-
1
-
-
0024670366
-
Familial pancreatic cancer (Part 1): Genetic pathology review
-
Lynch HT, Lanspa SJ, Fitzgibbons RJ Jr, Smyrk T, Fitzsimmons ML, McClellan J. Familial pancreatic cancer (Part 1): genetic pathology review. Nebr Med J 1989;74:109-12.
-
(1989)
Nebr. Med. J.
, vol.74
, pp. 109-112
-
-
Lynch, H.T.1
Lanspa, S.J.2
Fitzgibbons R.J., Jr.3
Smyrk, T.4
Fitzsimmons, M.L.5
McClellan, J.6
-
2
-
-
0034901004
-
Increased risk of incident pancreatic cancer among first-degree relatives of patients with familial pancreatic cancer
-
Tersmette AC, Petersen GM, Offerhaus GJ, Falatko FC, Brune KA, Goggins M, et al. Increased risk of incident pancreatic cancer among first-degree relatives of patients with familial pancreatic cancer. Clin Cancer Res 2001;7:738-44.
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 738-744
-
-
Tersmette, A.C.1
Petersen, G.M.2
Offerhaus, G.J.3
Falatko, F.C.4
Brune, K.A.5
Goggins, M.6
-
3
-
-
0032797516
-
Diabetes mellitus, other medical conditions and familial history of cancer as risk factors for pancreatic cancer
-
Silverman DT, Schiffman M, Everhart J, Goldstein A, Lillemoe KD, Swanson GM, et al. Diabetes mellitus, other medical conditions and familial history of cancer as risk factors for pancreatic cancer. Br J Cancer 1999; 80:1830-7.
-
(1999)
Br. J. Cancer
, vol.80
, pp. 1830-1837
-
-
Silverman, D.T.1
Schiffman, M.2
Everhart, J.3
Goldstein, A.4
Lillemoe, K.D.5
Swanson, G.M.6
-
4
-
-
0031950026
-
Recent discoveries in cancer genetics of exocrine pancreatic neoplasia
-
Hahn SA, Schmiegel WH. Recent discoveries in cancer genetics of exocrine pancreatic neoplasia. Digestion 1998;59:493-501.
-
(1998)
Digestion
, vol.59
, pp. 493-501
-
-
Hahn, S.A.1
Schmiegel, W.H.2
-
5
-
-
0032807116
-
Familial pancreatic cancer
-
Hruban RH, Petersen GM, Goggins M, Tersmette AC, Offerhaus GJ, Falatko F, et al. Familial pancreatic cancer. Ann Oncol 1999;10 Suppl 4:69-73.
-
(1999)
Ann. Oncol.
, vol.10
, Issue.SUPPL. 4
, pp. 69-73
-
-
Hruban, R.H.1
Petersen, G.M.2
Goggins, M.3
Tersmette, A.C.4
Offerhaus, G.J.5
Falatko, F.6
-
6
-
-
0025284650
-
Systemic cancer and the FAMMM syndrome
-
Bergman W, Watson P, de Jong J, Lynch HT, Fusaro RM. Systemic cancer and the FAMMM syndrome. Br J Cancer 1990;61:932-6.
-
(1990)
Br. J. Cancer
, vol.61
, pp. 932-936
-
-
Bergman, W.1
Watson, P.2
de Jong, J.3
Lynch, H.T.4
Fusaro, R.M.5
-
7
-
-
0025963801
-
Pancreatic cancer and the familial atypical multiple mole melanoma (FAMMM) syndrome
-
Lynch HT, Fusaro RM. Pancreatic cancer and the familial atypical multiple mole melanoma (FAMMM) syndrome. Pancreas 1991;6:127-31.
-
(1991)
Pancreas
, vol.6
, pp. 127-131
-
-
Lynch, H.T.1
Fusaro, R.M.2
-
8
-
-
0023192463
-
Increased risk of cancer in the Peutz-Jeghers syndrome
-
Giardiello FM, Welsh SB, Hamilton SR, Offerhaus GJ, Gittelsohn AM, Booker SV, et al. Increased risk of cancer in the Peutz-Jeghers syndrome. N Engl J Med 1987;316:1511-4.
-
(1987)
N. Engl. J. Med.
, vol.316
, pp. 1511-1514
-
-
Giardiello, F.M.1
Welsh, S.B.2
Hamilton, S.R.3
Offerhaus, G.J.4
Gittelsohn, A.M.5
Booker, S.V.6
-
9
-
-
15444350943
-
Increased risk for cancer in patients with the Peutz-Jeghers syndrome
-
Boardman LA, Thibodeau SN, Schaid DJ, Lindor NM, McDonnell SK, Burgart LJ, et al. Increased risk for cancer in patients with the Peutz-Jeghers syndrome. Ann Intern Med 1998;128:896-9.
-
(1998)
Ann. Intern Med.
, vol.128
, pp. 896-899
-
-
Boardman, L.A.1
Thibodeau, S.N.2
Schaid, D.J.3
Lindor, N.M.4
McDonnell, S.K.5
Burgart, L.J.6
-
10
-
-
0034464147
-
Very high risk of cancer in familial Peutz-Jeghers syndrome
-
Giardiello FM, Brensinger JD, Tersmette AC, Goodman SN, Petersen GM, Booker SV, et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 2000;119:1447-53.
-
(2000)
Gastroenterology
, vol.119
, pp. 1447-1453
-
-
Giardiello, F.M.1
Brensinger, J.D.2
Tersmette, A.C.3
Goodman, S.N.4
Petersen, G.M.5
Booker, S.V.6
-
11
-
-
0030975440
-
Hereditary pancreatitis and the risk of pancreatic cancer
-
International Hereditary Pancreatitis Study Group
-
Lowenfels AB, Maisonneuve P, DiMagno EP, Elitsur Y, Gates LJ, Perrault J, et al. Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group. J Natl Cancer Inst 1997;89: 442-6.
-
(1997)
J. Natl. Cancer Inst.
, vol.89
, pp. 442-446
-
-
Lowenfels, A.B.1
Maisonneuve, P.2
DiMagno, E.P.3
Elitsur, Y.4
Gates, L.J.5
Perrault, J.6
-
12
-
-
0027248156
-
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: An updated review
-
Lynch HT, Smyrk TC, Watson P, Lanspa SJ, Lynch JF, Lynch PM, et al. Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review. Gastroenterology 1993; 104:1535-49.
-
(1993)
Gastroenterology
, vol.104
, pp. 1535-1549
-
-
Lynch, H.T.1
Smyrk, T.C.2
Watson, P.3
Lanspa, S.J.4
Lynch, J.F.5
Lynch, P.M.6
-
13
-
-
0028068230
-
Neoplastic diseases in families of breast cancer patients
-
Tulinius H, Olafsdottir GH, Sigvaldason H, Tryggvadottir L, Bjarnadottir K. Neoplastic diseases in families of breast cancer patients. J Med Genet 1994;31:618-21.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 618-621
-
-
Tulinius, H.1
Olafsdottir, G.H.2
Sigvaldason, H.3
Tryggvadottir, L.4
Bjarnadottir, K.5
-
14
-
-
0026537747
-
The risk of upper gastrointestinal cancer in familial adenomatous polyposis
-
Offerhaus GJ, Giardiello FM, Krush AJ, Booker SV, Tersmette AC, Kelley NC, et al. The risk of upper gastrointestinal cancer in familial adenomatous polyposis. Gastroenterology 1992;102:1980-2.
-
(1992)
Gastroenterology
, vol.102
, pp. 1980-1982
-
-
Offerhaus, G.J.1
Giardiello, F.M.2
Krush, A.J.3
Booker, S.V.4
Tersmette, A.C.5
Kelley, N.C.6
-
15
-
-
0029102927
-
A familial syndrome of pancreatic carcinoma and melanoma with a mutation in the CDKN2 tumor suppressor gene
-
Whelan AJ, Bartsch D, Goodfellow PJ. A familial syndrome of pancreatic carcinoma and melanoma with a mutation in the CDKN2 tumor suppressor gene. N Engl J Med 1995;333:975-7.
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 975-977
-
-
Whelan, A.J.1
Bartsch, D.2
Goodfellow, P.J.3
-
16
-
-
0028059330
-
Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma
-
Caldas C, Hahn SA, da Costa LT, Redston MS, Schutte M, Seymour AB, et al. Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma. Nat Genet 1994;8:27-32.
-
(1994)
Nat. Genet.
, vol.8
, pp. 27-32
-
-
Caldas, C.1
Hahn, S.A.2
da Costa, L.T.3
Redston, M.S.4
Schutte, M.5
Seymour, A.B.6
-
17
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
Hemminki A, Markie D, Tomlinson I, Avizienyte E, Roth S, Loukola A, et al. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 1998;391:184-7.
-
(1998)
Nature
, vol.391
, pp. 184-187
-
-
Hemminki, A.1
Markie, D.2
Tomlinson, I.3
Avizienyte, E.4
Roth, S.5
Loukola, A.6
-
18
-
-
0031974516
-
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
-
Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, et al. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat Genet 1998;18:38-43.
-
(1998)
Nat. Genet.
, vol.18
, pp. 38-43
-
-
Jenne, D.E.1
Reimann, H.2
Nezu, J.3
Friedel, W.4
Loff, S.5
Jeschke, R.6
-
19
-
-
0032984141
-
Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers
-
Su GH, Hruban RH, Bansal RK, Bova GS, Tang DJ, Shekher MC, et al. Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers. Am J Pathol 1999;154:1835-40.
-
(1999)
Am. J. Pathol.
, vol.154
, pp. 1835-1840
-
-
Su, G.H.1
Hruban, R.H.2
Bansal, R.K.3
Bova, G.S.4
Tang, D.J.5
Shekher, M.C.6
-
20
-
-
0029041032
-
Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region
-
Schutte M, da Costa LT, Hahn SA, Moskaluk C, Hoque AT, Rozenblum E, et al. Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region. Proc Natl Acad Sci U S A 1995;92:5950-4.
-
(1995)
Proc. Natl. Acad. Sci. U. S. A.
, vol.92
, pp. 5950-5954
-
-
Schutte, M.1
da Costa, L.T.2
Hahn, S.A.3
Moskaluk, C.4
Hoque, A.T.5
Rozenblum, E.6
-
21
-
-
12644253827
-
Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas
-
Goggins M, Schutte M, Lu J, Moskaluk CA, Weinstein CL, Peterson GM, et al. Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas. Cancer Res 1996;56:5360-4.
-
(1996)
Cancer Res.
, vol.56
, pp. 5360-5364
-
-
Goggins, M.1
Schutte, M.2
Lu, J.3
Moskaluk, C.A.4
Weinstein, C.L.5
Peterson, G.M.6
-
22
-
-
0031137173
-
Germline BRCA26174delT mutations in Ashkenazi Jewish pancreatic cancer patients
-
Ozcelik H, Schmocker B, Di Nicola N, Shi XH, Langer B, Moore M, et al. Germline BRCA26174delT mutations in Ashkenazi Jewish pancreatic cancer patients. Nat Genet 1997;16:17-8.
-
(1997)
Nat. Genet.
, vol.16
, pp. 17-18
-
-
Ozcelik, H.1
Schmocker, B.2
Di Nicola, N.3
Shi, X.H.4
Langer, B.5
Moore, M.6
-
23
-
-
16044366988
-
The carrier frequency of the BRCA26174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, et al. The carrier frequency of the BRCA26174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat Genet 1996;14: 188-90.
-
(1996)
Nat. Genet.
, vol.14
, pp. 188-190
-
-
Oddoux, C.1
Struewing, J.P.2
Clayton, C.M.3
Neuhausen, S.4
Brody, L.C.5
Kaback, M.6
-
24
-
-
0034650411
-
Inherited predisposition to pancreatic adenocarcinoma: Role of family history and germ-line p16, BRCA1, and BRCA2 mutations
-
Lal G, Liu G, Schmocker B, Kaurah P, Ozcelik H, Narod SA, et al. Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations. Cancer Res 2000; 60:409-16.
-
(2000)
Cancer Res.
, vol.60
, pp. 409-416
-
-
Lal, G.1
Liu, G.2
Schmocker, B.3
Kaurah, P.4
Ozcelik, H.5
Narod, S.A.6
-
25
-
-
0035283898
-
A BRCA2 germ-line mutation in familial pancreatic carcinoma
-
White K, Held KR, Weber BH. A BRCA2 germ-line mutation in familial pancreatic carcinoma. Int J Cancer 2001;91:742-4.
-
(2001)
Int. J. Cancer
, vol.91
, pp. 742-744
-
-
White, K.1
Held, K.R.2
Weber, B.H.3
-
26
-
-
0036644884
-
Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: Deleterious BRCA2 mutations in 17%
-
Murphy KM, Brune KA, Griffin C, Sollenberger JE, Petersen GM, Bansal R, et al. Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: deleterious BRCA2 mutations in 17%. Cancer Res 2002;62:3789-93.
-
(2002)
Cancer Res.
, vol.62
, pp. 3789-3793
-
-
Murphy, K.M.1
Brune, K.A.2
Griffin, C.3
Sollenberger, J.E.4
Petersen, G.M.5
Bansal, R.6
-
27
-
-
0035552527
-
Update of familial pancreatic cancer in Germany
-
Bartsch D, Sina-Frey M, Ziegler A, Hahn SA, Przypadlo E, Kress R, et al. Update of familial pancreatic cancer in Germany. Pancreatology 2001;1: 510-6.
-
(2001)
Pancreatology
, vol.1
, pp. 510-516
-
-
Bartsch, D.1
Sina-Frey, M.2
Ziegler, A.3
Hahn, S.A.4
Przypadlo, E.5
Kress, R.6
-
28
-
-
0036269812
-
Familial pancreatic cancer-concept for study of the National Case Collection and early diagnosis program for high risk people
-
Gerdes B, Kress R, Rieder H, Sina-Frey M, Przypadlo E, Barth P, et al. Familial pancreatic cancer-concept for study of the National Case Collection and early diagnosis program for high risk people. Z Arztl Fortbild Qualitatssich 2002;96:251-5.
-
(2002)
Z. Arztl. Fortbild. Qualitatssich
, vol.96
, pp. 251-255
-
-
Gerdes, B.1
Kress, R.2
Rieder, H.3
Sina-Frey, M.4
Przypadlo, E.5
Barth, P.6
-
29
-
-
0034043609
-
Genetic testing. Counseling, laboratory, and regulatory issues and the EUROPAC protocol for ethical research in multicenter studies of inherited pancreatic diseases
-
Applebaum SE, Kant JA, Whitcomb DC, Ellis IH. Genetic testing. Counseling, laboratory, and regulatory issues and the EUROPAC protocol for ethical research in multicenter studies of inherited pancreatic diseases. Med Clin North Am 2000;84:575-88.
-
(2000)
Med. Clin. North Am.
, vol.84
, pp. 575-588
-
-
Applebaum, S.E.1
Kant, J.A.2
Whitcomb, D.C.3
Ellis, I.H.4
-
30
-
-
0034767957
-
Cancer burden in the year 2000. The global picture
-
Parkin DM, Bray FI, Devesa SS. Cancer burden in the year 2000. The global picture. Eur J Cancer 2001;37 Suppl 8:S4-66.
-
(2001)
Eur. J. Cancer
, vol.37
, Issue.SUPPL. 8
-
-
Parkin, D.M.1
Bray, F.I.2
Devesa, S.S.3
-
31
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, et al. Linkage disequilibrium in the human genome. Nature 2001;411:199-204.
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
-
32
-
-
0036466858
-
Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population
-
Meindl A. Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population. Int J Cancer 2002;97:472-80.
-
(2002)
Int. J. Cancer
, vol.97
, pp. 472-480
-
-
Meindl, A.1
-
33
-
-
0030137718
-
Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families
-
Phelan CM, Lancaster JM, Tonin P, Gumbs C, Cochran C, Carter R, et al. Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families. Nat Genet 1996;13:120-2.
-
(1996)
Nat. Genet.
, vol.13
, pp. 120-122
-
-
Phelan, C.M.1
Lancaster, J.M.2
Tonin, P.3
Gumbs, C.4
Cochran, C.5
Carter, R.6
-
34
-
-
0033842724
-
BRCA2 is inactivated late in the development of pancreatic intraepithelial neoplasia: Evidence and implications
-
Goggins M, Hruban RH, Kern SE. BRCA2 is inactivated late in the development of pancreatic intraepithelial neoplasia: evidence and implications. Am J Pathol 2000;156:1767-71.
-
(2000)
Am. J. Pathol.
, vol.156
, pp. 1767-1771
-
-
Goggins, M.1
Hruban, R.H.2
Kern, S.E.3
-
35
-
-
0030932869
-
Cancer-susceptibility genes. Gatekeepers and caretakers
-
Kinzler KW, Vogelstein B. Cancer-susceptibility genes. Gatekeepers and caretakers. Nature 1997;386:761, 763.
-
(1997)
Nature
, vol.386
, pp. 761-763
-
-
Kinzler, K.W.1
Vogelstein, B.2
-
36
-
-
0037169354
-
Cancer susceptibility and the functions of BRCA1 and BRCA2
-
Venkitaraman AR. Cancer susceptibility and the functions of BRCA1 and BRCA2. Cell 2002;108:171-82.
-
(2002)
Cell
, vol.108
, pp. 171-182
-
-
Venkitaraman, A.R.1
-
37
-
-
0028199186
-
Family history and the risk of liver, gallbladder, and pancreatic cancer
-
Fernandez E, La Vecchia C, D'Avanzo B, Negri E, Franceschi S. Family history and the risk of liver, gallbladder, and pancreatic cancer. Cancer Epidemiol Biomarkers Prev 1994;3:209-12.
-
(1994)
Cancer Epidemiol. Biomarkers Prev.
, vol.3
, pp. 209-212
-
-
Fernandez, E.1
La Vecchia, C.2
D'Avanzo, B.3
Negri, E.4
Franceschi, S.5
-
39
-
-
18344363182
-
A new susceptibility locus for autosomal dominant pancreatic cancer maps to chromosome 4q32-34
-
Eberle MA, Pfutzer R, Pogue-Geile KL, Bronner MP, Crispin D, Kimmey MB, et al. A new susceptibility locus for autosomal dominant pancreatic cancer maps to chromosome 4q32-34. Am J Hum Genet 2002;70:1044-8.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 1044-1048
-
-
Eberle, M.A.1
Pfutzer, R.2
Pogue-Geile, K.L.3
Bronner, M.P.4
Crispin, D.5
Kimmey, M.B.6
|