-
1
-
-
0025343444
-
Assessment of clonality in human tumors: A review
-
Wainscoat JS, Fey MF. Assessment of clonality in human tumors: A review. Cancer Res 1990;50:1355-1360.
-
(1990)
Cancer Res
, vol.50
, pp. 1355-1360
-
-
Wainscoat, J.S.1
Fey, M.F.2
-
2
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (Mus musculus L.)
-
Lyon MF. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature 1961;190:372-373.
-
(1961)
Nature
, vol.190
, pp. 372-373
-
-
Lyon, M.F.1
-
3
-
-
0002826398
-
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. Normal human female as a mosaic of X-chromosome activity: Studies using the gene for G6PD deficiency as a marker. Proc Natl Acad Sci USA 1962;48:9-16.
-
(1962)
Proc Natl Acad Sci USA
, vol.48
, pp. 9-16
-
-
Beutler, E.1
Yeh, M.2
Fairbanks, V.F.3
-
4
-
-
0023946968
-
X-chromosome inactivation and the location and expression of X-linked genes
-
Lyon MF. X-chromosome inactivation and the location and expression of X-linked genes. Am J Hum Genet 1988;42:8-16.
-
(1988)
Am J Hum Genet
, vol.42
, pp. 8-16
-
-
Lyon, M.F.1
-
5
-
-
0020987354
-
Mammalian X-chromosome inactivation
-
Gartler SM, Riggs, AD. Mammalian X-chromosome inactivation. Annu Rev Genet 1983;17:155-190.
-
(1983)
Annu Rev Genet
, vol.17
, pp. 155-190
-
-
Gartler, S.M.1
Riggs, A.D.2
-
6
-
-
0001872496
-
Glucose-6-dehydrogenase mosaicism: Utilization as a cell marker in the study of leiomyomas
-
Linder D, Gartler SM. Glucose-6-dehydrogenase mosaicism: Utilization as a cell marker in the study of leiomyomas. Science 1965;150: 67-69.
-
(1965)
Science
, vol.150
, pp. 67-69
-
-
Linder, D.1
Gartler, S.M.2
-
7
-
-
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
-
-
0015258886
-
Use of genetic markers to study cellular origin of development of tumors in human females
-
Fialkow PJ. Use of genetic markers to study cellular origin of development of tumors in human females. Adv Cancer Res 1972;15:191-226.
-
(1972)
Adv Cancer Res
, vol.15
, pp. 191-226
-
-
Fialkow, P.J.1
-
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
-
-
0022820116
-
Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-pluscytosine-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-pluscytosine-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
-
12
-
-
0023626415
-
Clonal analysis using recombinant DNA probes from the X-chromosome
-
Vogelstein B, Fearon ER, Hamilton SR. 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
-
13
-
-
0026678490
-
Methylation of HpaII and HpaI 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 HpaII and HpaI 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
-
-
0025324635
-
Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status
-
Boyd Y, Fraser NJ. Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status. Genomics 1990;7:182-187.
-
(1990)
Genomics
, vol.7
, pp. 182-187
-
-
Boyd, Y.1
Fraser, N.J.2
-
15
-
-
0027958082
-
Clonality and X-inactivation patterns in hematopoietic cell populations detected by the highly informative M27β DNA probe
-
Fey MF, Liechti-Gallati S, von Rohr A. Clonality and X-inactivation patterns in hematopoietic cell populations detected by the highly informative M27β 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
-
16
-
-
0027441009
-
Clonal analysis using X-linked DNA polymorphisms
-
Gale RE, Wainscoat, JS. Clonal analysis using X-linked DNA polymorphisms. Br J Haematol 1993;85:2-8.
-
(1993)
Br J Haematol
, vol.85
, pp. 2-8
-
-
Gale, R.E.1
Wainscoat, J.S.2
-
17
-
-
0025851838
-
Variable X-chromosome DNA methylation patterns detected with M27β probe in a series of lymphoid and myeloid malignancies
-
Hodges E, Howell WM, Boyd Y, Smith JL. Variable X-chromosome DNA methylation patterns detected with M27β probe in a series of lymphoid and myeloid malignancies. Br J Haematol 1991;77:315-322.
-
(1991)
Br J Haematol
, vol.77
, pp. 315-322
-
-
Hodges, E.1
Howell, W.M.2
Boyd, Y.3
Smith, J.L.4
-
18
-
-
0026710893
-
Assessment of X-chromosome inactivation patterns using HPRT and PGK polymorphisms in haematologically normal and post-chemotherapy females
-
Gale RE, Wheadon H, Linch DC. Assessment of X-chromosome inactivation patterns using HPRT and PGK polymorphisms in haematologically normal and post-chemotherapy females. Leukemia 1992; 6:649-655.
-
(1992)
Leukemia
, vol.6
, pp. 649-655
-
-
Gale, R.E.1
Wheadon, H.2
Linch, D.C.3
-
19
-
-
0027174362
-
A novel clonality assay based on transcriptional analysis of the active X chromosome in normal and clonal hematopoiesis
-
Prchal JT, Guan YL. A novel clonality assay based on transcriptional analysis of the active X chromosome in normal and clonal hematopoiesis. Stem Cells 1993;11:62-65.
-
(1993)
Stem Cells
, vol.11
, pp. 62-65
-
-
Prchal, J.T.1
Guan, Y.L.2
-
20
-
-
85084624169
-
Transcriptional analysis of the active X chromosome in normal and abnormal hematopoiesis
-
Prchal JT, Prchal JF, Barany F, Guan YL. Transcriptional analysis of the active X chromosome in normal and abnormal hematopoiesis. Blood 1993;81:269-271.
-
(1993)
Blood
, vol.81
, pp. 269-271
-
-
Prchal, J.T.1
Prchal, J.F.2
Barany, F.3
Guan, Y.L.4
-
21
-
-
0029421466
-
A novel clonality assay based on transcriptional polymorphism of X-chromosome gene p55
-
Luhovy M, Lin 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
Lin, Y.2
Belickova, M.3
Prchal, J.F.4
Prchal, J.T.5
-
22
-
-
0030909351
-
Rapid determination of clonality by detection of two closely linked X-chromosome exonic polymorphisms using allele-specific PCR
-
Liu Y, Phelan J, Go RCP, 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.P.3
Prchal, J.F.4
Prchal, J.T.5
-
23
-
-
0002713231
-
Allele specific enzymatic amplification of beta globin genomic DNA for diagnosis of sickle cell anemia
-
Wu DY, Ugozzoli L, Pal BK, Wallace RB. Allele specific enzymatic amplification of beta globin genomic DNA for diagnosis of sickle cell anemia Proc Natl Acad Sci USA 1989;86:2757-2760.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 2757-2760
-
-
Wu, D.Y.1
Ugozzoli, L.2
Pal, B.K.3
Wallace, R.B.4
-
24
-
-
0023022499
-
Analysis of enzymatically amplified β globin and HLA-DQ α DNA with allele-specific oligonucleotide probes
-
Saiki RK, Bugawan TL, Horn GT, Mullis KB, Erlich HA. Analysis of enzymatically amplified β globin and HLA-DQ α DNA with allele-specific oligonucleotide probes. Nature (London) 1986;324:163-166.
-
(1986)
Nature (London)
, vol.324
, pp. 163-166
-
-
Saiki, R.K.1
Bugawan, T.L.2
Horn, G.T.3
Mullis, K.B.4
Erlich, H.A.5
-
25
-
-
0026512912
-
PCR amplification of specific alleles (PASA) is a general method for rapidly detecting known single base changes
-
Sommer SS, Groszbach AR, Bottema CDK. PCR amplification of specific alleles (PASA) is a general method for rapidly detecting known single base changes. Biotechniques 1992;12:82-87.
-
(1992)
Biotechniques
, vol.12
, pp. 82-87
-
-
Sommer, S.S.1
Groszbach, A.R.2
Bottema, C.D.K.3
-
26
-
-
0026907536
-
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)
-
Bunge S, Steglich C, Bech M, Rosenkranz W, Schwinger E, Hopwood JJ, Gal A. Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome). Hum Mol Genet 1992;5:335-339.
-
(1992)
Hum Mol Genet
, vol.5
, pp. 335-339
-
-
Bunge, S.1
Steglich, C.2
Bech, M.3
Rosenkranz, W.4
Schwinger, E.5
Hopwood, J.J.6
Gal, A.7
-
27
-
-
0026660087
-
Detection of point mutations and a gross deletion in six Hunter syndrome patients
-
Flomen RH, Green PM, Bentley DR, Giannelli F, Green EP. Detection of point mutations and a gross deletion in six Hunter syndrome patients. Genomics 1992;13:543-550.
-
(1992)
Genomics
, vol.13
, pp. 543-550
-
-
Flomen, R.H.1
Green, P.M.2
Bentley, D.R.3
Giannelli, F.4
Green, E.P.5
-
28
-
-
0024519065
-
Further evidence localising the gene for Hunter's syndrome to the distal region of the X-chromosome long arm
-
Roberts SH, Upadhyaya M, Sarfarazi M, Harper PS. Further evidence localising the gene for Hunter's syndrome to the distal region of the X-chromosome long arm. J Med Genet 1989;26:309-313.
-
(1989)
J Med Genet
, vol.26
, pp. 309-313
-
-
Roberts, S.H.1
Upadhyaya, M.2
Sarfarazi, M.3
Harper, P.S.4
-
29
-
-
0029161632
-
Presence of IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome
-
Bondeson M-L, Malmgren H, Dahl N, Carlherg B-M, Pettersson U. Presence of IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome. Eur J Hum Genet 1995;3:219-227.
-
(1995)
Eur J Hum Genet
, vol.3
, pp. 219-227
-
-
Bondeson, M.-L.1
Malmgren, H.2
Dahl, N.3
Carlherg, B.-M.4
Pettersson, U.5
-
31
-
-
0024284028
-
A simple salting oui procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting oui procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988; 16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
32
-
-
0019738069
-
DNA analysis in the diagnosis of hemoglobin disorders
-
Goossens M, Kan YW. DNA analysis in the diagnosis of hemoglobin disorders. Methods Enzymol 1981;76:805-817.
-
(1981)
Methods Enzymol
, vol.76
, pp. 805-817
-
-
Goossens, M.1
Kan, Y.W.2
-
33
-
-
0026056970
-
Genetic disease detection and DNA amplification using cloned thermostable ligase
-
Barany F. Genetic disease detection and DNA amplification using cloned thermostable ligase. Proc Natl Acad Sci USA 1991;88:189-193.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 189-193
-
-
Barany, F.1
-
34
-
-
0025889025
-
Cloning expression and nucleotide sequence of a thermostable DNA ligase-encoding gene
-
Barany F, Gelfand D. Cloning expression and nucleotide sequence of a thermostable DNA ligase-encoding gene. Gene 1991;109:1-11.
-
(1991)
Gene
, vol.109
, pp. 1-11
-
-
Barany, F.1
Gelfand, D.2
-
36
-
-
0013786051
-
The approach to a random association of genotypes with random mating
-
Bennett JH, Oertel CR. The approach to a random association of genotypes with random mating. J Theor Biol 1965;9:67-76.
-
(1965)
J Theor Biol
, vol.9
, pp. 67-76
-
-
Bennett, J.H.1
Oertel, C.R.2
-
37
-
-
0004242267
-
-
Portola Valley: Bartlett and Jones Publishers, Inc.
-
Hedrick PW, editor. Genetics of Populations. Portola Valley: Bartlett and Jones Publishers, Inc.: 1974.
-
(1974)
Genetics of Populations
-
-
Hedrick, P.W.1
-
38
-
-
0016319012
-
Estimation of linkage disequilibrium in randomly mating populations
-
Hill WG. Estimation of linkage disequilibrium in randomly mating populations. Heredity 1974;33:229-239.
-
(1974)
Heredity
, vol.33
, pp. 229-239
-
-
Hill, W.G.1
-
39
-
-
0027178843
-
G6PD haplotypes spanning Xq28 from F8C to red/green color vision
-
Filosa S, Calahro V, Han D, Packer L. G6PD haplotypes spanning Xq28 from F8C to red/green color vision. Genomics 1993;17:6-14.
-
(1993)
Genomics
, vol.17
, pp. 6-14
-
-
Filosa, S.1
Calahro, V.2
Han, D.3
Packer, L.4
-
40
-
-
0026864937
-
The gene coding the palmitoylated erythrocyte membrane protein p55 originates CpG island 3′ to the Factor VIII gene
-
Metzenger AB, Gitschier J. The gene coding the palmitoylated erythrocyte membrane protein p55 originates CpG island 3′ to the Factor VIII gene. Hum Mol Genet 1996;1:97-101.
-
(1996)
Hum Mol Genet
, vol.1
, pp. 97-101
-
-
Metzenger, A.B.1
Gitschier, J.2
-
41
-
-
0002791380
-
Molecular and genetic studies of human X chromosome inactivation
-
Brown CJ, Willard HF. Molecular and genetic studies of human X chromosome inactivation. Adv Dev Biol 1993;2:37-76.
-
(1993)
Adv Dev Biol
, vol.2
, pp. 37-76
-
-
Brown, C.J.1
Willard, H.F.2
-
42
-
-
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
-
43
-
-
0019455210
-
Evidence for a multistep pathogenesis of chronic myelogenous leukemia
-
Fialkow PJ, Martin PJ, Najfeld V, Penfold GK, Jacobson RJ, Hansen JA. Evidence for a multistep pathogenesis of chronic myelogenous leukemia. Blood 1981;58:159-163.
-
(1981)
Blood
, vol.58
, pp. 159-163
-
-
Fialkow, P.J.1
Martin, P.J.2
Najfeld, V.3
Penfold, G.K.4
Jacobson, R.J.5
Hansen, J.A.6
-
44
-
-
0000453311
-
Clonality of myeloproliferative disorders
-
Gregg XT, Liu Y, Prchal JT, Gartland GL, Cooper MD, Prchal JF. Clonality of myeloproliferative disorders. Blood 1996;88:479a.
-
(1996)
Blood
, vol.88
-
-
Gregg, X.T.1
Liu, Y.2
Prchal, J.T.3
Gartland, G.L.4
Cooper, M.D.5
Prchal, J.F.6
-
45
-
-
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
|