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Results: 1-25 | 26-49
Results: 1-25/49
EUCLID - AUTOMATIC CLASSIFICATION OF PROTEINS IN FUNCTIONAL CLASSES BY THEIR DATABASE ANNOTATIONS
Authors: TAMAMES J OUZOUNIS C CASARI G SANDER C VALENCIA A
Citation: J. Tamames et al., EUCLID - AUTOMATIC CLASSIFICATION OF PROTEINS IN FUNCTIONAL CLASSES BY THEIR DATABASE ANNOTATIONS, BIOINFORMATICS, 14(6), 1998, pp. 542-543
GENOTYPE-PHENOTYPE CORRELATIONS IN NORMOTENSIVE PATIENTS WITH PRIMARYRENAL TUBULAR HYPOKALEMIC METABOLIC ALKALOSIS
Authors: BETTINELLI A VEZZOLI G COLUSSI G BIANCHETTI MG SERENI F CASARI G
Citation: A. Bettinelli et al., GENOTYPE-PHENOTYPE CORRELATIONS IN NORMOTENSIVE PATIENTS WITH PRIMARYRENAL TUBULAR HYPOKALEMIC METABOLIC ALKALOSIS, JN. Journal of nephrology, 11(2), 1998, pp. 61-69
GLUCOCORTICOID RECEPTOR POLYMORPHISM IN GENETIC-HYPERTENSION
Authors: KENYON CJ PANARELLI M ZAGATO L TORIELLI L HEELEY RP HOLLOWAY CD FRASER R CASARI G SUTCLIFFE RG BIANCHI G
Citation: Cj. Kenyon et al., GLUCOCORTICOID RECEPTOR POLYMORPHISM IN GENETIC-HYPERTENSION, Journal of molecular endocrinology, 21(1), 1998, pp. 41-50
AUTOSOMAL-DOMINANT MEDULLARY CYSTIC-DISEASE - A DISORDER WITH VARIABLE CLINICAL PICTURES AND EXCLUSION OF LINKAGE WITH THE NPH1 LOCUS
Authors: SCOLARI F GHIGGERI GM CASARI G AMOROSO A PUZZER D CARIDI GL VALZORIO B TARDANICO R VIZZARDI V SAVOLDI S VIOLA BF BOSSINI N PRATI E GUSMANO R MAIORCA R
Citation: F. Scolari et al., AUTOSOMAL-DOMINANT MEDULLARY CYSTIC-DISEASE - A DISORDER WITH VARIABLE CLINICAL PICTURES AND EXCLUSION OF LINKAGE WITH THE NPH1 LOCUS, Nephrology, dialysis, transplantation, 13(10), 1998, pp. 2536-2546
MODULATION OF IGE REACTIVITY OF ALLERGENS BY SITE-DIRECTED MUTAGENESIS - POTENTIAL USE OF HYPOALLERGENIC VARIANTS FOR IMMUNOTHERAPY
Authors: FERREIRA F EBNER C KRAMER B CASARI G BRIZA P KUNGL AJ GRIMM R JAHNSCHMID B BREITENEDER H KRAFT D BREITENBACH M RHEINBERGER H SCHEINER O
Citation: F. Ferreira et al., MODULATION OF IGE REACTIVITY OF ALLERGENS BY SITE-DIRECTED MUTAGENESIS - POTENTIAL USE OF HYPOALLERGENIC VARIANTS FOR IMMUNOTHERAPY, The FASEB journal, 12(2), 1998, pp. 231-242
VARIABLE PHENOTYPE OF LONG QT SYNDROME PATIENTS WITH THE SAME GENETIC-DEFECT
Authors: PRIORI SG NAPOLITANO C SCHWARTZ PJ MARK R MCDONALDS D DENJOY I GUICENEY P TOWBIN JA PAGANINI V CASARI G
Citation: Sg. Priori et al., VARIABLE PHENOTYPE OF LONG QT SYNDROME PATIENTS WITH THE SAME GENETIC-DEFECT, Journal of the American College of Cardiology, 31(2), 1998, pp. 349-349
A SEQUENCESPACE ANALYSIS OF LYS49 PHOSPHOLIPASES A(2) - CLUES TOWARDSIDENTIFICATION OF RESIDUES INVOLVED IN A NOVEL MECHANISM OF MEMBRANE DAMAGE AND IN MYOTOXICITY
Authors: WARD RJ ALVES AR NETO JR ARNI RK CASARI G
Citation: Rj. Ward et al., A SEQUENCESPACE ANALYSIS OF LYS49 PHOSPHOLIPASES A(2) - CLUES TOWARDSIDENTIFICATION OF RESIDUES INVOLVED IN A NOVEL MECHANISM OF MEMBRANE DAMAGE AND IN MYOTOXICITY, Protein engineering (Print), 11(4), 1998, pp. 285-294
GENETIC-ANALYSIS OF THE S-A AND NA+ K+-ATPASE ALPHA(1) GENES IN THE MILAN HYPERTENSIVE RAT/
Authors: LODWICK D ZAGATO L KAISER MA TORIELLI L CASARI G BIANCHI G SAMANI NJ
Citation: D. Lodwick et al., GENETIC-ANALYSIS OF THE S-A AND NA+ K+-ATPASE ALPHA(1) GENES IN THE MILAN HYPERTENSIVE RAT/, Journal of hypertension, 16(2), 1998, pp. 139-144
SPASTIC PARAPLEGIA AND OXPHOS IMPAIRMENT CAUSED BY MUTATIONS IN PARAPLEGIN, A NUCLEAR-ENCODED MITOCHONDRIAL METALLOPROTEASE
Authors: CASARI G DEFUSCO M CIARMATORI S ZEVIANI M MORA M FERNANDEZ P DEMICHELE G FILLA A COCOZZA S MARCONI R DURR A FONTAINE B BALLABIO A
Citation: G. Casari et al., SPASTIC PARAPLEGIA AND OXPHOS IMPAIRMENT CAUSED BY MUTATIONS IN PARAPLEGIN, A NUCLEAR-ENCODED MITOCHONDRIAL METALLOPROTEASE, Cell, 93(6), 1998, pp. 973-983
FUNCTIONAL-ANALYSIS OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REV PROTEIN OLIGOMERIZATION INTERFACE
Authors: THOMAS SL OFT M JAKSCHE H CASARI G HEGER P DOBROVNIK M BEVEC D HAUBER J
Citation: Sl. Thomas et al., FUNCTIONAL-ANALYSIS OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REV PROTEIN OLIGOMERIZATION INTERFACE, Journal of virology, 72(4), 1998, pp. 2935-2944
MULTIMER FORMATION IS NOT ESSENTIAL FOR NUCLEAR EXPORT OF HUMAN T-CELL LEUKEMIA-VIRUS TYPE-1 REX TRANSACTIVATOR PROTEIN
Authors: HEGER P ROSORIUS O KOCH C CASARI G GRASSMANN R HAUBER J
Citation: P. Heger et al., MULTIMER FORMATION IS NOT ESSENTIAL FOR NUCLEAR EXPORT OF HUMAN T-CELL LEUKEMIA-VIRUS TYPE-1 REX TRANSACTIVATOR PROTEIN, Journal of virology (Print), 72(11), 1998, pp. 8659-8668
GENOME-WIDE SEARCH FOR LINKAGE MAPPING OF SUSCEPTIBILITY GENES FOR FAMILIAL COMBINED HYPERLIPIDEMIA (FCHL)
Authors: ARCA M CAMPAGNA F MONTALI A FLORA L GADDI A GALLETTI P CASARI G DEVOTO M DAMBROSIO E VERNA R
Citation: M. Arca et al., GENOME-WIDE SEARCH FOR LINKAGE MAPPING OF SUSCEPTIBILITY GENES FOR FAMILIAL COMBINED HYPERLIPIDEMIA (FCHL), Atherosclerosis (Amsterdam), 138, 1998, pp. 25-25
A RECESSIVE VARIANT OF THE ROMANO-WARD-LONG-QT-SYNDROME
Authors: PRIORI SG SCHWARTZ PJ NAPOLITANO C BIANCHI L DENNIS A DEFUSCO M BROWN AM CASARI G
Citation: Sg. Priori et al., A RECESSIVE VARIANT OF THE ROMANO-WARD-LONG-QT-SYNDROME, Circulation, 97(24), 1998, pp. 2420-2425
A NEW LOCUS FOR AUTOSOMAL RECESSIVE HEREDITARY SPASTIC PARAPLEGIA MAPS TO CHROMOSOME 16Q24.3
Authors: DEMICHELE G DEFUSCO M CAVALCANTI F FILLA A MARCONI R VOLPE G MONTICELLI A BALLABIO A CASARI G COCOZZA S
Citation: G. Demichele et al., A NEW LOCUS FOR AUTOSOMAL RECESSIVE HEREDITARY SPASTIC PARAPLEGIA MAPS TO CHROMOSOME 16Q24.3, American journal of human genetics, 63(1), 1998, pp. 135-139
CHARACTERIZATION OF NEW PROTEINS FOUND BY ANALYSIS OF SHORT OPEN READING FRAMES FROM THE FULL YEAST GENOME
Authors: ANDRADE MA DARUVAR A CASARI G SCHNEIDER R TERMIER M SANDER C
Citation: Ma. Andrade et al., CHARACTERIZATION OF NEW PROTEINS FOUND BY ANALYSIS OF SHORT OPEN READING FRAMES FROM THE FULL YEAST GENOME, Yeast, 13(14), 1997, pp. 1363-1374
MOLECULAR ANALYSTS OF THE HERG-GENE IN 48 UNRELATED LONG QT SYNDROME PATIENTS - GENOTYPE PHENOTYPE CORRELATION IN 2 FAMILIES WITH NOVEL MUTATIONS/
Authors: PRIORI SG SCHWARTZ PJ NAPOLITANO C MASTROIANNI N PAGANINI V CANTU F LOCATI EH TOWBIN JA BALLABIO A CASARI G
Citation: Sg. Priori et al., MOLECULAR ANALYSTS OF THE HERG-GENE IN 48 UNRELATED LONG QT SYNDROME PATIENTS - GENOTYPE PHENOTYPE CORRELATION IN 2 FAMILIES WITH NOVEL MUTATIONS/, Journal of the American College of Cardiology, 29(2), 1997, pp. 7372-7372
CLASSIFICATION OF PROTEIN FAMILIES AND DETECTION OF THE DETERMINANT RESIDUES WITH AN IMPROVED SELF-ORGANIZING MAP
Authors: ANDRADE MA CASARI G SANDER C VALENCIA A
Citation: Ma. Andrade et al., CLASSIFICATION OF PROTEIN FAMILIES AND DETECTION OF THE DETERMINANT RESIDUES WITH AN IMPROVED SELF-ORGANIZING MAP, Biological cybernetics, 76(6), 1997, pp. 441-450
GLUCOCORTICOID RECEPTOR MUTATIONS IN GENETICALLY HYPERTENSIVE RATS - MARKERS OF GLUCOCORTICOID INSENSITIVITY
Authors: HEELEY RP CASARI G ZAGATO L TORIELLI L SUTCLIFFE RG BIANCHI G KENYON CJ
Citation: Rp. Heeley et al., GLUCOCORTICOID RECEPTOR MUTATIONS IN GENETICALLY HYPERTENSIVE RATS - MARKERS OF GLUCOCORTICOID INSENSITIVITY, Biochemical Society transactions, 25(2), 1997, pp. 236-236
PROBING THE STRUCTURE OF THE HIV-1 REV TRANSACTIVATOR PROTEIN BY FUNCTIONAL-ANALYSIS
Authors: THOMAS SL HAUBER J CASARI G
Citation: Sl. Thomas et al., PROBING THE STRUCTURE OF THE HIV-1 REV TRANSACTIVATOR PROTEIN BY FUNCTIONAL-ANALYSIS, Protein engineering, 10(2), 1997, pp. 103-107
SEQUENCE-ANALYSIS OF THE METHANOCOCCUS-JANNASCHII GENOME AND THE PREDICTION OF PROTEIN FUNCTION
Authors: ANDRADE M CASARI G DEDARUVAR A SANDER C SCHNEIDER R TAMAMES J VALENCIA A OUZOUNIS C
Citation: M. Andrade et al., SEQUENCE-ANALYSIS OF THE METHANOCOCCUS-JANNASCHII GENOME AND THE PREDICTION OF PROTEIN FUNCTION, Computer applications in the biosciences, 13(4), 1997, pp. 481-483
POLYMORPHISMS OF ALPHA-ADDUCIN AND SALT SENSITIVITY IN PATIENTS WITH ESSENTIAL-HYPERTENSION
Authors: CUSI D BARLASSINA C AZZANI T CASARI G CITTERIO L DEVOTO M GLORIOSO N LANZANI C MANUNTA P RIGHETTI M RIVERA R STELLA P TROFFA C ZAGATO L BIANCHI G
Citation: D. Cusi et al., POLYMORPHISMS OF ALPHA-ADDUCIN AND SALT SENSITIVITY IN PATIENTS WITH ESSENTIAL-HYPERTENSION, Lancet, 349(9062), 1997, pp. 1353-1357
MUTATIONAL ANALYSES SUPPORT A MODEL FOR THE HRV2 2A PROTEINASE
Authors: SOMMERGRUBER W SEIPELT J FESSL F SKERN T LIEBIG HD CASARI G
Citation: W. Sommergruber et al., MUTATIONAL ANALYSES SUPPORT A MODEL FOR THE HRV2 2A PROTEINASE, Virology, 234(2), 1997, pp. 203-214
CONSERVED CLUSTERS OF FUNCTIONALLY RELATED GENES IN 2 BACTERIAL GENOMES
Authors: TAMAMES J CASARI G OUZOUNIS C VALENCIA A
Citation: J. Tamames et al., CONSERVED CLUSTERS OF FUNCTIONALLY RELATED GENES IN 2 BACTERIAL GENOMES, Journal of molecular evolution, 44(1), 1997, pp. 66-73
IDENTIFICATION OF A LONG QT SYNDROME MOLECULAR DEFECT IN DRUG-INDUCEDTORSADES-DE-POINTES
Authors: NAPOLITANO C PRIORI SG SCHWARTZ PJ CANTU F PAGANINI V DEFUSCO M PINNAVAIA A AQUARO G CASARI G
Citation: C. Napolitano et al., IDENTIFICATION OF A LONG QT SYNDROME MOLECULAR DEFECT IN DRUG-INDUCEDTORSADES-DE-POINTES, Circulation, 96(8), 1997, pp. 1169-1169
IDENTIFICATION OF A MUTATIONAL HOT-SPOT IN HERG-RELATED LONG QT SYNDROME (LQT2) - PHENOTYPIC IMPLICATIONS
Authors: NAPOLITANO C PRIORI SG SCHWARTZ PJ TIMOTHY K PAGANINI V CANTU F BLOISI R DEFUSCO M SPAZZOLINI C CASARI G
Citation: C. Napolitano et al., IDENTIFICATION OF A MUTATIONAL HOT-SPOT IN HERG-RELATED LONG QT SYNDROME (LQT2) - PHENOTYPIC IMPLICATIONS, Circulation, 96(8), 1997, pp. 1173-1173
Risultati: 1-25 | 26-49