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Results 1 to 25 of 41

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Resistance of pseudomonas strains of formaldehydeSCHNITTGER, S.SÖFW. Seifen, Öle, Fette, Wachse. 1991, Vol 117, Num 9, pp 335-336, issn 0173-5500, 2 p.Article

Simulation des verkehrsflusses in Fernstrassennetzen unter Beachtung des Kraftstoffverbrauchs, der Abgaswerte und der Reisezeit = Traffic flow simulation on trunk road networks taking fuel consumption, exhaust gas levels and travel time into considerationLEUTZBACH, W; SCHNITTGER, S.Forschung Strassenbau und Strassenverkehrstechnik. 1988, Num 559, issn 0344-0788, 109 p.Serial Issue

Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemiaSCHNITTGER, S; BACHER, U; KERN, W et al.Leukemia. 2011, Vol 25, Num 8, pp 1297-1304, issn 0887-6924, 8 p.Article

NPM1-mutated acute myeloid leukaemia occurring in JAK2-V617F+ primary myelofibrosis : de-novo origin?PASQUALUCCI, L; LI, S; HAFERLACH, T et al.Leukemia. 2008, Vol 22, Num 7, pp 1459-1463, issn 0887-6924, 5 p.Article

Identification of additional cytogenetic and molecular genetic abnormalities in acute myeloid leukaemia with t(8;21)/AML1-ETOKUCHENBAUER, F; SCHNITTGER, S; LOOK, T et al.British journal of haematology. 2006, Vol 134, Num 6, pp 616-619, issn 0007-1048, 4 p.Article

Partial tandem duplications of the MLL gene are detectable in peripheral blood and bone marrow of nearly all healthy donorsSCHNITTGER, S; WÖRMANN, B; HIDDEMANN, W et al.Blood. 1998, Vol 92, Num 5, pp 1728-1734, issn 0006-4971Article

Regional sublocalization of the human CD69 gene to chromosome bands 12p12.3-p13.2, the predicted region of the human natural killer cell gene complexSCHNITTGER, S; HAMANN, J; DANNENBERG, C et al.European journal of immunology. 1993, Vol 23, Num 10, pp 2711-2713, issn 0014-2980Article

The quality of molecular response to chemotherapy is predictive for the outcome of AML 1-ETO-positive AML and is independent of pretreatment risk factorsWEISSER, M; HAFERLACH, C; HIDDEMANN, W et al.Leukemia. 2007, Vol 21, Num 6, pp 1177-1182, issn 0887-6924, 6 p.Article

A new polymorphic DNA probe pS43 derived from a flow sorted library is assigned to human chromosome 20q13SCHNITTGER, S; BEERMANN, F; HANSMANN, I et al.Human genetics. 1989, Vol 81, Num 4, pp 391-392, issn 0340-6717Article

Assignment of the human histone deacetylase 4 gene (HDAC4) to chromosome 2q37.2 by in situ hybridizationMAHLKNECHT, U; SCHNITTGER, S; HOELZER, D et al.Cytogenetics and cell genetics. 2001, Vol 93, Num 1-2, pp 137-138, issn 0301-0171Article

Interactive diagnostics in the indication to allogeneic SCT in AMLBACHER, U; HAFERLACH, C; SCHNITTGER, S et al.Bone marrow transplantation (Basingstoke). 2009, Vol 43, Num 10, pp 745-756, issn 0268-3369, 12 p.Article

High dose ara-C in the treatment of newly diagnosed acute promyelocytic leukemia: long-term results of the German AMLCGLENGFELDER, E; HAFERLACH, C; KERN, W et al.Leukemia. 2009, Vol 23, Num 12, pp 2248-2258, issn 0887-6924, 11 p.Article

New insights into MLL gene rearranged acute leukemias using gene expression profiling : shared pathways, lineage commitment, and partner genesKOHLMANN, A; SCHOCH, C; DUGAS, M et al.Leukemia. 2005, Vol 19, Num 6, pp 953-964, issn 0887-6924, 12 p.Article

Mapping of leukaemia-associated breakpoints in chromosome band 3q21 using a newly established PAC contigWIESER, R; VOLZ, A; SCHNITTGER, S et al.British journal of haematology. 2000, Vol 110, Num 2, pp 343-350, issn 0007-1048Article

Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26SCHNITTGER, S; DE SAUVAGE, F. J; LE PASLIER, D et al.Leukemia. 1996, Vol 10, Num 12, pp 1891-1896, issn 0887-6924Article

Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2SCHNITTGER, S; GOPAL RAO, V. V. N; ABRAHAMSON, M et al.Genomics (San Diego, Calif.). 1993, Vol 16, Num 1, pp 50-55, issn 0888-7543Article

A sterile male with 45,X0 and a Y;22 translocationARNEMANN, J; SCHNITTGER, S; HINKEL, G. K et al.Human genetics. 1991, Vol 87, Num 2, pp 134-138, issn 0340-6717Article

Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA librarySTOLZ, F.-M; PFAU, H.-P; REIPEN, G et al.Genomics (San Diego, Calif.). 1991, Vol 11, Num 4, pp 948-955, issn 0888-7543Article

Landscape of TET2 mutations in acute myeloid leukemiaWEISSMANN, S; ALPERMANN, T; KERN, W et al.Leukemia. 2012, Vol 26, Num 5, pp 934-942, issn 0887-6924, 9 p.Article

The inv(3)(q21q26)/t(3;3)(q21;q26) is frequently accompanied by alterations of the RUNX1, KRAS and NRAS and NF1 genes and mediates adverse prognosis both in MDS and in AML: a study in 39 cases of MDS or AMLHAFERLACH, C; BACHER, U; HAFERLACH, T et al.Leukemia. 2011, Vol 25, Num 5, pp 874-877, issn 0887-6924, 4 p.Article

Development of standardized approaches to reporting of minimal residual disease data using a reporting software package designed within the European LeukemiaNetØSTERGAARD, M; NYVOLD, C. G; SCHNITTGER, S et al.Leukemia. 2011, Vol 25, Num 7, pp 1168-1173, issn 0887-6924, 6 p.Article

AML with CBFB-MYH11 rearrangement demonstrate RAS pathway alterations in 92% of all cases including a high frequency of NF1 deletionsHAFERLACH, C; DICKER, F; KOHLMANN, A et al.Leukemia. 2010, Vol 24, Num 5, pp 1065-1069, issn 0887-6924, 5 p.Article

Rare CBFB-MYH11 fusion transcripts in AML with inv(16)/t(16;16) are associated with therapy-related AML M4eo, atypical cytomorphology, atypical immunophenotype, atypical additional chromosomal rearrangements and low white blood cell count : a study on 162 patientsSCHNITTGER, S; BACHER, U; HAFERLACH, C et al.Leukemia. 2007, Vol 21, Num 4, pp 725-731, issn 0887-6924, 7 p.Article

The MLL recombinome of acute leukemiasMEYER, C; SCHNEIDER, B; PIETERS, R et al.Leukemia. 2006, Vol 20, Num 5, pp 777-784, issn 0887-6924, 8 p.Article

Assignment of the human histone deacetylase 6 gene (HDAC6) to X chromosome p11.23 by in situ hybridizationMAHLKNECHT, U; SCHNITTGER, S; LANDGRAF, F et al.Cytogenetics and cell genetics. 2001, Vol 93, Num 1-2, pp 135-136, issn 0301-0171Article

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