-
1
-
-
0014008065
-
Job’s syndrome
-
Davis S, Schaller J, Wedgwood R, Harvard MD. Job’s syndrome. Lancet. 1966;287(7445):1013–5.
-
(1966)
Lancet
, vol.287
, Issue.7445
, pp. 1013-1015
-
-
Davis, S.1
Schaller, J.2
Wedgwood, R.3
Harvard, M.D.4
-
2
-
-
0015266954
-
Extreme hyperimmunoglobulinemia E and undue susceptibility to infection
-
COI: 1:STN:280:DyaE387gvFSitQ%3D%3D, PID: 5059313
-
Buckley RH, Wray BB, Belmaker EZ. Extreme hyperimmunoglobulinemia E and undue susceptibility to infection. Pediatrics. 1972;49(1):59–70.
-
(1972)
Pediatrics
, vol.49
, Issue.1
, pp. 59-70
-
-
Buckley, R.H.1
Wray, B.B.2
Belmaker, E.Z.3
-
3
-
-
0033522220
-
Hyper-IgE syndrome with recurrent infections–an autosomal dominant multisystem disorder
-
COI: 1:STN:280:DyaK1M7ltVSltQ%3D%3D, PID: 10053178
-
Grimbacher B, Holland SM, Gallin JI, Greenberg F, Hill SC, Malech HL, et al. Hyper-IgE syndrome with recurrent infections–an autosomal dominant multisystem disorder. N Engl J Med. 1999;340(9):692–702.
-
(1999)
N Engl J Med
, vol.340
, Issue.9
, pp. 692-702
-
-
Grimbacher, B.1
Holland, S.M.2
Gallin, J.I.3
Greenberg, F.4
Hill, S.C.5
Malech, H.L.6
-
4
-
-
35348960378
-
STAT3 mutations in the hyper-IgE syndrome
-
COI: 1:CAS:528:DC%2BD2sXht1SgurzL, PID: 17881745
-
Holland SM, DeLeo FR, Elloumi HZ, Hsu AP, Uzel G, Brodsky N, et al. STAT3 mutations in the hyper-IgE syndrome. N Engl J Med. 2007;357(16):1608–19.
-
(2007)
N Engl J Med
, vol.357
, Issue.16
, pp. 1608-1619
-
-
Holland, S.M.1
DeLeo, F.R.2
Elloumi, H.Z.3
Hsu, A.P.4
Uzel, G.5
Brodsky, N.6
-
5
-
-
34548317417
-
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
-
COI: 1:CAS:528:DC%2BD2sXps12nsLc%3D, PID: 17676033
-
Minegishi Y, Saito M, Tsuchiya S, Tsuge I, Takada H, Hara T, et al. Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature. 2007;448(7157):1058–62.
-
(2007)
Nature
, vol.448
, Issue.7157
, pp. 1058-1062
-
-
Minegishi, Y.1
Saito, M.2
Tsuchiya, S.3
Tsuge, I.4
Takada, H.5
Hara, T.6
-
6
-
-
35348997007
-
STAT3 mutation in the original patient with job’s syndrome
-
COI: 1:CAS:528:DC%2BD2sXht1Snsr7M, PID: 17942886
-
Renner ED, Torgerson TR, Rylaarsdam S, Anover-Sombke S, Golob K, LaFlam T, et al. STAT3 mutation in the original patient with job’s syndrome. N Engl J Med. 2007;357(16):1667–8.
-
(2007)
N Engl J Med
, vol.357
, Issue.16
, pp. 1667-1668
-
-
Renner, E.D.1
Torgerson, T.R.2
Rylaarsdam, S.3
Anover-Sombke, S.4
Golob, K.5
LaFlam, T.6
-
7
-
-
9144261081
-
Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity
-
COI: 1:CAS:528:DC%2BD2cXosFyh, PID: 14722525
-
Renner ED, Puck JM, Holland SM, Schmitt M, Weiss M, Frosch M, et al. Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity. J Pediatr. 2004;144(1):93–9.
-
(2004)
J Pediatr
, vol.144
, Issue.1
, pp. 93-99
-
-
Renner, E.D.1
Puck, J.M.2
Holland, S.M.3
Schmitt, M.4
Weiss, M.5
Frosch, M.6
-
8
-
-
71149115670
-
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
-
Engelhardt KR, McGhee S, Winkler S, Sassi A, Woellner C, Lopez-Herrera G, et al. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome. J Allergy Clin Immunol. 2009;124(6):1289--1302.
-
(2009)
J Allergy Clin Immunol
, vol.124
, Issue.6
-
-
Engelhardt, K.R.1
McGhee, S.2
Winkler, S.3
Sassi, A.4
Woellner, C.5
Lopez-Herrera, G.6
-
9
-
-
70949098060
-
Combined immunodeficiency associated with DOCK8 mutations
-
COI: 1:CAS:528:DC%2BD1MXhsVequ7bN, PID: 19776401
-
Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med. 2009;361(21):2046–55.
-
(2009)
N Engl J Med
, vol.361
, Issue.21
, pp. 2046-2055
-
-
Zhang, Q.1
Davis, J.C.2
Lamborn, I.T.3
Freeman, A.F.4
Jing, H.5
Favreau, A.J.6
-
10
-
-
84899692269
-
Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency
-
COI: 1:CAS:528:DC%2BC2cXpslCqsbk%3D, PID: 24743019
-
Al-Zahrani D, Raddadi A, Massaad M, Keles S, Jabara HH, Chatila TA, et al. Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency. Clin Immunol. 2014;153(1):104–8.
-
(2014)
Clin Immunol
, vol.153
, Issue.1
, pp. 104-108
-
-
Al-Zahrani, D.1
Raddadi, A.2
Massaad, M.3
Keles, S.4
Jabara, H.H.5
Chatila, T.A.6
-
11
-
-
84901807538
-
Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-alpha 2b therapy
-
COI: 1:CAS:528:DC%2BC2cXmvVWrt7k%3D, PID: 24767873
-
Keles S, Jabara HH, Reisli I, McDonald DR, Barlan I, Hanna-Wakim R, et al. Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-alpha 2b therapy. J Allergy Clin Immunol. 2014;133(6):1753–1755.
-
(2014)
J Allergy Clin Immunol
, vol.133
, Issue.6
, pp. 1753-1755
-
-
Keles, S.1
Jabara, H.H.2
Reisli, I.3
McDonald, D.R.4
Barlan, I.5
Hanna-Wakim, R.6
-
12
-
-
84899645392
-
Beneficial IFN-alpha treatment of tumorous herpes simplex blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency
-
COI: 1:CAS:528:DC%2BC2cXltl2ktLo%3D, PID: 24698314
-
Papan C, Hagl B, Heinz V, Albert MH, Ehrt O, Sawalle-Belohradsky J, et al. Beneficial IFN-alpha treatment of tumorous herpes simplex blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol. 2014;133(5):1456–8.
-
(2014)
J Allergy Clin Immunol
, vol.133
, Issue.5
, pp. 1456-1458
-
-
Papan, C.1
Hagl, B.2
Heinz, V.3
Albert, M.H.4
Ehrt, O.5
Sawalle-Belohradsky, J.6
-
13
-
-
78349303895
-
Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation
-
Bittner TC, Pannicke U, Renner ED, Notheis G, Hoffmann F, Belohradsky BH, et al. Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation. Klin Pädiatr. 2010;222(6):351–5.
-
(2010)
Klin Pädiatr
, vol.222
, Issue.6
, pp. 351-355
-
-
Bittner, T.C.1
Pannicke, U.2
Renner, E.D.3
Notheis, G.4
Hoffmann, F.5
Belohradsky, B.H.6
-
14
-
-
79953734130
-
Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation
-
COI: 1:CAS:528:DC%2BC3MXkt1Wqsb8%3D, PID: 20622910
-
Gatz SA, Benninghoff U, Schutz C, Schulz A, Honig M, Pannicke U, et al. Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation. Bone Marrow Transplant. 2011;46(4):552–6.
-
(2011)
Bone Marrow Transplant
, vol.46
, Issue.4
, pp. 552-556
-
-
Gatz, S.A.1
Benninghoff, U.2
Schutz, C.3
Schulz, A.4
Honig, M.5
Pannicke, U.6
-
15
-
-
84866945470
-
Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen
-
COI: 1:CAS:528:DC%2BC38XhsVehtLvL, PID: 22897717
-
Boztug H, Karitnig-Weiss C, Ausserer B, Renner ED, Albert MH, Sawalle-Belohradsky J, et al. Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen. Pediatr Hematol Oncol. 2012;29(7):585–94.
-
(2012)
Pediatr Hematol Oncol
, vol.29
, Issue.7
, pp. 585-594
-
-
Boztug, H.1
Karitnig-Weiss, C.2
Ausserer, B.3
Renner, E.D.4
Albert, M.H.5
Sawalle-Belohradsky, J.6
-
16
-
-
79961014871
-
Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency
-
Barlogis V, Galambrun C, Chambost H, Lamoureux-Toth S, Petit P, Stephan JL, et al. Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency. J Allergy Clin Immunol. 2011;128(2):420--422.
-
(2011)
J Allergy Clin Immunol
, vol.128
, Issue.2
-
-
Barlogis, V.1
Galambrun, C.2
Chambost, H.3
Lamoureux-Toth, S.4
Petit, P.5
Stephan, J.L.6
-
17
-
-
84897563653
-
Haploidentical stem cell transplantation in DOCK8 deficiency - successful control of pre-existing severe viremia with a TCRass/CD19-depleted graft and antiviral treatment
-
COI: 1:CAS:528:DC%2BC2cXmvVWltrw%3D, PID: 24667686
-
Ghosh S, Schuster FR, Adams O, Babor F, Borkhardt A, Comoli P, et al. Haploidentical stem cell transplantation in DOCK8 deficiency - successful control of pre-existing severe viremia with a TCRass/CD19-depleted graft and antiviral treatment. Clin Immunol. 2014;152(1–2):111–4.
-
(2014)
Clin Immunol
, vol.152
, Issue.1-2
, pp. 111-114
-
-
Ghosh, S.1
Schuster, F.R.2
Adams, O.3
Babor, F.4
Borkhardt, A.5
Comoli, P.6
-
18
-
-
84861194430
-
Successful bone marrow transplantation for DOCK8 deficient hyper IgE syndrome
-
PID: 22248482
-
Metin A, Tavil B, Azik F, Azkur D, Ok-Bozkaya I, Kocabas C, et al. Successful bone marrow transplantation for DOCK8 deficient hyper IgE syndrome. Pediatr Transplant. 2012;16(4):398–9.
-
(2012)
Pediatr Transplant
, vol.16
, Issue.4
, pp. 398-399
-
-
Metin, A.1
Tavil, B.2
Azik, F.3
Azkur, D.4
Ok-Bozkaya, I.5
Kocabas, C.6
-
19
-
-
84899629014
-
Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
-
Sassi A, Lazaroski S, Wu G, Haslam SM, Fliegauf M, Mellouli F, et al. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels. J Allergy Clin Immunol. 2014;133(5):1410--1419.
-
(2014)
J Allergy Clin Immunol
, vol.133
, Issue.5
-
-
Sassi, A.1
Lazaroski, S.2
Wu, G.3
Haslam, S.M.4
Fliegauf, M.5
Mellouli, F.6
-
20
-
-
84887595223
-
DOCK8 is critical for the survival and function of NKT cells
-
COI: 1:CAS:528:DC%2BC3sXhsFOhtrbF, PID: 23929855
-
Crawford G, Enders A, Gileadi U, Stankovic S, Zhang Q, Lambe T, et al. DOCK8 is critical for the survival and function of NKT cells. Blood. 2013;122(12):2052–61.
-
(2013)
Blood
, vol.122
, Issue.12
, pp. 2052-2061
-
-
Crawford, G.1
Enders, A.2
Gileadi, U.3
Stankovic, S.4
Zhang, Q.5
Lambe, T.6
-
21
-
-
84875454223
-
Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity
-
COI: 1:CAS:528:DC%2BC3sXksVynsbo%3D, PID: 23455509
-
Ham H, Guerrier S, Kim J, Schoon RA, Anderson EL, Hamann MJ, et al. Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity. J Immunol. 2013;190(7):3661–9.
-
(2013)
J Immunol
, vol.190
, Issue.7
, pp. 3661-3669
-
-
Ham, H.1
Guerrier, S.2
Kim, J.3
Schoon, R.A.4
Anderson, E.L.5
Hamann, M.J.6
-
22
-
-
84875226021
-
Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency
-
COI: 1:CAS:528:DC%2BC3sXitFKmsbY%3D, PID: 23380217
-
Mizesko MC, Banerjee PP, Monaco-Shawver L, Mace EM, Bernal WE, Sawalle-Belohradsky J, et al. Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol. 2013;131(3):840–8.
-
(2013)
J Allergy Clin Immunol
, vol.131
, Issue.3
, pp. 840-848
-
-
Mizesko, M.C.1
Banerjee, P.P.2
Monaco-Shawver, L.3
Mace, E.M.4
Bernal, W.E.5
Sawalle-Belohradsky, J.6
-
23
-
-
84856022081
-
Cutaneous manifestations of DOCK8 deficiency syndrome
-
COI: 1:CAS:528:DC%2BC38Xis1aqs70%3D, PID: 21931011
-
Chu EY, Freeman AF, Jing H, Cowen EW, Davis J, Su HC, et al. Cutaneous manifestations of DOCK8 deficiency syndrome. Arch Dermatol. 2012;148(1):79–84.
-
(2012)
Arch Dermatol
, vol.148
, Issue.1
, pp. 79-84
-
-
Chu, E.Y.1
Freeman, A.F.2
Jing, H.3
Cowen, E.W.4
Davis, J.5
Su, H.C.6
-
24
-
-
80054842183
-
Deficient T cell receptor excision circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: implications for pathogenesis and potential detection by newborn screening
-
COI: 1:CAS:528:DC%2BC3MXhtlKktLnJ, PID: 21763205
-
Dasouki M, Okonkwo KC, Ray A, Folmsbeel CK, Gozales D, Keles S, et al. Deficient T cell receptor excision circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: implications for pathogenesis and potential detection by newborn screening. Clin Immunol. 2011;141(2):128–32.
-
(2011)
Clin Immunol
, vol.141
, Issue.2
, pp. 128-132
-
-
Dasouki, M.1
Okonkwo, K.C.2
Ray, A.3
Folmsbeel, C.K.4
Gozales, D.5
Keles, S.6
-
25
-
-
78649878923
-
Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency
-
McDonald DR, Massaad MJ, Johnston A, Keles S, Chatila T, Geha RS, et al. Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol. 2010;126(6):1304--1305.
-
(2010)
J Allergy Clin Immunol
, vol.126
, Issue.6
-
-
McDonald, D.R.1
Massaad, M.J.2
Johnston, A.3
Keles, S.4
Chatila, T.5
Geha, R.S.6
-
26
-
-
80055107954
-
DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice
-
COI: 1:CAS:528:DC%2BC3MXhsVSru73N, PID: 22006977
-
Randall KL, Chan SS, Ma CS, Fung I, Mei Y, Yabas M, et al. DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice. J Exp Med. 2011;208(11):2305–20.
-
(2011)
J Exp Med
, vol.208
, Issue.11
, pp. 2305-2320
-
-
Randall, K.L.1
Chan, S.S.2
Ma, C.S.3
Fung, I.4
Mei, Y.5
Yabas, M.6
-
27
-
-
84863985331
-
Additional diverse findings expand the clinical presentation of DOCK8 deficiency
-
COI: 1:CAS:528:DC%2BC38XhtVSlsL%2FP, PID: 22476911
-
Sanal O, Jing H, Ozgur T, Ayvaz D, Strauss-Albee DM, Ersoy-Evans S, et al. Additional diverse findings expand the clinical presentation of DOCK8 deficiency. J Clin Immunol. 2012;32(4):698–708.
-
(2012)
J Clin Immunol
, vol.32
, Issue.4
, pp. 698-708
-
-
Sanal, O.1
Jing, H.2
Ozgur, T.3
Ayvaz, D.4
Strauss-Albee, D.M.5
Ersoy-Evans, S.6
-
28
-
-
0000120995
-
A class of K-sample tests for comparing the cumulative incidence of a competing risk
-
Gray R. A class of K-sample tests for comparing the cumulative incidence of a competing risk. Ann Stat. 1988;16(3):1141–54.
-
(1988)
Ann Stat
, vol.16
, Issue.3
, pp. 1141-1154
-
-
Gray, R.1
-
29
-
-
84876441426
-
Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients
-
COI: 1:CAS:528:DC%2BC3sXhslamtro%3D, PID: 22968740
-
Alsum Z, Hawwari A, Alsmadi O, Al-Hissi S, Borrero E, Abu-Staiteh A, et al. Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients. J Clin Immunol. 2013;33(1):55–67.
-
(2013)
J Clin Immunol
, vol.33
, Issue.1
, pp. 55-67
-
-
Alsum, Z.1
Hawwari, A.2
Alsmadi, O.3
Al-Hissi, S.4
Borrero, E.5
Abu-Staiteh, A.6
-
30
-
-
84861235270
-
Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait
-
COI: 1:CAS:528:DC%2BC38XlvFyqtrk%3D, PID: 22534316
-
Al-Herz W, Ragupathy R, Massaad MJ, Al-Attiyah R, Nanda A, Engelhardt KR, et al. Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait. Clin Immunol. 2012;143(3):266–72.
-
(2012)
Clin Immunol
, vol.143
, Issue.3
, pp. 266-272
-
-
Al-Herz, W.1
Ragupathy, R.2
Massaad, M.J.3
Al-Attiyah, R.4
Nanda, A.5
Engelhardt, K.R.6
-
31
-
-
84859875061
-
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival
-
COI: 1:CAS:528:DC%2BC38XmtVKgtL8%3D, PID: 22174160
-
Nehme NT, Pachlopnik Schmid J, Debeurme F, Andre-Schmutz I, Lim A, Nitschke P, et al. MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival. Blood. 2012;119(15):3458–68.
-
(2012)
Blood
, vol.119
, Issue.15
, pp. 3458-3468
-
-
Nehme, N.T.1
Pachlopnik Schmid, J.2
Debeurme, F.3
Andre-Schmutz, I.4
Lim, A.5
Nitschke, P.6
-
32
-
-
84901777686
-
Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype
-
COI: 1:CAS:528:DC%2BC2cXnslejtL0%3D, PID: 24797421
-
Jing H, Zhang Q, Zhang Y, Hill BJ, Dove CG, Gelfand EW, et al. Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype. J Allergy Clin Immunol. 2014;133(6):1667–75.
-
(2014)
J Allergy Clin Immunol
, vol.133
, Issue.6
, pp. 1667-1675
-
-
Jing, H.1
Zhang, Q.2
Zhang, Y.3
Hill, B.J.4
Dove, C.G.5
Gelfand, E.W.6
-
33
-
-
84903751001
-
-
Pai SY, de Boer H, Massaad MJ, Chatila TA, Keles S, Jabara HH, et al. Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency. J Allergy Clin Immunol. 2014;134(1):221.–223
-
Pai SY, de Boer H, Massaad MJ, Chatila TA, Keles S, Jabara HH, et al. Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency. J Allergy Clin Immunol. 2014;134(1):221.–223.
-
-
-
-
34
-
-
84895064425
-
Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies
-
COI: 1:CAS:528:DC%2BC3sXhs1OrtLjL, PID: 24139496
-
Nijman IJ, van Montfrans JM, Hoogstraat M, Boes ML, van de Corput L, Renner ED, et al. Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies. J Allergy Clin Immunol. 2014;133(2):529–34.
-
(2014)
J Allergy Clin Immunol
, vol.133
, Issue.2
, pp. 529-534
-
-
Nijman, I.J.1
van Montfrans, J.M.2
Hoogstraat, M.3
Boes, M.L.4
van de Corput, L.5
Renner, E.D.6
-
35
-
-
84896881838
-
STAT3 is a central regulator of lymphocyte differentiation and function
-
Kane A, Deenick EK, Ma CS, Cook MC, Uzel G, Tangye SG. STAT3 is a central regulator of lymphocyte differentiation and function. Curr Opin Immunol. 2014;28C:49–57.
-
(2014)
Curr Opin Immunol
, vol.28C
, pp. 49-57
-
-
Kane, A.1
Deenick, E.K.2
Ma, C.S.3
Cook, M.C.4
Uzel, G.5
Tangye, S.G.6
-
36
-
-
79851507687
-
Clinical spectrum, pathophysiology and treatment of the Wiskott-Aldrich syndrome
-
PID: 21076297
-
Albert MH, Notarangelo LD, Ochs HD. Clinical spectrum, pathophysiology and treatment of the Wiskott-Aldrich syndrome. Curr Opin Hematol. 2011;18(1):42–8.
-
(2011)
Curr Opin Hematol
, vol.18
, Issue.1
, pp. 42-48
-
-
Albert, M.H.1
Notarangelo, L.D.2
Ochs, H.D.3
-
37
-
-
84880961783
-
Aberrant humoral immune reactivity in DOCK8 deficiency with follicular hyperplasia and nodal plasmacytosis
-
Aan de Kerk DJ, van Leeuwen EM, Jansen MH, van den Berg JM, Alders M, Vermont CL, et al. Aberrant humoral immune reactivity in DOCK8 deficiency with follicular hyperplasia and nodal plasmacytosis. Clin Immunol. 2013;149(1):25–31.
-
(2013)
Clin Immunol
, vol.149
, Issue.1
, pp. 25-31
-
-
Aan de Kerk, D.J.1
van Leeuwen, E.M.2
Jansen, M.H.3
van den Berg, J.M.4
Alders, M.5
Vermont, C.L.6
-
38
-
-
84861078339
-
DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses
-
COI: 1:CAS:528:DC%2BC38Xnt1Gkt70%3D, PID: 22461490
-
Harada Y, Tanaka Y, Terasawa M, Pieczyk M, Habiro K, Katakai T, et al. DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses. Blood. 2012;119(19):4451–61.
-
(2012)
Blood
, vol.119
, Issue.19
, pp. 4451-4461
-
-
Harada, Y.1
Tanaka, Y.2
Terasawa, M.3
Pieczyk, M.4
Habiro, K.5
Katakai, T.6
-
39
-
-
84861236002
-
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation
-
COI: 1:CAS:528:DC%2BC38XmvFequ7Y%3D, PID: 22581261
-
Jabara HH, McDonald DR, Janssen E, Massaad MJ, Ramesh N, Borzutzky A, et al. DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation. Nat Immunol. 2012;13(6):612–20.
-
(2012)
Nat Immunol
, vol.13
, Issue.6
, pp. 612-620
-
-
Jabara, H.H.1
McDonald, D.R.2
Janssen, E.3
Massaad, M.J.4
Ramesh, N.5
Borzutzky, A.6
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