-
1
-
-
0000909935
-
Sur l'activité hemopoietique de serum au cours de la regeneration du sang
-
Carnot P., and Deflandre C. Sur l'activité hemopoietique de serum au cours de la regeneration du sang. C R Acad Sci 143 (1906) 432-435
-
(1906)
C R Acad Sci
, vol.143
, pp. 432-435
-
-
Carnot, P.1
Deflandre, C.2
-
2
-
-
0024502040
-
The molecular control of cell division, differentiation commitment and maturation in haematopoietic cells
-
Metcalf D. The molecular control of cell division, differentiation commitment and maturation in haematopoietic cells. Nature 339 (1989) 27-30
-
(1989)
Nature
, vol.339
, pp. 27-30
-
-
Metcalf, D.1
-
3
-
-
77049235105
-
Infantile genetic agranulocytosis
-
Kostmann R. Infantile genetic agranulocytosis. Acta Pediatr Scand 45 (1956) 1-78
-
(1956)
Acta Pediatr Scand
, vol.45
, pp. 1-78
-
-
Kostmann, R.1
-
4
-
-
0016612028
-
Infantile genetic agranulocytosis: A review with presentation of ten new cases
-
Kostmann R. Infantile genetic agranulocytosis: A review with presentation of ten new cases. Acta Pediatr Scand 64 (1975) 362-368
-
(1975)
Acta Pediatr Scand
, vol.64
, pp. 362-368
-
-
Kostmann, R.1
-
5
-
-
33845904894
-
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
-
Klein C., Grudzien M., Appaswamy G., Germeshausen M., Sandrock I., Schaffer A.A., et al. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet 39 (2007) 86-92
-
(2007)
Nat Genet
, vol.39
, pp. 86-92
-
-
Klein, C.1
Grudzien, M.2
Appaswamy, G.3
Germeshausen, M.4
Sandrock, I.5
Schaffer, A.A.6
-
6
-
-
0036899917
-
Mutant elastase in pathogenesis of cyclic and severe congenital neutropenia
-
Aprikyan A.A., Liles W.C., Boxer L.A., and Dale D.C. Mutant elastase in pathogenesis of cyclic and severe congenital neutropenia. J Pediatr Hematol Oncol 24 (2002) 784-786
-
(2002)
J Pediatr Hematol Oncol
, vol.24
, pp. 784-786
-
-
Aprikyan, A.A.1
Liles, W.C.2
Boxer, L.A.3
Dale, D.C.4
-
7
-
-
0034307655
-
Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia
-
Dale D.C., Person R.E., Bolyard A.A., Aprikyan A.G., Bos C., Bonilla M.A., Boxer L.A., et al. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 96 (2000) 2317-2322
-
(2000)
Blood
, vol.96
, pp. 2317-2322
-
-
Dale, D.C.1
Person, R.E.2
Bolyard, A.A.3
Aprikyan, A.G.4
Bos, C.5
Bonilla, M.A.6
Boxer, L.A.7
-
8
-
-
0032757863
-
Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoesis
-
Horwitz M., Benson K.F., Person R.E., Aprikyan A.G., and Dale D.C. Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoesis. Nat Genet 23 (1999) 433-436
-
(1999)
Nat Genet
, vol.23
, pp. 433-436
-
-
Horwitz, M.1
Benson, K.F.2
Person, R.E.3
Aprikyan, A.G.4
Dale, D.C.5
-
9
-
-
33749510883
-
LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia
-
Skokowa J., Cario G., Uenalan M., Schambach A., Germeshausen M., Battmer K., et al. LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia. Nat Med 12 (2006) 1191-1197
-
(2006)
Nat Med
, vol.12
, pp. 1191-1197
-
-
Skokowa, J.1
Cario, G.2
Uenalan, M.3
Schambach, A.4
Germeshausen, M.5
Battmer, K.6
-
11
-
-
0029129034
-
Mutations in the gene for the granulocyte-colony stimulating factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia
-
Dong F., Brynes R.K., Tidow N., Welte K., Lowenberg B., and Touw I.P. Mutations in the gene for the granulocyte-colony stimulating factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia. N Engl J Med 333 (1995) 487-493
-
(1995)
N Engl J Med
, vol.333
, pp. 487-493
-
-
Dong, F.1
Brynes, R.K.2
Tidow, N.3
Welte, K.4
Lowenberg, B.5
Touw, I.P.6
-
12
-
-
33845972945
-
Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: Results of a long-term survey
-
Germeshausen M., Ballmaier M., and Welte K. Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: Results of a long-term survey. Blood 109 (2007) 93-99
-
(2007)
Blood
, vol.109
, pp. 93-99
-
-
Germeshausen, M.1
Ballmaier, M.2
Welte, K.3
-
13
-
-
0018842744
-
Correction of infantile granulocytosis (Kostmann syndrome) by allogeneic bone marrow transplantation
-
Rappeport J., Parkman R., Newburger P., Camitta B.M., and Chusid M.J. Correction of infantile granulocytosis (Kostmann syndrome) by allogeneic bone marrow transplantation. Am J Med 68 (1980) 605-609
-
(1980)
Am J Med
, vol.68
, pp. 605-609
-
-
Rappeport, J.1
Parkman, R.2
Newburger, P.3
Camitta, B.M.4
Chusid, M.J.5
-
14
-
-
0022549329
-
Recombinant human granulocyte colony-stimulating factor: effects on normal and leukemic myeloid cells
-
Souza L., Boone T., Gabrilove J., Lai P.H., Zsebo K.M., Murdock D.C., et al. Recombinant human granulocyte colony-stimulating factor: effects on normal and leukemic myeloid cells. Science 232 (1986) 61-65
-
(1986)
Science
, vol.232
, pp. 61-65
-
-
Souza, L.1
Boone, T.2
Gabrilove, J.3
Lai, P.H.4
Zsebo, K.M.5
Murdock, D.C.6
-
15
-
-
0024317186
-
Effects of recombinant human granulocyte colony-stimulating factor on neutropenia in patients with congenital agranulocytosis
-
Bonilla M., Gillio A., Ruggeiro M., Kernan N.A., Brochstein J.A., Abboud M., et al. Effects of recombinant human granulocyte colony-stimulating factor on neutropenia in patients with congenital agranulocytosis. N Engl J Med 320 (1989) 1574-1580
-
(1989)
N Engl J Med
, vol.320
, pp. 1574-1580
-
-
Bonilla, M.1
Gillio, A.2
Ruggeiro, M.3
Kernan, N.A.4
Brochstein, J.A.5
Abboud, M.6
-
16
-
-
0027942372
-
Long-term safety of treatment with recombinant human granulocyte colony-stimulating factor (r-metHuG-CSF) in patients with severe congential neutropenias
-
Bonilla M., Dale D., Zeidler C., Last L., Reiter A., Ruggeiro M., et al. Long-term safety of treatment with recombinant human granulocyte colony-stimulating factor (r-metHuG-CSF) in patients with severe congential neutropenias. Br J Hematol 88 (1994) 723-730
-
(1994)
Br J Hematol
, vol.88
, pp. 723-730
-
-
Bonilla, M.1
Dale, D.2
Zeidler, C.3
Last, L.4
Reiter, A.5
Ruggeiro, M.6
-
17
-
-
19944430855
-
Analysis of risk factors for myelodysplasia/leukemia and infectious death among patients with congenital neutropenia: Experience of the French Severe Chronic Neutropenia Study Group
-
Donadieu J., Leblanc T., Meunier B.B., Barkaoui M., Fenneteau O., Bertrand Y., et al. Analysis of risk factors for myelodysplasia/leukemia and infectious death among patients with congenital neutropenia: Experience of the French Severe Chronic Neutropenia Study Group. Haematologica 90 (2005) 45-53
-
(2005)
Haematologica
, vol.90
, pp. 45-53
-
-
Donadieu, J.1
Leblanc, T.2
Meunier, B.B.3
Barkaoui, M.4
Fenneteau, O.5
Bertrand, Y.6
-
18
-
-
0027269718
-
A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (Filgrastim) for treatment of severe chronic neutropenia
-
Dale D., Bonilla M., Davis M., Nakanishi A.M., Hammond W.P., Kurtzberg J., et al. A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (Filgrastim) for treatment of severe chronic neutropenia. Blood 81 (1993) 2496-2502
-
(1993)
Blood
, vol.81
, pp. 2496-2502
-
-
Dale, D.1
Bonilla, M.2
Davis, M.3
Nakanishi, A.M.4
Hammond, W.P.5
Kurtzberg, J.6
-
19
-
-
0034086969
-
Management of Kostmann syndrome in the G-CSF era
-
Zeidler C., Boxer L., Dale D.C., Freedman M.H., Kinsey S., and Welte K. Management of Kostmann syndrome in the G-CSF era. Br J Haematol 109 (2000) 490-495
-
(2000)
Br J Haematol
, vol.109
, pp. 490-495
-
-
Zeidler, C.1
Boxer, L.2
Dale, D.C.3
Freedman, M.H.4
Kinsey, S.5
Welte, K.6
-
20
-
-
0025255616
-
Differential effects of granulocyte-macrophage colony-stimulating factor and granulocyte colony-stimulating factor in children with severe congenital neutropenia
-
Welte K., Zeidler C., Reiter A., Muller W., Odenwald E., Souza L., et al. Differential effects of granulocyte-macrophage colony-stimulating factor and granulocyte colony-stimulating factor in children with severe congenital neutropenia. Blood 75 (1990) 1056-1063
-
(1990)
Blood
, vol.75
, pp. 1056-1063
-
-
Welte, K.1
Zeidler, C.2
Reiter, A.3
Muller, W.4
Odenwald, E.5
Souza, L.6
-
21
-
-
4244209688
-
Beneficial effects of stem cell factor (SCF) in children with severe congenital neutropenias refractory to G-CSF
-
(abstr)
-
Zeidler C., Vogel R., Wyres M., and Welte K. Beneficial effects of stem cell factor (SCF) in children with severe congenital neutropenias refractory to G-CSF. Blood 92 (1998) 380a (abstr)
-
(1998)
Blood
, vol.92
-
-
Zeidler, C.1
Vogel, R.2
Wyres, M.3
Welte, K.4
-
22
-
-
0034651925
-
Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation
-
Zeidler C., Welte K., Barak Y., Barriga F., Bolyard A.A., Boxer L., et al. Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation. Blood 95 (2000) 1195-1198
-
(2000)
Blood
, vol.95
, pp. 1195-1198
-
-
Zeidler, C.1
Welte, K.2
Barak, Y.3
Barriga, F.4
Bolyard, A.A.5
Boxer, L.6
-
23
-
-
0014882993
-
Congenital agranulocytosis: Prolonged survival and terminal acute leukemia
-
Gilman P., Jackson D., and Guild H. Congenital agranulocytosis: Prolonged survival and terminal acute leukemia. Blood 36 (1970) 576-585
-
(1970)
Blood
, vol.36
, pp. 576-585
-
-
Gilman, P.1
Jackson, D.2
Guild, H.3
-
24
-
-
0018371661
-
Congenital agranulocytosis terminating in acute myelomonocytic leukemia
-
Rosen R., and Kang S. Congenital agranulocytosis terminating in acute myelomonocytic leukemia. J Pediatr 94 (1979) 406-408
-
(1979)
J Pediatr
, vol.94
, pp. 406-408
-
-
Rosen, R.1
Kang, S.2
-
25
-
-
33745096897
-
The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy
-
Rosenberg P.S., Alter B.P., Bolyard A.A., Bonilla M.A., Boxer L.A., Cham B., et al. The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy. Blood 107 (2005) 4628-4635
-
(2005)
Blood
, vol.107
, pp. 4628-4635
-
-
Rosenberg, P.S.1
Alter, B.P.2
Bolyard, A.A.3
Bonilla, M.A.4
Boxer, L.A.5
Cham, B.6
-
26
-
-
0022980521
-
Effect of human erythropoietin derived from recombinant DNA on the anemia of patients maintained by chronic haemodialysis
-
Winearls C.H., Oliver D.O., Pippard M.J., Reid C., Downing M.R., and Cotes P.M. Effect of human erythropoietin derived from recombinant DNA on the anemia of patients maintained by chronic haemodialysis. Lancet 2 (1986) 1175
-
(1986)
Lancet
, vol.2
, pp. 1175
-
-
Winearls, C.H.1
Oliver, D.O.2
Pippard, M.J.3
Reid, C.4
Downing, M.R.5
Cotes, P.M.6
-
27
-
-
0026448704
-
Serum immunoreactive erythropoietin in patients with idiopathic aplastic and Fanconi's anemias
-
Das R.E.G., Milne A., Rowley M., Smith E.C.G., and Cotes P.M. Serum immunoreactive erythropoietin in patients with idiopathic aplastic and Fanconi's anemias. Br J Haematol 82 (1992) 601
-
(1992)
Br J Haematol
, vol.82
, pp. 601
-
-
Das, R.E.G.1
Milne, A.2
Rowley, M.3
Smith, E.C.G.4
Cotes, P.M.5
-
28
-
-
0008952658
-
The erythrocyte-stimulating factor in serum and urine in congenital hypoplastic anemia
-
Hammond D., and Keighley G. The erythrocyte-stimulating factor in serum and urine in congenital hypoplastic anemia. Am J Dis Child 100 (1960) 466
-
(1960)
Am J Dis Child
, vol.100
, pp. 466
-
-
Hammond, D.1
Keighley, G.2
-
29
-
-
0032907438
-
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia
-
Draptchinskaia N., Gustavsson P., Andersson B., Pettersson M., Willig T.N., Dianzani I., et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat Genet 21 (1999) 169-175
-
(1999)
Nat Genet
, vol.21
, pp. 169-175
-
-
Draptchinskaia, N.1
Gustavsson, P.2
Andersson, B.3
Pettersson, M.4
Willig, T.N.5
Dianzani, I.6
-
30
-
-
33845303558
-
Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia
-
Gazda H.T., Grabowska A., Merida-Long L.B., Latawiec E., Schneider H.E., Lipton J.M., et al. Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia. Am J Hum Genet 79 (2006) 1110-1118
-
(2006)
Am J Hum Genet
, vol.79
, pp. 1110-1118
-
-
Gazda, H.T.1
Grabowska, A.2
Merida-Long, L.B.3
Latawiec, E.4
Schneider, H.E.5
Lipton, J.M.6
-
31
-
-
0026050010
-
Treatment trial with recombinant human erythropoietin in children with congenital hypoplastic anemia
-
Niemeyer C.M., Baumgarten E., Holldack J., Meier I., Trenn G., Jobke A., et al. Treatment trial with recombinant human erythropoietin in children with congenital hypoplastic anemia. Contrib Nephrol 88 (1991) 276-280
-
(1991)
Contrib Nephrol
, vol.88
, pp. 276-280
-
-
Niemeyer, C.M.1
Baumgarten, E.2
Holldack, J.3
Meier, I.4
Trenn, G.5
Jobke, A.6
-
32
-
-
0026075449
-
Treatment of Diamond-Blasckfan anemia with hematopoiesis growth factors, granulocyte-macrophage colony-stimulating factor and interleukin-3: Sustained remission following IL-3
-
Dunbar C.E., Smith D.A., Kimball J., Garrison J., Nienhues A.W., and Young N.S. Treatment of Diamond-Blasckfan anemia with hematopoiesis growth factors, granulocyte-macrophage colony-stimulating factor and interleukin-3: Sustained remission following IL-3. Br J Haematol 79 (1991) 316-321
-
(1991)
Br J Haematol
, vol.79
, pp. 316-321
-
-
Dunbar, C.E.1
Smith, D.A.2
Kimball, J.3
Garrison, J.4
Nienhues, A.W.5
Young, N.S.6
-
33
-
-
0027185538
-
Treatment of Diamond-Blackfan anemia with recombinant human interleukin-3
-
Gillio A.P., Faulkner L.B., Alter B.P., Reilly L., Klafter R., Heller G., et al. Treatment of Diamond-Blackfan anemia with recombinant human interleukin-3. Blood 82 (1993) 744-751
-
(1993)
Blood
, vol.82
, pp. 744-751
-
-
Gillio, A.P.1
Faulkner, L.B.2
Alter, B.P.3
Reilly, L.4
Klafter, R.5
Heller, G.6
-
34
-
-
0028354627
-
Failure of recombinant human interleukin-3 therapy to induce erythropoiesis in patients with refractory Diamond-Blackfan anemia
-
Olivieri F., Feig S.A., Valentino L., Berriman A.M., Shore R., and Freedman M.H. Failure of recombinant human interleukin-3 therapy to induce erythropoiesis in patients with refractory Diamond-Blackfan anemia. Blood 83 (1994) 2444-2450
-
(1994)
Blood
, vol.83
, pp. 2444-2450
-
-
Olivieri, F.1
Feig, S.A.2
Valentino, L.3
Berriman, A.M.4
Shore, R.5
Freedman, M.H.6
-
35
-
-
0032965427
-
No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type I
-
Tamary H., Shalev H., Pinsk V., Zoldan M., and Zaizov R. No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type I. Pediatr Hematol Oncol 16 (1999) 165-168
-
(1999)
Pediatr Hematol Oncol
, vol.16
, pp. 165-168
-
-
Tamary, H.1
Shalev, H.2
Pinsk, V.3
Zoldan, M.4
Zaizov, R.5
-
36
-
-
30144440213
-
Congenital dyserythropoietic anemia type I (CDA I): Molecular genetics, clinical appearance, and prognosis based on long-term observation
-
Heimpel H., Schwarz K., Ebnöther M., Goede J.S., Heydrich D., Kamp T., et al. Congenital dyserythropoietic anemia type I (CDA I): Molecular genetics, clinical appearance, and prognosis based on long-term observation. Blood 107 (2006) 334-340
-
(2006)
Blood
, vol.107
, pp. 334-340
-
-
Heimpel, H.1
Schwarz, K.2
Ebnöther, M.3
Goede, J.S.4
Heydrich, D.5
Kamp, T.6
-
37
-
-
33745496802
-
Inherited thrombocytopenia: Congenital amegakaryocytic thrombocytopenia and thrombocytopenia with absent radii
-
Geddis A.E. Inherited thrombocytopenia: Congenital amegakaryocytic thrombocytopenia and thrombocytopenia with absent radii. Semin Hematol 43 (2006) 196-203
-
(2006)
Semin Hematol
, vol.43
, pp. 196-203
-
-
Geddis, A.E.1
-
38
-
-
33644795087
-
Congenital amegakaryocytic thrombocytopenia: A retrospective clinical analysis of 20 patients
-
King S., Germeshausen M., Strauss G., Welte K., and Ballmaier M. Congenital amegakaryocytic thrombocytopenia: A retrospective clinical analysis of 20 patients. Br J Haematol 131 (2005) 636-644
-
(2005)
Br J Haematol
, vol.131
, pp. 636-644
-
-
King, S.1
Germeshausen, M.2
Strauss, G.3
Welte, K.4
Ballmaier, M.5
-
39
-
-
33745693042
-
c-mpl mutations in 23 patients suffering from congenital amegakaryocytic thrombocytopenia: the type of mutation predicts the course of the disease
-
Germeshausen M., Ballmaier M., and Welte K. c-mpl mutations in 23 patients suffering from congenital amegakaryocytic thrombocytopenia: the type of mutation predicts the course of the disease. Hum Mut 27 (2006) 296
-
(2006)
Hum Mut
, vol.27
, pp. 296
-
-
Germeshausen, M.1
Ballmaier, M.2
Welte, K.3
-
40
-
-
22044440491
-
Thrombopoietin regulates differentiation of Rhesus monkey embryonic stem cells to hematopoietic cells
-
Wang Z., Skokowa J., Pramono A., Ballmaier M., and Welte K. Thrombopoietin regulates differentiation of Rhesus monkey embryonic stem cells to hematopoietic cells. Ann N Y Acad Sci 1044 (2005) 29-40
-
(2005)
Ann N Y Acad Sci
, vol.1044
, pp. 29-40
-
-
Wang, Z.1
Skokowa, J.2
Pramono, A.3
Ballmaier, M.4
Welte, K.5
-
41
-
-
0037441757
-
A 20-year perspective on the International Fanconi Anemia Registry (IFAR)
-
Kutler D.I., Singh B., and Satagopan J. A 20-year perspective on the International Fanconi Anemia Registry (IFAR). Blood 101 (2003) 1249-1256
-
(2003)
Blood
, vol.101
, pp. 1249-1256
-
-
Kutler, D.I.1
Singh, B.2
Satagopan, J.3
-
42
-
-
0028125830
-
Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with fanconi anemia
-
Guinan E.C., Lopez K.D., Huhn R.D., Felser J.M., and Nathan D.G. Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with fanconi anemia. J Pediatr 124 (1994) 144-150
-
(1994)
J Pediatr
, vol.124
, pp. 144-150
-
-
Guinan, E.C.1
Lopez, K.D.2
Huhn, R.D.3
Felser, J.M.4
Nathan, D.G.5
-
43
-
-
0029844796
-
Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to patients with Fanconi anemia: A pilot study
-
Rackoff W.R., Orazi A., Robinson C.A., Cooper R.J., Alter B.P., Freedman M.H., et al. Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to patients with Fanconi anemia: A pilot study. Blood 88 (1996) 1588-1593
-
(1996)
Blood
, vol.88
, pp. 1588-1593
-
-
Rackoff, W.R.1
Orazi, A.2
Robinson, C.A.3
Cooper, R.J.4
Alter, B.P.5
Freedman, M.H.6
-
44
-
-
0031862437
-
Use of recombinant granulocyte colony-stimulating factor in Fanconi's anemia
-
Scagni P., Saracco P., Timeus F., Farinasso L., Dall'Aglio M., Bosa E.M., et al. Use of recombinant granulocyte colony-stimulating factor in Fanconi's anemia. Haematologica 83 (1998) 432-437
-
(1998)
Haematologica
, vol.83
, pp. 432-437
-
-
Scagni, P.1
Saracco, P.2
Timeus, F.3
Farinasso, L.4
Dall'Aglio, M.5
Bosa, E.M.6
-
45
-
-
0035892134
-
Mobilization and collection of peripheral blood CD34+ cells from patients with Fanconi anemia
-
Croop J.M., Cooper R., Fernandez C., Graves V., Kreissman S., Hanenberg H., et al. Mobilization and collection of peripheral blood CD34+ cells from patients with Fanconi anemia. Blood 98 (2001) 2917-2921
-
(2001)
Blood
, vol.98
, pp. 2917-2921
-
-
Croop, J.M.1
Cooper, R.2
Fernandez, C.3
Graves, V.4
Kreissman, S.5
Hanenberg, H.6
-
46
-
-
33845475198
-
Continuous in vivo infusion of interferon-gamma (IFN-gamma) enhances engraftment of syngeneic wild-type cells in Fanca-/-and Fancg-/- mice
-
Si Y., Ciccone S., Yang F.C., Yuan J., Zeng D., Chen S., et al. Continuous in vivo infusion of interferon-gamma (IFN-gamma) enhances engraftment of syngeneic wild-type cells in Fanca-/-and Fancg-/- mice. Blood 108 (2006) 4283-4287
-
(2006)
Blood
, vol.108
, pp. 4283-4287
-
-
Si, Y.1
Ciccone, S.2
Yang, F.C.3
Yuan, J.4
Zeng, D.5
Chen, S.6
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