AAAAAA

   
Results: 1-25 | 26-44
Results: 1-25/44
HOST RESPONSE TO EBV INFECTION IN X-LINKED LYMPHOPROLIFERATIVE DISEASE RESULTS FROM MUTATIONS IN AN SH2-DOMAIN ENCODING GENE
Authors: COFFEY AJ BROOKSBANK RA BRANDAU O OOHASHI T HOWELL GR BYE JM CAHN AP DURHAM J HEATH P WRAY P PAVITT R WILKINSON J LEVERSHA M HUCKLE E SHAWSMITH CJ DUNHAM A RHODES S SCHUSTER V PORTA G YIN L SERAFINI P SYLLA B ZOLLO M FRANCO B BOLINO A SERI M LANYI A DAVIS JR WEBSTER D HARRIS A LENOIR G STBASILE GD JONES A BEHLORADSKY BH ACHATZ H MURKEN J FASSLER R SUMEGI J ROMEO G VAUDIN M ROSS MT MEINDL A BENTLEY DR
Citation: Aj. Coffey et al., HOST RESPONSE TO EBV INFECTION IN X-LINKED LYMPHOPROLIFERATIVE DISEASE RESULTS FROM MUTATIONS IN AN SH2-DOMAIN ENCODING GENE, Nature genetics, 20(2), 1998, pp. 129-135
A NEW CANDIDATE REGION FOR THE POSITIONAL CLONING OF THE XLP GENE
Authors: BOLINO A YIN L SERI M CUSANO R CINTI R COFFEY A BROOKSBANK R HOWELL G BENTLEY D DAVIS JR LANYI A HUANG DL STARK M CREAVEN M BJORKHAUG L HEITZMANN F LAMARTINE J GAUDI S SYLLA BS LENOIR GM CASTAGNOLA E GIACCHINO R PORTA G FRANCO B ZOLLO M SUMEGI J ROMEO G
Citation: A. Bolino et al., A NEW CANDIDATE REGION FOR THE POSITIONAL CLONING OF THE XLP GENE, European journal of human genetics, 6(5), 1998, pp. 509-517
GENERATION OF A TRANSCRIPTION MAP OF A 1 MBASE REGION CONTAINING THE HFE GENE (6P22)
Authors: TOTARO A ROETTO A ROMMENS JM GRIFA A CARELLA M DAGRUMA L VALENTINO MA DAMBROSIO L CICILANO M CAMASCHELLA C FRANCO B GASPARINI P
Citation: A. Totaro et al., GENERATION OF A TRANSCRIPTION MAP OF A 1 MBASE REGION CONTAINING THE HFE GENE (6P22), European journal of human genetics, 6(2), 1998, pp. 105-113
IDENTIFICATION AND EXPRESSION STUDIES OF MAMMALIAN HOMOLOGS OF THE DROSOPHILA CDP-DIACYLGLYCEROL SYNTHASE (CDS) GENE - IMPLICATIONS FOR THEEVOLUTION OF PHOTOTRANSDUCTION MECHANISMS
Authors: VOLTA M BULFONE A ROSSI E MARIANI M CONSALES G ZUFFARDI O BALLABIO A BANFI S FRANCO B
Citation: M. Volta et al., IDENTIFICATION AND EXPRESSION STUDIES OF MAMMALIAN HOMOLOGS OF THE DROSOPHILA CDP-DIACYLGLYCEROL SYNTHASE (CDS) GENE - IMPLICATIONS FOR THEEVOLUTION OF PHOTOTRANSDUCTION MECHANISMS, European journal of human genetics, 6, 1998, pp. 6032-6032
FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS)
Authors: DENDUNNEN JT KRAAYENBRINK T VANSCHOONEVELD M VANDEVOSSE E DEJONG PTVM TENBRINK JB SCHUURMAN E TIJMES N VANOMMEN GJB BERGEN AAB ANDOLFI G MONTINI E LI Y OUDET C BOLZ H KAPLAN J ORTH U GAL A HANAUER A BARDELLI AM AYUSO C DIAZ FJ BITOUN P VENTRUTO V BALLABIO A FRANCO B HIRIYANNA KT BINGHAM EL MCHENRY C PAWAR H COATS C DARGA T RICHARDS JE SIEVING PA HUOPANIEMI L RANTALA A ROSENBERG T DAHL N WRIGHT A DELACHAPELLE A ALITALO T LENZNER S BRUNNER B FEIL S NIESLER B SCHULZ U PINCKERS A BLANKENNAGEL A RUETHER K KELLNER U RAPPOLD G ROPERS HH KALSCHEUER V BERGER W TRUMP D WALPOLE SM NICOLAOU A GAYTHOR SA PIMENIDES D GEORGE NDL MOORE UT YATES JRW
Citation: Jt. Dendunnen et al., FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS), Human molecular genetics (Print), 7(7), 1998, pp. 1185-1192
IDENTIFICATION AND CHARACTERIZATION OF A NOVEL SERINE-THREONINE KINASE GENE FROM THE XP22 REGION
Authors: MONTINI E ANDOLFI G CARUSO A BUCHNER G WALPOLE SM MARIANI M CONSALEZ GG TRUMP D BALLABIO A FRANCO B
Citation: E. Montini et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL SERINE-THREONINE KINASE GENE FROM THE XP22 REGION, Genomics (San Diego, Calif.), 51(3), 1998, pp. 427-433
CHARACTERIZATION OF CXORF5 (71-7A), A NOVEL HUMAN CDNA MAPPING TO XP22 AND ENCODING A PROTEIN CONTAINING COILED-COIL ALPHA-HELICAL DOMAINS
Authors: DECONCILIIS L MARCHITIELLO A WAPENAAR MC BORSANI G GIGLIO S MARIANI M CONSALEZ GG ZUFFARDI O FRANCO B BALLABIO A BANFI S
Citation: L. Deconciliis et al., CHARACTERIZATION OF CXORF5 (71-7A), A NOVEL HUMAN CDNA MAPPING TO XP22 AND ENCODING A PROTEIN CONTAINING COILED-COIL ALPHA-HELICAL DOMAINS, Genomics (San Diego, Calif.), 51(2), 1998, pp. 243-250
HUMAN FIGF - CLONING, GENE STRUCTURE, AND MAPPING TO CHROMOSOME XP22.1 BETWEEN THE PIGA AND THE GRPR GENES
Authors: ROCCHIGIANI M LESTINGI M LUDDI A ORLANDINI M FRANCO B ROSSI E BALLABIO A ZUFFARDI O OLIVIERO S
Citation: M. Rocchigiani et al., HUMAN FIGF - CLONING, GENE STRUCTURE, AND MAPPING TO CHROMOSOME XP22.1 BETWEEN THE PIGA AND THE GRPR GENES, Genomics, 47(2), 1998, pp. 207-216
XP CONTIGUOUS GENE SYNDROMES - FROM CLINICAL OBSERVATION TO DISEASE GENE IDENTIFICATION
Authors: FRANCO B
Citation: B. Franco, XP CONTIGUOUS GENE SYNDROMES - FROM CLINICAL OBSERVATION TO DISEASE GENE IDENTIFICATION, Cytogenetics and cell genetics, 81(2), 1998, pp. 6-6
IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE DYSTROBREVIN GENE FAMILY
Authors: PUCA AA NIGRO V PILUSO G BELSITO A SAMPAOLO S QUADERI N ROSSI E DIIORIO G BALLABIO A FRANCO B
Citation: Aa. Puca et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE DYSTROBREVIN GENE FAMILY, FEBS letters, 425(1), 1998, pp. 7-13
A 5' REGULATORY SEQUENCE CONTAINING 2 ETS MOTIFS CONTROLS THE EXPRESSION OF THE WISKOTT-ALDRICH-SYNDROME PROTEIN (WASP) GENE IN HUMAN HEMATOPOIETIC-CELLS
Authors: PETRELLA A DOTI I AGOSTI V GIARRUSSO PC VITALE D BOND HM CUOMO C TASSONE P FRANCO B BALLABIO A VENUTA S MORRONE G
Citation: A. Petrella et al., A 5' REGULATORY SEQUENCE CONTAINING 2 ETS MOTIFS CONTROLS THE EXPRESSION OF THE WISKOTT-ALDRICH-SYNDROME PROTEIN (WASP) GENE IN HUMAN HEMATOPOIETIC-CELLS, Blood, 91(12), 1998, pp. 4554-4560
MEASUREMENT OF HEPATIC GLUCOSE OUTPUT, KREBS CYCLE, AND GLUCONEOGENICFLUXES BY NMR ANALYSIS OF A SINGLE PLASMA-GLUCOSE SAMPLE
Authors: JONES JG CARVALHO RA FRANCO B SHERRY AD MALLOY CR
Citation: Jg. Jones et al., MEASUREMENT OF HEPATIC GLUCOSE OUTPUT, KREBS CYCLE, AND GLUCONEOGENICFLUXES BY NMR ANALYSIS OF A SINGLE PLASMA-GLUCOSE SAMPLE, Analytical biochemistry (Print), 263(1), 1998, pp. 39-45
OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN (VOL 63, PG 703, 1998)/
Authors: GAUDENZ K ROESSLER E QUADERI N FRANCO B FELDMAN G GASSER DL WITTWER B HORST J MONTINI E OPITZ JM BALLABIO A MUENKE M
Citation: K. Gaudenz et al., OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN (VOL 63, PG 703, 1998)/, American journal of human genetics, 63(5), 1998, pp. 1571-1571
OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN/
Authors: GAUDENZ K ROESSLER E QUADERI N FRANCO B FELDMAN G GASSER DL WITTWER B MONTINI E OPITZ JM BALLABIO A MUENKE M
Citation: K. Gaudenz et al., OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN/, American journal of human genetics, 63(3), 1998, pp. 703-710
OPITZ G BBB SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NEW RING FINGER GENE ON XP22/
Authors: QUADERI NA SCHWEIGER S GAUDENZ K FRANCO B RUGARLI EI BERGER W FELDMAN GJ VOLTA M ANDOLFI G GILGENKRANTZ S MARION RW HENNEKAM RCM OPITZ JM MUENKE M ROPERS HH BALLABIO A
Citation: Na. Quaderi et al., OPITZ G BBB SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NEW RING FINGER GENE ON XP22/, Nature genetics, 17(3), 1997, pp. 285-291
A NOVEL HUMAN SERINE-THREONINE PHOSPHATASE RELATED TO THE DROSOPHILA RETINAL-DEGENERATION-C (RDGC) GENE IS SELECTIVELY EXPRESSED IN SENSORYNEURONS OF NEURAL CREST ORIGIN
Authors: MONTINI E RUGARLI EI VANDEVOSSE E ANDOLFI G MARIANI M PUCA AA CONSALEZ GG DENDUNNEN JT BALLABIO A FRANCO B
Citation: E. Montini et al., A NOVEL HUMAN SERINE-THREONINE PHOSPHATASE RELATED TO THE DROSOPHILA RETINAL-DEGENERATION-C (RDGC) GENE IS SELECTIVELY EXPRESSED IN SENSORYNEURONS OF NEURAL CREST ORIGIN, Human molecular genetics, 6(7), 1997, pp. 1137-1145
IDENTIFICATION BY SHOTGUN SEQUENCING, GENOMIC ORGANIZATION, AND FUNCTIONAL-ANALYSIS OF A 4TH ARYLSULFATASE GENE (ARSF) FROM THE XP22.3 REGION
Authors: PUCA AA ZOLLO M REPETTO M ANDOLFI G GUFFANTI A SIMON G BALLABIO A FRANCO B
Citation: Aa. Puca et al., IDENTIFICATION BY SHOTGUN SEQUENCING, GENOMIC ORGANIZATION, AND FUNCTIONAL-ANALYSIS OF A 4TH ARYLSULFATASE GENE (ARSF) FROM THE XP22.3 REGION, Genomics, 42(2), 1997, pp. 192-199
EXCLUSION OF PPEF AS THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS
Authors: VANDEVOSSE E FRANCO B VANDERBENT P MONTINI E ORTH U HANAUER A TIJMES N VANOMMEN GJB BALLABIO A DENDUNNEN JT BERGEN AAB
Citation: E. Vandevosse et al., EXCLUSION OF PPEF AS THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS, Human genetics, 101(2), 1997, pp. 235-237
RESPONSES TO GLASSBERG,DAVID 'PUBLIC HISTORY AND THE STUDY OF MEMORY'- PUBLIC HISTORY AND MEMORY, A MUSEUM PERSPECTIVE
Authors: FRANCO B
Citation: B. Franco, RESPONSES TO GLASSBERG,DAVID 'PUBLIC HISTORY AND THE STUDY OF MEMORY'- PUBLIC HISTORY AND MEMORY, A MUSEUM PERSPECTIVE, The Public historian, 19(2), 1997, pp. 65-67
LEARNING FROM THINGS - METHOD AND THEORY OF MATERIAL CULTURE STUDIES - KINGERY,WD
Authors: FRANCO B
Citation: B. Franco, LEARNING FROM THINGS - METHOD AND THEORY OF MATERIAL CULTURE STUDIES - KINGERY,WD, The Public historian, 19(2), 1997, pp. 109-110
X-LINKED RECESSIVE CHONDRODYSPLASIA PUNCTATA DUE TO A NEW POINT MUTATION OF THE ARSE GENE
Authors: PARENTI G BUTTITTA P MERONI G FRANCO B BERNARD L RIZZOLO MG BRUNETTIPIERRI N BALLABIO A ANDRIA G
Citation: G. Parenti et al., X-LINKED RECESSIVE CHONDRODYSPLASIA PUNCTATA DUE TO A NEW POINT MUTATION OF THE ARSE GENE, American journal of medical genetics, 73(2), 1997, pp. 139-143
WOMEN IN MUSEUMS -TABLE DISCUSSION - A PROGRESS REPORT( A ROUND)
Authors: ODONNELL SC FRANKEL D SOUTHERN KD BECKER G FRANCO B CONWILL KH
Citation: Sc. Odonnell et al., WOMEN IN MUSEUMS -TABLE DISCUSSION - A PROGRESS REPORT( A ROUND), Museum news, 76(2), 1997, pp. 34-41
OPITZ-SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NOVEL RING FINGER GENE ON XP22
Authors: QUADERI NA SCHWEIGER S GAUDENZ K FRANCO B RUGARLI E FELDMAN GJ VOLTA M GILGENKRANTZ S BERGER W OPITZ J MUENCKE J ROPERS H BALLABIO A
Citation: Na. Quaderi et al., OPITZ-SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NOVEL RING FINGER GENE ON XP22, American journal of human genetics, 61(4), 1997, pp. 44-44
MAPPING OF 3 NEW LOCI FOR X-LINKED MENTAL RETARDATIONS
Authors: AHMAD W FUSCO MD HAQUE MF SARNO T ARIDON P AHMAD M ULHAQUE S SELICORNI A BEDESCHI C BALLABIO A FRANCO B CASARI G
Citation: W. Ahmad et al., MAPPING OF 3 NEW LOCI FOR X-LINKED MENTAL RETARDATIONS, American journal of human genetics, 61(4), 1997, pp. 1540-1540
REFINEMENT OF THE LOCALIZATION OF THE X-LINKED RETINOSCHISIS GENE
Authors: BERGEN AAB VANDEVOSSE E FRANCO B VANDERBENT P BAKKER E MONTINI E HANAUER A TIJMES E VANOMMEN GJB BALLABIO A DENDUNNEN JT
Citation: Aab. Bergen et al., REFINEMENT OF THE LOCALIZATION OF THE X-LINKED RETINOSCHISIS GENE, American journal of human genetics, 61(4), 1997, pp. 1559-1559
Risultati: 1-25 | 26-44