-
1
-
-
0028910402
-
Childhood monosomy 7: Epidemiology, biology and mechanistic implications
-
Luna-Fineman S, Shannon K, Lange BJ: Childhood monosomy 7: Epidemiology, biology and mechanistic implications. Blood 85:1985, 1995
-
(1995)
Blood
, vol.85
, pp. 1985
-
-
Luna-Fineman, S.1
Shannon, K.2
Lange, B.J.3
-
2
-
-
9044248952
-
Myelodysplastic syndromes in childhood: Report of 49 patients from a French multicentre study
-
Bader-Meunier B, Mielot F, Tchernia G, Buisine J, Delsol G, Duchayne E, Lemerle S, Leverger G, de Lumley L, Manel A-M, Nathanson M, Plantaz D, Robert A, Schaison G, Sommelet D, Vilmer E: Myelodysplastic syndromes in childhood: Report of 49 patients from a French multicentre study. Br J Haematol 92:344, 1996
-
(1996)
Br J Haematol
, vol.92
, pp. 344
-
-
Bader-Meunier, B.1
Mielot, F.2
Tchernia, G.3
Buisine, J.4
Delsol, G.5
Duchayne, E.6
Lemerle, S.7
Leverger, G.8
De Lumley, L.9
Manel, A.-M.10
Nathanson, M.11
Plantaz, D.12
Robert, A.13
Schaison, G.14
Sommelet, D.15
Vilmer, E.16
-
3
-
-
0028967873
-
Pediatric myelodysplasia: A study of 68 children and anew prognostic scoring system
-
Passmore SJ, Hann IM, Stiller CA, Ramani P, Swansbury GJ, Gibbons B, Reeves B, Chessells J: Pediatric myelodysplasia: A study of 68 children and anew prognostic scoring system. Blood 85:1743, 1995
-
(1995)
Blood
, vol.85
, pp. 1743
-
-
Passmore, S.J.1
Hann, I.M.2
Stiller, C.A.3
Ramani, P.4
Swansbury, G.J.5
Gibbons, B.6
Reeves, B.7
Chessells, J.8
-
4
-
-
0030843626
-
Juvenile myelomonocytic leukemia
-
Arico M, Biondi A, Pui C-H: Juvenile myelomonocytic leukemia. Blood 90:479, 1997
-
(1997)
Blood
, vol.90
, pp. 479
-
-
Arico, M.1
Biondi, A.2
Pui, C.-H.3
-
5
-
-
0026668362
-
Experience in pediatric myelodysplastic syndromes
-
Gadner H, Haas OA: Experience in pediatric myelodysplastic syndromes. Hematol Oncol Clin North Am 6:655, 1992
-
(1992)
Hematol Oncol Clin North Am
, vol.6
, pp. 655
-
-
Gadner, H.1
Haas, O.A.2
-
6
-
-
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 2:468475, 1996
-
(1996)
Mol Med Today
, vol.2
, pp. 468475
-
-
Emanuel, P.D.1
Shannon, K.M.2
Castleberry, R.P.3
-
7
-
-
0030977399
-
Chronic myelomonocytic leukemia in childhood: A retrospective analysis of 110 cases
-
Niemeyer C, Arico M, Basso G, Biondi A, Cantu Rajnoldi A, Creutzig U, Haas O, Harbott J, Hasle H, Kerndrup G, Locatelli F, Mann G, Stollmann-Gibbels B, van't Veer-Korthof ETh, van Wering E, Zimmermann M: Chronic myelomonocytic leukemia in childhood: A retrospective analysis of 110 cases. Blood 89:3534, 1997
-
(1997)
Blood
, vol.89
, pp. 3534
-
-
Niemeyer, C.1
Arico, M.2
Basso, G.3
Biondi, A.4
Cantu Rajnoldi, A.5
Creutzig, U.6
Haas, O.7
Harbott, J.8
Hasle, H.9
Kerndrup, G.10
Locatelli, F.11
Mann, G.12
Stollmann-Gibbels, B.13
Van't Veer-Korthof, E.Th.14
Van Wering, E.15
Zimmermann, M.16
-
9
-
-
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 70:969, 1994
-
(1994)
Br J Cancer
, vol.70
, pp. 969
-
-
Stiller, C.A.1
Chessells, J.M.2
Fitchett, M.3
-
10
-
-
0021233189
-
Subacute and chronic myelomonocytic leukemia in children (Juvenile CML)
-
Caitro-Malaspina H, Schaison G, Passe S, Pasquier A, Berger R, Bayle-Weisgerber C, Miller D, Seligmann M, Bernard J: Subacute and chronic myelomonocytic leukemia in children (Juvenile CML). Cancer 54:675, 1984
-
(1984)
Cancer
, vol.54
, pp. 675
-
-
Caitro-Malaspina, H.1
Schaison, G.2
Passe, S.3
Pasquier, A.4
Berger, R.5
Bayle-Weisgerber, C.6
Miller, D.7
Seligmann, M.8
Bernard, J.9
-
11
-
-
0026502986
-
Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: Epidemiology and molecular analysis
-
Shannon KM, Watterson J, Johnson P, O'Connell P, Lange B, Shah N, Kan YW, Priest JR: Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: Epidemiology and molecular analysis. Blood 79:1311, 1992
-
(1992)
Blood
, vol.79
, pp. 1311
-
-
Shannon, K.M.1
Watterson, J.2
Johnson, P.3
O'Connell, P.4
Lange, B.5
Shah, N.6
Kan, Y.W.7
Priest, J.R.8
-
12
-
-
0025201012
-
The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins
-
Ballester R, Marchuk D, Boguski M, Saulino A, Letcher R, Wigler M, Collins F: The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins. Cell 63:851, 1990
-
(1990)
Cell
, vol.63
, pp. 851
-
-
Ballester, R.1
Marchuk, D.2
Boguski, M.3
Saulino, A.4
Letcher, R.5
Wigler, M.6
Collins, F.7
-
13
-
-
0025091465
-
The neurofibromatosis type 1 gene encodes a protein related to GAP
-
Xu G, O'Connell P, Viskochil D, Cawthon R, Robertson M, Culver M, Dunn D, Stevens J, Gesteland R, White R, Weiss R: The neurofibromatosis type 1 gene encodes a protein related to GAP. Cell 62:599, 1990
-
(1990)
Cell
, vol.62
, pp. 599
-
-
Xu, G.1
O'Connell, P.2
Viskochil, D.3
Cawthon, R.4
Robertson, M.5
Culver, M.6
Dunn, D.7
Stevens, J.8
Gesteland, R.9
White, R.10
Weiss, R.11
-
14
-
-
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, Adler F, Zhang Y, Thompson P, Lange BJ, Freedman MH, McCormick F, Jacks T, Shannon K: Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in murine and human hematopoietic cells. Nat Genet 12:144, 1996
-
(1996)
Nat Genet
, vol.12
, pp. 144
-
-
Bollag, G.1
Clapp, D.W.2
Shih, S.3
Adler, F.4
Zhang, Y.5
Thompson, P.6
Lange, B.J.7
Freedman, M.H.8
McCormick, F.9
Jacks, T.10
Shannon, K.11
-
15
-
-
0028307836
-
Tumorigenic and developmental consequences of a targeted Nf1 mutation in the mouse
-
Jacks T, Shih S, Schmitt EM, Bronson RT, Bernards A, Weinberg RA: Tumorigenic and developmental consequences of a targeted Nf1 mutation in the mouse. Nat Genet 7:353, 1994
-
(1994)
Nat Genet
, vol.7
, pp. 353
-
-
Jacks, T.1
Shih, S.2
Schmitt, E.M.3
Bronson, R.T.4
Bernards, A.5
Weinberg, R.A.6
-
16
-
-
0030045594
-
Nf1 deficiency causes Ras-mediated granulocyte-macrophage colony stimulating factor hypersensitivity and chronic myeloid leukemia
-
Largaespada DA, Brannan CI, Jenkins NA, Copeland NG: Nf1 deficiency causes Ras-mediated granulocyte-macrophage colony stimulating factor hypersensitivity and chronic myeloid leukemia. Nat Genet 12:137, 1996
-
(1996)
Nat Genet
, vol.12
, pp. 137
-
-
Largaespada, D.A.1
Brannan, C.I.2
Jenkins, N.A.3
Copeland, N.G.4
-
17
-
-
0030947237
-
Homozygous inactivation of NF1 in the bone marrows of children with neurofibromatosis, type 1 and malignant myeloid disorders
-
Side L, Taylor B, Cayouette M, Connor E, Thompson P, Luce M, Shannon KM: Homozygous inactivation of NF1 in the bone marrows of children with neurofibromatosis, type 1 and malignant myeloid disorders. N Engl J Med 336:1713, 1997
-
(1997)
N Engl J Med
, vol.336
, pp. 1713
-
-
Side, L.1
Taylor, B.2
Cayouette, M.3
Connor, E.4
Thompson, P.5
Luce, M.6
Shannon, K.M.7
-
18
-
-
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, Paderanga D, Olson K, Dinndorf P, McCormick F: Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders. N Engl J Med 330:597, 1994
-
(1994)
N Engl J Med
, vol.330
, pp. 597
-
-
Shannon, K.M.1
O'Connell, P.2
Martin, G.A.3
Paderanga, D.4
Olson, K.5
Dinndorf, P.6
McCormick, F.7
-
20
-
-
0030957310
-
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2
-
Gutmann D, Aylsworth A, Carey J, Korf B, Marks J, Pyeritz R, Rubenstein A, Viskochil D: The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA 278:51, 1997
-
(1997)
JAMA
, vol.278
, pp. 51
-
-
Gutmann, D.1
Aylsworth, A.2
Carey, J.3
Korf, B.4
Marks, J.5
Pyeritz, R.6
Rubenstein, A.7
Viskochil, D.8
-
21
-
-
0018604894
-
Penetrance and variability in neurofibromatosis: A genetic study of 60 families
-
Carey JC, Lant JM, Hall BD: Penetrance and variability in neurofibromatosis: A genetic study of 60 families. Birth Defects 15:271, 1979
-
(1979)
Birth Defects
, vol.15
, pp. 271
-
-
Carey, J.C.1
Lant, J.M.2
Hall, B.D.3
-
22
-
-
0027427198
-
Genotype, malleotype, phenotype and randomness: Lessons from neurofibromatosis-1 (NF-1)
-
Riccardi VM: Genotype, malleotype, phenotype and randomness: Lessons from neurofibromatosis-1 (NF-1). Am J Hum Genet 53:301, 1993
-
(1993)
Am J Hum Genet
, vol.53
, pp. 301
-
-
Riccardi, V.M.1
-
23
-
-
0027379865
-
An analysis of variation in expression of neurofibromatosis type 1 (NF1): Evidence for modifying genes
-
Easton D, Ponder M, Huson S, Ponder B: An analysis of variation in expression of neurofibromatosis type 1 (NF1): Evidence for modifying genes. Am J Hum Genet 53:305, 1993
-
(1993)
Am J Hum Genet
, vol.53
, pp. 305
-
-
Easton, D.1
Ponder, M.2
Huson, S.3
Ponder, B.4
-
24
-
-
0028928718
-
Genomic organisation of the neurofibromatosis 1 gene (NF1)
-
Li Y, O'Connell P, Breidenbach HH, Cawthon R, Stevens J, Xu G, Neil S, Robertson M, White R, Viskochil D: Genomic organisation of the neurofibromatosis 1 gene (NF1). Genomics 25:1, 1995
-
(1995)
Genomics
, vol.25
, pp. 1
-
-
Li, Y.1
O'Connell, P.2
Breidenbach, H.H.3
Cawthon, R.4
Stevens, J.5
Xu, G.6
Neil, S.7
Robertson, M.8
White, R.9
Viskochil, D.10
-
25
-
-
0022924142
-
The genetic aspects of neurofibromatosis
-
Carey J, Baty B, Johnson J, Morrion T, Skolnick M, Kivlin J: The genetic aspects of neurofibromatosis. Ann NY Acad Sci 486:45, 1986
-
(1986)
Ann NY Acad Sci
, vol.486
, pp. 45
-
-
Carey, J.1
Baty, B.2
Johnson, J.3
Morrion, T.4
Skolnick, M.5
Kivlin, J.6
-
26
-
-
0029908346
-
Patterns of hematopoietic lineage involvement in children with neurofibromatosis, type 1, and malignant myeloid disorders
-
Miles DK, Freedman MH, Stephens K, Pallavicini M, Sievers E, Weaver M, Grunberger T, Thompson P, Shannon KM: Patterns of hematopoietic lineage involvement in children with neurofibromatosis, type 1, and malignant myeloid disorders. Blood 88:4314, 1996
-
(1996)
Blood
, vol.88
, pp. 4314
-
-
Miles, D.K.1
Freedman, M.H.2
Stephens, K.3
Pallavicini, M.4
Sievers, E.5
Weaver, M.6
Grunberger, T.7
Thompson, P.8
Shannon, K.M.9
-
27
-
-
0002440928
-
Molecular Cloning
-
New York, NY, Cold Spring Harbor Laboratory
-
Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning. A Laboratory Manual. New York, NY, Cold Spring Harbor Laboratory, 1989
-
(1989)
A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
28
-
-
0029002475
-
Distribution of 13 truncating mutations in the neurofibromatosis 1 gene
-
Heim R, Kam-Morgan L, Binnie C, Corns D, Cayouette M, Farber R, Aylsworth A, Silverman L, Luce M: Distribution of 13 truncating mutations in the neurofibromatosis 1 gene. Hum Mol Genet 4:975, 1995
-
(1995)
Hum Mol Genet
, vol.4
, pp. 975
-
-
Heim, R.1
Kam-Morgan, L.2
Binnie, C.3
Corns, D.4
Cayouette, M.5
Farber, R.6
Aylsworth, A.7
Silverman, L.8
Luce, M.9
-
29
-
-
0030977357
-
Rapid identification of RT-PCR clones containing translation-termination mutations
-
Binnie CG, Kam-Morgan LNW, Cayouette M, Marra G, Boland CR, Luce MC: Rapid identification of RT-PCR clones containing translation-termination mutations. Mutat Res 388:21, 1997
-
(1997)
Mutat Res
, vol.388
, pp. 21
-
-
Binnie, C.G.1
Kam-Morgan, L.N.W.2
Cayouette, M.3
Marra, G.4
Boland, C.R.5
Luce, M.C.6
-
30
-
-
0029560551
-
Identification of neurofibromatosis type l (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids
-
Purandare SM, Breidenbach H, Li Y, Zhu XL, Sawada S, Neil SM, Brothman A, White R, Cawthon R, Viskochil D: Identification of neurofibromatosis type l (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids. Genomics 30:476, 1995
-
(1995)
Genomics
, vol.30
, pp. 476
-
-
Purandare, S.M.1
Breidenbach, H.2
Li, Y.3
Zhu, X.L.4
Sawada, S.5
Neil, S.M.6
Brothman, A.7
White, R.8
Cawthon, R.9
Viskochil, D.10
-
31
-
-
0025293818
-
Detection of ras gene mutations in human lung cancers by single-strand conformation polymorphism analysis of polymerase chain reaction products
-
Suzuki Y, Orita M, Shiraishi M, Hayashi K, Sekiya T: Detection of ras gene mutations in human lung cancers by single-strand conformation polymorphism analysis of polymerase chain reaction products. Oncogene 5:1037, 1990
-
(1990)
Oncogene
, vol.5
, pp. 1037
-
-
Suzuki, Y.1
Orita, M.2
Shiraishi, M.3
Hayashi, K.4
Sekiya, T.5
-
33
-
-
0031059482
-
Evidence for the embryonic origin of partial chromosome 7 deletion in monozygotic twins with juvenile chronic myelogenous leukemia
-
Najfeld V, Vlachos A, Parker R, Burnett W, Scalise A, Fructman S: Evidence for the embryonic origin of partial chromosome 7 deletion in monozygotic twins with juvenile chronic myelogenous leukemia. Leukemia 11:306, 1997
-
(1997)
Leukemia
, vol.11
, pp. 306
-
-
Najfeld, V.1
Vlachos, A.2
Parker, R.3
Burnett, W.4
Scalise, A.5
Fructman, S.6
-
35
-
-
0025813519
-
An Alu polymorphism intragenic to the neurofibromatosis, type 1 gene
-
Xu G, Nelson L, O'Connell P, White R: An Alu polymorphism intragenic to the neurofibromatosis, type 1 gene. Nucleic Acids Res 19:3764, 1991
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 3764
-
-
Xu, G.1
Nelson, L.2
O'Connell, P.3
White, R.4
-
36
-
-
0027199643
-
A highly informative compound nucleotide repeat in the neurofibromatosis (NF1) gene
-
Andersen LB, Tarle SA, Marchuk DA, Legius E, Collins FS: A highly informative compound nucleotide repeat in the neurofibromatosis (NF1) gene. Hum Mol Genet 2:1083, 1993
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1083
-
-
Andersen, L.B.1
Tarle, S.A.2
Marchuk, D.A.3
Legius, E.4
Collins, F.S.5
-
37
-
-
0028013195
-
Two CA/GT repeat polymorphisms in intron 27 of the human NF1 gene
-
Lazaro C, Gaona A, Estivill X: Two CA/GT repeat polymorphisms in intron 27 of the human NF1 gene. Hum Genet 93:351, 1994
-
(1994)
Hum Genet
, vol.93
, pp. 351
-
-
Lazaro, C.1
Gaona, A.2
Estivill, X.3
-
38
-
-
2642606483
-
Interaction between NF1 and GMCSF in leukemogenesis and hematopoietic engraftment
-
abstr, suppl 1
-
Birnbaum R, O'Marcaigh A, Wardak Z, Zhang Y, Dranoff G, Jacks T, Clapp DW, Shannon KM: Interaction between NF1 and GMCSF in leukemogenesis and hematopoietic engraftment. Blood 90:411 a, 1997 (abstr, suppl 1)
-
(1997)
Blood
, vol.90
-
-
Birnbaum, R.1
O'Marcaigh, A.2
Wardak, Z.3
Zhang, Y.4
Dranoff, G.5
Jacks, T.6
Clapp, D.W.7
Shannon, K.M.8
-
39
-
-
26144432530
-
A mouse model of alkylator-induced leukemia
-
abstr, suppl 1
-
Mahgoub N, Taylor B, Le Beau M, Gratiot M, Carlson K, Jacks T, Shannon KM: A mouse model of alkylator-induced leukemia. Blood 90:385a, 1997 (abstr, suppl 1)
-
(1997)
Blood
, vol.90
-
-
Mahgoub, N.1
Taylor, B.2
Le Beau, M.3
Gratiot, M.4
Carlson, K.5
Jacks, T.6
Shannon, K.M.7
-
40
-
-
0028224348
-
Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
-
Golub TR, Barker GF, Lovett M, Gilliland DG: Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77:307, 1994
-
(1994)
Cell
, vol.77
, pp. 307
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
41
-
-
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 77:171, 1994
-
(1994)
Cell
, vol.77
, pp. 171
-
-
Sawyers, C.L.1
Denny, C.T.2
-
42
-
-
0027732538
-
Proteins regulating Ras and its relatives
-
Boguski M, McCormick F: Proteins regulating Ras and its relatives. Nature 366:643, 1993
-
(1993)
Nature
, vol.366
, pp. 643
-
-
Boguski, M.1
McCormick, F.2
-
43
-
-
0027454104
-
Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours
-
Friedman E, Gejman P, Martin G, McCormick F: Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours. Nat Genet 5:242, 1993
-
(1993)
Nat Genet
, vol.5
, pp. 242
-
-
Friedman, E.1
Gejman, P.2
Martin, G.3
McCormick, F.4
-
44
-
-
0029549724
-
The role of ras GTPase activating protein in human tumorigenesis
-
Friedman E: The role of ras GTPase activating protein in human tumorigenesis. Pathobiology 63:348, 1995
-
(1995)
Pathobiology
, vol.63
, pp. 348
-
-
Friedman, E.1
-
45
-
-
0028788570
-
Vascular system defects and neuronal apoptosis in mice lacking Ras GTPase activating protein
-
Henkemeyer M, Rossi D, Holmyard D, Puri M, Mbamalu G, Harpal K, Shih TS, Jacks T, Pawson T: Vascular system defects and neuronal apoptosis in mice lacking Ras GTPase activating protein. Nature 377:695, 1995
-
(1995)
Nature
, vol.377
, pp. 695
-
-
Henkemeyer, M.1
Rossi, D.2
Holmyard, D.3
Puri, M.4
Mbamalu, G.5
Harpal, K.6
Shih, T.S.7
Jacks, T.8
Pawson, T.9
-
46
-
-
0026063878
-
Seletive hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors
-
Emanuel PD, Bates LJ, Castleberry RP, Gualtieri RJ, Zuckerman KS: Seletive hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors. Blood 77:925, 1991
-
(1991)
Blood
, vol.77
, pp. 925
-
-
Emanuel, P.D.1
Bates, L.J.2
Castleberry, R.P.3
Gualtieri, R.J.4
Zuckerman, K.S.5
-
47
-
-
0031010989
-
Analysis of the coding sequence for the GM-CSF receptor α and β chains in patients with juvenile chronic myeloid leukemia (JCML)
-
Freeburn R, Gale R, Wagner H, Linch D: Analysis of the coding sequence for the GM-CSF receptor α and β chains in patients with juvenile chronic myeloid leukemia (JCML). Exp Hemat 25:306, 1997
-
(1997)
Exp Hemat
, vol.25
, pp. 306
-
-
Freeburn, R.1
Gale, R.2
Wagner, H.3
Linch, D.4
-
48
-
-
12944310935
-
Increased levels of the p85α subunit of phosphatidylinositol 3-OH kinase in cell lysates of juvenile myelomonocytic leukemia cells
-
abstr, suppl 1
-
Snyder RC, Wiley T, Castleberry RP, Emanuel PD: Increased levels of the p85α subunit of phosphatidylinositol 3-OH kinase in cell lysates of juvenile myelomonocytic leukemia cells. Blood 90:411a, 1997 (abstr, suppl 1)
-
(1997)
Blood
, vol.90
-
-
Snyder, R.C.1
Wiley, T.2
Castleberry, R.P.3
Emanuel, P.D.4
-
49
-
-
0028074316
-
Phosphatidylinositol3-OH kinase as a direct target of Ras
-
Rodriguez-Viciana P, Warne PH, Dhand R, Vanhaesebroeck B, Gout I, Fry MJ, Waterfield MD, Downward J: Phosphatidylinositol3-OH kinase as a direct target of Ras. Nature 370:527, 1994
-
(1994)
Nature
, vol.370
, pp. 527
-
-
Rodriguez-Viciana, P.1
Warne, P.H.2
Dhand, R.3
Vanhaesebroeck, B.4
Gout, I.5
Fry, M.J.6
Waterfield, M.D.7
Downward, J.8
-
50
-
-
0026655421
-
Loss of alleles in pheochromocytomas from patients with type 1 neurofibromatosis
-
Xu W, Mulligan L, Ponder MA, Liu L, Smith BA, Mathew CG, Ponder BA: Loss of alleles in pheochromocytomas from patients with type 1 neurofibromatosis. Genes Chromosomes Cancer 4:337, 1992
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 337
-
-
Xu, W.1
Mulligan, L.2
Ponder, M.A.3
Liu, L.4
Smith, B.A.5
Mathew, C.G.6
Ponder, B.A.7
-
51
-
-
0024957180
-
Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: Loss of heterozygosity for chromosome 17
-
Skuse GR, Kosciolek BA, Rowley PT: Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: Loss of heterozygosity for chromosome 17. Genes Chromosomes Cancer 1:36, 1989
-
(1989)
Genes Chromosomes Cancer
, vol.1
, pp. 36
-
-
Skuse, G.R.1
Kosciolek, B.A.2
Rowley, P.T.3
-
52
-
-
0025108408
-
Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis
-
Menon AG, Anderson KM, Riccardi VM, Chung RY, Whaley JM, Yandell DW, Farmer GE, Freiman RN, Lee JK, Li FP, Barker DF, Ledbetter DH, Kleider A, Martuza RL, Gusella JF, Seizinger BR: Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis. Proc Natl Acad Sci USA 87:5435, 1990
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 5435
-
-
Menon, A.G.1
Anderson, K.M.2
Riccardi, V.M.3
Chung, R.Y.4
Whaley, J.M.5
Yandell, D.W.6
Farmer, G.E.7
Freiman, R.N.8
Lee, J.K.9
Li, F.P.10
Barker, D.F.11
Ledbetter, D.H.12
Kleider, A.13
Martuza, R.L.14
Gusella, J.F.15
Seizinger, B.R.16
-
53
-
-
0026505197
-
Somatic mutations in the neurofibromatosis 1 gene in human tumors
-
Li Y, Bollag G, Clark R, Stevens J, Conroy L, Fults D, Ward K, Friedman E, Samowitz W, Robertson M, Bradley P, McCormick F, White R, Cawthon R: Somatic mutations in the neurofibromatosis 1 gene in human tumors. Cell 69:275, 1992
-
(1992)
Cell
, vol.69
, pp. 275
-
-
Li, Y.1
Bollag, G.2
Clark, R.3
Stevens, J.4
Conroy, L.5
Fults, D.6
Ward, K.7
Friedman, E.8
Samowitz, W.9
Robertson, M.10
Bradley, P.11
McCormick, F.12
White, R.13
Cawthon, R.14
|