-
1
-
-
0003675970
-
Australia, New Guinea, and the Pacific Islands
-
In: Cavalli-Sforza LL, Menozzi P, Piazza A (eds); Princeton University Press, Princeton
-
Cavalli-Sforza LL, Menozzi P, Piazza A (1994) Australia, New Guinea, and the Pacific Islands. In: Cavalli-Sforza LL, Menozzi P, Piazza A (eds) The History and Geography of Human Genes. Princeton University Press, Princeton, pp 343-371
-
(1994)
The History and Geography of Human Genes
, pp. 343-371
-
-
Cavalli-Sforza, L.L.1
Menozzi, P.2
Piazza, A.3
-
2
-
-
0032842164
-
Molecular analysis of secretor type α(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations
-
Chang J-G, Yang T-Y, Liu T-C, Lin T-P, Hu C-T, Kao M-C, Wang N-M, Tsai F-J, Peng C-T, Tsai C-H (1999) Molecular analysis of secretor type α(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations. Transfusion 39:1013-1017
-
(1999)
Transfusion
, vol.39
, pp. 1013-1017
-
-
Chang, J.-G.1
Yang, T.-Y.2
Liu, T.-C.3
Lin, T.-P.4
Hu, C.-T.5
Kao, M.-C.6
Wang, N.-M.7
Tsai, F.-J.8
Peng, C.-T.9
Tsai, C.-H.10
-
3
-
-
0031661279
-
Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups
-
Fernandez-Mateos P, Cailleau A, Henry S, Costache M, Elmgren A, Svensson L, Larson G, Samuelsson BE, Oriol R, Mollicone R (1998) Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups. Vox Sang 75:37-46
-
(1998)
Vox Sang
, vol.75
, pp. 37-46
-
-
Fernandez-Mateos, P.1
Cailleau, A.2
Henry, S.3
Costache, M.4
Elmgren, A.5
Svensson, L.6
Larson, G.7
Samuelsson, B.E.8
Oriol, R.9
Mollicone, R.10
-
4
-
-
0030821992
-
Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection
-
Fu YX (1997) Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics 147:915-925
-
(1997)
Genetics
, vol.147
, pp. 915-925
-
-
Fu, Y.X.1
-
5
-
-
0027453041
-
Statistical tests of neutrality of mutations
-
Fu YX, Li WH (1993) Statistical tests of neutrality of mutations. Genetics 133:693-709
-
(1993)
Genetics
, vol.133
, pp. 693-709
-
-
Fu, Y.X.1
Li, W.H.2
-
7
-
-
0029963803
-
Homozygous expression of a missense mutation at nucleotide 385 in the FUT2 gene associates with the Le(a+b+) partial-secretor phenotype in an Indonesian family
-
Henry S, Mollicone R, Fernandez P, Samuelsson B, Oriol R, Larson G (1996a) Homozygous expression of a missense mutation at nucleotide 385 in the FUT2 gene associates with the Le(a+b+) partial-secretor phenotype in an Indonesian family. Biochem Biophys Res Commun 219:675-678
-
(1996)
Biochem Biophys Res Commun
, vol.219
, pp. 675-678
-
-
Henry, S.1
Mollicone, R.2
Fernandez, P.3
Samuelsson, B.4
Oriol, R.5
Larson, G.6
-
8
-
-
0029773739
-
Molecular basis for erythrocyte Le(a+b+) and salivary ABH partial-secretor phenotypes: Expression of a FUT2 secretor allele with an A→T mutation at nucleotide 385 correlates with reduced α(1,2)fucosyltransferase activity
-
Henry S, Mollicone R, Fernandez P, Samuelson B, Oriol R, Larson G (1996b) Molecular basis for erythrocyte Le(a+b+) and salivary ABH partial-secretor phenotypes: Expression of a FUT2 secretor allele with an A→T mutation at nucleotide 385 correlates with reduced α(1,2)fucosyltransferase activity. Glycoconj J 13:985-993
-
(1996)
Glycoconj J
, vol.13
, pp. 985-993
-
-
Henry, S.1
Mollicone, R.2
Fernandez, P.3
Samuelson, B.4
Oriol, R.5
Larson, G.6
-
9
-
-
0030068036
-
A second nonsecretor allele of the blood group α(1,2)fucosyltransferase gene (FUT2)
-
Henry S, Mollicone R, Lowe JB, Samuelson B, Larson G (1996c) A second nonsecretor allele of the blood group α(1,2)fucosyltransferase gene (FUT2). Vox Sang 70:21-25
-
(1996)
Vox Sang
, vol.70
, pp. 21-25
-
-
Henry, S.1
Mollicone, R.2
Lowe, J.B.3
Samuelson, B.4
Larson, G.5
-
10
-
-
0033886350
-
A new statistic for detecting genetic differentiation
-
Hudson RT (2000) A new statistic for detecting genetic differentiation. Genetics 155:2011-2014
-
(2000)
Genetics
, vol.155
, pp. 2011-2014
-
-
Hudson, R.T.1
-
11
-
-
0026709389
-
Estimation of levels of gene flow from DNA sequence data
-
Hudson RR, Slatkin M, Maddison WP (1992) Estimation of levels of gene flow from DNA sequence data. Genetics 132:583-589
-
(1992)
Genetics
, vol.132
, pp. 583-589
-
-
Hudson, R.R.1
Slatkin, M.2
Maddison, W.P.3
-
12
-
-
0032470821
-
European Y-chromosomal lineages in Polynesians: A contrast to the population structure revealed by mtDNA
-
Hurles ME, Irven C, Nicholson J, Taylor PG, Santos FR, Loughlin J, Jobling MA, Sykes BC (1998) European Y-chromosomal lineages in Polynesians: A contrast to the population structure revealed by mtDNA. Am J Hum Genet 63:1793-1806
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1793-1806
-
-
Hurles, M.E.1
Irven, C.2
Nicholson, J.3
Taylor, P.G.4
Santos, F.R.5
Loughlin, J.6
Jobling, M.A.7
Sykes, B.C.8
-
13
-
-
0033912515
-
The distribution of human genetic diversity: A comparison of mitochondrial, autosomal, and Y-chromosome data
-
Jorde LB, Watkins WS, Bamshad MJ, Dixon ME, Ricker CE, Seielstad MT, Batzer MA (2000) The distribution of human genetic diversity: A comparison of mitochondrial, autosomal, and Y-chromosome data. Am J Hum Genet 66:979-988
-
(2000)
Am J Hum Genet
, vol.66
, pp. 979-988
-
-
Jorde, L.B.1
Watkins, W.S.2
Bamshad, M.J.3
Dixon, M.E.4
Ricker, C.E.5
Seielstad, M.T.6
Batzer, M.A.7
-
14
-
-
0035172065
-
Independent histories of human Y chromosomes from Melanesia and Australia
-
Kayser M, Brauer S, Weiss G, Schiefenhovel W, Underhill PA, Stoneking M (2001a) Independent histories of human Y chromosomes from Melanesia and Australia. Am J Hum Genet 68:173-190
-
(2001)
Am J Hum Genet
, vol.68
, pp. 173-190
-
-
Kayser, M.1
Brauer, S.2
Weiss, G.3
Schiefenhovel, W.4
Underhill, P.A.5
Stoneking, M.6
-
15
-
-
0035076030
-
An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations
-
Kayser M, Krawczak M, Excoffier L, Dieltjes P, Corach D, Pascali V, Gehrig C, Bernini LF, Jespersen J, Bakker E, Roewer L, De Knijff P (2001b) An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations. Am J Hum Genet 68:990-1018
-
(2001)
Am J Hum Genet
, vol.68
, pp. 990-1018
-
-
Kayser, M.1
Krawczak, M.2
Excoffier, L.3
Dieltjes, P.4
Corach, D.5
Pascali, V.6
Gehrig, C.7
Bernini, L.F.8
Jespersen, J.9
Bakker, E.10
Roewer, L.11
De Knijff, P.12
-
16
-
-
0028276829
-
Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals
-
Kelly RJ, Ernst LK, Larsen RD, Bryant JG, Robinson JS, Lowe JB (1994) Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals. Proc Natl Acad Sci USA 91:5843-5847
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 5843-5847
-
-
Kelly, R.J.1
Ernst, L.K.2
Larsen, R.D.3
Bryant, J.G.4
Robinson, J.S.5
Lowe, J.B.6
-
17
-
-
0028965558
-
Sequence and expression of a candidate for the human secretor blood group α(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype
-
Kelly RJ, Rouquier S, Giorgi D, Lennon GG, Lowe JB (1995) Sequence and expression of a candidate for the human secretor blood group α(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype. J Biol Chem 270:4640-4649
-
(1995)
J Biol Chem
, vol.270
, pp. 4640-4649
-
-
Kelly, R.J.1
Rouquier, S.2
Giorgi, D.3
Lennon, G.G.4
Lowe, J.B.5
-
18
-
-
0029816015
-
Molecular basis for secretor type α(1,2)-fucosyltransferase gene deficiency in a Japanese population: A fusion gene generated by unequal crossover responsible for the enzyme deficiency
-
Koda Y, Soejima M, Liu Y-H, Kimura H (1996) Molecular basis for secretor type α(1,2)-fucosyltransferase gene deficiency in a Japanese population: A fusion gene generated by unequal crossover responsible for the enzyme deficiency. Am J Hum Genet 59:343-350
-
(1996)
Am J Hum Genet
, vol.59
, pp. 343-350
-
-
Koda, Y.1
Soejima, M.2
Liu, Y.-H.3
Kimura, H.4
-
19
-
-
0031559828
-
Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system
-
Koda Y, Soejima M, Johnson PH, Smart E, Kimura H (1997) Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system. Biochem Biophys Res Commun 238:21-25
-
(1997)
Biochem Biophys Res Commun
, vol.238
, pp. 21-25
-
-
Koda, Y.1
Soejima, M.2
Johnson, P.H.3
Smart, E.4
Kimura, H.5
-
20
-
-
0034103155
-
An Alu-mediated large deletion of the FUT2 gene in individuals with the ABO-Bombay phenotype
-
Koda Y, Soejima M, Johnson PH, Smart E, Kimura H (2000a) An Alu-mediated large deletion of the FUT2 gene in individuals with the ABO-Bombay phenotype. Hum Genet 106:80-85
-
(2000)
Hum Genet
, vol.106
, pp. 80-85
-
-
Koda, Y.1
Soejima, M.2
Johnson, P.H.3
Smart, E.4
Kimura, H.5
-
22
-
-
0035056717
-
The polymorphisms of fucosyltransferases
-
Koda Y, Soejima M, Kimura H (2001a) The polymorphisms of fucosyltransferases. Legal Med 3:2-14
-
(2001)
Legal Med
, vol.3
, pp. 2-14
-
-
Koda, Y.1
Soejima, M.2
Kimura, H.3
-
23
-
-
0034972749
-
Contrasting patterns of polymorphisms of ABO-secretor gene (FUT2) and plasma α(1,3)fucosyltransferase gene (FUT6) in human populations
-
Koda Y, Tachida H, Pang H, Liu Y-H, Soejima M, Ghaderi AA, Takenaka O, Kimura H (2001b) Contrasting patterns of polymorphisms of ABO-secretor gene (FUT2) and plasma α(1,3)fucosyltransferase gene (FUT6) in human populations. Genetics 158:747-756
-
(2001)
Genetics
, vol.158
, pp. 747-756
-
-
Koda, Y.1
Tachida, H.2
Pang, H.3
Liu, Y.-H.4
Soejima, M.5
Ghaderi, A.A.6
Takenaka, O.7
Kimura, H.8
-
24
-
-
0031595630
-
Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa
-
Liu Y-H, Koda Y, Soejima M, Pang H, Schlaphoff T, Du Toit ED, Kimura H (1998) Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa. Hum Genet 103:204-210
-
(1998)
Hum Genet
, vol.103
, pp. 204-210
-
-
Liu, Y.-H.1
Koda, Y.2
Soejima, M.3
Pang, H.4
Schlaphoff, T.5
Du Toit, E.D.6
Kimura, H.7
-
25
-
-
0032944671
-
The fusion gene at the ABO-secretor locus (FUT2): Absence in Chinese populations
-
Liu Y-H, Koda Y, Soejima M, Pang H, Wang B-J, Kim D-S, Oh H-B, Kimura H (1999) The fusion gene at the ABO-secretor locus (FUT2): Absence in Chinese populations. J Hum Genet 544:181-184
-
(1999)
J Hum Genet
, vol.44
, pp. 181-184
-
-
Liu, Y.-H.1
Koda, Y.2
Soejima, M.3
Pang, H.4
Wang, B.-J.5
Kim, D.-S.6
Oh, H.-B.7
Kimura, H.8
-
26
-
-
0019346542
-
DNA polymorphism detectable by restriction endonucleases
-
Nei M, Tajima F (1981) DNA polymorphism detectable by restriction endonucleases. Genetics 97:145-163
-
(1981)
Genetics
, vol.97
, pp. 145-163
-
-
Nei, M.1
Tajima, F.2
-
27
-
-
0034268003
-
Two distinct Alu-mediated deletions of the human ABO-secretor (FUT2) locus in Samoan and Bangladeshi populations
-
Pang H, Fujitani H, Soejima M, Koda Y, Islam MN, Islam AK, Kimura H (2000) Two distinct Alu-mediated deletions of the human ABO-secretor (FUT2) locus in Samoan and Bangladeshi populations. Hum Mutat 16:274
-
(2000)
Hum Mutat
, vol.16
, pp. 274
-
-
Pang, H.1
Fujitani, H.2
Soejima, M.3
Koda, Y.4
Islam, M.N.5
Islam, A.K.6
Kimura, H.7
-
28
-
-
0035208811
-
Polymorphism of the human ABO-secretor locus (FUT2) in four populations in Asia: Indication of distinct Asian subpopulations
-
Pang H, Koda Y, Soejima M, Fujitani N, Ogaki T, Saito A, Kawasaki T, Kimura H (2001) Polymorphism of the human ABO-secretor locus (FUT2) in four populations in Asia: Indication of distinct Asian subpopulations. Ann Hum Genet 65:429-437
-
(2001)
Ann Hum Genet
, vol.65
, pp. 429-437
-
-
Pang, H.1
Koda, Y.2
Soejima, M.3
Fujitani, N.4
Ogaki, T.5
Saito, A.6
Kawasaki, T.7
Kimura, H.8
-
29
-
-
0032744252
-
Molecular characterization of secretor type α(1,2)fucosyltransferase gene deficiency in the Philippine population
-
Peng C-T, Tsai C-H, Lin T-P, Perng L-I, Kao M-C, Yang T-Y, Wang N-M, Liu T-C, Lin S-F, Chang J-G (1999) Molecular characterization of secretor type α(1,2)fucosyltransferase gene deficiency in the Philippine population. Ann Hematol 78:463-467
-
(1999)
Ann Hematol
, vol.78
, pp. 463-467
-
-
Peng, C.-T.1
Tsai, C.-H.2
Lin, T.-P.3
Perng, L.-I.4
Kao, M.-C.5
Yang, T.-Y.6
Wang, N.-M.7
Liu, T.-C.8
Lin, S.-F.9
Chang, J.-G.10
-
30
-
-
0033358569
-
Peopling of Sahul: mtDNA variation in aboriginal Australian and Papua New Guinea populations
-
Redd AJ, Stoneking M (1999) Peopling of Sahul: mtDNA variation in aboriginal Australian and Papua New Guinea populations. Am J Hum Genet 65:808-828
-
(1999)
Am J Hum Genet
, vol.65
, pp. 808-828
-
-
Redd, A.J.1
Stoneking, M.2
-
31
-
-
0029991274
-
An ancient common origin of aboriginal Australians and New Guinea highlanders is supported by alpha-globin haplotype analysis
-
Roberts-Thomson JM, Martinson JJ, Norwich JT, Harding RM, Clegg JB, Boettcher B (1996) An ancient common origin of aboriginal Australians and New Guinea highlanders is supported by alpha-globin haplotype analysis. Am J Hum Genet 58:1017-1024
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1017-1024
-
-
Roberts-Thomson, J.M.1
Martinson, J.J.2
Norwich, J.T.3
Harding, R.M.4
Clegg, J.B.5
Boettcher, B.6
-
32
-
-
0032972599
-
DnaSP version 3: An integrated program for molecular population genetics and molecular evolution analysis
-
Rozas J, Rozas R (1999) DnaSP version 3: An integrated program for molecular population genetics and molecular evolution analysis. Bioinformatics 15:174-175
-
(1999)
Bioinformatics
, vol.15
, pp. 174-175
-
-
Rozas, J.1
Rozas, R.2
-
33
-
-
0003300707
-
Arlequin ver. 2.000: A software for population genetics data analysis
-
University of Geneva, Switzerland
-
Schneider S, Roessli D, Excoffier L (2000) Arlequin ver. 2.000: A software for population genetics data analysis. Genetics and Biometry Laboratory, University of Geneva, Switzerland
-
(2000)
Genetics and Biometry Laboratory
-
-
Schneider, S.1
Roessli, D.2
Excoffier, L.3
-
34
-
-
0024313579
-
Statistical method for testing the neutral mutation hypothesis by DNA polymorphism
-
Tajima F (1989) Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123:585-595
-
(1989)
Genetics
, vol.123
, pp. 585-595
-
-
Tajima, F.1
-
35
-
-
0033794922
-
Short tandem-repeat polymorphism/Alu haplotype variation at the PLAT locus: Implications for modern human origins
-
Tishkoff SA, Pakstis AJ, Stoneking M, Kidd JR, Destro-Bisol G, Sanjantila A, Lu RB, Deinard AS, Sirugo G, Jenkins T, Kidd KK, Clark AG (2000) Short tandem-repeat polymorphism/Alu haplotype variation at the PLAT locus: Implications for modern human origins. Am J Hum Genet 67:901-925
-
(2000)
Am J Hum Genet
, vol.67
, pp. 901-925
-
-
Tishkoff, S.A.1
Pakstis, A.J.2
Stoneking, M.3
Kidd, J.R.4
Destro-Bisol, G.5
Sanjantila, A.6
Lu, R.B.7
Deinard, A.S.8
Sirugo, G.9
Jenkins, T.10
Kidd, K.K.11
Clark, A.G.12
-
36
-
-
0025017891
-
α-Globin gene markers identify genetic differences between Australian aborigines and Melanesians
-
Tsintsof AS, Hertzberg MS, Prior JF, Mickleson KN, Trent RJ (1990) α-Globin gene markers identify genetic differences between Australian aborigines and Melanesians. Am J Hum Genet 46:138-143
-
(1990)
Am J Hum Genet
, vol.46
, pp. 138-143
-
-
Tsintsof, A.S.1
Hertzberg, M.S.2
Prior, J.F.3
Mickleson, K.N.4
Trent, R.J.5
-
37
-
-
0031001398
-
Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles
-
Wagner FF, Flegel WA (1997) Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles. Transfusion 37:284-290
-
(1997)
Transfusion
, vol.37
, pp. 284-290
-
-
Wagner, F.F.1
Flegel, W.A.2
-
38
-
-
0035128918
-
A new h allele detected in Europe has a missense mutation in α(1,2)-fucosyltransferase motif II
-
Wagner T, Vadon M, Staudacher E, Schmarda A, Gassner C, Helmberg W, Lanzer G, Flegel WA, Wagner FF (2001) A new h allele detected in Europe has a missense mutation in α(1,2)-fucosyltransferase motif II. Transfusion 41:31-38
-
(2001)
Transfusion
, vol.41
, pp. 31-38
-
-
Wagner, T.1
Vadon, M.2
Staudacher, E.3
Schmarda, A.4
Gassner, C.5
Helmberg, W.6
Lanzer, G.7
Flegel, W.A.8
Wagner, F.F.9
-
39
-
-
0031017961
-
Two missense mutations of H type α(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype
-
Wang B-J, Koda Y, Soejima M, Kimura H (1997) Two missense mutations of H type α(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype. Vox Sang 72:31-35
-
(1997)
Vox Sang
, vol.72
, pp. 31-35
-
-
Wang, B.-J.1
Koda, Y.2
Soejima, M.3
Kimura, H.4
-
40
-
-
0016491430
-
On the number of segregating sites in genetical model without recombination
-
Watterson GA (1975) On the number of segregating sites in genetical model without recombination. Theor Popul Biol 7:256-276
-
(1975)
Theor Popul Biol
, vol.7
, pp. 256-276
-
-
Watterson, G.A.1
-
43
-
-
0030585360
-
Heterogeneity of the human secretor α(1,2)fucosyltransferase gene among Lewis(a+b-) non-secretors
-
Yu L-C, Broadberry RE, Yang Y-H, Chen Y-H, Lin M (1996) Heterogeneity of the human secretor α(1,2)fucosyltransferase gene among Lewis(a+b-) non-secretors. Biochem Biophys Res Commun 222:390-394
-
(1996)
Biochem Biophys Res Commun
, vol.222
, pp. 390-394
-
-
Yu, L.-C.1
Broadberry, R.E.2
Yang, Y.-H.3
Chen, Y.-H.4
Lin, M.5
-
44
-
-
0032971968
-
A newly identified nonsecretor allele of the human histo-blood group α(1,2)fucosyltransferase gene (FUT2)
-
Yu L-C, Lee H-L, Chu C-C, Broadberry RE, Lin M (1999) A newly identified nonsecretor allele of the human histo-blood group α(1,2)fucosyltransferase gene (FUT2). Vox Sang 76:115-119
-
(1999)
Vox Sang
, vol.76
, pp. 115-119
-
-
Yu, L.-C.1
Lee, H.-L.2
Chu, C.-C.3
Broadberry, R.E.4
Lin, M.5
|