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Results: 1-25 | 26-44 |
Results: 26-44/44
NARROWING THE CRITICAL DELETED REGION IN THE 5Q-SYNDROME
Authors: JAJU RJ BOULTWOOD J FIDLER C SHERIDAN H OLIVER F WALKER H PARKER N KOSTRZEWA M MUELLER U WAINSCOAT JS KEARNEY L
Citation: Rj. Jaju et al., NARROWING THE CRITICAL DELETED REGION IN THE 5Q-SYNDROME, Blood, 88(10), 1996, pp. 1467-1467
CHARACTERIZATION OF A T(10-11)(P13-14-Q14-21) IN THE MONOBLASTIC CELL-LINE U937
Authors: SHIPLEY J WILLIAMS S OBYRNE A KEARNEY L JONES T YOUNG B DYER M CATOVSKY D SHEER D GUSTERSON B
Citation: J. Shipley et al., CHARACTERIZATION OF A T(10-11)(P13-14-Q14-21) IN THE MONOBLASTIC CELL-LINE U937, Genes, chromosomes & cancer, 13(2), 1995, pp. 138-142
PHYSICAL MAPPING OF THE HUMAN T-CELL ANTIGEN RECEPTOR BETA-GENE COMPLEX USING YEAST ARTIFICIAL CHROMOSOMES
Authors: HASHIM Y RAGOUSSIS I KEARNEY L TOSI S SO AK
Citation: Y. Hashim et al., PHYSICAL MAPPING OF THE HUMAN T-CELL ANTIGEN RECEPTOR BETA-GENE COMPLEX USING YEAST ARTIFICIAL CHROMOSOMES, Cytogenetics and cell genetics, 71(1), 1995, pp. 24-25
CHARACTERIZATION OF 7Q ABNORMALITIES IN THE HUMAN MYELOID-LEUKEMIA CELL-LINE GFD8 BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)
Authors: TOSI S SCHERER SW RAMBALDI A HASHIM Y WAINSCOAT JS OSBORNE L BIONDI A TSUI LC KEARNEY L
Citation: S. Tosi et al., CHARACTERIZATION OF 7Q ABNORMALITIES IN THE HUMAN MYELOID-LEUKEMIA CELL-LINE GFD8 BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH), Cytogenetics and cell genetics, 71(1), 1995, pp. 28-28
INTERPHASE CYTOGENETICS OF THE T(8-21)(Q22-Q22) ASSOCIATED WITH ACUTEMYELOGENOUS LEUKEMIA BY 2-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: SACCHI N MAGNANI I KEARNEY L WIJSMAN T HAGEMEIJER A DARFLER M
Citation: N. Sacchi et al., INTERPHASE CYTOGENETICS OF THE T(8-21)(Q22-Q22) ASSOCIATED WITH ACUTEMYELOGENOUS LEUKEMIA BY 2-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION, Cancer genetics and cytogenetics, 79(2), 1995, pp. 97-103
CLINICAL AND HEMATOLOGIC ASPECTS OF THE X-LINKED ALPHA-THALASSEMIA MENTAL-RETARDATION SYNDROME (ATR-X)
Authors: GIBBONS RJ BRUETON L BUCKLE VJ BURN J CLAYTONSMITH J DAVISON BCC GARDNER RJM HOMFRAY T KEARNEY L KINGSTON HM NEWBURYECOB R PORTEOUS MEP WILKIE AOM HIGGS DR
Citation: Rj. Gibbons et al., CLINICAL AND HEMATOLOGIC ASPECTS OF THE X-LINKED ALPHA-THALASSEMIA MENTAL-RETARDATION SYNDROME (ATR-X), American journal of medical genetics, 55(3), 1995, pp. 288-299
PHYSICAL MAPPING OF THE HUMAN T-CELL RECEPTOR-BETA GENE-COMPLEX, USING YEAST ARTIFICIAL CHROMOSOMES
Authors: HASHIM Y RAGOUSSIS I KEARNEY L TOSI S SO AK
Citation: Y. Hashim et al., PHYSICAL MAPPING OF THE HUMAN T-CELL RECEPTOR-BETA GENE-COMPLEX, USING YEAST ARTIFICIAL CHROMOSOMES, Immunogenetics, 41(6), 1995, pp. 337-342
CHARACTERIZATION AND VARIATION OF A HUMAN INWARDLY-RECTIFYING K-CHANNEL GENE (KCNJ6) - A PUTATIVE ATP-SENSITIVE K-CHANNEL SUBUNIT
Authors: SAKURA H BOND C WARRENPERRY M HORSLEY S KEARNEY L TUCKER S ADELMAN J TURNER R ASHCROFT FM
Citation: H. Sakura et al., CHARACTERIZATION AND VARIATION OF A HUMAN INWARDLY-RECTIFYING K-CHANNEL GENE (KCNJ6) - A PUTATIVE ATP-SENSITIVE K-CHANNEL SUBUNIT, FEBS letters, 367(2), 1995, pp. 193-197
MOLECULAR CYTOGENETIC ANALYSIS OF 7Q DELETIONS IN HEMATOLOGICAL MALIGNANCIES
Authors: TOSI S HARBOTT J HAAS QA DOUGLAS A HUGHES D ROSS F BIONDI A SCHERER SW KEARNEY L
Citation: S. Tosi et al., MOLECULAR CYTOGENETIC ANALYSIS OF 7Q DELETIONS IN HEMATOLOGICAL MALIGNANCIES, Blood, 86(10), 1995, pp. 2965-2965
ACUTE MYELOMONOCYTIC LEUKEMIA WITH T(10 11)(P 13Q23) - HETEROGENEITY OF BREAKPOINTS AT 11Q23 AND ASSOCIATION WITH RECOMBINASE ACTIVATION
Authors: HEIGHT SE DAINTON MG KEARNEY L SWANSBURY GJ MATUTES E DYER MJS TRELEAVEN JG POWLES RL CATOVSKY D
Citation: Se. Height et al., ACUTE MYELOMONOCYTIC LEUKEMIA WITH T(10 11)(P 13Q23) - HETEROGENEITY OF BREAKPOINTS AT 11Q23 AND ASSOCIATION WITH RECOMBINASE ACTIVATION, Genes, chromosomes & cancer, 11(2), 1994, pp. 136-139
FLUORESCENCE IN-SITU HYBRIDIZATION STUDIES TO CHARACTERIZE COMPLETE AND PARTIAL MONOSOMY-7 IN MYELOID DISORDERS
Authors: GIBBONS B LILLINGTON DM MONARD S YOUNG BD CHEUNG KL LISTER TA KEARNEY L
Citation: B. Gibbons et al., FLUORESCENCE IN-SITU HYBRIDIZATION STUDIES TO CHARACTERIZE COMPLETE AND PARTIAL MONOSOMY-7 IN MYELOID DISORDERS, Genes, chromosomes & cancer, 10(4), 1994, pp. 244-249
MOLECULAR-CLONING OF A NOVEL 11Q23 BREAKPOINT ASSOCIATED WITH NON-HODGKINS-LYMPHOMA
Authors: MEERABUX JM COTTER FE KEARNEY L NIZETIC D DHUT S GIBBONS B LISTER TA YOUNG BD
Citation: Jm. Meerabux et al., MOLECULAR-CLONING OF A NOVEL 11Q23 BREAKPOINT ASSOCIATED WITH NON-HODGKINS-LYMPHOMA, Oncogene, 9(3), 1994, pp. 893-898
A CASE OF ACUTE MONOCYTIC LEUKEMIA WITH T(1117) INVOLVING A REARRANGEMENT OF MLL-1 AND A REGION PROXIMAL TO THE RARA GENE
Authors: REEVES BR KEMPSKI H JANI K BORROW J HOWE K SOLOMON E KEARNEY L COTTER F
Citation: Br. Reeves et al., A CASE OF ACUTE MONOCYTIC LEUKEMIA WITH T(1117) INVOLVING A REARRANGEMENT OF MLL-1 AND A REGION PROXIMAL TO THE RARA GENE, Cancer genetics and cytogenetics, 74(1), 1994, pp. 50-53
THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16
Authors: WARD CJ PERAL B HUGHES J THOMAS S GAMBLE V MACCARTHY AB SLOANESTANLEY J BUCKLE VJ KEARNEY L HIGGS DR RATCLIFFE PJ HARRIS PC ROELFSEMA JH SPRUIT L SARIS JJ DAUWERSE HG PETERS DJM BREUNING MH NELLIST M BROOKCARTER PT MAHESHWAR MM CORDEIRO I SANTOS H CABRAL P SAMPSON JR JANSSEN B HESSELINGJANSSEN ALW VANDENOUWELAND AMW EUSSEN B VERHOEF S LINDHOUT D HALLEY DJJ
Citation: Cj. Ward et al., THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16, Cell, 77(6), 1994, pp. 881-894
UNTWIRLING DIRVISH
Authors: BUCKLE VJ KEARNEY L
Citation: Vj. Buckle et L. Kearney, UNTWIRLING DIRVISH, Nature genetics, 5(1), 1993, pp. 4-5
IN-SITU HYBRIDIZATION ANALYSIS OF A HOMOGENEOUSLY STAINING REGION AT 11Q23-24 IN AN ACUTE MYELOID-LEUKEMIA (M5) USING YEAST ARTIFICIAL CHROMOSOMES
Authors: NACHEVA E KEARNEY L BOWER M CHAPLIN T DOUEK E DAS S YOUNG BD
Citation: E. Nacheva et al., IN-SITU HYBRIDIZATION ANALYSIS OF A HOMOGENEOUSLY STAINING REGION AT 11Q23-24 IN AN ACUTE MYELOID-LEUKEMIA (M5) USING YEAST ARTIFICIAL CHROMOSOMES, Genes, chromosomes & cancer, 7(3), 1993, pp. 123-127
THE ISOLATION OF A YEAST ARTIFICIAL CHROMOSOME WHICH SPANS THE CHROMOSOME 11Q23 REGION INVOLVED IN A NUMBER OF TRANSLOCATIONS IN ACUTE LEUKEMIAS
Authors: BOWER M CHAPLIN T DAS S KEARNEY L GIBBONS B RILEY JH LISTER TA YOUNG BD
Citation: M. Bower et al., THE ISOLATION OF A YEAST ARTIFICIAL CHROMOSOME WHICH SPANS THE CHROMOSOME 11Q23 REGION INVOLVED IN A NUMBER OF TRANSLOCATIONS IN ACUTE LEUKEMIAS, Leukemia, 7, 1993, pp. 190000034-190000039
LEUKEMIA ARISING IN DONOR CELLS FOLLOWING ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR BETA-THALASSEMIA DEMONSTRATED BY IMMUNOLOGICAL, DNA AND MOLECULAR CYTOGENETIC ANALYSIS
Authors: KATZ F REEVES BR ALEXANDER S KEARNEY L CHESSELLS J
Citation: F. Katz et al., LEUKEMIA ARISING IN DONOR CELLS FOLLOWING ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR BETA-THALASSEMIA DEMONSTRATED BY IMMUNOLOGICAL, DNA AND MOLECULAR CYTOGENETIC ANALYSIS, British Journal of Haematology, 85(2), 1993, pp. 326-331
ACUTE MYELOMONOCYTIC LEUKEMIA WITH T(10-11)(P13-Q23) - HETEROGENEITY OF BREAKPOINTS INVOLVING 11Q23 AND ASSOCIATION WITH ACTIVATION OF RECOMBINASE
Authors: HEIGHT S DAINTON MG MATUTES E KEARNEY L SWANSBURY GJ DYER MJS ZELENT A TRELEAVEN JG POWLES R CATOVSKY D
Citation: S. Height et al., ACUTE MYELOMONOCYTIC LEUKEMIA WITH T(10-11)(P13-Q23) - HETEROGENEITY OF BREAKPOINTS INVOLVING 11Q23 AND ASSOCIATION WITH ACTIVATION OF RECOMBINASE, Blood, 82(10), 1993, pp. 10000035-10000035
Risultati: 1-25 | 26-44 |