-
1
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
(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
Bignell, G.7
Warren, W.8
Aminoff, M.9
Hoglund, P.10
Jarvinen, U.11
Kristo, P.12
Pelin, K.13
Ridanpaa, 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..
-
2
-
-
0031974516
-
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
-
(1998)
Nature Genet
, vol.18
, pp. 38-43
-
-
Jenne, D.E.1
Reimann, U.2
Nezu, J.3
Friedel, W.4
Loff, S.5
Jeschke, R.6
Muller, O.7
Back, W.8
Zimmer, M.9
-
3
-
-
0030820394
-
Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p
-
(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
-
4
-
-
0031012344
-
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
-
(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
Salovaara, R.8
Bodmer, W.9
Shibata, D.10
De La Chapelle, A.11
Aaltonen, L.A.12
-
6
-
-
0000043603
-
A very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane
-
(1921)
(Dutch) Nederl Maandschr Geneesk
, vol.10
, pp. 134-146
-
-
Peutz, J.L.1
-
8
-
-
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
-
10
-
-
15444350943
-
Increased risk for cancer in patients with the Peutz-Jeghers syndrome
-
(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
Ahlquist, D.A.7
Podratz, K.C.8
Pittelkow, M.9
Hartmann, L.C.10
-
11
-
-
13144251118
-
Mutations of the STK11 gene in sporadic gastric carcinoma
-
(1998)
Int J Oncol
, vol.13
, pp. 601-604
-
-
Park, W.S.1
Moon, Y.W.2
Yang, Y.M.3
Kim, Y.S.4
Kim, Y.D.5
Fuller, B.G.6
Vortmeyer, A.O.7
Fogt, F.8
Lubensky, I.A.9
Zhuang, Z.10
-
13
-
-
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
-
14
-
-
0032523997
-
Somatic mutations in LKB1 are rare in sporadic colorectal and testicular tumors
-
(1998)
Cancer Res
, vol.58
, pp. 2087-2090
-
-
Avizienyte, E.1
Roth, S.2
Loukola, A.3
Hemminki, A.4
Lothe, R.A.5
Stenwig, A.E.6
Fossa, S.D.7
Salovaara, R.8
Aaltonen, L.A.9
-
15
-
-
0033054479
-
LKB1 somatic mutations in sporadic tumors
-
(1999)
Am J Pathol
, vol.154
, pp. 677-681
-
-
Avizienyte, E.1
Loukola, A.2
Roth, S.3
Hemminki, A.4
Tarkkanen, M.5
Salovaara, R.6
Arola, J.7
Butzow, R.8
Husgafvel-Pursiainen, K.9
Kokkola, A.10
Jarvinen, H.11
Aaltonen, L.A.12
-
16
-
-
0033522144
-
Somatic mutations of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma
-
(1999)
Oncogene
, vol.18
, pp. 1777-1780
-
-
Guldberg, P.1
Thor Straten, P.2
Ahrenkiel, V.3
Seremet, T.4
Kirkin, A.F.5
Zeuthen, J.6
-
18
-
-
0032984141
-
Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers
-
(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
Westerman, A.M.7
Entius, M.M.8
Goggins, M.9
Yeo, C.J.10
Kern, S.E.11
-
19
-
-
0032949434
-
Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours
-
(1999)
Br J Cancer
, vol.80
, pp. 70-72
-
-
Wang, Z.J.1
Churchman, M.2
Campbell, I.G.3
Xu, W.H.4
Yan, Z.Y.5
McCluggage, W.G.6
Foulkes, W.D.7
Tomlinson, I.P.8
-
20
-
-
0032791288
-
Mutational analysis of STK11 gene in ovarian carcinomas
-
(1999)
Jpn J Cancer Res
, vol.90
, pp. 629-632
-
-
Nischioka, Y.1
Kobayashi, K.2
Sagae, S.3
Sugimura, M.4
Ishioka, S.5
Nagata, M.6
Terasawa, K.7
Tokino, T.8
Kudo, R.9
-
21
-
-
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
-
23
-
-
0030817576
-
PTEN gene mutations are seen in high-grade but not in low-grade gliomas
-
(1997)
Cancer Res
, vol.57
, pp. 4187-4190
-
-
Rasheed, B.K.A.1
Stenzel, T.T.2
McLendon, R.E.3
Parsons, R.4
Friedman, A.H.5
Friedman, H.S.6
Bigner, D.D.7
Bigner, S.H.8
-
25
-
-
1842301690
-
The putative tumor suppressor gene FHIT at 3p14.2 is rarely affected by loss of heterozygosity in primary human brain tumors
-
(1997)
Cancer Res
, vol.57
, pp. 2638-2641
-
-
Frank, S.1
Müller, J.2
Plaschke, J.3
Hahn, M.4
Hampl, J.5
Hampl, M.6
Pistorius, S.7
Schackert, G.8
Schackert, H.K.9
-
26
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5264 microsatellites
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
27
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
(1997)
Science
, vol.275
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
Podsypanina, K.4
Bose, S.5
Wang, S.I.6
Puc, J.7
Miliaresis, C.8
Rodgers, L.9
McCombie, R.10
Bigner, S.H.11
Giovanella, B.C.12
Ittmann, M.13
Tycko, B.14
Hibshoosh, H.15
Wigler, M.U.16
Parsons, R.17
-
28
-
-
0027973944
-
Frequency of allele loss of DCC, p53, RB1, WT1, NF1, NM23 and APC/MCC in colorectal cancer assayed by fluorescent multiplex polymerase chain reaction
-
(1994)
Br J Cancer
, vol.70
, pp. 813-818
-
-
Cawkwell, L.1
Lewis, F.A.2
Quirke, P.3
-
30
-
-
0031662147
-
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome
-
(1998)
Hum Genet
, vol.103
, pp. 168-172
-
-
Nakagawa, H.1
Koyama, K.2
Miyoshi, Y.3
Ando, H.4
Baba, S.5
Watatani, M.6
Yasutomi, M.7
Matsuura, N.8
Monden, M.9
Nakamura, Y.10
-
31
-
-
0032471851
-
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1641-1650
-
-
Mehenni, H.1
Gehrig, C.2
Nezu, J.3
Oku, A.4
Shimane, M.5
Rossier, C.6
Guex, N.7
Blouin, J.L.8
Scott, H.S.9
Antonarakis, S.E.10
-
32
-
-
0032906537
-
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer
-
(1999)
Hum Mol Genet
, vol.8
, pp. 45-51
-
-
Ylikorkala, A.1
Avizienyte, E.2
Tomlison, I.P.3
Tiainen, M.4
Roth, S.5
Loukala, A.6
Hemminiki, A.7
Johansson, M.8
Sistonen, P.9
Markie, D.10
Neale, K.11
Phillips, R.12
Zauber, P.13
Twama, T.14
Sampson, J.15
Jarvinen, H.16
Makela, T.P.17
Aaltonen, L.A.18
-
33
-
-
0032947283
-
Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients
-
(1999)
J Med Genet
, vol.36
, pp. 365-368
-
-
Wang, Z.J.1
Churchman, M.2
Avizienyte, E.3
McKeown, C.4
Davies, S.5
Evans, D.G.6
Ferguson, A.7
Ellis, I.8
Xu, W.H.9
Yan, Z.Y.10
Aaltonen, L.A.11
Tomlinson, I.P.12
-
34
-
-
0033012429
-
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families
-
(1999)
Hum Mutat
, vol.13
, pp. 476-481
-
-
Westerman, A.M.1
Entius, M.M.2
Boor, P.P.3
Koole, R.4
De Baar, E.5
Offerhaus, G.J.6
Lubinski, J.7
Lindhout, D.8
Halley, D.J.9
De Rooij, F.W.10
Wilson, J.H.11
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