Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Pamela Himadewi"'
Autor:
Pamela Himadewi, Xue Qing David Wang, Fan Feng, Haley Gore, Yushuai Liu, Lei Yu, Ryo Kurita, Yukio Nakamura, Gerd P Pfeifer, Jie Liu, Xiaotian Zhang
Publikováno v:
eLife, Vol 10 (2021)
Mutations in the adult β-globin gene can lead to a variety of hemoglobinopathies, including sickle cell disease and β-thalassemia. An increase in fetal hemoglobin expression throughout adulthood, a condition named hereditary persistence of fetal he
Externí odkaz:
https://doaj.org/article/f57b54ffcd06452fa3926ecc23940b5f
Autor:
Xiaotian Zhang, Liling Wan, Shasha Chong, Jianzhong Su, Jolanta Grembecka, Tomasz Cierpicki, Gerd P. Pfeifer, Pamela Himadewi, Haley Gore, Dong Chen, Qinglan Li, Xinyu Wang, Hongzhi Miao, Yiman Liu, Qinyu Han, Dandan Fan, Xue Qing David Wang
Supplementary Table S3 shows the differential expressed genes in NPM1c-koncked in HOXB8 cell lines vs parental cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6be70e59c5f88c06fb2cde76de7d127c
https://doi.org/10.1158/2159-8290.22542205
https://doi.org/10.1158/2159-8290.22542205
Autor:
Xiaotian Zhang, Liling Wan, Shasha Chong, Jianzhong Su, Jolanta Grembecka, Tomasz Cierpicki, Gerd P. Pfeifer, Pamela Himadewi, Haley Gore, Dong Chen, Qinglan Li, Xinyu Wang, Hongzhi Miao, Yiman Liu, Qinyu Han, Dandan Fan, Xue Qing David Wang
Supplementary Figure S1 is associated with Figure1 and it shows the NPM1-WT binds to the rDNA arrays and NPM1c binds to non-repetitive genomic regions. Supplementary Figure S2 is associated with Figure1 and it shows NPM1c’s chromatin binding and as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b6c5e5faf66b8dd4c3853b4ea1b03d6
https://doi.org/10.1158/2159-8290.22542214.v1
https://doi.org/10.1158/2159-8290.22542214.v1
Autor:
Xue Qing David Wang, Dandan Fan, Qinyu Han, Yiman Liu, Hongzhi Miao, Xinyu Wang, Qinglan Li, Dong Chen, Haley Gore, Pamela Himadewi, Gerd P. Pfeifer, Tomasz Cierpicki, Jolanta Grembecka, Jianzhong Su, Shasha Chong, Liling Wan, Xiaotian Zhang
Nucleophosmin (NPM1) is a ubiquitously expressed nucleolar protein with a wide range of biological functions. In 30% of acute myeloid leukemia (AML), the terminal exon of NPM1 is often found mutated, resulting in the addition of a nuclear export sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44cf32ef68e893c5e381926d6f4487ab
https://resolver.caltech.edu/CaltechAUTHORS:20230322-270078000.2
https://resolver.caltech.edu/CaltechAUTHORS:20230322-270078000.2
Autor:
Xue Qing David Wang, Dandan Fan, Yiman Liu, Hongzhi Miao, Dong Chen, Xinyu Wang, Haley Gore, Pamela Himadewi, Gerd Pfeifer, Tomasz Cierpicki, Jolanta Su, Liling Wan, Xiaotian Zhang
Publikováno v:
Blood Cancer Discovery. 4:A34-A34
Nucleophosmin (NPM1) is a ubiquitously expressed nucleolar protein with a wide range of functions including ribosome biogenesis, mRNA processing, and maintenance of genomic stability. In acute myeloid leukemia (AML), the terminal exon of NPM1 is ofte
Autor:
Benjamin K. Johnson, Mary Rhodes, Marc Wegener, Pamela Himadewi, Kelly Foy, Joshua L. Schipper, Rebecca A. Siwicki, Larissa L. Rossell, Emily J. Siegwald, Dave W. Chesla, Jose M. Teixeira, Rachael T. C. Sheridan, Marie Adams, Timothy J. Triche, Hui Shen
We present Single-cell TOtal RNA Miniaturized sequencing (STORM-seq), a full-length single-cell ribo-reduced RNA sequencing protocol, optimized to profile thousands of cells per run. Using off-the-shelf reagents and random hexamer priming, STORM-seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbfeedabe75f94243bbb7d80995fdaf0
https://doi.org/10.1101/2022.03.14.484332
https://doi.org/10.1101/2022.03.14.484332
Autor:
Lei Yu, Jie Liu, Xiaotian Zhang, Yushuai Liu, Fan Feng, Gerd P. Pfeifer, Haley Gore, Ryo Kurita, Xue Qing David Wang, Yukio Nakamura, Pamela Himadewi
Publikováno v:
eLife, Vol 10 (2021)
eLife
eLife
Mutations in the adult β-globin gene can lead to a variety of hemoglobinopathies, including sickle cell disease and β-thalassemia. An increase in fetal hemoglobin expression throughout adulthood, a condition named hereditary persistence of fetal he
Autor:
Haley Gore, Xiaotian Zhang, Yukio Nakamura, Pamela Himadewi, Gerd P. Pfeifer, Fan Feng, Xue Qing David Wang, Jie Liu, Lei Yu, Yushuai Liu, Ryo Kurita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::442db03bbc568a875c4bf7ce46703ea9
https://doi.org/10.7554/elife.70557.sa2
https://doi.org/10.7554/elife.70557.sa2
Autor:
Pamela Himadewi, David N. Arnosti, Philipp Kapranov, Rima Mouawad, Jaideep Prasad, Dominic Thorley, Nathan R. Wilson, Dhruva Kadiyala
Publikováno v:
Mol Biol Evol
Retinoblastoma proteins are eukaryotic transcriptional co-repressors that play central roles in cell cycle control, among other functions. Although most metazoan genomes encode a single retinoblastoma protein, gene duplications have occurred at least
Autor:
Yukio Nakamura, Fan Feng, Jie Liu, Xue Qing David Wang, Haley Gore, Yushuai Liu, Ryo Kurita, Xiaotian Zhang, Lei Yu, Pamela Himadewi, Gerd P. Pfeifer
SummaryMutations in the adult β-globin gene can lead to a variety of hemoglobinopathies, including sickle cell disease and β-thalassemia. An increase in fetal hemoglobin expression throughout adulthood, a condition named Hereditary Persistence of F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::debe144485c8749e733e91ee76e73ebd
https://doi.org/10.1101/2021.05.18.444713
https://doi.org/10.1101/2021.05.18.444713