-
2
-
-
0035934019
-
Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients
-
Wang LL, Levy ML, Lewis RA, Chintagumpala MM, Lev D, Rogers M, Plon SE. Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients. Am J Med Genet 2001;102:11-7.
-
(2001)
Am J Med Genet
, vol.102
, pp. 11-17
-
-
Wang, L.L.1
Levy, M.L.2
Lewis, R.A.3
Chintagumpala, M.M.4
Lev, D.5
Rogers, M.6
Plon, S.E.7
-
3
-
-
0000041048
-
Uber Kataract in Vebindung mit Einer Eugntumliche Haut Degeneration
-
Rothmund A. Uber Kataract in Vebindung mit Einer Eugntumliche Haut Degeneration. Arch Ophthalmol 1887;4:159.
-
(1887)
Arch Ophthalmol
, vol.4
, pp. 159
-
-
Rothmund, A.1
-
4
-
-
0001743196
-
A hitherto undescribed familial disease
-
Thomson M. A hitherto undescribed familial disease. Br J Dermatol 1923;35:455-62.
-
(1923)
Br J Dermatol
, vol.35
, pp. 455-462
-
-
Thomson, M.1
-
5
-
-
0038288850
-
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome
-
Wang LL, Gannavarapu A, Kozinetz CA, et al. Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. J Natl Cancer Inst 2003;95:669-74.
-
(2003)
J Natl Cancer Inst
, vol.95
, pp. 669-674
-
-
Wang, L.L.1
Gannavarapu, A.2
Kozinetz, C.A.3
-
6
-
-
0032939991
-
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
-
Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, Lindor NM, Furuichi Y. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat Genet 1999;22:82-4.
-
(1999)
Nat Genet
, vol.22
, pp. 82-84
-
-
Kitao, S.1
Shimamoto, A.2
Goto, M.3
Miller, R.W.4
Smithson, W.A.5
Lindor, N.M.6
Furuichi, Y.7
-
9
-
-
0030076795
-
Myelodysplastic syndrome in a child with Rothmund-Thomson syndrome: a case report
-
Rizzari C, Bacchiocchi D, Rovelli A, Biondi A, CantuRajnoldi A, Uderzo C, Masera G. Myelodysplastic syndrome in a child with Rothmund-Thomson syndrome: a case report. J Pediatr Hematol Oncol 1996;18:96-7.
-
(1996)
J Pediatr Hematol Oncol
, vol.18
, pp. 96-97
-
-
Rizzari, C.1
Bacchiocchi, D.2
Rovelli, A.3
Biondi, A.4
CantuRajnoldi, A.5
Uderzo, C.6
Masera, G.7
-
12
-
-
33846998643
-
Clinicopathologic features of osteosarcoma in patients with Rothmund-Thomson syndrome
-
Hicks MJ, Roth JR, Kozinetz CA, Wang LL. Clinicopathologic features of osteosarcoma in patients with Rothmund-Thomson syndrome. J Clin Oncol 2007;25:370-5.
-
(2007)
J Clin Oncol
, vol.25
, pp. 370-375
-
-
Hicks, M.J.1
Roth, J.R.2
Kozinetz, C.A.3
Wang, L.L.4
-
13
-
-
9344253898
-
Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism
-
Lindor NM, Devries EMG, Michels VV, Schad CR, Jalal SM, Donovan KM, Smithson WA, Kvols LK, Thibodeau SN, Dewald GW. Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism. Clin Genet 1996;49:124-9.
-
(1996)
Clin Genet
, vol.49
, pp. 124-129
-
-
Lindor, N.M.1
Devries, E.M.G.2
Michels, V.V.3
Schad, C.R.4
Jalal, S.M.5
Donovan, K.M.6
Smithson, W.A.7
Kvols, L.K.8
Thibodeau, S.N.9
Dewald, G.W.10
-
14
-
-
33846007694
-
Treatment of relapsed acute leukemia after allogeneic transplantation: a single center experience
-
Arellano ML, Langston A, Winton E, Flowers CR, Waller EK. Treatment of relapsed acute leukemia after allogeneic transplantation: a single center experience. Biol Blood Marrow Transplant 2007;13:116-23.
-
(2007)
Biol Blood Marrow Transplant
, vol.13
, pp. 116-123
-
-
Arellano, M.L.1
Langston, A.2
Winton, E.3
Flowers, C.R.4
Waller, E.K.5
-
15
-
-
0037108181
-
Second malignant neoplasms in long-term survivors of osteosarcoma - Memorial Sloan-Kettering Cancer Center Experience
-
Aung L, Gorlick RG, Shi W, Thaler H, Shorter NA, Healey JH, Huvos AG, Meyers PA. Second malignant neoplasms in long-term survivors of osteosarcoma - Memorial Sloan-Kettering Cancer Center Experience. Cancer 2002;95:1728-34.
-
(2002)
Cancer
, vol.95
, pp. 1728-1734
-
-
Aung, L.1
Gorlick, R.G.2
Shi, W.3
Thaler, H.4
Shorter, N.A.5
Healey, J.H.6
Huvos, A.G.7
Meyers, P.A.8
-
16
-
-
0033008437
-
Secondary leukemia or myelodysplastic syndrome after treatment with epipodophyllotoxins
-
Smith MA, Rubinstein L, Anderson JR, et al. Secondary leukemia or myelodysplastic syndrome after treatment with epipodophyllotoxins. J Clin Oncol 1999;17:569-77.
-
(1999)
J Clin Oncol
, vol.17
, pp. 569-577
-
-
Smith, M.A.1
Rubinstein, L.2
Anderson, J.R.3
-
17
-
-
69849099149
-
Therapy-related myeloid neoplasms
-
Czader M, Orazi A. Therapy-related myeloid neoplasms. Am J Clin Pathol 2009;132:410-25.
-
(2009)
Am J Clin Pathol
, vol.132
, pp. 410-425
-
-
Czader, M.1
Orazi, A.2
-
18
-
-
0028110040
-
Incidence and characterization of secondary myelodysplastic syndrome and acute myelogenous leukemia following high-dose chemoradiotherapy and autologous stem-cell transplantation for lymphoid malignancies
-
Darrington DL, Vose JM, Anderson JR, Bierman PJ, Bishop MR, Chan WC, Morris ME, Reed EC, Sanger WG, Tarantolo SR. Incidence and characterization of secondary myelodysplastic syndrome and acute myelogenous leukemia following high-dose chemoradiotherapy and autologous stem-cell transplantation for lymphoid malignancies. J Clin Oncol 1994;12:2527-34.
-
(1994)
J Clin Oncol
, vol.12
, pp. 2527-2534
-
-
Darrington, D.L.1
Vose, J.M.2
Anderson, J.R.3
Bierman, P.J.4
Bishop, M.R.5
Chan, W.C.6
Morris, M.E.7
Reed, E.C.8
Sanger, W.G.9
Tarantolo, S.R.10
-
19
-
-
66349111700
-
Therapy-related myeloid neoplasms
-
Larson RA. Therapy-related myeloid neoplasms. Haematologica 2009;94:454-9.
-
(2009)
Haematologica
, vol.94
, pp. 454-459
-
-
Larson, R.A.1
-
20
-
-
0038305924
-
Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series
-
Smith SM, Le Beau MM, Huo D, Karrison T, Sobecks RM, Anastasi J, Vardiman JW, Rowley JD, Larson RA. Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series. Blood 2003;102:43-52.
-
(2003)
Blood
, vol.102
, pp. 43-52
-
-
Smith, S.M.1
Le Beau, M.M.2
Huo, D.3
Karrison, T.4
Sobecks, R.M.5
Anastasi, J.6
Vardiman, J.W.7
Rowley, J.D.8
Larson, R.A.9
-
21
-
-
30144443817
-
The myelodysplastic syndromes: diagnosis and treatment
-
Steensma DP, Bennett JM. The myelodysplastic syndromes: diagnosis and treatment. Mayo Clin Proc 2006;81:104-30.
-
(2006)
Mayo Clin Proc
, vol.81
, pp. 104-130
-
-
Steensma, D.P.1
Bennett, J.M.2
-
22
-
-
33847228012
-
RECQL, a member of the RecQ family of DNA helicases, suppresses chromosomal instability
-
Sharma S, Stumpo DJ, Balajee AS, Bock CB, Lansdorp PM, Brosh RM, Blackshear PJ. RECQL, a member of the RecQ family of DNA helicases, suppresses chromosomal instability. Mol Cell Biol 2007;27:1784-94.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 1784-1794
-
-
Sharma, S.1
Stumpo, D.J.2
Balajee, A.S.3
Bock, C.B.4
Lansdorp, P.M.5
Brosh, R.M.6
Blackshear, P.J.7
-
23
-
-
77749330814
-
Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation
-
Thangavel S, Mendoza-Maldonado R, Tissino E, Sidorova JM, Yin JH, Wang WD, Monnat RJ, Falaschi A, Vindigni A. Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation. Mol Cell Biol 2010;30:1382-96.
-
(2010)
Mol Cell Biol
, vol.30
, pp. 1382-1396
-
-
Thangavel, S.1
Mendoza-Maldonado, R.2
Tissino, E.3
Sidorova, J.M.4
Yin, J.H.5
Wang, W.D.6
Monnat, R.J.7
Falaschi, A.8
Vindigni, A.9
-
24
-
-
62049085034
-
Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4
-
Xu XH, Liu YL. Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4. EMBO J 2009;28:568-77.
-
(2009)
EMBO J
, vol.28
, pp. 568-577
-
-
Xu, X.H.1
Liu, Y.L.2
-
25
-
-
69449097526
-
Direct and indirect roles of RECQL4 in modulating base excision repair capacity
-
Schurman SH, Hedayati M, Wang ZM, et al. Direct and indirect roles of RECQL4 in modulating base excision repair capacity. Hum Mol Genet 2009;18:3470-83.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3470-3483
-
-
Schurman, S.H.1
Hedayati, M.2
Wang, Z.M.3
-
26
-
-
33646399211
-
RECQL4-deficient cells are hypersensitive to oxidative stress/damage: insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndrome
-
Werner SR, Prahalad AK, Yang J, Hock JM. RECQL4-deficient cells are hypersensitive to oxidative stress/damage: insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndrome. Biochem Biophys Res Commun 2006;345:403-9.
-
(2006)
Biochem Biophys Res Commun
, vol.345
, pp. 403-409
-
-
Werner, S.R.1
Prahalad, A.K.2
Yang, J.3
Hock, J.M.4
-
27
-
-
0028837378
-
Fanconi-anemia
-
Auerbach AD. Fanconi-anemia. Dermatol Clin 1995;13:41-9.
-
(1995)
Dermatol Clin
, vol.13
, pp. 41-49
-
-
Auerbach, A.D.1
-
28
-
-
77952600845
-
Susceptibility pathways in Fanconi's anemia and breast cancer
-
Schwartz RS, D'Andrea AD. Susceptibility pathways in Fanconi's anemia and breast cancer. N Engl J Med 2010;362:1909-19.
-
(2010)
N Engl J Med
, vol.362
, pp. 1909-1919
-
-
Schwartz, R.S.1
D'Andrea, A.D.2
-
29
-
-
0037439356
-
Cancer in Fanconi anemia, 1927-2001
-
Alter BP. Cancer in Fanconi anemia, 1927-2001. Cancer 2003;97:425-40.
-
(2003)
Cancer
, vol.97
, pp. 425-440
-
-
Alter, B.P.1
-
30
-
-
34548504331
-
Therapy-related acute myelogenous leukemia and myelodysplastic syndrome
-
Borthakur G, Estey E. Therapy-related acute myelogenous leukemia and myelodysplastic syndrome. Curr Oncol Rep 2007;9:373-7.
-
(2007)
Curr Oncol Rep
, vol.9
, pp. 373-377
-
-
Borthakur, G.1
Estey, E.2
-
31
-
-
77950361766
-
Allogeneic transplantation for therapy-related myelodysplastic syndrome and acute myeloid leukemia
-
Litzow MR, Tarima S, Perez WS, et al. Allogeneic transplantation for therapy-related myelodysplastic syndrome and acute myeloid leukemia. Blood 2010;115:1850-7.
-
(2010)
Blood
, vol.115
, pp. 1850-1857
-
-
Litzow, M.R.1
Tarima, S.2
Perez, W.S.3
-
32
-
-
42949122111
-
High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated
-
Lugthart S, van Drunen E, van Norden Y, van Hoven A, Erpelinck CAJ, Valk PJM, Beverloo HB, Lowenberg B, Delwel R. High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated. Blood 2008;111:4329-37.
-
(2008)
Blood
, vol.111
, pp. 4329-4337
-
-
Lugthart, S.1
van Drunen, E.2
van Norden, Y.3
van Hoven, A.4
Erpelinck, C.A.J.5
Valk, P.J.M.6
Beverloo, H.B.7
Lowenberg, B.8
Delwel, R.9
|