Matches in Nanopublications for { ?s ?p "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP213106.RAAIr1kQ71zgNlJb7Ihb0W1E4sd5VpqaYoBTg2ZMwuLcY130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213106.RAAIr1kQ71zgNlJb7Ihb0W1E4sd5VpqaYoBTg2ZMwuLcY130_provenance.
- NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898145.RAqMWGV-NfKRNO9BasREq2boO8COFe8i3NYtLvWMDRMSM130_provenance.
- NP696984.RAnYPRDaqwt2_uYu2CZwOSEWPIkgpdgcd6ivvkz0-3HTE130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696984.RAnYPRDaqwt2_uYu2CZwOSEWPIkgpdgcd6ivvkz0-3HTE130_provenance.
- NP871087.RAWaTF3CqqyhIYnWVpBiM4DGp4d8nSs6Rc0reC5FMSFtc130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871087.RAWaTF3CqqyhIYnWVpBiM4DGp4d8nSs6Rc0reC5FMSFtc130_provenance.
- NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317879.RA6EQhzkty-SAFnyJJcDm6EQocS_PJ3qg1atK_JvTEtyM130_provenance.
- assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP732052.RA_4XCfeohHYmU4P0CLLDGMMW1aebqU85eFrEsEmWEG_4130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP732052.RA_4XCfeohHYmU4P0CLLDGMMW1aebqU85eFrEsEmWEG_4130_provenance.
- NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP562589.RAGtuKRYYm5CytuWbE9Awy5_uas_I_cyqp9W0sPkne9Hs130_provenance.
- NP359302.RAXEhwmlkxFISCG4f5WHh8LK5W9c4bqPtXGFfJ8cnDqow130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359302.RAXEhwmlkxFISCG4f5WHh8LK5W9c4bqPtXGFfJ8cnDqow130_provenance.
- NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933655.RAPpLNWPM17kvcmaoNgfZMJ52c3TRfYkQIjpsTm0Bzfvk130_provenance.
- NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_assertion description "[One mutation in a DR1 site causes elevated gamma-globin transcription in human HPFH (hereditary persistence of fetal hemoglobin) syndrome, and we show that this mutation reduces TR2/TR4 binding in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444648.RAKJAiSB6Wbhtbqhl5zSX8Pk_oAf5dP2EToO7aUGHy6no130_provenance.