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Results: 1-15 |
Results: 15
PSYCHIATRIC-DISORDER IN A FAMILIAL 15-18 TRANSLOCATION AND SUBLOCALIZATION OF MYELIN BASIC-PROTEIN TO 18Q22.3
Authors: CALZOLARI E AIELLO V PALAZZI P SENSI A CALZOLARI S ORRICO D CALLIARI L HOLLER H MARZI C BELLI S BERNARDI F PATRACCHINI P
Citation: E. Calzolari et al., PSYCHIATRIC-DISORDER IN A FAMILIAL 15-18 TRANSLOCATION AND SUBLOCALIZATION OF MYELIN BASIC-PROTEIN TO 18Q22.3, American journal of medical genetics, 67(2), 1996, pp. 154-161
MOLECULAR DEFECTS IN CRM-VII DEFICIENCIES - MODELING OF MISSENSE MUTATIONS IN THE CATALYTIC DOMAIN OF FVII( FACTOR)
Authors: BERNARDI F LINEY DL PATRACCHINI P GEMMATI D LEGNANI C ARCIERI P PINOTTI M REDAELLI R BALLERINI G PEMBERTON S WACEY AI MARIANI G TUDDENHAM EGD MARCHETTI G
Citation: F. Bernardi et al., MOLECULAR DEFECTS IN CRM-VII DEFICIENCIES - MODELING OF MISSENSE MUTATIONS IN THE CATALYTIC DOMAIN OF FVII( FACTOR), British Journal of Haematology, 86(3), 1994, pp. 610-618
A MISSENSE MUTATION ((178)CYS-]TYR) AND 2 NEUTRAL DIMORPHISMS ((115)HIS AND (333)SER) IN THE HUMAN COAGULATION FACTOR-VII GENE
Authors: MARCHETTI G FERRATI M PATRACCHINI P REDAELLI R BERNARDI F
Citation: G. Marchetti et al., A MISSENSE MUTATION ((178)CYS-]TYR) AND 2 NEUTRAL DIMORPHISMS ((115)HIS AND (333)SER) IN THE HUMAN COAGULATION FACTOR-VII GENE, Human molecular genetics, 2(7), 1993, pp. 1055-1056
IN-FRAME DELETION OF VONWILLEBRAND FACTOR-A DOMAINS IN A DOMINANT TYPE OF VONWILLEBRAND DISEASE
Authors: BERNARDI F PATRACCHINI P GEMMATI D PINOTTI M SCHWIENBACHER C BALLERINI G MARCHETTI G
Citation: F. Bernardi et al., IN-FRAME DELETION OF VONWILLEBRAND FACTOR-A DOMAINS IN A DOMINANT TYPE OF VONWILLEBRAND DISEASE, Human molecular genetics, 2(5), 1993, pp. 545-548
MOLECULAR ANALYSIS OF FACTOR-VII DEFICIENCY IN ITALY - A FREQUENT MUTATION (FVII-LAZIO) IN A REPEATED INTRONIC REGION
Authors: BERNARDI F PATRACCHINI P GEMMATI D FERRATI M ARCIERI P PAPACCHINI M REDAELLI R BAUDO F MARIANI G MARCHETTI G
Citation: F. Bernardi et al., MOLECULAR ANALYSIS OF FACTOR-VII DEFICIENCY IN ITALY - A FREQUENT MUTATION (FVII-LAZIO) IN A REPEATED INTRONIC REGION, Human genetics, 92(5), 1993, pp. 446-450
TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION (GLY 381 GREATER-THAN SER) IN THE SUBSTRATE-BINDING POCKET
Authors: MARCHETTI G PATRACCHINI P GEMMATI D CASTAMAN G RODEGHIERO F WACEY A COOPER DN TUDDENHAM EGD BERNARDI F
Citation: G. Marchetti et al., TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION (GLY 381 GREATER-THAN SER) IN THE SUBSTRATE-BINDING POCKET, Thrombosis and haemostasis, 69(6), 1993, pp. 722-722
STUDY OF A PROTEIN-S GENE POLYMORPHISM AT DNA AND MESSENGER-RNA LEVELIN A FAMILY WITH SYMPTOMATIC PROTEIN-S DEFICIENCY
Authors: MARCHETTI G LEGNANI C FERRATI M PATRACCHINI P LUNGHI B SACCHI E PALARETI G COCCHERI S BERNARDI F
Citation: G. Marchetti et al., STUDY OF A PROTEIN-S GENE POLYMORPHISM AT DNA AND MESSENGER-RNA LEVELIN A FAMILY WITH SYMPTOMATIC PROTEIN-S DEFICIENCY, Thrombosis and haemostasis, 69(6), 1993, pp. 930-930
DETECTION OF A PROTEIN-C GENE MUTATION PRESENT IN THE ASYMPTOMATIC AND NOT IN THE THROMBOSIS-PRONE LINEAGE
Authors: GEMMATI D PATRACCHINI P MARCHETTI G SERINO ML MORATELLI S GUERRA S BALLERINI G BERNARDI F
Citation: D. Gemmati et al., DETECTION OF A PROTEIN-C GENE MUTATION PRESENT IN THE ASYMPTOMATIC AND NOT IN THE THROMBOSIS-PRONE LINEAGE, Thrombosis and haemostasis, 69(6), 1993, pp. 1253-1253
DETECTION OF NEW POLYMORPHIC MARKERS AND HAPLOTYPE STUDIES IN THE FACTOR-VII GENE
Authors: PATRACCHINI P MARCHETTI G FERRATI M PAPACCHINI M ARCIERI P REDAELLI R BARONCINI C BALLERINI G BERNARDI F
Citation: P. Patracchini et al., DETECTION OF NEW POLYMORPHIC MARKERS AND HAPLOTYPE STUDIES IN THE FACTOR-VII GENE, Thrombosis and haemostasis, 69(6), 1993, pp. 1291-1291
MOLECULAR DEFECTS IN CONGENITAL FACTOR-VII DEFICIENCIES
Authors: BERNARDI F PATRACCHINI P GEMMATI D PINOTTI M BAUDO F DEROSA V MARIANI G MARCHETTI G
Citation: F. Bernardi et al., MOLECULAR DEFECTS IN CONGENITAL FACTOR-VII DEFICIENCIES, Thrombosis and haemostasis, 69(6), 1993, pp. 1292-1292
DELETION OF EXONS 26-34 (DOMAIN D3-A3) OF VONWILLEBRAND-FACTOR GENE IN THE VONWILLEBRAND DISEASE TYPE-II
Authors: PATRACCHINI P MARCHETTI G GEMMATI D SERINO ML BALLERINI G BERNARDI F
Citation: P. Patracchini et al., DELETION OF EXONS 26-34 (DOMAIN D3-A3) OF VONWILLEBRAND-FACTOR GENE IN THE VONWILLEBRAND DISEASE TYPE-II, Thrombosis research, 70, 1993, pp. 19-19
DETECTION AND CHARACTERIZATION OF POLYMORPHIC MARKERS IN THE FACTOR-VII GENE
Authors: GEMMATI D MARCHETTI G PATRACCHINI P PAPACCHINI P PINOTTI M ARCIERI P MARIANI G BERNARDI F
Citation: D. Gemmati et al., DETECTION AND CHARACTERIZATION OF POLYMORPHIC MARKERS IN THE FACTOR-VII GENE, Thrombosis research, 70, 1993, pp. 19-19
CHARACTERIZATION OF MOLECULAR LESIONS CAUSING PROTEIN-C DEFICIENCY (TYPE-I AND TYPE-II)
Authors: MARCHETTI G GEMMATI D PATRACCHINI P CASTAMAN G MORATELLI S PALARETI G RODEGHIERO F BALLERINI G BERNARDI F
Citation: G. Marchetti et al., CHARACTERIZATION OF MOLECULAR LESIONS CAUSING PROTEIN-C DEFICIENCY (TYPE-I AND TYPE-II), Thrombosis research, 70, 1993, pp. 20-20
STUDY OF A PROTEIN-S GENE POLYMORPHISM AT DNA AND MESSENGER-RNA LEVELIN A FAMILY WITH SYMPTOMATIC PROTEIN-S DEFICIENCY
Authors: MARCHETTI G LEGNANI C PATRACCHINI P GEMMATI D FERRATI M PALARETI G COCCHERI S BERNARDI F
Citation: G. Marchetti et al., STUDY OF A PROTEIN-S GENE POLYMORPHISM AT DNA AND MESSENGER-RNA LEVELIN A FAMILY WITH SYMPTOMATIC PROTEIN-S DEFICIENCY, British Journal of Haematology, 85(1), 1993, pp. 173-175
SYMPTOMATIC TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION (GLY-381-]SER) IN THE SUBSTRATE-BINDING POCKET
Authors: MARCHETTI G PATRACCHINI P GEMMATI D CASTAMAN G RODEGHIERO F WACEY A COOPER DN TUDDENHAM EGD BERNARDI F
Citation: G. Marchetti et al., SYMPTOMATIC TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION (GLY-381-]SER) IN THE SUBSTRATE-BINDING POCKET, British Journal of Haematology, 84(2), 1993, pp. 285-289
Risultati: 1-15 |