-
1
-
-
0000043603
-
On a very remarkable case of familial polyposis of the mucous membrane of the intestinal tract and nasopharynx accompanied by peculiar pigmentations of the skin and mucous membrane
-
(1921)
Ned. Tijdschr. Geneeskd.
, vol.10
, pp. 134-146
-
-
Peutz, J.L.A.1
-
3
-
-
0023192463
-
Increased risk of cancer in the Peutz-Jeghers syndrome
-
(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.A.4
Gittelsohn, A.M.5
Booker, S.V.6
Krush, A.J.7
Yardley, J.H.8
Luk, G.D.9
-
5
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
(1998)
Nature (Lond.)
, vol.391
, pp. 184-187
-
-
Hemminki, A.1
Markie, D.2
Tomlinson, I.3
Avizienyte, E.4
Roth, S.5
Loukola, A.6
Bignell, G.7
Warren, W.8
Aminoff, M.9
Höglund, P.10
Jävinen, H.11
Kristo, P.12
Pelin, K.13
Ridanpää, M.14
Salovaara, R.15
Toro, T.16
Bodmer, W.17
Olschwang, S.18
Olsen, A.S.19
Stratton, M.R.20
De la Chapelle, A.21
Aaltonen, L.A.22
more..
-
6
-
-
0031974516
-
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
-
(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
Muller, O.7
Back, W.8
Zimmer, M.9
-
8
-
-
0031012344
-
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
-
(1997)
Nat. Genet.
, vol.15
, pp. 87-90
-
-
Hemminki, A.1
Torminson, I.2
Markie, D.3
Järvinen, H.4
Sistonen, P.5
Björkqvist, A.-M.6
Knuutila, S.7
Salovaara, R.8
Bodmer, W.9
Shibata, D.10
De la Chapelle, A.11
Aaltonen, L.A.12
-
9
-
-
0032403068
-
Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome
-
(1998)
Cancer Res.
, vol.58
, pp. 5267-5270
-
-
Gruber, S.B.1
Entius, M.M.2
Petersen, G.M.3
Laken, S.J.4
Longo, P.A.5
Boyer, R.6
Levin, A.M.7
Mujumdar, U.J.8
Trent, J.M.9
Kinzler, K.W.10
Vogelstein, B.11
Hamilton, S.R.12
Polymeropoulos, M.H.13
Offerhaus, G.J.14
Giardiello, F.M.15
-
10
-
-
14444272759
-
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer
-
(1998)
Cancer Res.
, vol.58
, pp. 4799-4801
-
-
Resta, N.1
Simone, C.2
Mareni, C.3
Montera, M.4
Gentile, M.5
Susca, F.6
Gristina, R.7
Pozzi, S.8
Bertario, L.9
Bufo, P.10
Carlomagno, N.11
Ingrosso, M.12
Rossini, F.P.13
Tenconi, R.14
Guanti, G.15
-
11
-
-
0032893658
-
Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence
-
(1999)
J. Pathol.
, vol.188
, pp. 9-13
-
-
Wang, Z.-J.1
Ellis, I.2
Zauber, P.3
Iwama, T.4
Marchese, C.5
Talbot, I.6
Xue, W.-H.7
Yan, Z.-Y.8
Tomlison, I.9
-
12
-
-
0033692749
-
Somatic mutations of LKB1 and β-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome
-
(2000)
Cancer Res.
, vol.60
, pp. 6311-6313
-
-
Miyaki, M.1
Iijima, T.2
Hosono, K.3
Ishii, R.4
Yasuno, M.5
Mori, T.6
Toi, M.7
Hishima, T.8
Shitara, N.9
Tamura, K.10
Utsunomiya, J.11
Kobayashi, N.12
Kuroki, T.13
Iwama, T.14
-
13
-
-
0035142924
-
Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome
-
(2001)
J. Clin. Pathol.
, vol.54
, pp. 126-131
-
-
Entius, M.M.1
Keller, J.J.2
Westerman, A.M.3
Van Rees, B.P.4
Van Velthuysen, M.-L.F.5
De Goeij, A.F.P.M.6
Wilson, J.H.P.7
Giardiello, F.M.8
Offerhaus, G.J.A.9
-
16
-
-
0035375261
-
433is essential for LKB1 to suppress cell growth
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 19469-19482
-
-
Sapkota, G.P.1
Kieloch, A.2
Lizcano, J.M.3
Lain, S.4
Arthur, J.S.C.5
Williams, M.R.6
Morrice, N.7
Deak, M.8
Alessi, D.R.9
-
18
-
-
0034964446
-
The Peutz-Jegher gene product LKB1 is a mediator of p53-dependent cell death
-
(2001)
Mol. Cell
, vol.7
, pp. 1307-1319
-
-
Karuman, P.1
Gozani, O.2
Odze, R.D.3
Zhou, X.C.4
Zhu, H.5
Shaw, R.6
Brien, T.P.7
Bozzuto, C.D.8
Ooi, D.9
Cantley, L.C.10
Yuan, J.11
-
26
-
-
0032524069
-
Mutations in the SMAD4/DPC4 gene in juvenile polyposis
-
(1998)
Science (Wash. DC)
, vol.280
, pp. 1086-1088
-
-
Howe, J.R.1
Roth, S.2
Ringold, J.C.3
Summers, R.W.4
Jarvinen, H.J.5
Sistonen, P.6
Tomlinson, I.P.M.7
Houlston, R.S.8
Bevan, S.9
Mitros, F.A.10
Stone, E.M.11
Aaltonen, L.A.12
-
29
-
-
0032830638
-
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukemia
-
(1999)
Nat. Genet.
, vol.23
, pp. 166-175
-
-
Song, W.-J.1
Sullivan, M.G.2
Legare, R.D.3
Hutchings, S.4
Tan, X.5
Kufrin, D.6
Ratajczak, J.7
Resende, I.C.8
Haworth, C.9
Hock, R.10
Loh, M.11
Felix, C.12
Roy, D.-C.13
Busque, L.14
Kurnit, D.15
Williman, C.16
Gewirtz, A.M.17
Speck, N.A.18
Bushweller, J.H.19
Li, F.P.20
Gardiner, K.21
Poncz, M.22
Maris, J.M.23
Gilliland, D.G.24
more..
|