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La ricerca find articoli where authors phrase all words ' Lohse, P' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 36 riferimenti
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    1. Pihusch, R; Buchholz, T; Lohse, P; Rubsamen, H; Rogenhofer, N; Hasbargen, U; Hiller, E; Thaler, CJ
      Thrombophilic gene mutations and recurrent spontaneous abortion: Prothrombin mutation increases the risk in the first trimester

      AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY
    2. Tietge, UJF; Sun, GS; Czarnecki, S; Yu, QC; Lohse, P; Du, H; Grabowski, GA; Glick, JM; Rader, DJ
      Phenotypic correction of lipid storage and growth arrest in Wolman diseasefibroblasts by gene transfer of lysosomal acid lipase

      HUMAN GENE THERAPY
    3. Hasbargen, U; Thaler, CJ; Ruebsamen, H; Fuchshuber, S; Lohse, P
      S680N substitution of the follicle-stimulating hormone receptor is a common polymorphism not associated with spontaneous human twinning

      EUROPEAN JOURNAL OF MEDICAL RESEARCH
    4. Muller-Koch, Y; Kopp, R; Lohse, P; Baretton, G; Stoetzer, A; Aust, D; Daum, J; Kerker, B; Gross, M; Dietmeier, W; Holinksi-Feder, E
      Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: Mutations or polymorphisms?

      EUROPEAN JOURNAL OF MEDICAL RESEARCH
    5. Rassoul, F; Richter, V; Lohse, P; Naumann, A; Purschwitz, K; Keller, E
      Long-term administration of the HMG-CoA reductase inhibitor lovastatin in two patients with cholesteryl ester storage disease

      INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS
    6. Fischereder, M; Schneeberger, H; Lohse, P; Kramer, BK; Schlondorff, D; Land, W
      Increased rate of renal transplant failure in patients with the G20210A mutation of the prothrombin gene

      AMERICAN JOURNAL OF KIDNEY DISEASES
    7. Holinski-Feder, E; Muller-Koch, Y; Friedl, W; Moselein, G; Keller, G; Plaschke, J; Ballhausen, W; Gross, M; Baldwin-Jedele, K; Jungck, M; Mangold, E; Vogelsang, H; Schackert, HK; Lohse, P; Murken, J; Meitinger, T
      DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    8. Ascherl, J; Schmidbaur, W; Wienbeck, M; Lohse, P
      Case study - Familial Mediterranean fever

      INTERNIST
    9. Teupser, D; Rupprecht, W; Lohse, P; Thiery, J
      Fluorescence-based detection of the CETP TaqIB polymorphism: False positives with the TaqMan-based exonuclease assay attributable to a previously unknown gene variant

      CLINICAL CHEMISTRY
    10. Hasbargen, U; Lohse, P; Thaler, CJ
      The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C -> T mutation

      HUMAN REPRODUCTION
    11. Elleder, M; Chlumska, A; Hyanek, J; Poupetova, H; Ledvinova, J; Maas, S; Lohse, P
      Subclinical course of cholesteryl ester storage disease in an adult with hypercholesterolemia, accelerated atherosclerosis, and liver cancer

      JOURNAL OF HEPATOLOGY
    12. Lohse, P; Maas, S; Lohse, P; Elleder, M; Kirk, JM; Besley, GTN; Seidel, D
      Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease

      JOURNAL OF LIPID RESEARCH
    13. Mangold, E; Diepolder, H; Lohse, P; Pape, GR; Ritter, MM
      Porphyria cutanea tarda related to genetically linked iron overload in compound heterozygous anlage for 2 mutations in the hemochromatosis gene

      INTERNIST
    14. Tischer, J; Forstpointner, R; Lohse, P; Hiller, E
      Central pulmonary embolism found in prothrombin dimorphism (hereditary thrombophilia)

      INTERNIST
    15. Lohse, P; Maas, S; Lohse, P; Sewell, AC; van Diggelen, OP; Seidel, D
      Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease

      JOURNAL OF LIPID RESEARCH
    16. ZACHOVAL R; RUEBSAMEN H; PAPE GR; LOHSE P
      THE FREQUENCY OF THE HEMOCHROMATOSIS CYS282TYR MUTATION IS NOT INCREASED IN GERMAN PATIENTS WITH CHRONIC HEPATITIS-C

      Hepatology
    17. FISCHEREDER M; GOHRING P; SCHNEEBERGER H; LOHSE P; VONAPPEN K; SAMTLEBEN W; SCHLONDORFF D; LAND W
      EARLY LOSS OF RENAL-TRANSPLANTS IN PATIENTS WITH THROMBOPHILIA

      Transplantation
    18. OSSENDORF M; HAFNER G; LOHSE P; PRELLWITZ W
      EVALUATION OF A NOVEL PCR-RFLP TECHNIQUE FOR APOLIPOPROTEIN-E GENOTYPING

      Clinical chemistry
    19. JAEGER BR; GOEHRING P; UHRIG S; LOHSE P; THIERY J; SEIDEL D
      AN EXTRACORPOREAL DEVICE TO REMOVE CLOTTING FACTORS FROM THE BLOOD-CIRCULATION VIA PRECIPITATION WITH HEPARIN (HELP)

      Circulation
    20. FISCHEREDER M; GOHRING P; SCHNEEBERGER H; LOHSE P; VONAPPEN K; SAMTLEBEN W; SCHLONDORFF D; LAND W
      EARLY LOSS OF RENAL-TRANSPLANTS IN PATIENTS WITH THROMBOPHILIA

      Journal of the American Society of Nephrology
    21. IGNATIUS A; UNTERRICKER K; WENGER K; RICHTER M; CLAES L; LOHSE P; HIRST H
      A NEW COMPOSITE MADE OF POLYURETHANE AND GLASS-CERAMIC IN A LOADED IMPLANT MODEL - A BIOMECHANICAL AND HISTOLOGICAL ANALYSIS

      Journal of materials science. Materials in medicine
    22. LOHSE P; LOHSE P; CHAHROKHZADEH S; SEIDEL D
      HUMAN LYSOSOMAL ACID LIPASE CHOLESTERYL ESTER HYDROLASE AND HUMAN GASTRIC LIPASE - SITE-DIRECTED MUTAGENESIS OF CYS(227) AND CYS(236) RESULTS IN SUBSTRATE-DEPENDENT REDUCTION OF ENZYMATIC-ACTIVITY/

      Journal of lipid research
    23. LOHSE P; LOHSE P; CHAHROKHZADEH S; SEIDEL D
      THE ACID-LIPASE GENE FAMILY - 3 ENZYMES, ONE HIGHLY CONSERVED GENE STRUCTURE

      Journal of lipid research
    24. LOHSE P; CHAHROKHZADEH S; LOHSE P; SEIDEL D
      HUMAN LYSOSOMAL ACID LIPASE CHOLESTERYL ESTER HYDROLASE AND HUMAN GASTRIC LIPASE - IDENTIFICATION OF THE CATALYTICALLY ACTIVE SERINE, ASPARTIC-ACID, AND HISTIDINE-RESIDUES

      Journal of lipid research
    25. RASSOUL F; KELLER E; NAUMANN A; LOHSE P; PURSCHWITZ K; LASSNER D; RICHTER V
      CHOLESTERYL ESTER STORAGE DISEASE - MOLECULAR DEFECTS AND TREATMENT WITH THE HMGCOA-REDUCTASE INHIBITOR LOVASTATIN

      Atherosclerosis
    26. SZOSTAK JW; BARTEL D; HAGER A; DAS A; LOHSE P
      ISOLATION OF NEW RIBOZYMES FORM POOLS OF RANDOM SEQUENCES

      The FASEB journal
    27. RADER D; TSUKAMOTO K; LOHSE P; CZARNECKI S
      EXPRESSION OF ADENOVIRAL VECTOR CONTAINING THE CDNA FOR HUMAN LYSOSOMAL ACID LIPASE IN HELA AND WOLMAN CELLS

      The FASEB journal
    28. ROUIS M; LOHSE P; DUGI KA; LOHSE P; BEG OU; RONAN R; TALLEY GD; BRUNZELL JD; SANTAMARINAFOJO S
      HOMOZYGOSITY FOR 2 POINT MUTATIONS IN THE LIPOPROTEIN-LIPASE (LPL) GENE IN A PATIENT WITH FAMILIAL LPL DEFICIENCY - LPL(ASP(9)-]ASN, TYR(262)-]HIS)

      Journal of lipid research
    29. LOHSE P; OBERHAUSER B; OBERHAUSERHOFBAUER B; BASCHANG G; ESCHENMOSER A
      CHEMISTRY OF ALPHA-AMINONITRILES .17. OLI GO(NUCLEODIPEPTAMIDINIUM) SALTS

      Croatica chemica acta
    30. PFEIFFER M; LEAVER N; ALI R; CREMER P; FRAUNBERGER P; LOHSE P; ROSE ML; SEIDEL D
      SYVA EMIT(R) CYCLOSPORINE ASSAY - A NOVEL WHOLE-BLOOD PRETREATMENT REAGENT

      Clinical chemistry
    31. CZARNECKI S; TSUKAMOTO K; LOHSE P; RADER D
      CONSTRUCTION AND EXPRESSION OF A REPLICATION-DEFECTIVE ADENOVIRUS CONTAINING THE HUMAN CDNA FOR LYSOSOMAL ACID LIPASE

      Molecular biology of the cell
    32. MANN WA; LOHSE P; GREGG RE; RONAN R; HOEG JM; ZECH LA; BREWER HB
      DOMINANT EXPRESSION OF TYPE-III HYPERLIPOPROTEINEMIA - PATHOPHYSIOLOGICAL INSIGHTS DERIVED FROM THE STRUCTURAL AND KINETIC CHARACTERISTICS OF APOE-1(LYS(146)-]GLU)

      The Journal of clinical investigation
    33. PFEIFFER M; CREMER P; LOHSE P; SEIDEL D
      EVALUATION OF 5 NON-PRETREATMENT DIGOXIN IMMUNOASSAYS

      Clinical chemistry
    34. RADER DJ; SCHAEFER JR; LOHSE P; IKEWAKI K; THOMAS F; HARRIS WA; ZECH LA; DUJOVNE CA; BREWER HB
      INCREASED PRODUCTION OF APOLIPOPROTEIN-A-I ASSOCIATED WITH ELEVATED PLASMA-LEVELS OF HIGH-DENSITY-LIPOPROTEINS, APOLIPOPROTEIN-A-I, AND LIPOPROTEIN-A-I IN A PATIENT WITH FAMILIAL HYPERALPHALIPOPROTEINEMIA

      Metabolism, clinical and experimental
    35. RADER DJ; SCHAFER J; LOHSE P; VERGES B; KINDT M; ZECH LA; STEINMETZ A; BREWER HB
      RAPID IN-VIVO TRANSPORT AND CATABOLISM OF HUMAN APOLIPOPROTEIN A-VI-1AND SLOWER CATABOLISM OF THE APOA-IV-2 ISOPROTEIN

      The Journal of clinical investigation
    36. LOHSE P; CHAHROKHZADEH S; LOHSE P; SEIDEL D
      HUMAN LYSOSOMAL ACID LIPASE - STRUCTURE-FUNCTION ANALYSIS BY DNA-SEQUENCING AND SITE-DIRECTED MUTAGENESIS

      Circulation


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 17:10:21