-
1
-
-
0017174101
-
Polycythemia vera: Stem-cell and probable clonal origin of the disease
-
Adamson JW, Fialkow PJ, Murphy S, Prchal JF, Steinmann L. Polycythemia vera: stem-cell and probable clonal origin of the disease. N Engl J Med. 1976;295:913-916.
-
(1976)
N Engl J Med
, vol.295
, pp. 913-916
-
-
Adamson, J.W.1
Fialkow, P.J.2
Murphy, S.3
Prchal, J.F.4
Steinmann, L.5
-
2
-
-
0018138805
-
A common progenitor for human myeloid and lymphoid cells
-
Prchal JT, Throckmorton DW, Carroll AJ III, Fuson EW, Gams RA, Prchal JF. A common progenitor for human myeloid and lymphoid cells. Nature. 1978;274:590-591.
-
(1978)
Nature
, vol.274
, pp. 590-591
-
-
Prchal, J.T.1
Throckmorton, D.W.2
Carroll A.J. III3
Fuson, E.W.4
Gams, R.A.5
Prchal, J.F.6
-
4
-
-
0019818299
-
Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell
-
Fialkow PJ, Faguet GB, Jacobson RJ, Vaidya K, Murphy S. Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. Blood. 1981;58:916-919.
-
(1981)
Blood
, vol.58
, pp. 916-919
-
-
Fialkow, P.J.1
Faguet, G.B.2
Jacobson, R.J.3
Vaidya, K.4
Murphy, S.5
-
5
-
-
0026091590
-
Clonal granulocytes and bone marrow cells in the cellular phase of agnogenic myeloid metaplasia
-
Kreipe H, Jaquet K, Feigner J, Radzun HJ, Parwaresch MR. Clonal granulocytes and bone marrow cells in the cellular phase of agnogenic myeloid metaplasia. Blood. 1991;78:1814-1817.
-
(1991)
Blood
, vol.78
, pp. 1814-1817
-
-
Kreipe, H.1
Jaquet, K.2
Feigner, J.3
Radzun, H.J.4
Parwaresch, M.R.5
-
6
-
-
7144223296
-
Gene action in the X chromosome of the mouse
-
Lyon MF. Gene action in the X chromosome of the mouse. Nature. 1961;190:372-373.
-
(1961)
Nature
, vol.190
, pp. 372-373
-
-
Lyon, M.F.1
-
7
-
-
0002826398
-
The normal human female as a mosaic of X-chromosome activity: Studies using the gene for G6PD deficiency as a marker
-
Beutler E, Yeh M, Fairbanks VF. The normal human female as a mosaic of X-chromosome activity: studies using the gene for G6PD deficiency as a marker. Proc Natl Acad Sci U S A. 1962;48:9-16.
-
(1962)
Proc Natl Acad Sci U S A
, vol.48
, pp. 9-16
-
-
Beutler, E.1
Yeh, M.2
Fairbanks, V.F.3
-
8
-
-
0014208048
-
Value of genetic variants of glucose-6-phosphate dehydrogenase in tracing the origin of malignant tumors
-
Beutler E, Collins Z, Irwin LE. Value of genetic variants of glucose-6-phosphate dehydrogenase in tracing the origin of malignant tumors. N Engl J Med. 1967;276:389-391.
-
(1967)
N Engl J Med
, vol.276
, pp. 389-391
-
-
Beutler, E.1
Collins, Z.2
Irwin, L.E.3
-
9
-
-
0022820116
-
Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5′ end of the gene for phosphoglycerate kinase
-
Keith DH, Singer-Sam J, Riggs AD. Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5′ end of the gene for phosphoglycerate kinase. Mol Cell Biol. 1986;6:4122-4125.
-
(1986)
Mol Cell Biol
, vol.6
, pp. 4122-4125
-
-
Keith, D.H.1
Singer-Sam, J.2
Riggs, A.D.3
-
10
-
-
0021992165
-
Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors
-
Vogelstein B, Fearon ER, Hamilton SR, Feinberg AP. Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors. Science. 1985;227:642-645.
-
(1985)
Science
, vol.227
, pp. 642-645
-
-
Vogelstein, B.1
Fearon, E.R.2
Hamilton, S.R.3
Feinberg, A.P.4
-
11
-
-
0023626415
-
Clonal analysis using recombinant DNA probes from the X-chromosome
-
Vogelstein B, Fearon ER, Hamilton SR, et al. Clonal analysis using recombinant DNA probes from the X-chromosome. Cancer Res. 1987;47:4806-4813.
-
(1987)
Cancer Res
, vol.47
, pp. 4806-4813
-
-
Vogelstein, B.1
Fearon, E.R.2
Hamilton, S.R.3
-
12
-
-
0025324635
-
Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27 beta): Correlation with X-inactivation status
-
Boyd Y, Fraser NJ. Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27 beta): correlation with X-inactivation status. Genomics. 1990;7:182-187.
-
(1990)
Genomics
, vol.7
, pp. 182-187
-
-
Boyd, Y.1
Fraser, N.J.2
-
13
-
-
0026678490
-
Methylation of Hpall and Hhal sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
-
Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW. Methylation of Hpall and Hhal sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet. 1992;51:1229-1239.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1229-1239
-
-
Allen, R.C.1
Zoghbi, H.Y.2
Moseley, A.B.3
Rosenblatt, H.M.4
Belmont, J.W.5
-
14
-
-
0027958082
-
Clonality and X-inactivation patterns in hematopoietic cell populations detected by the highly informative M27 beta DNA probe
-
Fey MF, Liechti-Gallati S, von Rohr A, et al. Clonality and X-inactivation patterns in hematopoietic cell populations detected by the highly informative M27 beta DNA probe. Blood. 1994;83:931-938.
-
(1994)
Blood
, vol.83
, pp. 931-938
-
-
Fey, M.F.1
Liechti-Gallati, S.2
Von Rohr, A.3
-
15
-
-
0027174362
-
A novel clonality assay based on transcriptional analysis of the active X chromosome
-
Prchal JT, Guan YL. A novel clonality assay based on transcriptional analysis of the active X chromosome. Stem Cells. 1993;11(suppl 1):62-65.
-
(1993)
Stem Cells
, vol.11
, Issue.SUPPL. 1
, pp. 62-65
-
-
Prchal, J.T.1
Guan, Y.L.2
-
16
-
-
0027454606
-
Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis
-
Prchal JT, Guan YL, Prchal JF, Barany F. Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis. Blood. 1993;81:269-271.
-
(1993)
Blood
, vol.81
, pp. 269-271
-
-
Prchal, J.T.1
Guan, Y.L.2
Prchal, J.F.3
Barany, F.4
-
17
-
-
0029421466
-
A novel clonality assay based on transcriptional polymorphism of X chromosome gene p55
-
Luhovy M, Liu Y, Belickova M, Prchal JF, Prchal JT. A novel clonality assay based on transcriptional polymorphism of X chromosome gene p55. Biol Blood Marrow Transplant. 1995;1:81-87.
-
(1995)
Biol Blood Marrow Transplant
, vol.1
, pp. 81-87
-
-
Luhovy, M.1
Liu, Y.2
Belickova, M.3
Prchal, J.F.4
Prchal, J.T.5
-
18
-
-
0030909351
-
Rapid determination of clonality by detection of two closely-linked X chromosome exonic polymorphisms using allele-specific PCR
-
Liu Y, Phelan J, Go RC, Prchal JF, Prchal JT. Rapid determination of clonality by detection of two closely-linked X chromosome exonic polymorphisms using allele-specific PCR. J Clin Invest. 1997;99:1984-1990.
-
(1997)
J Clin Invest
, vol.99
, pp. 1984-1990
-
-
Liu, Y.1
Phelan, J.2
Go, R.C.3
Prchal, J.F.4
Prchal, J.T.5
-
19
-
-
0034019735
-
A polymorphism of the X-linked gene IDS increases the number of females informative for transcriptional clonality assays
-
Gregg XT, Kralovics R, Prchal JT. A polymorphism of the X-linked gene IDS increases the number of females informative for transcriptional clonality assays. Am J Hematol. 2000;63:184-191.
-
(2000)
Am J Hematol
, vol.63
, pp. 184-191
-
-
Gregg, X.T.1
Kralovics, R.2
Prchal, J.T.3
-
20
-
-
0036362911
-
Clonality studies in cancer based on X chromosome inactivation phenomenon
-
Phelan JT II, Prchal JT. Clonality studies in cancer based on X chromosome inactivation phenomenon. Methods Mol Med. 2002;68:251-270.
-
(2002)
Methods Mol Med
, vol.68
, pp. 251-270
-
-
Phelan J.T. II1
Prchal, J.T.2
-
21
-
-
0031972966
-
X-chromosome inactivation in healthy females: Incidence of excessive lyonization with age and comparison of assays involving DNA methylation and transcript polymorphisms
-
El-Kassar N, Hetet G, Briere J, Grandchamp B. X-chromosome inactivation in healthy females: incidence of excessive lyonization with age and comparison of assays involving DNA methylation and transcript polymorphisms. Clin Chem. 1998;44:61-67.
-
(1998)
Clin Chem
, vol.44
, pp. 61-67
-
-
El-Kassar, N.1
Hetet, G.2
Briere, J.3
Grandchamp, B.4
-
23
-
-
0031019581
-
Clonality analysis of hematopoiesis in essential thrombocythemia: Advantages of studying T lymphocytes and platelets
-
El-Kassar N, Hetet G, Briere J, Grandchamp B. Clonality analysis of hematopoiesis in essential thrombocythemia: advantages of studying T lymphocytes and platelets. Blood. 1997;89:128-134.
-
(1997)
Blood
, vol.89
, pp. 128-134
-
-
El-Kassar, N.1
Hetet, G.2
Briere, J.3
Grandchamp, B.4
-
24
-
-
0027374141
-
Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome)
-
Bunge S, Steglich C, Zuther C, et al. Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome). Hum Mol Genet. 1993;2:1871-1875.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1871-1875
-
-
Bunge, S.1
Steglich, C.2
Zuther, C.3
-
25
-
-
0016391236
-
Bone-marrow responses in polycythemia vera
-
Prchal JF, Axelrad AA. Bone-marrow responses in polycythemia vera [letter]. N Engl J Med. 1974;290:1382.
-
(1974)
N Engl J Med
, vol.290
, pp. 1382
-
-
Prchal, J.F.1
Axelrad, A.A.2
-
26
-
-
0018163444
-
Erythropoietin (Ep) dose-response curves for three classes of erythroid progenitors in normal human marrow and in patients with polycythemia vera
-
Eaves CJ, Eaves AC. Erythropoietin (Ep) dose-response curves for three classes of erythroid progenitors in normal human marrow and in patients with polycythemia vera. Blood. 1978;52:1196-1210.
-
(1978)
Blood
, vol.52
, pp. 1196-1210
-
-
Eaves, C.J.1
Eaves, A.C.2
-
27
-
-
0034656066
-
Cloning of PRV-1, a novel member of the uPAR receptor superfamily, which is overexpressed in polycythemia rubra vera
-
Temednac S, Klippel S, Strunck E, et al. Cloning of PRV-1, a novel member of the uPAR receptor superfamily, which is overexpressed in polycythemia rubra vera. Blood. 2000;95:2569-2576.
-
(2000)
Blood
, vol.95
, pp. 2569-2576
-
-
Temednac, S.1
Klippel, S.2
Strunck, E.3
-
28
-
-
79960971629
-
Quantification of PRV-1 expression, a molecular marker for the diagnosis of polycythemia vera
-
Klippel S, Strunck E, Temerinac S, et al. Quantification of PRV-1 expression, a molecular marker for the diagnosis of polycythemia vera [abstract]. Blood. 2001;98:470a.
-
(2001)
Blood
, vol.98
-
-
Klippel, S.1
Strunck, E.2
Temerinac, S.3
-
29
-
-
79960971482
-
Development of a new quantitative PCR-based assay for the polycythemia rubra vera-1 (PRV-1) gene: Diagnostic and therapeutic implications
-
Fruehauf S, Topaly J, Villalobos M, et al. Development of a new quantitative PCR-based assay for the polycythemia rubra vera-1 (PRV-1) gene: diagnostic and therapeutic implications [abstract]. Blood. 2001;98:629a.
-
(2001)
Blood
, vol.98
-
-
Fruehauf, S.1
Topaly, J.2
Villalobos, M.3
-
30
-
-
0003415792
-
Polycythemia vera
-
Hoffman R, Benz EJJ, Shattil SJ, et al, eds. New York, NY: Churchill Livingstone
-
Hoffman R. Polycythemia vera. In: Hoffman R, Benz EJJ, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 3rd ed. New York, NY: Churchill Livingstone; 2000;1130-1151.
-
(2000)
Hematology: Basic Principles and Practice. 3rd Ed.
, pp. 1130-1151
-
-
Hoffman, R.1
-
31
-
-
0030882659
-
Detection of rifampin resistance by single-strand conformation polymorphism analysis of cerebrospinal fluid of patients with tuberculosis of the central nervous system
-
Scarpellini P, Braglia S, Brambilla AM, et al. Detection of rifampin resistance by single-strand conformation polymorphism analysis of cerebrospinal fluid of patients with tuberculosis of the central nervous system. J Clin Microbiol. 1997;35:2802-2806.
-
(1997)
J Clin Microbiol
, vol.35
, pp. 2802-2806
-
-
Scarpellini, P.1
Braglia, S.2
Brambilla, A.M.3
-
32
-
-
0032128336
-
Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia
-
Kralovics R, Sokol L, Prchal JT. Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia. J Clin Invest. 1998;102:124-129.
-
(1998)
J Clin Invest
, vol.102
, pp. 124-129
-
-
Kralovics, R.1
Sokol, L.2
Prchal, J.T.3
-
33
-
-
0028237666
-
Isolation of cosmid and cDNA clones in the region surrounding the BTK gene at Xq21.3-q22
-
Vorechovsky I, Vetrie D, Holland J, et al. Isolation of cosmid and cDNA clones in the region surrounding the BTK gene at Xq21.3-q22. Genomics. 1994;21:517-524.
-
(1994)
Genomics
, vol.21
, pp. 517-524
-
-
Vorechovsky, I.1
Vetrie, D.2
Holland, J.3
-
34
-
-
0032541324
-
Chromosomal mapping, tissue distribution and cDNA sequence of four-and-a-half LIM domain protein 1 (FHL1)
-
Lee SM, Tsui SK, Chan KK, et al. Chromosomal mapping, tissue distribution and cDNA sequence of four-and-a-half LIM domain protein 1 (FHL1). Gene. 1998;216:163-170.
-
(1998)
Gene
, vol.216
, pp. 163-170
-
-
Lee, S.M.1
Tsui, S.K.2
Chan, K.K.3
-
35
-
-
0020034279
-
Primary thrombocythemia: Clonal origin of platelets, erythrocytes, and granulocytes in a GdB/Gd Mediterranean subject
-
Gaetani GF, Ferraris AM, Galiano S, Giuntini P, Canepa L, d'Urso M. Primary thrombocythemia: clonal origin of platelets, erythrocytes, and granulocytes in a GdB/Gd Mediterranean subject. Blood. 1982;59:76-79.
-
(1982)
Blood
, vol.59
, pp. 76-79
-
-
Gaetani, G.F.1
Ferraris, A.M.2
Galiano, S.3
Giuntini, P.4
Canepa, L.5
D'Urso, M.6
-
36
-
-
0028362575
-
Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: Demonstration of heterogeneity in lineage involvement
-
Tsukamoto N, Morita K, Maehara T, et al. Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: demonstration of heterogeneity in lineage involvement. Br J Haematol. 1994;86:253-258.
-
(1994)
Br J Haematol
, vol.86
, pp. 253-258
-
-
Tsukamoto, N.1
Morita, K.2
Maehara, T.3
-
37
-
-
0028295482
-
Expression of Bruton's agammaglobulinemia tyrosine kinase gene, BTK, is selectively downregulated in T lymphocytes and plasma cells
-
Smith CI, Baskin B, Humire-Greiff P, et al. Expression of Bruton's agammaglobulinemia tyrosine kinase gene, BTK, is selectively downregulated in T lymphocytes and plasma cells. J Immunol. 1994;152:557-565.
-
(1994)
J Immunol
, vol.152
, pp. 557-565
-
-
Smith, C.I.1
Baskin, B.2
Humire-Greiff, P.3
-
38
-
-
0024756969
-
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
-
Orita M, Suzuki Y, Sekiya T, Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics. 1989;5:874-879.
-
(1989)
Genomics
, vol.5
, pp. 874-879
-
-
Orita, M.1
Suzuki, Y.2
Sekiya, T.3
Hayashi, K.4
-
39
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
-
Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc Natl Acad Sci U S A. 1989;86:2766-2770.
-
(1989)
Proc Natl Acad Sci U S A
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
40
-
-
0026207465
-
PCR-SSCP: A simple and sensitive method for detection of mutations in the genomic DNA
-
Hayashi K. PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA. PCR Methods Appl. 1991;1:34-38.
-
(1991)
PCR Methods Appl
, vol.1
, pp. 34-38
-
-
Hayashi, K.1
-
41
-
-
0028137136
-
Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase
-
Conley ME, Fitch-Hilgenberg ME, Cleveland JL, Parolini O, Rohrer J. Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase. Hum Mol Genet. 1994;3:1751-1756.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1751-1756
-
-
Conley, M.E.1
Fitch-Hilgenberg, M.E.2
Cleveland, J.L.3
Parolini, O.4
Rohrer, J.5
-
42
-
-
0023109203
-
Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation
-
Fearon ER, Winkelstein JA, Civin CI, Pardoll DM, Vogelstein B. Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation. N Engl J Med. 1987;316:427-431.
-
(1987)
N Engl J Med
, vol.316
, pp. 427-431
-
-
Fearon, E.R.1
Winkelstein, J.A.2
Civin, C.I.3
Pardoll, D.M.4
Vogelstein, B.5
-
43
-
-
0035106628
-
Pathogenetic mechanisms of polycythemia vera and congenital polycythemic disorders
-
Prchal JT. Pathogenetic mechanisms of polycythemia vera and congenital polycythemic disorders. Semin Hematol. 2001;38:10-20.
-
(2001)
Semin Hematol
, vol.38
, pp. 10-20
-
-
Prchal, J.T.1
-
44
-
-
0030021624
-
Clonal stability of blood cell lineages indicated by X-chromosomal transcriptional polymorphism
-
Prchal JT, Prchal JF, Belickova M, et al. Clonal stability of blood cell lineages indicated by X-chromosomal transcriptional polymorphism. J Exp Med. 1996;183:561-567.
-
(1996)
J Exp Med
, vol.183
, pp. 561-567
-
-
Prchal, J.T.1
Prchal, J.F.2
Belickova, M.3
-
45
-
-
0032576744
-
X inactivation in females with X-linked disease
-
Puck JM, Willard HF. X inactivation in females with X-linked disease. N Engl J Med. 1998;338:325-328.
-
(1998)
N Engl J Med
, vol.338
, pp. 325-328
-
-
Puck, J.M.1
Willard, H.F.2
-
46
-
-
0019212580
-
Wiskott-Aldrich syndrome: Cellular impairments and their implication for carrier detection
-
Prchal JT, Carroll AJ, Prchal JF, et al. Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection. Blood. 1980;56:1048-1054.
-
(1980)
Blood
, vol.56
, pp. 1048-1054
-
-
Prchal, J.T.1
Carroll, A.J.2
Prchal, J.F.3
-
47
-
-
0037441601
-
Mutations in the VHL gene in sporadic apparently congenital polycythemia
-
Pastore YD, Jelinek J, Ang S, et al. Mutations in the VHL gene in sporadic apparently congenital polycythemia. Blood. 2003;101:1591-1595.
-
(2003)
Blood
, vol.101
, pp. 1591-1595
-
-
Pastore, Y.D.1
Jelinek, J.2
Ang, S.3
-
48
-
-
0033954268
-
Diagnosis and treatment of polycythemia vera and possible future study designs of the PVSG
-
Michiels JJ, Barbui T, Finazzi G, et al. Diagnosis and treatment of polycythemia vera and possible future study designs of the PVSG. Leuk Lymphoma. 2000;36:239-253.
-
(2000)
Leuk Lymphoma
, vol.36
, pp. 239-253
-
-
Michiels, J.J.1
Barbui, T.2
Finazzi, G.3
-
49
-
-
0033555392
-
A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications
-
Harrison CN, Gale RE, Machin SJ, Linch DC. A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications. Blood. 1999;93:417-424.
-
(1999)
Blood
, vol.93
, pp. 417-424
-
-
Harrison, C.N.1
Gale, R.E.2
Machin, S.J.3
Linch, D.C.4
-
50
-
-
0034669997
-
Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia
-
Axelrad AA, Eskinazi D, Correa PN, Amato D. Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia. Blood. 2000;96:3310-3321.
-
(2000)
Blood
, vol.96
, pp. 3310-3321
-
-
Axelrad, A.A.1
Eskinazi, D.2
Correa, P.N.3
Amato, D.4
-
51
-
-
0028055045
-
Identification of masked polycythemia vera from patients with idiopathic marked thrombocytosis by endogenous erythroid colony assay
-
Shih LY, Lee CT. Identification of masked polycythemia vera from patients with idiopathic marked thrombocytosis by endogenous erythroid colony assay. Blood. 1994;83:744-748.
-
(1994)
Blood
, vol.83
, pp. 744-748
-
-
Shih, L.Y.1
Lee, C.T.2
-
53
-
-
0033575003
-
Direct comparison of GAPDH, beta-actin, cyclophilin, and 28S rRNA as internal standards for quantifying RNA levels under hypoxia
-
Zhong H, Simons JW. Direct comparison of GAPDH, beta-actin, cyclophilin, and 28S rRNA as internal standards for quantifying RNA levels under hypoxia. Biochem Biophys Res Commun. 1999;259:523-526.
-
(1999)
Biochem Biophys Res Commun
, vol.259
, pp. 523-526
-
-
Zhong, H.1
Simons, J.W.2
-
54
-
-
18744373593
-
Congenital Chuvash polycythemia: Altered oxygen homeostasis due to homozygosity for a hypomorphic VHL allele
-
Ang SO, Chen H, Hirota K, et al. Congenital Chuvash polycythemia: altered oxygen homeostasis due to homozygosity for a hypomorphic VHL allele. Nat Genet. 2002;32:614-621.
-
(2002)
Nat Genet
, vol.32
, pp. 614-621
-
-
Ang, S.O.1
Chen, H.2
Hirota, K.3
-
55
-
-
0036265158
-
Quantitative assessment of gene expression in highly purified hematopoietic cells using real-time reverse transcriptase polymerase chain reaction
-
Raaijmakers MH, van Emst L, de Witte T, Mensink E, Raymakers RA. Quantitative assessment of gene expression in highly purified hematopoietic cells using real-time reverse transcriptase polymerase chain reaction. Exp Hematol. 2002;30:481-487.
-
(2002)
Exp Hematol
, vol.30
, pp. 481-487
-
-
Raaijmakers, M.H.1
Van Emst, L.2
De Witte, T.3
Mensink, E.4
Raymakers, R.A.5
|