
-
-
0037730140
-
An ancestral Ashkenazi haplotype at the HPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
-
Jaeger, A. C. et al. An ancestral Ashkenazi haplotype at the HPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome. Am. J. Hum. Genet. 72, 1261-1267 (2003).
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 1261-1267
-
-
Jaeger, A.C.1
-
64
-
-
0002874089
-
A distinct tumor suppressor gene locus on chromosome 15q21. 1 in sporadic form of colorectal cancer
-
Park, W. S. et al. A distinct tumor suppressor gene locus on chromosome 15q21. 1 in sporadic form of colorectal cancer. Cancer Res. 60, 70-73 (2000).
-
(2000)
Cancer Res.
, vol.60
, pp. 70-73
-
-
Park, W.S.1
-
65
-
-
0038636429
-
Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excel of allelic imbalance in chromosome 10q in familial cases
-
Laiho, P. et al. Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excel of allelic imbalance in chromosome 10q in familial cases. Oncogene 22, 2206-2214 (2003).
-
(2003)
Oncogene
, vol.22
, pp. 2206-2214
-
-
Laiho, P.1
-
66
-
-
0029803949
-
Functional evidence for a colorectal cancer tumor suppressor gene at chromosome 8p22-23 by monochromosome transfer
-
Gustafson, C. E. et al. Functional evidence for a colorectal cancer tumor suppressor gene at chromosome 8p22-23 by monochromosome transfer. Cancer Res. 56, 5238-5245 (1996).
-
(1996)
Cancer Res.
, vol.56
, pp. 5238-5245
-
-
Gustafson, C.E.1
-
67
-
-
16944365288
-
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC
-
Laken, S. J. et al. Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC. Nature Genet. 17, 79-83 (1997). The first convincing description of a common low-penetrance allele predisposing to colorectal cancer.
-
(1997)
Nature Genet.
, vol.17
, pp. 79-83
-
-
Laken, S.J.1
-
68
-
-
0032946973
-
Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer
-
Rozen, P. et al. Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer. Gastroenterology 116, 54-57 (1999).
-
(1999)
Gastroenterology
, vol.116
, pp. 54-57
-
-
Rozen, P.1
-
69
-
-
0031595693
-
The APC I1307K allele and cancer risk in a community-based study of Ashkenazi Jews
-
Woodage, T. et al. The APC I1307K allele and cancer risk in a community-based study of Ashkenazi Jews. Nature Genet 20, 62-65 (1998).
-
(1998)
Nature Genet.
, vol.20
, pp. 62-65
-
-
Woodage, T.1
-
70
-
-
0032530139
-
Somatic instability of the APC I1307K allele in colorectal neoplasia
-
Gryfe, R., DiNicola, N., Gallinger, S. & Redston, M. Somatic instability of the APC I1307K allele in colorectal neoplasia. Cancer Res. 58, 440-4043 (1998).
-
(1998)
Cancer Res.
, vol.58
, pp. 440-4043
-
-
Gryfe, R.1
DiNicola, N.2
Gallinger, S.3
Redston, M.4
-
71
-
-
0034651671
-
Adenomatous polyposis coli I1307K mutation in Jewish patients with different ethnicity
-
Drucker, L. et al. Adenomatous polyposis coli I1307K mutation in Jewish patients with different ethnicity. Cancer 88, 755-760 (2000).
-
(2000)
Cancer
, vol.88
, pp. 755-760
-
-
Drucker, L.1
-
72
-
-
0037314547
-
The characterization of somatic APC mutations in colonic adenomas and carcinomas in Ashkenazi Jews with the APC I1307K variant using linkage disequilibrium
-
Zauber, N. P., Sabbath-Solitare, M., Marotta, S. P. & Bishop, D. T. The characterization of somatic APC mutations in colonic adenomas and carcinomas in Ashkenazi Jews with the APC I1307K variant using linkage disequilibrium. J. Pathol. 199, 146-151 (2003).
-
(2003)
J. Pathol.
, vol.199
, pp. 146-151
-
-
Zauber, N.P.1
Sabbath-Solitare, M.2
Marotta, S.P.3
Bishop, D.T.4
-
73
-
-
10744222509
-
The I1307K adenomatous polyposis coli gene variant does not contribute in the assessment of the risk for colorectal cancer in Ashkenazi Jews
-
Strul, H. et al. The I1307K adenomatous polyposis coli gene variant does not contribute in the assessment of the risk for colorectal cancer in Ashkenazi Jews. Cancer Epidemiol. Biomarkers Prev. 12, 1012-1015 (2003).
-
(2003)
Cancer Epidemiol. Biomarkers Prev.
, vol.12
, pp. 1012-1015
-
-
Strul, H.1
-
74
-
-
0037314617
-
Colorectal tumorigenesis in carriers of the APC I1307K variant: Lone gunman or conspiracy?
-
Sieber, O., Lipton, L., Heinimann, K. & Tomlinson, I. Colorectal tumorigenesis in carriers of the APC I1307K variant: lone gunman or conspiracy? J. Pathol. 199, 137-139 (2003).
-
(2003)
J. Pathol.
, vol.199
, pp. 137-139
-
-
Sieber, O.1
Lipton, L.2
Heinimann, K.3
Tomlinson, I.4
-
75
-
-
0032930429
-
I1307K polymorphism of the APC gene in colorectal cancer
-
Prior, T. W. et al. I1307K polymorphism of the APC gene in colorectal cancer. Gastroenterology 116, 58-63 (1999).
-
(1999)
Gastroenterology
, vol.116
, pp. 58-63
-
-
Prior, T.W.1
-
76
-
-
0032809994
-
Common origin of the I1307K APC polymorphism in Ashkenazi and non-Ashkenazi Jews
-
Patael, Y. et al. Common origin of the I1307K APC polymorphism in Ashkenazi and non-Ashkenazi Jews. Eur. J. Hum. Genet. 7, 555-559 (1999).
-
(1999)
Eur. J. Hum. Genet.
, vol.7
, pp. 555-559
-
-
Patael, Y.1
-
77
-
-
0034878803
-
The I1307K APC polymorphism: Prevalence in Non-Ashkenazi Jews and evidence for a founder effect
-
Shtoyerman-Chen, R. et al. The I1307K APC polymorphism: prevalence in Non-Ashkenazi Jews and evidence for a founder effect. Genet. Testing 5, 141-146 (2001).
-
(2001)
Genet. Testing
, vol.5
, pp. 141-146
-
-
Shtoyerman-Chen, R.1
-
78
-
-
0347362521
-
Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: Evidence of genetic drift within the Ashkenazim
-
Niell, B. L., Long J. C., Rennert, G. & Gruber, S. B. Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim. Am. J. Hum. Genet. 73, 1250-1260 (2003).
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1250-1260
-
-
Niell, B.L.1
Long, J.C.2
Rennert, G.3
Gruber, S.B.4
-
79
-
-
0037093967
-
Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effect
-
Rozen, P. et al. Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effect. Cancer 94, 2561-2568 (2002).
-
(2002)
Cancer
, vol.94
, pp. 2561-2568
-
-
Rozen, P.1
-
80
-
-
0034948519
-
A review of adjusted estimators of attributable risk
-
Benichou, J. A review of adjusted estimators of attributable risk. Stat. Methods Med. Res. 10, 195-216 (2001).
-
(2001)
Stat. Methods Med. Res.
, vol.10
, pp. 195-216
-
-
Benichou, J.1
-
81
-
-
0141465131
-
TGFBR1*6A and cancer risk: A meta-analysis of seven case-control studies
-
Kaklamani, V. G. et al. TGFBR1*6A and cancer risk: a meta-analysis of seven case-control studies. J. Clin. Oncol. 21, 3236-3243 (2003).
-
(2003)
J. Clin. Oncol.
, vol.21
, pp. 3236-3243
-
-
Kaklamani, V.G.1
-
82
-
-
1442356678
-
TBFBR1*6A and cancer: A meta-analysis of 12 case-control studies
-
Pasche, B. et al. TBFBR1*6A and cancer: a meta-analysis of 12 case-control studies. J. Clin. Oncol. 22, 756-758 (2004).
-
(2004)
J. Clin. Oncol.
, vol.22
, pp. 756-758
-
-
Pasche, B.1
-
83
-
-
0035890942
-
TβR-I(6A) Polymorphism is not a tumor susceptibility allele in Macedonian colorectal cancer patients
-
Stefanovska, A.-M. et al. TβR-I(6A) Polymorphism is not a tumor susceptibility allele in Macedonian colorectal cancer patients. Cancer Res. 61, 8351-8352 (2001).
-
(2001)
Cancer Res.
, vol.61
, pp. 8351-8352
-
-
Stefanovska, A.-M.1
-
84
-
-
0033516627
-
Structural alterations of transforming growth factor-β receptor genes in human cervical carcinoma
-
Chen, T. et al. Structural alterations of transforming growth factor-β receptor genes in human cervical carcinoma. Int. J. Cancer 82, 43-51 (1999).
-
(1999)
Int. J. Cancer
, vol.82
, pp. 43-51
-
-
Chen, T.1
-
85
-
-
0033570376
-
TβR-I(6A) is a candidate tumor susceptibility allele
-
Pasche, B. et al. TβR-I(6A) is a candidate tumor susceptibility allele. Cancer Res. 59, 5678-5682 (1999).
-
(1999)
Cancer Res.
, vol.59
, pp. 5678-5682
-
-
Pasche, B.1
-
86
-
-
3042700124
-
The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer
-
Lipkin, S. M. et al. The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer. Nature Genet. 36, 694-699 (2004).
-
(2004)
Nature Genet.
, vol.36
, pp. 694-699
-
-
Lipkin, S.M.1
-
87
-
-
0034909923
-
Polymorphisms and colorectal tumor risk
-
Houlston, R. S. & Tomlinson, I. P. M. Polymorphisms and colorectal tumor risk. Gastroenterology 121, 282-301 (2001). An extensive critical review of published papers on polymorphisms thought to affect colorectal cancer risk.
-
(2001)
Gastroenterology
, vol.121
, pp. 282-301
-
-
Houlston, R.S.1
Tomlinson, I.P.M.2
-
88
-
-
0035760845
-
Genotype and phenotype in hereditary nonpolyposis colon cancer: A study of families with different vs. shared predisposing mutations
-
Peltomäki, P., Gao, X. & Mecklin, J. P. Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations. Fam. Cancer. 1, 9-15 (2001).
-
(2001)
Fam. Cancer
, vol.1
, pp. 9-15
-
-
Peltomäki, P.1
Gao, X.2
Mecklin, J.P.3
-
89
-
-
0025015168
-
A dominant mutation that predisposes to multiple intestinal neoplasia in the mouse
-
Moser, A. R., Pitot, H. C. & Dove, W. F. A dominant mutation that predisposes to multiple intestinal neoplasia in the mouse. Science 247, 322-324 (1990).
-
(1990)
Science
, vol.247
, pp. 322-324
-
-
Moser, A.R.1
Pitot, H.C.2
Dove, W.F.3
-
90
-
-
0027363063
-
Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
-
Dietrich, W. et al. Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse. Cell 75, 631-639 (1993).
-
(1993)
Cell
, vol.75
, pp. 631-639
-
-
Dietrich, W.1
-
91
-
-
0030797904
-
Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis
-
Cormier, R. T. et al. Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis. Nature Genet. 17, 88-91 (1997).
-
(1997)
Nature Genet.
, vol.17
, pp. 88-91
-
-
Cormier, R.T.1
-
92
-
-
0035287508
-
Modifier genes in mice and humans
-
Nadeau, J. H. Modifier genes in mice and humans. Nature Rev. Genet. 2, 165-174 (2001).
-
(2001)
Nature Rev. Genet.
, vol.2
, pp. 165-174
-
-
Nadeau, J.H.1
-
93
-
-
0030882943
-
Loss of the PLA2G24 gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAP
-
Nimmrich, I. et al. Loss of the PLA2G24 gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAP. Hum. Genet. 100, 345-349 (1997).
-
(1997)
Hum. Genet.
, vol.100
, pp. 345-349
-
-
Nimmrich, I.1
-
94
-
-
0035804663
-
Fruit, vegetables, dietary fiber, and risk of colorectal cancer
-
Terry, P. et al. Fruit, vegetables, dietary fiber, and risk of colorectal cancer. J. Natl Cancer Inst. 93, 525-533 (2001).
-
(2001)
J. Natl Cancer Inst.
, vol.93
, pp. 525-533
-
-
Terry, P.1
-
95
-
-
0025828430
-
A note on multiple testing procedures in linkage analysis
-
Risch, N. A note on multiple testing procedures in linkage analysis. Am. J. Hum. Genet. 48, 1058-1064 (1991).
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 1058-1064
-
-
Risch, N.1
-
96
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for Mendelian disease, future approaches for complex disease
-
Botstein, D. & Risch, N. Discovering genotypes underlying human phenotypes: past successes for Mendelian disease, future approaches for complex disease. Nature Genet. Suppl. 33, 228-237 (2003).
-
(2003)
Nature Genet. Suppl.
, vol.33
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
97
-
-
0034927358
-
The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches
-
Risch, N. The genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches. Cancer Epidemiol. Biomarkers Prev. 10, 733-741 (2001). An insightful interpretation and evaluation of studies into the heritability of cancer.
-
(2001)
Cancer Epidemiol. Biomarkers Prev.
, vol.10
, pp. 733-741
-
-
Risch, N.1
-
98
-
-
0028143018
-
Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands
-
Goldgar, D. E., Easton, D. F., Cannon-Albright, L. A. & Skolnick, M. H. Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J. Natl Cancer Inst. 21, 1600-1608 (1994).
-
(1994)
J. Natl Cancer Inst.
, vol.21
, pp. 1600-1608
-
-
Goldgar, D.E.1
Easton, D.F.2
Cannon-Albright, L.A.3
Skolnick, M.H.4
-
99
-
-
0035314017
-
Modification of cancer risks in offspring by sibling and parental cancers from 2, 122,616 nuclear families
-
Dong, C. & Hemminki, K. Modification of cancer risks in offspring by sibling and parental cancers from 2, 122,616 nuclear families. Int. J. Cancer 92, 144-150 (2001).
-
(2001)
Int. J. Cancer
, vol.92
, pp. 144-150
-
-
Dong, C.1
Hemminki, K.2
-
100
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer
-
Lichtenstein, P. et al. Environmental and heritable factors in the causation of cancer. New Engl. J. Med. 343, 78-85 (2000).
-
(2000)
New Engl. J. Med.
, vol.343
, pp. 78-85
-
-
Lichtenstein, P.1
-
101
-
-
0028845693
-
Founding mutations and Alu-mediated recombination in hereditary colon cancer
-
Nyström-Lahti, M. et al. Founding mutations and Alu-mediated recombination in hereditary colon cancer. Nature Med. 1, 1203-1206 (1995). The first demonstration of widespread founder mutations in Lynch syndrome.
-
(1995)
Nature Med.
, vol.1
, pp. 1203-1206
-
-
Nyström-Lahti, M.1
-
102
-
-
0029851496
-
Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer
-
Moisio, A.-L., Sistonen, P., Weissenbach, J., de la Chapelle, A. & Peltomäki, P. Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer. Am. J. Hum. Genet. 59, 1243-1251 (1996).
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1243-1251
-
-
Moisio, A.-L.1
Sistonen, P.2
Weissenbach, J.3
De La Chapelle, A.4
Peltomäki, P.5
-
103
-
-
19244362382
-
Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation
-
Hutter, P. et al. Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation. J. Med. Genet. 33, 636-640 (1996).
-
(1996)
J. Med. Genet.
, vol.33
, pp. 636-640
-
-
Hutter, P.1
-
104
-
-
0029075583
-
Genetic linkage analysis in hereditary nonpolyposis colon cancer syndrome
-
Froggatt, N. J. et al. Genetic linkage analysis in hereditary nonpolyposis colon cancer syndrome. J. Med. Genet. 32, 352-357 (1995).
-
(1995)
J. Med. Genet.
, vol.32
, pp. 352-357
-
-
Froggatt, N.J.1
-
105
-
-
0036732650
-
Impact of gender and parent of origin on the phenotypic expression of hereditary nonpolyposis colorectal cancer in a large Newfoundland kindred with a common MSH2 mutation
-
Green, J. et al. Impact of gender and parent of origin on the phenotypic expression of hereditary nonpolyposis colorectal cancer in a large Newfoundland kindred with a common MSH2 mutation. Dis. Colon Rect. 45, 1223-1232, (2002).
-
(2002)
Dis. Colon Rect.
, vol.45
, pp. 1223-1232
-
-
Green, J.1
-
106
-
-
0036917758
-
The founder mutation MSH2*1906G→C is an important cause of hereditary non-polyposis colorectal cancer in the Ashkenszi Jewish population
-
Foulkes, W. D. et al. The founder mutation MSH2*1906G→C is an important cause of hereditary non-polyposis colorectal cancer in the Ashkenszi Jewish population. Am. J. Hum. Genet. 71, 1395-1412 (2002).
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1395-1412
-
-
Foulkes, W.D.1
-
107
-
-
0037730214
-
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: High mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene
-
Wagner, A. et al. Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. Am. J. Hum. Genet. 72, 1088-1100 (2003).
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 1088-1100
-
-
Wagner, A.1
-
108
-
-
0142124795
-
Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques
-
Nakagawa, H., Hampel, H. & de la Chapelle, A. Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques. Hum. Mut. 22, 258 (2003).
-
(2003)
Hum. Mut.
, vol.22
, pp. 258
-
-
Nakagawa, H.1
Hampel, H.2
De La Chapelle, A.3
-
109
-
-
10744223648
-
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States
-
Lynch, H. T. et al. A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States. JAMA 291, 718-724 (2004).
-
(2004)
JAMA
, vol.291
, pp. 718-724
-
-
Lynch, H.T.1
-
110
-
-
18544386262
-
BLM heterozygosity and the risk of colorectal cancer
-
Gruber, S. B. et al. BLM heterozygosity and the risk of colorectal cancer. Science 297, 2013 (2002).
-
(2002)
Science
, vol.297
, pp. 2013
-
-
Gruber, S.B.1
-
111
-
-
0037440257
-
Association between hemochromatosis (HFE) gene mutation carrier status and the risk of colon cancer
-
Shaheen, N. J. et al. Association between hemochromatosis (HFE) gene mutation carrier status and the risk of colon cancer. J. Natl. Cancer Inst. 95, 154-159 (2003).
-
(2003)
J. Natl. Cancer Inst.
, vol.95
, pp. 154-159
-
-
Shaheen, N.J.1
-
112
-
-
85047697181
-
Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer
-
Porter, T. R. et al. Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer. Oncogene 21, 1928-1933 (2002).
-
(2002)
Oncogene
, vol.21
, pp. 1928-1933
-
-
Porter, T.R.1
-
113
-
-
0344953576
-
ASH mutation and cancer risk
-
ASH mutation and cancer risk. Cancer Res. 63, 1769-1771 (2003).
-
(2003)
Cancer Res.
, vol.63
, pp. 1769-1771
-
-
Cleary, S.P.1
|