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Results: 1-25 | 26-27
Results: 1-25/27
FLUORESCENCE IN-SITU HYBRIDIZATION CHARACTERIZATION OF THE CHROMOSOMAL BREAKPOINTS IN A CASE WITH INS(17-3) (Q11.2-Q21Q26.3) AND ACUTE MONOCYTIC LEUKEMIA
Authors: SCHNITTGER S JOACHIMMAYER E SCHOCH C FUCHS R FONATSCH C
Citation: S. Schnittger et al., FLUORESCENCE IN-SITU HYBRIDIZATION CHARACTERIZATION OF THE CHROMOSOMAL BREAKPOINTS IN A CASE WITH INS(17-3) (Q11.2-Q21Q26.3) AND ACUTE MONOCYTIC LEUKEMIA, Cancer genetics and cytogenetics, 106(2), 1998, pp. 122-127
CELL LINEAGE-SPECIFIC INVOLVEMENT IN ACUTE-PROMYELOCYTIC-LEUKEMIA (APL) USING A COMBINATION OF MAY-GRUNWALD-GIEMSA STAINING AND FLUORESCENCE IN-SITU HYBRIDIZATION TECHNIQUES FOR THE DETECTION OF THE TRANSLOCATION T(15-17)(Q22-Q12)
Authors: HAFERLACH T LOFFLER H NICKENIG C RAMMPETERSEN L MEEDER M SCHOCH R SCHLEGELBERGER B SCHNITTGER S SCHOCH C HIDDEMANN W
Citation: T. Haferlach et al., CELL LINEAGE-SPECIFIC INVOLVEMENT IN ACUTE-PROMYELOCYTIC-LEUKEMIA (APL) USING A COMBINATION OF MAY-GRUNWALD-GIEMSA STAINING AND FLUORESCENCE IN-SITU HYBRIDIZATION TECHNIQUES FOR THE DETECTION OF THE TRANSLOCATION T(15-17)(Q22-Q12), British Journal of Haematology, 103(1), 1998, pp. 93-99
AML1-ETO FUSION TRANSCRIPTS ARE SPECIFICALLY ASSOCIATED WITH T(8-21)(Q22-Q22) AND AML M1 AND M2
Authors: SCHNITTGER S STICHWEH S KINKELIN U SCHOCH C HAASE D WORMANN B BUCHNER T LOFFLER H HAFERLACH T HIDDEMANN W
Citation: S. Schnittger et al., AML1-ETO FUSION TRANSCRIPTS ARE SPECIFICALLY ASSOCIATED WITH T(8-21)(Q22-Q22) AND AML M1 AND M2, British Journal of Haematology, 102(1), 1998, pp. 32-32
MLL-TANDEM DUPLICATIONS CAN BE FOUND IN THE HEMATOPOIESIS OF ALMOST-ALL HEALTHY-INDIVIDUALS
Authors: SCHNITTGER S WORMANN B HIDDEMANN W GRIESINGER F
Citation: S. Schnittger et al., MLL-TANDEM DUPLICATIONS CAN BE FOUND IN THE HEMATOPOIESIS OF ALMOST-ALL HEALTHY-INDIVIDUALS, British Journal of Haematology, 102(1), 1998, pp. 277-277
PARTIAL TANDEM DUPLICATIONS OF THE MLL GENE ARE DETECTABLE IN PERIPHERAL-BLOOD AND BONE-MARROW OF NEARLY ALL HEALTHY DONORS
Authors: SCHNITTGER S WORMANN B HIDDEMANN WG GRIESINGER F
Citation: S. Schnittger et al., PARTIAL TANDEM DUPLICATIONS OF THE MLL GENE ARE DETECTABLE IN PERIPHERAL-BLOOD AND BONE-MARROW OF NEARLY ALL HEALTHY DONORS, Blood, 92(5), 1998, pp. 1728-1734
A CASE OF ATYPICAL MYELODYSPLASTIC SYNDROME WITH MICROMEGAKARYOCYTES,NORMAL PLATELET COUNT, AND T(3-12)(Q21-P13) WITH INV(3)(Q21Q26)
Authors: SCHNITTGER S SCHOCH C STREUBEL B HINRICHS HF OTREMBA B PARWARESCH R FONATSCH C
Citation: S. Schnittger et al., A CASE OF ATYPICAL MYELODYSPLASTIC SYNDROME WITH MICROMEGAKARYOCYTES,NORMAL PLATELET COUNT, AND T(3-12)(Q21-P13) WITH INV(3)(Q21Q26), Genes, chromosomes & cancer, 20(3), 1997, pp. 292-298
LEUKEMIA BREAKPOINT REGION IN 3Q21 IS GENE RICH
Authors: RYNDITCH A PEKARSKY Y SCHNITTGER S GARDINER K
Citation: A. Rynditch et al., LEUKEMIA BREAKPOINT REGION IN 3Q21 IS GENE RICH, Gene, 193(1), 1997, pp. 49-57
CHARACTERIZATION, MAPPING AND PARTIAL CDNA SEQUENCE OF THE 57-KD INTRACELLULAR KI-1 ANTIGEN
Authors: KOBARG J SCHNITTGER S FONATSCH C LEMKE H BOWEN MA BUCK F HANSEN HP
Citation: J. Kobarg et al., CHARACTERIZATION, MAPPING AND PARTIAL CDNA SEQUENCE OF THE 57-KD INTRACELLULAR KI-1 ANTIGEN, Experimental and clinical immunogenetics, 14(4), 1997, pp. 273-280
SIGNIFICANT ASSOCIATION OF ABERRANT CD13 COEXPRESSION WITH TEL-AML-1 POSITIVE CHILDHOOD C-ALL
Authors: GRIESINGER F RENZIEHAUSEN A SCHNITTGER S RITTER J LUDWIG WD HIDDEMANN W WORMANN B
Citation: F. Griesinger et al., SIGNIFICANT ASSOCIATION OF ABERRANT CD13 COEXPRESSION WITH TEL-AML-1 POSITIVE CHILDHOOD C-ALL, Blood, 90(10), 1997, pp. 3592-3592
GENOMIC DELETION OF EXON-8 OF THE MLL-GENE IS A RARE EVENT IN T-ALL AND DOES NOT REPRESENT A SUITABLE GENETIC-MARKER FOR MRD-STUDIES
Authors: GRIESINGER F KAUL S RENZIEHAUSEN A PODLESCHNY M SCHNITTGER S HIDDEMANN W WORMANN B
Citation: F. Griesinger et al., GENOMIC DELETION OF EXON-8 OF THE MLL-GENE IS A RARE EVENT IN T-ALL AND DOES NOT REPRESENT A SUITABLE GENETIC-MARKER FOR MRD-STUDIES, Blood, 90(10), 1997, pp. 3693-3693
UNUSUAL MLL-EXON5 AF4-EXON7 FUSION GENE IN INFANT PRE-PRE-B-ALL - SIGNIFICANCE FOR PRIMER SELECTION AND PATHOGENETIC MECHANISM OF MLL-AF4 FUSION TRANSCRIPTS/
Authors: SCHNITTGER S HIDDEMANN W WORMANN B GRIESINGER F
Citation: S. Schnittger et al., UNUSUAL MLL-EXON5 AF4-EXON7 FUSION GENE IN INFANT PRE-PRE-B-ALL - SIGNIFICANCE FOR PRIMER SELECTION AND PATHOGENETIC MECHANISM OF MLL-AF4 FUSION TRANSCRIPTS/, Blood, 90(10), 1997, pp. 3733-3733
PARTIAL TANDEM DUPLICATION WITHIN THE MLL-GENE IN THE NORMAL POPULATION
Authors: SCHNITTGER S HIDDEMANN W WORMANN B GRIESINGER F
Citation: S. Schnittger et al., PARTIAL TANDEM DUPLICATION WITHIN THE MLL-GENE IN THE NORMAL POPULATION, Blood, 90(10), 1997, pp. 185-185
CELL LINEAGE-SPECIFIC INVOLVEMENT IN ACUTE PROMYELOCYTIC LEUKEMIA (APL) USING A COMBINATION OF MAY-GRUNWALD-GIEMSA STAINING AND FLUORESCENCE IN-SITU HYBRIDIZATION TECHNIQUES FOR THE DETECTION OF THE TRANSLOCATION T(15-17)
Authors: HAFERLACH T LOFFLER H NICKENIG C RAMMPETERSEN L MEEDER M SCHOCH R SCHLEGELBERGER B SCHNITTGER S SCHOCH C HIDDEMANN W
Citation: T. Haferlach et al., CELL LINEAGE-SPECIFIC INVOLVEMENT IN ACUTE PROMYELOCYTIC LEUKEMIA (APL) USING A COMBINATION OF MAY-GRUNWALD-GIEMSA STAINING AND FLUORESCENCE IN-SITU HYBRIDIZATION TECHNIQUES FOR THE DETECTION OF THE TRANSLOCATION T(15-17), Blood, 90(10), 1997, pp. 291-291
SCREENING FOR PARTIAL TANDEM DUPLICATION WITHIN THE MLL-GENE IN PATIENTS WITH ACUTE MYELOID-LEUKEMIA
Authors: SCHNITTGER S KINKELIN U SCHOCH C HAASE D HAFERLACH T LOFFLER H WORMANN B HIDDEMANN W GRIESINGER F
Citation: S. Schnittger et al., SCREENING FOR PARTIAL TANDEM DUPLICATION WITHIN THE MLL-GENE IN PATIENTS WITH ACUTE MYELOID-LEUKEMIA, Blood, 90(10), 1997, pp. 2482-2482
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 3Q26
Authors: SCHNITTGER S DESAUVAGE FJ LEPASLIER D FONATSCH C
Citation: S. Schnittger et al., 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 3Q26, Leukemia, 10(12), 1996, pp. 1891-1896
DIC(9-20) - A NEW RECURRENT CHROMOSOME ABNORMALITY IN ADULT ACUTE LYMPHOBLASTIC-LEUKEMIA
Authors: RIEDER H SCHNITTGER S BODENSTEIN H SCHWONZEN M WORMANN B BERKOVIC D LUDWIG WD HOELZER D FONATSCH C
Citation: H. Rieder et al., DIC(9-20) - A NEW RECURRENT CHROMOSOME ABNORMALITY IN ADULT ACUTE LYMPHOBLASTIC-LEUKEMIA, Genes, chromosomes & cancer, 13(1), 1995, pp. 54-61
YEAST ARTIFICIAL CHROMOSOME MAPPING AND FISH MAPPING OF 3Q
Authors: SCHNITTGER S
Citation: S. Schnittger, YEAST ARTIFICIAL CHROMOSOME MAPPING AND FISH MAPPING OF 3Q, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 142-142
LOCALIZATION OF THE UNDULIN GENE (UND) TO HUMAN-CHROMOSOME BAND 8Q23
Authors: SCHNITTGER S HERBST H SCHUPPAN D DANNENBERG C BAUER M FONATSCH C
Citation: S. Schnittger et al., LOCALIZATION OF THE UNDULIN GENE (UND) TO HUMAN-CHROMOSOME BAND 8Q23, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 233-234
MAPPING OF THE MALIGNANT HYPERTHERMIA SUSCEPTIBILITY (MHS) REGION ON CHROMOSOME 3Q13.1
Authors: SUDBRAK R MULLER CR SCHNITTGER S WEISSENBACH J DEUFEL T
Citation: R. Sudbrak et al., MAPPING OF THE MALIGNANT HYPERTHERMIA SUSCEPTIBILITY (MHS) REGION ON CHROMOSOME 3Q13.1, American journal of human genetics, 57(4), 1995, pp. 1173-1173
CORRELATION OF CYTOGENETIC FINDINGS WITH CLINICAL-FEATURES IN 18 PATIENTS WITH INV(3)(Q21Q26) OR T(3,3)(Q21,Q26)
Authors: FONATSCH C GUDAT H LENGFELDER E WANDT H SILLINGENGELHARDT G LUDWIG WD THIEL E FREUND M BODENSTEIN H SCHWIEDER G GRUNEISEN A AUL C SCHNITTGER S RIEDER H HAASE D HILD F
Citation: C. Fonatsch et al., CORRELATION OF CYTOGENETIC FINDINGS WITH CLINICAL-FEATURES IN 18 PATIENTS WITH INV(3)(Q21Q26) OR T(3,3)(Q21,Q26), Leukemia, 8(8), 1994, pp. 1318-1326
THE HUMAN VIGILIN GENE - IDENTIFICATION, CHROMOSOMAL LOCALIZATION ANDEXPRESSION PATTERN
Authors: PLENZ G KUGLER S SCHNITTGER S RIEDER H FONATSCH C MULLER PK
Citation: G. Plenz et al., THE HUMAN VIGILIN GENE - IDENTIFICATION, CHROMOSOMAL LOCALIZATION ANDEXPRESSION PATTERN, Human genetics, 93(5), 1994, pp. 575-582
PHYSICAL MAPPING OF YAC CONTIGS FROM 3Q
Authors: SCHNITTGER S MIRGHOMIZADEH F RIEDER H DANNENBERG C FONATSCH C
Citation: S. Schnittger et al., PHYSICAL MAPPING OF YAC CONTIGS FROM 3Q, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 44-45
THE HUMAN OX40 HOMOLOG - CDNA STRUCTURE, EXPRESSION AND CHROMOSOMAL ASSIGNMENT OF THE ACT35 ANTIGEN
Authors: LATZA U DURKOP H SCHNITTGER S RINGELING J EITELBACH F HUMMEL M FONATSCH C STEIN H
Citation: U. Latza et al., THE HUMAN OX40 HOMOLOG - CDNA STRUCTURE, EXPRESSION AND CHROMOSOMAL ASSIGNMENT OF THE ACT35 ANTIGEN, European Journal of Immunology, 24(3), 1994, pp. 677-683
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-20P11.2 (VOL 16, PG 50, 1993)
Authors: SCHNITTGER S RAO VVNG ABRAHAMSON M HANSMANN I
Citation: S. Schnittger et al., 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-20P11.2 (VOL 16, PG 50, 1993), Genomics, 17(2), 1993, pp. 533-533
REGIONAL SUBLOCALIZATION OF THE HUMAN CD69 GENE TO CHROMOSOME BANDS 12P12.3-P13.2, THE PREDICTED REGION OF THE HUMAN NATURAL-KILLER-CELL GENE-COMPLEX
Authors: SCHNITTGER S HAMANN J DANNENBERG C FIEBIG H STRAUSS M FONATSCH C
Citation: S. Schnittger et al., REGIONAL SUBLOCALIZATION OF THE HUMAN CD69 GENE TO CHROMOSOME BANDS 12P12.3-P13.2, THE PREDICTED REGION OF THE HUMAN NATURAL-KILLER-CELL GENE-COMPLEX, European Journal of Immunology, 23(10), 1993, pp. 2711-2713
Risultati: 1-25 | 26-27