-
1
-
-
0029554515
-
Molecular genetics of dilated cardiomyopathies
-
Mestroni L, Krajinovic M, Severini GM et al (1995) Molecular genetics of dilated cardiomyopathies. Eur Heart J 16(Suppl O):5-9
-
(1995)
Eur Heart J
, vol.16
, Issue.SUPPL. O
, pp. 5-9
-
-
Mestroni, L.1
Krajinovic, M.2
Severini, G.M.3
-
2
-
-
30944435503
-
Sarcomeric protein mutations in dilated cardiomyopathy
-
Chang AN, Potter JD (2005) Sarcomeric protein mutations in dilated cardiomyopathy. Heart Fail Rev 10:225-235
-
(2005)
Heart Fail Rev
, vol.10
, pp. 225-235
-
-
Chang, A.N.1
Potter, J.D.2
-
4
-
-
84856703950
-
Genetics of inherited cardiomyopathy
-
Jacoby D, McKenna WJ (2012) Genetics of inherited cardiomyopathy. Eur Heart J 33:296-304
-
(2012)
Eur Heart J
, vol.33
, pp. 296-304
-
-
Jacoby, D.1
McKenna, W.J.2
-
5
-
-
0027193330
-
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
-
Towbin JA, Hejtmancik JF, Brink P et al (1993) X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation 87:1854-1865
-
(1993)
Circulation
, vol.87
, pp. 1854-1865
-
-
Towbin, J.A.1
Hejtmancik, J.F.2
Brink, P.3
-
6
-
-
80155210139
-
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: Results from the German Competence Network Heart Failure
-
Waldmüller S, Erdmann J, Binner P et al (2011) Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure. Eur J Heart Fail 13:1185-1192
-
(2011)
Eur J Heart Fail
, vol.13
, pp. 1185-1192
-
-
Waldmüller, S.1
Erdmann, J.2
Binner, P.3
-
7
-
-
39749103537
-
Sarcomeric proteins and inherited cardiomyopathies
-
Morimoto S (2008) Sarcomeric proteins and inherited cardiomyopathies. Cardiovasc Res 77:659-666
-
(2008)
Cardiovasc Res
, vol.77
, pp. 659-666
-
-
Morimoto, S.1
-
8
-
-
79959741856
-
Contribution of genetic factors to the pathogenesis of dilated cardiomyopathy: The cause of dilated cardiomyopathy: Genetic or acquired? (genetic-side
-
Kimura A (2011) Contribution of genetic factors to the pathogenesis of dilated cardiomyopathy: the cause of dilated cardiomyopathy: genetic or acquired? (genetic-side). Circ J 75:1756-1765
-
(2011)
Circ J
, vol.75
, pp. 1756-1765
-
-
Kimura, A.1
-
9
-
-
18444408379
-
Titin mutations as the molecular basis for dilated cardiomyopathy
-
Itoh-Satoh M, Hayashi T, Nishi H et al (2002) Titin mutations as the molecular basis for dilated cardiomyopathy. Biochem Biophys Res Commun 291:385-393
-
(2002)
Biochem Biophys Res Commun
, vol.291
, pp. 385-393
-
-
Itoh-Satoh, M.1
Hayashi, T.2
Nishi, H.3
-
10
-
-
0037184992
-
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
-
Knöll R, Hoshijima M, Hoffman HM et al (2002) The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell 111:943-955
-
(2002)
Cell
, vol.111
, pp. 943-955
-
-
Knöll, R.1
Hoshijima, M.2
Hoffman, H.M.3
-
11
-
-
84863116641
-
Truncations of titin causing dilated cardiomyopathy
-
Herman DS, Lam L, Taylor MR et al (2012) Truncations of titin causing dilated cardiomyopathy. N Engl J Med 366:619-628
-
(2012)
N Engl J Med
, vol.366
, pp. 619-628
-
-
Herman, D.S.1
Lam, L.2
Taylor, M.R.3
-
12
-
-
85047687537
-
Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human
-
Haghighi K, Kolokathis F, Pater L et al (2003) Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human. J Clin Invest 111:869-876
-
(2003)
J Clin Invest
, vol.111
, pp. 869-876
-
-
Haghighi, K.1
Kolokathis, F.2
Pater, L.3
-
13
-
-
0037470512
-
Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban
-
Schmitt JP, Kamisago M, Asahi M et al (2003) Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban. Science 299:1410-1413
-
(2003)
Science
, vol.299
, pp. 1410-1413
-
-
Schmitt, J.P.1
Kamisago, M.2
Asahi, M.3
-
15
-
-
0027985787
-
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
-
Bione S, Maestrini E, Rivella S et al (1994) Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nat Genet 8:323-327
-
(1994)
Nat Genet
, vol.8
, pp. 323-327
-
-
Bione, S.1
Maestrini, E.2
Rivella, S.3
-
16
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
Bonne G, Di Barletta MR, Varnous S et al (1999) Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet 21:285-288
-
(1999)
Nat Genet
, vol.21
, pp. 285-288
-
-
Bonne, G.1
Di Barletta, M.R.2
Varnous, S.3
-
17
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
Fatkin D, MacRae C, Sasaki T et al (1999) Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med 341:1715-1724
-
(1999)
N Engl J Med
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
Macrae, C.2
Sasaki, T.3
-
18
-
-
0032928462
-
Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophy
-
Funakoshi M, Tsuchiya Y, Arahata K (1999) Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophy. Neuromuscul Disord 9:108-114
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 108-114
-
-
Funakoshi, M.1
Tsuchiya, Y.2
Arahata, K.3
-
19
-
-
0035169030
-
The A-type lamins: Nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases
-
Mounkes LC, Burke B, Stewart CL (2001) The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases. Trends Cardiovasc Med 11:280-285
-
(2001)
Trends Cardiovasc Med
, vol.11
, pp. 280-285
-
-
Mounkes, L.C.1
Burke, B.2
Stewart, C.L.3
-
20
-
-
26444469463
-
No positive association between adrenergic receptor variants of ?2cDel322-325, ?1Ser49, ?1Arg389 and the risk for heart failure in the Japanese population
-
Nonen S, Okamoto H, Akino M et al (2005) No positive association between adrenergic receptor variants of ?2cDel322-325, ?1Ser49, ?1Arg389 and the risk for heart failure in the Japanese population. Br J Clin Pharmacol 60:414-417
-
(2005)
Br J Clin Pharmacol
, vol.60
, pp. 414-417
-
-
Nonen, S.1
Okamoto, H.2
Akino, M.3
-
21
-
-
69249211016
-
1- and 2-adrenoceptor polymorphisms and cardiovascular diseases
-
Leineweber K, Heusch G (2009) 1- and 2-adrenoceptor polymorphisms and cardiovascular diseases. Br J Pharmacol 158:61-69
-
(2009)
Br J Pharmacol
, vol.158
, pp. 61-69
-
-
Leineweber, K.1
Heusch, G.2
-
22
-
-
37549002858
-
Role of ?-adrenergic receptor polymorphisms in heart failure: Systematic review and meta-analysis
-
Muthumala A, Drenos F, Elliott PM, Humphries SE (2008) Role of ?-adrenergic receptor polymorphisms in heart failure: systematic review and meta-analysis. Eur J Heart Fail 10:3-13
-
(2008)
Eur J Heart Fail
, vol.10
, pp. 3-13
-
-
Muthumala, A.1
Drenos, F.2
Elliott, P.M.3
Humphries, S.E.4
-
23
-
-
0036023337
-
Suppressive effect of the Gly389 allele of the ?1-adrenergic receptor gene on the occurrence of ventricular tachycardia in dilated cardiomyopathy
-
Iwai C, Akita H, Shiga N et al (2002) Suppressive effect of the Gly389 allele of the ?1-adrenergic receptor gene on the occurrence of ventricular tachycardia in dilated cardiomyopathy. Circ J 66:723-728
-
(2002)
Circ J
, vol.66
, pp. 723-728
-
-
Iwai, C.1
Akita, H.2
Shiga, N.3
-
24
-
-
34547652660
-
1- and 2-Adrenergic receptor polymorphisms affect susceptibility to idiopathic dilated cardiomyopathy
-
Forleo C, Sorrentino S, Guida P et al (2007) 1- and 2-Adrenergic receptor polymorphisms affect susceptibility to idiopathic dilated cardiomyopathy. J Cardiovasc Med (Hagerstown) 8:589-595
-
(2007)
J Cardiovasc Med (Hagerstown)
, vol.8
, pp. 589-595
-
-
Forleo, C.1
Sorrentino, S.2
Guida, P.3
-
25
-
-
42549164339
-
The alpha 2C Del322-325 adrenergic receptor polymorphism is not associated with heart failure due to idiopathic dilated cardiomyopathy in black Africans
-
Du Preez J, Matolweni LO, Greenberg J et al (2008) The alpha 2C Del322-325 adrenergic receptor polymorphism is not associated with heart failure due to idiopathic dilated cardiomyopathy in black Africans. Cardiovasc J Afr 19:15-16
-
(2008)
Cardiovasc J Afr
, vol.19
, pp. 15-16
-
-
Du Preez, J.1
Matolweni, L.O.2
Greenberg, J.3
-
26
-
-
66149093539
-
Polymorphisms of the 1- and 2-adrenergic receptors in Polish patients with idiopathic dilated cardiomyopathy
-
Paczkowska A, Szperl M, Maek et al (2009) Polymorphisms of the ?1- and ?2-adrenergic receptors in Polish patients with idiopathic dilated cardiomyopathy. Kardiol Pol 67:235-241
-
(2009)
Kardiol Pol
, vol.67
, pp. 235-241
-
-
Paczkowska, A.1
Szperl, M.2
Maek3
-
27
-
-
32144444496
-
2C-Adrenoceptor polymorphism is associated with improved event-free survival in patients with dilated cardiomyopathy
-
Regitz-Zagrosek V, Hocher B, Bettmann M et al (2006) 2C-Adrenoceptor polymorphism is associated with improved event-free survival in patients with dilated cardiomyopathy. Eur Heart J 27:454-459
-
(2006)
Eur Heart J
, vol.27
, pp. 454-459
-
-
Regitz-Zagrosek, V.1
Hocher, B.2
Bettmann, M.3
-
28
-
-
41749107345
-
Molecular biology and pathogenesis of viral myocarditis
-
Esfandiarei M, McManus BM (2008) Molecular biology and pathogenesis of viral myocarditis. Annu Rev Pathol 3:127-155
-
(2008)
Annu Rev Pathol
, vol.3
, pp. 127-155
-
-
Esfandiarei, M.1
McManus, B.M.2
-
30
-
-
79953309886
-
Impaired thymic tolerance to ?-myosin directs autoimmunity to the heart in mice and humans
-
Lv H, Havari E, Pinto S et al (2011) Impaired thymic tolerance to ?-myosin directs autoimmunity to the heart in mice and humans. J Clin Invest 121:1561-1573
-
(2011)
J Clin Invest
, vol.121
, pp. 1561-1573
-
-
Lv, H.1
Havari, E.2
Pinto, S.3
-
31
-
-
79953303209
-
Myocarditis: A defect in central immune tolerance?
-
Metzger TC, Anderson MS (2011) Myocarditis: a defect in central immune tolerance? J Clin Invest 121:1251-1253
-
(2011)
J Clin Invest
, vol.121
, pp. 1251-1253
-
-
Metzger, T.C.1
Anderson, M.S.2
-
32
-
-
84865299726
-
PAMPs and DAMPs: Signal 0s that spur autophagy and immunity
-
Tang D, Kang R, Coyne CB et al (2012) PAMPs and DAMPs: signal 0s that spur autophagy and immunity. Immunol Rev 249:158-175
-
(2012)
Immunol Rev
, vol.249
, pp. 158-175
-
-
Tang, D.1
Kang, R.2
Coyne, C.B.3
-
33
-
-
1842683764
-
Immunopathological basis of virus-induced myocarditis
-
Maier R, Krebs P, Ludewig B (2004) Immunopathological basis of virus-induced myocarditis. Clin Dev Immunol 11:1-5
-
(2004)
Clin Dev Immunol
, vol.11
, pp. 1-5
-
-
Maier, R.1
Krebs, P.2
Ludewig, B.3
-
34
-
-
77950926741
-
The innate immune response: An important partner in shaping coxsackievirus-mediated autoimmunity
-
Richer MJ, Horwitz MS (2009) The innate immune response: an important partner in shaping coxsackievirus-mediated autoimmunity. J Innate Immun 1:421-434
-
(2009)
J Innate Immun
, vol.1
, pp. 421-434
-
-
Richer, M.J.1
Horwitz, M.S.2
-
35
-
-
79955601433
-
The emerging role of innate immunity in the heart and vascular system: For whom the cell tolls
-
Mann DL (2011) The emerging role of innate immunity in the heart and vascular system: for whom the cell tolls. Circ Res 108:1133-1145
-
(2011)
Circ Res
, vol.108
, pp. 1133-1145
-
-
Mann, D.L.1
-
36
-
-
79956062189
-
Viral myocarditis: Potential defense mechanisms within the cardiomyocyte against virus infection
-
Yajima T (2011) Viral myocarditis: potential defense mechanisms within the cardiomyocyte against virus infection. Future Microbiol 6:551-566
-
(2011)
Future Microbiol
, vol.6
, pp. 551-566
-
-
Yajima, T.1
-
37
-
-
84855372880
-
Inflammation in myocardial diseases
-
Marchant DJ, Boyd JH et al (2012) Inflammation in myocardial diseases. Circ Res 110:126-144
-
(2012)
Circ Res
, vol.110
, pp. 126-144
-
-
Marchant, D.J.1
Boyd, J.H.2
-
38
-
-
84865794084
-
Cooperation of Th1 and Th17 cells determines transition from autoimmune myocarditis to dilated cardiomyopathy
-
Nindl V, Maier R, Ratering D et al (2012) Cooperation of Th1 and Th17 cells determines transition from autoimmune myocarditis to dilated cardiomyopathy. Eur J Immunol 42:2311-2321
-
(2012)
Eur J Immunol
, vol.42
, pp. 2311-2321
-
-
Nindl, V.1
Maier, R.2
Ratering, D.3
-
39
-
-
37649006061
-
Genetic complexity of autoimmune myocarditis
-
Li HS, Ligons DL, Rose NR (2008) Genetic complexity of autoimmune myocarditis. Autoimmun Rev 7:168-173
-
(2008)
Autoimmun Rev
, vol.7
, pp. 168-173
-
-
Li, H.S.1
Ligons, D.L.2
Rose, N.R.3
-
40
-
-
58149481806
-
HLA-DQB1* polymorphism and associations with dilated cardiomyopathy, inflammatory dilated cardiomyopathy and myocarditis
-
Portig I, Sandmoeller A, Kreilinger S, Maisch B (2009) HLA-DQB1* polymorphism and associations with dilated cardiomyopathy, inflammatory dilated cardiomyopathy and myocarditis. Autoimmunity 42:33-40
-
(2009)
Autoimmunity
, vol.42
, pp. 33-40
-
-
Portig, I.1
Sandmoeller, A.2
Kreilinger, S.3
Maisch, B.4
-
41
-
-
31744450847
-
Relationship of CTLA-4 exon 1 A49G polymorphism with sCTLA-4 and Th1/Th2 bias in idiopathic dilated cardiomyopathy
-
(in Chinese
-
Liu W, Li WM, Gao C et al (2005) Relationship of CTLA-4 exon 1 A49G polymorphism with sCTLA-4 and Th1/Th2 bias in idiopathic dilated cardiomyopathy (in Chinese) Zhonghua Yi Xue Za Zhi 85:3221-3224
-
(2005)
Zhonghua Yi Xue Za Zhi
, vol.85
, pp. 3221-3224
-
-
Liu, W.1
Li, W.M.2
Gao, C.3
-
42
-
-
77952668175
-
Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathy
-
Ruppert V, Meyer T, Struwe C et al (2010) Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathy. Eur J Hum Genet 18:694-699
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 694-699
-
-
Ruppert, V.1
Meyer, T.2
Struwe, C.3
-
43
-
-
0034139830
-
CTLA-4 in autoimmune diseases - A general susceptibility gene to autoimmunity?
-
Kristiansen OP, Larsen ZM, Pociot F (2000) CTLA-4 in autoimmune diseases - a general susceptibility gene to autoimmunity? Genes Immun 1:170-184
-
(2000)
Genes Immun
, vol.1
, pp. 170-184
-
-
Kristiansen, O.P.1
Larsen, Z.M.2
Pociot, F.3
-
45
-
-
0037648405
-
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
-
Ueda H, Howson JM, Esposito L et al (2003) Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature 423:506-511
-
(2003)
Nature
, vol.423
, pp. 506-511
-
-
Ueda, H.1
Howson, J.M.2
Esposito, L.3
-
46
-
-
4444369694
-
B7-1 and B7-2 selectively recruit CTLA-4 and CD28 to the immunological synapse
-
Pentcheva-Hoang T, Egen JG, Wojnoonski K, Allison JP (2004) B7-1 and B7-2 selectively recruit CTLA-4 and CD28 to the immunological synapse. Immunity 21:401-413
-
(2004)
Immunity
, vol.21
, pp. 401-413
-
-
Pentcheva-Hoang, T.1
Egen, J.G.2
Wojnoonski, K.3
Allison, J.P.4
-
47
-
-
49649129944
-
CTLA4 expression is an indicator and regulator of steady-state CD4+FoxP3+T cell homeostasis
-
Tang AL, Teijaro JR, Njau MN et al (2008) CTLA4 expression is an indicator and regulator of steady-state CD4+FoxP3+T cell homeostasis. J Immunol 181:1806-1813
-
(2008)
J Immunol
, vol.181
, pp. 1806-1813
-
-
Tang, A.L.1
Teijaro, J.R.2
Njau, M.N.3
-
48
-
-
63049090504
-
CD4+ regulatory T cells require CTLA-4 for the maintenance of systemic tolerance
-
Friedline RH, Brown DS, Nguyen H et al (2009) CD4+ regulatory T cells require CTLA-4 for the maintenance of systemic tolerance. J Exp Med 206:421-434
-
(2009)
J Exp Med
, vol.206
, pp. 421-434
-
-
Friedline, R.H.1
Brown, D.S.2
Nguyen, H.3
-
49
-
-
0035346140
-
CTLA-4 gene expression is influenced by promoter and exon 1 polymorphisms
-
Ligers A, Teleshova N, Masterman T et al (2001) CTLA-4 gene expression is influenced by promoter and exon 1 polymorphisms. Genes Immun 2:145-152
-
(2001)
Genes Immun
, vol.2
, pp. 145-152
-
-
Ligers, A.1
Teleshova, N.2
Masterman, T.3
-
50
-
-
0036256007
-
A polymorphism in the human cytotoxic T-lymphocyte antigen 4 (CTLA4) gene (exon 1 +49) alters T-cell activation
-
Mäurer M, Loserth S, Kolb-Mäurer A et al (2002) A polymorphism in the human cytotoxic T-lymphocyte antigen 4 (CTLA4) gene (exon 1 +49) alters T-cell activation. Immunogenetics 54:1-8
-
(2002)
Immunogenetics
, vol.54
, pp. 1-8
-
-
Mäurer, M.1
Loserth, S.2
Kolb-Mäurer, A.3
-
51
-
-
2242465734
-
A common autoimmunity predisposing signal peptide variant of the cytotoxic T-lymphocyte antigen 4 results in inefficient glycosylation of the susceptibility allele
-
Anjos S, Nguyen A, Ounissi-Benkalha H et al (2002) A common autoimmunity predisposing signal peptide variant of the cytotoxic T-lymphocyte antigen 4 results in inefficient glycosylation of the susceptibility allele. J Biol Chem 277:46478-46486
-
(2002)
J Biol Chem
, vol.277
, pp. 46478-46486
-
-
Anjos, S.1
Nguyen, A.2
Ounissi-Benkalha, H.3
-
52
-
-
0028867420
-
Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4
-
Tivol EA, Borriello F, Schweitzer AN et al (1995) Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. Immunity 3:541-547
-
(1995)
Immunity
, vol.3
, pp. 541-547
-
-
Tivol, E.A.1
Borriello, F.2
Schweitzer, A.N.3
-
53
-
-
0028791059
-
Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4
-
Waterhouse P, Penninger JM, Timms E et al (1995) Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4. Science 270:985-988
-
(1995)
Science
, vol.270
, pp. 985-988
-
-
Waterhouse, P.1
Penninger, J.M.2
Timms, E.3
-
54
-
-
0031405867
-
Lymphoproliferation in CTLA-4-deficient mice is mediated by costimulation-dependent activation of CD4+ T cells
-
Chambers CA, Sullivan TJ, Allison JP (1997) Lymphoproliferation in CTLA-4-deficient mice is mediated by costimulation-dependent activation of CD4+ T cells. Immunity 7:885-895
-
(1997)
Immunity
, vol.7
, pp. 885-895
-
-
Chambers, C.A.1
Sullivan, T.J.2
Allison, J.P.3
-
55
-
-
0033563265
-
Lymphoproliferative disorder in CTLA-4 knockout mice is characterized by CD28-regulated activation of Th2 responses
-
Khattri R, Auger JA, Griffin MD et al (1999) Lymphoproliferative disorder in CTLA-4 knockout mice is characterized by CD28-regulated activation of Th2 responses. J Immunol 162:5784-5791
-
(1999)
J Immunol
, vol.162
, pp. 5784-5791
-
-
Khattri, R.1
Auger, J.A.2
Griffin, M.D.3
-
56
-
-
0033579816
-
B7-1 or B7-2 is required to produce the lymphoproliferative phenotype in mice lacking cytotoxic T lymphocyte-associated antigen 4 (CTLA-4
-
Mandelbrot DA, McAdam AJ, Sharpe AH (1999) B7-1 or B7-2 is required to produce the lymphoproliferative phenotype in mice lacking cytotoxic T lymphocyte-associated antigen 4 (CTLA-4). J Exp Med 189:435-440
-
(1999)
J Exp Med
, vol.189
, pp. 435-440
-
-
Mandelbrot, D.A.1
McAdam, A.J.2
Sharpe, A.H.3
-
57
-
-
33846301634
-
Signatures of strong population differentiation shape extended haplotypes across the human CD28, CTLA4, and ICOS costimulatory genes
-
Butty V, Roy M, Sabeti P et al (2007) Signatures of strong population differentiation shape extended haplotypes across the human CD28, CTLA4, and ICOS costimulatory genes. Proc Natl Acad Sci USA 104:570-575
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 570-575
-
-
Butty, V.1
Roy, M.2
Sabeti, P.3
|