-
1
-
-
76949133404
-
Pedigree of a family with hereditary chronic relapsing pancreatitis
-
M.W. Comfort, and A.G. Steinberg Pedigree of a family with hereditary chronic relapsing pancreatitis Gastroenterology 21 1952 54 63
-
(1952)
Gastroenterology
, vol.21
, pp. 54-63
-
-
Comfort, M.W.1
Steinberg, A.G.2
-
2
-
-
7444266818
-
Hereditary pancreatitis
-
B. Gerber Hereditary pancreatitis Arch Surg 87 1963 70 80
-
(1963)
Arch Surg
, vol.87
, pp. 70-80
-
-
Gerber, B.1
-
3
-
-
7444267384
-
Some recent developments pertaining to the pancreas
-
J. Gross Some recent developments pertaining to the pancreas Ann Intern Med 49 1958 796 836
-
(1958)
Ann Intern Med
, vol.49
, pp. 796-836
-
-
Gross, J.1
-
4
-
-
0001523374
-
Hereditary pancreatitis: Report on two additional families
-
J. Gross, and M.W. Comfort Hereditary pancreatitis: report on two additional families Gastroenterology 32 1957 829 854
-
(1957)
Gastroenterology
, vol.32
, pp. 829-854
-
-
Gross, J.1
Comfort, M.W.2
-
6
-
-
0035702382
-
Clinical characterization of patients with hereditary pancreatitis and mutations in the cationic trypsinogen gene
-
V. Keim, N. Bauer, N. Teich, P. Simon, M.M. Lerch, and J. Mossner Clinical characterization of patients with hereditary pancreatitis and mutations in the cationic trypsinogen gene Am J Med 111 8 2001 622 626
-
(2001)
Am J Med
, vol.111
, Issue.8
, pp. 622-626
-
-
Keim, V.1
Bauer, N.2
Teich, N.3
Simon, P.4
Lerch, M.M.5
Mossner, J.6
-
7
-
-
0030848153
-
Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multi-center Pancreatic Study Group
-
M.J. Sossenheimer, C.E. Aston, R.A. Preston, L.K. Gates Jr., C.D. Ulrich, and S.P. Martin Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multi-center Pancreatic Study Group Am J Gastroenterol 92 1997 1113 1116
-
(1997)
Am J Gastroenterol
, vol.92
, pp. 1113-1116
-
-
Sossenheimer, M.J.1
Aston, C.E.2
Preston, R.A.3
Gates Jr., L.K.4
Ulrich, C.D.5
Martin, S.P.6
-
8
-
-
0018150025
-
Hereditary pancreatitis in England and Wales
-
J.R. Sibert Hereditary pancreatitis in England and Wales J Med Genet 15 1978 189 201
-
(1978)
J Med Genet
, vol.15
, pp. 189-201
-
-
Sibert, J.R.1
-
9
-
-
0030017252
-
An exceptional genealogy for hereditary chronic pancreatitis
-
L. Le Bodic, M. Schnee, T. Georgelin, F. Soulard, C. Ferec, and J.D. Bignon An exceptional genealogy for hereditary chronic pancreatitis Dig Dis Sci 41 7 1996 1504 1510
-
(1996)
Dig Dis Sci
, vol.41
, Issue.7
, pp. 1504-1510
-
-
Le Bodic, L.1
Schnee, M.2
Georgelin, T.3
Soulard, F.4
Ferec, C.5
Bignon, J.D.6
-
10
-
-
0035080006
-
Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins
-
S.T. Amann, L.K. Gates, C.E. Aston, A. Pandya, and D.C. Whitcomb Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins Gut 48 4 2001 542 547
-
(2001)
Gut
, vol.48
, Issue.4
, pp. 542-547
-
-
Amann, S.T.1
Gates, L.K.2
Aston, C.E.3
Pandya, A.4
Whitcomb, D.C.5
-
11
-
-
10144246566
-
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene
-
D.C. Whitcomb, M.C. Gorry, R.A. Preston, W. Furey, M.J. Sossenheimer, and C.D. Ulrich Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene Nat Genet 14 1996 141 145
-
(1996)
Nat Genet
, vol.14
, pp. 141-145
-
-
Whitcomb, D.C.1
Gorry, M.C.2
Preston, R.A.3
Furey, W.4
Sossenheimer, M.J.5
Ulrich, C.D.6
-
12
-
-
0030813082
-
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis
-
M.C. Gorry, D. Gabbaizedeh, W. Furey, L.K. Gates Jr., R.A. Preston, and C.E. Aston Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis Gastroenterology 113 1997 1063 1068
-
(1997)
Gastroenterology
, vol.113
, pp. 1063-1068
-
-
Gorry, M.C.1
Gabbaizedeh, D.2
Furey, W.3
Gates Jr., L.K.4
Preston, R.A.5
Aston, C.E.6
-
13
-
-
0030017526
-
The complete 685-kilobase DNA sequence of the human beta T cell receptor locus
-
L. Rowen, B.F. Koop, and L. Hood The complete 685-kilobase DNA sequence of the human beta T cell receptor locus Science 272 5269 1996 1755 1762
-
(1996)
Science
, vol.272
, Issue.5269
, pp. 1755-1762
-
-
Rowen, L.1
Koop, B.F.2
Hood, L.3
-
14
-
-
2442723724
-
Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis
-
C. Ferec, O. Raguenes, R. Salomon, C. Roche, J.P. Bernard, and M. Guillot Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis J Med Genet 36 1999 228 232
-
(1999)
J Med Genet
, vol.36
, pp. 228-232
-
-
Ferec, C.1
Raguenes, O.2
Salomon, R.3
Roche, C.4
Bernard, J.P.5
Guillot, M.6
-
15
-
-
0032993541
-
A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis
-
H. Witt, W. Luck, and M. Becker A signal peptide cleavage site mutation in the cationic trypsinogen gene is strongly associated with chronic pancreatitis Gastroenterology 117 1999 7 10
-
(1999)
Gastroenterology
, vol.117
, pp. 7-10
-
-
Witt, H.1
Luck, W.2
Becker, M.3
-
16
-
-
0033866202
-
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation
-
N. Teich, J. Ockenga, A. Hoffmeister, M. Manns, J. Mossner, and V. Keim Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation Gastroenterology 119 2000 461 465
-
(2000)
Gastroenterology
, vol.119
, pp. 461-465
-
-
Teich, N.1
Ockenga, J.2
Hoffmeister, A.3
Manns, M.4
Mossner, J.5
Keim, V.6
-
17
-
-
0242582422
-
Evolution of trypsinogen activation peptides
-
J.M. Chen, Z. Kukor, C. Le Marechal, M. Toth, L. Tsakiris, and O. Raguenes Evolution of trypsinogen activation peptides Mol Biol Evol 20 11 2003 1767 1777
-
(2003)
Mol Biol Evol
, vol.20
, Issue.11
, pp. 1767-1777
-
-
Chen, J.M.1
Kukor, Z.2
Le Marechal, C.3
Toth, M.4
Tsakiris, L.5
Raguenes, O.6
-
18
-
-
0036177587
-
Mutational screening of patients with nonalcoholic chronic pancreatitis: Identification of further trypsinogen variants
-
N. Teich, N. Bauer, J. Mossner, and V. Keim Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants Am J Gastroenterol 97 2 2002 341 346
-
(2002)
Am J Gastroenterol
, vol.97
, Issue.2
, pp. 341-346
-
-
Teich, N.1
Bauer, N.2
Mossner, J.3
Keim, V.4
-
19
-
-
0035193087
-
Identification of a novel pancreatitis-associated missense mutation, R116C, in the human cationic trypsinogen gene (PRSS1)
-
C. Le Marechal, J.F. Bretagne, O. Raguenes, I. Quere, J.M. Chen, and C. Ferec Identification of a novel pancreatitis-associated missense mutation, R116C, in the human cationic trypsinogen gene (PRSS1) Mol Genet Metab 74 3 2001 342 344
-
(2001)
Mol Genet Metab
, vol.74
, Issue.3
, pp. 342-344
-
-
Le Marechal, C.1
Bretagne, J.F.2
Raguenes, O.3
Quere, I.4
Chen, J.M.5
Ferec, C.6
-
20
-
-
0036151004
-
Novel Cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis
-
R. Pfutzer, E. Myers, S. Applebaum-Shapiro, R. Finch, I. Eliis, and J. Neoptolemos Novel Cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis Gut 50 2002 271 272
-
(2002)
Gut
, vol.50
, pp. 271-272
-
-
Pfutzer, R.1
Myers, E.2
Applebaum-Shapiro, S.3
Finch, R.4
Eliis, I.5
Neoptolemos, J.6
-
21
-
-
18544365392
-
Hereditary pancreatitis caused by a Novel PRSS1 mutation (Arg-122 right-arrow Cys) that alters autoactivation and autodegradation of cationic trypsinogen
-
P. Simon, F.U. Weiss, M. Sahin-Toth, M. Parry, O. Nayler, and B. Lenfers Hereditary pancreatitis caused by a Novel PRSS1 mutation (Arg-122 right-arrow Cys) that alters autoactivation and autodegradation of cationic trypsinogen J Biol Chem 277 7 2002 5404 5410
-
(2002)
J Biol Chem
, vol.277
, Issue.7
, pp. 5404-5410
-
-
Simon, P.1
Weiss, F.U.2
Sahin-Toth, M.3
Parry, M.4
Nayler, O.5
Lenfers, B.6
-
22
-
-
0035128513
-
A new polymorphism for the RI22H mutation in hereditary pancreatitis
-
N. Howes, W. Greenhalf, S. Rutherford, M. O'Donnell, R. Mountford, and I. Ellis A new polymorphism for the RI22H mutation in hereditary pancreatitis Gut 48 2 2001 247 250
-
(2001)
Gut
, vol.48
, Issue.2
, pp. 247-250
-
-
Howes, N.1
Greenhalf, W.2
Rutherford, S.3
O'Donnell, M.4
Mountford, R.5
Ellis, I.6
-
23
-
-
0035093636
-
Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitis
-
J.M. Chen, A. Piepoli Bis, L. Le Bodic, P. Ruszniewski, M. Robaszkiewicz, and P.H. Deprez Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitis Clin Genet 59 3 2001 189 193
-
(2001)
Clin Genet
, vol.59
, Issue.3
, pp. 189-193
-
-
Chen, J.M.1
Piepoli Bis, A.2
Le Bodic, L.3
Ruszniewski, P.4
Robaszkiewicz, M.5
Deprez, P.H.6
-
24
-
-
9144233558
-
Interaction between trypsinogen isoforms in genetically determined pancreatitis: Mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2)
-
N. Teich, C. Le Marechal, Z. Kukor, K. Caca, H. Witzigmann, and J.M. Chen Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2) Hum Mutat 23 1 2004 22 31
-
(2004)
Hum Mutat
, vol.23
, Issue.1
, pp. 22-31
-
-
Teich, N.1
Le Marechal, C.2
Kukor, Z.3
Caca, K.4
Witzigmann, H.5
Chen, J.M.6
-
25
-
-
0038183810
-
Loss of function mutations in the cationic trypsinogen gene (PRSS1) may act as a protective factor against pancreatitis
-
J.M. Chen, C. Le Marechal, D. Lucas, O. Raguenes, and C. Ferec Loss of function mutations in the cationic trypsinogen gene (PRSS1) may act as a protective factor against pancreatitis Mol Genet Metab 79 1 2003 67 70
-
(2003)
Mol Genet Metab
, vol.79
, Issue.1
, pp. 67-70
-
-
Chen, J.M.1
Le Marechal, C.2
Lucas, D.3
Raguenes, O.4
Ferec, C.5
-
26
-
-
2442727497
-
Screening for mutations of the cationic trypsinogen gene: Are they of relevance in chronic alcoholic pancreatitis?
-
N. Teich, J. Mossner, and V. Keim Screening for mutations of the cationic trypsinogen gene: are they of relevance in chronic alcoholic pancreatitis? Gut 44 1999 413 416
-
(1999)
Gut
, vol.44
, pp. 413-416
-
-
Teich, N.1
Mossner, J.2
Keim, V.3
-
27
-
-
0031695080
-
Lack of R117H mutation in the cationic trypsinogen gene in patients with tropical pancreatitis from Bangladesh
-
L. Rossi, D.C. Whitcomb, G.D. Ehrlich, M.C. Gorry, S. Parvin, and S. Sattar Lack of R117H mutation in the cationic trypsinogen gene in patients with tropical pancreatitis from Bangladesh Pancreas 17 1998 278 280
-
(1998)
Pancreas
, vol.17
, pp. 278-280
-
-
Rossi, L.1
Whitcomb, D.C.2
Ehrlich, G.D.3
Gorry, M.C.4
Parvin, S.5
Sattar, S.6
-
28
-
-
0037032399
-
Spontaneous and sporadic trypsinogen mutations in idiopathic pancreatitis
-
P. Simon, F.U. Weiss, K.P. Zimmer, S. Rand, B. Brinkmann, and W. Domschke Spontaneous and sporadic trypsinogen mutations in idiopathic pancreatitis JAMA 288 17 2002 2122
-
(2002)
JAMA
, vol.288
, Issue.17
, pp. 2122
-
-
Simon, P.1
Weiss, F.U.2
Zimmer, K.P.3
Rand, S.4
Brinkmann, B.5
Domschke, W.6
-
29
-
-
10744233747
-
Clinical and genetic characteristics of hereditary pancreatitis in Europe
-
N. Howes, M.M. Lerch, W. Greenhalf, D.D. Stocken, I. Ellis, and P. Simon Clinical and genetic characteristics of hereditary pancreatitis in Europe Clin Gastroenterol Hepatol 2 2004 252 261
-
(2004)
Clin Gastroenterol Hepatol
, vol.2
, pp. 252-261
-
-
Howes, N.1
Lerch, M.M.2
Greenhalf, W.3
Stocken, D.D.4
Ellis, I.5
Simon, P.6
-
30
-
-
0035554034
-
Hereditary pancreatitis in Japan: A review of pancreatitis-associated gene mutations
-
I. Nishimori, and S. Onishi Hereditary pancreatitis in Japan: a review of pancreatitis-associated gene mutations Pancreatol 1 2001 444 447
-
(2001)
Pancreatol
, vol.1
, pp. 444-447
-
-
Nishimori, I.1
Onishi, S.2
-
31
-
-
0032988134
-
Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis
-
I. Nishimori, M. Kamakura, K. Fujikawa-Adachi, M. Morita, S. Onishi, and K. Yokoyama Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis Gut 44 1999 259 263
-
(1999)
Gut
, vol.44
, pp. 259-263
-
-
Nishimori, I.1
Kamakura, M.2
Fujikawa-Adachi, K.3
Morita, M.4
Onishi, S.5
Yokoyama, K.6
-
32
-
-
0035553707
-
Hereditary pancreatitis in North America: The Pittsburgh-Midwest Multi-Center Pancreatic Study Group Study
-
S.E. Applebaum-Shapiro, R. Finch, R.H. Pfutzer, L.A. Hepp, L. Gates, and S. Amann Hereditary pancreatitis in North America: the Pittsburgh-Midwest Multi-Center Pancreatic Study Group Study Pancreatology 1 5 2001 439 443
-
(2001)
Pancreatology
, vol.1
, Issue.5
, pp. 439-443
-
-
Applebaum-Shapiro, S.E.1
Finch, R.2
Pfutzer, R.H.3
Hepp, L.A.4
Gates, L.5
Amann, S.6
-
33
-
-
0034043830
-
Genetic predispositions to acute and chronic pancreatitis
-
D.C. Whitcomb Genetic predispositions to acute and chronic pancreatitis Med Clin North Am 84 3 2000 531 547 [vii]
-
(2000)
Med Clin North Am
, vol.84
, Issue.3
, pp. 531-547
-
-
Whitcomb, D.C.1
-
34
-
-
0042061201
-
Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor alpha (TNF-α) promoter region or the TNF receptor 1 (TNFR1) gene
-
A. Schneider, K. Pogue-Geile, M.M. Barmada, E. Myers-Fong, B.S. Thompson, and D.C. Whitcomb Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor alpha (TNF-α) promoter region or the TNF receptor 1 (TNFR1) gene Genet Med 5 2 2003 120 125
-
(2003)
Genet Med
, vol.5
, Issue.2
, pp. 120-125
-
-
Schneider, A.1
Pogue-Geile, K.2
Barmada, M.M.3
Myers-Fong, E.4
Thompson, B.S.5
Whitcomb, D.C.6
-
35
-
-
0034129667
-
Risk factors for cancer in hereditary pancreatitis. International Hereditary Pancreatitis Study Group
-
A.B. Lowenfels, P. Maisonneuve, and D.C. Whitcomb Risk factors for cancer in hereditary pancreatitis. International Hereditary Pancreatitis Study Group Med Clin North Am 84 3 2000 565 573
-
(2000)
Med Clin North Am
, vol.84
, Issue.3
, pp. 565-573
-
-
Lowenfels, A.B.1
Maisonneuve, P.2
Whitcomb, D.C.3
-
36
-
-
0033953518
-
Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis
-
J.E. Creighton, R. Lyall, D.I. Wilson, A. Curtis, and R.M. Charnley Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis Br J Surg 87 2000 170 175
-
(2000)
Br J Surg
, vol.87
, pp. 170-175
-
-
Creighton, J.E.1
Lyall, R.2
Wilson, D.I.3
Curtis, A.4
Charnley, R.M.5
-
37
-
-
0027294719
-
Pancreatitis and the risk of pancreatic cancer. International Pancreatitis Study Group
-
A.B. Lowenfels, P. Maisonneuve, G. Cavallini, R.W. Ammann, P.G. Lankisch, and J.R. Andersen Pancreatitis and the risk of pancreatic cancer. International Pancreatitis Study Group N Engl J Med 328 1993 1433 1437
-
(1993)
N Engl J Med
, vol.328
, pp. 1433-1437
-
-
Lowenfels, A.B.1
Maisonneuve, P.2
Cavallini, G.3
Ammann, R.W.4
Lankisch, P.G.5
Andersen, J.R.6
-
38
-
-
0035158207
-
Trypsinogen gene mutations in patients with chronic or recurrent acute pancreatitis
-
K. Truninger, J. Kock, H.P. Wirth, B. Muellhaupt, C. Arnold, and F. von Weizsacker Trypsinogen gene mutations in patients with chronic or recurrent acute pancreatitis Pancreas 22 2001 18 23
-
(2001)
Pancreas
, vol.22
, pp. 18-23
-
-
Truninger, K.1
Kock, J.2
Wirth, H.P.3
Muellhaupt, B.4
Arnold, C.5
Von Weizsacker, F.6
-
39
-
-
0027168349
-
Long-term follow-up of young patients with chronic hereditary or idiopathic pancreatitis
-
K.M. Konzen, J. Perrault, C. Moir, and A.R. Zinsmeister Long-term follow-up of young patients with chronic hereditary or idiopathic pancreatitis Mayo Clin Proc 68 1993 449 453
-
(1993)
Mayo Clin Proc
, vol.68
, pp. 449-453
-
-
Konzen, K.M.1
Perrault, J.2
Moir, C.3
Zinsmeister, A.R.4
-
40
-
-
0027946488
-
The different courses of early and late-onset idiopathic and alcoholic chronic pancreatitis
-
P. Layer, H. Yamamoto, L. Kalthoff, J.E. Clain, L.J. Bakken, and E.P. DiMagno The different courses of early and late-onset idiopathic and alcoholic chronic pancreatitis Gastroenterology 107 1994 1481 1487
-
(1994)
Gastroenterology
, vol.107
, pp. 1481-1487
-
-
Layer, P.1
Yamamoto, H.2
Kalthoff, L.3
Clain, J.E.4
Bakken, L.J.5
Dimagno, E.P.6
-
41
-
-
0015548234
-
Hereditary pancreatitis: Three new kindreds and a critical review of the literature
-
J. Kattwinkel, A. Lapey, P.A. Di Sant'Agnese, and W.A. Edwards Hereditary pancreatitis: three new kindreds and a critical review of the literature Pediatrics 51 1973 55 69
-
(1973)
Pediatrics
, vol.51
, pp. 55-69
-
-
Kattwinkel, J.1
Lapey, A.2
Di Sant'Agnese, P.A.3
Edwards, W.A.4
-
42
-
-
0031662469
-
The natural history of hereditary chronic pancreatitis: A study of 12 cases compared to chronic alcoholic pancreatitis
-
O. Paolini, P. Hastier, M. Buckley, B. Maes, J.F. Demarquay, and P. Staccini The natural history of hereditary chronic pancreatitis: a study of 12 cases compared to chronic alcoholic pancreatitis Pancreas 17 1998 266 271
-
(1998)
Pancreas
, vol.17
, pp. 266-271
-
-
Paolini, O.1
Hastier, P.2
Buckley, M.3
Maes, B.4
Demarquay, J.F.5
Staccini, P.6
-
43
-
-
0030975440
-
Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group
-
A.B. Lowenfels, P. Maisonneuve, E.P. DiMagno, Y. Elitsur, L.K. Gates Jr., and J. Perrault Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group J Natl Cancer Inst 89 1997 442 446
-
(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 Jr., L.K.5
Perrault, J.6
-
44
-
-
0034940538
-
Cigarette smoking as a risk factor for pancreatic cancer in patients with hereditary pancreatitis
-
A.B. Lowenfels, P. Maisonneuve, D.C. Whitcomb, M.M. Lerch, and E.P. DiMagno Cigarette smoking as a risk factor for pancreatic cancer in patients with hereditary pancreatitis JAMA 286 2 2001 169 170
-
(2001)
JAMA
, vol.286
, Issue.2
, pp. 169-170
-
-
Lowenfels, A.B.1
Maisonneuve, P.2
Whitcomb, D.C.3
Lerch, M.M.4
Dimagno, E.P.5
-
45
-
-
0033590960
-
Maternal inheritance pattern of hereditary pancreatitis in patients with pancreatic carcinoma
-
M.M. Lerch, I. Ellis, D.C. Whitcomb, V. Keim, P. Simon, and N. Howes Maternal inheritance pattern of hereditary pancreatitis in patients with pancreatic carcinoma J Natl Cancer Inst 91 1999 723 724
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 723-724
-
-
Lerch, M.M.1
Ellis, I.2
Whitcomb, D.C.3
Keim, V.4
Simon, P.5
Howes, N.6
-
46
-
-
0025688248
-
Increased cell division as a cause of human cancer
-
S. Preston-Martin, M.C. Pike, R.K. Ross, P.A. Jones, and B.E. Henderson Increased cell division as a cause of human cancer Cancer Res 50 23 1990 7415 7421
-
(1990)
Cancer Res
, vol.50
, Issue.23
, pp. 7415-7421
-
-
Preston-Martin, S.1
Pike, M.C.2
Ross, R.K.3
Jones, P.A.4
Henderson, B.E.5
-
47
-
-
0028913443
-
Matrix metalloproteinase 7 (matrilysin) from human rectal carcinoma cells. Activation of the precursor, interaction with other matrix metalloproteinases and enzymic properties
-
K. Imai, Y. Yokohama, I. Nakanishi, E. Ohuchi, Y. Fujii, and N. Nakai Matrix metalloproteinase 7 (matrilysin) from human rectal carcinoma cells. Activation of the precursor, interaction with other matrix metalloproteinases and enzymic properties J Biol Chem 270 12 1995 6691 6697
-
(1995)
J Biol Chem
, vol.270
, Issue.12
, pp. 6691-6697
-
-
Imai, K.1
Yokohama, Y.2
Nakanishi, I.3
Ohuchi, E.4
Fujii, Y.5
Nakai, N.6
-
48
-
-
0036266409
-
Matrix metalloproteinase-7 is expressed by pancreatic cancer precursors and regulates acinar-to-ductal metaplasia in exocrine pancreas
-
H.C. Crawford, C.R. Scoggins, M.K. Washington, L.M. Matrisian, and S.D. Leach Matrix metalloproteinase-7 is expressed by pancreatic cancer precursors and regulates acinar-to-ductal metaplasia in exocrine pancreas J Clin Invest 109 11 2002 1437 1444
-
(2002)
J Clin Invest
, vol.109
, Issue.11
, pp. 1437-1444
-
-
Crawford, H.C.1
Scoggins, C.R.2
Washington, M.K.3
Matrisian, L.M.4
Leach, S.D.5
-
49
-
-
0034039578
-
Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis
-
H. Witt, W. Luck, H.C. Hennies, M. Classen, A. Kage, and U. Lass Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis Nat Genet 25 2000 213 216
-
(2000)
Nat Genet
, vol.25
, pp. 213-216
-
-
Witt, H.1
Luck, W.2
Hennies, H.C.3
Classen, M.4
Kage, A.5
Lass, U.6
-
50
-
-
0023594933
-
Primary structure of human pancreatic secretory trypsin inhibitor (PSTI) gene
-
A. Horii, T. Kobayashi, N. Tomita, T. Yamamoto, S. Fukushige, and T. Murotsu Primary structure of human pancreatic secretory trypsin inhibitor (PSTI) gene Biochem Biophys Res Commun 149 2 1987 635 641
-
(1987)
Biochem Biophys Res Commun
, vol.149
, Issue.2
, pp. 635-641
-
-
Horii, A.1
Kobayashi, T.2
Tomita, N.3
Yamamoto, T.4
Fukushige, S.5
Murotsu, T.6
-
51
-
-
0017335059
-
The primary structure of the human pancreatic secretory trypsin inhibitor. Amino acid sequence of the reduced S-aminoethylated protein
-
D.C. Bartelt, R. Shapanka, and L.J. Greene The primary structure of the human pancreatic secretory trypsin inhibitor. Amino acid sequence of the reduced S-aminoethylated protein Arch Biochem Biophys 179 1 1977 189 199
-
(1977)
Arch Biochem Biophys
, vol.179
, Issue.1
, pp. 189-199
-
-
Bartelt, D.C.1
Shapanka, R.2
Greene, L.J.3
-
52
-
-
0033857452
-
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis
-
R.H. Pfutzer, M.M. Barmada, A.P. Brunskill, R. Finch, P.S. Hart, and J. Neoptolemos SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis Gastroenterology 119 3 2000 615 623
-
(2000)
Gastroenterology
, vol.119
, Issue.3
, pp. 615-623
-
-
Pfutzer, R.H.1
Barmada, M.M.2
Brunskill, A.P.3
Finch, R.4
Hart, P.S.5
Neoptolemos, J.6
-
53
-
-
0034111551
-
Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis
-
J.M. Chen, B. Mercier, M.P. Audrezet, and C. Ferec Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis J Med Genet 37 2000 67 69
-
(2000)
J Med Genet
, vol.37
, pp. 67-69
-
-
Chen, J.M.1
Mercier, B.2
Audrezet, M.P.3
Ferec, C.4
-
54
-
-
0036102601
-
The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancreatitis but does not cause the disease
-
J. Threadgold, W. Greenhalf, I. Ellis, N. Howes, M.M. Lerch, and P. Simon The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancreatitis but does not cause the disease Gut 50 5 2002 675 681
-
(2002)
Gut
, vol.50
, Issue.5
, pp. 675-681
-
-
Threadgold, J.1
Greenhalf, W.2
Ellis, I.3
Howes, N.4
Lerch, M.M.5
Simon, P.6
-
55
-
-
0037387886
-
SPINK1 mutations and phenotypic expression in patients with pancreatitis associated with trypsinogen mutations
-
F.U. Weiss, P. Simon, H. Witt, J. Mayerle, V. Hlouschek, and K.P. Zimmer SPINK1 mutations and phenotypic expression in patients with pancreatitis associated with trypsinogen mutations J Med Genet 40 4 2003 e40
-
(2003)
J Med Genet
, vol.40
, Issue.4
, pp. 40
-
-
Weiss, F.U.1
Simon, P.2
Witt, H.3
Mayerle, J.4
Hlouschek, V.5
Zimmer, K.P.6
-
56
-
-
0036789203
-
Tropical calcific pancreatitis: Strong association with SPINK1 trypsin inhibitor mutations
-
E. Bhatia, G. Choudhuri, S.S. Sikora, O. Landt, A. Kage, and M. Becker Tropical calcific pancreatitis: strong association with SPINK1 trypsin inhibitor mutations Gastroenterology 123 4 2002 1020 1025
-
(2002)
Gastroenterology
, vol.123
, Issue.4
, pp. 1020-1025
-
-
Bhatia, E.1
Choudhuri, G.2
Sikora, S.S.3
Landt, O.4
Kage, A.5
Becker, M.6
-
57
-
-
19044400563
-
SPINK1 is a susceptibility gene for fibrocalculous pancreatic diabetes in subjects from the Indian subcontinent
-
Z. Hassan, V. Mohan, L. Ali, R. Allotey, K. Barakat, and M.O. Faruque SPINK1 is a susceptibility gene for fibrocalculous pancreatic diabetes in subjects from the Indian subcontinent Am J Hum Genet 71 4 2002 964 968
-
(2002)
Am J Hum Genet
, vol.71
, Issue.4
, pp. 964-968
-
-
Hassan, Z.1
Mohan, V.2
Ali, L.3
Allotey, R.4
Barakat, K.5
Faruque, M.O.6
-
58
-
-
0346846759
-
Absence of association between SPINK1 trypsin inhibitor mutations and type 1 or 2 diabetes mellitus in India and Germany
-
E. Bhatia, O. Kordonouri, K. Balasubramanium, J. Rajeswari, O. Landt, and P. Simon Absence of association between SPINK1 trypsin inhibitor mutations and type 1 or 2 diabetes mellitus in India and Germany Diabetologia 46 2003 1710 1711
-
(2003)
Diabetologia
, vol.46
, pp. 1710-1711
-
-
Bhatia, E.1
Kordonouri, O.2
Balasubramanium, K.3
Rajeswari, J.4
Landt, O.5
Simon, P.6
-
59
-
-
0028098005
-
Hereditary pancreatitis in the children of West Virginia
-
Y. Elitsur, J.A. Hunt, and B.S. Chertow Hereditary pancreatitis in the children of West Virginia Pediatrics 93 1994 528 531
-
(1994)
Pediatrics
, vol.93
, pp. 528-531
-
-
Elitsur, Y.1
Hunt, J.A.2
Chertow, B.S.3
|