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Results: 1-14 |
Results: 14
PROPIDIUM IODIDE QUENCHES THE FLUORESCENCE OF TDT-INCORPORATED FITC-LABELED DUTP IN APOPTOTIC CELLS
Authors: STOKKE T SOLBERG K DEANGELIS P STEEN HB
Citation: T. Stokke et al., PROPIDIUM IODIDE QUENCHES THE FLUORESCENCE OF TDT-INCORPORATED FITC-LABELED DUTP IN APOPTOTIC CELLS, Cytometry, 33(4), 1998, pp. 428-434
SCANNER FOR AUTOMATED HIGH-PRECISION MEASUREMENTS OF WIRE POSITIONS IN WIRE CHAMBERS
Authors: CARMAN DS BILODEAU D BLAND LC EADS A RINCKEL T SOLBERG K
Citation: Ds. Carman et al., SCANNER FOR AUTOMATED HIGH-PRECISION MEASUREMENTS OF WIRE POSITIONS IN WIRE CHAMBERS, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 394(3), 1997, pp. 409-414
WHATS IN A NAME (ARTISTS EXHIBITING IN THE 5TH ANNUAL NEW-YORK DIGITAL-SALON)
Authors: SOLBERG K
Citation: K. Solberg, WHATS IN A NAME (ARTISTS EXHIBITING IN THE 5TH ANNUAL NEW-YORK DIGITAL-SALON), Leonardo, 30(5), 1997, pp. 390-391
A COMMON MISSENSE MUTATION (C210G) IN THE LDL RECEPTOR GENE AMONG NORWEGIAN FAMILIAL HYPERCHOLESTEROLEMIA SUBJECTS
Authors: SUNDVOLD H SOLBERG K TONSTAD S RODNINGEN OK OSE L BERG K LEREN TP
Citation: H. Sundvold et al., A COMMON MISSENSE MUTATION (C210G) IN THE LDL RECEPTOR GENE AMONG NORWEGIAN FAMILIAL HYPERCHOLESTEROLEMIA SUBJECTS, Human mutation, 7(1), 1996, pp. 70-71
SCREENING FOR KNOWN MUTATIONS IN THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA (VOL 95, PG 671, 1995)
Authors: LEREN TP SUNDVOLD H RODNINGEN OK TONSTAD S SOLBERG K OSE L BERG K
Citation: Tp. Leren et al., SCREENING FOR KNOWN MUTATIONS IN THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA (VOL 95, PG 671, 1995), Human genetics, 97(2), 1996, pp. 268-268
THE 4TH-ANNUAL NEW-YORK-DIGITAL-SALON + INTRODUCTION, ARTISTS STATEMENTS AND WORKS BY EXHIBITING ARTISTS
Authors: SOLBERG K
Citation: K. Solberg, THE 4TH-ANNUAL NEW-YORK-DIGITAL-SALON + INTRODUCTION, ARTISTS STATEMENTS AND WORKS BY EXHIBITING ARTISTS, Leonardo, 29(5), 1996, pp. 405
2 NOVEL MISSENSE MUTATIONS IN THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA
Authors: GUNDERSEN KE SOLBERG K RODNINGEN OK TONSTAD S OSE L BERG K LEREN TP
Citation: Ke. Gundersen et al., 2 NOVEL MISSENSE MUTATIONS IN THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA, Clinical genetics, 49(2), 1996, pp. 85-87
2 NOVEL POINT MUTATIONS IN THE EGF PRECURSOR HOMOLOGY DOMAIN OF THE LDL-RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA
Authors: LEREN TP SOLBERG K RODNINGEN OK TONSTAD S OSE L
Citation: Tp. Leren et al., 2 NOVEL POINT MUTATIONS IN THE EGF PRECURSOR HOMOLOGY DOMAIN OF THE LDL-RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA, Human genetics, 96(2), 1995, pp. 241-242
SCREENING FOR KNOWN MUTATIONS IN THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA
Authors: LEREN TP SUNDVOLD H RODNINGEN OK TONSTAD S SOLBERG K OSE L BERG K
Citation: Tp. Leren et al., SCREENING FOR KNOWN MUTATIONS IN THE LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA, Human genetics, 95(6), 1995, pp. 671-676
FAMILIAL HYPERCHOLESTEROLEMIA CAUSED BY A NONSENSE MUTATION IN CODON-329 OF THE LDL RECEPTOR GENE
Authors: SOLBERG K RODNINGEN OK TONSTAD S OSE L LEREN TP
Citation: K. Solberg et al., FAMILIAL HYPERCHOLESTEROLEMIA CAUSED BY A NONSENSE MUTATION IN CODON-329 OF THE LDL RECEPTOR GENE, Scandinavian journal of clinical & laboratory investigation, 54(8), 1994, pp. 605-609
2 FOUNDER MUTATIONS IN THE LDL RECEPTOR GENE IN NORWEGIAN FAMILIAL HYPERCHOLESTEROLEMIA SUBJECTS
Authors: LEREN TP SOLBERG K RODNINGEN OK TONSTAD S OSE L
Citation: Tp. Leren et al., 2 FOUNDER MUTATIONS IN THE LDL RECEPTOR GENE IN NORWEGIAN FAMILIAL HYPERCHOLESTEROLEMIA SUBJECTS, Atherosclerosis, 111(2), 1994, pp. 175-182
EVALUATION OF RUNNING CONDITIONS FOR SSCP ANALYSIS - APPLICATION OF SSCP FOR DETECTION OF POINT MUTATIONS IN THE LDL-RECEPTOR CONE
Authors: LEREN TP SOLBERG K RODNINGEN OK OSE L TONSTAD S BERG K
Citation: Tp. Leren et al., EVALUATION OF RUNNING CONDITIONS FOR SSCP ANALYSIS - APPLICATION OF SSCP FOR DETECTION OF POINT MUTATIONS IN THE LDL-RECEPTOR CONE, PCR methods and applications, 3(3), 1993, pp. 159-162
SCREENING FOR POINT MUTATIONS IN EXON-10 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE BY ANALYSIS OF SINGLE-STRAND CONFORMATION POLYMORPHISMS - DETECTION OF A NONSENSE MUTATION FH(469-]STOP)
Authors: LEREN TP SOLBERG K RODNINGEN OK ROSBY O TONSTAD S OSE L BERG K
Citation: Tp. Leren et al., SCREENING FOR POINT MUTATIONS IN EXON-10 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE BY ANALYSIS OF SINGLE-STRAND CONFORMATION POLYMORPHISMS - DETECTION OF A NONSENSE MUTATION FH(469-]STOP), Human genetics, 92(1), 1993, pp. 6-10
MSPL RFLP IN EXON 18 OF THE LDL RECEPTOR GENE DETECTABLE BY PCR
Authors: SOLBERG K RODNINGEN OK TONSTAD S OSE L BERG K LEREN TP
Citation: K. Solberg et al., MSPL RFLP IN EXON 18 OF THE LDL RECEPTOR GENE DETECTABLE BY PCR, Clinical genetics, 44(2), 1993, pp. 111-111
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