-
1
-
-
15244360381
-
The multiple causes of human SCID
-
Buckley RH. The multiple causes of human SCID. J Clin Invest 2004;114:1409-11.
-
(2004)
J Clin Invest
, vol.114
, pp. 1409-1411
-
-
Buckley, R.H.1
-
2
-
-
0037442176
-
Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: Report of the European experience 1968-99
-
Antoine C, Muller S, Cant A, Cavazzana-Calvo M, Veys F, Vossen J, et al. Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968-99. Lancet 2003;361:553-60.
-
(2003)
Lancet
, vol.361
, pp. 553-560
-
-
Antoine, C.1
Muller, S.2
Cant, A.3
Cavazzana-Calvo, M.4
Veys, F.5
Vossen, J.6
-
3
-
-
2542461255
-
Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution
-
Buckley RH. Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution. Annu Rev Immunol 2004;22:625-55.
-
(2004)
Annu Rev Immunol
, vol.22
, pp. 625-655
-
-
Buckley, R.H.1
-
4
-
-
13144249155
-
Severe combined immunodeficiency. A model disease for molecular immunology and therapy
-
Fischer A, Le Deist F, Hacein-Bey-Abina S, Andre-Schmutz I, Basile Gde S, de Villartay JP, et al. Severe combined immunodeficiency. A model disease for molecular immunology and therapy. Immunol Rev 2005;203:98-109.
-
(2005)
Immunol Rev
, vol.203
, pp. 98-109
-
-
Fischer, A.1
Le Deist, F.2
Hacein-Bey-Abina, S.3
Andre-Schmutz, I.4
Basile Gde, S.5
de Villartay, J.P.6
-
5
-
-
0242380235
-
Have we seen the last variant of severe combined immunodeficiency?
-
Fischer A. Have we seen the last variant of severe combined immunodeficiency? N Engl J Med 2003;349:1789-92.
-
(2003)
N Engl J Med
, vol.349
, pp. 1789-1792
-
-
Fischer, A.1
-
6
-
-
10144253125
-
RAG mutations in human B cell-negative SCID
-
Schwarz K, Gauss GH, Ludwig L, Pannicke U, Li Z, Lindner D, et al. RAG mutations in human B cell-negative SCID. Science 1996;274:97-9.
-
(1996)
Science
, vol.274
, pp. 97-99
-
-
Schwarz, K.1
Gauss, G.H.2
Ludwig, L.3
Pannicke, U.4
Li, Z.5
Lindner, D.6
-
7
-
-
3242888974
-
-
Schatz DG. V(D)J recombination. Immunol Rev 2004;200:5-11.
-
Schatz DG. V(D)J recombination. Immunol Rev 2004;200:5-11.
-
-
-
-
8
-
-
0035917489
-
Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency
-
Moshous D, Callebaut I, de Chasseval R, Corneo B, Cavazzana-Calvo M, Le Deist F, et al. Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency. Cell 2001;105:177-86.
-
(2001)
Cell
, vol.105
, pp. 177-186
-
-
Moshous, D.1
Callebaut, I.2
de Chasseval, R.3
Corneo, B.4
Cavazzana-Calvo, M.5
Le Deist, F.6
-
9
-
-
0037441592
-
Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow
-
Noordzij JG, Verkaik NS, Van der Burg M, Van Veelen LR, De Bruin-Versteeg S, Wiegant W, et al. Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow. Blood 2003;101:1446-52.
-
(2003)
Blood
, vol.101
, pp. 1446-1452
-
-
Noordzij, J.G.1
Verkaik, N.S.2
Van der Burg, M.3
Van Veelen, L.R.4
De Bruin-Versteeg, S.5
Wiegant, W.6
-
10
-
-
0037097787
-
A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans
-
Li L, Moshous D, Zhou Y, Wang J, Xie G, Salido E, et al. A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans. J Immunol 2002;168:6323-9.
-
(2002)
J Immunol
, vol.168
, pp. 6323-6329
-
-
Li, L.1
Moshous, D.2
Zhou, Y.3
Wang, J.4
Xie, G.5
Salido, E.6
-
11
-
-
0037809601
-
Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families
-
Kobayashi N, Agematsu K, Sugita K, Sako M, Nonoyama S, Yachie A, et al. Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families. Hum Genet 2003;112:348-52.
-
(2003)
Hum Genet
, vol.112
, pp. 348-352
-
-
Kobayashi, N.1
Agematsu, K.2
Sugita, K.3
Sako, M.4
Nonoyama, S.5
Yachie, A.6
-
12
-
-
3242881897
-
An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome
-
O'Driscoll M, Gennery AR, Seidel J, Concannon P, Jeggo PA. An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome. DNA Repair (Amst) 2004;3:1227-35.
-
(2004)
DNA Repair (Amst)
, vol.3
, pp. 1227-1235
-
-
O'Driscoll, M.1
Gennery, A.R.2
Seidel, J.3
Concannon, P.4
Jeggo, P.A.5
-
13
-
-
31044446450
-
A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation
-
Van der Burg M, van Veelen LR, Verkaik NS, Wiegant WW, Hartwig NG, Barendregt BH, et al. A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation. J Clin Invest 2006;116:137-45.
-
(2006)
J Clin Invest
, vol.116
, pp. 137-145
-
-
Van der Burg, M.1
van Veelen, L.R.2
Verkaik, N.S.3
Wiegant, W.W.4
Hartwig, N.G.5
Barendregt, B.H.6
-
14
-
-
0033512908
-
Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell-depleted bone marrow transplantation: A retrospective European survey from the European group for bone marrow transplantation and the european society for immunodeficiency
-
Bertrand Y, Landais P, Friedrich W, Gerritsen B, Morgan G, Fasth A, et al. Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell-depleted bone marrow transplantation: a retrospective European survey from the European group for bone marrow transplantation and the european society for immunodeficiency. J Pediatr 1999;134:740-8.
-
(1999)
J Pediatr
, vol.134
, pp. 740-748
-
-
Bertrand, Y.1
Landais, P.2
Friedrich, W.3
Gerritsen, B.4
Morgan, G.5
Fasth, A.6
-
15
-
-
18244411938
-
Long-term immune reconstitution and outcome after HLA-nonidentical T-cell-depleted bone marrow transplantation for severe combined immunodeficiency: A European retrospective study of 116 patients
-
Haddad E, Landais F, Friedrich W, Gerritsen B, Cavazzana-Calvo M, Morgan G, et al. Long-term immune reconstitution and outcome after HLA-nonidentical T-cell-depleted bone marrow transplantation for severe combined immunodeficiency: a European retrospective study of 116 patients. Blood 1998;91:3646-53.
-
(1998)
Blood
, vol.91
, pp. 3646-3653
-
-
Haddad, E.1
Landais, F.2
Friedrich, W.3
Gerritsen, B.4
Cavazzana-Calvo, M.5
Morgan, G.6
-
16
-
-
0035042875
-
Bone marrow transplantation for T-B- severe combined immunodeficiency disease in Athabascan-speaking native Americans
-
O'Marcaigh AS, DeSantes K, Hu D, Pabst H, Horn B, Li L, et al. Bone marrow transplantation for T-B- severe combined immunodeficiency disease in Athabascan-speaking native Americans. Bone Marrow Transplant 2001;27:703-9.
-
(2001)
Bone Marrow Transplant
, vol.27
, pp. 703-709
-
-
O'Marcaigh, A.S.1
DeSantes, K.2
Hu, D.3
Pabst, H.4
Horn, B.5
Li, L.6
-
17
-
-
0037105535
-
The immunophenotypic and immunogenotypic B-cell differentiation arrest in bone marrow of RAG deficient SCID patients corresponds to residual recombination activities of mutated RAG proteins
-
Noordzij JG, De Bruin-Versteeg S, Verkaik NS, Vossen JMJJ, De Groot R, Bernatowska E, et al. The immunophenotypic and immunogenotypic B-cell differentiation arrest in bone marrow of RAG deficient SCID patients corresponds to residual recombination activities of mutated RAG proteins. Blood 2002;100:2145-52.
-
(2002)
Blood
, vol.100
, pp. 2145-2152
-
-
Noordzij, J.G.1
De Bruin-Versteeg, S.2
Verkaik, N.S.3
Vossen, J.M.J.J.4
De Groot, R.5
Bernatowska, E.6
-
18
-
-
0036152373
-
Composition of precursor B-cell compartment in bone marrow from patients with X-linked agammaglobulinemia compared with healthy children
-
Noordzij JG, De Bruin-Versteeg S, Comans-Bitter WM, Hartwig NG, Hendriks RW, De Groot R, et al. Composition of precursor B-cell compartment in bone marrow from patients with X-linked agammaglobulinemia compared with healthy children. Pediatr Res 2002;51:159-68.
-
(2002)
Pediatr Res
, vol.51
, pp. 159-168
-
-
Noordzij, J.G.1
De Bruin-Versteeg, S.2
Comans-Bitter, W.M.3
Hartwig, N.G.4
Hendriks, R.W.5
De Groot, R.6
-
19
-
-
33644845081
-
Microenvironmental niches in the bone marrow required for B-cell development
-
Nagasawa T. Microenvironmental niches in the bone marrow required for B-cell development. Nat Rev Immunol 2006;6:107-16.
-
(2006)
Nat Rev Immunol
, vol.6
, pp. 107-116
-
-
Nagasawa, T.1
-
20
-
-
27144461642
-
Ig gene rearrangement steps are initiated in early human precursor B cell subsets and correlate with specific transcription factor expression
-
van Zelm MC, van der Burg M, de Ridder D, Barendregt BH, de Haas EF, Reinders MJ, et al. Ig gene rearrangement steps are initiated in early human precursor B cell subsets and correlate with specific transcription factor expression. J Immunol 2005;175:5912-22
-
(2005)
J Immunol
, vol.175
, pp. 5912-5922
-
-
van Zelm, M.C.1
van der Burg, M.2
de Ridder, D.3
Barendregt, B.H.4
de Haas, E.F.5
Reinders, M.J.6
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