AAAAAA

   
Results: 1-25 | 26-49
Results: 1-25/49
WISKOTT-ALDRICH-SYNDROME PROTEIN-DEFICIENT MICE REVEAL A ROLE FOR WASP IN T-CELL BUT NOT B-CELL ACTIVATION
Authors: SNAPPER SB ROSEN FS MIZOGUCHI E COHEN P KHAN W LIU CH HAGEMANN TL KWAN SP FERRINI R DAVIDSON L BHAN AK ALT FW
Citation: Sb. Snapper et al., WISKOTT-ALDRICH-SYNDROME PROTEIN-DEFICIENT MICE REVEAL A ROLE FOR WASP IN T-CELL BUT NOT B-CELL ACTIVATION, Immunity (Cambridge, Mass.), 9(1), 1998, pp. 81-91
PLATELET DESTRUCTION IN PATIENTS WITH WISKOTT-ALDRICH-SYNDROME
Authors: SHCHERBINA AY ROSEN FS REMOLDODONNELL E
Citation: Ay. Shcherbina et al., PLATELET DESTRUCTION IN PATIENTS WITH WISKOTT-ALDRICH-SYNDROME, Molecular immunology, 35(11-12), 1998, pp. 735-735
A RANDOMIZED, CONTROLLED TRIAL TO STUDY THE EFFICACY AND SAFETY OF C1INHIBITOR CONCENTRATE IN TREATING HEREDITARY ANGIOEDEMA
Authors: KUNSCHAK M ENGL W MARITSCH F ROSEN FS EDER G ZERLAUTH G SCHWARZ HP
Citation: M. Kunschak et al., A RANDOMIZED, CONTROLLED TRIAL TO STUDY THE EFFICACY AND SAFETY OF C1INHIBITOR CONCENTRATE IN TREATING HEREDITARY ANGIOEDEMA, Transfusion, 38(6), 1998, pp. 540-549
A 54-DAY-OLD PREMATURE GIRL WITH RESPIRATORY-DISTRESS AND PERSISTENT PULMONARY-INFILTRATES - SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE-DEAMINASE DEFICIENCY
Authors: ROSEN FS BHAN AK CONNOLLY SA EZEKOWITZ ARB MARK EJ SHANNON DC ROBINSON JC
Citation: Fs. Rosen et al., A 54-DAY-OLD PREMATURE GIRL WITH RESPIRATORY-DISTRESS AND PERSISTENT PULMONARY-INFILTRATES - SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE-DEAMINASE DEFICIENCY, The New England journal of medicine, 338(24), 1998, pp. 1752-1758
THE GENERATION OF DIVERSITY - CLONAL SELECTION THEORY AND THE RISE OFMOLECULAR IMMUNOLOGY - PODOLSKY,SH, TAUBER,A
Authors: ROSEN FS
Citation: Fs. Rosen, THE GENERATION OF DIVERSITY - CLONAL SELECTION THEORY AND THE RISE OFMOLECULAR IMMUNOLOGY - PODOLSKY,SH, TAUBER,A, Nature, 395(6699), 1998, pp. 235-236
MOLECULAR DEFECTS IN HEREDITARY ANGIONEUROTIC-EDEMA
Authors: BISSLER JJ AULAK KS DONALDSON VH ROSEN FS CICARDI M HARRISON RA DAVIS AE
Citation: Jj. Bissler et al., MOLECULAR DEFECTS IN HEREDITARY ANGIONEUROTIC-EDEMA, Proceedings of the Association of American Physicians, 109(2), 1997, pp. 164-173
A COMMOTION IN THE BLOOD - LIFE, DEATH AND THE IMMUNE-SYSTEM - HALL,SS
Authors: ROSEN FS
Citation: Fs. Rosen, A COMMOTION IN THE BLOOD - LIFE, DEATH AND THE IMMUNE-SYSTEM - HALL,SS, Nature, 388(6645), 1997, pp. 841-841
SEVERE COMBINED IMMUNODEFICIENCY - A PEDIATRIC EMERGENCY
Authors: ROSEN FS
Citation: Fs. Rosen, SEVERE COMBINED IMMUNODEFICIENCY - A PEDIATRIC EMERGENCY, The Journal of pediatrics, 130(3), 1997, pp. 345-346
ENDOTOXIN-SHOCK IN ANTIBODY-DEFICIENT MICE - UNRAVELING THE ROLE OF NATURAL ANTIBODY AND COMPLEMENT IN THE CLEARANCE OF LIPOPOLYSACCHARIDE
Authors: REID RR PRODEUS AP KHAN W HSU T ROSEN FS CARROLL MC
Citation: Rr. Reid et al., ENDOTOXIN-SHOCK IN ANTIBODY-DEFICIENT MICE - UNRAVELING THE ROLE OF NATURAL ANTIBODY AND COMPLEMENT IN THE CLEARANCE OF LIPOPOLYSACCHARIDE, The Journal of immunology, 159(2), 1997, pp. 970-975
INCREASED SUSCEPTIBILITY TO ENDOTOXIN-SHOCK IN COMPLEMENT-C3-DEFICIENT AND COMPLEMENT-C4-DEFICIENT MICE IS CORRECTED BY C1-INHIBITOR REPLACEMENT
Authors: FISCHER MB PRODEUS AP NICHOLSONWELLER A MA MH MURROW J REID RR WARREN HB LAGE AL MOORE FD ROSEN FS CARROLL MC
Citation: Mb. Fischer et al., INCREASED SUSCEPTIBILITY TO ENDOTOXIN-SHOCK IN COMPLEMENT-C3-DEFICIENT AND COMPLEMENT-C4-DEFICIENT MICE IS CORRECTED BY C1-INHIBITOR REPLACEMENT, The Journal of immunology, 159(2), 1997, pp. 976-982
VARIABLE EXPRESSION OF WASP IN B-CELL LINES OF WISKOTT-ALDRICH-SYNDROME PATIENTS
Authors: REMOLDODONNELL E COOLEY J SHCHERBINA A HAGEMANN TL KWAN SP KENNEY DM ROSEN FS
Citation: E. Remoldodonnell et al., VARIABLE EXPRESSION OF WASP IN B-CELL LINES OF WISKOTT-ALDRICH-SYNDROME PATIENTS, The Journal of immunology, 158(9), 1997, pp. 4021-4025
PRIMARY IMMUNODEFICIENCY DISEASES
Authors: ROSEN FS WEDGWOOD RJP EIBL M FISCHER A AIUTI F NOTARANGELO L KISHIMOTO T RESNICK IB HAMMARSTROM L SEGER R CHAPEL H THOMPSON RA COOPER MD GEHA RS GOOD RA WALDMANN TA
Citation: Fs. Rosen et al., PRIMARY IMMUNODEFICIENCY DISEASES, Clinical and experimental immunology, 109, 1997, pp. 1-28
DISEASE MECHANISM - UNRAVELING WISKOTT-ALDRICH SYNDROME
Authors: KIRCHHAUSEN T ROSEN FS
Citation: T. Kirchhausen et Fs. Rosen, DISEASE MECHANISM - UNRAVELING WISKOTT-ALDRICH SYNDROME, Current biology, 6(6), 1996, pp. 676-678
EXQUISITE SPECIFICITY - THE MONOCLONAL-ANTIBODY REVOLUTION - CAMBROSIO,A, KEATING,P
Authors: ROSEN FS
Citation: Fs. Rosen, EXQUISITE SPECIFICITY - THE MONOCLONAL-ANTIBODY REVOLUTION - CAMBROSIO,A, KEATING,P, Nature, 383(6603), 1996, pp. 777-777
IMMUNOLOGY - THE MAKING OF A MODERN SCIENCE - GALLAGHER,RB, GILDER,J,NOSSAL,GIV, SALVATORE,G
Authors: ROSEN FS
Citation: Fs. Rosen, IMMUNOLOGY - THE MAKING OF A MODERN SCIENCE - GALLAGHER,RB, GILDER,J,NOSSAL,GIV, SALVATORE,G, Nature, 379(6560), 1996, pp. 36-36
SPECIES AND SPECIFICITY - AN INTERPRETATION OF THE HISTORY OF IMMUNOLOGY - MAZUMDAR,PMH
Authors: ROSEN FS
Citation: Fs. Rosen, SPECIES AND SPECIFICITY - AN INTERPRETATION OF THE HISTORY OF IMMUNOLOGY - MAZUMDAR,PMH, Nature, 379(6560), 1996, pp. 36-36
DIRECT INTERACTION OF THE WISKOTT-ALDRICH SYNDROME PROTEIN WITH THE GTPASE CDC42
Authors: KOLLURI R TOLIAS KF CARPENTER CL ROSEN FS KIRCHHAUSEN T
Citation: R. Kolluri et al., DIRECT INTERACTION OF THE WISKOTT-ALDRICH SYNDROME PROTEIN WITH THE GTPASE CDC42, Proceedings of the National Academy of Sciences of the United Statesof America, 93(11), 1996, pp. 5615-5618
REGULATION OF THE B-CELL RESPONSE TO T-DEPENDENT ANTIGENS BY CLASSICAL PATHWAY COMPLEMENT
Authors: FISCHER MB MA MH GOERG S ZHOU XN XIA JR FINCO O HAN SH KELSOE G HOWARD RG ROTHSTEIN TL KREMMER E ROSEN FS CARROLL MC
Citation: Mb. Fischer et al., REGULATION OF THE B-CELL RESPONSE TO T-DEPENDENT ANTIGENS BY CLASSICAL PATHWAY COMPLEMENT, The Journal of immunology, 157(2), 1996, pp. 549-556
MULTIPLE ANTIGENS ARE ALTERED ON T-LYMPHOCYTE AND B-LYMPHOCYTE FROM PERIPHERAL-BLOOD AND SPLEEN OF PATIENTS WITH WISKOTT-ALDRICH SYNDROME
Authors: GERWIN N FRIEDRICH C PEREZATAYDE A ROSEN FS GUTIERREZRAMOS JC
Citation: N. Gerwin et al., MULTIPLE ANTIGENS ARE ALTERED ON T-LYMPHOCYTE AND B-LYMPHOCYTE FROM PERIPHERAL-BLOOD AND SPLEEN OF PATIENTS WITH WISKOTT-ALDRICH SYNDROME, Clinical and experimental immunology, 106(2), 1996, pp. 208-217
EZRIN AND MOESIN IN HUMAN BLOOD-CELLS - POSSIBLE ROLE IN WISKOTT-ALDRICH SYNDROME
Authors: SHCHERBINA A RECZEK D BRETSCHER A KENNEY DM ROSEN FS REMOLDODONNELL E
Citation: A. Shcherbina et al., EZRIN AND MOESIN IN HUMAN BLOOD-CELLS - POSSIBLE ROLE IN WISKOTT-ALDRICH SYNDROME, Blood, 88(10), 1996, pp. 1272-1272
DEFECTS IN WISKOTT-ALDRICH SYNDROME BLOOD-CELLS
Authors: REMOLDODONNELL E ROSEN FS KENNEY DM
Citation: E. Remoldodonnell et al., DEFECTS IN WISKOTT-ALDRICH SYNDROME BLOOD-CELLS, Blood, 87(7), 1996, pp. 2621-2631
DEFECTIVE B-CELL DEVELOPMENT AND FUNCTION IN BTK-DEFICIENT MICE
Authors: KHAN WN ALT FW GERSTEIN RM MALYNN BA LARSSON I RATHBUN G DAVIDSON L MULLER S KANTOR AB HERZENBERG LA ROSEN FS SIDERAS P
Citation: Wn. Khan et al., DEFECTIVE B-CELL DEVELOPMENT AND FUNCTION IN BTK-DEFICIENT MICE, Immunity, 3(3), 1995, pp. 283-299
CHARACTERIZATION OF GERMLINE MUTATIONS OF THE GENE ENCODING BRUTONS TYROSINE KINASE IN FAMILIES WITH X-LINKED AGAMMAGLOBULINEMIA
Authors: HAGEMANN TL ROSEN FS KWAN SP
Citation: Tl. Hagemann et al., CHARACTERIZATION OF GERMLINE MUTATIONS OF THE GENE ENCODING BRUTONS TYROSINE KINASE IN FAMILIES WITH X-LINKED AGAMMAGLOBULINEMIA, Human mutation, 5(4), 1995, pp. 296-302
A POINT MUTATION IN EXON-2 OF THE CD40 LIGAND GENE CAUSES THE SIMULTANEOUS EXPRESSION OF 2 DEFECTIVE MESSENGER-RNA SPECIES IN X-LINKED HYPERIMMUNOGLOBULINEMIA-M
Authors: RAMESH N FULEIHAN R SWINTON P ROSEN FS GEHA R
Citation: N. Ramesh et al., A POINT MUTATION IN EXON-2 OF THE CD40 LIGAND GENE CAUSES THE SIMULTANEOUS EXPRESSION OF 2 DEFECTIVE MESSENGER-RNA SPECIES IN X-LINKED HYPERIMMUNOGLOBULINEMIA-M, Human molecular genetics, 4(4), 1995, pp. 759-761
SCANNING OF THE WISKOTT-ALDRICH SYNDROME (WAS) GENE - IDENTIFICATION OF 18 NOVEL ALTERATIONS INCLUDING A POSSIBLE MUTATION HOTSPOT AT ARG86RESULTING IN THROMBOCYTOPENIA, A MILD WAS PHENOTYPE
Authors: KWAN SP HAGEMANN TL BLAESE RM KNUTSEN A ROSEN FS
Citation: Sp. Kwan et al., SCANNING OF THE WISKOTT-ALDRICH SYNDROME (WAS) GENE - IDENTIFICATION OF 18 NOVEL ALTERATIONS INCLUDING A POSSIBLE MUTATION HOTSPOT AT ARG86RESULTING IN THROMBOCYTOPENIA, A MILD WAS PHENOTYPE, Human molecular genetics, 4(10), 1995, pp. 1995-1998
Risultati: 1-25 | 26-49