-
1
-
-
0037591410
-
Inherited aplastic anaemia
-
Dokal I. Inherited aplastic anaemia. Hematology J 2003;4:3-9.
-
(2003)
Hematology J
, vol.4
, pp. 3-9
-
-
Dokal, I.1
-
2
-
-
12144288675
-
Heterogeneity in Fanconi anemia: Evidence for two new genetic subtypes
-
Levitus M, Rooimans MA, Steltenpool J, Cool NF, Oostra AB, Mathew CG, et al. Heterogeneity in Fanconi anemia: evidence for two new genetic subtypes. Blood 2004;103:2498-503.
-
(2004)
Blood
, vol.103
, pp. 2498-2503
-
-
Levitus, M.1
Rooimans, M.A.2
Steltenpool, J.3
Cool, N.F.4
Oostra, A.B.5
Mathew, C.G.6
-
3
-
-
0344406186
-
Abnormal telomere metabolism in Fanconi's anaemia correlates withgenomic instability and the probability of developing severe aplastic anaemia
-
Li X, Leteurtre F, Rocha V, Guardiola P, Berger R, Daniel MT, et al. Abnormal telomere metabolism in Fanconi's anaemia correlates withgenomic instability and the probability of developing severe aplastic anaemia. Br J Haematol 2003:120:836-45.
-
(2003)
Br J Haematol
, vol.120
, pp. 836-845
-
-
Li, X.1
Leteurtre, F.2
Rocha, V.3
Guardiola, P.4
Berger, R.5
Daniel, M.T.6
-
4
-
-
0037148271
-
Telomerase in the human organism
-
Collins K, Mitchell JR.Telomerase in the human organism. Oncogene 2002;21:564-79.
-
(2002)
Oncogene
, vol.21
, pp. 564-579
-
-
Collins, K.1
Mitchell, J.R.2
-
5
-
-
0035960043
-
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
-
Vulliamy T, Marrone A, Goldman F, Dearlove A, Bessler M, Mason P, et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature 2001;413:432-5.
-
(2001)
Nature
, vol.413
, pp. 432-435
-
-
Vulliamy, T.1
Marrone, A.2
Goldman, F.3
Dearlove, A.4
Bessler, M.5
Mason, P.6
-
6
-
-
0037157582
-
Association between aplastic anaemia and mutations in telomerase RNA
-
Vulliamy T, Marrone A, Dokal I, Mason PJ. Association between aplastic anaemia and mutations in telomerase RNA. Lancet 2002;359:2168-70.
-
(2002)
Lancet
, vol.359
, pp. 2168-2170
-
-
Vulliamy, T.1
Marrone, A.2
Dokal, I.3
Mason, P.J.4
-
7
-
-
0037121254
-
Aplastic anaemia and telomerase RNA mutations
-
Calado RT, Pintao MC, Suva WA, Falcao RP, Zago MA. Aplastic anaemia and telomerase RNA mutations. Lancet 2002;360:1608.
-
(2002)
Lancet
, vol.360
, pp. 1608
-
-
Calado, R.T.1
Pintao, M.C.2
Suva, W.A.3
Falcao, R.P.4
Zago, M.A.5
-
8
-
-
0041592752
-
Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome
-
Yamaguchi H, Baerlocher GM, Lansdorp PL, Chanock SJ, Nunez O, Sloand EM, et al. Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome. Blood 2003:102:916-8.
-
(2003)
Blood
, vol.102
, pp. 916-918
-
-
Yamaguchi, H.1
Baerlocher, G.M.2
Lansdorp, P.L.3
Chanock, S.J.4
Nunez, O.5
Sloand, E.M.6
-
9
-
-
0038543124
-
Human telomerase RNA mutations and bone marrow failure
-
Wilson DB, Ivanovich J, Whelan A, Goodfellow PJ, Bessler M. Human telomerase RNA mutations and bone marrow failure. Lancet 2003:361:1993-4.
-
(2003)
Lancet
, vol.361
, pp. 1993-1994
-
-
Wilson, D.B.1
Ivanovich, J.2
Whelan, A.3
Goodfellow, P.J.4
Bessler, M.5
-
10
-
-
0344851536
-
Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA
-
Fogarty PF, Yamaguchi H, Wiestner A, Baerlocher GM, Sloand E, Zeng WS, et al. Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA. Lancet 2003:362:1628-30.
-
(2003)
Lancet
, vol.362
, pp. 1628-1630
-
-
Fogarty, P.F.1
Yamaguchi, H.2
Wiestner, A.3
Baerlocher, G.M.4
Sloand, E.5
Zeng, W.S.6
-
11
-
-
0141557781
-
Comprehensive structure-function analysis of the core domain of human telomerase RNA
-
Ly H, Blackburn EH, Parslow TG. Comprehensive structure-function analysis of the core domain of human telomerase RNA. Mol Cell Biol 2004:23:6849-56.
-
(2004)
Mol Cell Biol
, vol.23
, pp. 6849-6856
-
-
Ly, H.1
Blackburn, E.H.2
Parslow, T.G.3
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