-
2
-
-
0000043603
-
Very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane
-
Peutz JLA. Very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane. Nederl Maandschr Geneesk 1921;10: 134-146.
-
(1921)
Nederl Maandschr Geneesk
, vol.10
, pp. 134-146
-
-
Peutz, J.L.A.1
-
3
-
-
76549223053
-
Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits
-
Jeghers H, McKusick VA, Katz KH. Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits. NEJM 1949; 241:993-1005,1031-1036.
-
(1949)
NEJM
, vol.241
, pp. 993-1005
-
-
Jeghers, H.1
McKusick, V.A.2
Katz, K.H.3
-
4
-
-
0005758211
-
Peutz-Jeghers syndrome with metastasizing duodenal carcinoma
-
Williams JP, Knudsen A. Peutz-Jeghers syndrome with metastasizing duodenal carcinoma. Gut 1965;6:179-184.
-
(1965)
Gut
, vol.6
, pp. 179-184
-
-
Williams, J.P.1
Knudsen, A.2
-
5
-
-
0020443317
-
Peutz-Jeghers syndrome: A clinicopathologic study of a large family with a 27-year follow-up
-
Burdick D, Prior JT. Peutz-Jeghers syndrome: a clinicopathologic study of a large family with a 27-year follow-up. Cancer 1982;50:2139-2146.
-
(1982)
Cancer
, vol.50
, pp. 2139-2146
-
-
Burdick, D.1
Prior, J.T.2
-
6
-
-
0022591876
-
Pancreatic adenocarcinoma in an adolescent male with Peutz-Jeghers syndrome
-
Bowlby LS. Pancreatic adenocarcinoma in an adolescent male with Peutz-Jeghers syndrome. Hum Pathol 1986; 17:97-99.
-
(1986)
Hum Pathol
, vol.17
, pp. 97-99
-
-
Bowlby, L.S.1
-
9
-
-
0025970813
-
An aromatase-producing sex-cord tumor resulting in prepubertal gynecomastia
-
Coen P, Kulin H, Ballantine T, Zaino R, Frauenhoffer E, Boal D, Inkster S, Brodie A, Santen R. An aromatase-producing sex-cord tumor resulting in prepubertal gynecomastia. NEJM 1991;324:317-322.
-
(1991)
NEJM
, vol.324
, pp. 317-322
-
-
Coen, P.1
Kulin, H.2
Ballantine, T.3
Zaino, R.4
Frauenhoffer, E.5
Boal, D.6
Inkster, S.7
Brodie, A.8
Santen, R.9
-
11
-
-
0031012344
-
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
-
Hemminki A, Tomlinson I, Markie D, Jarvinen H, Sistonen P, Bjorkqvist AM, Knuutila S, Salovara R, Bodmer W, Shibata D, de la Chapelle A, Aaltonen LA. Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. Nature Genet 1997;15:87-90.
-
(1997)
Nature Genet
, vol.15
, pp. 87-90
-
-
Hemminki, A.1
Tomlinson, I.2
Markie, D.3
Jarvinen, H.4
Sistonen, P.5
Bjorkqvist, A.M.6
Knuutila, S.7
Salovara, R.8
Bodmer, W.9
Shibata, D.10
De La Chapelle, A.11
Aaltonen, L.A.12
-
12
-
-
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, Muller O, Back W, Zimmer M. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nature Genet 1998;18:38-43.
-
(1998)
Nature 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
Muller, O.7
Back, W.8
Zimmer, M.9
-
13
-
-
0035317252
-
A phenotype II triploid pregnancy and fluorescence microsatellite analysis to study the parental origin of the extra set of chromosomes
-
Chang SD, Chu DC, Lin EW, Chen DP, Lin PY, Soong YK. A phenotype II triploid pregnancy and fluorescence microsatellite analysis to study the parental origin of the extra set of chromosomes Chang Gung Med J 2001;24: 258-262.
-
(2001)
Chang Gung Med J
, vol.24
, pp. 258-262
-
-
Chang, S.D.1
Chu, D.C.2
Lin, E.W.3
Chen, D.P.4
Lin, P.Y.5
Soong, Y.K.6
-
14
-
-
0030820394
-
Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p
-
Amos CI, Bali D, Thiel TJ, Anderson JP, Gourley I, Frazier ML, Lynch PM, Luchtefeld MA, Young A, McGarrity TJ, Seldin MF. Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p. Cancer Res 1997; 57:3653-3656.
-
(1997)
Cancer Res
, vol.57
, pp. 3653-3656
-
-
Amos, C.I.1
Bali, D.2
Thiel, T.J.3
Anderson, J.P.4
Gourley, I.5
Frazier, M.L.6
Lynch, P.M.7
Luchtefeld, M.A.8
Young, A.9
McGarrity, T.J.10
Seldin, M.F.11
-
15
-
-
0036691603
-
A case of pulmonary adenocarcinoma accompanied by superior vena caval thrombosis in a patient with Peutz-Jeghers syndrome
-
Hirano S, Takiguchi Y, Igari H, Hiroshima K, Shingyoji M, Watanabe R, Moriya T, Tanabe N, Tatsumi K, Kuriyama T. A case of pulmonary adenocarcinoma accompanied by superior vena caval thrombosis in a patient with Peutz-Jeghers syndrome. Jpn J Clin Oncol 2002;32:307-309.
-
(2002)
Jpn J Clin Oncol
, vol.32
, pp. 307-309
-
-
Hirano, S.1
Takiguchi, Y.2
Igari, H.3
Hiroshima, K.4
Shingyoji, M.5
Watanabe, R.6
Moriya, T.7
Tanabe, N.8
Tatsumi, K.9
Kuriyama, T.10
-
17
-
-
0034988818
-
Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma
-
Olschwang S, Boisson C, Thomas G. Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma. J Med Genet 2001;38:356-360.
-
(2001)
J Med Genet
, vol.38
, pp. 356-360
-
-
Olschwang, S.1
Boisson, C.2
Thomas, G.3
-
18
-
-
0034056507
-
Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p
-
Chen J, Lindblom A. Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p. Clin Genet 2000;57:394-397.
-
(2000)
Clin Genet
, vol.57
, pp. 394-397
-
-
Chen, J.1
Lindblom, A.2
-
19
-
-
0038498340
-
Clinicopathologic and molecular features of pancreatic adenocarcinoma associated with Peutz-Jeghers syndrome
-
Yee NS, Furth EE, Pack M. Clinicopathologic and molecular features of pancreatic adenocarcinoma associated with Peutz-Jeghers syndrome. Cancer Biol Ther 2003;2:38-47.
-
(2003)
Cancer Biol Ther
, vol.2
, pp. 38-47
-
-
Yee, N.S.1
Furth, E.E.2
Pack, M.3
-
20
-
-
0037255043
-
Mutations in the STK11 gene characterize minimal deviation adenocarcinoma of the uterine cervix
-
Kuragaki C, Enomoto T, Ueno Y, Sun H, Fujita M, Nakashima R, Ueda Y, Wada H, Murata Y, Toki T, Konishi I, Fujii S. Mutations in the STK11 gene characterize minimal deviation adenocarcinoma of the uterine cervix. Lab Invest 2003;83:35-45.
-
(2003)
Lab Invest
, vol.83
, pp. 35-45
-
-
Kuragaki, C.1
Enomoto, T.2
Ueno, Y.3
Sun, H.4
Fujita, M.5
Nakashima, R.6
Ueda, Y.7
Wada, H.8
Murata, Y.9
Toki, T.10
Konishi, I.11
Fujii, S.12
-
21
-
-
0036321766
-
Ovarian tumors associated with multiple endocrine neoplasias and related syndromes (Carney complex, Peutz-Jeghers syndrome, von Hippel-Lindau disease, Cowden's disease)
-
Papageorgiou T, Stratakis CA. Ovarian tumors associated with multiple endocrine neoplasias and related syndromes (Carney complex, Peutz-Jeghers syndrome, von Hippel-Lindau disease, Cowden's disease). Int J Gynecol Cancer 2002;12:337-347.
-
(2002)
Int J Gynecol Cancer
, vol.12
, pp. 337-347
-
-
Papageorgiou, T.1
Stratakis, C.A.2
-
22
-
-
0034490014
-
Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brain
-
Sobottka SB, Haase M, Fitze G, Hahn M, Schackert HK, Schackert G. Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brain. J Neurooncol 2000; 49:187-195.
-
(2000)
J Neurooncol
, vol.49
, pp. 187-195
-
-
Sobottka, S.B.1
Haase, M.2
Fitze, G.3
Hahn, M.4
Schackert, H.K.5
Schackert, G.6
-
23
-
-
0033915012
-
5′-CpG island methylation of the LKB1/STK11 promoter and allelic loss at chromosome 19p13.3 in sporadic colorectal cancer
-
Trojan J, Brieger A, Raedle J, Esteller M, Zeuzem S. 5′-CpG island methylation of the LKB1/STK11 promoter and allelic loss at chromosome 19p13.3 in sporadic colorectal cancer. Gut 2000;47:272-276.
-
(2000)
Gut
, vol.47
, pp. 272-276
-
-
Trojan, J.1
Brieger, A.2
Raedle, J.3
Esteller, M.4
Zeuzem, S.5
-
24
-
-
0000268205
-
Peutz-Jeghers syndrome maps to chromosome 1p
-
abstract #1067
-
Bali D, Gourley IS, McGarrity TJ, Spencer CA, Howard L, Frazier ML, Lynch PM, Seldin MF, Amos CI. Peutz-Jeghers syndrome maps to chromosome 1p. Am J Hum Genet 1995; 57(Supp): abstract #1067.
-
(1995)
Am J Hum Genet
, vol.57
, Issue.SUPPL.
-
-
Bali, D.1
Gourley, I.S.2
McGarrity, T.J.3
Spencer, C.A.4
Howard, L.5
Frazier, M.L.6
Lynch, P.M.7
Seldin, M.F.8
Amos, C.I.9
-
25
-
-
0029934902
-
A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map
-
Markie D, Huson S, Maher E, Davies A, Tomlinson I, Bodmer WF. A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map. Hum Genet 1996;98:125-128.
-
(1996)
Hum Genet
, vol.98
, pp. 125-128
-
-
Markie, D.1
Huson, S.2
Maher, E.3
Davies, A.4
Tomlinson, I.5
Bodmer, W.F.6
-
26
-
-
0036048868
-
Search for the second Peutz-Jeghers syndrome locus: Exclusion of STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and STK11IP gene on chromosome 2
-
Buchet-Poyau K, Mehenni H, Radhakrishna U, Antonarakis SE. Search for the second Peutz-Jeghers syndrome locus: exclusion of STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and STK11IP gene on chromosome 2. Cytogenet Genome Res 2002;97:171-178.
-
(2002)
Cytogenet Genome Res
, vol.97
, pp. 171-178
-
-
Buchet-Poyau, K.1
Mehenni, H.2
Radhakrishna, U.3
Antonarakis, S.E.4
-
27
-
-
0037173013
-
Role of LKB1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis
-
Jishage K, Nezu J, Kawase Y, Iwata T, Watanabe M, Miyoshi A, Ose A, Habu K, Kake T, Kamada N, Ueda O, Kinoshita M, Jenne DE, Shimane M, Suzuki H. Role of LKB1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis. PNAS USA. 2002;99: 8903-8908.
-
(2002)
PNAS USA
, vol.99
, pp. 8903-8908
-
-
Jishage, K.1
Nezu, J.2
Kawase, Y.3
Iwata, T.4
Watanabe, M.5
Miyoshi, A.6
Ose, A.7
Habu, K.8
Kake, T.9
Kamada, N.10
Ueda, O.11
Kinoshita, M.12
Jenne, D.E.13
Shimane, M.14
Suzuki, H.15
-
28
-
-
0034106282
-
Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients
-
Yoon KA, Ku JL, Choi HS, Heo SC, Jeong SY, Park YJ, Kim NK, Kim JC, Jung PM, Park JG. Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients. Br J Cancer 2000;82:1403-1406.
-
(2000)
Br J Cancer
, vol.82
, pp. 1403-1406
-
-
Yoon, K.A.1
Ku, J.L.2
Choi, H.S.3
Heo, S.C.4
Jeong, S.Y.5
Park, Y.J.6
Kim, N.K.7
Kim, J.C.8
Jung, P.M.9
Park, J.G.10
|