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Results: 1-25 |
Results: 25
CORTICAL PIONEER CELLS ACQUIRE SPECIFIC TANGENTIAL DISTRIBUTIONS DURING RAT CORTICOGENESIS
Authors: SORIA JM MEYER G FAIREN A
Citation: Jm. Soria et al., CORTICAL PIONEER CELLS ACQUIRE SPECIFIC TANGENTIAL DISTRIBUTIONS DURING RAT CORTICOGENESIS, European journal of neuroscience, 10, 1998, pp. 1009-1009
DIFFERENT ORIGINS AND DEVELOPMENTAL HISTORIES OF TRANSIENT NEURONS INTHE MARGINAL ZONE OF THE FETAL AND NEONATAL RAT CORTEX
Authors: MEYER G SORIA JM MARTINEZGALAN JR MARTINCLEMENTE B FAIREN A
Citation: G. Meyer et al., DIFFERENT ORIGINS AND DEVELOPMENTAL HISTORIES OF TRANSIENT NEURONS INTHE MARGINAL ZONE OF THE FETAL AND NEONATAL RAT CORTEX, Journal of comparative neurology, 397(4), 1998, pp. 493-518
SUMMER PHYTOPLANKTON ASSEMBLAGES ACROSS TROPHIC GRADIENTS IN HARD-WATER RESERVOIRS
Authors: DASI MJ MIRACLE MR CAMACHO A SORIA JM VICENTE E
Citation: Mj. Dasi et al., SUMMER PHYTOPLANKTON ASSEMBLAGES ACROSS TROPHIC GRADIENTS IN HARD-WATER RESERVOIRS, Hydrobiologia, 370, 1998, pp. 27-43
LATE MIOCENE-PLEISTOCENE TECTONOSEDIMENTARY EVOLUTION AND SUBSIDENCE HISTORY OF THE CENTRAL BETIC CORDILLERA (SPAIN) - A CASE-STUDY IN THE GUADIX INTRAMONTANE BASIN
Authors: SORIA JM VISERAS C FERNANDEZ J
Citation: Jm. Soria et al., LATE MIOCENE-PLEISTOCENE TECTONOSEDIMENTARY EVOLUTION AND SUBSIDENCE HISTORY OF THE CENTRAL BETIC CORDILLERA (SPAIN) - A CASE-STUDY IN THE GUADIX INTRAMONTANE BASIN, Geological Magazine, 135(4), 1998, pp. 565-574
PREVALENCE OF FACTOR-V-LEIDEN (FV R506Q) IN SPANISH FAMILIES WITH HEREDITARY DEFICIENCIES OF HEMOSTATIC PROTEINS
Authors: TIRADO I LLOBET D SORIA JM COLL I MARTINEZ E BORRELL M MATEO J SOUTO JC MORELL M SALA N FONTCUBERTA J
Citation: I. Tirado et al., PREVALENCE OF FACTOR-V-LEIDEN (FV R506Q) IN SPANISH FAMILIES WITH HEREDITARY DEFICIENCIES OF HEMOSTATIC PROTEINS, Thrombosis and haemostasis, 1997, pp. 915-915
IDENTIFICATION OF TRANSCRIPTION INITIATION SITES IN THE HUMAN PROTEIN-S GENE
Authors: SORIA JM BERTINA R
Citation: Jm. Soria et R. Bertina, IDENTIFICATION OF TRANSCRIPTION INITIATION SITES IN THE HUMAN PROTEIN-S GENE, Thrombosis and haemostasis, 1997, pp. 3088-3088
SOFT-SEDIMENT DEFORMATION STRUCTURES INDUCED BY EARTHQUAKES (SEISMITES) IN PLIOCENE LACUSTRINE DEPOSITS (GUADIX-BAZA BASIN, CENTRAL BETIC CORDILLERA)
Authors: ALFARO P MORETTI M SORIA JM
Citation: P. Alfaro et al., SOFT-SEDIMENT DEFORMATION STRUCTURES INDUCED BY EARTHQUAKES (SEISMITES) IN PLIOCENE LACUSTRINE DEPOSITS (GUADIX-BAZA BASIN, CENTRAL BETIC CORDILLERA), Eclogae Geologicae Helvetiae, 90(3), 1997, pp. 531-540
RECURRENCE OF THE PROC GENE MUTATION R178Q - INDEPENDENT ORIGINS IN SPANISH PROTEIN-C DEFICIENCY PATIENTS
Authors: SORIA JM MORELL M ESTIVILL X SALA N
Citation: Jm. Soria et al., RECURRENCE OF THE PROC GENE MUTATION R178Q - INDEPENDENT ORIGINS IN SPANISH PROTEIN-C DEFICIENCY PATIENTS, Human mutation, 8(1), 1996, pp. 71-73
ABERRANT RNA SPLICING OF THE PROTEIN-C AND PROTEIN-S GENES IN HEALTHY-INDIVIDUALS
Authors: BERG LP SORIA JM FORMSTONE CJ MORELL M KAKKAR VV ESTIVILL X SALA N COOPER DN
Citation: Lp. Berg et al., ABERRANT RNA SPLICING OF THE PROTEIN-C AND PROTEIN-S GENES IN HEALTHY-INDIVIDUALS, Blood coagulation & fibrinolysis, 7(6), 1996, pp. 625-631
HOMOZYGOSITY FOR R87H MISSENSE MUTATION AND FOR A RARE INTRON-7 DNA VARIANT (7054G-]A) IN THE PROC GENES OF 3 SIBLINGS INITIALLY CLASSIFIEDAS HETEROZYGOTES FOR PROTEIN-C DEFICIENCY
Authors: SORIA JM MORELL M NICOLAU I ESTIVILL X SALA N
Citation: Jm. Soria et al., HOMOZYGOSITY FOR R87H MISSENSE MUTATION AND FOR A RARE INTRON-7 DNA VARIANT (7054G-]A) IN THE PROC GENES OF 3 SIBLINGS INITIALLY CLASSIFIEDAS HETEROZYGOTES FOR PROTEIN-C DEFICIENCY, Blood coagulation & fibrinolysis, 7(1), 1996, pp. 15-23
ECTOPIC TRANSCRIPT ANALYSIS INDICATES THAT ALLELIC EXCLUSION IS AN IMPORTANT CAUSE OF TYPE-I PROTEIN-C DEFICIENCY IN PATIENTS WITH NONSENSEAND FRAMESHIFT MUTATIONS IN THE PROC GENE
Authors: SORIA JM BERG LP FONTCUBERTA J KAKKAR VV ESTIVILL X COOPER DN SALA N
Citation: Jm. Soria et al., ECTOPIC TRANSCRIPT ANALYSIS INDICATES THAT ALLELIC EXCLUSION IS AN IMPORTANT CAUSE OF TYPE-I PROTEIN-C DEFICIENCY IN PATIENTS WITH NONSENSEAND FRAMESHIFT MUTATIONS IN THE PROC GENE, Thrombosis and haemostasis, 75(6), 1996, pp. 870-876
ABNORMAL POLYMERIZATION AND NORMAL BINDING OF PLASMINOGEN AND T-PA IN3 NEW DYSFIBRINOGENAEMIAS - BARCELONA-III AND BARCELONA-IV (GAMMA-ARG275-]HIS) AND VILLAJOYOSA (GAMMA-ARG 275-]CYS)
Authors: BORRELL M GARI M COLL I VALLVE C TIRADO I SORIA JM SALA N MUNOZ C OLIVER A GARCIA A FONTCUBERTA J
Citation: M. Borrell et al., ABNORMAL POLYMERIZATION AND NORMAL BINDING OF PLASMINOGEN AND T-PA IN3 NEW DYSFIBRINOGENAEMIAS - BARCELONA-III AND BARCELONA-IV (GAMMA-ARG275-]HIS) AND VILLAJOYOSA (GAMMA-ARG 275-]CYS), Blood coagulation & fibrinolysis, 6(3), 1995, pp. 198-206
A NOVEL POLYMORPHISM (6376-G T) IN INTRON-7 OF THE HUMAN PROTEIN-C GENE/
Authors: SORIA JM MORELL M ESTIVILL X SALA N
Citation: Jm. Soria et al., A NOVEL POLYMORPHISM (6376-G T) IN INTRON-7 OF THE HUMAN PROTEIN-C GENE/, Human genetics, 96(2), 1995, pp. 243-244
SEVERE TYPE-I PROTEIN-C DEFICIENCY IN A COMPOUND HETEROZYGOTE FOR Y124C AND Q132X MUTATIONS IN EXON-6 OF THE PROC GENE
Authors: SORIA JM MORELL M JIMENEZASTORGA C ESTIVILL X SALA N
Citation: Jm. Soria et al., SEVERE TYPE-I PROTEIN-C DEFICIENCY IN A COMPOUND HETEROZYGOTE FOR Y124C AND Q132X MUTATIONS IN EXON-6 OF THE PROC GENE, Thrombosis and haemostasis, 74(5), 1995, pp. 1215-1220
MOLECULAR ANALYSIS OF THE PROTEIN-S GENE (PS-ALPHA) IN 8 FAMILIES BY SOUTHERN BLOT
Authors: TIRADO I LLOBET D SORIA JM MARTINEZ E MURILLO J URRUTIA T SALA N FONTCUBERTA J
Citation: I. Tirado et al., MOLECULAR ANALYSIS OF THE PROTEIN-S GENE (PS-ALPHA) IN 8 FAMILIES BY SOUTHERN BLOT, Thrombosis and haemostasis, 73(6), 1995, pp. 940-940
A SINGLE-POINT MUTATION-1,691 G-]A IN BLOOD-COAGULATION FACTOR-V IN 12 PATIENTS WITH RESISTANCE TO ACTIVATED PROTEIN-C
Authors: TIRADO I LLOBET D SORIA JM SOUTO JC VALLVE C DELRIO E BORRELL M SALA N FONTCUBERTA J
Citation: I. Tirado et al., A SINGLE-POINT MUTATION-1,691 G-]A IN BLOOD-COAGULATION FACTOR-V IN 12 PATIENTS WITH RESISTANCE TO ACTIVATED PROTEIN-C, Thrombosis and haemostasis, 73(6), 1995, pp. 1126-1126
MESSENGER-RNA ANALYSIS OF 3 PROTEIN-C GENE-MUTATIONS THAT GENERATE PREMATURE STOP CODONS
Authors: SORIA JM BERG LP FONTCUBERTA J ESTIVILL X COOPER DN SALA N
Citation: Jm. Soria et al., MESSENGER-RNA ANALYSIS OF 3 PROTEIN-C GENE-MUTATIONS THAT GENERATE PREMATURE STOP CODONS, Thrombosis and haemostasis, 73(6), 1995, pp. 1254-1254
LINKAGE DISEQUILIBRIUM BETWEEN THE PROTEIN-S HEERLEN ALLELE AND PROTEIN-S DEFICIENCY IN SPANISH FAMILIES
Authors: SALA N MORELL M TIRADO I ESPINOSA Y LLOBET D FONTCUBERTA J SORIA JM VOLPINI V ESTIVIJL X
Citation: N. Sala et al., LINKAGE DISEQUILIBRIUM BETWEEN THE PROTEIN-S HEERLEN ALLELE AND PROTEIN-S DEFICIENCY IN SPANISH FAMILIES, Thrombosis and haemostasis, 73(6), 1995, pp. 1259-1259
DETECTION OF AN HOMOZYGOTE AND 16 HETEROZYGOTES FOR A 1,691, G-]A MUTATION IN THE FACTOR-V-GENE, IN A LARGE FAMILY WITH RESISTANCE TO ACTIVATED PROTEIN-C, PREVIOUSLY CLASSIFIED AS FUNCTIONAL PROTEIN-S DEFICIENCY
Authors: LLOBET D TIRADO I SORIA JM MATEO J BORRELL M FELICES R RODRIGUEZ M SALA N FONTCUBERTA J
Citation: D. Llobet et al., DETECTION OF AN HOMOZYGOTE AND 16 HETEROZYGOTES FOR A 1,691, G-]A MUTATION IN THE FACTOR-V-GENE, IN A LARGE FAMILY WITH RESISTANCE TO ACTIVATED PROTEIN-C, PREVIOUSLY CLASSIFIED AS FUNCTIONAL PROTEIN-S DEFICIENCY, Thrombosis and haemostasis, 73(6), 1995, pp. 1363-1363
A NEW-TYPE OF SEISMITES IN THE UPPER MIOC ENE OF ALICANTE (EASTERN BETIC CORDILLERA, SPAIN) - DETRITAL WEDGES
Authors: ESTEVEZ A SORIA JM ALFARO P
Citation: A. Estevez et al., A NEW-TYPE OF SEISMITES IN THE UPPER MIOC ENE OF ALICANTE (EASTERN BETIC CORDILLERA, SPAIN) - DETRITAL WEDGES, Comptes rendus de l'Academie des sciences. Serie II. Mecanique, physique, chimie, astronomie, 318(4), 1994, pp. 507-512
2 NOVEL MUTATIONS IN EXON-5 OF THE PROTEIN-C GENE IN 2 SPANISH FAMILIES WITH THROMBOPHILIA DUE TO PROTEIN-C DEFICIENCY
Authors: SORIA JM FONTCUBERTA J BORRELL M ESTIVILL X SALA N
Citation: Jm. Soria et al., 2 NOVEL MUTATIONS IN EXON-5 OF THE PROTEIN-C GENE IN 2 SPANISH FAMILIES WITH THROMBOPHILIA DUE TO PROTEIN-C DEFICIENCY, Human molecular genetics, 3(7), 1994, pp. 1205-1206
SEVERE HOMOZYGOUS PROTEIN-C DEFICIENCY - IDENTIFICATION OF A SPLICE-SITE MISSENSE MUTATION-(184,Q-]H) IN EXON-7 OF THE PROTEIN-C GENE
Authors: SORIA JM BRITO D BARCELO J FONTCUBERTA J BOTERO L MALDONADO J ESTIVILL X SALA N
Citation: Jm. Soria et al., SEVERE HOMOZYGOUS PROTEIN-C DEFICIENCY - IDENTIFICATION OF A SPLICE-SITE MISSENSE MUTATION-(184,Q-]H) IN EXON-7 OF THE PROTEIN-C GENE, Thrombosis and haemostasis, 72(1), 1994, pp. 65-69
ACCEPTOR SPLICE-SITE MUTATION IN THE INVARIANT AG OF INTRON-5 OF THE PROTEIN-C GENE, CAUSING TYPE-I PROTEIN-C DEFICIENCY
Authors: SORIA JM FONTCUBERTA J CHILLON M BORRELL M ESTIVILL X SALA N
Citation: Jm. Soria et al., ACCEPTOR SPLICE-SITE MUTATION IN THE INVARIANT AG OF INTRON-5 OF THE PROTEIN-C GENE, CAUSING TYPE-I PROTEIN-C DEFICIENCY, Human genetics, 92(5), 1993, pp. 506-508
ACCEPTOR SPLICE-SITE MUTATION IN THE INVARIANT AG OF INTRON-E OF THE PROTEIN-C GENE OF A TYPE-I PROTEIN-C DEFICIENT FAMILY
Authors: SORIA JM FONTCUBERTA J BORRELL M ESTIVILL X SALA N
Citation: Jm. Soria et al., ACCEPTOR SPLICE-SITE MUTATION IN THE INVARIANT AG OF INTRON-E OF THE PROTEIN-C GENE OF A TYPE-I PROTEIN-C DEFICIENT FAMILY, Thrombosis and haemostasis, 69(6), 1993, pp. 720-720
THE USE OF SSCPS IN THE ANALYSIS OF PROTEIN-C GENE - IDENTIFICATION OF 6 DIFFERENT MUTATIONS IN PROTEIN-C DEFICIENT SPANISH FAMILIES
Authors: SORIA JM FONTCUBERTA J BRITO D ESTIVILL X SALA N
Citation: Jm. Soria et al., THE USE OF SSCPS IN THE ANALYSIS OF PROTEIN-C GENE - IDENTIFICATION OF 6 DIFFERENT MUTATIONS IN PROTEIN-C DEFICIENT SPANISH FAMILIES, Thrombosis and haemostasis, 69(6), 1993, pp. 720-720
Risultati: 1-25 |