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genome browser reference sequence (refseq) gene track  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology genome browser reference sequence (refseq) gene track
    Genome Browser Reference Sequence (Refseq) Gene Track, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/genome+browser+reference+sequence+(refseq)+gene+track/genome+sequences/pm32277283-64-15-13
    Average 90 stars, based on 1 article reviews
    genome browser reference sequence (refseq) gene track - by Bioz Stars, 2026-11
    90/100 stars

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    Article Title: Clustering of genomic breakpoints at the MLL locus in therapy-related acute leukemia with t(4;11)(q21;q23).
    Article Snippet: Syed Khizer Hasan,* Gianluca Barba, Markus Metzler, Mariadomenica Divona, Tiziana Ottone, Laura Cicconi, Brunangelo Falini, Cristina Mecucci, and Francesco Lo-Coco Departmentof Biomedicine and Prevention,Universityof TorVergata,Rome,Italy Laboratorio di Neuro-Oncoematologia,Fondazione Santa Lucia,Rome,Italy Hematology Unit,Universityof Perugia,Polo Unico S.M.Misericordia,Perugia,Italy Departmentof Paediatrics,Universityof Erlangen-Nuremberg,Germany Institute of Hematology,Universityof Perugia,Perugia,Italy

    Article Title: Characterization of therapy-related acute leukemia in hereditary breast-ovarian carcinoma patients: role of BRCA1 mutation and topoisomerase II-directed therapy.
    Article Snippet: Therapy-related acute leukemias (t-ALs) represent approximately 10–20% of all acute leukemias, are frequently resistant to chemotherapy, and are associated with guarded outcomes.. The national comprehensive cancer network data suggest that t-AL cases are diagnosed at increasing rates in breast cancer patients treated with chemotherapeutic agents targeting topoisomerase II.. Two cases of BRCA1-mutated ovarian and breast carcinoma who developed therapy-related APL and ALL, respectively, following topoisomerase II-directed therapy were characterized.

    Article Title: Identification of a potential "hotspot" DNA region in the RUNX1 gene targeted by mitoxantrone in therapy-related acute myeloid leukemia with t(16;21) translocation.
    Article Snippet: Tiziana Ottone, Syed Khizer Hasan, Enrico Montefusco, Paola Curzi, Ashley N. Mays, Luciana Chessa, Antonella Ferrari, Esmeralda Conte, Nelida Inés Noguera, Serena Lavorgna, Emanuele Ammatuna, Mariadomenica Divona, Katia Bovetti, Sergio Amadori, David Grimwade, and Francesco Lo-Coco* Dipartimento di Biopatologia e Diagnostica per Immagini,University‘‘TorVergata,’’Rome,Italy Azienda Ospedaliera Sant’Andrea,University‘‘La Sapienza,’’Rome,Italy Dipartimento di Medicina di Laboratorio,PoliclinicoTorVergata,Rome,Italy Departmentof Medical and Molecular Genetics,King’s College London School of Medicine,London,UK



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    Santa Cruz Biotechnology genome browser reference sequence (refseq) gene track
    Genome Browser Reference Sequence (Refseq) Gene Track, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/genome+browser+reference+sequence+(refseq)+gene+track/genome+sequences/pm32277283-64-15-13
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    MLV and SIV Integration Sites Distribution (Reported to <t> UCSC </t> <t> RefSeq </t> Genes) Compared to In Silico-Generated Random Integration Sites
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    Image Search Results


    Journal: PLoS Biology

    Article Title: Distinct Genomic Integration of MLV and SIV Vectors in Primate Hematopoietic Stem and Progenitor Cells

    doi: 10.1371/journal.pbio.0020423

    Figure Lengend Snippet: MLV and SIV Integration Sites Distribution (Reported to UCSC RefSeq Genes) Compared to In Silico-Generated Random Integration Sites

    Article Snippet: We correlated the 760 integration sites (432 for MLV and 328 for SIV) that unequivocally mapped to a unique position in the genome to the locations of annotated genes, using the UCSC Genome Browser Reference Sequence (RefSeq) Genes track, which displays the positions of National Center for Biotechnology Information mRNA Reference Sequences ( ).

    Techniques:

    Shown are integrations that landed within RefSeq gene introns (arrows) in comparison to in silico-generated integration sites (bars). Black indicates MLV and gray indicates SIV. * p < 0.0001 by a Chi 2 test.

    Journal: PLoS Biology

    Article Title: Distinct Genomic Integration of MLV and SIV Vectors in Primate Hematopoietic Stem and Progenitor Cells

    doi: 10.1371/journal.pbio.0020423

    Figure Lengend Snippet: Shown are integrations that landed within RefSeq gene introns (arrows) in comparison to in silico-generated integration sites (bars). Black indicates MLV and gray indicates SIV. * p < 0.0001 by a Chi 2 test.

    Article Snippet: We correlated the 760 integration sites (432 for MLV and 328 for SIV) that unequivocally mapped to a unique position in the genome to the locations of annotated genes, using the UCSC Genome Browser Reference Sequence (RefSeq) Genes track, which displays the positions of National Center for Biotechnology Information mRNA Reference Sequences ( ).

    Techniques: Comparison, In Silico, Generated

    (A) Distribution of MLV and SIV integration sites relative to gene density within a 1-Mbp window compared to in silico-generated random integration sites. Each bar corresponds to the percentage of integration sites within the corresponding gene density region. (B) Location of MLV and SIV integration sites and gene density on human Chromosome 6. MLV and SIV integrations were aligned to Chromosome 6 (obtained from the UCSC custom annotation track feature) and shown in relation to RefSeq gene density (blue). 73% of the SIV integration events are within the 20-Mbp unique ridge of Chromosome 6, compared to 29% for MLV. Distance between thick black bars is 20 Mbp; centromere is represented by the black circle.

    Journal: PLoS Biology

    Article Title: Distinct Genomic Integration of MLV and SIV Vectors in Primate Hematopoietic Stem and Progenitor Cells

    doi: 10.1371/journal.pbio.0020423

    Figure Lengend Snippet: (A) Distribution of MLV and SIV integration sites relative to gene density within a 1-Mbp window compared to in silico-generated random integration sites. Each bar corresponds to the percentage of integration sites within the corresponding gene density region. (B) Location of MLV and SIV integration sites and gene density on human Chromosome 6. MLV and SIV integrations were aligned to Chromosome 6 (obtained from the UCSC custom annotation track feature) and shown in relation to RefSeq gene density (blue). 73% of the SIV integration events are within the 20-Mbp unique ridge of Chromosome 6, compared to 29% for MLV. Distance between thick black bars is 20 Mbp; centromere is represented by the black circle.

    Article Snippet: We correlated the 760 integration sites (432 for MLV and 328 for SIV) that unequivocally mapped to a unique position in the genome to the locations of annotated genes, using the UCSC Genome Browser Reference Sequence (RefSeq) Genes track, which displays the positions of National Center for Biotechnology Information mRNA Reference Sequences ( ).

    Techniques: In Silico, Generated