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Results: 1-25 | 26-50 | 51-67
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INTRACELLULAR METABOLISM OF HUMAN APOLIPOPROTEIN(A) IN STABLY TRANSFECTED HEP G2 CELLS
Authors: LOBENTANZ EM KRASZNAI K GRUBER A BRUNNER C MULLER HJ SATTLER J KRAFT HG UTERMANN G DIEPLINGER H
Citation: Em. Lobentanz et al., INTRACELLULAR METABOLISM OF HUMAN APOLIPOPROTEIN(A) IN STABLY TRANSFECTED HEP G2 CELLS, Biochemistry, 37(16), 1998, pp. 5417-5425
FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) ON PERIPHERAL-BLOOD SMEARS FOR MONITORING PHILADELPHIA-CHROMOSOME-POSITIVE CHRONIC MYELOID-LEUKEMIA (CML) DURING INTERFERON TREATMENT - A NEW STRATEGY FOR REMISSION ASSESSMENT
Authors: MUHLMANN J THALER J HILBE W BECHTER O ERDEL M UTERMANN G DUBA HC
Citation: J. Muhlmann et al., FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) ON PERIPHERAL-BLOOD SMEARS FOR MONITORING PHILADELPHIA-CHROMOSOME-POSITIVE CHRONIC MYELOID-LEUKEMIA (CML) DURING INTERFERON TREATMENT - A NEW STRATEGY FOR REMISSION ASSESSMENT, Genes, chromosomes & cancer, 21(2), 1998, pp. 90-100
CONCENTRATIONS OF THE ATHEROGENIC LP(A) ARE ELEVATED IN FH
Authors: LINGENHEL A KRAFT HG KOTZE M PEETERS AV KRONENBERG F KRUSE R UTERMANN G
Citation: A. Lingenhel et al., CONCENTRATIONS OF THE ATHEROGENIC LP(A) ARE ELEVATED IN FH, European journal of human genetics, 6(1), 1998, pp. 50-60
NAIL-PATELLA SYNDROME IN A CYTOGENETICALLY BALANCED T(9-17)(Q34.1-Q25) CARRIER
Authors: DUBA HC ERDEL M LOFFLER J WIRTH J UTERMANN B UTERMANN G
Citation: Hc. Duba et al., NAIL-PATELLA SYNDROME IN A CYTOGENETICALLY BALANCED T(9-17)(Q34.1-Q25) CARRIER, European journal of human genetics, 6(1), 1998, pp. 75-79
SIGNIFICANT IMPACT OF THE -C(93)T-POLYMORPHISM IN THE APOLIPOPROTEIN(A) GENE ON LP(A) CONCENTRATIONS IN AFRICANS BUT NOT IN CAUCASIANS - CONFOUNDING EFFECT OF LINKAGE DISEQUILIBRIUM/
Authors: KRAFT HG WINDEGGER M MENZEL HJ UTERMANN G
Citation: Hg. Kraft et al., SIGNIFICANT IMPACT OF THE -C(93)T-POLYMORPHISM IN THE APOLIPOPROTEIN(A) GENE ON LP(A) CONCENTRATIONS IN AFRICANS BUT NOT IN CAUCASIANS - CONFOUNDING EFFECT OF LINKAGE DISEQUILIBRIUM/, Human molecular genetics, 7(2), 1998, pp. 257-264
GENOMIC ORGANIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN SGK PROTEIN-KINASE GENE
Authors: WALDEGGER S ERDEL M NAGL UO BARTH P RABER G STEUER S UTERMANN G PAULMICHL M LANG F
Citation: S. Waldegger et al., GENOMIC ORGANIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN SGK PROTEIN-KINASE GENE, Genomics (San Diego, Calif.), 51(2), 1998, pp. 299-302
CHARACTERIZATION OF THE HUMAN GENE CODING FOR THE SWELLING-DEPENDENT CHLORIDE CHANNEL I-CLN AT POSITION 11Q13.5-14.1 (CLNS1A) AND FURTHER CHARACTERIZATION OF THE CHROMOSOME-6 (CLNS1B) LOCALIZATION
Authors: NAGL UO ERDEL M BERGMANN F OEHL B SCANDELLA E MUSANTE L GALIETTA LJV GSCHWENTNER M FURST J SCHMARDA A HOFER S UTERMANN G DEETJEN P PAULMICHL M
Citation: Uo. Nagl et al., CHARACTERIZATION OF THE HUMAN GENE CODING FOR THE SWELLING-DEPENDENT CHLORIDE CHANNEL I-CLN AT POSITION 11Q13.5-14.1 (CLNS1A) AND FURTHER CHARACTERIZATION OF THE CHROMOSOME-6 (CLNS1B) LOCALIZATION, Gene, 209(1-2), 1998, pp. 59-63
THE NUMBER OF KRINGLE-IV REPEATS 3-10 IS INVARIABLE IN THE HUMAN APO(A) GENE
Authors: HAIBACH C KRAFT HG KOCHL S ABE A UTERMANN G
Citation: C. Haibach et al., THE NUMBER OF KRINGLE-IV REPEATS 3-10 IS INVARIABLE IN THE HUMAN APO(A) GENE, Gene, 208(2), 1998, pp. 253-258
THE HUMAN GENE ENCODING SCYB9B, A PUTATIVE NOVEL CXC CHEMOKINE, MAPS TO HUMAN-CHROMOSOME 4Q21 LIKE THE CLOSELY-RELATED GENES FOR MIG (SCYB9) AND INP10 (SCYB10)
Authors: ERDEL M LAICH A UTERMANN G WERNER ER WERNERFELMAYER G
Citation: M. Erdel et al., THE HUMAN GENE ENCODING SCYB9B, A PUTATIVE NOVEL CXC CHEMOKINE, MAPS TO HUMAN-CHROMOSOME 4Q21 LIKE THE CLOSELY-RELATED GENES FOR MIG (SCYB9) AND INP10 (SCYB10), Cytogenetics and cell genetics, 81(3-4), 1998, pp. 271-272
INFLUENCE OF HEMATOCRIT ON THE MEASUREMENT OF LIPOPROTEINS DEMONSTRATED BY THE EXAMPLE OF LIPOPROTEIN(A)
Authors: KRONENBERG F TRENKWALDER E KRONENBERG MF KONIG P UTERMANN G DIEPLINGER H
Citation: F. Kronenberg et al., INFLUENCE OF HEMATOCRIT ON THE MEASUREMENT OF LIPOPROTEINS DEMONSTRATED BY THE EXAMPLE OF LIPOPROTEIN(A), Kidney international, 54(4), 1998, pp. 1385-1389
MUTATIONS IN THE DELTA-7-STEROL REDUCTASE GENE IN PATIENTS WITH THE SMITH-LEMLI-OPITZ-SYNDROME
Authors: FITZKY BU WITSCHBAUMGARTNER M ERDEL M GLOSSMANN H UTERMANN G MOEBIUS FF
Citation: Bu. Fitzky et al., MUTATIONS IN THE DELTA-7-STEROL REDUCTASE GENE IN PATIENTS WITH THE SMITH-LEMLI-OPITZ-SYNDROME, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 22-22
MUTATIONS IN THE DELTA-7-STEROL REDUCTASE GENE IN PATIENTS WITH THE SMITH-LEMLI-OPITZ-SYNDROME
Authors: FITZKY BU WITSCHBAUMGARTNER M ERDEL M LEE JN PAIK YK GLOSSMANN H UTERMANN G MOEBIUS FF
Citation: Bu. Fitzky et al., MUTATIONS IN THE DELTA-7-STEROL REDUCTASE GENE IN PATIENTS WITH THE SMITH-LEMLI-OPITZ-SYNDROME, Proceedings of the National Academy of Sciences of the United Statesof America, 95(14), 1998, pp. 8181-8186
MOLECULAR CHARACTERIZATION OF THE HUMAN PROTEIN-KINASE-C 0-ASTERISK GENE LOCUS (PRKCQ)
Authors: KOFLER K KOCHL S PARSON W ERDEL M UTERMANN G BAIER G
Citation: K. Kofler et al., MOLECULAR CHARACTERIZATION OF THE HUMAN PROTEIN-KINASE-C 0-ASTERISK GENE LOCUS (PRKCQ), MGG. Molecular & general genetics, 259(4), 1998, pp. 398-403
PHYSICAL INTERACTION OF APOE WITH AMYLOID PRECURSOR PROTEIN INDEPENDENT OF THE AMYLOID A-BETA REGION IN-VITRO
Authors: HASS S FRESSER F KOCHL S BEYREUTHER K UTERMANN G BAIER G
Citation: S. Hass et al., PHYSICAL INTERACTION OF APOE WITH AMYLOID PRECURSOR PROTEIN INDEPENDENT OF THE AMYLOID A-BETA REGION IN-VITRO, The Journal of biological chemistry, 273(22), 1998, pp. 13892-13897
GENETIC SERVICES IN AUSTRIA
Authors: UTERMANN G
Citation: G. Utermann, GENETIC SERVICES IN AUSTRIA, European journal of human genetics, 5, 1997, pp. 31-34
CLONING, STRUCTURAL-ANALYSIS, AND CHROMOSOMAL LOCALIZATION OF THE HUMAN CSRP2 GENE ENCODING THE LIM DOMAIN PROTEIN CRP2
Authors: WEISKIRCHEN R ERDEL M UTERMANN G BISTER K
Citation: R. Weiskirchen et al., CLONING, STRUCTURAL-ANALYSIS, AND CHROMOSOMAL LOCALIZATION OF THE HUMAN CSRP2 GENE ENCODING THE LIM DOMAIN PROTEIN CRP2, Genomics, 44(1), 1997, pp. 83-93
COMPARATIVE GENOMIC HYBRIDIZATION REVEALS A PARTIAL DE-NOVO TRISOMY 6Q23-QTER IN AN INFANT WITH CONGENITAL-MALFORMATIONS - DELINEATION OF THE PHENOTYPE
Authors: ERDEL M DUBA HC VERDORFER I LINGENHEL A GEIGER R GUTENBERGER KH LUDESCHER E UTERMANN B UTERMANN G
Citation: M. Erdel et al., COMPARATIVE GENOMIC HYBRIDIZATION REVEALS A PARTIAL DE-NOVO TRISOMY 6Q23-QTER IN AN INFANT WITH CONGENITAL-MALFORMATIONS - DELINEATION OF THE PHENOTYPE, Human genetics, 99(5), 1997, pp. 596-601
CHROMOSOMAL INSTABILITY IN A WOMAN WITH INFERTILITY AND 2 UNAFFECTED BROTHERS - A NEW FAMILIAL CHROMOSOMAL BREAKAGE SYNDROME
Authors: DUBA HC WEIRICH HG WEIRICHSCHWAIGER H UTERMANN B NACHBAUR D SOLDER E UTERMANN G
Citation: Hc. Duba et al., CHROMOSOMAL INSTABILITY IN A WOMAN WITH INFERTILITY AND 2 UNAFFECTED BROTHERS - A NEW FAMILIAL CHROMOSOMAL BREAKAGE SYNDROME, Human genetics, 100(3-4), 1997, pp. 431-440
ASSOCIATION OF SERUM LIPOPROTEIN(A) LEVELS AND APOLIPOPROTEIN(A) SIZEPOLYMORPHISM WITH TARGET-ORGAN DAMAGE IN ARTERIAL-HYPERTENSION
Authors: SECHI LA KRONENBERG F DECARLI S FALLETI E ZINGARO L CATENA C UTERMANN G BARTOLI E
Citation: La. Sechi et al., ASSOCIATION OF SERUM LIPOPROTEIN(A) LEVELS AND APOLIPOPROTEIN(A) SIZEPOLYMORPHISM WITH TARGET-ORGAN DAMAGE IN ARTERIAL-HYPERTENSION, JAMA, the journal of the American Medical Association, 277(21), 1997, pp. 1689-1695
DETECTION OF A DE-NOVO DUPLICATION OF 1Q32-QTER BY FLUORESCENCE IN-SITU HYBRIDIZATION IN A BOY WITH MULTIPLE MALFORMATIONS - FURTHER DELINEATION OF THE TRISOMY 1Q SYNDROME
Authors: DUBA HC ERDEL M LOFFLER J BEREUTHER L FISCHER H UTERMANN B UTERMANN G
Citation: Hc. Duba et al., DETECTION OF A DE-NOVO DUPLICATION OF 1Q32-QTER BY FLUORESCENCE IN-SITU HYBRIDIZATION IN A BOY WITH MULTIPLE MALFORMATIONS - FURTHER DELINEATION OF THE TRISOMY 1Q SYNDROME, Journal of Medical Genetics, 34(4), 1997, pp. 309-313
RENOVASCULAR ARTERIOVENOUS DIFFERENCES IN LP[A] PLASMA-CONCENTRATIONSSUGGEST REMOVAL OF LP[A] FROM THE RENAL CIRCULATION
Authors: KRONENBERG F TRENKWALDER E LINGENHEL A FRIEDRICH G LHOTTA K SCHOBER M MOES N KONIG P UTERMANN G DIEPLINGER H
Citation: F. Kronenberg et al., RENOVASCULAR ARTERIOVENOUS DIFFERENCES IN LP[A] PLASMA-CONCENTRATIONSSUGGEST REMOVAL OF LP[A] FROM THE RENAL CIRCULATION, Journal of lipid research, 38(9), 1997, pp. 1755-1763
SIB-PAIR ANALYSIS DETECTS ELEVATED LP(A) LEVELS AND LARGE VARIATION OF LP(A) CONCENTRATION IN SUBJECTS WITH FAMILIAR DEFECTIVE APO-B
Authors: VANDERHOEK YY LINGENHEL A KRAFT HG DEFESCHE JC KASTELEIN JJP UTERMANN G
Citation: Yy. Vanderhoek et al., SIB-PAIR ANALYSIS DETECTS ELEVATED LP(A) LEVELS AND LARGE VARIATION OF LP(A) CONCENTRATION IN SUBJECTS WITH FAMILIAR DEFECTIVE APO-B, The Journal of clinical investigation, 99(9), 1997, pp. 2269-2273
GENETIC-CONTROL OF LP(A) CONCENTRATIONS
Authors: UTERMANN G
Citation: G. Utermann, GENETIC-CONTROL OF LP(A) CONCENTRATIONS, Atherosclerosis, 134(1-2), 1997, pp. 13-13
THE C T-POLYMORPHISM IN THE APO(A) GENE EFFECTS LP(A) LEVELS IN AFRICANS BUT NOT IN CAUCASIANS - CONFOUNDING EFFECT OF LINKAGE DISEQUILIBRIUM/
Authors: KRAFT HG WINDEGGER M UTERMANN G
Citation: Hg. Kraft et al., THE C T-POLYMORPHISM IN THE APO(A) GENE EFFECTS LP(A) LEVELS IN AFRICANS BUT NOT IN CAUCASIANS - CONFOUNDING EFFECT OF LINKAGE DISEQUILIBRIUM/, Atherosclerosis, 134(1-2), 1997, pp. 80-80
SCREENING FOR MUTATIONS IN THE APOLIPOPROTEIN(A) UNIQUE KRINGLES TYPE-6, TYPE-9 AND TYPE-10
Authors: OGORELKOVA M TROMMSDORFF M KRAFT HG UTERMANN G
Citation: M. Ogorelkova et al., SCREENING FOR MUTATIONS IN THE APOLIPOPROTEIN(A) UNIQUE KRINGLES TYPE-6, TYPE-9 AND TYPE-10, Atherosclerosis, 134(1-2), 1997, pp. 146-146
Risultati: 1-25 | 26-50 | 51-67