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Results: 1-23 |
Results: 23
Hypogammaglobulinemia and reduced numbers of B-cells in children with myelodysplastic syndrome
Authors: Srivannaboon, K Conley, ME Coustan-Smith, E Wang, WC
Citation: K. Srivannaboon et al., Hypogammaglobulinemia and reduced numbers of B-cells in children with myelodysplastic syndrome, J PED H ONC, 23(2), 2001, pp. 122-125
Negative selection at the pre-BCR checkpoint elicited by human mu heavy chains with unusual CDR3 regions
Authors: Minegishi, Y Conley, ME
Citation: Y. Minegishi et Me. Conley, Negative selection at the pre-BCR checkpoint elicited by human mu heavy chains with unusual CDR3 regions, IMMUNITY, 14(5), 2001, pp. 631-641
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappa B signaling
Authors: Doffinger, R Smahi, A Bessia, C Geissmann, F Feinberg, J Durandy, A Bodemer, C Kenwrick, S Dupuis-Girod, S Blanche, S Wood, P Rabia, SH Headon, DJ Overbeek, PA Le Deist, F Holland, SM Belani, K Kumararatne, DS Fischer, A Shapiro, R Conley, ME Reimund, E Kalhoff, H Abinun, M Munnich, A Israel, A Courtois, G Casanova, JL
Citation: R. Doffinger et al., X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappa B signaling, NAT GENET, 27(3), 2001, pp. 277-285
A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness
Authors: Richter, D Conley, ME Rohrer, J Myers, LA Zahradka, K Kelecic, J Sertic, J Stavljenic-Rukavina, A
Citation: D. Richter et al., A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness, PEDIAT A IM, 12(2), 2001, pp. 107-111
Variations in the human phospholipase C gamma 2 gene in patients with B-cell defects of unknown etiology
Authors: Wang, DM Boylin, EC Minegishi, Y Wen, RR Smith, CIE Ihle, JN Conley, ME
Citation: Dm. Wang et al., Variations in the human phospholipase C gamma 2 gene in patients with B-cell defects of unknown etiology, IMMUNOGENET, 53(7), 2001, pp. 550-556
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations
Authors: Villa, A Sobacchi, C Notarangelo, LD Bozzi, F Abinun, M Abrahamsen, TG Arkwright, PD Baniyash, M Brooks, EG Conley, ME Cortes, P Duse, M Fasth, A Filipovich, AM Infante, AJ Jones, A Mazzolari, E Muller, SM Pasic, S Rechavi, G Sacco, MG Santagata, S Schroeder, ML Seger, R Strina, D Ugazio, A Valiaho, J Vihinen, M Vogler, LB Ochs, H Vezzoni, P Friedrich, W Schwarz, K
Citation: A. Villa et al., V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations, BLOOD, 97(1), 2001, pp. 81-88
Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome
Authors: Minegishi, Y Lavoie, A Cunningham-Rundles, C Bedard, PM Hebert, J Cote, L Dan, K Sedlak, D Buckley, RH Fischer, A Durandy, A Conley, ME
Citation: Y. Minegishi et al., Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome, CLIN IMMUNO, 97(3), 2000, pp. 203-210
X-linked agammaglobulinemia
Authors: Conley, ME Rohrer, J Minegishi, Y
Citation: Me. Conley et al., X-linked agammaglobulinemia, CL R ALL IM, 19(2), 2000, pp. 183-204
Molecular evidence of ocular Epstein-Barr virus infection
Authors: Slobod, KS Sandlund, JT Spiegel, PH Haik, B Hurwitz, JL Conley, ME Bowman, LC Benaim, E Jenkins, JJ Stocks, RMS Gan, YJ Sixbey, JW
Citation: Ks. Slobod et al., Molecular evidence of ocular Epstein-Barr virus infection, CLIN INF D, 31(1), 2000, pp. 184-188
Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouse
Authors: Conley, ME Rohrer, J Rapalus, L Boylin, EC Minegishi, Y
Citation: Me. Conley et al., Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouse, IMMUNOL REV, 178, 2000, pp. 75-90
The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease
Authors: Webb, CF Yamashita, Y Ayers, N Evetts, S Paulin, Y Conley, ME Smith, EA
Citation: Cf. Webb et al., The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease, J IMMUNOL, 165(12), 2000, pp. 6956-6965
Early B cell defects
Authors: Gaspar, HB Conley, ME
Citation: Hb. Gaspar et Me. Conley, Early B cell defects, CLIN EXP IM, 119(3), 2000, pp. 383-389
Nijmegen breakage syndrome
Authors: Hiel, JA Weemaes, CM van den Heuvel, LP van Engelen, BG Gabreels, FJ Smeets, DF van der Burgt, I Chrzanovska, KH Bernatowska, E Krajewska-Walasek, M Bialecka, M Abramczuk, D Gregorek, H Michalkiewicz, I Perek, D Midro, AT Seemanova, E Belohradsky, BH Solder, B Barbi, G Wegner, RD Sperling, K Dixon, J Maraschio, P Marseglia, GL Green, A Taylor, AM Der Kaloustian, VM Komatsu, K Matsuura, S Conley, ME Concannon, P Gatti, RA
Citation: Ja. Hiel et al., Nijmegen breakage syndrome, ARCH DIS CH, 82(5), 2000, pp. 400-406
Diagnostic guidelines - An international consensus document
Authors: Conley, ME
Citation: Me. Conley, Diagnostic guidelines - An international consensus document, CLIN IMMUNO, 93(3), 1999, pp. 189-189
Diagnostic criteria for primary immunodeficiencies
Authors: Conley, ME Notarangelo, LD Etzioni, A
Citation: Me. Conley et al., Diagnostic criteria for primary immunodeficiencies, CLIN IMMUNO, 93(3), 1999, pp. 190-197
Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1
Authors: Conley, ME Rapalus, L Boylin, EC Rohrer, J Minegishi, Y
Citation: Me. Conley et al., Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1, CLIN IMMUNO, 93(2), 1999, pp. 162-167
Unusual mutations in Btk: An insertion, a duplication, an inversion, and four large deletions
Authors: Rohrer, J Minegishi, Y Richter, D Eguiguren, J Conley, ME
Citation: J. Rohrer et al., Unusual mutations in Btk: An insertion, a duplication, an inversion, and four large deletions, CLIN IMMUNO, 90(1), 1999, pp. 28-37
Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia
Authors: Vihinen, M Kwan, SP Lester, T Ochs, HD Resnick, I Valiaho, J Conley, ME Smith, CIE
Citation: M. Vihinen et al., Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia, HUM MUTAT, 13(4), 1999, pp. 280-285
Genetic effects on immunity - New genes - how do they fit? Editorial overview
Authors: Conley, ME
Citation: Me. Conley, Genetic effects on immunity - New genes - how do they fit? Editorial overview, CURR OP IM, 11(4), 1999, pp. 427-430
An essential role for BLNK in human B cell development
Authors: Minegishi, Y Rohrer, J Coustan-Smith, E Lederman, HM Pappu, R Campana, D Chan, AC Conley, ME
Citation: Y. Minegishi et al., An essential role for BLNK in human B cell development, SCIENCE, 286(5446), 1999, pp. 1954-1957
Novel mechanisms control the folding and assembly of lambda 5/14.1 and VpreB to produce an intact surrogate light chain
Authors: Minegishi, Y Hendershot, LM Conley, ME
Citation: Y. Minegishi et al., Novel mechanisms control the folding and assembly of lambda 5/14.1 and VpreB to produce an intact surrogate light chain, P NAS US, 96(6), 1999, pp. 3041-3046
Mutations in Ig alpha (CD79a) result in in B-cell development
Authors: Minegishi, Y Coustan-Smith, E Rapalus, L Ersoy, F Campana, D Conley, ME
Citation: Y. Minegishi et al., Mutations in Ig alpha (CD79a) result in in B-cell development, J CLIN INV, 104(8), 1999, pp. 1115-1121
Correction of X-linked immunodeficient mice by competitive reconstitution with limiting numbers of normal bone marrow cells
Authors: Rohrer, J Conley, ME
Citation: J. Rohrer et Me. Conley, Correction of X-linked immunodeficient mice by competitive reconstitution with limiting numbers of normal bone marrow cells, BLOOD, 94(10), 1999, pp. 3358-3365
Risultati: 1-23 |