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La ricerca find articoli where authors phrase all words 'Stumm, M' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 49 riferimenti
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    1. Lemke, J; Chudoba, I; Senger, G; Stumm, M; Loncarevic, IF; Henry, C; Zabel, B; Claussen, U
      Improved definition of chromosomal breakpoints using high-resolution multicolour banding

      HUMAN GENETICS
    2. Musebeck, J; Mohnike, K; Beye, P; Tonnies, H; Neitzel, H; Schnabel, D; Gruters, A; Wieacker, PF; Stumm, M
      Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature

      EUROPEAN JOURNAL OF PEDIATRICS
    3. Tonnies, H; Stumm, M; Wegner, RD; Chudoba, I; Kalscheuer, V; Neitzel, H
      Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics

      CYTOGENETICS AND CELL GENETICS
    4. Stumm, M; Neubauer, S; Keindorff, S; Wegner, RD; Wieacker, P; Sauer, R
      High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome

      CYTOGENETICS AND CELL GENETICS
    5. Arutyunyan, R; Neubauer, S; Martus, P; Dork, T; Stumm, M; Gebhart, E
      Intercellular distribution of aberrations detected by means of chromosome painting in cells of patients with cancer prone chromosome instability syndromes

      EXPERIMENTAL ONCOLOGY
    6. Sieber, CC; Sumanovski, LT; Stumm, M; van der Kooij, M; Battegay, E
      In vivo angiogenesis in normal and portal hypertensive rats: role of basicfibroblast growth factor and nitric oxide

      JOURNAL OF HEPATOLOGY
    7. Volleth, M; Stumm, M; Mohnike, K; Kalscheuer, VM; Jakubiczka, S; Wieacker, P
      Preferential inactivation of a dupX(q23 -> q27-28) chromosome in a girl with mental retardation and dysmorphy

      HUMAN HEREDITY
    8. Stumm, M; Wieacker, P; Kessel-Weiner, E; Theile, U; Pascu, F; Ottolenghi, C
      Deletion of the DM-domain gene cluster in a fetus with ring chromosome 9 and sex reversal

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    9. Struk, B; Cai, L; Zach, S; Chung, WJJ; Lumsden, A; Stumm, M; Huber, M; Schaen, L; Kim, CA; Goldsmith, LA; Viljoen, D; Figuera, LE; Fuchs, W; Munier, F; Ramesar, R; Hohl, D; Richards, R; Neldner, KH; Lindpaintner, K
      Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

      JOURNAL OF MOLECULAR MEDICINE-JMM
    10. Cai, L; Struk, B; Adams, MD; Ji, W; Haaf, T; Kang, HL; Dho, SH; Xu, XQ; Ringpfeil, F; Nancarrow, J; Zach, S; Schaen, L; Stumm, M; Niu, TH; Chung, J; Lunze, K; Verrecchia, B; Goldsmith, LA; Viljoen, D; Figuera, LE; Fuchs, W; Lebwohl, M; Uitto, J; Richards, R; Hohl, D; Ramesar, R; Callen, DF; Kim, UJ; Doggett, NA; Neldner, KH; Lindpainter, K
      A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structure

      JOURNAL OF MOLECULAR MEDICINE-JMM
    11. Wieacker, P; Grumpelt, U; Schulz, TO; Gharavi, B; Avenarius, S; Jakubiczka, S; Stumm, M
      Female pseudohermaphroditism caused by caudal dysgenesis

      CYTOGENETICS AND CELL GENETICS
    12. Jakubiczka, S; Mitulla, B; Liehr, T; Arnemann, J; Lehrach, H; Sudbrak, R; Stumm, M; Wieacker, PF; Bettecken, T
      Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing

      PRENATAL DIAGNOSIS
    13. Bruckner, R; Jentsch-Ullrich, K; Franke, A; Wieacker, P; Stumm, M
      A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia

      CANCER GENETICS AND CYTOGENETICS
    14. Stumm, M; Sieber, C
      Portal hypertension and angiogenesis

      SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT
    15. Girard, PM; Foray, N; Stumm, M; Waugh, A; Riballo, E; Maser, RS; Phillips, WP; Petrini, J; Arlett, CF; Jeggo, PA
      Radiosensitivity in Nijmegen Breakage syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects

      CANCER RESEARCH
    16. Stanulla, M; Stumm, M; Dieckvoss, BO; Seidemann, K; Schemmel, V; Brechlin, AM; Schrappe, M; Welte, K; Reiter, A
      No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence

      BRITISH JOURNAL OF HAEMATOLOGY
    17. Bartsch, O; Wagner, A; Hinkel, GK; Krebs, P; Stumm, M; Schmalenberger, B; Bohm, S; Balci, S; Majewski, F
      FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy

      EUROPEAN JOURNAL OF HUMAN GENETICS
    18. Antoccia, A; Stumm, M; Saar, K; Ricordy, R; Maraschio, P; Tanzarella, C
      Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines

      INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
    19. Winter, C; tom Dieck, S; Boeckers, TM; Bockmann, J; Kampf, U; Sanmarti-Vila, L; Langnaese, K; Altrock, W; Stumm, M; Soyke, A; Wieacker, P; Garner, CC; Gundelfinger, ED
      The presynaptic cytomatrix protein bassoon: Sequence and chromosomal localization of the human BSN gene

      GENOMICS
    20. Elliott, DG; Stumm, M; Snelgrove, WM; Cojocaru, C; McKenzie, R
      Computational RAM: Implementing processors in memory

      IEEE DESIGN & TEST OF COMPUTERS
    21. Stumm, M; Tonnies, H; Wieacker, PF
      Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease

      EUROPEAN JOURNAL OF PEDIATRICS
    22. Stumm, M; Tonnies, H; Mandon, U; Gotze, A; Krebs, P; Wieacker, PF
      Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: cytogenetic and molecular-cytogenetic studies

      EUROPEAN JOURNAL OF PEDIATRICS
    23. Stumm, M; Reuter, M; Mandon, U; Bruckner, R; Wieacker, P
      Trisomy 4p as result of a maternal translocation t(4;8) (q11;p23)

      KLINISCHE PADIATRIE
    24. Sumanovski, LT; Battegay, E; Stumm, M; van der Kooij, M; Sieber, CC
      Increased angiogenesis in portal hypertensive rats: Role of nitric oxide

      HEPATOLOGY
    25. Jakubiczka, S; Bettecken, T; Stumm, M; Nickel, I; Musebeck, J; Krebs, P; Fischer, C; Kleinstein, J; Wieacker, P
      Frequency of CFTR gene mutations in males participating in an ICSI programme

      HUMAN REPRODUCTION
    26. Konig, B; Steinbach, F; Janocha, B; Drynda, A; Stumm, M; Philipp, C; Allhoff, EP; Konig, W
      The differential expression of proinflammatory cytokines IL-6, IL-8 and TNF-alpha in renal cell carcinoma

      ANTICANCER RESEARCH
    27. Stumm, M; Koch, A; Wieacker, PF; Phillip, C; Steinbach, F; Allhoff, EP; Buhtz, P; Walter, H; Tonnies, H; Wirth, J
      Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma

      CANCER GENETICS AND CYTOGENETICS
    28. Gotze, A; Krebs, P; Stumm, M; Wieacker, P; Allhoff, EP
      Trisomy 8 mosaicism in a patient with tetraamelia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    29. DIECK ST; SANMARTIVILA L; STUMM M; KAMPF U; LANGNASE K; DRESBACH R; WIEACKER P; GUNDELFINGER ED
      BASSOON, A NOVEL PRESYNAPTIC CYTOMATRIX PROTEIN, CONTAINS N-TERMINAL ZN2-FINGER MOTIFS AND A C-TERMINAL POLY-GLUTAMINE STRETCH()

      European journal of neuroscience
    30. Soyke, A; Stumm, M; Krebs, P; Kloos, DU; Wieacker, P; Elsner, J; Mohnike, K
      Familial occurrence of a del(Xp-) chromosome: Pitfall in karyotype/phenotype correlation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    31. VARON R; VISSINGA C; PLATZER M; CEROSALETTI KM; CHRZANOWSKA KH; SAAR K; BECKMANN G; SEEMANOVA E; COOPER PR; NOWAK NJ; STUMM M; WEEMAES CMR; GATTI RA; WILSON RK; DIGWEED M; ROSENTHAL A; SPERLING K; CONCANNON P; REIS A
      NIBRIN, A NOVEL DNA DOUBLE-STRAND BREAK REPAIR PROTEIN, IS MUTATED INNIJMEGEN BREAKAGE SYNDROME

      Cell
    32. DIECK ST; SANMARTIVILA L; LANGNAESE K; RICHTER K; KINDLER S; SOYKE A; WEX H; SMALLA KH; KAMPF U; FRANZER JT; STUMM M; GARNER CC; GUNDELFINGER ED
      BASSOON, A NOVEL ZINC-FINGER CAG GLUTAMINE-REPEAT PROTEIN SELECTIVELYLOCALIZED AT THE ACTIVE ZONE OF PRESYNAPTIC NERVE-TERMINALS/

      The Journal of cell biology
    33. KRIEGER O; STUMM M
      HFS - A PERFORMANCE-ORIENTED FLEXIBLE FILE SYSTEM BASED ON BUILDING-BLOCK COMPOSITIONS

      ACM transactions on computer systems
    34. ANTOCCIA A; RICORDY R; STUMM M; TANZARELLA C
      X-RAY-INDUCED P53 ACCUMULATION, G1 S-BLOCK AND CHROMOSOMAL DAMAGE IN NIJMEGEN BREAKAGE SYNDROME CELLS/

      European journal of cell biology
    35. MERTSALOV IB; STUMM M; WIEACKER P; DIECK ST; GUNDELFINGER E; TSETLIN VI
      THE STRUCTURE AND CHROMOSOMAL LOCALIZATIO N OF THE HUMAN NEUROGRANIN GENE

      Bioorganiceskaa himia
    36. BIRKENHAKE S; NEUBAUER S; STUMM M; DUNST J; GEBHART E; SAUER R
      INCREASED RADIOSENSITIVITY IN ATAXIA-TELANGIECTASIA PATIENTS (A-T), A-T HETEROZYGOTES AND CANCER-PATIENTS

      Radiology
    37. SRBLJIC S; VRANESIC ZG; STUMM M; BUDIN L
      ANALYTICAL PREDICTION OF PERFORMANCE FOR CACHE COHERENCE PROTOCOLS

      I.E.E.E. transactions on computers
    38. KULKARNI D; STUMM M
      LINEAR AND EXTENDED LINEAR TRANSFORMATIONS FOR SHARED-MEMORY MULTIPROCESSORS

      Computer journal
    39. CHRZANOWSKA K; STUMM M; BIALECKA M; SAAR K; BERNATOWSKAMATUSZKIEWICZ E; MICHALKIEWICZ J; BARSZCZ S; REIS A; WEGNER RD
      LINKAGE STUDIES EXCLUDE THE AT-V GENE(S) FROM THE TRANSLOCATION BREAKPOINTS IN AN AT-V PATIENT

      Clinical genetics
    40. STUMM M; SPERLING K; WEGNER RD
      NONCOMPLEMENTATION OF RADIATION-INDUCED CHROMOSOME-ABERRATIONS IN ATAXIA-TELANGIECTASIA ATAXIA-TELANGIECTASIA-VARIANT HETERODIKARYONS/

      American journal of human genetics
    41. SAAR K; CHRZANOWSKA KH; STUMM M; JUNG M; NURNBERG G; WIENKER TF; SEEMANOVA E; WEGNER RD; REIS A; SPERLING K
      THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21

      American journal of human genetics
    42. RAVINDRAN G; STUMM M
      A COMPARISON OF BLOCKING AND NONBLOCKING PACKET-SWITCHING TECHNIQUES IN HIERARCHICAL RING NETWORKS

      IEICE transactions on information and systems
    43. WEGNER RD; SCHROCK E; OBLADEN M; BECKER R; STUMM M; SPERLING K
      PARTIAL TRISOMY MONOSOMY 6Q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE/

      Prenatal diagnosis
    44. UNRAU RC; KRIEGER O; GAMSA B; STUMM M
      HIERARCHICAL-CLUSTERING - A STRUCTURE FOR SCALABLE MULTIPROCESSOR OPERATING SYSTEM-DESIGN

      Journal of supercomputing
    45. FARKAS K; VRANESIC Z; STUMM M
      SCALABLE CACHE CONSISTENCY FOR HIERARCHICALLY STRUCTURED MULTIPROCESSORS

      Journal of supercomputing
    46. SCHUFFENHAUER S; BARTSCH O; STUMM M; BUCHHOLZ T; PETROPOULOU T; KRAFT S; BELOHRADSKY B; HINKEL GK; MEITINGER T; WEGNER RD
      DNA, FISH AND COMPLEMENTATION STUDIES IN ICF SYNDROME - DNA HYPOMETHYLATION OF REPETITIVE AND SINGLE-COPY LOCI AND EVIDENCE FOR A TRANS-ACTING FACTOR

      Human genetics
    47. STUMM M; GATTI RA; REIS A; UDAR N; CHRZANOWSKA K; SEEMANOVA E; SPERLING K; WEGNER RD
      THE ATAXIA-TELANGIECTASIA-VARIANT GENE-1 AND GENE-2 ARE DISTINCT FROMTHE ATAXIA-TELANGIECTASIA GENE ON CHROMOSOME-11Q23.1

      American journal of human genetics
    48. HOLLIDAY M; STUMM M
      PERFORMANCE EVALUATION OF HIERARCHICAL RING-BASED SHARED-MEMORY MULTIPROCESSORS

      I.E.E.E. transactions on computers
    49. KRIEGER O; STUMM M; UNRAU R
      THE ALLOC STREAM FACILITY - A REDESIGN OF APPLICATION-LEVEL STREAM I O/

      Computer


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 19:24:12