-
2
-
-
0034069237
-
Cancer, aging and cellular senescence
-
Campisi J. Cancer, aging and cellular senescence. In Vivo 14 (2000) 183-188
-
(2000)
In Vivo
, vol.14
, pp. 183-188
-
-
Campisi, J.1
-
3
-
-
0036856474
-
The significance of telomerase activation and cellular immortalization in human cancer
-
Newbold R.F. The significance of telomerase activation and cellular immortalization in human cancer. Mutagenesis 17 (2002) 539-550
-
(2002)
Mutagenesis
, vol.17
, pp. 539-550
-
-
Newbold, R.F.1
-
4
-
-
0034503870
-
Cellular senescence mechanisms independent of telomere shortening and telomerase: Other barriers to cell immortalization and carcinogenesis
-
Horikawa I., Yawata T., and Barrett J.C. Cellular senescence mechanisms independent of telomere shortening and telomerase: Other barriers to cell immortalization and carcinogenesis. J. Anti-Aging Med. 3 (2000) 373-382
-
(2000)
J. Anti-Aging Med.
, vol.3
, pp. 373-382
-
-
Horikawa, I.1
Yawata, T.2
Barrett, J.C.3
-
5
-
-
0035059672
-
From cells to organisms: can we learn about aging from cells in culture?
-
Campisi J. From cells to organisms: can we learn about aging from cells in culture?. Exp. Gerontol. 36 (2001) 607-618
-
(2001)
Exp. Gerontol.
, vol.36
, pp. 607-618
-
-
Campisi, J.1
-
6
-
-
0031835444
-
Repression of the telomerase catalytic subunit by a gene on human chromosome 3 that induces cellular senescence
-
Horikawa I., Oshimura M., and Barrett J.C. Repression of the telomerase catalytic subunit by a gene on human chromosome 3 that induces cellular senescence. Mol. Carcinog. 22 (1998) 65-72
-
(1998)
Mol. Carcinog.
, vol.22
, pp. 65-72
-
-
Horikawa, I.1
Oshimura, M.2
Barrett, J.C.3
-
7
-
-
15844428981
-
Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries
-
Diatchenko L., Lau Y.F., Campbell A.P., Chenchik A., Moqadam F., Huang B., Lukyanov S., Lukyanov K., Gurskaya N., Sverdlov E.D., and Siebert P.D. Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries. Proc. Natl. Acad. Sci. USA 93 (1996) 6025-6030
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 6025-6030
-
-
Diatchenko, L.1
Lau, Y.F.2
Campbell, A.P.3
Chenchik, A.4
Moqadam, F.5
Huang, B.6
Lukyanov, S.7
Lukyanov, K.8
Gurskaya, N.9
Sverdlov, E.D.10
Siebert, P.D.11
-
8
-
-
0034898892
-
Upregulation of the gene encoding a cytoplasmic dynein intermediate chain in senescent human cells
-
Horikawa I., Parker E.S., Solomon G.G., and Barrett J.C. Upregulation of the gene encoding a cytoplasmic dynein intermediate chain in senescent human cells. J. Cell. Biochem. 82 (2001) 415-421
-
(2001)
J. Cell. Biochem.
, vol.82
, pp. 415-421
-
-
Horikawa, I.1
Parker, E.S.2
Solomon, G.G.3
Barrett, J.C.4
-
9
-
-
0028294621
-
A gene involved in control of human cellular senescence on human chromosome 1q
-
Hensler P.J., Annab L.A., Barrett J.C., and Pereira-Smith O.M. A gene involved in control of human cellular senescence on human chromosome 1q. Mol. Cell. Biol. 14 (1994) 2291-2297
-
(1994)
Mol. Cell. Biol.
, vol.14
, pp. 2291-2297
-
-
Hensler, P.J.1
Annab, L.A.2
Barrett, J.C.3
Pereira-Smith, O.M.4
-
10
-
-
4944240745
-
Transcriptional activation of hTERT through the NF-kappaB pathway in HTLV-I-transformed cells
-
Sinha-Datta U., Horikawa I., Michishita E., Datta A., Sigler-Nicot J.C., Brown M., Kazanji M., Barrett J.C., and Nicot C. Transcriptional activation of hTERT through the NF-kappaB pathway in HTLV-I-transformed cells. Blood 104 (2004) 2523-2531
-
(2004)
Blood
, vol.104
, pp. 2523-2531
-
-
Sinha-Datta, U.1
Horikawa, I.2
Michishita, E.3
Datta, A.4
Sigler-Nicot, J.C.5
Brown, M.6
Kazanji, M.7
Barrett, J.C.8
Nicot, C.9
-
11
-
-
0346881534
-
Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss
-
Abe S., Usami S., and Nakamura Y. Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss. J. Hum. Genet. 48 (2003) 564-570
-
(2003)
J. Hum. Genet.
, vol.48
, pp. 564-570
-
-
Abe, S.1
Usami, S.2
Nakamura, Y.3
-
12
-
-
0034603782
-
Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2
-
Scott D.A., Drury S., Sundstrom R.A., Bishop J., Swiderski R.E., Carmi R., Ramesh A., Elbedour K., Srikumari Srisailapathy C.R., Keats B.J., Sheffield V.C., and Smith R.J. Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2. Gene 246 (2000) 265-274
-
(2000)
Gene
, vol.246
, pp. 265-274
-
-
Scott, D.A.1
Drury, S.2
Sundstrom, R.A.3
Bishop, J.4
Swiderski, R.E.5
Carmi, R.6
Ramesh, A.7
Elbedour, K.8
Srikumari Srisailapathy, C.R.9
Keats, B.J.10
Sheffield, V.C.11
Smith, R.J.12
-
13
-
-
0042169025
-
Transcriptional regulation of the telomerase hTERT gene as a target for cellular and viral oncogenic mechanisms
-
Horikawa I., and Barrett J.C. Transcriptional regulation of the telomerase hTERT gene as a target for cellular and viral oncogenic mechanisms. Carcinogenesis 24 (2003) 1167-1176
-
(2003)
Carcinogenesis
, vol.24
, pp. 1167-1176
-
-
Horikawa, I.1
Barrett, J.C.2
-
14
-
-
0036645284
-
A novel low-penetrance locus for familial glioma at 15q23-q26.3
-
Paunu N., Lahermo P., Onkamo P., Ollikainen V., Rantala I., Helen P., Simola K.O., Kere J., and Haapasalo H. A novel low-penetrance locus for familial glioma at 15q23-q26.3. Cancer Res. 62 (2002) 3798-3802
-
(2002)
Cancer Res.
, vol.62
, pp. 3798-3802
-
-
Paunu, N.1
Lahermo, P.2
Onkamo, P.3
Ollikainen, V.4
Rantala, I.5
Helen, P.6
Simola, K.O.7
Kere, J.8
Haapasalo, H.9
-
15
-
-
0034780110
-
Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinoma
-
Zweemer R.P., Ryan A., Snijders A.M., Hermsen M.A., Meijer G.A., Beller U., Menko F.H., Jacobs I.J., Baak J.P., Verheijen R.H., Kenemans P., and van Diest P.J. Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinoma. Lab. Invest. 81 (2001) 1363-1370
-
(2001)
Lab. Invest.
, vol.81
, pp. 1363-1370
-
-
Zweemer, R.P.1
Ryan, A.2
Snijders, A.M.3
Hermsen, M.A.4
Meijer, G.A.5
Beller, U.6
Menko, F.H.7
Jacobs, I.J.8
Baak, J.P.9
Verheijen, R.H.10
Kenemans, P.11
van Diest, P.J.12
-
16
-
-
0343049059
-
Recurrent allelic deletions of chromosome arms 15q and 16q in human small cell lung carcinomas
-
Stanton S.E., Shin S.W., Johnson B.E., and Meyerson M. Recurrent allelic deletions of chromosome arms 15q and 16q in human small cell lung carcinomas. Genes Chromosomes Cancer 27 (2000) 323-331
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 323-331
-
-
Stanton, S.E.1
Shin, S.W.2
Johnson, B.E.3
Meyerson, M.4
|