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    1. Brabender, J; Lord, RV; Danenberg, KD; Metzger, R; Schneider, PM; Uetake, H; Kawakami, K; Park, JM; Salonga, D; Peters, JH; DeMeester, TR; Holscher, AH; Danenberg, PV
      Upregulation of ornithine decarboxylase mRNA expression in Barrett's esophagus and Barrett's - Associated adenocarcinoma

      JOURNAL OF GASTROINTESTINAL SURGERY
    2. Brabender, J; Danenberg, KD; Metzger, R; Schneider, PM; Park, JM; Salonga, D; Holscher, AH; Danenberg, PV
      Epidermal growth factor receptor and HER2-neu mRNA expression in non-smallcell lung cancer is correlated with survival

      CLINICAL CANCER RESEARCH
    3. Witzel-Schlomp, K; Rittner, C; Schneider, PM
      The human complement C9 gene: structural analysis of the 5 ' gene region and genetic polymorphism studies

      EUROPEAN JOURNAL OF IMMUNOGENETICS
    4. Brabender, J; Usadel, H; Danenberg, KD; Metzger, R; Schneider, PM; Lord, RV; Wickramasinghe, K; Lum, CE; Park, J; Salonga, D; Singer, J; Sidransky, D; Holscher, AH; Meltzer, SJ; Danenberg, PV
      Adenomatous polyposis coli gene promoter hypermethylation in non-small cell lung cancer is associated with survival

      ONCOGENE
    5. Gill, P; Brenner, C; Brinkmann, B; Budowle, B; Carracedo, A; Jobling, MA; de Knijff, P; Kayser, M; Krawczak, M; Mayr, WR; Morling, N; Olaisen, B; Pascali, V; Prinz, M; Roewer, L; Schneider, PM; Sajantila, A; Tyler-Smith, C
      DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    6. Martin, PD; Schmitter, H; Schneider, PM
      A brief history of the formation of DNA databases in forensic science within Europe

      FORENSIC SCIENCE INTERNATIONAL
    7. Schneider, PM; Martin, PD
      Criminal DNA databases: the European situation

      FORENSIC SCIENCE INTERNATIONAL
    8. Carracedo, A; Beckmann, A; Bengs, A; Brinkman, B; Caglia, A; Capelli, C; Gill, P; Gusmao, L; Hagelberg, C; Hohoff, C; Hoste, B; Kihlgren, A; Kloosterman, A; Dupuy, BM; Morling, N; O'Donnell, G; Parson, W; Phillips, C; Pouwels, M; Scheithauer, R; Schmitter, H; Schneider, PM; Schumm, J; Skitsa, I; Stradmann-Bellinghausen, B; Stuart, M; Court, DS; Vide, C
      Results of a collaborative study of the EDNAP group regarding the reproducibility and robustness of the Y-chromosome STRs DYS19, DYS389 I and II, DYS390 and DYS393 in a PCR pentaplex format

      FORENSIC SCIENCE INTERNATIONAL
    9. Roewer, L; Krawczak, M; Willuweit, S; Nagy, M; Alves, C; Amorim, A; Anslinger, K; Augustin, C; Betz, A; Bosch, E; Caglia, A; Carracedo, A; Corach, D; Dekairelle, AF; Dobosz, T; Dupuy, BM; Furedi, S; Gehrig, C; Gusmao, L; Henke, J; Henke, L; Hidding, M; Hohoff, C; Hoste, B; Jobling, MA; Kargel, HJ; de Knijff, P; Lessig, R; Liebeherr, E; Lorente, M; Martinez-Jarreta, B; Nievas, P; Nowak, M; Parson, W; Pascali, VL; Penacino, G; Ploski, R; Rolf, B; Sala, A; Schmidt, U; Schmitt, C; Schneider, PM; Szibor, R; Teifel-Greding, J; Kayser, M
      Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypes

      FORENSIC SCIENCE INTERNATIONAL
    10. Kreiter, S; Winkelmann, N; Schneider, PM; Schuler, M; Fischer, T; Ullmann, AJ; Huber, C; Derigs, HG; Kolbe, K
      Failure of sustained engraftment after non-myeloablative conditioning withlow-dose TBI and T cell-reduced allogeneic peripheral stem cell transplantation

      BONE MARROW TRANSPLANTATION
    11. Schneider, PM; Witzel-Schlomp, K; Steinhauer, C; Stradmann-Bellinghausen, B; Rittner, C
      Rapid detection of the ERV-K(C4) retroviral insertion reveals further structural polymorphism of the complement C4 genes in old world primates

      EXPERIMENTAL AND CLINICAL IMMUNOGENETICS
    12. Schneider, PM; Witzel-Schlomp, K; Rittner, C; Zhang, L
      The endogenous retroviral insertion in the human complement C4 gene modulates the expression of homologous genes by antisense inhibition

      IMMUNOGENETICS
    13. Baldus, SE; Schneider, PM; Monig, SP; Zirbes, TK; Fromm, S; Meyer, W; Glossmann, J; Schuler, S; Thiele, J; Holscher, AH; Dienes, HP
      p21/waf1/cip1 In gastric cancer: Associations with histopathological subtypes, lymphonodal metastasis, prognosis and p53 status

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    14. Baldus, SE; Zirbes, T; Glossmann, J; Fromm, S; Hanisch, FG; Monig, SP; Schroder, W; Schneider, PM; Flucke, U; Karsten, U; Thiele, J; Holscher, AH; Dienes, HP
      Immunoreactivity of monoclonal antibody BW835 represents a marker of progression and prognosis in early gastric cancer

      ONCOLOGY
    15. Brabender, J; Lord, RV; Danenberg, KD; Metzger, R; Schneider, PM; Park, JM; Salonga, D; Groshen, S; Tsao-Wei, DD; DeMeester, TR; Holscher, AH; Danenberg, PV
      Increased c-myb mRNA expression in Barrett's esophagus and Barrett's-associated adenocarcinoma

      JOURNAL OF SURGICAL RESEARCH
    16. Muller-Tidow, C; Metzger, R; Kugler, K; Diederichs, S; Idos, G; Thomas, M; Dockhorn-Dworniczak, B; Schneider, PM; Koeffler, HP; Berdel, WE; Serve, H
      Cyclin E is the only cyclin-dependent kinase 2-associated cyclin that predicts metastasis and survival in early stage non-small cell lung cancer

      CANCER RESEARCH
    17. Muller-Tidow, C; Kugler, K; Diederichs, S; Klumpen, S; Moller, M; Vogt, U; Metzger, R; Schneider, PM; Berdel, WE; Serve, H
      Loss of expression of HDAC-recruiting methyl-CpG-binding domain proteins in human cancer

      BRITISH JOURNAL OF CANCER
    18. Schneider, PM; Stoeltzing, O; Roth, JA; Hoelscher, AH; Wegerer, S; Mizumoto, S; Becker, K; Dittler, HJ; Fink, U; Siewert, JR
      p53 mutational status improves estimation of prognosis in patients with curatively resected adenocarcinoma in Barrett's esophagus

      CLINICAL CANCER RESEARCH
    19. Bar, W; Brinkmann, B; Budowle, B; Carracedo, A; Gill, P; Holland, M; Lincoln, PJ; Mayr, W; Morling, N; Olaisen, B; Schneider, PM; Tully, G; Wilson, M
      DNA Commission of the International Society for Forensic Genetics: Guidelines for mitochondrial DNA typing

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    20. Bender, K; Schneider, PM; Rittner, C
      Application of mtDNA sequence analysis in forensic casework for the identification of human remains

      FORENSIC SCIENCE INTERNATIONAL
    21. Wittig, H; Augustin, C; Baasner, A; Bulnheim, U; Dimo-Simonin, N; Edelmann, J; Hering, S; Jung, S; Lutz, S; Michael, M; Parson, W; Poetsch, M; Schneider, PM; Weichhold, G; Krause, D
      Mitochondrial DNA in the central european population Human identification with the help of the forensic mt-DNA D-Loop-Base Database

      FORENSIC SCIENCE INTERNATIONAL
    22. Boorboor, P; Drescher, BE; Hartung, K; Sachse, C; Tsao, BP; Schneider, PM; Kalden, JR; Lakomek, HJ; Peter, HH; Schmidt, RE; Witte, T
      Poly(ADP-ribose) polymerase polymorphisms are not a genetic risk factor for systemic lupus erythematosus in German Caucasians

      JOURNAL OF RHEUMATOLOGY
    23. Holscher, AH; Metzger, R; Schneider, PM
      Preoperative radiochemotherapy of esophageal cancer. Light at the end of the tunnel?

      ZENTRALBLATT FUR CHIRURGIE
    24. Bar, W; Brinkmann, B; Budowle, B; Carracedo, A; Gill, P; Holland, M; Lincoln, PJ; Mayr, W; Morling, N; Olaisen, B; Schneider, PM; Tully, G; Wilson, M
      Guidelines for mitochondrial DNA typing

      VOX SANGUINIS
    25. Zirbes, TK; Baldus, SE; Moenig, SP; Nolden, S; Kunze, D; Shafizadeh, ST; Schneider, PM; Thiele, J; Hoelscher, AH; Dienes, HP
      Prognostic impact of p21/waf1/cip1 in colorectal cancer

      INTERNATIONAL JOURNAL OF CANCER
    26. Baldus, SE; Zirbes, TK; Hanisch, FG; Kunze, D; Shafizadeh, ST; Nolden, S; Monig, SP; Schneider, PM; Karsten, U; Thiele, J; Holscher, AH; Dienes, HP
      Thomsen-Friedenreich antigen presents as a prognostic factor in colorectalcarcinoma - A clinicopathologic study of 264 patients

      CANCER
    27. Schneider, PM; Praeuer, HW; Stoeltzing, O; Boehm, J; Manning, J; Metzger, R; Fink, U; Wegerer, S; Hoelscher, AH; Roth, JA
      Multiple molecular marker testing (p53, C-Ki-ras, c-erbB-2) improves estimation of prognosis in potentially curative resected non small cell lung cancer

      BRITISH JOURNAL OF CANCER
    28. Schneider, PM; Zirbes, TK; Metzger, R; Baldus, S; Dienes, HP; Holscher, AH
      Histomorphologic regression grading and apoptotic-index as objective response parameters for adenocarcinomas of the stomach and esophagogastric junction treated with neoadjuvant chemotherapy

      LANGENBECKS ARCHIVES OF SURGERY
    29. Schneider, PM; Seo, Y; Rittner, C
      Forensic mtDNA hair analysis excludes a dog from having caused a traffic accident

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    30. Schneider, PM; d'Aloja, E; Dupuy, BM; Eriksen, B; Jangblad, A; Kloosterman, AD; Kratzer, A; Lareu, MV; Pfitzinger, H; Rand, S; Scheithauer, R; Schmitter, H; Skitsa, I; Syndercombe-Court, D; Vide, MC
      Results of a collaborative study regarding the standardization of the Y-linked STR system DYS385 by the European DNA Profiling (EDNAP) group

      FORENSIC SCIENCE INTERNATIONAL
    31. Zhang, L; Stradmann-Bellinghausen, B; Rittner, C; Schneider, PM
      Genetic polymorphism of human complement factor I (C3b inactivator) in theChinese Han population

      EXPERIMENTAL AND CLINICAL IMMUNOGENETICS
    32. Schneider, PM; Wurzner, R
      Complement genetics: biological implications of polymorphisms and deficiencies

      IMMUNOLOGY TODAY
    33. Hohler, T; Leininger, S; Schneider, PM
      A new polymorphism in the human HFE gene

      IMMUNOGENETICS
    34. Hohler, T; Hug, R; Schneider, PM; Krummenauer, F; Gripenberg-Lerche, C; Granfors, K; Marker-Hermann, E
      Ankylosing spondylitis in monozygotic twins: studies on immunological parameters

      ANNALS OF THE RHEUMATIC DISEASES
    35. BEIN G; DRILLER B; SCHURMANN M; SCHNEIDER PM; KIRCHNER H
      PSEUDO-EXCLUSION FROM PATERNITY DUE TO MATERNAL UNIPARENTAL DISOMY-16

      International journal of legal medicine
    36. WAIYAWUTH W; ZHANG L; RITTNER C; SCHNEIDER PM
      GENETIC-ANALYSIS OF THE SHORT TANDEM REPEAT SYSTEM D12S391 IN THE GERMAN AND 3 ASIAN POPULATIONS

      Forensic science international
    37. Seo, Y; Stradmann-Bellinghausen, B; Rittner, C; Takahama, K; Schneider, PM
      Sequence polymorphism of mitochondrial DNA control region in Japanese

      FORENSIC SCIENCE INTERNATIONAL
    38. Schneider, PM; Meuser, S; Waiyawuth, W; Seo, Y; Rittner, C
      Tandem repeat structure of the duplicated Y-chromosomal STR locus DYS385 and frequency studies in the German and three Asian populations

      FORENSIC SCIENCE INTERNATIONAL
    39. HOHLER T; WUNSCHEL M; GERKEN G; SCHNEIDER PM; ZUMBUSCHENFELDE KHM; RITTNER C
      NO ASSOCIATION BETWEEN MANNOSE-BINDING LECTIN ALLELES AND SUSCEPTIBILITY TO CHRONIC HEPATITIS-B VIRUS-INFECTION IN GERMAN PATIENTS

      Experimental and clinical immunogenetics
    40. Mauff, G; Luther, B; Schneider, PM; Rittner, C; Stradmann-Bellinghausen, B; Dawkins, R; Moulds, JM
      Reference typing report for complement component C4

      EXPERIMENTAL AND CLINICAL IMMUNOGENETICS
    41. Geserick, G; Otremba, P; Schroder, H; Stradmann-Bellinghausen, B; Schneider, PM
      Reference typing report for complement factor B

      EXPERIMENTAL AND CLINICAL IMMUNOGENETICS
    42. HOHLER T; MEYER CU; NOTGHI A; STRADMANNBELLINGHAUSEN B; SCHNEIDER PM; STARKE R; ZEPP F; SANGER R; CLEMENS R; ZUMBUSCHENFELDE KHM; RITTNER C
      THE INFLUENCE OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II GENES AND T-CELL V-BETA REPERTOIRE ON RESPONSE TO IMMUNIZATION WITH HBSAG

      Human immunology
    43. FREDRIKSON GN; GULLSTRAND B; SCHNEIDER PM; WITZELSCHLOMP K; SJOHOLM AG; ALPER CA; AWDEH Z; TRUEDSSON L
      CHARACTERIZATION OF NONEXPRESSED C4 GENES IN A CASE OF COMPLETE C4 DEFICIENCY - IDENTIFICATION OF A NOVEL POINT MUTATION LEADING TO A PREMATURE STOP CODON

      Human immunology
    44. MORLEY BJ; BARTOK I; SPATH PJ; VYSE TJ; SCHNEIDER PM; WALPORT MJ
      MOLECULAR-BASIS OF HEREDITARY FACTOR-I DEFICIENCY

      Molecular immunology
    45. FRANK A; STRADMANNBELLINGHAUSEN B; SCHNEIDER PM; RITTNER C; HOHLER T
      MOLECULAR-BASIS OF SEVERAL RARE VARIANTS AND GENOMIC ORGANIZATION OF THE HUMAN C3 GENE

      Molecular immunology
    46. WITZELSCHLOMP K; RITTNER C; SCHNEIDER PM
      STRUCTURAL ORGANIZATION, DEFICIENCY MUTATIONS AND GENETIC-POLYMORPHISM OF THE HUMAN-COMPLEMENT C9 GENE

      Molecular immunology
    47. HOHLER T; KRUGER A; GERKEN G; SCHNEIDER PM; ZUMBUSCHENFELDE KHM; RITTNER C
      TURNER NECROSIS FACTOR-ALPHA PROMOTER POLYMORPHISM AT POSITION-238 ISASSOCIATED WITH CHRONIC ACTIVE HEPATITIS-C INFECTION

      Journal of medical virology
    48. WITZELSCHLOMP K; HOBART MJ; FERNIE BA; ORREN A; WURZNER R; RITTNER C; KAUFMANN T; SCHNEIDER PM
      HETEROGENEITY IN THE GENETIC-BASIS OF HUMAN-COMPLEMENT C9 DEFICIENCY

      Immunogenetics (New York)
    49. HORIUCHI T; NISHIZAKA H; KOJIMA T; SAWABE T; NIHO Y; SCHNEIDER PM; INABA S; SAKAI K; HAYASHI K; HASHIMURA C; FUKUMORI Y
      A NONSENSE MUTATION AT ARG(95) IS PREDOMINANT IN COMPLEMENT-9 DEFICIENCY IN JAPANESE

      The Journal of immunology
    50. HOHLER T; KRUGER A; GERKEN G; SCHNEIDER PM; ZUMBUSCHENFELDE KHM; RITTNER C
      A TUMOR-NECROSIS-FACTOR-ALPHA (TNF-ALPHA) PROMOTER POLYMORPHISM IS ASSOCIATED WITH CHRONIC HEPATITIS-B INFECTION

      Clinical and experimental immunology
    51. HOHLER T; SCHAAPER T; SCHNEIDER PM; ZUMBUUSCHENFELDE KHM; MARKERHERMANN E
      DIFFERENCES IN TNF-ALPHA PROMOTER ALLELE FREQUENCIES ARE ASSOCIATED WITH ANKYLOSING-SPONDYLITIS IN HLA-B27 POSITIVE INDIVIDUALS

      Arthritis and rheumatism
    52. HOHLER T; SCHAPER T; SCHNEIDER PM; ZUMBUSCHENFELDE KHM; MARKERHERMANN E
      ASSOCIATION OF DIFFERENT TUMOR-NECROSIS-FACTOR-ALPHA PROMOTER ALLELE FREQUENCIES WITH ANKYLOSING-SPONDYLITIS IN HLA-B27 POSITIVE INDIVIDUALS

      Arthritis and rheumatism
    53. SCHNEIDER PM; FELLBAUM C; FINK U; BOLLSCHWEILER E; PRAUER HW
      PROGNOSTIC IMPORTANCE OF HISTOMORPHOLOGIC SUBCLASSIFICATION FOR EPITHELIAL THYMIC TUMORS

      Annals of surgical oncology
    54. KAYSER M; CAGLIA A; CORACH D; FRETWELL N; GEHRIG C; GRAZIOSI G; HEIDORN F; HERRMANN S; HERZOG B; HIDDING M; HONDA K; JOBLING M; KRAWCZAK M; LEIM K; MEUSER S; MEYER E; OESTERREICH W; PANDYA A; PARSON W; PENACINO G; PEREZLEZAUN A; PICCININI A; PRINZ M; SCHMITT C; SCHNEIDER PM; SZIBOR R; TEIFELGREDING J; WEICHOLD G; DEKNIJFF P; ROEWER L
      EVALUATION OF Y-CHROMOSOMAL STRS - A MULTICENTER STUDY

      International journal of legal medicine
    55. DEKNIJFF P; KAYSER M; CAGLIA A; CORACH D; FRETWELL N; GEHRIG C; GRAZIOSI G; HEIDORN F; HERRMANN S; HERZOG B; HIDDING M; HONDA K; JOBLING M; KRAWCZAK M; LEIM K; MEUSER S; MEYER E; OESTERREICH W; PANDYA A; PARSON W; PENACINO G; PEREZLEZAUN A; PICCININI A; PRINZ M; SCHMITT C; SCHNEIDER PM; SZIBOR R; TEIFELGREDING J; WEICHHOLD G; ROEWER L
      CHROMOSOME-Y MICROSATELLITES - POPULATION GENETIC AND EVOLUTIONARY ASPECTS

      International journal of legal medicine
    56. SCHNEIDER PM; RITTER C; MARTIN PD
      SPECIAL ISSUE - PROCEEDINGS OF THE EUROPEAN SYMPOSIUM - ETHICAL AND LEGAL ISSUES OF DNA TYPING IN FORENSIC MEDICINE

      Forensic science international
    57. SCHNEIDER PM
      BASIC ISSUES IN FORENSIC DNA TYPING

      Forensic science international
    58. SCHMITTER H; SCHNEIDER PM
      LEGAL-ASPECTS OF FORENSIC DNA ANALYSIS IN GERMANY

      Forensic science international
    59. MORLING N; RITTNER C; SCHMITTER H; BEYLEVELD D; MARTIN PD; SCHNEIDER PM; SCHEITHAUER R; WERRETT DJ; OLAISEN B; KLOOSTERMAN A
      SPECIAL ISSUE - PROCEEDINGS OF THE EUROPEAN SYMPOSIUM - ETHICAL AND LEGAL ISSUES OF DNA TYPING IN FORENSIC MEDICINE - SUMMARY OF THE DISCUSSION

      Forensic science international
    60. SCHNEIDER PM
      CHANGES IN THE DNA PROFILE CAUSED BY TOXIC-SUBSTANCES

      Forensic science international
    61. SCHNEIDER PM
      MOLECULAR PATHOGENESIS OF ADENOCARCINOMAS IN BARRETTS-ESOPHAGUS - ROLE OF TUMOR-SUPPRESSOR GENE P53 (VOL 20, PG 36, 1997)

      Onkologie
    62. SCHNEIDER PM; CASSON AG; HOLSCHER AH; SCHWEIGHART S; MIZUMOTO S; SIEWERT JR; ROTH JA
      MOLECULAR PATHOGENESIS OF ADENOCARCINOMAS IN BARRETTS-ESOPHAGUS - ROLE OF THE TUMOR-SUPPRESSOR GENE P53

      Onkologie
    63. WEGREMERS S; BRENDEN M; SCHWARZ E; WITZEL K; SCHNEIDER PM; GUERRA LK; REHFELDT IR; LIMA MT; HARTMANN D; PETZLERLER ML; DEMESSIAS IJT; MAUFF G
      MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) CLASS-III GENETICS IN 2 AMERINDIAN TRIBES FROM SOUTHERN BRAZIL - THE KAINGANG AND THE GUARANI

      Human genetics
    64. HOHLER T; MEYER CU; NOTGHI A; STRADMANNBELLINGHAUSEN B; SCHNEIDER PM; STARKE R; ZEPP F; SANGER R; CLEMENS R; ZUMBUSCHENFELDE KHM; RITTNER C
      THE INFLUENCE OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II GENES AND T-CELL V-BETA REPERTOIRE ON RESPONSE TO IMMUNIZATION WITH HBSAG

      Hepatology
    65. HOHLER T; GERKEN G; NOTGHI A; KNOLLE P; LUBJUHN R; TAHERI H; SCHNEIDER PM; ZUMBUSCHENFELDE KHM; RITTNER C
      MHC CLASS-II GENES INFLUENCE THE SUSCEPTIBILITY TO CHRONIC ACTIVE HEPATITIS-C

      Journal of hepatology
    66. HOHLER T; GERKEN G; NOTGHI A; LUBJUHN R; TAHERI H; PROTZER U; LOHR HF; SCHNEIDER PM; ZUMBUSCHENFELDE KHM; RITTNER C
      HLA-DRB1-ASTERISK-1301 AND ASTERISK-1302 PROTECT AGAINST CHRONIC HEPATITIS-B

      Journal of hepatology
    67. SCHEURER B; RITTNER C; SCHNEIDER PM
      EXPRESSION OF THE HUMAN-COMPLEMENT C8 SUBUNITS IS INDEPENDENTLY REGULATED BY INTERLEUKIN-1-BETA, INTERLEUKIN-6, AND INTERFERON-GAMMA

      Immunopharmacology
    68. KOTNIK V; LUZNIKBUFON T; SCHNEIDER PM; KIRSCHFINK M
      MOLECULAR, GENETIC, AND FUNCTIONAL-ANALYSIS OF HOMOZYGOUS C8 BETA-CHAIN DEFICIENCY IN 2 SIBLINGS

      Immunopharmacology
    69. HOHLER T; KRUGER A; SCHNEIDER PM; SCHOPF RE; KNOP J; RITTNER C; ZUMBUSCHENFELDE KHM; MARKERHERMANN E
      A TNF-ALPHA PROMOTER POLYMORPHISM IS ASSOCIATED WITH JUVENILE-ONSET PSORIASIS AND PSORIATIC-ARTHRITIS

      Journal of investigative dermatology
    70. WITZELSCHLOMP K; SPATH PJ; HOBART MJ; FERNIE BA; RITTNER C; KAUFMANN T; SCHNEIDER PM
      THE HUMAN-COMPLEMENT C9 GENE - IDENTIFICATION OF 2 MUTATIONS CAUSING DEFICIENCY AND REVISION OF THE GENE STRUCTURE

      The Journal of immunology
    71. HOLSCHER AH; BOLLSCHWEILER E; SCHNEIDER PM; SIEWERT JR
      EARLY ADENOCARCINOMA IN BARRETTS-ESOPHAGUS

      British Journal of Surgery
    72. HOHLER T; KRUGER A; SCHNEIDER PM; SCHOPF RE; KNOP J; RITTNER C; ZUMBUSCHENFELDE KHM; MARKERHERMANN E
      A TNF-ALPHA PROMOTER POLYMORPHISM IS ASSOCIATED WITH PSORIATIC-ARTHRITIS AND JUVENILE-ONSET PSORIASIS

      Arthritis and rheumatism
    73. HOHLER T; SCHAPER T; SCHNEIDER PM; KRUMMENAUER F; RITTNER C; ZUMBUSCHENFELDE KHM; MARKERHERMANN E
      NO PRIMARY ASSOCIATION BETWEEN LMP2 POLYMORPHISMS AND EXTRASPINAL MANIFESTATIONS IN SPONDYLOARTHROPATHIES

      Annals of the Rheumatic Diseases
    74. SCHNEIDER PM; STRADMANNBELLINGHAUSEN B; RITTNER C
      GENETIC-POLYMORPHISM OF THE 4TH COMPONENT OF HUMAN-COMPLEMENT - POPULATION STUDY AND PROPOSAL FOR A REVISED NOMENCLATURE BASED ON GENOMIC PCR TYPING OF RODGERS AND CHIDO DETERMINANTS

      European journal of immunogenetics
    75. HOHLER T; SCHNEIDER PM; RITTNER C; HASENCLEVER P; ZUMBUSCHENFELDE KHM; MARKERHERMANN E
      LMP POLYMORPHISMS DO NOT INFLUENCE DISEASE EXPRESSION IN PSORIATIC-ARTHRITIS

      Clinical and experimental rheumatology
    76. BELLAVIA D; SCHNEIDER PM; RITTNER C; MALFITANO G; KAUFMANN TJ; BRAI M
      DETECTION OF HETEROZYGOUS C8-BETA DEFICIENCY BY PCR IN A HEALTHY ITALIAN POPULATION

      Experimental and clinical immunogenetics
    77. HOHLER T; GERKEN G; SCHNEIDER PM; ZUMBUSCHENFELDE KH; RITTNER C
      ANTIGEN-PROCESSING POLYMORPHISMS IN CHRONIC HEPATITIS-C INFECTION

      Experimental and clinical immunogenetics
    78. HOHLER T; WEINMANN A; SCHNEIDER PM; RITTNER C; SCHOPF RE; KNOP J; HASENCLEVER P; ZUMBUSCHENFELDE KHM; MARKERHERMANN E
      TAP-POLYMORPHISMS IN JUVENILE-ONSET PSORIASIS AND PSORIATIC-ARTHRITIS

      Human immunology
    79. SCHNEIDER PM; CASSON AG; LEVIN B; GAREWAL HS; HOELSCHER AH; BECKER K; DITTLER HJ; CLEARY KR; TROSTER M; SIEWERT JR; ROTH JA
      MUTATIONS OF P53 IN BARRETTS-ESOPHAGUS AND BARRETTS-CANCER - A PROSPECTIVE-STUDY OF 98 CASES

      Journal of thoracic and cardiovascular surgery
    80. RICE TW; SCHNEIDER PM; RICE TW; RUSCH VW; TRASTEK VF; THOMAS AN
      MUTATIONS OF P53 IN BARRETTS-ESOPHAGUS AND BARRETTS-CANCER - A PROSPECTIVE-STUDY OF 98 CASES - DISCUSSION

      Journal of thoracic and cardiovascular surgery
    81. HEIKE M; SCHLAAK J; SCHULZEBERGKAMEN H; HEYL S; HERR W; SCHMITT U; SCHNEIDER PM; ZUMBUSCHENFELDE KHM
      SPECIFICITIES AND FUNCTIONS OF CD4(-RESTRICTED T-CELL CLONES AGAINST A HUMAN SARCOMA - EVIDENCE FOR SEVERAL RECOGNIZED ANTIGENS() HLA CLASSII)

      The Journal of immunology
    82. KIMPTON C; GILL P; DALOJA E; ANDERSEN JF; BAR W; HOLGERSSON S; JACOBSEN S; JOHNSSON V; KLOOSTERMAN AD; LAREU MV; NELLEMANN L; PFITZINGER H; PHILLIPS CP; RAND S; SCHMITTER H; SCHNEIDER PM; STERNERSEN M; VIDE MC
      REPORT ON THE 2ND EDNAP COLLABORATIVE STR EXERCISE

      Forensic science international
    83. HOHLER T; BOTTO M; RITTNER C; SCHNEIDER PM; ZUMBUSCHENFELDE KHM
      COMPLEMENT COMPONENT C3 - MOLECULAR-BASIS OF THE C3-ASTERISK-S025 VARIANT AND EVIDENCE FOR MOLECULAR HETEROGENEITY OF OTHER VARIANTS

      Human genetics
    84. ZHANG L; RITTNER C; SODETZ JM; SCHNEIDER PM; KAUFMANN T
      THE 8TH COMPONENT OF HUMAN-COMPLEMENT - MOLECULAR-BASIS OF C8A (C81) POLYMORPHISM

      Human genetics
    85. CHU XL; RITTNER C; SCHNEIDER PM
      LENGTH POLYMORPHISM OF THE HUMAN-COMPLEMENT COMPONENT C4 GENE IS DUE TO AN ANCIENT RETROVIRAL INTEGRATION

      Experimental and clinical immunogenetics
    86. SPATH GF; RAMADORI G; RITTNER C; SCHNEIDER PM
      EXPRESSION OF THE COMPLEMENT C8 GENES DURING INTERLEUKIN-6-MEDIATED IN-VITRO INDUCTION OF THE ACUTE-PHASE RESPONSE

      Experimental and clinical immunogenetics
    87. WITZEL K; CHU XL; RITTNER C; SCHNEIDER PM
      POLYMERASE CHAIN-REACTION ANALYSIS OF THE XBA-I POLYMORPHISM OF THE HUMAN-COMPLEMENT C4 GENES PROVIDES EVIDENCE FOR STRONG HAPLOTYPE CONSERVATION

      Human immunology
    88. SCHNEIDER PM; DAVEY SB
      SEDIMENT CONTAMINANTS OFF THE COAST OF SYDNEY, AUSTRALIA - A MODEL FOR THEIR DISTRIBUTION

      Marine pollution bulletin
    89. HOHLER T; HUNDT M; RITTNER C; SCHNEIDER PM; ZUMBUSCHENFELDE KHM
      CHOLINESTERASE VARIANTS - RAPID CHARACTERIZATION BY PCR SSCP AND EVIDENCE FOR MOLECULAR HOMOGENEITY/

      Journal of Medical Genetics
    90. RODER JD; SCHNEIDER PM; STEIN HJ; SIEWERT JR
      CARCINOMA OF THE PERIAMPULLARY REGION - WHY ARE THERE PROGNOSTIC DIFFERENCES

      Gastroenterology
    91. HOLSCHER AH; BOLLSCHWEILER E; SCHNEIDER PM; SIEWERT JR
      PROGNOSIS OF EARLY ESOPHAGEAL CANCER - COMPARISON BETWEEN ADENOCARCINOMA AND SQUAMOUS-CELL CARCINOMA

      Cancer
    92. RODER JD; SCHNEIDER PM; STEIN HJ; SIEWERT JR
      NUMBER OF LYMPH-NODE METASTASES IS SIGNIFICANTLY ASSOCIATED WITH SURVIVAL IN PATIENTS WITH RADICALLY RESECTED CARCINOMA OF THE AMPULLA OF VATER

      British Journal of Surgery
    93. BARBA GMR; BRAUNHEIMER L; RITTNER C; SCHNEIDER PM
      A NEW PCR-BASED TYPING OF THE RODGERS AND CHIDO ANTIGENIC DETERMINANTS OF THE 4TH COMPONENT OF HUMAN-COMPLEMENT

      European journal of immunogenetics
    94. SCHNEIDER PM
      STERILIZATION - LOW-TEMPERATURE STERILIZATION ALTERNATIVES IN THE 1990S

      Tappi journal
    95. GILL P; KIMPTON C; DALOJA E; ANDERSEN JF; BAR W; BRINKMANN B; HOLGERSSON S; JOHNSSON V; KLOOSTERMAN AD; LAREU MV; NELLEMANN L; PFITZINGER H; PHILLIPS CP; SCHMITTER H; SCHNEIDER PM; STENERSEN M
      REPORT OF THE EUROPEAN DNA PROFILING GROUP (EDNAP) - TOWARDS STANDARDIZATION OF SHORT TANDEM REPEAT (STR) LOCI

      Forensic science international
    96. ZHANG L; WURZNER R; STRADMANNBELLINGHAUSEN B; RITTNER C; SCHNEIDER PM
      A COMBINED STUDY OF HUMAN-COMPLEMENT C7 IEF AND C7 M N POLYMORPHISMS IN THE CHINESE HAN POPULATION/

      Experimental and clinical immunogenetics
    97. BRENNER CH; RITTNER C; SCHNEIDER PM
      CALCULATION OF PATERNITY PROBABILITIES FROM MULTILOCUS DNA PROFILES

      Electrophoresis
    98. WENDT RE; MURPHY PH; SCHNEIDER PM; TREFFERT JD; GROCH MW; FORD PV; MOORE WH
      LOSSY COMPRESSION OF DYNAMIC STUDIES USING EIGENIMAGE METHODS

      The Journal of nuclear medicine
    99. BARBA GMR; KAUFMANN TJ; SCHNEIDER PM; RITTNER C; BRAI M
      POLYMORPHISM OF THE COMPLEMENT C8A AND C8B GENES IN 2 FAMILIES WITH C8-BETA DEFICIENCY AND NEISSERIAL INFECTIONS

      Clinical immunology and immunopathology
    100. ROTH JA; HOLSCHER AH; SCHNEIDER PM
      MARKERS OF MALIGNANT POTENTIAL AND CLINIC AL MANAGEMENT OF DYSPLASIA IN BARRETT-ESOPHAGUS

      Chirurg


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 23/01/21 alle ore 13:06:42