-
1
-
-
0025938038
-
Identification and characterization of the familial adenomatous polyposis coli gene
-
3
-
J Groden A Thliveris 1991 Identification and characterization of the familial adenomatous polyposis coli gene Cell 66 3 589 600
-
(1991)
Cell
, vol.66
, pp. 589-600
-
-
Groden, J.1
Thliveris, A.2
-
2
-
-
0028864589
-
Multiple APC messenger RNA isoforms encoding exon 15 short open reading frames are expressed in the context of a novel exon 10A-derived sequence
-
3
-
Z Sulekova J Reina-Sanchez 1995 Multiple APC messenger RNA isoforms encoding exon 15 short open reading frames are expressed in the context of a novel exon 10A-derived sequence Int J Cancer 63 3 435 41
-
(1995)
Int J Cancer
, vol.63
, pp. 435-41
-
-
Sulekova, Z.1
Reina-Sanchez, J.2
-
3
-
-
0027401792
-
Mutational analysis of patients with adenomatous polyposis: Identical inactivating mutations in unrelated individuals
-
2
-
J Groden L Gelbert 1993 Mutational analysis of patients with adenomatous polyposis: Identical inactivating mutations in unrelated individuals Am J Hum Genet 52 2 263 72
-
(1993)
Am J Hum Genet
, vol.52
, pp. 263-72
-
-
Groden, J.1
Gelbert, L.2
-
4
-
-
0002358598
-
Germline hMSH2 and differential somatic mutations in patients with Turcot's syndrome
-
2
-
TL Chan ST Yuen 1999 Germline hMSH2 and differential somatic mutations in patients with Turcot's syndrome Genes Chromosomes Cancer 25 2 75 81
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 75-81
-
-
Chan, T.L.1
Yuen, S.T.2
-
5
-
-
0029088536
-
The APC gene in Turcot's syndrome
-
8
-
WH Yong C Raffel 1995 The APC gene in Turcot's syndrome N Engl J Med 333 8 524
-
(1995)
N Engl J Med
, vol.333
, pp. 524
-
-
Yong, W.H.1
Raffel, C.2
-
6
-
-
0023572211
-
The gene for familial polyposis coli maps to the long arm of chromosome 5
-
4832
-
M Leppert M Dobbs 1987 The gene for familial polyposis coli maps to the long arm of chromosome 5 Science 238 4832 1411 3
-
(1987)
Science
, vol.238
, pp. 1411-3
-
-
Leppert, M.1
Dobbs, M.2
-
7
-
-
0031781181
-
Genotype-phenotype correlations in attenuated adenomatous polyposis coli
-
6
-
C Soravia T Berk 1998 Genotype-phenotype correlations in attenuated adenomatous polyposis coli Am J Hum Genet 62 6 1290 301
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1290-301
-
-
Soravia, C.1
Berk, T.2
-
8
-
-
0027724691
-
Alleles of the APC gene: An attenuated form of familial polyposis
-
5
-
L Spirio S Olschwang 1993 Alleles of the APC gene: An attenuated form of familial polyposis Cell 75 5 951 7
-
(1993)
Cell
, vol.75
, pp. 951-7
-
-
Spirio, L.1
Olschwang, S.2
-
9
-
-
6844252957
-
Germline mutations in the 3′ part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli
-
6
-
RB van der Luijt P Meera Khan 1996 Germline mutations in the 3′ part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli Hum Genet 98 6 727 34
-
(1996)
Hum Genet
, vol.98
, pp. 727-34
-
-
Van Der Luijt, R.B.1
Meera Khan, P.2
-
10
-
-
0034703393
-
Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q
-
15
-
H Lamlum N Al Tassan 2000 Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q Hum Mol Genet 9 15 2215 21
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2215-21
-
-
Lamlum, H.1
Al Tassan, N.2
-
11
-
-
18344367618
-
Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or multiple colorectal adenomas
-
5
-
OM Sieber H Lamlum 2002 Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or multiple colorectal adenomas Proc Natl Acad Sci USA 99 5 2954 8
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 2954-8
-
-
Sieber, O.M.1
Lamlum, H.2
-
12
-
-
0035750483
-
Repair of oxidative DNA damage: Mechanisms and functions
-
2
-
AL Lu X Li 2001 Repair of oxidative DNA damage: Mechanisms and functions Cell Biochem Biophys 35 2 141 70
-
(2001)
Cell Biochem Biophys
, vol.35
, pp. 141-70
-
-
Lu, A.L.1
Li, X.2
-
13
-
-
0037133042
-
Replication-associated repair of adenine:8-oxoguanine mispairs by MYH
-
4
-
H Hayashi Y Tominaga 2002 Replication-associated repair of adenine:8-oxoguanine mispairs by MYH Curr Biol 12 4 335 9
-
(2002)
Curr Biol
, vol.12
, pp. 335-9
-
-
Hayashi, H.1
Tominaga, Y.2
-
14
-
-
0025981359
-
Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG
-
S Shibutani M Takeshita 1991 Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG Nature 349 431 4
-
(1991)
Nature
, vol.349
, pp. 431-4
-
-
Shibutani, S.1
Takeshita, M.2
-
15
-
-
0030004207
-
Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative damage
-
13
-
MM Slupska C Baikalov 1996 Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative damage J Bacteriol 178 13 3885 92
-
(1996)
J Bacteriol
, vol.178
, pp. 3885-92
-
-
Slupska, M.M.1
Baikalov, C.2
-
16
-
-
0032840464
-
Functional expression of hMYH, a human homolog of the Escherichia coli MutY protein
-
19
-
MM Slupska WM Luther 1999 Functional expression of hMYH, a human homolog of the Escherichia coli MutY protein J Bacteriol 181 19 6210 3
-
(1999)
J Bacteriol
, vol.181
, pp. 6210-3
-
-
Slupska, M.M.1
Luther, W.M.2
-
17
-
-
0036478899
-
Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors
-
2
-
N Al-Tassan NH Chmiel 2002 Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors Nat Genet 30 2 227 32
-
(2002)
Nat Genet
, vol.30
, pp. 227-32
-
-
Al-Tassan, N.1
Chmiel, N.H.2
-
18
-
-
0038501052
-
Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH
-
9377
-
JR Sampson S Dolwani 2003 Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH Lancet 362 9377 39 41
-
(2003)
Lancet
, vol.362
, pp. 39-41
-
-
Sampson, J.R.1
Dolwani, S.2
-
19
-
-
0037468517
-
Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH
-
9
-
OM Sieber L Lipton 2003 Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH N Engl J Med 348 9 791 9
-
(2003)
N Engl J Med
, vol.348
, pp. 791-9
-
-
Sieber, O.M.1
Lipton, L.2
-
20
-
-
0037408432
-
Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers
-
5
-
SE Halford AJ Rowan 2003 Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers Am J Pathol 162 5 1545 8
-
(2003)
Am J Pathol
, vol.162
, pp. 1545-8
-
-
Halford, S.E.1
Rowan, A.J.2
-
21
-
-
12144289614
-
Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas
-
5
-
V Gismondi M Meta 2004 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 5 680 4
-
(2004)
Int J Cancer
, vol.109
, pp. 680-4
-
-
Gismondi, V.1
Meta, M.2
-
22
-
-
10744220394
-
Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway
-
22
-
L Lipton SE Halford 2003 Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway Cancer Res 63 22 7595 9
-
(2003)
Cancer Res
, vol.63
, pp. 7595-9
-
-
Lipton, L.1
Halford, S.E.2
-
23
-
-
0041423452
-
Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients
-
3
-
S Enholm T Hienonen 2003 Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients Am J Pathol 163 3 827 32
-
(2003)
Am J Pathol
, vol.163
, pp. 827-32
-
-
Enholm, S.1
Hienonen, T.2
-
24
-
-
0036848267
-
Bi-allelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C→T:A mutations
-
23
-
S Jones P Emmerson 2002 Bi-allelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C→T:A mutations Hum Mol Genet 11 23 2961 7
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2961-7
-
-
Jones, S.1
Emmerson, P.2
-
25
-
-
1542719919
-
Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer
-
4
-
C Fleischmann J Peto 2004 Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer Int J Cancer 109 4 554 8
-
(2004)
Int J Cancer
, vol.109
, pp. 554-8
-
-
Fleischmann, C.1
Peto, J.2
-
26
-
-
11144355687
-
Role of inherited defects of MYH in the development of sporadic colorectal cancer
-
1
-
T Kambara VL Whitehall 2004 Role of inherited defects of MYH in the development of sporadic colorectal cancer Genes Chromosomes Cancer 40 1 1 9
-
(2004)
Genes Chromosomes Cancer
, vol.40
, pp. 1-9
-
-
Kambara, T.1
Whitehall, V.L.2
-
27
-
-
7944225535
-
Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk
-
Croitoru ME, Cleary SP, Di Nicola N, et al. Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk. J Natl Cancer Inst 2004; 96:1631-4
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 1631-1634
-
-
Croitoru, M.E.1
Cleary, S.P.2
Di Nicola, N.3
-
28
-
-
20544452084
-
Germline susceptibility to colorectal cancer due to base-excision repair gene defects
-
Farrington SM, Tenesa A, Barnetson R, et al. Germline susceptibility to colorectal cancer due to base-excision repair gene defects. Am J Hum Genet 2005; 77:112-9
-
(2005)
Am J Hum Genet
, vol.77
, pp. 112-119
-
-
Farrington, S.M.1
Tenesa, A.2
Barnetson, R.3
-
29
-
-
0031048855
-
Clinical and molecular features of the hereditary mixed polyposis syndrome
-
2
-
SC Whitelaw VA Murday 1997 Clinical and molecular features of the hereditary mixed polyposis syndrome Gastroenterology 112 2 327 34
-
(1997)
Gastroenterology
, vol.112
, pp. 327-34
-
-
Whitelaw, S.C.1
Murday, V.A.2
-
30
-
-
0037730140
-
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
-
EEM Jaeger KL Woodford-Richens 2003 An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome Am J Hum Genet 72 1261 7
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1261-7
-
-
Jaeger, E.E.M.1
Woodford-Richens, K.L.2
-
31
-
-
19144370572
-
Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q
-
4
-
HJ Thomas SC Whitelaw 1996 Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q Am J Hum Genet 58 4 770 6
-
(1996)
Am J Hum Genet
, vol.58
, pp. 770-6
-
-
Thomas, H.J.1
Whitelaw, S.C.2
-
32
-
-
0033067274
-
Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22
-
4
-
I Tomlinson N Rahman 1999 Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22 Gastroenterology 116 4 789 95
-
(1999)
Gastroenterology
, vol.116
, pp. 789-95
-
-
Tomlinson, I.1
Rahman, N.2
-
33
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
6663
-
A Hemminki D Markie 1998 A serine/threonine kinase gene defective in Peutz-Jeghers syndrome Nature 391 6663 184 7
-
(1998)
Nature
, vol.391
, pp. 184-7
-
-
Hemminki, A.1
Markie, D.2
-
34
-
-
0032947283
-
Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients
-
5
-
ZJ Wang M Churchman 1999 Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients J Med Genet 36 5 365 8
-
(1999)
J Med Genet
, vol.36
, pp. 365-8
-
-
Wang, Z.J.1
Churchman, M.2
-
35
-
-
0032524069
-
Mutations in the SMAD4/DPC4 gene in juvenile polyposis
-
5366
-
JR Howe S Roth 1998 Mutations in the SMAD4/DPC4 gene in juvenile polyposis Science 280 5366 1086 8
-
(1998)
Science
, vol.280
, pp. 1086-8
-
-
Howe, J.R.1
Roth, S.2
-
36
-
-
0034829630
-
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
-
4
-
XP Zhou K Woodford-Richens 2001 Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes Am J Hum Genet 69 4 704 11
-
(2001)
Am J Hum Genet
, vol.69
, pp. 704-11
-
-
Zhou, X.P.1
Woodford-Richens, K.2
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