-
1
-
-
0037298128
-
The myelodysplastic syndrome(s): A perspective and review highlighting current controversies
-
Steensma D.P., Tefferi A. The myelodysplastic syndrome(s): a perspective and review highlighting current controversies. Leuk. Res. 27:2003;95-120
-
(2003)
Leuk. Res.
, vol.27
, pp. 95-120
-
-
Steensma, D.P.1
Tefferi, A.2
-
2
-
-
0038470905
-
Molecular mechanisms of myelodysplastic syndrome
-
Hirai H. Molecular mechanisms of myelodysplastic syndrome. Jpn. J. Clin. Oncol. 33:2003;153-160
-
(2003)
Jpn. J. Clin. Oncol.
, vol.33
, pp. 153-160
-
-
Hirai, H.1
-
3
-
-
0037097597
-
Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome
-
Boultwood C., Fidler A.J., Strickson F., et al. Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome. Blood. 99:2002;4638-4641
-
(2002)
Blood
, vol.99
, pp. 4638-4641
-
-
Boultwood, C.1
Fidler, A.J.2
Strickson, F.3
-
4
-
-
0027315865
-
Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases
-
Le Beau M.M., Espinosa R., Neuman W.L., et al. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases. Proc. Natl. Acad. Sci. U.S.A. 90:1993;5484-5488
-
(1993)
Proc. Natl. Acad. Sci. U.S.A.
, vol.90
, pp. 5484-5488
-
-
Le Beau, M.M.1
Espinosa, R.2
Neuman, W.L.3
-
5
-
-
0028871987
-
Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia
-
Pedersen-Bjergaard J., Pedersen M., Roulston D., et al. Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia. Blood. 86:1995;3542-3552
-
(1995)
Blood
, vol.86
, pp. 3542-3552
-
-
Pedersen-Bjergaard, J.1
Pedersen, M.2
Roulston, D.3
-
6
-
-
0031788987
-
Cytogenetically unrelated clones in therapy-related myelodysplasia and acute myeloid leukemia: Experience from the Copenhagen series updated to 180 consecutive cases
-
Pedersen-Bjergaard J., Timshel S., Andersen M.K., et al. Cytogenetically unrelated clones in therapy-related myelodysplasia and acute myeloid leukemia: experience from the Copenhagen series updated to 180 consecutive cases. Genes Chromosomes Cancer. 23:1998;337-349
-
(1998)
Genes Chromosomes Cancer
, vol.23
, pp. 337-349
-
-
Pedersen-Bjergaard, J.1
Timshel, S.2
Andersen, M.K.3
-
7
-
-
0022873443
-
Multiple chromosomally distinct cell populations in myelodysplastic syndromes and their possible significance in the evolution of the disease
-
Mecucci C., Rege-Cambrin G., Michaux J.L., et al. Multiple chromosomally distinct cell populations in myelodysplastic syndromes and their possible significance in the evolution of the disease. Br. J. Haematol. 64:1986;699-706
-
(1986)
Br. J. Haematol.
, vol.64
, pp. 699-706
-
-
Mecucci, C.1
Rege-Cambrin, G.2
Michaux, J.L.3
-
8
-
-
0027465728
-
Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia
-
Willman C.L., Sever C.E., Pallavicini M.G., et al. Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia. Science. 259:1993;968-971
-
(1993)
Science
, vol.259
, pp. 968-971
-
-
Willman, C.L.1
Sever, C.E.2
Pallavicini, M.G.3
-
9
-
-
0028214564
-
Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: Delineation of the critical region on 5q and identification of a 5q- breakpoint
-
Boultwood J., Fidler C., Lewis S., Kelly S., Sheridan H., Littlewood T.J., et al. Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint. Genomics. 19:1994;425-432
-
(1994)
Genomics
, vol.19
, pp. 425-432
-
-
Boultwood, J.1
Fidler, C.2
Lewis, S.3
Kelly, S.4
Sheridan, H.5
Littlewood, T.J.6
-
11
-
-
0034177514
-
Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31
-
Horrigan S.K., Arbieva Z.H., Xie H.Y., et al. Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31. Blood. 95:2000;2372-2377
-
(2000)
Blood
, vol.95
, pp. 2372-2377
-
-
Horrigan, S.K.1
Arbieva, Z.H.2
Xie, H.Y.3
-
12
-
-
0026053173
-
Deletion of one GM-CSF allele and rearrangement of the other in a patient with myelodysplastic syndrome: Possible loss of functions of a tumour suppressor gene closely linked to the GM-CSF locus on chromosome 5
-
Li Y.S., Luke B., Wang H.S., et al. Deletion of one GM-CSF allele and rearrangement of the other in a patient with myelodysplastic syndrome: possible loss of functions of a tumour suppressor gene closely linked to the GM-CSF locus on chromosome 5. Br. J. Haematol. 79:1991;126-127
-
(1991)
Br. J. Haematol.
, vol.79
, pp. 126-127
-
-
Li, Y.S.1
Luke, B.2
Wang, H.S.3
-
13
-
-
0027479684
-
Anti-oncogenic and oncogenic potentials of interferon regulatory factors-1 and -2
-
Harada H., Kitagawa M., Tanaka N., et al. Anti-oncogenic and oncogenic potentials of interferon regulatory factors-1 and -2. Science. 259:1993;971-974
-
(1993)
Science
, vol.259
, pp. 971-974
-
-
Harada, H.1
Kitagawa, M.2
Tanaka, N.3
-
14
-
-
0030240574
-
Chromosomal assignment of three rat and human H-rev genes, putative tumor suppressors, down-regulated in malignantly HRAS-transformed cells
-
Szpirer C., Szpirer J., Riviere M., et al. Chromosomal assignment of three rat and human H-rev genes, putative tumor suppressors, down-regulated in malignantly HRAS-transformed cells. Mamm. Genome. 7:1996;701-703
-
(1996)
Mamm. Genome
, vol.7
, pp. 701-703
-
-
Szpirer, C.1
Szpirer, J.2
Riviere, M.3
-
15
-
-
0023944394
-
The human genes for GM-CSF and IL 3 are closely linked in tandem on chromosome 5
-
Yang Y.C., Kovacic S., Kriz R., et al. The human genes for GM-CSF and IL 3 are closely linked in tandem on chromosome 5. Blood. 71:1988;958-961
-
(1988)
Blood
, vol.71
, pp. 958-961
-
-
Yang, Y.C.1
Kovacic, S.2
Kriz, R.3
-
16
-
-
0025744150
-
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion
-
Boultwood J., Rack K., Kelly S., Madden J., Sakaguchi A.Y., Wang L.M., et al. Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion. Proc. Natl. Acad. Sci. U.S.A. 88:1991;6176-6180
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 6176-6180
-
-
Boultwood, J.1
Rack, K.2
Kelly, S.3
Madden, J.4
Sakaguchi, A.Y.5
Wang, L.M.6
-
17
-
-
0032532741
-
Human CDC23: CDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias
-
Zhao N., Lai F., Fernald A.A., Eisenbart J.D., et al. Human CDC23: cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias. Genomics. 53:1998;184-190
-
(1998)
Genomics
, vol.53
, pp. 184-190
-
-
Zhao, N.1
Lai, F.2
Fernald, A.A.3
Eisenbart, J.D.4
-
18
-
-
0033199116
-
TTID: A novel gene at 5q31 encoding a protein with titin-like features
-
Godley L.A., Lai F., Liu J., et al. TTID: A novel gene at 5q31 encoding a protein with titin-like features. Genomics. 60:1999;226-233
-
(1999)
Genomics
, vol.60
, pp. 226-233
-
-
Godley, L.A.1
Lai, F.2
Liu, J.3
-
19
-
-
0034672586
-
CDNA cloning and genomic structure of three genes localized to human chromosome band 5q31 encoding potential nuclear proteins
-
Lai F., Godley L.A., Fernald A.A., Orelli B.J., et al. cDNA cloning and genomic structure of three genes localized to human chromosome band 5q31 encoding potential nuclear proteins. Genomics. 70:2000;123-130
-
(2000)
Genomics
, vol.70
, pp. 123-130
-
-
Lai, F.1
Godley, L.A.2
Fernald, A.A.3
Orelli, B.J.4
-
20
-
-
0032733441
-
Lack of IRF-1 expression in acute promyelocytic leukemia and in a subset of acute myeloid leukemias with del (5)(q31)
-
Green W.B., Slovak M.L., Chen I.M., et al. Lack of IRF-1 expression in acute promyelocytic leukemia and in a subset of acute myeloid leukemias with del (5)(q31). Leukemia. 13:1999;1960-1971
-
(1999)
Leukemia
, vol.13
, pp. 1960-1971
-
-
Green, W.B.1
Slovak, M.L.2
Chen, I.M.3
-
21
-
-
0033566759
-
Identification of NKIAMRE, the human homologue to the mitogen-activated protein kinase-/cyclin-dependent kinase-related protein kinase NKIATRE, and its loss in leukemic blasts with chromosome arm 5q deletion
-
Midmer M., Haq R., Squire J.A., et al. Identification of NKIAMRE, the human homologue to the mitogen-activated protein kinase-/cyclin-dependent kinase-related protein kinase NKIATRE, and its loss in leukemic blasts with chromosome arm 5q deletion. Cancer Res. 59:1999;4069-4074
-
(1999)
Cancer Res.
, vol.59
, pp. 4069-4074
-
-
Midmer, M.1
Haq, R.2
Squire, J.A.3
-
22
-
-
0034983827
-
Deletions of PURA, at 5q31 and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia
-
Lezon-Geyda K., Najfeld V., Johnson E.M. Deletions of PURA, at 5q31 and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia. Leukemia. 15:2001;954-962
-
(2001)
Leukemia
, vol.15
, pp. 954-962
-
-
Lezon-Geyda, K.1
Najfeld, V.2
Johnson, E.M.3
-
23
-
-
0036540314
-
Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene
-
Dubourg C., Toutain B., Helias C., et al. Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene. Cancer Genet. Cytogenet. 134:2002;33-37
-
(2002)
Cancer Genet. Cytogenet.
, vol.134
, pp. 33-37
-
-
Dubourg, C.1
Toutain, B.2
Helias, C.3
-
24
-
-
8444224048
-
Simplified and rapid approach for the selection of cDNAs encoded by YACs
-
Xagorari A, Anagnou NP. Simplified and rapid approach for the selection of cDNAs encoded by YACs. Trends Genet 1997. http://www.tto.trends.com/T4002.
-
(1997)
Trends Genet
-
-
Xagorari, A.1
Anagnou, N.P.2
-
25
-
-
8444236499
-
First stage construction of a physical and transcriptional map of the 5q31 "critical region" associated with the 5q- syndrome
-
Kamakari S., Konstantinopoulou V., Anagnou N.P. First stage construction of a physical and transcriptional map of the 5q31 "critical region" associated with the 5q- syndrome. Eur. J. Hum. Genet. 6:1998;116
-
(1998)
Eur. J. Hum. Genet.
, vol.6
, pp. 116
-
-
Kamakari, S.1
Konstantinopoulou, V.2
Anagnou, N.P.3
-
26
-
-
8444222910
-
Construction of a physical and transcript map of the 5q31 "critical region" associated with the 5q- syndrome
-
Kamakari S., Konstantinopoulou V., Anagnou N.P. Construction of a physical and transcript map of the 5q31 "critical region" associated with the 5q- syndrome. Blood. 92:1998;420a
-
(1998)
Blood
, vol.92
-
-
Kamakari, S.1
Konstantinopoulou, V.2
Anagnou, N.P.3
-
27
-
-
8444232644
-
Construction of a physical and transcript map of the 5q31 "critical region" associated with the 5q- syndrome
-
Kamakari S, Konstantinopoulou V, Anagnou NP. Construction of a physical and transcript map of the 5q31 "critical region" associated with the 5q- syndrome. Eur J Hum Genet 1999;132.
-
(1999)
Eur J Hum Genet
, pp. 132
-
-
Kamakari, S.1
Konstantinopoulou, V.2
Anagnou, N.P.3
-
28
-
-
8444246922
-
Physical and hematopoietic transcript map of a 5q31 "critical subregion" associated with the 5q- syndrome
-
Kamakari S., Konstantinopoulou V., Anagnou N.P. Physical and hematopoietic transcript map of a 5q31 "critical subregion" associated with the 5q- syndrome. Am. J. Hum. Genet. 67:2000;75
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 75
-
-
Kamakari, S.1
Konstantinopoulou, V.2
Anagnou, N.P.3
-
29
-
-
0012416827
-
Physical and hematopoietic transcript map of a 5q31 "critical subregion" associated with the 5q- syndrome
-
Konstantinopoulou V., Kamakari S., Ragoussis I., et al. Physical and hematopoietic transcript map of a 5q31 "critical subregion" associated with the 5q- syndrome. Leuk. Res. 25:2001;83
-
(2001)
Leuk. Res.
, vol.25
, pp. 83
-
-
Konstantinopoulou, V.1
Kamakari, S.2
Ragoussis, I.3
-
30
-
-
0036615791
-
A complex translocation event between the two homologues of chromosomes 5 leading to a del (5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: Characterization of the aberration by multicolor banding
-
Heller A., Starke H., Trifonov V., et al. A complex translocation event between the two homologues of chromosomes 5 leading to a del (5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding. Int. J. Oncol. 20:2002;1179-1181
-
(2002)
Int. J. Oncol.
, vol.20
, pp. 1179-1181
-
-
Heller, A.1
Starke, H.2
Trifonov, V.3
-
31
-
-
0141702288
-
Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: A potential modifier of phenotype?
-
Hutchinson S., Furger A., Halliday D., et al. Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype? Hum. Mol. Genet. 12:2003;2269-2276
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2269-2276
-
-
Hutchinson, S.1
Furger, A.2
Halliday, D.3
-
32
-
-
0033858202
-
Patterns of variant polyadenylation signal usage in human genes
-
Beaudoing E., Freier S., Wyatt J.R., et al. Patterns of variant polyadenylation signal usage in human genes. Genome Res. 10:2000;1001-1010
-
(2000)
Genome Res.
, vol.10
, pp. 1001-1010
-
-
Beaudoing, E.1
Freier, S.2
Wyatt, J.R.3
-
33
-
-
0033804469
-
Genomic sequence, splicing, and gene annotation
-
Mount S.M. Genomic sequence, splicing, and gene annotation. Am. J. Hum. Genet. 67:2000;788-792
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 788-792
-
-
Mount, S.M.1
-
34
-
-
0033429143
-
AF5q31, a newly identified AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia with ins(5;11)(q31;q13q23)
-
Taki T., Kano H., Taniwaki M., et al. AF5q31, a newly identified AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia with ins(5;11)(q31;q13q23). Proc. Natl. Acad. Sci. U.S.A. 96:1999;14535-14540
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 14535-14540
-
-
Taki, T.1
Kano, H.2
Taniwaki, M.3
-
35
-
-
0033042659
-
Regulatory role of SH3 domain-mediated protein-protein interactions in synaptic vesicle endocytosis
-
McPherson P.S. Regulatory role of SH3 domain-mediated protein-protein interactions in synaptic vesicle endocytosis. Cell Signal. 11:1999;229-238
-
(1999)
Cell Signal
, vol.11
, pp. 229-238
-
-
McPherson, P.S.1
-
36
-
-
0036157980
-
The WW domain: Linking cell signalling to the membrane cytoskeleton
-
Ilsley J.L., Sudol M., Winder S.J. The WW domain: linking cell signalling to the membrane cytoskeleton. Cell Signal. 14:2002;183-189
-
(2002)
Cell Signal
, vol.14
, pp. 183-189
-
-
Ilsley, J.L.1
Sudol, M.2
Winder, S.J.3
-
37
-
-
0026572737
-
Structure and evolution of the lipase superfamily
-
Hide W.A., Chan L., Li W.-H. Structure and evolution of the lipase superfamily. J. Lipid Res. 33:1992;167-178
-
(1992)
J. Lipid Res.
, vol.33
, pp. 167-178
-
-
Hide, W.A.1
Chan, L.2
Li, W.-H.3
-
38
-
-
0033575277
-
P125 is a novel mammalian Sec23p-interacting protein with structural similarity to phospholipid-modifying proteins
-
Tani K., Mizoguchi T., Iwamatsu A., et al. p125 is a novel mammalian Sec23p-interacting protein with structural similarity to phospholipid-modifying proteins. J. Biol. Chem. 274:1999;20505-20512
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 20505-20512
-
-
Tani, K.1
Mizoguchi, T.2
Iwamatsu, A.3
-
39
-
-
0034627220
-
Determination of functional regions of p125, a novel mammalian Sec23p-interacting protein
-
Mizoguchi T., Nakajima K., Hatsuzawa K., et al. Determination of functional regions of p125, a novel mammalian Sec23p-interacting protein. Biochem. Biophys. Res. Commun. 279:2000;144-149
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.279
, pp. 144-149
-
-
Mizoguchi, T.1
Nakajima, K.2
Hatsuzawa, K.3
-
40
-
-
8444252291
-
Multicolour banding fluorescence in situ hybridisation technique in the evaluation of 5q deletions
-
Sindelarova L., Zemanova Z., Brezinova S., et al. Multicolour banding fluorescence in situ hybridisation technique in the evaluation of 5q deletions. Leuk. Res. 27:2003;S29
-
(2003)
Leuk. Res.
, vol.27
, pp. 29
-
-
Sindelarova, L.1
Zemanova, Z.2
Brezinova, S.3
-
41
-
-
0036337915
-
A genomic view of alternative splicing
-
Modrek B., Lee C. A genomic view of alternative splicing. Nat. Genet. 30:2002;13-19
-
(2002)
Nat. Genet.
, vol.30
, pp. 13-19
-
-
Modrek, B.1
Lee, C.2
-
42
-
-
0033950653
-
Genomic interval engineering of mice identifies a novel modulator of triglyceride production
-
Zhu Y., Jong M.C., Frazer K.A., et al. Genomic interval engineering of mice identifies a novel modulator of triglyceride production. Proc. Natl. Acad. Sci. U.S.A. 97:2000;11371142
-
(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 11371142
-
-
Zhu, Y.1
Jong, M.C.2
Frazer, K.A.3
-
43
-
-
0000235244
-
A prototypical cytidylyltransferase: CTP:glycerol-3-phosphate cytidylyltransferase from Bacillus subtilis
-
Weber C.H., Park Y.S., Sanker S., et al. A prototypical cytidylyltransferase: CTP:glycerol-3-phosphate cytidylyltransferase from Bacillus subtilis. Struct. Fold Des. 7:1999;1113-1124
-
(1999)
Struct. Fold Des.
, vol.7
, pp. 1113-1124
-
-
Weber, C.H.1
Park, Y.S.2
Sanker, S.3
-
44
-
-
1542399170
-
'Slip, sliding away': Phospholipase D and the Golgi apparatus
-
Freyberg Z., Siddhanta A., Shields D. 'Slip, sliding away': phospholipase D and the Golgi apparatus. Trends Cell Biol. 13:2003;540-546
-
(2003)
Trends Cell Biol.
, vol.13
, pp. 540-546
-
-
Freyberg, Z.1
Siddhanta, A.2
Shields, D.3
-
45
-
-
0034053069
-
Wnt signaling in oncogenesis and embryogenesis - A look outside the nucleus
-
Peifer M., Polakis P. Wnt signaling in oncogenesis and embryogenesis - a look outside the nucleus. Science. 287:2000;1606-1609
-
(2000)
Science
, vol.287
, pp. 1606-1609
-
-
Peifer, M.1
Polakis, P.2
-
46
-
-
0037126331
-
The DIX domain targets dishevelled to actin stress fibres and vesicular membranes
-
Capelluto D.G., Kutateladze T.G., Habas R., et al. The DIX domain targets dishevelled to actin stress fibres and vesicular membranes. Nature. 419:2002;726-729
-
(2002)
Nature
, vol.419
, pp. 726-729
-
-
Capelluto, D.G.1
Kutateladze, T.G.2
Habas, R.3
-
47
-
-
0037142086
-
A global analysis of Caenorhabditis elegans operons
-
Blumenthal T., Evans D., Link C.D., et al. A global analysis of Caenorhabditis elegans operons. Nature. 417:2002;851-854
-
(2002)
Nature
, vol.417
, pp. 851-854
-
-
Blumenthal, T.1
Evans, D.2
Link, C.D.3
-
48
-
-
0037737726
-
Wnt proteins are lipid-modified and can act as stem cell growth factors
-
Willert K., Brown J.D., Danenberg E., et al. Wnt proteins are lipid-modified and can act as stem cell growth factors. Nature. 423:2003;448-452
-
(2003)
Nature
, vol.423
, pp. 448-452
-
-
Willert, K.1
Brown, J.D.2
Danenberg, E.3
-
49
-
-
0031457622
-
Signaling through scaffold, anchoring, and adaptor proteins
-
Pawson T., Scott J.D. Signaling through scaffold, anchoring, and adaptor proteins. Science. 278:1997;2075-2080
-
(1997)
Science
, vol.278
, pp. 2075-2080
-
-
Pawson, T.1
Scott, J.D.2
-
50
-
-
0033950079
-
The importance of being proline: The interaction of proline-rich motifs in signaling proteins with their cognate domains
-
Kay B.K., Williamson M.P., Sudol M. The importance of being proline: the interaction of proline-rich motifs in signaling proteins with their cognate domains. FASEB J. 14:2000;231-241
-
(2000)
FASEB J.
, vol.14
, pp. 231-241
-
-
Kay, B.K.1
Williamson, M.P.2
Sudol, M.3
-
51
-
-
0031456158
-
Wnt signaling: A common theme in animal development
-
Cadigan K.M., Nusse R. Wnt signaling: a common theme in animal development. Genes Dev. 11:1997;3286-3305
-
(1997)
Genes Dev.
, vol.11
, pp. 3286-3305
-
-
Cadigan, K.M.1
Nusse, R.2
-
52
-
-
0037737728
-
A role for Wnt signalling in self-renewal of haematopoietic stem cells
-
Reya T., Duncan A.W., Ailles L., et al. A role for Wnt signalling in self-renewal of haematopoietic stem cells. Nature. 423:2003;409-414
-
(2003)
Nature
, vol.423
, pp. 409-414
-
-
Reya, T.1
Duncan, A.W.2
Ailles, L.3
-
53
-
-
0035499267
-
Stem cells, cancer, and cancer stem cells
-
Reya T., Morrison S.J., Clarke M.F., et al. Stem cells, cancer, and cancer stem cells. Nature. 414:2001;105-111
-
(2001)
Nature
, vol.414
, pp. 105-111
-
-
Reya, T.1
Morrison, S.J.2
Clarke, M.F.3
|