-
1
-
-
0027157843
-
Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis
-
BARDI G, PANDIS N, FENGER C, KRONBORG O AND HEIM S. (1993). Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis. Cancer Res., 53, 1895-1898.
-
(1993)
Cancer Res.
, vol.53
, pp. 1895-1898
-
-
Bardi, G.1
Pandis, N.2
Fenger, C.3
Kronborg, O.4
Heim, S.5
-
2
-
-
0027155128
-
Two distinct regions involved in 1p deletion in human primary breast cancer
-
BIECHE I, CHAMPEME M-H, MATIFAS F, CROPP CS, CALLAHAN R AND LIDEREAU R. (1993). Two distinct regions involved in 1p deletion in human primary breast cancer. Cancer Res., 53, 1990-1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 1990-1993
-
-
Bieche, I.1
Champeme, M.-H.2
Matifas, F.3
Cropp, C.S.4
Callahan, R.5
Lidereau, R.6
-
3
-
-
0023223152
-
Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line
-
EZ
-
DENG G, LU Y, CHEN S, MIAO J, LU G, LI H, CAI H, XU X, EZ AND LIU P. (1987). Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line. Cancer Res., 47, 3195-3198.
-
(1987)
Cancer Res.
, vol.47
, pp. 3195-3198
-
-
Deng, G.1
Lu, Y.2
Chen, S.3
Miao, J.4
Lu, G.5
Li, H.6
Cai, H.7
Xu, X.8
Liu, P.9
-
4
-
-
0028311249
-
Report of the first international workshop on human chromosome 1 mapping 1994
-
DRACOPOLI NC, BRUNS GAP, BRODEUR GM, LANDES GM, MATISE TC, SELDIN MF, VANCE JM AND WEITH A. (1994). Report of the first international workshop on human chromosome 1 mapping 1994. Cytogenet. Cell Genet., 67, 144-174.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 144-174
-
-
Dracopoli, N.C.1
Bruns, G.A.P.2
Brodeur, G.M.3
Landes, G.M.4
Matise, T.C.5
Seldin, M.F.6
Vance, J.M.7
Weith, A.8
-
5
-
-
0021381028
-
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
-
FEINBERG AP AND VOGELSTEIN B. (1984). A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem., 137, 266-267.
-
(1984)
Anal. Biochem.
, vol.137
, pp. 266-267
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
6
-
-
0024670859
-
Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-myc amplification
-
FONG C-T, DRACOPOLI NC, WHITE PS, MERRILL PT, GRIFFITH RC, HOUSMAN DE AND BRODEUR GM. (1989). Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-myc amplification. Proc. Natl Acad. Sci., 86, 3753-3757.
-
(1989)
Proc. Natl Acad. Sci.
, vol.86
, pp. 3753-3757
-
-
Fong, C.-T.1
Dracopoli, N.C.2
White, P.S.3
Merrill, P.T.4
Griffith, R.C.5
Housman, D.E.6
Brodeur, G.M.7
-
7
-
-
0022253232
-
Purification of DNA from formaldehyde fixed and paraffin embedded human tissue
-
GOELZ SE, HAMILTON SR AND VOGELSTEIN B. (1985). Purification of DNA from formaldehyde fixed and paraffin embedded human tissue. Biochem. Biophys. Res. Commun., 130, 118-126.
-
(1985)
Biochem. Biophys. Res. Commun.
, vol.130
, pp. 118-126
-
-
Goelz, S.E.1
Hamilton, S.R.2
Vogelstein, B.3
-
8
-
-
0027363208
-
Genetic in stability in pancreatic cancer and poorly differentiated type of gastric cancer
-
HAN H-J, YANAGISAWA A, KATO Y, PARK J-G AND NAKAMURA Y. (1993). Genetic in stability in pancreatic cancer and poorly differentiated type of gastric cancer. Cancer Res., 53, 5087-5089.
-
(1993)
Cancer Res.
, vol.53
, pp. 5087-5089
-
-
Han, H.-J.1
Yanagisawa, A.2
Kato, Y.3
Park, J.-G.4
Nakamura, Y.5
-
9
-
-
0025365350
-
K-sam, an amplified gene in stomach cancer, is a member of the heparin-binding growth factor receptor genes
-
HATTORI Y, ODAGIRI H, NAKATANI H, MIYAGAWA K, NAITO K, SAKAMOTO H, KATOH O, YOSHIDA T, SUGIMURA T AND TERADA M. (1990). K-sam, an amplified gene in stomach cancer, is a member of the heparin-binding growth factor receptor genes. Proc. Natl Acad. Sci. USA, 87, 5983-5987
-
(1990)
Proc. Natl Acad. Sci. USA
, vol.87
, pp. 5983-5987
-
-
Hattori, Y.1
Odagiri, H.2
Nakatani, H.3
Miyagawa, K.4
Naito, K.5
Sakamoto, H.6
Katoh, O.7
Yoshida, T.8
Sugimura, T.9
Terada, M.10
-
10
-
-
0023890047
-
Isolation and mapping of a polymorphic DNA sequence (pTHI54) on chromosome 1p (D1S62)
-
HOLM T, NAKAMURA Y, BALLARD L, LEPPERT L, O'CONNELL P, LATHROP GM, LALOUEL J-M AND WHITE R. (1988). Isolation and mapping of a polymorphic DNA sequence (pTHI54) on chromosome 1p (D1S62). Nucleic Acids Res., 16, 3115.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 3115
-
-
Holm, T.1
Nakamura, Y.2
Ballard, L.3
Leppert, L.4
O'Connell, P.5
Lathrop, G.M.6
Lalouel, J.-M.7
White, R.8
-
11
-
-
0026734665
-
The APC gene, responsible for familial adenomatous polyposis, is mutated in human gastric cancer
-
HORII A, NAKATSURU S, MIYOSHI Y, ICHII S, NAGASE H, KATO Y, YANAGISAWA A AND NAKAMURA Y. (1992). The APC gene, responsible for familial adenomatous polyposis, is mutated in human gastric cancer. Cancer Res., 52, 3231-3233.
-
(1992)
Cancer Res.
, vol.52
, pp. 3231-3233
-
-
Horii, A.1
Nakatsuru, S.2
Miyoshi, Y.3
Ichii, S.4
Nagase, H.5
Kato, Y.6
Yanagisawa, A.7
Nakamura, Y.8
-
12
-
-
0028308161
-
Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers
-
HORII A, HAN H-J, SHIMADA M, YANAGISAWA A, KATO Y, OHTA H, YASUI W, TAHARA E AND NAKAMURA Y. (1994). Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers. Cancer Res., 54, 3373-3375.
-
(1994)
Cancer Res.
, vol.54
, pp. 3373-3375
-
-
Horii, A.1
Han, H.-J.2
Shimada, M.3
Yanagisawa, A.4
Kato, Y.5
Ohta, H.6
Yasui, W.7
Tahara, E.8
Nakamura, Y.9
-
13
-
-
0025785216
-
Assignment of the human granulocyte colony-stimulating factor receptor gene (CSF3R) to chromosome 1 at region p35-p34.3
-
INAZAWA J, FUKUNAGA R, SETO Y, NAKAGAWA H, MISAWA S, ABE T AND NAGATA S. (1991). Assignment of the human granulocyte colony-stimulating factor receptor gene (CSF3R) to chromosome 1 at region p35-p34.3. Genomics, 10, 1075-1078.
-
(1991)
Genomics
, vol.10
, pp. 1075-1078
-
-
Inazawa, J.1
Fukunaga, R.2
Seto, Y.3
Nakagawa, H.4
Misawa, S.5
Abe, T.6
Nagata, S.7
-
14
-
-
0027081368
-
Physical ordering of three polymorphic DNA markers spanning the regions containing a tumor suppressor gene of renal cell carcinoma by three-color fluorescent in situ hybridization
-
INAZAWA J, ARIYAMA T AND ABE T. (1992). Physical ordering of three polymorphic DNA markers spanning the regions containing a tumor suppressor gene of renal cell carcinoma by three-color fluorescent in situ hybridization. Jpn. J. Cancer Res., 83, 1248-1252.
-
(1992)
Jpn. J. Cancer Res.
, vol.83
, pp. 1248-1252
-
-
Inazawa, J.1
Ariyama, T.2
Abe, T.3
-
15
-
-
0027209470
-
High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridization
-
INAZAWA J, SAITO H, ARIYAMA T, ABE T AND NAKAMURA Y. (1993). High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridization. Genomics, 17, 153-162.
-
(1993)
Genomics
, vol.17
, pp. 153-162
-
-
Inazawa, J.1
Saito, H.2
Ariyama, T.3
Abe, T.4
Nakamura, Y.5
-
16
-
-
0025965097
-
Point mutation of C-Ki-ras oncogene in gastric adenoma and adenocarcinoma with tubular differentiation
-
KIHANA T, TSUDA H, HIROTA T, SHIMOSATO Y, SAKAMOTO H, TERADA M AND HIROHASHI S. (1991). Point mutation of C-Ki-ras oncogene in gastric adenoma and adenocarcinoma with tubular differentiation. Jpn. J. Cancer Res., 82, 308-314.
-
(1991)
Jpn. J. Cancer Res.
, vol.82
, pp. 308-314
-
-
Kihana, T.1
Tsuda, H.2
Hirota, T.3
Shimosato, Y.4
Sakamoto, H.5
Terada, M.6
Hirohashi, S.7
-
17
-
-
0028037032
-
Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas
-
KUNIYASU H, YASUI W, YOKOZAKI H, AKAGI M, AKAMA Y, KITAHARA K, FUJII K AND TAHARA E. (1994). Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas. Int. J. Cancer, 59, 597-600.
-
(1994)
Int. J. Cancer
, vol.59
, pp. 597-600
-
-
Kuniyasu, H.1
Yasui, W.2
Yokozaki, H.3
Akagi, M.4
Akama, Y.5
Kitahara, K.6
Fujii, K.7
Tahara, E.8
-
18
-
-
0025221248
-
Human colorectal cancer: High frequency of deletions at chromosomes 1p35
-
LEISTER I, WEITH A, BRÜDERLINE S, CZIEPLUCH C, KANGWANPONG D, SCHLAG P AND SCHWAB M. (1990). Human colorectal cancer: high frequency of deletions at chromosomes 1p35. Cancer Res., 50, 7232-7235.
-
(1990)
Cancer Res.
, vol.50
, pp. 7232-7235
-
-
Leister, I.1
Weith, A.2
Brüderline, S.3
Cziepluch, C.4
Kangwanpong, D.5
Schlag, P.6
Schwab, M.7
-
19
-
-
0028853419
-
Allelic imbalance on chromosome 1 in human breast cancer. I. minisatellite and RFLP analysis
-
LOUPART M-L, ARMOUR J, WALKER R, ADAMS S, BRAMMAR W AND VARLEY J. (1995). Allelic imbalance on chromosome 1 in human breast cancer. I. minisatellite and RFLP analysis. Genes Chrom. Cancer, 12, 16-23.
-
(1995)
Genes Chrom. Cancer
, vol.12
, pp. 16-23
-
-
Loupart, M.-L.1
Armour, J.2
Walker, R.3
Adams, S.4
Brammar, W.5
Varley, J.6
-
20
-
-
0023228919
-
Deletion of genes on chromosome 1 in endocrine neoplasia
-
MATHEW CGP, SMITH BA, THORPE K, WONG Z, ROYLE NJ, JEFFERYS AJ AND PONDER BAJ. (1987). Deletion of genes on chromosome 1 in endocrine neoplasia. Nature, 328, 524-526.
-
(1987)
Nature
, vol.328
, pp. 524-526
-
-
Mathew, C.G.P.1
Smith, B.A.2
Thorpe, K.3
Wong, Z.4
Royle, N.J.5
Jefferys, A.J.6
Ponder, B.A.J.7
-
21
-
-
0026548844
-
Consistent association of 1p LOH with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes
-
MOLEY JF, BROTHER MB, FONG C-T, WHITE PS, BAYLIN SB, NELKIN B, WELLS SA AND BRODEUR GM. (1992). Consistent association of 1p LOH with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes. Cancer Res., 52, 770-774.
-
(1992)
Cancer Res.
, vol.52
, pp. 770-774
-
-
Moley, J.F.1
Brother, M.B.2
Fong, C.-T.3
White, P.S.4
Baylin, S.B.5
Nelkin, B.6
Wells, S.A.7
Brodeur, G.M.8
-
22
-
-
0023806041
-
Isolation and mapping of a polymorphic DNA sequence (pMCT58) on chromosome 1p (D1S77)
-
NAKAMURA Y, CARLSON M, KRAPCHO K AND WHITE R. (1988a). Isolation and mapping of a polymorphic DNA sequence (pMCT58) on chromosome 1p (D1S77). Nucleic Acids Res., 16, 9367.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 9367
-
-
Nakamura, Y.1
Carlson, M.2
Krapcho, K.3
White, R.4
-
23
-
-
16744366502
-
Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p (D1S77)
-
NAKAMURA Y, CULVER M, SERGEANT L, LEPPERT M, O'CONNELL P, LATHROP GM, LALOUEL J-M AND WHITE R. (1988b). Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p (D1S77). Nucleic Acids Res., 16, 4747.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 4747
-
-
Nakamura, Y.1
Culver, M.2
Sergeant, L.3
Leppert, M.4
O'Connell, P.5
Lathrop, G.M.6
Lalouel, J.-M.7
White, R.8
-
24
-
-
0025111437
-
Isolation of an amplified DNA sequence in stomach cancer
-
NAKATANI H, SAKAMOTO H, YOSHIDA T, YOKOTA J, TAMARA E, SUGIMURA T AND TERADA M. (1990). Isolation of an amplified DNA sequence in stomach cancer. Jpn. J. Cancer Res., 81, 707-710.
-
(1990)
Jpn. J. Cancer Res.
, vol.81
, pp. 707-710
-
-
Nakatani, H.1
Sakamoto, H.2
Yoshida, T.3
Yokota, J.4
Tamara, E.5
Sugimura, T.6
Terada, M.7
-
25
-
-
0026948827
-
Somatic mutation of the APC gene in gastric cancer: Frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma
-
NAKATSURU S, YANAGISAWA A. ICHII S, TAHARA E, KATO Y, NAKAMURA Y AND HORII A. (1992). Somatic mutation of the APC gene in gastric cancer: frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma. Hum. Mol. Genet., 1, 559-563.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 559-563
-
-
Nakatsuru, S.1
Yanagisawa, A.2
Ichii, S.3
Tahara, E.4
Kato, Y.5
Nakamura, Y.6
Horii, A.7
-
26
-
-
0023902853
-
Estimates of the worldwide frequency of sixteen major cancers in 1980
-
PARKIN DM, LÄÄRÄ E AND MUIR CS. (1988). Estimates of the worldwide frequency of sixteen major cancers in 1980. Int. J. Cancer. 41, 184-197.
-
(1988)
Int. J. Cancer.
, vol.41
, pp. 184-197
-
-
Parkin, D.M.1
Läärä, E.2
Muir, C.S.3
-
27
-
-
0025807514
-
Frequent loss of heterozygosity on chromosomes 1q, 5q, and 17p in human gastric carcinomas
-
SANO T, TSUJINO T, YOSHIDA K, NAKAYAMA H, HARUMA K, ITO H, NAKAMURA Y, KAJIYAMA G AND TAHARA E. (1991). Frequent loss of heterozygosity on chromosomes 1q, 5q, and 17p in human gastric carcinomas. Cancer Res., 51, 2926-2931.
-
(1991)
Cancer Res.
, vol.51
, pp. 2926-2931
-
-
Sano, T.1
Tsujino, T.2
Yoshida, K.3
Nakayama, H.4
Haruma, K.5
Ito, H.6
Nakamura, Y.7
Kajiyama, G.8
Tahara, E.9
-
28
-
-
0025250745
-
Allelotype of breast cancer: Cumulative allele losses promote tumour progression in primary breast cancer
-
SATO T, TANIGAMI A, YAMAKAWA K, AKIYAMA F, KASUMI F, SAKAMOTO G AND NAKAMURA Y. (1990). Allelotype of breast cancer: cumulative allele losses promote tumour progression in primary breast cancer. Cancer Res., 50, 7184-7189.
-
(1990)
Cancer Res.
, vol.50
, pp. 7184-7189
-
-
Sato, T.1
Tanigami, A.2
Yamakawa, K.3
Akiyama, F.4
Kasumi, F.5
Sakamoto, G.6
Nakamura, Y.7
-
29
-
-
0028067338
-
Two distinct deleted regions in the short arm of chromosome 1 in neuroblastoma
-
SCHLEIERMACHFR G, PETER M, MICHON J, HUGOT J-P, VIELH P, ZUCKER J-M, MAGDELÉNAT H, THOMAS G AND DELATTRE O. (1994). Two distinct deleted regions in the short arm of chromosome 1 in neuroblastoma. Genes Chrom. Cancer. 10, 275-281.
-
(1994)
Genes Chrom. Cancer.
, vol.10
, pp. 275-281
-
-
Schleiermachfr, G.1
Peter, M.2
Michon, J.3
Hugot, J.-P.4
Vielh, P.5
Zucker, J.-M.6
Magdelénat, H.7
Thomas, G.8
Delattre, O.9
-
30
-
-
0025801654
-
Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas
-
SIMON D, KNOWLES BB AND WEITH A. (1991). Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas. Oncogene, 6, 765-770.
-
(1991)
Oncogene
, vol.6
, pp. 765-770
-
-
Simon, D.1
Knowles, B.B.2
Weith, A.3
-
31
-
-
0028169368
-
p53 mutations and microsatellite instability in sporadic gastric cancer: When Guardians fail
-
STRICKLER JS, ZHENG J, SHU Q, BURGART LJ, ALBERTS SR AND SHIBATA D. (1994). p53 mutations and microsatellite instability in sporadic gastric cancer: When Guardians fail. Cancer Res., 54, 4750-4755.
-
(1994)
Cancer Res.
, vol.54
, pp. 4750-4755
-
-
Strickler, J.S.1
Zheng, J.2
Shu, Q.3
Burgart, L.J.4
Alberts, S.R.5
Shibata, D.6
-
32
-
-
0025200279
-
R-banding and nonisotopic in situ hybridization: Precise localisation of the type Il collagen gene (COL2A1)
-
TAKAHASHI E, HORI T, O'CONNELL P, LEPPERT M AND WHITE R. (1990). R-banding and nonisotopic in situ hybridization: precise localisation of the type Il collagen gene (COL2A1). Hum. Genet., 86, 14-16.
-
(1990)
Hum. Genet.
, vol.86
, pp. 14-16
-
-
Takahashi, E.1
Hori, T.2
O'Connell, P.3
Leppert, M.4
White, R.5
-
33
-
-
0028258815
-
There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma
-
TAKEDA O, HOMMA C, MASEKI N, SAKURAI M, KANDA N, SCHWAB M, NAKAMURA Y AND KANEKO Y. (1994). There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma. Genes Chrom. Cancer. 10, 30-39.
-
(1994)
Genes Chrom. Cancer.
, vol.10
, pp. 30-39
-
-
Takeda, O.1
Homma, C.2
Maseki, N.3
Sakurai, M.4
Kanda, N.5
Schwab, M.6
Nakamura, Y.7
Kaneko, Y.8
-
34
-
-
0025880420
-
Detection of frequent p53 gene mutations in primary gastric cancer by cell sorting and polymerase chain reaction single-strand conformation polymorphism analysis
-
TAMURA G, KIHANA T, NOMURA K, TERADA M, SUGIMURA T AND HIROHASHI S. (1991). Detection of frequent p53 gene mutations in primary gastric cancer by cell sorting and polymerase chain reaction single-strand conformation polymorphism analysis. Cancer Res., 51, 3056-3058.
-
(1991)
Cancer Res.
, vol.51
, pp. 3056-3058
-
-
Tamura, G.1
Kihana, T.2
Nomura, K.3
Terada, M.4
Sugimura, T.5
Hirohashi, S.6
-
35
-
-
0026642513
-
Frequent loss of heterozygosity at the DCC locus in gastric cancer
-
UCHINO S, TSUDA H, NOGUCHI M, YOKOTA J, TERADA M, SAITO T. KOBAYASHI M, SUGIMURA T AND HIROHASHI S. (1992). Frequent loss of heterozygosity at the DCC locus in gastric cancer. Cancer Res., 52, 3099-3102.
-
(1992)
Cancer Res.
, vol.52
, pp. 3099-3102
-
-
Uchino, S.1
Tsuda, H.2
Noguchi, M.3
Yokota, J.4
Terada, M.5
Saito, T.6
Kobayashi, M.7
Sugimura, T.8
Hirohashi, S.9
-
36
-
-
0026446099
-
A second-generation linkage map of the human genome
-
WEISSENBACH J, GYAPAY G, DIB C, VIGNAL A, MORISSETTE J, MILLASSEAU P, VAYSSEIX G AND LATHROP M. (1992). A second-generation linkage map of the human genome. Nature, 359, 794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
37
-
-
0024887501
-
Neuroblastoma consensus deletion maps to 1p36.1-2
-
WEITH A. MARTlNSSON T, CZIEPLUCH C, BRÜDERLEIN S, AMLER LC AND BERTHOLD F. (1989). Neuroblastoma consensus deletion maps to 1p36.1-2. Genes Chrom. Cancer., 1, 159-166.
-
(1989)
Genes Chrom. Cancer.
, vol.1
, pp. 159-166
-
-
Weith, A.1
Martlnsson, T.2
Cziepluch, C.3
Brüderlein, S.4
Amler, L.C.5
Berthold, F.6
-
38
-
-
0025942634
-
c-Ki-ras point mutations in ductectatic-type mucinous cystic neoplasms of the pancreas
-
YANAGlSAWA A, KATO Y, OHTAKE K, KITAGAWA T, OHASHI K, HORI M, TAKAGI K AND SUGANO H. (1991). c-Ki-ras point mutations in ductectatic-type mucinous cystic neoplasms of the pancreas. Jpn. J. Cancer Res., 82, 1057-1060.
-
(1991)
Jpn. J. Cancer Res.
, vol.82
, pp. 1057-1060
-
-
Yanaglsawa, A.1
Kato, Y.2
Ohtake, K.3
Kitagawa, T.4
Ohashi, K.5
Hori, M.6
Takagi, K.7
Sugano, H.8
-
39
-
-
0028111570
-
Frequent genetic alterations at the distal region of chromosome Ip in human hepatocellular carcinomas
-
YEH S-H, CHEN P-J, CHEN H-L, LAI M-Y, WANG C-C AND CHEN D-S. (1994). Frequent genetic alterations at the distal region of chromosome Ip in human hepatocellular carcinomas. Cancer Res., 54, 4188-4192.
-
(1994)
Cancer Res.
, vol.54
, pp. 4188-4192
-
-
Yeh, S.-H.1
Chen, P.-J.2
Chen, H.-L.3
Lai, M.-Y.4
Wang, C.-C.5
Chen, D.-S.6
-
40
-
-
0023829645
-
Genetic alterations of the c-erbB-2 oncogene occur frequently in tubular adenocarcinoma of the stomach and are often accompanied by amplification of the v-erbA homologue
-
YOKOTA J. YAMAMOTO T, MIYAJIMA N, TOYOSHIMA K, NOMURA N, SAKAMOTO H, YOSHIDA T, TERADA M AND SUGIMURA T. (1988). Genetic alterations of the c-erbB-2 oncogene occur frequently in tubular adenocarcinoma of the stomach and are often accompanied by amplification of the v-erbA homologue. Oncogene, 2, 283-287.
-
(1988)
Oncogene
, vol.2
, pp. 283-287
-
-
Yokota, J.1
Yamamoto, T.2
Miyajima, N.3
Toyoshima, K.4
Nomura, N.5
Sakamoto, H.6
Yoshida, T.7
Terada, M.8
Sugimura, T.9
|