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2
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0006854346
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G. F. Van de Woode and C. Klein, Eds. Academic Press, San Diego
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L. A. Loeb, in Advances in Cancer Research, G. F. Van de Woode and C. Klein, Eds. (Academic Press, San Diego, 1998) vol. 72, pp. 26-56.
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Advances in Cancer Research
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Loeb, L.A.1
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9
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0342576911
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note
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Peripheral blood samples were obtained from patients at the time of diagnosis with ALL and from patients previously treated for ALL at the Pediatric Oncology Clinic at the University of Vermont. Patients at the time of bone marrow relapse were also recruited from other Pediatric Oncology Group (POG) institutions before treatment began. Informed consent was obtained, and procedures approved by the Committee on Human Research at the University of Vermont and other POG institutions were followed.
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10
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0028147748
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Peripheral blood was separated and the mononuclear cell fraction was obtained for the T cell cloning assay within 12 to 24 hours of its collection. The T cell cloning assay and analysis have been described [see B. A. Finette et al., Mutat. Res. 308, 223 (1994)].
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(1994)
Mutat. Res.
, vol.308
, pp. 223
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Finette, B.A.1
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12
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0342576909
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note
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Mutant frequencies in subjects at diagnoses, remission, and relapse were compared with normal controls by the nonparametric Kruskal-Wallis test. Pairwise differences between groups were assessed by Mann-Whitney tests, with a Bonferroni adjustment for multiple comparisons. Linear regression analysis was used to examine the relationship between the logarithm of Mf (InMf) and months since diagnosis.
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15
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0025282802
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R. A. Gibbs, P.-N. Nguyen, A. Edwards, A. B. Civitello, C. T. Caskey, Genomics 7, 235 (1990).
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(1990)
Genomics
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Gibbs, R.A.1
Nguyen, P.-N.2
Edwards, A.3
Civitello, A.B.4
Caskey, C.T.5
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17
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0031752252
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B. A. Finette, J. P. O'Neill, P. M. Vacek, R. J. Albertini, Nat. Med. 4, 1144 (1998).
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(1998)
Nat. Med.
, vol.4
, pp. 1144
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Finette, B.A.1
O'Neill, J.P.2
Vacek, P.M.3
Albertini, R.J.4
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19
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0031752252
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Because the HPRT gene is located on the X chromosome, molecular analysis at the DNA/RNA level was performed in a different way for mutant isolates from males and females [B. A. Finette, J. P. O'Neill, P. M. Vacek, R. J. Albertini, Nat. Med. 4, 1144 (1998)].
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(1998)
Nat. Med.
, vol.4
, pp. 1144
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Finette, B.A.1
O'Neill, J.P.2
Vacek, P.M.3
Albertini, R.J.4
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20
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0020534965
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S. Tonegawa, Nature 302, 575 (1983).
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(1983)
Nature
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Tonegawa, S.1
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21
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0032565554
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R. J. Albertini, J. A. Nicklas, T. R. Skopeck, Ł. Recio, J. P. O'Neill, Mutat. Res. 400, 381 (1998).
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Mutat. Res.
, vol.400
, pp. 381
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Albertini, R.J.1
Nicklas, J.A.2
Skopeck, T.R.3
Recio, L.4
O'Neill, J.P.5
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22
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0342576905
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note
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β consensus primer mix. The resulting PCR product was purified and the highly polymorphic CDR3/variable regions of TCRβ were sequenced.
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23
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0343882722
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Supplementary material is available at www. sciencemag.org/feature/data/1047822.shl
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24
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0343011207
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note
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Single-letter abbreviations for amino acid residues are as follows: A, Ala; C, Cys; D, Asp; E, Glu; F, Phe; G, Gly; H, His; I, Iie; K, Lys; L, Leu; M, Met; N, Asn; P, Pro; Q, Gln; R, Arg; S, Ser; T, Thr; V, Val; W, Trp; and Y, Tyr.
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25
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0026350934
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R. F. Branda, J. P. O'Neil, L. M. Sullivan, R. J. Albertini, Cancer Res. 51, 6603 (1991).
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Cancer Res.
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Branda, R.F.1
O'Neil, J.P.2
Sullivan, L.M.3
Albertini, R.J.4
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29
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0031023159
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E. F. Mao, L. Lane, J. Lee, J. H. Miller, J. Bacteriol. 179, 417 (1997).
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J. Bacteriol.
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Mao, E.F.1
Lane, L.2
Lee, J.3
Miller, J.H.4
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31
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0343882718
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note
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Supported by National Institute of Child Health & Human Development grant 1R29HD35309, National Cancer Institute (NCI) grant 1K01CA77737, grant 6103-98 from the Leukemia Society of America, the Lake Champlain Cancer Research Organization, the Vermont Chapter of the American Cancer Society, the Art Ehrmann Cancer Fund and NCI grant P30CA22435 to the University of Vermont Cancer Center DNA Analysis Facility. We thank C-C. Duriex-Lu, H. Kendall, and J. Rivers for technical assistance; S. Billado for assistance with blood samples; and P. Vacek for statistical analyses.
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