-
1
-
-
0030280090
-
Juvenile myelomonocytic leukemia: Molecular understanding and prospects for therapy
-
Emanuel PD, Shannon KM, Castleberry RP. Juvenile myelomonocytic leukemia: molecular understanding and prospects for therapy. Mol Med Today. 1996;2:468-475.
-
(1996)
Mol Med Today
, vol.2
, pp. 468-475
-
-
Emanuel, P.D.1
Shannon, K.M.2
Castleberry, R.P.3
-
2
-
-
0030843626
-
Juvenile myelomonocytic leukemia
-
Arico M, Biondi A, Pui C-H. Juvenile myelomonocytic leukemia. Blood. 1997;90:479-488.
-
(1997)
Blood
, vol.90
, pp. 479-488
-
-
Arico, M.1
Biondi, A.2
Pui, C.-H.3
-
3
-
-
0026063878
-
Selective hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors
-
Emanuel PD, Bates LJ, Castleberry RP, Gualtieri RJ, Zuckerman KS. Selective hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors. Blood. 1991;77:925-929.
-
(1991)
Blood
, vol.77
, pp. 925-929
-
-
Emanuel, P.D.1
Bates, L.J.2
Castleberry, R.P.3
Gualtieri, R.J.4
Zuckerman, K.S.5
-
4
-
-
0028344097
-
Mutations of the N-ras gene in juvenile chronic myelogenous leukemia
-
Miyauchi J, Asada M, Sasaki M,Tsunematsu Y, Kojima S, Mizutani S. Mutations of the N-ras gene in juvenile chronic myelogenous leukemia. Blood. 1994;83:2248-2254.
-
(1994)
Blood
, vol.83
, pp. 2248-2254
-
-
Miyauchi, J.1
Asada, M.2
Sasaki, M.3
Tsunematsu, Y.4
Kojima, S.5
Mizutani, S.6
-
6
-
-
0017880413
-
Neurofibromatosis and childhood leukemia
-
Bader JL, Miller RW. Neurofibromatosis and childhood leukemia. J Pediatr. 1978;92:925-929.
-
(1978)
J Pediatr
, vol.92
, pp. 925-929
-
-
Bader, J.L.1
Miller, R.W.2
-
7
-
-
0027974256
-
Neurofibromatosis and childhood leukemia/lymphoma: A population-based UKCCSG study
-
Stiller CA, Chessells JM, Fitchett M. Neurofibromatosis and childhood leukemia/lymphoma: a population-based UKCCSG study. Br J Cancer. 1994;70:969-972.
-
(1994)
Br J Cancer
, vol.70
, pp. 969-972
-
-
Stiller, C.A.1
Chessells, J.M.2
Fitchett, M.3
-
8
-
-
0027732538
-
Proteins regulating Ras and its relatives
-
Boguski M, McCormick F. Proteins regulating Ras and its relatives. Nature. 1993;366:643-653.
-
(1993)
Nature
, vol.366
, pp. 643-653
-
-
Boguski, M.1
McCormick, F.2
-
9
-
-
0347725620
-
Hyperactivation of protein kinase B and ERK have discrete effects on survival, proliferation, and cytokine expression in Nf1-deficient myeloid cells
-
Donovan S, See W, Bonifas J, Stockoe D, Shannon KM. Hyperactivation of protein kinase B and ERK have discrete effects on survival, proliferation, and cytokine expression in Nf1-deficient myeloid cells. Cancer Cell. 2002;2:507-514.
-
(2002)
Cancer Cell
, vol.2
, pp. 507-514
-
-
Donovan, S.1
See, W.2
Bonifas, J.3
Stockoe, D.4
Shannon, K.M.5
-
10
-
-
0027979146
-
Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders
-
Shannon KM, O'Connell P, Martin GA, et al. Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders. N Engl J Med. 1994;330:597-601.
-
(1994)
N Engl J Med
, vol.330
, pp. 597-601
-
-
Shannon, K.M.1
O'Connell, P.2
Martin, G.A.3
-
11
-
-
9044251606
-
Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in murine and human hematopoietic cells
-
Bollag G, Clapp DW, Shih S, et al. Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in murine and human hematopoietic cells. Nat Genet. 1996;12:144-148.
-
(1996)
Nat Genet
, vol.12
, pp. 144-148
-
-
Bollag, G.1
Clapp, D.W.2
Shih, S.3
-
12
-
-
0030947237
-
Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders
-
Side L, Taylor B, Cayouette M, et al. Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders. N Engl J Med. 1997;336:1713-1720.
-
(1997)
N Engl J Med
, vol.336
, pp. 1713-1720
-
-
Side, L.1
Taylor, B.2
Cayouette, M.3
-
13
-
-
0032125716
-
Mutations of the NF1 gene in children with juvenile myelomonocytic leukemia without evidence of neurofibromatosis, type 1
-
Side L, Emanuel P, Taylor B, et al. Mutations of the NF1 gene in children with juvenile myelomonocytic leukemia without evidence of neurofibromatosis, type 1. Blood. 1998;92:267-272.
-
(1998)
Blood
, vol.92
, pp. 267-272
-
-
Side, L.1
Emanuel, P.2
Taylor, B.3
-
14
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M, Mehler EL, Goldberg R, et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet. 2001;29:465-468.
-
(2001)
Nat Genet
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
-
15
-
-
18344370436
-
PTPN11 mutations in Noonan syndrome: Molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity
-
Tartaglia M, Kalidas K, Shaw A, et al. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet. 2002;70:1555-1563.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1555-1563
-
-
Tartaglia, M.1
Kalidas, K.2
Shaw, A.3
-
16
-
-
0032521428
-
Revealing mechanisms for SH2 domain mediated regulation of the protein tyrosine phosphatase SHP-2
-
Barford D, Neel BG. Revealing mechanisms for SH2 domain mediated regulation of the protein tyrosine phosphatase SHP-2. Structure. 1998;6:249-254.
-
(1998)
Structure
, vol.6
, pp. 249-254
-
-
Barford, D.1
Neel, B.G.2
-
17
-
-
0038771965
-
The 'Shp'ing news: SH2 domain-containing tyrosine phosphatases in cell signaling
-
Neel BG, Gu H, Pao L. The 'Shp'ing news: SH2 domain-containing tyrosine phosphatases in cell signaling. Trends Biochem Sci. 2003;28:284-293.
-
(2003)
Trends Biochem Sci
, vol.28
, pp. 284-293
-
-
Neel, B.G.1
Gu, H.2
Pao, L.3
-
18
-
-
0032548830
-
Crystal structure of the tyrosine phosphatase SHP-2
-
Hof P, Pluskey S, Dhe-Paganon S, Eck MJ, Shoelson SE. Crystal structure of the tyrosine phosphatase SHP-2. Cell. 1998;92:441-450.
-
(1998)
Cell
, vol.92
, pp. 441-450
-
-
Hof, P.1
Pluskey, S.2
Dhe-Paganon, S.3
Eck, M.J.4
Shoelson, S.E.5
-
20
-
-
0033604644
-
Shp-2 tyrosine phosphatase: Signaling one cell or many
-
Feng GS. Shp-2 tyrosine phosphatase: signaling one cell or many. Exp Cell Res. 1999;253:47-54.
-
(1999)
Exp Cell Res
, vol.253
, pp. 47-54
-
-
Feng, G.S.1
-
21
-
-
0031931409
-
Definition of the role of tyrosine residues of the common beta subunit regulating multiple signaling pathways of granulocyte-macrophage colony-stimulating factor receptor
-
Itoh T, Liu R, Yokota T, Arai KI, Watanabe S. Definition of the role of tyrosine residues of the common beta subunit regulating multiple signaling pathways of granulocyte-macrophage colony-stimulating factor receptor. Mol Cell Biol. 1998;18:742-752.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 742-752
-
-
Itoh, T.1
Liu, R.2
Yokota, T.3
Arai, K.I.4
Watanabe, S.5
-
22
-
-
0032985421
-
Differential influence of tyrosine residues of the common receptor beta subunit on multiple signals induced by human GM-CSF
-
Itoh T, Liu R, Arai K, Watanabe S. Differential influence of tyrosine residues of the common receptor beta subunit on multiple signals induced by human GM-CSF. J Allergy Clin Immunol. 1999;103:S462-S470.
-
(1999)
J Allergy Clin Immunol
, vol.103
-
-
Itoh, T.1
Liu, R.2
Arai, K.3
Watanabe, S.4
-
23
-
-
0034091647
-
Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesis
-
Chen B, Bronson RT, Klaman LD, et al. Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesis. Nat Genet. 2000;24:296-299.
-
(2000)
Nat Genet
, vol.24
, pp. 296-299
-
-
Chen, B.1
Bronson, R.T.2
Klaman, L.D.3
-
24
-
-
0030797548
-
A deletion mutation in the SH2-N domain of Shp-2 severely suppresses hematopoietic cell development
-
Qu CK, Shi ZQ, Shen R, Tsai FY, Orkin SH, Feng GS. A deletion mutation in the SH2-N domain of Shp-2 severely suppresses hematopoietic cell development. Mol Cell Biol. 1997;17:5499-5507.
-
(1997)
Mol Cell Biol
, vol.17
, pp. 5499-5507
-
-
Qu, C.K.1
Shi, Z.Q.2
Shen, R.3
Tsai, F.Y.4
Orkin, S.H.5
Feng, G.S.6
-
25
-
-
0031708674
-
Biased suppression of hematopoiesis and multiple developmental defects in chimeric mice containing Shp-2 mutant cells
-
Qu CK, Yu WM, Azzarelli B, Cooper S, Broxmeyer HE, Feng GS. Biased suppression of hematopoiesis and multiple developmental defects in chimeric mice containing Shp-2 mutant cells. Mol Cell Biol. 1998;18:6075-6082.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 6075-6082
-
-
Qu, C.K.1
Yu, W.M.2
Azzarelli, B.3
Cooper, S.4
Broxmeyer, H.E.5
Feng, G.S.6
-
26
-
-
0035865690
-
Requirement of Shp-2 tyrosine phosphatase in lymphoid and hematopoietic cell development
-
Qu CK, Nguyen S, Chen J, Feng GS. Requirement of Shp-2 tyrosine phosphatase in lymphoid and hematopoietic cell development. Blood. 2001;97:911-914.
-
(2001)
Blood
, vol.97
, pp. 911-914
-
-
Qu, C.K.1
Nguyen, S.2
Chen, J.3
Feng, G.S.4
-
27
-
-
0037064549
-
Role of the SHP-2 tyrosine phosphatase in cytokine-induced signaling and cellular response
-
Qu CK. Role of the SHP-2 tyrosine phosphatase in cytokine-induced signaling and cellular response. Biochim Biophys Acta. 2002;1592:297-301.
-
(2002)
Biochim Biophys Acta
, vol.1592
, pp. 297-301
-
-
Qu, C.K.1
-
28
-
-
0030712155
-
Occurrence of myeloproliferative disorder in patients with the Noonan syndrome
-
Bader-Meunier B, Tchernia G, Miélot F, et al. Occurrence of myeloproliferative disorder in patients with the Noonan syndrome. J Pediatr. 1997;130:885-889.
-
(1997)
J Pediatr
, vol.130
, pp. 885-889
-
-
Bader-Meunier, B.1
Tchernia, G.2
Miélot, F.3
-
29
-
-
0033504544
-
Juvenile myelomonocytic leukemia and Noonan syndrome
-
Choong K, Freedman MH, Chitayat D, Kelly EN, Taylor G, Zipursky A. Juvenile myelomonocytic leukemia and Noonan syndrome. J Pediatr Hematol Oncol. 1999;21:523-527.
-
(1999)
J Pediatr Hematol Oncol
, vol.21
, pp. 523-527
-
-
Choong, K.1
Freedman, M.H.2
Chitayat, D.3
Kelly, E.N.4
Taylor, G.5
Zipursky, A.6
-
30
-
-
0030665934
-
Myeloid disorders in infants with Noonan syndrome and a resident's "rule" recalled
-
Side LE, Shannon KM. Myeloid disorders in infants with Noonan syndrome and a resident's "rule" recalled. J Pediatr. 1997;130:857-859.
-
(1997)
J Pediatr
, vol.130
, pp. 857-859
-
-
Side, L.E.1
Shannon, K.M.2
-
31
-
-
0038278866
-
Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia
-
Tartaglia M, Niemeyer CM, Fragale A, et al. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia. Nat Genet. 2003;34:148-150.
-
(2003)
Nat Genet
, vol.34
, pp. 148-150
-
-
Tartaglia, M.1
Niemeyer, C.M.2
Fragale, A.3
-
32
-
-
0034999807
-
Denaturing high-performance liquid chromatography: A review
-
Xiao W, Oefner PJ. Denaturing high-performance liquid chromatography: a review. Hum Mutat. 2001;17:439-474.
-
(2001)
Hum Mutat
, vol.17
, pp. 439-474
-
-
Xiao, W.1
Oefner, P.J.2
-
33
-
-
0028385758
-
Versatile retroviral vectors for potential use in gene therapy
-
Hawley RG, Lieu FH, Fong AZ, Hawley TS. Versatile retroviral vectors for potential use in gene therapy. Gene Ther. 1994;1:136-138.
-
(1994)
Gene Ther
, vol.1
, pp. 136-138
-
-
Hawley, R.G.1
Lieu, F.H.2
Fong, A.Z.3
Hawley, T.S.4
-
34
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, et al. Mutations of the BRAF gene in human cancer. Nature. 2002;417:949-954.
-
(2002)
Nature
, vol.417
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
-
35
-
-
0028082464
-
Deletions spanning the neurofibromatosis 1 gene: Identification and phenotype of five patients
-
Kayes LM, Burke W, Riccardi VM, et al. Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients. Am J Hum Genet. 1994;54:424-436.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 424-436
-
-
Kayes, L.M.1
Burke, W.2
Riccardi, V.M.3
-
36
-
-
0036340975
-
PTPN11 mutations in LEOPARD syndrome
-
Legius E, Schrander-Stumpel C, Schollen E, Pulles-Heintzberger C, Gewillig M, Fryns JP. PTPN11 mutations in LEOPARD syndrome. J Med Genet. 2002;39:571-574.
-
(2002)
J Med Genet
, vol.39
, pp. 571-574
-
-
Legius, E.1
Schrander-Stumpel, C.2
Schollen, E.3
Pulles-Heintzberger, C.4
Gewillig, M.5
Fryns, J.P.6
-
37
-
-
0028351698
-
Chronic myelomonocytic leukemia: Tel-a-kinase what Ets all about
-
Sawyers CL, Denny CT. Chronic myelomonocytic leukemia: Tel-a-kinase what Ets all about. Cell. 1994;77:171-173.
-
(1994)
Cell
, vol.77
, pp. 171-173
-
-
Sawyers, C.L.1
Denny, C.T.2
-
38
-
-
0033614446
-
Chronic myeloid leukemia
-
Sawyers CL. Chronic myeloid leukemia. N Engl J Med. 1999;340:1330-1340.
-
(1999)
N Engl J Med
, vol.340
, pp. 1330-1340
-
-
Sawyers, C.L.1
-
39
-
-
0026101050
-
Mutations of the ras proto-oncogenes in childhood monosomy 7
-
Neubauer A, Shannon KM, Liu E. Mutations of the ras proto-oncogenes in childhood monosomy 7. Blood. 1991;77:594-598.
-
(1991)
Blood
, vol.77
, pp. 594-598
-
-
Neubauer, A.1
Shannon, K.M.2
Liu, E.3
-
40
-
-
0028210052
-
Mutations in the Ras proto-oncogenes in patients with myelodysplastic syndromes
-
Neubauer A, Greenberg P, Negrin R, Ginzton N, Liu ET. Mutations in the Ras proto-oncogenes in patients with myelodysplastic syndromes. Leukemia. 1994;8:638-641.
-
(1994)
Leukemia
, vol.8
, pp. 638-641
-
-
Neubauer, A.1
Greenberg, P.2
Negrin, R.3
Ginzton, N.4
Liu, E.T.5
-
41
-
-
0026502986
-
Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: Epidemiology and molecular analysis
-
Shannon KM, Watterson J, Johnson P, et al. Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis. Blood. 1992;79:1311-1318.
-
(1992)
Blood
, vol.79
, pp. 1311-1318
-
-
Shannon, K.M.1
Watterson, J.2
Johnson, P.3
-
42
-
-
0024538098
-
Chromosome patterns in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis
-
Kaneko Y, Maseki N, Sakuri M, et al. Chromosome patterns in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis. Leukemia. 1989;3:36-41.
-
(1989)
Leukemia
, vol.3
, pp. 36-41
-
-
Kaneko, Y.1
Maseki, N.2
Sakuri, M.3
-
43
-
-
0028783986
-
Possible coexistence of RAS activation and monosomy 7 in the leukaemic transformation of myelodysplastic syndromes
-
Stephenson J, Lizhen H, Mufti GJ. Possible coexistence of RAS activation and monosomy 7 in the leukaemic transformation of myelodysplastic syndromes. Leuk Res. 1995;19:741-748.
-
(1995)
Leuk Res
, vol.19
, pp. 741-748
-
-
Stephenson, J.1
Lizhen, H.2
Mufti, G.J.3
-
44
-
-
0030974476
-
Characterization of two SHP-2-associated binding proteins and potential substrates in hematopoietic cells
-
Gu H, Griffin JD, Neel BG. Characterization of two SHP-2-associated binding proteins and potential substrates in hematopoietic cells. J Biol Chem. 1997;272:16421-16430.
-
(1997)
J Biol Chem
, vol.272
, pp. 16421-16430
-
-
Gu, H.1
Griffin, J.D.2
Neel, B.G.3
-
45
-
-
0033826512
-
New role for Shc in activation of the phosphatidylinositol 3-kinase/Akt pathway
-
Gu H, Maeda H, Moon JJ, et al. New role for Shc in activation of the phosphatidylinositol 3-kinase/Akt pathway. Mol Cell Biol. 2000;20:7109-7120.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 7109-7120
-
-
Gu, H.1
Maeda, H.2
Moon, J.J.3
-
46
-
-
0036156348
-
Molecular interactions of SHP1 and SHP2 in IL-3-signalling
-
Wheadon H, Paling NR, Welham MJ. Molecular interactions of SHP1 and SHP2 in IL-3-signalling. Cell Signal. 2002;14:219-229.
-
(2002)
Cell Signal
, vol.14
, pp. 219-229
-
-
Wheadon, H.1
Paling, N.R.2
Welham, M.J.3
-
47
-
-
0029759926
-
Reversal of apoptosis by the leukaemia-associated E2A-HLF chimaeric transcription factor
-
Inaba T, Inukai T, Yoshihara T, et al. Reversal of apoptosis by the leukaemia-associated E2A-HLF chimaeric transcription factor. Nature. 1996;382:541-544.
-
(1996)
Nature
, vol.382
, pp. 541-544
-
-
Inaba, T.1
Inukai, T.2
Yoshihara, T.3
-
48
-
-
0034678609
-
Signal transduction and transforming properties of the TELTRKC fusions associated with t(12;15)(p13;q25) in congenital fibrosarcoma and acute myelogenous leukemia
-
Liu Q, Schwaller J, Kutok J, et al. Signal transduction and transforming properties of the TELTRKC fusions associated with t(12;15)(p13;q25) in congenital fibrosarcoma and acute myelogenous leukemia. EMBO J. 2000;19:1827-1838.
-
(2000)
EMBO J
, vol.19
, pp. 1827-1838
-
-
Liu, Q.1
Schwaller, J.2
Kutok, J.3
-
49
-
-
0013102301
-
CT53518, a novel selective FLT3 antagonist for the treatment of acute myelogenous leukemia (AML)
-
Kelly LM, Yu JC, Boulton CL, et al. CT53518, a novel selective FLT3 antagonist for the treatment of acute myelogenous leukemia (AML). Cancer Cell. 2002;1:421-432.
-
(2002)
Cancer Cell
, vol.1
, pp. 421-432
-
-
Kelly, L.M.1
Yu, J.C.2
Boulton, C.L.3
-
50
-
-
0142119964
-
PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRalpha-induced myeloproliferative disease
-
Cools J, Stover EH, Boulton CL, et al. PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRalpha-induced myeloproliferative disease. Cancer Cell. 2003;3:459-469.
-
(2003)
Cancer Cell
, vol.3
, pp. 459-469
-
-
Cools, J.1
Stover, E.H.2
Boulton, C.L.3
-
51
-
-
0036799356
-
Inhibition of the transforming activity of FLT3 internal tandem duplication mutants from AML patients by a tyrosine kinase inhibitor
-
Tse KF, Allebach J, Levis M, Smith BD, Bohmer FD, Small D. Inhibition of the transforming activity of FLT3 internal tandem duplication mutants from AML patients by a tyrosine kinase inhibitor. Leukemia. 2002;16:2027-2036.
-
(2002)
Leukemia
, vol.16
, pp. 2027-2036
-
-
Tse, K.F.1
Allebach, J.2
Levis, M.3
Smith, B.D.4
Bohmer, F.D.5
Small, D.6
-
52
-
-
0033989423
-
Activated mutants of SHP-2 preferentially induce elongation of Xenopus animal caps
-
O'Reilly AM, Pluskey S, Shoelson SE, Neel BG. Activated mutants of SHP-2 preferentially induce elongation of Xenopus animal caps. Mol Cell Biol. 2000;20:299-311.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 299-311
-
-
O'Reilly, A.M.1
Pluskey, S.2
Shoelson, S.E.3
Neel, B.G.4
-
53
-
-
0347725620
-
Hyperactivation of protein kinase B and ERK have discrete effects on survival, proliferation, and cytokine expression in Nf1-deficient myeloid cells
-
Donovan S, See W, Bonifas J, Stokoe D, Shannon KM. Hyperactivation of protein kinase B and ERK have discrete effects on survival, proliferation, and cytokine expression in Nf1-deficient myeloid cells. Cancer Cell. 2002;2:507-514.
-
(2002)
Cancer Cell
, vol.2
, pp. 507-514
-
-
Donovan, S.1
See, W.2
Bonifas, J.3
Stokoe, D.4
Shannon, K.M.5
-
54
-
-
0032238275
-
Opposing actions of CSW and RasGAP modulate the strength of Torso RTK signaling in the Drosophila terminal pathway
-
Cleghon V, Feldmann P, Ghiglione C, et al. Opposing actions of CSW and RasGAP modulate the strength of Torso RTK signaling in the Drosophila terminal pathway. Mol Cell. 1998;2:719-727.
-
(1998)
Mol Cell
, vol.2
, pp. 719-727
-
-
Cleghon, V.1
Feldmann, P.2
Ghiglione, C.3
-
55
-
-
0032238298
-
Cloning of p97/Gab2, the major SHP2-binding protein in hematopoietic cells, reveals a novel pathway for cytokine-induced gene activation
-
Gu H, Pratt JC, Burakoff SJ, Neel BG. Cloning of p97/Gab2, the major SHP2-binding protein in hematopoietic cells, reveals a novel pathway for cytokine-induced gene activation. Mol Cell. 1998;2:729-740.
-
(1998)
Mol Cell
, vol.2
, pp. 729-740
-
-
Gu, H.1
Pratt, J.C.2
Burakoff, S.J.3
Neel, B.G.4
-
56
-
-
0030045594
-
Nfl deficiency causes Ras-mediated granulocyte-macrophage colony stimulating factor hypersensitivity and chronic myeloid leukemia
-
Largaespada DA, Brannan CI, Jenkins NA, Copeland NG. Nfl deficiency causes Ras-mediated granulocyte-macrophage colony stimulating factor hypersensitivity and chronic myeloid leukemia. Nat Genet. 1996;12:137-143.
-
(1996)
Nat Genet
, vol.12
, pp. 137-143
-
-
Largaespada, D.A.1
Brannan, C.I.2
Jenkins, N.A.3
Copeland, N.G.4
-
57
-
-
0033982718
-
Nf1 and Gmcsf interact in myeloid leukemogenesis
-
Birnbaum RA, O'Marcaigh A, Wardak Z, et al. Nf1 and Gmcsf interact in myeloid leukemogenesis. Mol Cell. 2000;5:189-195.
-
(2000)
Mol Cell
, vol.5
, pp. 189-195
-
-
Birnbaum, R.A.1
O'Marcaigh, A.2
Wardak, Z.3
|