-
1
-
-
33749430257
-
Genetics of epidermodysplasia verruciformis: Insights into host defense against papillomaviruses
-
Orth G, (2006) Genetics of epidermodysplasia verruciformis: Insights into host defense against papillomaviruses. Semin Immunol 18: 362-374.
-
(2006)
Semin Immunol
, vol.18
, pp. 362-374
-
-
Orth, G.1
-
2
-
-
51149111202
-
Host defenses against human papillomaviruses: lessons from epidermodysplasia verruciformis
-
Orth G, (2008) Host defenses against human papillomaviruses: lessons from epidermodysplasia verruciformis. Curr Top Microbiol Immunol 321: 59-83.
-
(2008)
Curr Top Microbiol Immunol
, vol.321
, pp. 59-83
-
-
Orth, G.1
-
4
-
-
18744369886
-
Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis
-
Ramoz N, Rueda LA, Bouadjar B, Montoya LS, Orth G, et al. (2002) Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis. Nat Genet 32: 579-581.
-
(2002)
Nat Genet
, vol.32
, pp. 579-581
-
-
Ramoz, N.1
Rueda, L.A.2
Bouadjar, B.3
Montoya, L.S.4
Orth, G.5
-
5
-
-
22944461763
-
Inborn errors of immunity to infection: the rule rather than the exception
-
Casanova JL, Abel L, (2005) Inborn errors of immunity to infection: the rule rather than the exception. J Exp Med 202: 197-201.
-
(2005)
J Exp Med
, vol.202
, pp. 197-201
-
-
Casanova, J.L.1
Abel, L.2
-
6
-
-
34547732069
-
Primary immunodeficiencies: a field in its infancy
-
Casanova JL, Abel L, (2007) Primary immunodeficiencies: a field in its infancy. Science 317: 617-619.
-
(2007)
Science
, vol.317
, pp. 617-619
-
-
Casanova, J.L.1
Abel, L.2
-
7
-
-
70349220934
-
Human genetics of infectious diseases: between proof of principle and paradigm
-
Alcais A, Abel L, Casanova JL, (2009) Human genetics of infectious diseases: between proof of principle and paradigm. J Clin Invest 119: 2506-2514.
-
(2009)
J Clin Invest
, vol.119
, pp. 2506-2514
-
-
Alcais, A.1
Abel, L.2
Casanova, J.L.3
-
8
-
-
77957020774
-
Life-threatening infectious diseases of childhood: single-gene inborn errors of immunity
-
Alcais A, Quintana-Murci L, Thaler DS, Schurr E, Abel L, et al. (2010) Life-threatening infectious diseases of childhood: single-gene inborn errors of immunity? Ann N Y Acad Sci 1214: 18-33.
-
(2010)
Ann N Y Acad Sci
, vol.1214
, pp. 18-33
-
-
Alcais, A.1
Quintana-Murci, L.2
Thaler, D.S.3
Schurr, E.4
Abel, L.5
-
9
-
-
38749086503
-
Regulation of cellular zinc balance as a potential mechanism of EVER-mediated protection against pathogenesis by cutaneous oncogenic human papillomaviruses
-
Lazarczyk M, Pons C, Mendoza JA, Cassonnet P, Jacob Y, et al. (2008) Regulation of cellular zinc balance as a potential mechanism of EVER-mediated protection against pathogenesis by cutaneous oncogenic human papillomaviruses. J Exp Med 205: 35-42.
-
(2008)
J Exp Med
, vol.205
, pp. 35-42
-
-
Lazarczyk, M.1
Pons, C.2
Mendoza, J.A.3
Cassonnet, P.4
Jacob, Y.5
-
10
-
-
36148975407
-
A novel homozygous mutation of the EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis
-
Aochi S, Nakanishi G, Suzuki N, Setsu N, Suzuki D, et al. (2007) A novel homozygous mutation of the EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis. Br J Dermatol 157: 1265-1266.
-
(2007)
Br J Dermatol
, vol.157
, pp. 1265-1266
-
-
Aochi, S.1
Nakanishi, G.2
Suzuki, N.3
Setsu, N.4
Suzuki, D.5
-
11
-
-
34147160203
-
Treatment of a patient with epidermodysplasia verruciformis carrying a novel EVER2 mutation with imiquimod
-
Berthelot C, Dickerson MC, Rady P, He Q, Niroomand F, et al. (2007) Treatment of a patient with epidermodysplasia verruciformis carrying a novel EVER2 mutation with imiquimod. J Am Acad Dermatol 56: 882-886.
-
(2007)
J Am Acad Dermatol
, vol.56
, pp. 882-886
-
-
Berthelot, C.1
Dickerson, M.C.2
Rady, P.3
He, Q.4
Niroomand, F.5
-
12
-
-
33947263257
-
Novel homozygous frameshift mutation of EVER1 gene in an epidermodysplasia verruciformis patient
-
Gober MD, Rady PL, He Q, Tucker SB, Tyring SK, et al. (2007) Novel homozygous frameshift mutation of EVER1 gene in an epidermodysplasia verruciformis patient. J Invest Dermatol 127: 817-820.
-
(2007)
J Invest Dermatol
, vol.127
, pp. 817-820
-
-
Gober, M.D.1
Rady, P.L.2
He, Q.3
Tucker, S.B.4
Tyring, S.K.5
-
13
-
-
33751170449
-
Identification of a novel mutation and a genetic polymorphism of EVER1 gene in two families with epidermodysplasia verruciformis
-
Zuo YG, Ma D, Zhang Y, Qiao J, Wang B, (2006) Identification of a novel mutation and a genetic polymorphism of EVER1 gene in two families with epidermodysplasia verruciformis. J Dermatol Sci 44: 153-159.
-
(2006)
J Dermatol Sci
, vol.44
, pp. 153-159
-
-
Zuo, Y.G.1
Ma, D.2
Zhang, Y.3
Qiao, J.4
Wang, B.5
-
14
-
-
23044509522
-
A homozygous nonsense mutation in the EVER2 gene leads to epidermodysplasia verruciformis
-
Sun XK, Chen JF, Xu AE, (2005) A homozygous nonsense mutation in the EVER2 gene leads to epidermodysplasia verruciformis. Clin Exp Dermatol 30: 573-574.
-
(2005)
Clin Exp Dermatol
, vol.30
, pp. 573-574
-
-
Sun, X.K.1
Chen, J.F.2
Xu, A.E.3
-
15
-
-
2442694458
-
Novel mutations of EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis
-
Tate G, Suzuki T, Kishimoto K, Mitsuya T, (2004) Novel mutations of EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis. J Hum Genet 49: 223-225.
-
(2004)
J Hum Genet
, vol.49
, pp. 223-225
-
-
Tate, G.1
Suzuki, T.2
Kishimoto, K.3
Mitsuya, T.4
-
16
-
-
34548580630
-
Novel homozygous nonsense TMC8 mutation detected in patients with epidermodysplasia verruciformis from a Brazilian family
-
Rady PL, De Oliveira WR, He Q, Festa C, Rivitti EA, et al. (2007) Novel homozygous nonsense TMC8 mutation detected in patients with epidermodysplasia verruciformis from a Brazilian family. Br J Dermatol 157: 831-833.
-
(2007)
Br J Dermatol
, vol.157
, pp. 831-833
-
-
Rady, P.L.1
de Oliveira, W.R.2
He, Q.3
Festa, C.4
Rivitti, E.A.5
-
17
-
-
84865426636
-
Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections
-
in Press
-
Crequer A, Troeger A, Patin E, Ma CS, Picard C, et al. (2012) Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections. Journal of Clinical Investigation in Press.
-
(2012)
Journal of Clinical Investigation
-
-
Crequer, A.1
Troeger, A.2
Patin, E.3
Ma, C.S.4
Picard, C.5
-
18
-
-
58149328497
-
Acquired epidermodysplasia verruciformis
-
Rogers HD, Macgregor JL, Nord KM, Tyring S, Rady P, et al. (2009) Acquired epidermodysplasia verruciformis. J Am Acad Dermatol 60: 315-320.
-
(2009)
J Am Acad Dermatol
, vol.60
, pp. 315-320
-
-
Rogers, H.D.1
Macgregor, J.L.2
Nord, K.M.3
Tyring, S.4
Rady, P.5
-
19
-
-
84857971327
-
Epidermodysplasia verruciformis and human immunodeficiency virus infection: a distinct entity?
-
Daly ML, Hay RJ (2012) Epidermodysplasia verruciformis and human immunodeficiency virus infection: a distinct entity? Curr Opin Infect Dis.
-
(2012)
Curr Opin Infect Dis
-
-
Daly, M.L.1
Hay, R.J.2
-
20
-
-
0022138199
-
Papillomavirus lesions in immunodepression and immunosuppression
-
Lutzner MA, (1985) Papillomavirus lesions in immunodepression and immunosuppression. Clin Dermatol 3: 165-169.
-
(1985)
Clin Dermatol
, vol.3
, pp. 165-169
-
-
Lutzner, M.A.1
-
21
-
-
45449126315
-
Epidermodysplasia verruciformis in a patient with Hodgkin's disease: characterization of a new papillomavirus type and interferon treatment
-
Gross G, Ellinger K, Roussaki A, Fuchs PG, Peter HH, et al. (1988) Epidermodysplasia verruciformis in a patient with Hodgkin's disease: characterization of a new papillomavirus type and interferon treatment. J Invest Dermatol 91: 43-48.
-
(1988)
J Invest Dermatol
, vol.91
, pp. 43-48
-
-
Gross, G.1
Ellinger, K.2
Roussaki, A.3
Fuchs, P.G.4
Peter, H.H.5
-
22
-
-
2942648153
-
Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common gammac cytokine receptor subunit or JAK-3 deficiency
-
Laffort C, Le Deist F, Favre M, Caillat-Zucman S, Radford-Weiss I, et al. (2004) Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common gammac cytokine receptor subunit or JAK-3 deficiency. Lancet 363: 2051-2054.
-
(2004)
Lancet
, vol.363
, pp. 2051-2054
-
-
Laffort, C.1
Le Deist, F.2
Favre, M.3
Caillat-Zucman, S.4
Radford-Weiss, I.5
-
23
-
-
78149325696
-
Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma
-
Byun M, Abhyankar A, Lelarge V, Plancoulaine S, Palanduz A, et al. (2010) Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma. J Exp Med 207: 2307-2312.
-
(2010)
J Exp Med
, vol.207
, pp. 2307-2312
-
-
Byun, M.1
Abhyankar, A.2
Lelarge, V.3
Plancoulaine, S.4
Palanduz, A.5
-
24
-
-
78649772960
-
Whole-exome-sequencing-based discovery of human FADD deficiency
-
Bolze A, Byun M, McDonald D, Morgan NV, Abhyankar A, et al. (2010) Whole-exome-sequencing-based discovery of human FADD deficiency. Am J Hum Genet 87: 873-881.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 873-881
-
-
Bolze, A.1
Byun, M.2
McDonald, D.3
Morgan, N.V.4
Abhyankar, A.5
-
25
-
-
79961154447
-
Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
-
Liu L, Okada S, Kong XF, Kreins AY, Cypowyj S,et al. Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis. J Exp Med 208: 1635-1648.
-
J Exp Med
, vol.208
, pp. 1635-1648
-
-
Liu, L.1
Okada, S.2
Kong, X.F.3
Kreins, A.Y.4
Cypowyj, S.5
-
26
-
-
33947687864
-
Four functionally distinct populations of human effector-memory CD8+ T lymphocytes
-
Romero P, Zippelius A, Kurth I, Pittet MJ, Touvrey C, et al. (2007) Four functionally distinct populations of human effector-memory CD8+ T lymphocytes. J Immunol 178: 4112-4119.
-
(2007)
J Immunol
, vol.178
, pp. 4112-4119
-
-
Romero, P.1
Zippelius, A.2
Kurth, I.3
Pittet, M.J.4
Touvrey, C.5
-
27
-
-
0030785521
-
Enhancement of DNA repair in human skin cells by thymidine dinucleotides: evidence for a p53-mediated mammalian SOS response
-
Eller MS, Maeda T, Magnoni C, Atwal D, Gilchrest BA, (1997) Enhancement of DNA repair in human skin cells by thymidine dinucleotides: evidence for a p53-mediated mammalian SOS response. Proc Natl Acad Sci U S A 94: 12627-12632.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 12627-12632
-
-
Eller, M.S.1
Maeda, T.2
Magnoni, C.3
Atwal, D.4
Gilchrest, B.A.5
-
28
-
-
0026008883
-
Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome
-
Weeda G, Ma LB, van Ham RC, van der Eb AJ, Hoeijmakers JH, (1991) Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome. Nucleic Acids Res 19: 6301-6308.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 6301-6308
-
-
Weeda, G.1
Ma, L.B.2
van Ham, R.C.3
van der Eb, A.J.4
Hoeijmakers, J.H.5
-
29
-
-
33750922149
-
Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome
-
Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, et al. (2006) Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome. Hum Mutat 27: 1092-1103.
-
(2006)
Hum Mutat
, vol.27
, pp. 1092-1103
-
-
Oh, K.S.1
Khan, S.G.2
Jaspers, N.G.3
Raams, A.4
Ueda, T.5
-
30
-
-
84859875061
-
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T cells survival
-
10.1182/blood-2011-09-378364
-
Nehme NT, Pachlopnik Schmid J, Debeurme F, Andre-Schmutz I, Lim A, et al. (2011) MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T cells survival. Blood 10.1182/blood-2011-09-378364.
-
(2011)
Blood
-
-
Nehme, N.T.1
Pachlopnik Schmid, J.2
Debeurme, F.3
Andre-Schmutz, I.4
Lim, A.5
-
31
-
-
84859837132
-
The phenotype of human STK4 deficiency
-
10.1182/blood-2011-09-378158
-
Abdollahpour H, Appaswamy G, Kotlarz D, Diestelhorst J, Beier R, et al. (2012) The phenotype of human STK4 deficiency. Blood 10.1182/blood-2011-09-378158.
-
(2012)
Blood
-
-
Abdollahpour, H.1
Appaswamy, G.2
Kotlarz, D.3
Diestelhorst, J.4
Beier, R.5
-
32
-
-
58149520083
-
The Nore1B/Mst1 complex restrains antigen receptor-induced proliferation of naive T cells
-
Zhou D, Medoff BD, Chen L, Li L, Zhang XF, et al. (2008) The Nore1B/Mst1 complex restrains antigen receptor-induced proliferation of naive T cells. Proc Natl Acad Sci U S A 105: 20321-20326.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 20321-20326
-
-
Zhou, D.1
Medoff, B.D.2
Chen, L.3
Li, L.4
Zhang, X.F.5
-
33
-
-
70349313125
-
A cell-intrinsic role for Mst1 in regulating thymocyte egress
-
Dong Y, Du X, Ye J, Han M, Xu T, et al. (2009) A cell-intrinsic role for Mst1 in regulating thymocyte egress. J Immunol 183: 3865-3872.
-
(2009)
J Immunol
, vol.183
, pp. 3865-3872
-
-
Dong, Y.1
Du, X.2
Ye, J.3
Han, M.4
Xu, T.5
-
34
-
-
78650885839
-
Mst1/2 signalling to Yap: gatekeeper for liver size and tumour development
-
Avruch J, Zhou D, Fitamant J, Bardeesy N, (2011) Mst1/2 signalling to Yap: gatekeeper for liver size and tumour development. Br J Cancer 104: 24-32.
-
(2011)
Br J Cancer
, vol.104
, pp. 24-32
-
-
Avruch, J.1
Zhou, D.2
Fitamant, J.3
Bardeesy, N.4
-
35
-
-
42449101282
-
A crucial role of WW45 in developing epithelial tissues in the mouse
-
Lee JH, Kim TS, Yang TH, Koo BK, Oh SP, et al. (2008) A crucial role of WW45 in developing epithelial tissues in the mouse. EMBO J 27: 1231-1242.
-
(2008)
EMBO J
, vol.27
, pp. 1231-1242
-
-
Lee, J.H.1
Kim, T.S.2
Yang, T.H.3
Koo, B.K.4
Oh, S.P.5
-
36
-
-
79952298459
-
Yap1 acts downstream of alpha-catenin to control epidermal proliferation
-
Schlegelmilch K, Mohseni M, Kirak O, Pruszak J, Rodriguez JR, et al. (2011) Yap1 acts downstream of alpha-catenin to control epidermal proliferation. Cell 144: 782-795.
-
(2011)
Cell
, vol.144
, pp. 782-795
-
-
Schlegelmilch, K.1
Mohseni, M.2
Kirak, O.3
Pruszak, J.4
Rodriguez, J.R.5
-
37
-
-
84861875855
-
Cutaneous beta-human papillomavirus E6 proteins bind Mastermind-like coactivators and repress Notch signaling
-
Tan MJ, White EA, Sowa ME, Harper JW, Aster JC, et al. (2012) Cutaneous beta-human papillomavirus E6 proteins bind Mastermind-like coactivators and repress Notch signaling. Proc Natl Acad Sci U S A 109: E1473-1480.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
-
-
Tan, M.J.1
White, E.A.2
Sowa, M.E.3
Harper, J.W.4
Aster, J.C.5
-
38
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR, (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
39
-
-
57149093420
-
Modeling genetic inheritance of copy number variations
-
Wang K, Chen Z, Tadesse MG, Glessner J, Grant SF, et al. (2008) Modeling genetic inheritance of copy number variations. Nucleic Acids Res 36: e138.
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Wang, K.1
Chen, Z.2
Tadesse, M.G.3
Glessner, J.4
Grant, S.F.5
-
40
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R, (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25: 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
41
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20: 1297-1303.
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
-
42
-
-
68549104404
-
The Sequence Alignment/Map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics 25: 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
-
43
-
-
0024415971
-
The majority of human CD3 epitopes are conferred by the epsilon chain
-
Tunnacliffe A, Olsson C, de la Hera A, (1989) The majority of human CD3 epitopes are conferred by the epsilon chain. Int Immunol 1: 546-550.
-
(1989)
Int Immunol
, vol.1
, pp. 546-550
-
-
Tunnacliffe, A.1
Olsson, C.2
de la Hera, A.3
-
44
-
-
0037072113
-
Immune reconstitution without graft-versus-host disease after haemopoietic stem-cell transplantation: a phase 1/2 study
-
Andre-Schmutz I, Le Deist F, Hacein-Bey-Abina S, Vitetta E, Schindler J, et al. (2002) Immune reconstitution without graft-versus-host disease after haemopoietic stem-cell transplantation: a phase 1/2 study. Lancet 360: 130-137.
-
(2002)
Lancet
, vol.360
, pp. 130-137
-
-
Andre-Schmutz, I.1
Le Deist, F.2
Hacein-Bey-Abina, S.3
Vitetta, E.4
Schindler, J.5
-
45
-
-
14544288042
-
Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3
-
de Saint Basile G, Geissmann F, Flori E, Uring-Lambert B, Soudais C, et al. (2004) Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3. J Clin Invest 114: 1512-1517.
-
(2004)
J Clin Invest
, vol.114
, pp. 1512-1517
-
-
de Saint Basile, G.1
Geissmann, F.2
Flori, E.3
Uring-Lambert, B.4
Soudais, C.5
-
46
-
-
27644559049
-
A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection
-
de Villartay JP, Lim A, Al-Mousa H, Dupont S, Dechanet-Merville J, et al. (2005) A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection. J Clin Invest 115: 3291-3299.
-
(2005)
J Clin Invest
, vol.115
, pp. 3291-3299
-
-
de Villartay, J.P.1
Lim, A.2
Al-Mousa, H.3
Dupont, S.4
Dechanet-Merville, J.5
-
47
-
-
0347758636
-
Population-based hematologic and immunologic reference values for a healthy Ugandan population
-
Lugada ES, Mermin J, Kaharuza F, Ulvestad E, Were W, et al. (2004) Population-based hematologic and immunologic reference values for a healthy Ugandan population. Clin Diagn Lab Immunol 11: 29-34.
-
(2004)
Clin Diagn Lab Immunol
, vol.11
, pp. 29-34
-
-
Lugada, E.S.1
Mermin, J.2
Kaharuza, F.3
Ulvestad, E.4
Were, W.5
-
48
-
-
0242550686
-
Lymphocyte subsets in healthy children from birth through 18 years of age: the Pediatric AIDS Clinical Trials Group P1009 study
-
Shearer WT, Rosenblatt HM, Gelman RS, Oyomopito R, Plaeger S, et al. (2003) Lymphocyte subsets in healthy children from birth through 18 years of age: the Pediatric AIDS Clinical Trials Group P1009 study. J Allergy Clin Immunol 112: 973-980.
-
(2003)
J Allergy Clin Immunol
, vol.112
, pp. 973-980
-
-
Shearer, W.T.1
Rosenblatt, H.M.2
Gelman, R.S.3
Oyomopito, R.4
Plaeger, S.5
-
49
-
-
1342322721
-
Reference values for peripheral blood lymphocyte phenotypes applicable to the healthy adult population in Switzerland
-
Bisset LR, Lung TL, Kaelin M, Ludwig E, Dubs RW, (2004) Reference values for peripheral blood lymphocyte phenotypes applicable to the healthy adult population in Switzerland. Eur J Haematol 72: 203-212.
-
(2004)
Eur J Haematol
, vol.72
, pp. 203-212
-
-
Bisset, L.R.1
Lung, T.L.2
Kaelin, M.3
Ludwig, E.4
Dubs, R.W.5
-
50
-
-
33845461937
-
Familial NK cell deficiency associated with impaired IL-2- and IL-15-dependent survival of lymphocytes
-
Eidenschenk C, Jouanguy E, Alcais A, Mention JJ, Pasquier B, et al. (2006) Familial NK cell deficiency associated with impaired IL-2- and IL-15-dependent survival of lymphocytes. J Immunol 177: 8835-8843.
-
(2006)
J Immunol
, vol.177
, pp. 8835-8843
-
-
Eidenschenk, C.1
Jouanguy, E.2
Alcais, A.3
Mention, J.J.4
Pasquier, B.5
|