-
1
-
-
0040061124
-
Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: Frequent loss of 19p13.3 and gain of 19q13.1-13.2
-
Hoglund M, Gorunova L, Andren-Sandberg A, Dawiskiba S, Mitelman F, Johansson R (1998) Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: frequent loss of 19p13.3 and gain of 19q13.1-13.2. Genes Chromosomes Cancer 21: 8-16
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 8-16
-
-
Hoglund, M.1
Gorunova, L.2
Andren-Sandberg, A.3
Dawiskiba, S.4
Mitelman, F.5
Johansson, R.6
-
2
-
-
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 (1998) Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nature Genet 18: 38-4-3
-
(1998)
Nature Genet
, vol.18
-
-
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
-
3
-
-
0031911792
-
ZIP kinase, a novel serine/threonin kinase which mediates apoptosis
-
Kawai T, Matsumoto M, Takeda K, Sanjo H, Akira S (1998) ZIP kinase, a novel serine/threonin kinase which mediates apoptosis. Mol Cell Biol 18: 1642-1651
-
(1998)
Mol Cell Biol
, vol.18
, pp. 1642-1651
-
-
Kawai, T.1
Matsumoto, M.2
Takeda, K.3
Sanjo, H.4
Akira, S.5
-
4
-
-
0008916601
-
A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix
-
Lee JY, Dona SM, Kim HS, Kim SY, Na EY, Shin MS, Lee SH, Park WS, Kim KM, Lee YS, Jang JJ, Yoo NJ (1998) A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix. Cancer Res 58: 1140-1143
-
(1998)
Cancer Res
, vol.58
, pp. 1140-1143
-
-
Lee, J.Y.1
Dona, S.M.2
Kim, H.S.3
Kim, S.Y.4
Na, E.Y.5
Shin, M.S.6
Lee, S.H.7
Park, W.S.8
Kim, K.M.9
Lee, Y.S.10
Jang, J.J.11
Yoo, N.J.12
-
5
-
-
18344416870
-
Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3
-
Nakagawa H, Koyama K, Tanaka T, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Monden M, Nakamura Y (1998) Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3. Hum Genet 102. 203-206
-
(1998)
Hum Genet
, vol.102
, pp. 203-206
-
-
Nakagawa, H.1
Koyama, K.2
Tanaka, T.3
Miyoshi, Y.4
Ando, H.5
Baba, S.6
Watatani, M.7
Yasutomi, M.8
Monden, M.9
Nakamura, Y.10
-
6
-
-
0025064238
-
Chromosomal translocation t(1:19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor
-
Nourse J, Mellentin JD, Galili N, Wilkinson J, Stanbridge E, Smith SD, Cleary ML (1990) Chromosomal translocation t(1:19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Cell 60: 535-545
-
(1990)
Cell
, vol.60
, pp. 535-545
-
-
Nourse, J.1
Mellentin, J.D.2
Galili, N.3
Wilkinson, J.4
Stanbridge, E.5
Smith, S.D.6
Cleary, M.L.7
-
7
-
-
15644380741
-
Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21
-
Ohira M, Seki N, Nagase T, Suzuki E, Nomura N, Ohara O, Hattori M, Sakaki Y, Eki T, Murakami Y, Saito T, Ichikawa H, Oki M (1997) Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21. Genome Res 7: 47-58
-
(1997)
Genome Res
, vol.7
, pp. 47-58
-
-
Ohira, M.1
Seki, N.2
Nagase, T.3
Suzuki, E.4
Nomura, N.5
Ohara, O.6
Hattori, M.7
Sakaki, Y.8
Eki, T.9
Murakami, Y.10
Saito, T.11
Ichikawa, H.12
Oki, M.13
-
8
-
-
17344367301
-
Peutz-Jeghers disease: Most, but not all, families are compatible with linkage to 19p13.3
-
Olschwang S, Markie D, Seal S, Neale K, Phillips R, Cottrell S, Ellis I, Hodgson S, Zauber P, Spigelman A, Iwama T, Loff S, McKeown C, Marchese C, Sampson J, Davies S, Talbot I, Wyke J, Thomas G, Bodmer W, Hemminki A, Avizienyte E, de la Chapette A, Aaltonen L, Tomlinson I, et al. (1998) Peutz-Jeghers disease: Most, but not all, families are compatible with linkage to 19p13.3. J Med Genet 35: 42-44
-
(1998)
J Med Genet
, vol.35
, pp. 42-44
-
-
Olschwang, S.1
Markie, D.2
Seal, S.3
Neale, K.4
Phillips, R.5
Cottrell, S.6
Ellis, I.7
Hodgson, S.8
Zauber, P.9
Spigelman, A.10
Iwama, T.11
Loff, S.12
McKeown, C.13
Marchese, C.14
Sampson, J.15
Davies, S.16
Talbot, I.17
Wyke, J.18
Thomas, G.19
Bodmer, W.20
Hemminki, A.21
Avizienyte, E.22
De la Chapette, A.23
Aaltonen, L.24
Tomlinson, I.25
more..
-
9
-
-
0028922296
-
Identification of the human ERK gene as a putative receptor tyrosine kinase and its chromosomal localization to 1p36.1: A comparative mapping of human, mouse, and rat chromosomes
-
Saito T, Seki N, Matsuda Y, Kitahara M, Murata M, Kanda N, Nomura N, Yamamoto T, Hori T (1995) Identification of the human ERK gene as a putative receptor tyrosine kinase and its chromosomal localization to 1p36.1: a comparative mapping of human, mouse, and rat chromosomes. Genomics 26: 382-384
-
(1995)
Genomics
, vol.26
, pp. 382-384
-
-
Saito, T.1
Seki, N.2
Matsuda, Y.3
Kitahara, M.4
Murata, M.5
Kanda, N.6
Nomura, N.7
Yamamoto, T.8
Hori, T.9
-
10
-
-
0031592729
-
Complementary DNA cloning and chromosomal mapping of a novel phosphatidylinositol kinase gene
-
Saito T, Seki N, Ishii H, Ohira M, Hayashi A, Kozuma S, Hori T (1997) Complementary DNA cloning and chromosomal mapping of a novel phosphatidylinositol kinase gene DNA Res 4: 301-305
-
(1997)
DNA Res
, vol.4
, pp. 301-305
-
-
Saito, T.1
Seki, N.2
Ishii, H.3
Ohira, M.4
Hayashi, A.5
Kozuma, S.6
Hori, T.7
-
11
-
-
0031592814
-
Identification and chromosome assignment of a human gene encoding a novel phosphatidylinositol-3 kinase
-
Seki N, Nimura Y, Ohira M, Saito T, Ichimiya S, Nomura N, Nakagawara A (1997) Identification and chromosome assignment of a human gene encoding a novel phosphatidylinositol-3 kinase. DNA Res 4: 355-358
-
(1997)
DNA Res
, vol.4
, pp. 355-358
-
-
Seki, N.1
Nimura, Y.2
Ohira, M.3
Saito, T.4
Ichimiya, S.5
Nomura, N.6
Nakagawara, A.7
-
12
-
-
0032032348
-
Establishment of a novel cell line (TS-2) of pre-B acute lymphoblastic leukemia with a t(1;19) not involving the E2A gene
-
Yoshinari M, Imaizumi M, Eguchi M, Ogasawara M, Saito T, Suzuki H, Koizumi Y, Cui Y, Sato A, Saisho T, Ichinohasama R, Matsubara Y, Kamada N, Iinuma K (1998) Establishment of a novel cell line (TS-2) of pre-B acute lymphoblastic leukemia with a t(1;19) not involving the E2A gene. Cancer Genet Cytogenet 101: 95-102
-
(1998)
Cancer Genet Cytogenet
, vol.101
, pp. 95-102
-
-
Yoshinari, M.1
Imaizumi, M.2
Eguchi, M.3
Ogasawara, M.4
Saito, T.5
Suzuki, H.6
Koizumi, Y.7
Cui, Y.8
Sato, A.9
Saisho, T.10
Ichinohasama, R.11
Matsubara, Y.12
Kamada, N.13
Iinuma, K.14
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