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Results: 1-25/107
MUTATIONS IN THE DELTA(1)-PYRROLINE 5-CARBOXYLATE DEHYDROGENASE GENE CAUSE TYPE-II HYPERPROLINEMIA
Authors: GERAGHTY MT VAUGHN D NICHOLSON AJ LIN WW JIMENEZSANCHEZ G OBIE C FLYNN MP VALLE D HU CAA
Citation: Mt. Geraghty et al., MUTATIONS IN THE DELTA(1)-PYRROLINE 5-CARBOXYLATE DEHYDROGENASE GENE CAUSE TYPE-II HYPERPROLINEMIA, Human molecular genetics (Print), 7(9), 1998, pp. 1411-1415
AN ISOFORM OF PEX5P, THE HUMAN PTS1 RECEPTOR, IS REQUIRED FOR THE IMPORT OF PTS2 PROTEINS INTO PEROXISOMES
Authors: BRAVERMAN N DODT G GOULD SJ VALLE D
Citation: N. Braverman et al., AN ISOFORM OF PEX5P, THE HUMAN PTS1 RECEPTOR, IS REQUIRED FOR THE IMPORT OF PTS2 PROTEINS INTO PEROXISOMES, Human molecular genetics (Print), 7(8), 1998, pp. 1195-1205
EVALUATION OF THE VASCULAR PATTERN OF HEPATOCELLULAR-CARCINOMA WITH DYNAMIC COMPUTED-TOMOGRAPHY AND ITS USE IN IDENTIFYING OPTIMAL TEMPORALWINDOWS FOR HELICAL COMPUTED-TOMOGRAPHY
Authors: PACELLA CM BIZZARRI G ANELLI V VALLE D FABBRINI R BIANCHINI A FENDERICO P ROSSI Z
Citation: Cm. Pacella et al., EVALUATION OF THE VASCULAR PATTERN OF HEPATOCELLULAR-CARCINOMA WITH DYNAMIC COMPUTED-TOMOGRAPHY AND ITS USE IN IDENTIFYING OPTIMAL TEMPORALWINDOWS FOR HELICAL COMPUTED-TOMOGRAPHY, European radiology, 8(1), 1998, pp. 30-35
IDENTIFICATION AND CHARACTERIZATION OF THE HUMAN ORTHOLOG OF RAT STXBP1, A PROTEIN IMPLICATED IN VESICLE TRAFFICKING AND NEUROTRANSMITTER RELEASE
Authors: SWANSON DA STEEL JM VALLE D
Citation: Da. Swanson et al., IDENTIFICATION AND CHARACTERIZATION OF THE HUMAN ORTHOLOG OF RAT STXBP1, A PROTEIN IMPLICATED IN VESICLE TRAFFICKING AND NEUROTRANSMITTER RELEASE, Genomics, 48(3), 1998, pp. 373-376
GENOMIC ORGANIZATION OF THE 70-KDA PEROXISOMAL MEMBRANE-PROTEIN GENE (PXMP1)
Authors: GARTNER J JIMENEZSANCHEZ G ROERIG P VALLE D
Citation: J. Gartner et al., GENOMIC ORGANIZATION OF THE 70-KDA PEROXISOMAL MEMBRANE-PROTEIN GENE (PXMP1), Genomics, 48(2), 1998, pp. 203-208
MANAGEMENT OF CERVICAL INTRAEPITHELIAL NEOPLASIA OF THE UTERINE CERVIX - 110 CASES TREATED BY COLD-KNIFE CONIZATION
Authors: MARGARITI PA BALSAMO G GULLOTTA G RABITTI C VALLE D MANCUSO S
Citation: Pa. Margariti et al., MANAGEMENT OF CERVICAL INTRAEPITHELIAL NEOPLASIA OF THE UTERINE CERVIX - 110 CASES TREATED BY COLD-KNIFE CONIZATION, European journal of gynaecological oncology, 19(3), 1998, pp. 253-256
EVALUATION OF PRE-PRANDIAL AND POSTPRANDIAL GROWTH-HORMONE (GH)-RELEASING HORMONE-INDUCED GH RESPONSE IN SUBJECTS WITH PERSISTENT BODY-WEIGHT NORMALIZATION AFTER BILIOPANCREATIC DIVERSION
Authors: DEMARINIS L MANCINI A VALLE D TACCHINO RM BIANCHI A GENTILELLA R PERRELLI M CASTAGNETO M GASBARRINI G
Citation: L. Demarinis et al., EVALUATION OF PRE-PRANDIAL AND POSTPRANDIAL GROWTH-HORMONE (GH)-RELEASING HORMONE-INDUCED GH RESPONSE IN SUBJECTS WITH PERSISTENT BODY-WEIGHT NORMALIZATION AFTER BILIOPANCREATIC DIVERSION, International journal of obesity, 22(10), 1998, pp. 1011-1018
NALTREXONE EFFECT ON GROWTH-HORMONE AND INSULIN-SECRETION IN HYPERANDROGENIC AND NORMAL OBESE PATIENTS
Authors: VILLA P PAVONE V VALLE D DEMARINIS L MANCINI A FULGHESU AM BELOSI C PIERRO E LANZONE A MANCUSO S
Citation: P. Villa et al., NALTREXONE EFFECT ON GROWTH-HORMONE AND INSULIN-SECRETION IN HYPERANDROGENIC AND NORMAL OBESE PATIENTS, Human reproduction (Oxford. Print), 13, 1998, pp. 238-238
RESTORATION OF PEX2 PEROXISOME ASSEMBLY DEFECTS BY OVEREXPRESSION OF PMP70
Authors: GARTNER J BROSIUS U OBIE C WATKINS PA VALLE D
Citation: J. Gartner et al., RESTORATION OF PEX2 PEROXISOME ASSEMBLY DEFECTS BY OVEREXPRESSION OF PMP70, European journal of cell biology, 76(4), 1998, pp. 237-245
MAMMALIAN ORTHOLOGS OF C-ELEGANS UNC-119 HIGHLY EXPRESSED IN PHOTORECEPTORS
Authors: SWANSON DA CHANG JT CAMPOCHIARO PA ZACK DJ VALLE D
Citation: Da. Swanson et al., MAMMALIAN ORTHOLOGS OF C-ELEGANS UNC-119 HIGHLY EXPRESSED IN PHOTORECEPTORS, Investigative ophthalmology & visual science, 39(11), 1998, pp. 2085-2094
PROVOCATIVE HYPOTHALAMOPITUITARY AXIS TESTS IN SEVERE HEAD-INJURY - CORRELATIONS WITH SEVERITY AND PROGNOSIS
Authors: DELLACORTE F MANCINI A VALLE D GALLIZZI F CARDUCCI P MIGNANI V DEMARINIS L
Citation: F. Dellacorte et al., PROVOCATIVE HYPOTHALAMOPITUITARY AXIS TESTS IN SEVERE HEAD-INJURY - CORRELATIONS WITH SEVERITY AND PROGNOSIS, Critical care medicine, 26(8), 1998, pp. 1419-1426
NEW GOALS FOR THE US HUMAN-GENOME-PROJECT - 1998-2003
Authors: COLLINS FS PATRINOS A JORDAN E CHAKRAVARTI A GESTELAND R WALTERS L FEARON E HARTWELT L LANGLEY CH MATHIES RA OLSON M PAWSON AJ POLLARD T WILLIAMSON A WOLD B BUETOW K BRANSCOMB E CAPECCHI M CHURCH G GARNER H GIBBS RA HAWKINS T HODGSON K KNOTEK M MEISLER M RUBIN GM SMITH LM SMITH RF WESTERFIELD M CLAYTON EW FISHER NL LERMAN CE MCINERNEY JD NEBO W PRESS N VALLE D
Citation: Fs. Collins et al., NEW GOALS FOR THE US HUMAN-GENOME-PROJECT - 1998-2003, Science, 282(5389), 1998, pp. 682-689
SUPERPARAMAGNETIC IRON OXIDE-ENHANCED MRI (SPIO-MRI) - OPTIMAL PULSE SEQUENCES FOR HEPATOCELLULAR-CARCINOMA DETECTION IN CIRRHOTIC-PATIENTS
Authors: PACELLA CM BIZZARRI G ANELLI V BIANCHINI A DILELLA GM VALLE D
Citation: Cm. Pacella et al., SUPERPARAMAGNETIC IRON OXIDE-ENHANCED MRI (SPIO-MRI) - OPTIMAL PULSE SEQUENCES FOR HEPATOCELLULAR-CARCINOMA DETECTION IN CIRRHOTIC-PATIENTS, Radiology, 209P, 1998, pp. 1035-1035
GYRATE ATROPHY OF THE CHOROID AND RETINA - LYMPHOCYTE ORNITHINE-DELTA-AMINOTRANSFERASE ACTIVITY IN DIFFERENT MUTATIONS AND CARRIERS
Authors: HEINANEN K NANTOSALONEN K LEINO L PULKKI K HEINONEN O VALLE D SIMELL O
Citation: K. Heinanen et al., GYRATE ATROPHY OF THE CHOROID AND RETINA - LYMPHOCYTE ORNITHINE-DELTA-AMINOTRANSFERASE ACTIVITY IN DIFFERENT MUTATIONS AND CARRIERS, Pediatric research, 44(3), 1998, pp. 381-385
MOLECULAR ANALYSIS OF THE THIRD COMPONENT OF CANINE COMPLEMENT-(C3) AND IDENTIFICATION OF THE MUTATION RESPONSIBLE FOR HEREDITARY CANINE C3DEFICIENCY
Authors: AMERATUNGA R WINKELSTEIN JA BRODY L BINNS M CORK LC COLOMBANI P VALLE D
Citation: R. Ameratunga et al., MOLECULAR ANALYSIS OF THE THIRD COMPONENT OF CANINE COMPLEMENT-(C3) AND IDENTIFICATION OF THE MUTATION RESPONSIBLE FOR HEREDITARY CANINE C3DEFICIENCY, The Journal of immunology, 160(6), 1998, pp. 2824-2830
EXPRESSION OF PEX11-BETA MEDIATES PEROXISOME PROLIFERATION IN THE ABSENCE OF EXTRACELLULAR STIMULI
Authors: SCHRADER M REUBER BE MORRELL JC JIMENEZSANCHEZ G OBIE C STROH TA VALLE D SCHROER TA GOULD SJ
Citation: M. Schrader et al., EXPRESSION OF PEX11-BETA MEDIATES PEROXISOME PROLIFERATION IN THE ABSENCE OF EXTRACELLULAR STIMULI, The Journal of biological chemistry, 273(45), 1998, pp. 29607-29614
DELTA(3,5)-DELTA(2,4)-DIENOYL-COA ISOMERASE FROM RAT-LIVER - MOLECULAR CHARACTERIZATION
Authors: FILPPULA SA YAGI AI KILPELAINEN SH NOVIKOV D FITZPATRICK DR VIHINEN M VALLE D HILTUNEN JK
Citation: Sa. Filppula et al., DELTA(3,5)-DELTA(2,4)-DIENOYL-COA ISOMERASE FROM RAT-LIVER - MOLECULAR CHARACTERIZATION, The Journal of biological chemistry, 273(1), 1998, pp. 349-355
IDENTIFICATION OF PEX10, THE GENE DEFECTIVE IN COMPLEMENTATION GROUP-7 OF THE PEROXISOME-BIOGENESIS DISORDERS
Authors: WARREN DS MORRELL JC MOSER HW VALLE D GOULD SJ
Citation: Ds. Warren et al., IDENTIFICATION OF PEX10, THE GENE DEFECTIVE IN COMPLEMENTATION GROUP-7 OF THE PEROXISOME-BIOGENESIS DISORDERS, American journal of human genetics, 63(2), 1998, pp. 347-359
MUTATIONS IN PEX1 ARE THE MOST COMMON-CAUSE OF PEROXISOME BIOGENESIS DISORDERS
Authors: REUBER BE GERMAINLEE E COLLINS CS MORRELL JC AMERITUNGA R MOSER HW VALLE D GOULD SJ
Citation: Be. Reuber et al., MUTATIONS IN PEX1 ARE THE MOST COMMON-CAUSE OF PEROXISOME BIOGENESIS DISORDERS, Nature genetics, 17(4), 1997, pp. 445-448
HUMAN PEX7 ENCODES THE PEROXISOMAL PTS2 RECEPTOR AND IS RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA
Authors: BRAVERMAN N STEEL G OBIE C MOSER A MOSER H GOULD SJ VALLE D
Citation: N. Braverman et al., HUMAN PEX7 ENCODES THE PEROXISOMAL PTS2 RECEPTOR AND IS RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, Nature genetics, 15(4), 1997, pp. 369-376
ISOLATION OF THE HUMAN PEX12 GENE, MUTATED IN GROUP-3 OF THE PEROXISOME BIOGENESIS DISORDERS
Authors: CHANG CC LEE WH MOSER H VALLE D GOULD SJ
Citation: Cc. Chang et al., ISOLATION OF THE HUMAN PEX12 GENE, MUTATED IN GROUP-3 OF THE PEROXISOME BIOGENESIS DISORDERS, Nature genetics, 15(4), 1997, pp. 385-388
CLONING OF THE 47KD HUMAN PEROXISOMAL MEMBRANE-PROTEIN GENE AND ANALYSIS OF THE TARGETING AND FUNCTION OF ITS PROTEIN PRODUCT
Authors: BIERY BJ BRAVERMAN N VALLE D
Citation: Bj. Biery et al., CLONING OF THE 47KD HUMAN PEROXISOMAL MEMBRANE-PROTEIN GENE AND ANALYSIS OF THE TARGETING AND FUNCTION OF ITS PROTEIN PRODUCT, Molecular biology of the cell, 8, 1997, pp. 663-663
A PEROXISOMAL ABC TRANSPORTER EXHIBITS CONTRASTING RELATIONSHIPS WITHDIFFERENT FATTY-ACID ACTIVATORS
Authors: SHANI N STEEL G VALLE D
Citation: N. Shani et al., A PEROXISOMAL ABC TRANSPORTER EXHIBITS CONTRASTING RELATIONSHIPS WITHDIFFERENT FATTY-ACID ACTIVATORS, Molecular biology of the cell, 8, 1997, pp. 665-665
DEFECTS IN PEX1, A PEROXISOME-ASSOCIATED ATPASE THAT INTERACTS WITH PEX5 AND PEX6, DISRUPT PEROXISOMAL MATRIX PROTEIN IMPORT AND ARE THE MOST COMMON-CAUSE OF THE PEROXISOME BIOGENESIS DISORDERS
Authors: REUBER BE GERMAINLEE E MORRELL JC GEISBRECHT B COLLINS C AMERITUNGA R MOSER HW VALLE D GOULD SJ
Citation: Be. Reuber et al., DEFECTS IN PEX1, A PEROXISOME-ASSOCIATED ATPASE THAT INTERACTS WITH PEX5 AND PEX6, DISRUPT PEROXISOMAL MATRIX PROTEIN IMPORT AND ARE THE MOST COMMON-CAUSE OF THE PEROXISOME BIOGENESIS DISORDERS, Molecular biology of the cell, 8, 1997, pp. 668-668
A DIFFERENTIAL HYBRIDIZATION SCHEME TO IDENTIFY PHOTORECEPTOR-SPECIFIC GENES
Authors: SWANSON DA FREUND CL STEEL JM XU SB PLODER L MCINNES RR VALLE D
Citation: Da. Swanson et al., A DIFFERENTIAL HYBRIDIZATION SCHEME TO IDENTIFY PHOTORECEPTOR-SPECIFIC GENES, PCR methods and applications, 7(5), 1997, pp. 513-521
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>