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Results: 1-16 |
Results: 16
GENOMIC ORGANIZATION OF THE HUMAN INTEGRIN BETA-4 GENE
Authors: IACOVACCI S GAGNOUXPALACIOS L ZAMBRUNO G MENEGUZZI G DALESSIO M
Citation: S. Iacovacci et al., GENOMIC ORGANIZATION OF THE HUMAN INTEGRIN BETA-4 GENE, Mammalian genome, 8(6), 1997, pp. 448-450
COMPARATIVE-ANALYSIS OF FIBRILLAR AND BASEMENT-MEMBRANE COLLAGEN EXPRESSION IN EMBRYOS OF THE SEA-URCHIN, STRONGYLOCENTROTUS-PURPURATUS
Authors: SUZUKI HR REITER RS DALESSIO M DILIBERTO M RAMIREZ F EXPOSITO JY GAMBINO R SOLURSH M
Citation: Hr. Suzuki et al., COMPARATIVE-ANALYSIS OF FIBRILLAR AND BASEMENT-MEMBRANE COLLAGEN EXPRESSION IN EMBRYOS OF THE SEA-URCHIN, STRONGYLOCENTROTUS-PURPURATUS, Zoological science, 14(3), 1997, pp. 449-454
CULTURAL HIGHLIGHTS OF 1996-1997 (EXHIBIT S AND CONFERENCES IN AND AROUND ROME)
Authors: PELLEGRINI E GASBARRO R DOGLIO F GALLAVOTTI DC BEVILACQUA M MELASECCHI O DALESSIO M ROSSI D PARLATO G BARBAROSSA L
Citation: E. Pellegrini et al., CULTURAL HIGHLIGHTS OF 1996-1997 (EXHIBIT S AND CONFERENCES IN AND AROUND ROME), Studi romani, 45(3-4), 1997, pp. 474-502
A HOMOZYGOUS NONSENSE MUTATION IN THE COL17A1 GENE CAUSES SKIPPING OFTHE CONSTITUTIVE EXON AND A WILD GABEB PHENOTYPE
Authors: RUZZI L MAZZANTI C POSTERARO P GOBELLO T MENEGUZZI G ZAMBRUNO G DALESSIO M
Citation: L. Ruzzi et al., A HOMOZYGOUS NONSENSE MUTATION IN THE COL17A1 GENE CAUSES SKIPPING OFTHE CONSTITUTIVE EXON AND A WILD GABEB PHENOTYPE, Journal of investigative dermatology, 109(3), 1997, pp. 410-410
A HOMOZYGOUS MUTATION IN THE GENE ENCODING INTEGRIN ALPHA-6 IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA
Authors: DALESSIO M RUZZI L GAGNOUXPALACIOS L PINOLA M BELLI S MENEGUZZI G ZAMBRUNO G
Citation: M. Dalessio et al., A HOMOZYGOUS MUTATION IN THE GENE ENCODING INTEGRIN ALPHA-6 IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA, Journal of investigative dermatology, 108(4), 1997, pp. 25-25
A HOMOZYGOUS MUTATION IN THE INTEGRIN ALPHA-6 GENE IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA
Authors: RUZZI L GAGNOUXPALACIOS L PINOLA M BELLI S MENEGUZZI G DALESSIO M ZAMBRUNO G
Citation: L. Ruzzi et al., A HOMOZYGOUS MUTATION IN THE INTEGRIN ALPHA-6 GENE IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA, The Journal of clinical investigation, 99(12), 1997, pp. 2826-2831
EARLY DETECTION SMALL FIBERS NEUROPATHY IN INSULIN-DEPENDENT AND NON-INSULIN-DEPENDENT DIABETIC-PATIENTS
Authors: GABRIELE A MORANO S ROSSI P FROIO C MOROCUTTI A DALESSIO M GUIDOBALDI L CIPRIANI R VALLE E POZZESSERE G
Citation: A. Gabriele et al., EARLY DETECTION SMALL FIBERS NEUROPATHY IN INSULIN-DEPENDENT AND NON-INSULIN-DEPENDENT DIABETIC-PATIENTS, Diabetologia, 40, 1997, pp. 2201-2201
MSH MAY PLAY A CONSERVED ROLE IN DORSOVENTRAL PATTERNING OF THE NEUROECTODERM AND MESODERM
Authors: DALESSIO M FRASCH M
Citation: M. Dalessio et M. Frasch, MSH MAY PLAY A CONSERVED ROLE IN DORSOVENTRAL PATTERNING OF THE NEUROECTODERM AND MESODERM, Mechanisms of development, 58(1-2), 1996, pp. 217-231
PUPILLOMETRIC EVALUATION AND ANALYSIS OF LIGHT REFLEX IN HEALTHY-SUBJECTS AS A TOOL TO STUDY AUTONOMIC NERVOUS-SYSTEM CHANGES WITH AGING
Authors: POZZESSERE G VALLE E ROSSI P PETRUCCI B AMBROSINI A DALESSIO M PIERELLI F GIACOMINI P
Citation: G. Pozzessere et al., PUPILLOMETRIC EVALUATION AND ANALYSIS OF LIGHT REFLEX IN HEALTHY-SUBJECTS AS A TOOL TO STUDY AUTONOMIC NERVOUS-SYSTEM CHANGES WITH AGING, Aging, 8(1), 1996, pp. 55-60
GENOMIC ORGANIZATION OF THE SEQUENCES CODING FOR INTEGRIN BETA-4, THEDEFECTIVE GENE-PRODUCT IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA (PA-JEB)
Authors: IACOVACCI S RUZZI L POSTERARO P ZAMBRUNO G MENEGUZZI G DALESSIO M
Citation: S. Iacovacci et al., GENOMIC ORGANIZATION OF THE SEQUENCES CODING FOR INTEGRIN BETA-4, THEDEFECTIVE GENE-PRODUCT IN JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA (PA-JEB), Journal of investigative dermatology, 107(3), 1996, pp. 195-195
A COMMON INSERTION MUTATION IN COL7A1 IN 2 ITALIAN FAMILIES WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA
Authors: CHRISTIANO AM DALESSIO M PARADISI M ANGELO C MAZZANTI C PUDDU P UITTO J
Citation: Am. Christiano et al., A COMMON INSERTION MUTATION IN COL7A1 IN 2 ITALIAN FAMILIES WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA, Journal of investigative dermatology, 106(4), 1996, pp. 679-684
EXPRESSION OF RAT INTESTINAL DEFENSINS IN HEMORRHAGIC-SHOCK
Authors: DIAMOND G DALESSIO M CONDON M
Citation: G. Diamond et al., EXPRESSION OF RAT INTESTINAL DEFENSINS IN HEMORRHAGIC-SHOCK, Journal of cellular biochemistry, 1995, pp. 245-245
CRURAL AMYOTROPHY ASSOCIATED WITH A PARIETAL LESION - A CASE-REPORT
Authors: POZZESSERE G VALLE E TOMASELLI M DALESSIO M BIANCO F PIERELLI F MOROCUTTI C
Citation: G. Pozzessere et al., CRURAL AMYOTROPHY ASSOCIATED WITH A PARIETAL LESION - A CASE-REPORT, Acta neurologica belgica, 95(2), 1995, pp. 96-100
DESCRIPTIVE ANALYSIS OF THE PREVALENCE OF ANEMIA IN A RANDOMLY SELECTED SAMPLE OF ELDERLY PEOPLE LIVING AT HOME - SOME RESULTS OF AN ITALIAN MULTICENTRIC STUDY
Authors: INELMEN EM DALESSIO M GATTO MRA BAGGIO MB JIMENEZ G BIZZOTTO MG ENZI G
Citation: Em. Inelmen et al., DESCRIPTIVE ANALYSIS OF THE PREVALENCE OF ANEMIA IN A RANDOMLY SELECTED SAMPLE OF ELDERLY PEOPLE LIVING AT HOME - SOME RESULTS OF AN ITALIAN MULTICENTRIC STUDY, Aging, 6(2), 1994, pp. 81-89
GENOMIC ORGANIZATION OF THE SEQUENCE CODING FOR FIBRILLIN, THE DEFECTIVE GENE-PRODUCT IN MARFAN-SYNDROME
Authors: PEREIRA L DALESSIO M RAMIREZ F LYNCH JR SYKES B PANGILINAN T BONADIO J
Citation: L. Pereira et al., GENOMIC ORGANIZATION OF THE SEQUENCE CODING FOR FIBRILLIN, THE DEFECTIVE GENE-PRODUCT IN MARFAN-SYNDROME, Human molecular genetics, 2(7), 1993, pp. 961-968
GENOMIC ORGANIZATION OF THE SEQUENCE CODING FOR FIBRILLIN, THE DEFECTIVE GENE-PRODUCT IN MARFAN-SYNDROME (VOL 2, PG 961, 1993)
Authors: PEREIRA L DALESSIO M RAMIREZ F LYNCH JR SYKES B PANGILINAN T BONADIO J
Citation: L. Pereira et al., GENOMIC ORGANIZATION OF THE SEQUENCE CODING FOR FIBRILLIN, THE DEFECTIVE GENE-PRODUCT IN MARFAN-SYNDROME (VOL 2, PG 961, 1993), Human molecular genetics, 2(10), 1993, pp. 1762-1762
Risultati: 1-16 |