Generation and Characterization of a Transgenic Mouse Carrying a Functional Human β -Globin Gene with the IVSI-6 Thalassemia Mutation.

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Generation and Characterization of a Transgenic Mouse Carrying a Functional Human β -Globin Gene with the IVSI-6 Thalassemia Mutation.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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Generation and Characterizatio ...... e IVSI-6 Thalassemia Mutation.

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Generation and Characterizatio ...... e IVSI-6 Thalassemia Mutation.

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Generation and Characterizatio ...... e IVSI-6 Thalassemia Mutation.

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P1476

Generation and Characterizatio ...... he IVSI-6 Thalassemia Mutation

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Fiorella Altruda

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Gianni Carandina

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Irene Mancini

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Lucia C Cosenza

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Vincenzo Aiello

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P2860

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Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides

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Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients

Upstream stimulatory factors are involved in the P1 promoter directed transcription of the A beta H-J-J locus

Targeted correction of a thalassemia-associated beta-globin mutation induced by pseudo-complementary peptide nucleic acids

Mouse model of human beta zero thalassemia: targeted deletion of the mouse beta maj- and beta min-globin genes in embryonic stem cells.

Abnormally spliced beta-globin mRNAs: a single point mutation generates transcripts sensitive and insensitive to nonsense-mediated mRNA decay.

Restoration of human beta-globin gene expression in murine and human IVS2-654 thalassemic erythroid cells by free uptake of antisense oligonucleotides.

Genetic diseases of hemoglobin: diagnostic methods for elucidating beta-thalassemia mutations.

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687635

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scholarly article

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10.1155/2015/687635

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English

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2015

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P577

2015-05-04T00:00:00Z

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272022967

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26097845

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4434229

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