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THE SPECTRUM OF SOMATIC MUTATIONS IN THE PIG-A GENE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA INCLUDES LARGE DELETIONS AND SMALL DUPLICATIONS
Authors: NAFA K BESSLER M CASTROMALASPINA B JHANWAR S LUZZATTO L
Citation: K. Nafa et al., THE SPECTRUM OF SOMATIC MUTATIONS IN THE PIG-A GENE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA INCLUDES LARGE DELETIONS AND SMALL DUPLICATIONS, Blood cells, molecules, & diseases (Print), 24(18), 1998, pp. 370-384
DYSKERATOSIS AND RIBOSOMAL REBELLION
Authors: LUZZATTO L KARADIMITRIS A
Citation: L. Luzzatto et A. Karadimitris, DYSKERATOSIS AND RIBOSOMAL REBELLION, Nature genetics, 19(1), 1998, pp. 6-7
AN UNUSUAL CASE OF FAMILIAL APLASTIC-ANEMIA - IN-VITRO AND IN-VIVO EVIDENCE FOR A MULTIPOTENT PROGENITOR RESPONSIVE TO G-CSF
Authors: DUFOUR C MAHER J MURRAY N MANNING M DOKAL I LUZZATTO L ROBERTS IAG
Citation: C. Dufour et al., AN UNUSUAL CASE OF FAMILIAL APLASTIC-ANEMIA - IN-VITRO AND IN-VIVO EVIDENCE FOR A MULTIPOTENT PROGENITOR RESPONSIVE TO G-CSF, European journal of haematology, 60(3), 1998, pp. 209-212
FROM THE GENETIC-BASIS OF BLOOD DISORDERS TO GENE-TRANSFER FOR THE PURPOSE OF GENE-THERAPY - INTRODUCTION
Authors: LUZZATTO L
Citation: L. Luzzatto, FROM THE GENETIC-BASIS OF BLOOD DISORDERS TO GENE-TRANSFER FOR THE PURPOSE OF GENE-THERAPY - INTRODUCTION, Seminars in hematology, 35(2), 1998, pp. 89-92
X-LINKED WISKOTT-ALDRICH-SYNDROME IN A GIRL
Authors: LUZZATTO L MARTINI G
Citation: L. Luzzatto et G. Martini, X-LINKED WISKOTT-ALDRICH-SYNDROME IN A GIRL, The New England journal of medicine, 338(25), 1998, pp. 1850-1851
TYPE-I TRANSFORMING-GROWTH-FACTOR-BETA RECEPTOR MAPS TO 9Q22 AND EXHIBITS A POLYMORPHISM AND A RARE VARIANT WITHIN A POLYALANINE TRACT
Authors: PASCHE B LUO Y RAO PH NIMER SD DMITROVSKY E CARON P LUZZATTO L OFFIT K CORDONCARDO C RENAULT B SATAGOPAN JM MURTY VVVS MASSAGUE J
Citation: B. Pasche et al., TYPE-I TRANSFORMING-GROWTH-FACTOR-BETA RECEPTOR MAPS TO 9Q22 AND EXHIBITS A POLYMORPHISM AND A RARE VARIANT WITHIN A POLYALANINE TRACT, Cancer research, 58(13), 1998, pp. 2727-2732
CLINICAL AND HEMATOLOGICAL CONSEQUENCES OF RECURRENT G6PD MUTATIONS AND A SINGLE NEW MUTATION CAUSING CHRONIC NONSPHEROCYTIC HEMOLYTIC-ANEMIA
Authors: VULLIAMY TJ KAEDA JS AITCHAFA D MANGERINI R ROPER D BARBOT J MEHTA AB ATHANASSIOUMETAXA M LUZZATTO L MASON PJ
Citation: Tj. Vulliamy et al., CLINICAL AND HEMATOLOGICAL CONSEQUENCES OF RECURRENT G6PD MUTATIONS AND A SINGLE NEW MUTATION CAUSING CHRONIC NONSPHEROCYTIC HEMOLYTIC-ANEMIA, British Journal of Haematology, 101(4), 1998, pp. 670-675
NEW SOMATIC MUTATION IN THE PIG-A GENE EMERGES AT RELAPSE OF PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
Authors: NAFA K BESSLER M DEEG HJ LUZZATTO L
Citation: K. Nafa et al., NEW SOMATIC MUTATION IN THE PIG-A GENE EMERGES AT RELAPSE OF PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA, Blood, 92(9), 1998, pp. 3422-3427
EARLY PHAGOCYTOSIS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD)-DEFICIENT ERYTHROCYTES PARASITIZED BY PLASMODIUM-FALCIPARUM MAY EXPLAIN MALARIA PROTECTION IN G6PD DEFICIENCY
Authors: CAPPADORO M GIRIBALDI G OBRIEN E TURRINI F MANNU F ULLIERS D SIMULA G LUZZATTO L ARESE P
Citation: M. Cappadoro et al., EARLY PHAGOCYTOSIS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD)-DEFICIENT ERYTHROCYTES PARASITIZED BY PLASMODIUM-FALCIPARUM MAY EXPLAIN MALARIA PROTECTION IN G6PD DEFICIENCY, Blood, 92(7), 1998, pp. 2527-2534
SOMATIC MUTATION IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
Authors: LUZZATTO L
Citation: L. Luzzatto, SOMATIC MUTATION IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA, Hospital practice, 32(9), 1997, pp. 125
HEMATOLOGICALLY IMPORTANT MUTATIONS - GLUCOSE-6-PHOSPHATE-DEHYDROGENASE
Authors: VULLIAMY T LUZZATTO L HIRONO A BEUTLER E
Citation: T. Vulliamy et al., HEMATOLOGICALLY IMPORTANT MUTATIONS - GLUCOSE-6-PHOSPHATE-DEHYDROGENASE, Blood cells, molecules, & diseases, 23(15), 1997, pp. 302-313
IMMUNOGENE-THERAPY COMES INTO ITS OWN
Authors: SADELAIN M LUZZATTO L
Citation: M. Sadelain et L. Luzzatto, IMMUNOGENE-THERAPY COMES INTO ITS OWN, Gene therapy, 4(11), 1997, pp. 1129-1131
SOMATIC MUTATIONS IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - A BLESSINGIN DISGUISE
Authors: LUZZATTO L BESSLER M ROTOLI B
Citation: L. Luzzatto et al., SOMATIC MUTATIONS IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - A BLESSINGIN DISGUISE, Cell, 88(1), 1997, pp. 1-4
IN-VIVO TELOMERE DYNAMICS OF HUMAN HEMATOPOIETIC STEM-CELLS
Authors: NOTARO R CIMMINO A TABARINI D ROTOLI B LUZZATTO L
Citation: R. Notaro et al., IN-VIVO TELOMERE DYNAMICS OF HUMAN HEMATOPOIETIC STEM-CELLS, Proceedings of the National Academy of Sciences of the United Statesof America, 94(25), 1997, pp. 13782-13785
MURINE EMBRYONIC STEM-CELLS WITHOUT PIG-A GENE ACTIVITY ARE COMPETENTFOR HEMATOPOIESIS WITH THE PNH PHENOTYPE BUT NOT FOR CLONAL EXPANSION
Authors: ROSTI V TREMML G SOARES V PANDOLFI PP LUZZATTO L BESSLER M
Citation: V. Rosti et al., MURINE EMBRYONIC STEM-CELLS WITHOUT PIG-A GENE ACTIVITY ARE COMPETENTFOR HEMATOPOIESIS WITH THE PNH PHENOTYPE BUT NOT FOR CLONAL EXPANSION, The Journal of clinical investigation, 100(5), 1997, pp. 1028-1036
CHROMOSOMAL-ABNORMALITIES IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH)
Authors: ARATEN D BESSLER M NAFA K LONGO L KARADIMITRIS A FREEMAN J ANASTAGNOPOULOUS N BERIS P BOULAD F CASTROMALASPINA H CHASE A CHILDS B KUTLAR A MAZIARZ R TSATALAS C WEISS M JHANWAR S LUZZATTO L
Citation: D. Araten et al., CHROMOSOMAL-ABNORMALITIES IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH), Blood, 90(10), 1997, pp. 2694-2694
SEARCH FOR GENETIC-FACTORS THROMBOSIS IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - THE POSSIBLE ROLE OF A MUTANT METHYLENETETRAHYDROFOLATE REDUCTASE (C677T)
Authors: NAFA K BESSLER M CASTROMALASPINA H LUZZATTO L
Citation: K. Nafa et al., SEARCH FOR GENETIC-FACTORS THROMBOSIS IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - THE POSSIBLE ROLE OF A MUTANT METHYLENETETRAHYDROFOLATE REDUCTASE (C677T), Blood, 90(10), 1997, pp. 3249-3249
PATTERN OF EXPRESSION OF NPM ALK FUSION TRANSCRIPTS IN PEDIATRIC LYMPHOMAS/
Authors: LANZA C VOLPE G BASSO G LUZZATTO L GOTTARDI E SPINELLI M PIGLIONE M MADON E LINARI A DIMONTEZEMOLO LC SAGLIO G
Citation: C. Lanza et al., PATTERN OF EXPRESSION OF NPM ALK FUSION TRANSCRIPTS IN PEDIATRIC LYMPHOMAS/, Blood, 90(10), 1997, pp. 3921-3921
RETROVIRAL-MEDIATED TRANSFER AND EXPRESSION OF THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) GENE IN MOUSE BONE-MARROW CELLS
Authors: ROVIRA A GALLARDO H DEANGIOLETTI M MURPHY C ROSTI V LIU D SADELAIN M LUZZATTO L
Citation: A. Rovira et al., RETROVIRAL-MEDIATED TRANSFER AND EXPRESSION OF THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) GENE IN MOUSE BONE-MARROW CELLS, Blood, 90(10), 1997, pp. 517-517
PNH-LIKE LYMPHOCYTES ARE COMPETENT FOR GENERATING THE ENTIRE IMMUNE-SYSTEM IN RAG NULL MICE
Authors: ROSTI V DRAPPA J TREMML G CATTORETTI G ELKON KB LUZZATTO L BESSLER M
Citation: V. Rosti et al., PNH-LIKE LYMPHOCYTES ARE COMPETENT FOR GENERATING THE ENTIRE IMMUNE-SYSTEM IN RAG NULL MICE, Blood, 90(10), 1997, pp. 698-698
SURVEY OF MUTATIONS OF THE PIG-A GENE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - PHENOTYPE-GENOTYPE CORRELATIONS
Authors: NAFA K BESSLER M LUZZATTO L
Citation: K. Nafa et al., SURVEY OF MUTATIONS OF THE PIG-A GENE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - PHENOTYPE-GENOTYPE CORRELATIONS, Blood, 90(10), 1997, pp. 1204-1204
MICE HETEROZYGOUS FOR COMPLETE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) DEFICIENCY ARE VIABLE AND SHOW SOMATIC-CELL SELECTION
Authors: LONGO L ROSTI V GABOLI M TABARINI D PANDOLFI PP LUZZATTO L
Citation: L. Longo et al., MICE HETEROZYGOUS FOR COMPLETE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) DEFICIENCY ARE VIABLE AND SHOW SOMATIC-CELL SELECTION, Blood, 90(10), 1997, pp. 1812-1812
MUTATIONS OF THE PIG-A GENE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH) - AN UPDATE SURVEY
Authors: NAFA K BESSLER M LUZZATTO L
Citation: K. Nafa et al., MUTATIONS OF THE PIG-A GENE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH) - AN UPDATE SURVEY, American journal of human genetics, 61(4), 1997, pp. 1027-1027
GENETIC-EVIDENCE FOR A COMMON ORIGIN AMONG ROMAN JEWS AND ASHKENAZI JEWS
Authors: ODDOUX C GUILLENNAVARRO E CLAYTON CM NELSON H PERETZ H SELIGSOHN U LUZZATTO L NARDI M KARPATKIN M DITIVOLI C DICAVE E AXELROD F OSTRER H
Citation: C. Oddoux et al., GENETIC-EVIDENCE FOR A COMMON ORIGIN AMONG ROMAN JEWS AND ASHKENAZI JEWS, American journal of human genetics, 61(4), 1997, pp. 1200-1200
HEMATOLOGICALLY IMPORTANT MUTATIONS - GLUCOSE-6-PHOSPHATE-DEHYDROGENASE
Authors: BEUTLER E VULLIAMY T LUZZATTO L
Citation: E. Beutler et al., HEMATOLOGICALLY IMPORTANT MUTATIONS - GLUCOSE-6-PHOSPHATE-DEHYDROGENASE, Blood cells, molecules, & diseases, 22(4), 1996, pp. 49-56
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