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    1. Srivannaboon, K; Conley, ME; Coustan-Smith, E; Wang, WC
      Hypogammaglobulinemia and reduced numbers of B-cells in children with myelodysplastic syndrome

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    2. Minegishi, Y; Conley, ME
      Negative selection at the pre-BCR checkpoint elicited by human mu heavy chains with unusual CDR3 regions

      IMMUNITY
    3. 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
      X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappa B signaling

      NATURE GENETICS
    4. Richter, D; Conley, ME; Rohrer, J; Myers, LA; Zahradka, K; Kelecic, J; Sertic, J; Stavljenic-Rukavina, A
      A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness

      PEDIATRIC ALLERGY AND IMMUNOLOGY
    5. Wang, DM; Boylin, EC; Minegishi, Y; Wen, RR; Smith, CIE; Ihle, JN; Conley, ME
      Variations in the human phospholipase C gamma 2 gene in patients with B-cell defects of unknown etiology

      IMMUNOGENETICS
    6. 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
      V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations

      BLOOD
    7. 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
      Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome

      CLINICAL IMMUNOLOGY
    8. Conley, ME; Rohrer, J; Minegishi, Y
      X-linked agammaglobulinemia

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    9. Slobod, KS; Sandlund, JT; Spiegel, PH; Haik, B; Hurwitz, JL; Conley, ME; Bowman, LC; Benaim, E; Jenkins, JJ; Stocks, RMS; Gan, YJ; Sixbey, JW
      Molecular evidence of ocular Epstein-Barr virus infection

      CLINICAL INFECTIOUS DISEASES
    10. Conley, ME; Rohrer, J; Rapalus, L; Boylin, EC; Minegishi, Y
      Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouse

      IMMUNOLOGICAL REVIEWS
    11. Webb, CF; Yamashita, Y; Ayers, N; Evetts, S; Paulin, Y; Conley, ME; Smith, EA
      The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease

      JOURNAL OF IMMUNOLOGY
    12. Gaspar, HB; Conley, ME
      Early B cell defects

      CLINICAL AND EXPERIMENTAL IMMUNOLOGY
    13. 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
      Nijmegen breakage syndrome

      ARCHIVES OF DISEASE IN CHILDHOOD
    14. Conley, ME
      Diagnostic guidelines - An international consensus document

      CLINICAL IMMUNOLOGY
    15. Conley, ME; Notarangelo, LD; Etzioni, A
      Diagnostic criteria for primary immunodeficiencies

      CLINICAL IMMUNOLOGY
    16. Conley, ME; Rapalus, L; Boylin, EC; Rohrer, J; Minegishi, Y
      Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1

      CLINICAL IMMUNOLOGY
    17. Rohrer, J; Minegishi, Y; Richter, D; Eguiguren, J; Conley, ME
      Unusual mutations in Btk: An insertion, a duplication, an inversion, and four large deletions

      CLINICAL IMMUNOLOGY
    18. Vihinen, M; Kwan, SP; Lester, T; Ochs, HD; Resnick, I; Valiaho, J; Conley, ME; Smith, CIE
      Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia

      HUMAN MUTATION
    19. Conley, ME
      Genetic effects on immunity - New genes - how do they fit? Editorial overview

      CURRENT OPINION IN IMMUNOLOGY
    20. Minegishi, Y; Rohrer, J; Coustan-Smith, E; Lederman, HM; Pappu, R; Campana, D; Chan, AC; Conley, ME
      An essential role for BLNK in human B cell development

      SCIENCE
    21. Minegishi, Y; Hendershot, LM; Conley, ME
      Novel mechanisms control the folding and assembly of lambda 5/14.1 and VpreB to produce an intact surrogate light chain

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    22. Minegishi, Y; Coustan-Smith, E; Rapalus, L; Ersoy, F; Campana, D; Conley, ME
      Mutations in Ig alpha (CD79a) result in in B-cell development

      JOURNAL OF CLINICAL INVESTIGATION
    23. Rohrer, J; Conley, ME
      Correction of X-linked immunodeficient mice by competitive reconstitution with limiting numbers of normal bone marrow cells

      BLOOD
    24. CONLEY ME; COOPER MD
      GENETIC-BASIS OF ABNORMAL B-CELL DEVELOPMENT

      Current opinion in immunology
    25. MINEGISHI Y; CONLEY ME
      FAILURE OF IMMUNOGLOBULIN LIGHT-CHAIN REARRANGEMENT TO RESCUE B-CELL DEVELOPMENT IN A PATIENT WITH LAMBDA-5 14.1 DEFICIENCY/

      The FASEB journal
    26. ROHRER J; CONLEY ME
      CORRECTION OF BTK DEFICIENT MICE BY COMPETITIVE REPOPULATION OF BONE-MARROW CELLS

      The FASEB journal
    27. CONLEY ME
      GENETIC-COUNSELING FOR PRIMARY IMMUNODEFICIENCIES

      Molecular immunology
    28. YEL L; CONLEY ME; HERROD HG
      IMMUNOLOGICAL FINDINGS IN INFANTS WITH WISKOTT-ALDRICH-SYNDROME

      Journal of allergy and clinical immunology
    29. MINEGISHI Y; COUSTANSMITH E; WANG YH; COOPER MD; CAMPANA D; CONLEY ME
      MUTATIONS IN THE HUMAN LAMBDA-5 14.1 GENE RESULT IN B-CELL DEFICIENCYAND AGAMMAGLOBULINEMIA/

      The Journal of experimental medicine
    30. KITANAKA A; MANO H; CONLEY ME; CAMPANA D
      EXPRESSION AND ACTIVATION OF THE NONRECEPTOR TYROSINE KINASE TEC IN HUMAN B-CELLS

      Blood
    31. ROHRER J; CONLEY ME
      TRANSCRIPTIONAL REGULATORY ELEMENTS WITHIN THE FIRST INTRON OF BRUTONS TYROSINE KINASE

      Blood
    32. CONLEY ME; MATHIAS D; TREADAWAY J; MINEGISHI Y; ROHRER J
      MUTATIONS IN BTK IN PATIENTS WITH PRESUMED X-LINKED AGAMMAGLOBULINEMIA

      American journal of human genetics
    33. YEL L; TRUBEL H; BUCKLEY RH; PACHMAN LM; CONLEY ME
      CLINICAL-FEATURES IN PATIENTS WITH MUTATIONS IN THE IMMUNOGLOBULIN-MUHEAVY-CHAIN GENE

      Journal of allergy and clinical immunology
    34. ROHRER J; CONLEY ME
      TRANSCRIPTION CONTROL ELEMENTS IN THE FIRST INTRON OF BTK

      Journal of allergy and clinical immunology
    35. CONLEY ME
      AN EVOLVING VIEW OF HYPER-IGM SYNDROME

      The Journal of pediatrics
    36. KITANAKA A; MANO H; CONLEY ME; CAMPANA D
      EXPRESSION AND ACTIVATION OF THE NONRECEPTOR TYROSINE KINASE TEC IN HUMAN B-CELLS

      Blood
    37. PUCK JM; PEPPER AE; HENTHORN PS; CANDOTTI F; ISAKOV J; WHITWAM T; CONLEY ME; FISCHER RE; ROSENBLATT HM; SMALL TN; BUCKLEY RH
      MUTATION ANALYSIS OF IL2RG IN HUMAN X-LINKED SEVERE COMBINED IMMUNODEFICIENCY

      Blood
    38. GROSS TG; FILIPOVICH AH; CONLEY ME; PRACHER E; SCHMIEGELOW K; VERDIRAME JD; VOWELS M; WILLIAMS LL; SEEMAYER TA
      CURE OF X-LINKED LYMPHOPROLIFERATIVE DISEASE (XLP) WITH ALLOGENEIC HEMATOPOIETIC STEM-CELL TRANSPLANTATION (HSCT) - REPORT FROM THE XLP REGISTRY

      Bone marrow transplantation
    39. HERROD HG; RABY RB; VALENSKI WR; HUTCHINSON SR; NASTASI KJ; CONLEY ME
      CYTOKINE PRODUCTION AND IGE IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS

      Journal of allergy and clinical immunology
    40. NASTASI KJ; RABY RB; VALENSKI WR; CONLEY ME; HERROD HG
      ANALYSIS OF IN-VITRO AND SERUM IGM PRODUCTION IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS

      Journal of allergy and clinical immunology
    41. FARRAR JE; ROHRER J; CONLEY ME
      NEUTROPENIA IN X-LINKED AGAMMAGLOBULINEMIA

      Clinical immunology and immunopathology
    42. NASTASI KJ; RABY RB; VALENSKI WR; HUTCHINSON SR; CONLEY ME; HERROD HG
      CYTOKINE PRODUCTION AND IGE IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS

      Pediatric research
    43. YEL L; MINEGISHI Y; COUSTANSMITH E; BUCKLEY RH; TRUBEL H; PACHMAN LM; KITCHINGMAN GR; CAMPANA D; ROHRER J; CONLEY ME
      MUTATIONS IN THE MU HEAVY-CHAIN GENE IN PATIENTS WITH AGAMMAGLOBULINEMIA

      The New England journal of medicine
    44. ROHRER J; RIBEIRO RC; AUERBACH AD; MIRRO B; CONLEY ME
      WISKOTT-ALDRICH SYNDROME IN A FAMILY WITH FANCONI-ANEMIA

      The Journal of pediatrics
    45. SILVENNOINEN O; NISHIGAKI H; KITANAKA A; KUMAGAI MA; ITO C; MALAVASI F; LIN Q; CONLEY ME; CAMPANA D
      CD38 SIGNAL-TRANSDUCTION IN HUMAN B-CELL PRECURSORS - RAPID INDUCTIONOF TYROSINE PHOSPHORYLATION, ACTIVATION OF SYK TYROSINE KINASE, AND PHOSPHORYLATION OF PHOSPHOLIPASE C-GAMMA AND PHOSPHATIDYLINOSITOL 3-KINASE

      The Journal of immunology
    46. LIN Q; ROHRER J; ALLEN RC; LARCHE M; GREENE JM; SHIGEOKA AO; GATTI RA; DERAUF DC; BELMONT JW; CONLEY ME
      A SINGLE-STRAND CONFORMATION POLYMORPHISM STUDY OF CD40 LIGAND - EFFICIENT MUTATION ANALYSIS AND CARRIER DETECTION FOR X-LINKED HYPER IGM SYNDROME

      The Journal of clinical investigation
    47. CONLEY ME; PAPAROZZI ET; PAIR JC; STROUP WW
      LEAF TATTER IN ACER-SACCHARUM - AN ANATOMICAL LINK

      International journal of plant sciences
    48. MATHEW P; CONLEY ME
      EFFECT OF INTRAVENOUS GAMMA-GLOBULIN (IVIG) ON THE PLATELET COUNT IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME

      Pediatric allergy and immunology
    49. CONLEY ME
      PRIMARY IMMUNODEFICIENCIES - A FLURRY OF NEW GENES

      Immunology today
    50. PAROLINI O; ROHRER J; SHAPIRO LH; CONLEY ME
      B-CELL SPECIFIC DEMETHYLATION OF BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA

      Immunogenetics
    51. ROHRER J; PAROLINO O; BELMONT JW; CONLEY ME
      THE GENOMIC STRUCTURE OF HUMAN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA (VOL 40, PG 319, 1994)

      Immunogenetics
    52. CONLEY ME; ROHRER J
      THE SPECTRUM OF MUTATIONS IN BTK THAT CAUSE X-LINKED AGAMMAGLOBULINEMIA

      Clinical immunology and immunopathology
    53. CONLEY ME; FITCHHILGENBERG ME; CLEVELAND JL; PAROLINI O; ROHRER J
      SCREENING OF GENOMIC DNA TO IDENTIFY MUTATIONS IN THE GENE FOR BRUTONS TYROSINE KINASE

      Human molecular genetics
    54. WANG WC; CORDOBA J; INFANTE AJ; CONLEY ME
      SUCCESSFUL TREATMENT OF NEUTROPENIA IN THE HYPER-IMMUNOGLOBULIN-M SYNDROME WITH GRANULOCYTE-COLONY-STIMULATING FACTOR

      The American journal of pediatric hematology/oncology
    55. CONLEY ME; PAROLINI O; ROHRER J; CAMPANA D
      X-LINKED AGAMMAGLOBULINEMIA - NEW APPROACHES TO OLD QUESTIONS BASED ON THE IDENTIFICATION OF THE DEFECTIVE GENE

      Immunological reviews
    56. ROHRER J; PAROLINO O; BELMONT JW; CONLEY ME
      THE GENOMIC STRUCTURE OF HUMAN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA

      Immunogenetics
    57. CONLEY ME; ROHRER J; FITCHHILGENBERG MF; PAROLINI O
      VARIABLE CLINICAL CONSEQUENCES OF PREMATURE STOP CODONS IN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA (XLA)

      Pediatric research
    58. PAROLINI O; ROHRER J; CONLEY ME
      ATYPICAL X-LINKED AGAMMAGLOBULINEMIA - REPLY

      The New England journal of medicine
    59. SAFFRAN DC; PAROLINI O; FITCHHILGENBERG ME; RAWLINGS DJ; AFAR DEH; WITTE ON; CONLEY ME
      A POINT MUTATION IN THE SH2 DOMAIN OF BRUTONS TYROSINE KINASE IN ATYPICAL X-LINKED AGAMMAGLOBULINEMIA - BRIEF REPORT

      The New England journal of medicine
    60. CONLEY ME; LARCHE M; BONAGURA VR; LAWTON AR; BUCKLEY RH; FU SM; COUSTANSMITH E; HERROD HG; CAMPANA D
      HYPER IGM SYNDROME-ASSOCIATED WITH DEFECTIVE CD40-MEDIATED B-CELL ACTIVATION

      The Journal of clinical investigation
    61. WILLIAMS LL; ROONEY CM; CONLEY ME; BRENNER MK; KRANCE RA; HESLOP HE
      CORRECTION OF DUNCAN SYNDROME BY ALLOGENEIC BONE-MARROW TRANSPLANTATION

      Lancet
    62. PUCK JM; CONLEY ME; BAILEY LC
      REFINEMENT OF LINKAGE OF HUMAN SEVERE COMBINED IMMUNODEFICIENCY (SCIDX1) TO POLYMORPHIC MARKERS IN XQ13

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/01/21 alle ore 21:54:05