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Results: 1-7 |
Results: 7
MOLECULAR-CLONING OF THE BREAKPOINTS OF THE HEREDITARY PERSISTENCE OFFETAL HEMOGLOBIN TYPE-6 (HPFH-6) DELETION AND SEQUENCE-ANALYSIS OF THE NOVEL JUXTAPOSED REGION FROM THE 3'-END OF THE BETA-GLOBIN GENE-CLUSTER
Authors: KOSTEAS T PALENA A ANAGNOU NP
Citation: T. Kosteas et al., MOLECULAR-CLONING OF THE BREAKPOINTS OF THE HEREDITARY PERSISTENCE OFFETAL HEMOGLOBIN TYPE-6 (HPFH-6) DELETION AND SEQUENCE-ANALYSIS OF THE NOVEL JUXTAPOSED REGION FROM THE 3'-END OF THE BETA-GLOBIN GENE-CLUSTER, Human genetics, 100(3-4), 1997, pp. 441-445
STRUCTURAL AND FUNCTIONAL-ANALYSIS OF 2 DEVELOPMENTAL MUTANTS WITH DISCRETE PHENOTYPES USING CHROMOSOME MEDIATED GENE-TRANSFER
Authors: KOSTEAS T PALENA A PAPAYANNOPOULOU T ANAGNOU NP
Citation: T. Kosteas et al., STRUCTURAL AND FUNCTIONAL-ANALYSIS OF 2 DEVELOPMENTAL MUTANTS WITH DISCRETE PHENOTYPES USING CHROMOSOME MEDIATED GENE-TRANSFER, Blood, 90(10), 1997, pp. 566-566
YY1 BINDS TO MULTIPLE SITES OF A SILENCER ELEMENT LOCATED 1.6 KB 3' TO THE FETAL AY-GLOBIN GENE
Authors: SOULTANAS P KOSTEAS T ANAGNOU NP
Citation: P. Soultanas et al., YY1 BINDS TO MULTIPLE SITES OF A SILENCER ELEMENT LOCATED 1.6 KB 3' TO THE FETAL AY-GLOBIN GENE, Blood, 88(10), 1996, pp. 577-577
THE MOLECULAR-BASIS FOR THE PHENOTYPIC DIFFERENCES BETWEEN DELTA-BETA-THALASSEMIA AND HPFH - THE ROLE OF THE 2 SILENCERS UPSTREAM OF THE DELTA-GLOBIN GENE
Authors: KOSTEAS T MOSCHONAS N ANAGNOU NP
Citation: T. Kosteas et al., THE MOLECULAR-BASIS FOR THE PHENOTYPIC DIFFERENCES BETWEEN DELTA-BETA-THALASSEMIA AND HPFH - THE ROLE OF THE 2 SILENCERS UPSTREAM OF THE DELTA-GLOBIN GENE, Blood, 88(10), 1996, pp. 587-587
COMPLETE SEQUENCING AND FUNCTIONAL-ANALYSIS OF THE HPFH-6 ENHANCER - DETECTION OF MULTIPLE MOTIFS FOR TRANSCRIPTION FACTORS AND IDENTIFICATION OF AN OPEN READING FRAME
Authors: KOSTEAS T PAVLOU O PALENA A MOSCHONAS N ANAGNOU NP
Citation: T. Kosteas et al., COMPLETE SEQUENCING AND FUNCTIONAL-ANALYSIS OF THE HPFH-6 ENHANCER - DETECTION OF MULTIPLE MOTIFS FOR TRANSCRIPTION FACTORS AND IDENTIFICATION OF AN OPEN READING FRAME, Blood, 88(10), 1996, pp. 588-588
SEQUENCES LOCATED 3' TO THE BREAKPOINT OF THE HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN-3 DELETION EXHIBIT ENHANCER ACTIVITY AND CAN MODIFY THE DEVELOPMENTAL EXPRESSION OF THE HUMAN FETAL A-GAMMA-GLOBIN GENE IN TRANSGENIC MICE
Authors: ANAGNOU NP PEREZSTABLE C GELINAS R COSTANTINI F LIAPAKI K CONSTANTOPOULOU M KOSTEAS T MOSCHONAS NK STAMATOYANNOPOULOS G
Citation: Np. Anagnou et al., SEQUENCES LOCATED 3' TO THE BREAKPOINT OF THE HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN-3 DELETION EXHIBIT ENHANCER ACTIVITY AND CAN MODIFY THE DEVELOPMENTAL EXPRESSION OF THE HUMAN FETAL A-GAMMA-GLOBIN GENE IN TRANSGENIC MICE, The Journal of biological chemistry, 270(17), 1995, pp. 10256-10263
FUNCTIONAL-ANALYSIS OF THE A-GAMMA-TO-SIGMA-GLOBIN GENE REGION OF THEBETA-CLUSTER - EVIDENCE FOR MULTIPLE NEGATIVE REGULATORY ELEMENTS
Authors: KOSTEAS T MANIFAVA M MOSCHONAS N ANAGNOU NP
Citation: T. Kosteas et al., FUNCTIONAL-ANALYSIS OF THE A-GAMMA-TO-SIGMA-GLOBIN GENE REGION OF THEBETA-CLUSTER - EVIDENCE FOR MULTIPLE NEGATIVE REGULATORY ELEMENTS, Blood, 84(10), 1994, pp. 10000506-10000506
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