-
1
-
-
4544345577
-
Detection of retroviral antisense transcripts and promoter activity of the HERV-K(C4) insertion in the MHC class III region
-
Mack M, Bender K, Schneider PM. Detection of retroviral antisense transcripts and promoter activity of the HERV-K(C4) insertion in the MHC class III region. Immunogenetics 2004; 56: 321-332.
-
(2004)
Immunogenetics
, vol.56
, pp. 321-332
-
-
MacK, M.1
Bender, K.2
Schneider, P.M.3
-
2
-
-
0034686608
-
Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease
-
Blanchong CA, Zhou B, Rupert KL, Chung EK, Jones KN, Sotos JF et al. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease. J Exp Med 2000; 191: 2183-2196.
-
(2000)
J Exp Med
, vol.191
, pp. 2183-2196
-
-
Blanchong, C.A.1
Zhou, B.2
Rupert, K.L.3
Chung, E.K.4
Jones, K.N.5
Sotos, J.F.6
-
3
-
-
0042929924
-
Diversity in intrinsic strengths of the human complement system: Serum C4 protein concentrations correlate with C4 gene size and polygenic variations, hemolytic activities, and body mass index
-
Yang Y, Chung EK, Zhou B, Blanchong CA, Yu CY, Fust G et al. Diversity in intrinsic strengths of the human complement system: serum C4 protein concentrations correlate with C4 gene size and polygenic variations, hemolytic activities, and body mass index. J Immunol 2003; 171: 2734-2745.
-
(2003)
J Immunol
, vol.171
, pp. 2734-2745
-
-
Yang, Y.1
Chung, E.K.2
Zhou, B.3
Blanchong, C.A.4
Yu, C.Y.5
Fust, G.6
-
4
-
-
0030053692
-
The reaction mechanism of the internal thioester in the human complement component C4
-
Dodds AW, Ren XD, Willis AC, Law SK. The reaction mechanism of the internal thioester in the human complement component C4. Nature 1996; 379: 177-179.
-
(1996)
Nature
, vol.379
, pp. 177-179
-
-
Dodds, A.W.1
Ren, X.D.2
Willis, A.C.3
Law, S.K.4
-
5
-
-
1442288762
-
The intricate role of complement component C4 in human systemic lupus erythematosus
-
Yang Y, Chung EK, Zhou B, Lhotta K, Hebert LA, Birmingham DJ et al. The intricate role of complement component C4 in human systemic lupus erythematosus. Curr Dir Autoimmun 2004; 7: 98-132.
-
(2004)
Curr Dir Autoimmun
, vol.7
, pp. 98-132
-
-
Yang, Y.1
Chung, E.K.2
Zhou, B.3
Lhotta, K.4
Hebert, L.A.5
Birmingham, D.J.6
-
6
-
-
62549120802
-
Diseases associated with the low copy number of the C4B gene encoding C4, the fourth component of complement
-
Szilagyi A, Fust G. Diseases associated with the low copy number of the C4B gene encoding C4, the fourth component of complement. Cytogenet Genome Res 2008; 123: 118-130.
-
(2008)
Cytogenet Genome Res
, vol.123
, pp. 118-130
-
-
Szilagyi, A.1
Fust, G.2
-
7
-
-
0034454269
-
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
White PC, Speiser PW. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev 2000; 21: 245-291.
-
(2000)
Endocr Rev
, vol.21
, pp. 245-291
-
-
White, P.C.1
Speiser, P.W.2
-
9
-
-
0344688165
-
Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region
-
Lehner B, Semple JI, Brown SE, Counsell D, Campbell RD, Sanderson CM. Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region. Genomics 2004; 83: 153-167.
-
(2004)
Genomics
, vol.83
, pp. 153-167
-
-
Lehner, B.1
Semple, J.I.2
Brown, S.E.3
Counsell, D.4
Campbell, R.D.5
Sanderson, C.M.6
-
10
-
-
62549090133
-
Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: A comparison of Asian-Indian and European American populations
-
Saxena K, Kitzmiller KJ, Wu YL, Zhou B, Esack N, Hiremath L et al. Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations. Mol Immunol 2009; 46: 1289-1303.
-
(2009)
Mol Immunol
, vol.46
, pp. 1289-1303
-
-
Saxena, K.1
Kitzmiller, K.J.2
Wu, Y.L.3
Zhou, B.4
Esack, N.5
Hiremath, L.6
-
11
-
-
0036782903
-
Determining the one, two, three, or four long and short loci of human complement C4 in a major histocompatibility complex haplotype encoding C4A or C4B proteins
-
Chung EK, Yang Y, Rupert KL, Jones KN, Rennebohm RM, Blanchong CA et al. Determining the one, two, three, or four long and short loci of human complement C4 in a major histocompatibility complex haplotype encoding C4A or C4B proteins. Am J Hum Genet 2002; 71: 810-822.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 810-822
-
-
Chung, E.K.1
Yang, Y.2
Rupert, K.L.3
Jones, K.N.4
Rennebohm, R.M.5
Blanchong, C.A.6
-
12
-
-
0042165029
-
Inheritable variable sizes of DNA stretches in the human MHC: Conserved extended haplotypes and their fragments or blocks
-
Yunis EJ, Larsen CE, Fernandez-Vina M, Awdeh ZL, Romero T, Hansen JA et al. Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks. Tissue Antigens 2003; 62: 1-20.
-
(2003)
Tissue Antigens
, vol.62
, pp. 1-20
-
-
Yunis, E.J.1
Larsen, C.E.2
Fernandez-Vina, M.3
Awdeh, Z.L.4
Romero, T.5
Hansen, J.A.6
-
13
-
-
77952546708
-
Frequent occurrence of conserved extended haplotypes (CEHs) in two Caucasian populations
-
Szilagyi A, Banlaki Z, Pozsonyi E, Yunis EJ, Awdeh ZL, Hosso A et al. Frequent occurrence of conserved extended haplotypes (CEHs) in two Caucasian populations. Mol Immunol 2010; 47: 1899-1904.
-
(2010)
Mol Immunol
, vol.47
, pp. 1899-1904
-
-
Szilagyi, A.1
Banlaki, Z.2
Pozsonyi, E.3
Yunis, E.J.4
Awdeh, Z.L.5
Hosso, A.6
-
14
-
-
85099490694
-
-
Bánlaki Z, Szabó JA, Szilágyi Á, Patócs A, Prohászka Z, Füst G et al. Intraspecific evolution of human RCCX copy number variation traced by the haplotypes of CYP21A2 gene (Submitted).
-
Intraspecific Evolution of Human RCCX Copy Number Variation Traced by the Haplotypes of CYP21A2 Gene (Submitted)
-
-
Bánlaki, Z.1
Szabó, J.A.2
Szilágyi, Á.3
Patócs, A.4
Prohászka, Z.5
Füst, G.6
-
15
-
-
34250841166
-
Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): Low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans
-
Yang Y, Chung EK, Wu YL, Savelli SL, Nagaraja HN, Zhou B et al. Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans. Am J Hum Genet 2007; 80: 1037-1054.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 1037-1054
-
-
Yang, Y.1
Chung, E.K.2
Wu, Y.L.3
Savelli, S.L.4
Nagaraja, H.N.5
Zhou, B.6
-
16
-
-
33748302972
-
Conserved extended haplotypes of the major histocompatibility complex: Further characterization
-
Dorak MT, Shao W, Machulla HK, Lobashevsky ES, Tang J, Park MH et al. Conserved extended haplotypes of the major histocompatibility complex: further characterization. Genes Immun 2006; 7: 450-467.
-
(2006)
Genes Immun
, vol.7
, pp. 450-467
-
-
Dorak, M.T.1
Shao, W.2
MacHulla, H.K.3
Lobashevsky, E.S.4
Tang, J.5
Park, M.H.6
-
17
-
-
0026615212
-
Identification of the recombination site within the steroid 21-hydroxylase gene (CYP21) of the HLA-B47,DR7 haplotype
-
Chu X, Braun-Heimer L, Rittner C, Schneider PM. Identification of the recombination site within the steroid 21-hydroxylase gene (CYP21) of the HLA-B47,DR7 haplotype. Exp Clin Immunogenet 1992; 9: 80-85.
-
(1992)
Exp Clin Immunogenet
, vol.9
, pp. 80-85
-
-
Chu, X.1
Braun-Heimer, L.2
Rittner, C.3
Schneider, P.M.4
-
18
-
-
66949132906
-
TNF block haplotypes associated with conserved MHC haplotypes in European, Asian and Australian Aboriginal donors
-
Valente FP, Tan C, Phipps M, Witt CS, Kaur G, Gut I et al. TNF block haplotypes associated with conserved MHC haplotypes in European, Asian and Australian Aboriginal donors. Tissue Antigens 2009; 74: 57-61.
-
(2009)
Tissue Antigens
, vol.74
, pp. 57-61
-
-
Valente, F.P.1
Tan, C.2
Phipps, M.3
Witt, C.S.4
Kaur, G.5
Gut, I.6
-
19
-
-
0036780616
-
Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complex
-
Chung EK, Yang Y, Rennebohm RM, Lokki ML, Higgins GC, Jones KN et al. Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complex. Am J Hum Genet 2002; 71: 823-837.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 823-837
-
-
Chung, E.K.1
Yang, Y.2
Rennebohm, R.M.3
Lokki, M.L.4
Higgins, G.C.5
Jones, K.N.6
-
20
-
-
38349100266
-
Variation analysis and gene annotation of eight MHC haplotypes: The MHC Haplotype Project
-
Horton R, Gibson R, Coggill P, Miretti M, Allcock RJ, Almeida J et al. Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project. Immunogenetics 2008; 60: 1-18.
-
(2008)
Immunogenetics
, vol.60
, pp. 1-18
-
-
Horton, R.1
Gibson, R.2
Coggill, P.3
Miretti, M.4
Allcock, R.J.5
Almeida, J.6
-
21
-
-
62549109138
-
Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: Complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus
-
Wu YL, Yang Y, Chung EK, Zhou B, Kitzmiller KJ, Savelli SL et al. Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus. Cytogenet Genome Res 2008; 123: 131-141.
-
(2008)
Cytogenet Genome Res
, vol.123
, pp. 131-141
-
-
Wu, Y.L.1
Yang, Y.2
Chung, E.K.3
Zhou, B.4
Kitzmiller, K.J.5
Savelli, S.L.6
-
22
-
-
11844263256
-
Diversity of the CYP21P-like gene in CYP21 deficiency
-
Lee HH. Diversity of the CYP21P-like gene in CYP21 deficiency. DNA Cell Biol 2005; 24: 1-9.
-
(2005)
DNA Cell Biol
, vol.24
, pp. 1-9
-
-
Lee, H.H.1
-
23
-
-
33746295401
-
Diversity of the CYP21A2 gene: A 6.2-kb TaqI fragment and a 3.2-kb TaqI fragment mistaken as CYP21A1P
-
Lee HH, Tsai FJ, Lee YJ, Yang YC. Diversity of the CYP21A2 gene: a 6.2-kb TaqI fragment and a 3.2-kb TaqI fragment mistaken as CYP21A1P. Mol Genet Metab 2006; 88: 372-377.
-
(2006)
Mol Genet Metab
, vol.88
, pp. 372-377
-
-
Lee, H.H.1
Tsai, F.J.2
Lee, Y.J.3
Yang, Y.C.4
-
24
-
-
0036821001
-
Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: Characteristics of three unusual haplotypes
-
Koppens PF, Hoogenboezem T, Degenhart HJ. Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes. Hum Genet 2002; 111: 405-410.
-
(2002)
Hum Genet
, vol.111
, pp. 405-410
-
-
Koppens, P.F.1
Hoogenboezem, T.2
Degenhart, H.J.3
-
25
-
-
38449101999
-
Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: Elucidation of C4 CNVs in 50 consanguineous subjects with defined HLA genotypes
-
Wu YL, Savelli SL, Yang Y, Zhou B, Rovin BH, Birmingham DJ et al. Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: elucidation of C4 CNVs in 50 consanguineous subjects with defined HLA genotypes. J Immunol 2007; 179: 3012-3025.
-
(2007)
J Immunol
, vol.179
, pp. 3012-3025
-
-
Wu, Y.L.1
Savelli, S.L.2
Yang, Y.3
Zhou, B.4
Rovin, B.H.5
Birmingham, D.J.6
-
26
-
-
33747843105
-
The HLA 8.1 ancestral haplotype is strongly linked to the C allele of-429 T4C promoter polymorphism of receptor of the advanced glycation endproduct (RAGE) gene, Haplotype-independent association of the-429C allele with high hemoglobinA1C levels in diabetic patients
-
Laki J, Kiszel P, Vatay A, Blasko B, Kovacs M, Korner A et al. The HLA 8.1 ancestral haplotype is strongly linked to the C allele of-429 T4C promoter polymorphism of receptor of the advanced glycation endproduct (RAGE) gene. Haplotype-independent association of the-429C allele with high hemoglobinA1C levels in diabetic patients. Mol Immunol 2007; 44: 648-655.
-
(2007)
Mol Immunol
, vol.44
, pp. 648-655
-
-
Laki, J.1
Kiszel, P.2
Vatay, A.3
Blasko, B.4
Kovacs, M.5
Korner, A.6
-
27
-
-
0242684511
-
Relationship between complement components C4A and C4B diversities and two TNFA promoter polymorphisms in two healthy Caucasian populations
-
Vatay A, Yang Y, Chung EK, Zhou B, Blanchong CA, Kovacs M et al. Relationship between complement components C4A and C4B diversities and two TNFA promoter polymorphisms in two healthy Caucasian populations. Hum Immunol 2003; 64: 543-552.
-
(2003)
Hum Immunol
, vol.64
, pp. 543-552
-
-
Vatay, A.1
Yang, Y.2
Chung, E.K.3
Zhou, B.4
Blanchong, C.A.5
Kovacs, M.6
-
28
-
-
33947511469
-
Predisposition for de novo gene aberrations in the offspring of mothers with a duplicated CYP21A2 gene
-
Baumgartner-Parzer SM, Fischer G, Vierhapper H. Predisposition for de novo gene aberrations in the offspring of mothers with a duplicated CYP21A2 gene. J Clin Endocrinol Metab 2007; 92: 1164-1167.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 1164-1167
-
-
Baumgartner-Parzer, S.M.1
Fischer, G.2
Vierhapper, H.3
-
29
-
-
33745326638
-
Multi-SNP analysis of MHC region: Remarkable conservation of HLA-A1-B8-DR3 haplotype
-
Aly TA, Eller E, Ide A, Gowan K, Babu SR, Erlich HA et al. Multi-SNP analysis of MHC region: remarkable conservation of HLA-A1-B8-DR3 haplotype. Diabetes 2006; 55: 1265-1269.
-
(2006)
Diabetes
, vol.55
, pp. 1265-1269
-
-
Aly, T.A.1
Eller, E.2
Ide, A.3
Gowan, K.4
Babu, S.R.5
Erlich, H.A.6
-
30
-
-
35748942904
-
Genetic control of immune response in carriers of the 8.1 ancestral haplotype: Correlation with levels of IgG subclasses: Its relevance in the pathogenesis of autoimmune diseases
-
Candore G, Campagna AM, Cuppari I, Di Carlo D, Mineo C, Caruso C. Genetic control of immune response in carriers of the 8.1 ancestral haplotype: correlation with levels of IgG subclasses: its relevance in the pathogenesis of autoimmune diseases. Ann N Y Acad Sci 2007; 1110: 151-158.
-
(2007)
Ann N y Acad Sci
, vol.1110
, pp. 151-158
-
-
Candore, G.1
Campagna, A.M.2
Cuppari, I.3
Di Carlo, D.4
Mineo, C.5
Caruso, C.6
-
31
-
-
84855903891
-
Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patients
-
Corvol H, Beucher J, Boelle PY, Busson PF, Muselet-Charlier C, Clement A et al. Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patients. J Cyst Fibros 2012; 11: 63-67.
-
(2012)
J Cyst Fibros
, vol.11
, pp. 63-67
-
-
Corvol, H.1
Beucher, J.2
Boelle, P.Y.3
Busson, P.F.4
Muselet-Charlier, C.5
Clement, A.6
-
32
-
-
79960540929
-
The association of sporadic inclusion body myositis and Sjogren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype
-
Rojana-udomsart A, Needham M, Luo YB, Fabian V, Walters S, Zilko PJ et al. The association of sporadic inclusion body myositis and Sjogren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype. Clin Neurol Neurosurg 2011; 113: 559-563.
-
(2011)
Clin Neurol Neurosurg
, vol.113
, pp. 559-563
-
-
Rojana-Udomsart, A.1
Needham, M.2
Luo, Y.B.3
Fabian, V.4
Walters, S.5
Zilko, P.J.6
-
33
-
-
77952424727
-
Human leukocyte antigen (HLA) A1-B8-DR3 (8.1) haplotype, tumor necrosis factor (TNF) G-308 A, and risk of non-Hodgkin lymphoma
-
Abdou AM, Gao X, Cozen W, Cerhan JR, Rothman N, Martin MP et al. Human leukocyte antigen (HLA) A1-B8-DR3 (8.1) haplotype, tumor necrosis factor (TNF) G-308 A, and risk of non-Hodgkin lymphoma. Leukemia 2010; 24: 1055-1058.
-
(2010)
Leukemia
, vol.24
, pp. 1055-1058
-
-
Abdou, A.M.1
Gao, X.2
Cozen, W.3
Cerhan, J.R.4
Rothman, N.5
Martin, M.P.6
-
34
-
-
77249089237
-
IgA deficiency and the MHC: Assessment of relative risk and micro-heterogeneity within the HLA A1 B8, DR3 (8.1) haplotype
-
Mohammadi J, Ramanujam R, Jarefors S, Rezaei N, Aghamohammadi A, Gregersen PK et al. IgA deficiency and the MHC: assessment of relative risk and micro-heterogeneity within the HLA A1 B8, DR3 (8.1) haplotype. J Clin Immunol 2010; 30: 138-143.
-
(2010)
J Clin Immunol
, vol.30
, pp. 138-143
-
-
Mohammadi, J.1
Ramanujam, R.2
Jarefors, S.3
Rezaei, N.4
Aghamohammadi, A.5
Gregersen, P.K.6
-
35
-
-
21044451157
-
The implication of de novo 21-hydroxylase mutation in clinical and prenatal molecular diagnoses
-
Mao R, McDonald J, Cantwell M, Tang W, Ward K. The implication of de novo 21-hydroxylase mutation in clinical and prenatal molecular diagnoses. Genet Test 2005; 9: 121-125.
-
(2005)
Genet Test
, vol.9
, pp. 121-125
-
-
Mao, R.1
McDonald, J.2
Cantwell, M.3
Tang, W.4
Ward, K.5
-
36
-
-
79959392760
-
Complex disease: Ups and downs at the MHC
-
Muers M. Complex disease: ups and downs at the MHC. Nat Rev Genet 2011; 12: 456-457.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 456-457
-
-
Muers, M.1
-
37
-
-
43549121020
-
Human MHC architecture and evolution: Implications for disease association studies
-
Traherne JA. Human MHC architecture and evolution: implications for disease association studies. Int J Immunogenet 2008; 35: 179-192.
-
(2008)
Int J Immunogenet
, vol.35
, pp. 179-192
-
-
Traherne, J.A.1
-
38
-
-
0038051439
-
Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome
-
Zweers MC, Bristow J, Steijlen PM, Dean WB, Hamel BC, Otero M et al. Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome. Am J Hum Genet 2003; 73: 214-217.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 214-217
-
-
Zweers, M.C.1
Bristow, J.2
Steijlen, P.M.3
Dean, W.B.4
Hamel, B.C.5
Otero, M.6
-
39
-
-
13444293140
-
Confirmation of the association of the C4B null allelle in autism
-
Odell D, Maciulis A, Cutler A, Warren L, McMahon WM, Coon H et al. Confirmation of the association of the C4B null allelle in autism. Hum Immunol 2005; 66: 140-145.
-
(2005)
Hum Immunol
, vol.66
, pp. 140-145
-
-
Odell, D.1
MacIulis, A.2
Cutler, A.3
Warren, L.4
McMahon, W.M.5
Coon, H.6
-
40
-
-
48249100020
-
Complement C4B protein in schizophrenia
-
Mayilyan KR, Dodds AW, Boyajyan AS, Soghoyan AF, Sim RB. Complement C4B protein in schizophrenia. World J Biol Psychiatry 2008; 9: 225-230.
-
(2008)
World J Biol Psychiatry
, vol.9
, pp. 225-230
-
-
Mayilyan, K.R.1
Dodds, A.W.2
Boyajyan, A.S.3
Soghoyan, A.F.4
Sim, R.B.5
-
41
-
-
59449090701
-
Genetic deficiency of complement isoforms C4A or C4B predicts improved survival of metastatic renal cell carcinoma
-
discussion 34
-
Zafar GI, Grimm EA, Wei W, Johnson MM, Ellerhorst JA. Genetic deficiency of complement isoforms C4A or C4B predicts improved survival of metastatic renal cell carcinoma. J Urol 2009; 181: 1028-1034; discussion 34.
-
(2009)
J Urol
, vol.181
, pp. 1028-1034
-
-
Zafar, G.I.1
Grimm, E.A.2
Wei, W.3
Johnson, M.M.4
Ellerhorst, J.A.5
-
42
-
-
30844470456
-
Real-time PCR quantification of human complement C4A and C4B genes
-
Szilagyi A, Blasko B, Szilassy D, Fust G, Sasvari-Szekely M, Ronai Z. Real-time PCR quantification of human complement C4A and C4B genes. BMC Genet 2006; 7: 1.
-
(2006)
BMC Genet
, vol.7
, pp. 1
-
-
Szilagyi, A.1
Blasko, B.2
Szilassy, D.3
Fust, G.4
Sasvari-Szekely, M.5
Ronai, Z.6
-
43
-
-
85007110786
-
Arlequin (version 3.0): An integrated software package for population genetics data analysis
-
Excoffier L, Laval G, Schneider S. Arlequin (version 3.0): an integrated software package for population genetics data analysis. Evol Bioinform Online 2005; 1: 47-50.
-
(2005)
Evol Bioinform Online
, vol.1
, pp. 47-50
-
-
Excoffier, L.1
Laval, G.2
Schneider, S.3
|