-
1
-
-
0035054991
-
Relationship of chromosome 21 and acute leukemia in children with down syndrome
-
DOI 10.1097/00043426-200103000-00012
-
Taub JW. Relationship of chromosome 21 and acute leukemia in children with Down syndrome. J Pediatr Hematol Oncol. 2001;23:175-178. (Pubitemid 32332047)
-
(2001)
Journal of Pediatric Hematology/Oncology
, vol.23
, Issue.3
, pp. 175-178
-
-
Taub, J.W.1
-
2
-
-
0028213440
-
Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome
-
DOI 10.1016/0145-2126(94)90111-2
-
Zipursky A, Thorner P, De Harven E, Christensen H, Doyle J. Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome. Leuk Res. 1994;18:163-171. (Pubitemid 24127571)
-
(1994)
Leukemia Research
, vol.18
, Issue.3
, pp. 163-171
-
-
Zipursky, A.1
Thorner, P.2
De Harven, E.3
Christensen, H.4
Doyle, J.5
-
3
-
-
0037355255
-
Transient leukaemia - A benign form of leukaemia in newborn infants with trisomy 21
-
DOI 10.1046/j.1365-2141.2003.04229.x
-
Zipursky A. Transient leukaemia - a benign form of leukaemia in newborn infants with trisomy 21. Br J Haematol. 2003;120:930-938. (Pubitemid 36411551)
-
(2003)
British Journal of Haematology
, vol.120
, Issue.6
, pp. 930-938
-
-
Zipursky, A.1
-
4
-
-
0036727413
-
Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome
-
DOI 10.1038/ng955
-
Wechsler J, Greene M, McDevitt MA, et al. Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome. Nat Genet. 2002;32:148-152. (Pubitemid 34977210)
-
(2002)
Nature Genetics
, vol.32
, Issue.1
, pp. 148-152
-
-
Wechsler, J.1
Greene, M.2
McDevitt, M.A.3
Anastasi, J.4
Karp, J.E.5
Le Beau, M.M.6
Crispino, J.D.7
-
5
-
-
0038142390
-
Mutagenesis of GATA1 is an initiating event in Down syndrome leukemogenesis
-
DOI 10.1182/blood-2002-12-3904
-
Mundschau G, Gurbuxani S, Gamis AS, Greene ME, Arceci RJ, Crispino JD. Mutagenesis of GATA1 is an initiating event in Down syndrome leukemogenesis. Blood. 2003;101:4298-4300. (Pubitemid 36857792)
-
(2003)
Blood
, vol.101
, Issue.11
, pp. 4298-4300
-
-
Mundschau, G.1
Gurbuxani, S.2
Gamis, A.S.3
Greene, M.E.4
Arceci, R.J.5
Crispino, J.D.6
-
6
-
-
0038142350
-
GATA1 mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndrome
-
DOI 10.1182/blood-2003-01-0013
-
Hitzler JK, Cheung J, Li Y, Scherer SW, Zipursky A. GATA1 mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndrome. Blood. 2003;101:4301-4304. (Pubitemid 36857793)
-
(2003)
Blood
, vol.101
, Issue.11
, pp. 4301-4304
-
-
Hitzler, J.K.1
Cheung, J.2
Li, Y.3
Scherer, S.W.4
Zipursky, A.5
-
7
-
-
0042243593
-
Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
-
DOI 10.1182/blood-2002-11-3599
-
Rainis L, Bercovich D, Strehl S, et al. Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21. Blood. 2003;102:981-986. (Pubitemid 36917793)
-
(2003)
Blood
, vol.102
, Issue.3
, pp. 981-986
-
-
Rainis, L.1
Bercovich, D.2
Strehl, S.3
Teigler-Schlegel, A.4
Stark, B.5
Trka, J.6
Amariglio, N.7
Biondi, A.8
Muler, I.9
Rechavi, G.10
Kempski, H.11
Haas, O.A.12
Izraeli, S.13
-
8
-
-
0037906527
-
Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder
-
DOI 10.1016/S0140-6736(03)13266-7
-
Groet J, McElwaine S, Spinelli M, et al. Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder. Lancet. 2003;361:1617-1620. (Pubitemid 36579001)
-
(2003)
Lancet
, vol.361
, Issue.9369
, pp. 1617-1620
-
-
Groet, J.1
McElwaine, S.2
Spinelli, M.3
Rinaldi, A.4
Burtscher, I.5
Mulligan, C.6
Mensah, A.7
Cavani, S.8
Dagna-Bricarelli, F.9
Basso, G.10
Cotter, F.E.11
Nizetic, D.12
-
9
-
-
0141889275
-
Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome
-
DOI 10.1182/blood-2003-02-0390
-
Xu G, Nagano M, Kanezaki R, Toki T, et al. Frequent mutations in the GATA1 gene in the transient myeloproliferative disorder of Down's syndrome. Blood. 2003;102:2960-2968. (Pubitemid 37248871)
-
(2003)
Blood
, vol.102
, Issue.8
, pp. 2960-2968
-
-
Xu, G.1
Nagano, M.2
Kanezaki, R.3
Toki, T.4
Hayashi, Y.5
Taketani, T.6
Taki, T.7
Mitui, T.8
Koike, K.9
Kato, K.10
Imaizumi, M.11
Sekine, I.12
Ikeda, Y.13
Hanada, R.14
Sako, M.15
Kudo, K.16
Kojima, S.17
Ohneda, O.18
Yamamoto, M.19
Ito, E.20
more..
-
10
-
-
0346966816
-
Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndrome
-
DOI 10.1182/blood-2003-09-3219
-
Shimada A, Xu G, Toki T, Kimura H, Hayashi Y, Ito E. Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndrome. Blood. 2004;103:366. (Pubitemid 38029962)
-
(2004)
Blood
, vol.103
, Issue.1
, pp. 366
-
-
Shimada, A.1
Xu, G.2
Toki, T.3
Kimura, H.4
Hayashi, Y.5
Ito, E.6
-
11
-
-
4444347949
-
Prenatal origin of GATA1 mutations may be an initiating step in the development of megakaryocytic leukemia in Down syndrome [7]
-
DOI 10.1182/blood-2004-04-1563
-
Taub JW, Mundschau G, Ge Y, et al. Prenatal origin of GATA1 mutations may be an initiating step in the development of leukemia in Down syndrome. Blood. 2004;104:1588-1589. (Pubitemid 39166547)
-
(2004)
Blood
, vol.104
, Issue.5
, pp. 1588-1589
-
-
Taub, J.W.1
Mundschau, G.2
Ge, Y.3
Poulik, J.M.4
Qureshi, F.5
Jensen, T.6
James, S.J.7
Matherly, L.H.8
Wechsler, J.9
Crispino, J.D.10
-
12
-
-
54349086521
-
Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome
-
Bercovich D, Ganmore I, Scott LM, et al. Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome. Lancet. 2008;372:1484-1492.
-
(2008)
Lancet
, vol.372
, pp. 1484-1492
-
-
Bercovich, D.1
Ganmore, I.2
Scott, L.M.3
-
13
-
-
0032540912
-
Atypical background somatic mutant frequencies at the HPRT locus in children and adults with down syndrome
-
DOI 10.1016/S0027-5107(98)00024-4, PII S0027510798000244
-
Finette BA, Rood B, Poseno T, Vacek P, Pueschel S, Homans AC. Atypical background somatic mutant frequencies at the HPRT locus in children and adults with Down syndrome. Mutat Res. 1998;403:35-43. (Pubitemid 28383645)
-
(1998)
Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
, vol.403
, Issue.1-2
, pp. 35-43
-
-
Finette, B.A.1
Rood, B.2
Poseno, T.3
Vacek, P.4
Pueschel, S.5
Homans, A.C.6
-
14
-
-
0033566994
-
Expression of chromosome 21-localized genes in acute myeloid leukemia: Differences between Down syndrome and non-Down syndrome blast cells and relationship to in vitro sensitivity to cytosine arabinoside and daunorubicin
-
Taub JW, Huang X, Matherly LH, et al. Expression of chromosome 21-localized genes in acute myeloid leukemia: differences between Down syndrome and non-Down syndrome blast cells and relationship to in vitro sensitivity to cytosine arabinoside and daunorubicin. Blood. 1999;94:1393-1400. (Pubitemid 29380420)
-
(1999)
Blood
, vol.94
, Issue.4
, pp. 1393-1400
-
-
Taub, J.W.1
Huang, X.2
Matherly, L.H.3
Stout, M.L.4
Buck, S.A.5
Massey, G.V.6
Becton, D.L.7
Chang, M.N.8
Weinstein, H.J.9
Ravindranath, Y.10
-
15
-
-
13744252262
-
GATA1, cytidine deaminase, and the high cure rate of Down syndrome children with acute megakaryocytic leukemia
-
DOI 10.1093/jnci/dji026
-
Ge Y, Stout ML, Tatman DA, et al. GATA1, cytidine deaminase and the high cure rate of Down syndrome children with acute megakaryocytic leukemia. J Natl Cancer Institute. 2005;97:226-231. (Pubitemid 40277373)
-
(2005)
Journal of the National Cancer Institute
, vol.97
, Issue.3
, pp. 226-231
-
-
Ge, Y.1
Stout, M.L.2
Tatman, D.A.3
Jensen, T.L.4
Buck, S.A.5
Thomas, R.L.6
Ravindranath, Y.7
Matherly, L.H.8
Taub, J.W.9
-
17
-
-
0141731310
-
Base excision repair deficiency caused by polymerase beta haploinsufficiency: Accelerated DNA damage and increased mutational response to carcinogens
-
Cabelof DC, Guo Z, Raffoul JJ, et al. Base excision repair deficiency caused by polymerase beta haploinsufficiency: accelerated DNA damage and increased mutational response to carcinogens. Cancer Res. 2003;63:5799-5807. (Pubitemid 37187477)
-
(2003)
Cancer Research
, vol.63
, Issue.18
, pp. 5799-5807
-
-
Cabelof, D.C.1
Guo, Z.2
Raffoul, J.J.3
Sobol, R.W.4
Wilson, S.H.5
Richardson, A.6
Heydari, A.R.7
-
18
-
-
0028276746
-
2-Isoprostanes produced by non- Cyclooxygenase free radical-catalyzed mechanism
-
DOI 10.1016/S0076-6879(94)33019-0
-
Morrow JD, Roberts LJ 2nd. Mass spectrometry of prostanoids: F2-isoprostanes produced by non-cyclooxygenase free radical-catalyzed mechanism. Methods Enzymol. 1994;233:163-174. (Pubitemid 24177539)
-
(1994)
Methods in Enzymology
, vol.233
, pp. 163-174
-
-
Morrow, J.D.1
Roberts II, L.J.2
-
19
-
-
0029162684
-
Deletions at short direct repeats and base substitutions are characteristic mutations for bleomycin-induced double- And single-strand breaks, respectively, in a human shuttle vector system
-
Dar ME, Jorgensen TJ. Deletions at short direct repeats and base substitutions are characteristic mutations for bleomycin-induced double- and single-strand breaks, respectively, in a human shuttle vector system. Nucleic Acids Res. 1995;23:3224-3230.
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 3224-3230
-
-
Dar, M.E.1
Jorgensen, T.J.2
-
20
-
-
0031917762
-
DNA polymerase fidelity: From genetics toward a biochemical understanding
-
Goodman MF, Fygenson DK. DNA polymerase fidelity: from genetics toward a biochemical understanding. Genetics. 1998;148:1475-1482.
-
(1998)
Genetics
, vol.148
, pp. 1475-1482
-
-
Goodman, M.F.1
Fygenson, D.K.2
-
21
-
-
20044369162
-
Parp-1 deficiency causes an increase of deletion mutations and insertions/rearrangements in vivo after treatment with an alkylating agent
-
DOI 10.1038/sj.onc.1208289
-
Shibata A, Kamada N, Masumura K, et al. Parp-1 deficiency causes an increase of deletion mutations and insertions/rearrangements in vivo after treatment with an alkylating agent. Oncogene. 2005;24:1328-1337. (Pubitemid 40343113)
-
(2005)
Oncogene
, vol.24
, Issue.8
, pp. 1328-1337
-
-
Shibata, A.1
Kamada, N.2
Masumura, K.-I.3
Nohmi, T.4
Kobayashi, S.5
Teraoka, H.6
Nakagama, H.7
Sugimura, T.8
Suzuki, H.9
Masutani, M.10
-
22
-
-
24344505990
-
Microdeletions and microinsertions causing human genetic disease: Common mechanisms of mutagenesis and the role of local DNA sequence complexity
-
DOI 10.1002/humu.20212
-
Ball EV, Stenson PD, Abeysinghe SS, Krawczak M, Cooper DN, Chuzhanova NA. Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity. Human Mutat. 2005;26:205-213. (Pubitemid 41254376)
-
(2005)
Human Mutation
, vol.26
, Issue.3
, pp. 205-213
-
-
Ball, E.V.1
Stenson, P.D.2
Abeysinghe, S.S.3
Krawczak, M.4
Cooper, D.N.5
Chuzhanova, N.A.6
-
23
-
-
0022443767
-
Deoxyuridine misincorporation causes site-specific mutational lesions in the lacI gene of Escherichia coli
-
Sedwick WD, Brown OE, Glickman BW. Deoxyuridine misincorporation causes site-specific mutational lesions in the lacI gene of Escherichia coli. Mutat Res. 1986;162:7-20.
-
(1986)
Mutat Res
, vol.162
, pp. 7-20
-
-
Sedwick, W.D.1
Brown, O.E.2
Glickman, B.W.3
-
24
-
-
0023392392
-
Asymmetric cytosine deamination revealed by spontaneous mutational specificity in an Ung- Strain of Escherichia coli
-
Fix DF, Glickman BW. Asymmetric cytosine deamination revealed by spontaneous mutational specificity in an Ung- strain of Escherichia coli. Mol Gen Genet. 1987;209:78-82.
-
(1987)
Mol Gen Genet
, vol.209
, pp. 78-82
-
-
Fix, D.F.1
Glickman, B.W.2
-
25
-
-
0025344222
-
A sensitive genetic assay for the detection of cytosine deaminastion: Determination of rate constants and the activation energy
-
Frederico LA, Kunkel TA. Shaw BR. A sensitive genetic assay for the detection of cytosine deaminastion: determination of rate constants and the activation energy. Biochemistry. 1990;29:2532-2537.
-
(1990)
Biochemistry
, vol.29
, pp. 2532-2537
-
-
Frederico, L.A.1
Kunkel, T.A.2
Shaw, B.R.3
-
26
-
-
0025790276
-
The spectrum of spontaneous mutations in a Saccharomyces cerevisiae uracil-DNA-glycosylase mutatant limits the function of this enzyme to cytosine deamination repair
-
Impellizzeri KJ, Anderson B, Burgers PM. The spectrum of spontaneous mutations in a Saccharomyces cerevisiae uracil-DNA-glycosylase mutatant limits the function of this enzyme to cytosine deamination repair. J Bacteriol. 1991;173:6807-6810.
-
(1991)
J Bacteriol
, vol.173
, pp. 6807-6810
-
-
Impellizzeri, K.J.1
Anderson, B.2
Burgers, P.M.3
-
27
-
-
0020461949
-
Specific mutator effects of ung (uracil-DNA glycosylase) mutations in Escherichia coli
-
Duncan BK, Weiss B. Specific mutator effects of ung (Uracil-DNA Glycosylase) mutations in Escherichia coli. J Bacteriol. 1982;151:750-755. (Pubitemid 13230469)
-
(1982)
Journal of Bacteriology
, vol.151
, Issue.2
, pp. 750-755
-
-
Duncan, B.K.1
Weiss, B.2
-
28
-
-
0034969415
-
Homocysteine metabolism in children with down syndrome: In vitro modulation
-
DOI 10.1086/321262
-
Pogribna M, Melnyk S, Pogribny I, Chango A, Yi P, James SJ. Homocysteine metabolism in children with Down syndrome: in vitro modulation. Am J Hum Genet. 2001;69:88-95. (Pubitemid 32614021)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.1
, pp. 88-95
-
-
Pogribna, M.1
Melnyk, S.2
Pogribny, I.3
Chango, A.4
Yi, P.5
James, S.J.6
-
29
-
-
0021875707
-
Mechanism of mutation by thymine starvation in Escherichia coli: Clues from mutagenic specificity
-
Kunz BA, Glickman BW. Mechanism of mutation by thymine starvation in Escherichia coli: clues from mutagenic specificity. J Bacteriol. 1985;162:859-864.
-
(1985)
J Bacteriol
, vol.162
, pp. 859-864
-
-
Kunz, B.A.1
Glickman, B.W.2
-
30
-
-
21844464297
-
C3T mutagenesis and -radiation sensitivity due to deficiency in the Smug1 and Ung DNA glycosylases
-
An Q, Robins P, Lindahl T, Barnes DE. C3T mutagenesis and -radiation sensitivity due to deficiency in the Smug1 and Ung DNA glycosylases. EMBO J. 2005;24:2205-2213.
-
(2005)
EMBO J
, vol.24
, pp. 2205-2213
-
-
An, Q.1
Robins, P.2
Lindahl, T.3
Barnes, D.E.4
-
31
-
-
0032509749
-
Trisomy 21 and accelerated aging: DNA-repair parameters in peripheral lymphocytes of Down's syndrome patients
-
Raji NS, Rao KS. Trisomy 21 and accelerated aging: DNA-repair parameters in peripheral lymphocytes of Down's syndrome patients. Mech Ageing Dev. 1998;100:85-101.
-
(1998)
Mech Ageing Dev
, vol.100
, pp. 85-101
-
-
Raji, N.S.1
Rao, K.S.2
-
32
-
-
0014702519
-
DNA polymerase activity as an index of lymphocyte stimulation: Studies in Down's syndrome
-
Agarwal SS, Blumberg BS, Gerstley BJ, London WT, Sutnick AI, Loeb LA. DNA polymerase activity as an index of lymphocyte stimulation: studies in Down's syndrome. J Clin Invest. 1970;49:161-169.
-
(1970)
J Clin Invest
, vol.49
, pp. 161-169
-
-
Agarwal, S.S.1
Blumberg, B.S.2
Gerstley, B.J.3
London, W.T.4
Sutnick, A.I.5
Loeb, L.A.6
-
33
-
-
0018879295
-
Decreased repair of X-ray induced DNA single strand breaks in lymphocytes in Down's syndrome
-
Athanasiou K, Sideris EG, Bartsocas C. Decreased repair of x-ray induced DNA single-strand breaks in lymphocytes in Down's syndrome. Pediatr Res. 1980;14:336-338. (Pubitemid 10156097)
-
(1980)
Pediatric Research
, vol.14
, Issue.4 I
, pp. 336-338
-
-
Athanasiou, K.1
Sideris, E.G.2
Bartsocas, C.3
-
34
-
-
0034981492
-
Fetal hydrops and hepatosplenomegaly in the second half of pregnancy: A sign of myeloproliferative disorder in fetuses with trisomy 21
-
DOI 10.1046/j.1469-0705.2001.00384.x
-
Smrcek JM, Baschat AA, Germer U, Gloeckner-Hofmann K, Gembruch U. Fetal hydrops and hepatosplenomegaly in the second half of pregnancy: a sign of myeloproliferative disorder in fetuses with trisomy 21. Ultrasound Obstet Gynecol. 2001;17:403-409. (Pubitemid 32499871)
-
(2001)
Ultrasound in Obstetrics and Gynecology
, vol.17
, Issue.5
, pp. 403-409
-
-
Smrcek, J.M.1
Baschat, A.A.2
Germer, U.3
Gloeckner-Hofmann, K.4
Gembruch, U.5
-
35
-
-
0037852192
-
Prenatal diagnosis of congenital leukemia in a fetus at 25 weeks' gestation with Down syndrome: Case report and review of the literature
-
DOI 10.1002/uog.87
-
Robertson M, De Jong G, Mansvelt E. Prenatal diagnosis of congenital leukemia in a fetus at 25 weeks' gestation with Down syndrome: case report and review of the literature. Ultrasound Obstet Gynecol. 2003;21:486-489. (Pubitemid 36605713)
-
(2003)
Ultrasound in Obstetrics and Gynecology
, vol.21
, Issue.5
, pp. 486-489
-
-
Robertson, M.1
De Jong, G.2
Mansvelt, E.3
-
36
-
-
33747256270
-
Multiple evidence for an early age pro-oxidant state in Down Syndrome patients
-
DOI 10.1007/s10522-006-9002-5
-
Pallardo FV, Degan P, d'Ischia M, et al. Multiple evidence for an early age pro-oxidant state in Down syndrome patients. Biogerontology. 2006;7:211-220. (Pubitemid 44237302)
-
(2006)
Biogerontology
, vol.7
, Issue.4
, pp. 211-220
-
-
Pallardo, F.V.1
Degan, P.2
D'Ischia, M.3
Kelly, F.J.4
Zatterale, A.5
Calzone, R.6
Castello, G.7
Fernandez-Delgado, R.8
Dunster, C.9
Lloret, A.10
Manini, P.11
Pisanti, M.A.12
Vuttariello, E.13
Pagano, G.14
-
37
-
-
34247109650
-
Protein carbonyls as a biomarker of foetal-neonatal hypoxic stress
-
DOI 10.1016/j.clinbiochem.2006.10.013, PII S0009912006003705
-
Zitnanová I, Sumegova K, Simko M, et al. Protein carbonyls as a biomarker of foetal-neonatal hypoxic stress. Clin Biochem. 2007;40:567-570 (Pubitemid 46601415)
-
(2007)
Clinical Biochemistry
, vol.40
, Issue.8
, pp. 567-570
-
-
Zitnanová, I.1
Sumegova, K.2
Simko, M.3
Maruniakova, A.4
Chovanova, Z.5
Chavko, M.6
Durackova, Z.7
-
38
-
-
0033761958
-
Down's syndrome is associated with increased 8,12-isoi-PF2alpha-VI levels: Evidence for enhanced lipid peroxidation in vivo
-
Praticò D, Iuliano L, Amerio G, et al. Down's syndrome is associated with increased 8,12-isoi-PF2alpha-VI levels: evidence for enhanced lipid peroxidation in vivo. Ann Neurol. 2000;48:795-798.
-
(2000)
Ann Neurol
, vol.48
, pp. 795-798
-
-
Praticò, D.1
Iuliano, L.2
Amerio, G.3
-
39
-
-
0042932786
-
Enhanced brain levels of 8,12-iso-iPF2alpha-VI differentiate AD from frontotemporal dementia
-
Yao Y, Zhukareva V, Sung S, et al. Enhanced brain levels of 8,12-iso-iPF2alpha-VI differentiate AD from frontotemporal dementia. Neurology. 2003;61:475-478.
-
(2003)
Neurology
, vol.61
, pp. 475-478
-
-
Yao, Y.1
Zhukareva, V.2
Sung, S.3
-
40
-
-
0042432072
-
Brain isoprostanes: A marker of lipid peroxidation and oxidative stress in AD
-
Irizarry MC, Hyman BT. Brain isoprostanes: a marker of lipid peroxidation and oxidative stress in AD. Neurology. 2003;61:436-437.
-
(2003)
Neurology
, vol.61
, pp. 436-437
-
-
Irizarry, M.C.1
Hyman, B.T.2
-
41
-
-
33846237755
-
Early oxidative stress in amniotic fluid of pregnancies with Down syndrome
-
DOI 10.1016/j.clinbiochem.2006.10.019, PII S0009912006003778
-
Perrone S, Longini M, Bellieni CV, et al. Early oxidative stress in amniotic fluid of pregnancies with Down syndrome. Clin Biochem. 2007;40:177-180. (Pubitemid 46108711)
-
(2007)
Clinical Biochemistry
, vol.40
, Issue.3-4
, pp. 177-180
-
-
Perrone, S.1
Longini, M.2
Bellieni, C.V.3
Centini, G.4
Kenanidis, A.5
De Marco, L.6
Petraglia, F.7
Buonocore, G.8
-
42
-
-
0034711007
-
The quantitatively important relationship between homocysteine metabolism and glutathione synthesis by the transsulfuration pathway and its regulation by redox changes
-
DOI 10.1021/bi001088w
-
Mosharov E, Cranford MR, Banerjee R. The quantitatively important relationship between homocysteine metabolism and glutathione synthesis by the transsulfuration pathway and its regulation by redox changes. Biochemistry. 2000;39:13005-13011. (Pubitemid 30825904)
-
(2000)
Biochemistry
, vol.39
, Issue.42
, pp. 13005-13011
-
-
Mosharov, E.1
Cranford, M.R.2
Banerjee, R.3
-
43
-
-
3042698674
-
Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia
-
DOI 10.1152/ajpregu.00036.2004
-
Vitvitsky V, Dayal S, Stabler S, et al. Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia. Am J Physiol Regul Intergr Comp Physiol. 2004;287:R39-46. (Pubitemid 38856309)
-
(2004)
American Journal of Physiology - Regulatory Integrative and Comparative Physiology
, vol.287
, Issue.1
-
-
Vitvitsky, V.1
Dayal, S.2
Stabler, S.3
Zhou, Y.4
Wang, H.5
Lentz, S.R.6
Banerjee, R.7
-
44
-
-
0022453174
-
Effect of the variations of S-adenosyl-L-methionine liver content on fat accumulation and ethanol metabolism in ethanol-intoxicated rats
-
Feo F, Pascale R, Garcea R, et al. Effect of the variations of S-adenosyl-L-methionine liver content on fat accumulation and ethanol metabolism in ethanol-intoxicated rats. Toxicol Appl Pharmacol. 1986;83:331-341. (Pubitemid 16079418)
-
(1986)
Toxicology and Applied Pharmacology
, vol.83
, Issue.2
, pp. 331-341
-
-
Feo, F.1
Pascale, R.2
Garcea, R.3
-
45
-
-
0035882353
-
Influence of age on activities of antioxidant enzymes and lipid peroxidation products in erythrocytes and neutrophils of down syndrome patients
-
DOI 10.1016/S0891-5849(01)00609-8, PII S0891584901006098
-
Muchová J, Sustrova M, Garaiova I, et al. Influence of age on activities of antioxidant enzymes and lipid peroxidation products in erythrocytes and neutrophils of Down syndrome patients. Free Radic Biol Med. 2001;31:499-508. (Pubitemid 32728437)
-
(2001)
Free Radical Biology and Medicine
, vol.31
, Issue.4
, pp. 499-508
-
-
Muchova, J.1
Sustrova, M.2
Garaiova, I.3
Liptakova, A.4
Blazicek, P.5
Kvasnicka, P.6
Pueschel, S.7
Durackova, Z.8
-
46
-
-
0035118930
-
Effect of overexpression of wild-type and mutant CU/ZN-superoxide dismutases on oxidative damage and antioxidant defences: Relevance to Down's syndrome and familial amyotrophic lateral sclerosis
-
DOI 10.1046/j.1471-4159.2001.00107.x
-
Lee M, Hyun D. Jenner P, Halliwell B. Effect of overexpression of wild-type and mutant Cu/Zn-superoxide dismutases on oxidative damage and antioxidant defences: relevance to Down's syndrome and familial amyotrophic lateral sclerosis. J Neurochem. 2001;76:957-965. (Pubitemid 32167369)
-
(2001)
Journal of Neurochemistry
, vol.76
, Issue.4
, pp. 957-965
-
-
Lee, M.1
Hyun, D.-H.2
Jenner, P.3
Halliwell, B.4
-
47
-
-
0034905452
-
Evaluation of superoxide dismutase and glutathione peroxidase enzymes and their cofactors in Egyptian children with Down's syndrome
-
Meguid NA, Kholoussi NM, Afifi HH. Evaluation of superoxide dismutase and glutathione peroxidase enzymes and their cofactors in Egyptian children with Down's syndrome. Biol Trace Elem Res. 2001;81:21-28.
-
(2001)
Biol Trace Elem Res
, vol.81
, pp. 21-28
-
-
Meguid, N.A.1
Kholoussi, N.M.2
Afifi, H.H.3
-
48
-
-
0037089414
-
High frequency of leukemic clones in newborn screening blood samples of children with B-precursor acute lymphoblastic leukemia
-
DOI 10.1182/blood.V99.8.2992
-
Taub JW, Konrad MA, Ge Y, et al. High frequency of leukemic clones in newborn screening blood samples of children with B-precursor acute lymphoblastic leukemia. Blood. 2002;99:2992-2996. (Pubitemid 34525390)
-
(2002)
Blood
, vol.99
, Issue.8
, pp. 2992-2996
-
-
Taub, J.W.1
Konrad, M.A.2
Ge, Y.3
Naber, J.M.4
Scott, J.S.5
Matherly, L.H.6
Ravindranath, Y.7
-
49
-
-
0023006905
-
Excessive chemotherapy-related myelotoxicity in children with Down syndrome and acute lymphoblastic leukaemia
-
Blatt J, Albo V, Prin W, et al. Excessive chemotherapy-related myleotoxicity in children with Down's syndrome and acute lymphoblastic leukemia. Lancet. 1986;2:914. (Pubitemid 17170655)
-
(1986)
Lancet
, vol.2
, Issue.8512
, pp. 914
-
-
Blatt, J.1
Albo, V.2
Prin, W.3
-
50
-
-
0023187384
-
Down syndrome and leukemia: Unusual clinical aspects and unexpected methotrexate sensitivity
-
Peeters M, Poon A. Down syndrome and leukaemia: unusual clinical aspects and unexpected methotrexate sensitivity. Eur J Pediatr. 1987;146:416-422. (Pubitemid 17130864)
-
(1987)
European Journal of Pediatrics
, vol.146
, Issue.4
, pp. 416-422
-
-
Peeters, M.1
Poon, A.2
-
51
-
-
0028951430
-
In vivo folic acid supplementation partially corrects in vitro methotrexate toxicity in patients with Down syndrome
-
Peeters MA, Rethore MO, Lejeune J. In vivo folic acid supplementation partially corrects in vitro methotrexate toxicity in patients with Down syndrome. Br J Haematol. 1995;89:678-680.
-
(1995)
Br J Haematol
, vol.89
, pp. 678-680
-
-
Peeters, M.A.1
Rethore, M.O.2
Lejeune, J.3
-
52
-
-
0019486066
-
Methotrexate accumulation and folate depletion in cells as a possible mechanism of chronic toxicity to the drug
-
Kamen BA, Nylen PA, Camitta BM, et al. Methotrexate accumulation and folate depletion in cells as a possible mechanism of chronic toxicity to the drug. Br J Haematol. 1981;49:355-360.
-
(1981)
Br J Haematol
, vol.49
, pp. 355-360
-
-
Kamen, B.A.1
Nylen, P.A.2
Camitta, B.M.3
-
53
-
-
58149380865
-
Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutations
-
Tunstall-Pedoe O, Roy A, Karadimitris A, et al. Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutations. Blood. 2008;112:4507-4511.
-
(2008)
Blood
, vol.112
, pp. 4507-4511
-
-
Tunstall-Pedoe, O.1
Roy, A.2
Karadimitris, A.3
-
54
-
-
52649166735
-
Megacaryocyte hyperproliferation without GATA1 mutation in foetal liver of a case of Down syndrome with hydrops foetalis
-
De Vita S, Devoy A, Groet J, et al. Megacaryocyte hyperproliferation without GATA1 mutation in foetal liver of a case of Down syndrome with hydrops foetalis. Br J Haematol. 2008;143:300-303.
-
(2008)
Br J Haematol
, vol.143
, pp. 300-303
-
-
De Vita, S.1
Devoy, A.2
Groet, J.3
|