Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Charles H Li"'
Publikováno v:
Canadian Journal of Gastroenterology, Vol 22, Iss 1, Pp 37-40 (2008)
BACKGROUND AND METHODS: Elevated serum ferritin is a common clinical finding. The etiology of hyperferritinemia in the Asia-Pacific population is less clear due to a low prevalence of known HFE mutations such as C282Y and H63D, as well as an increase
Externí odkaz:
https://doaj.org/article/92e85be050244dea959541190df7db10
Autor:
Charles H Li, Maria Cervantes, Deborah J Springer, Teun Boekhout, Rosa M Ruiz-Vazquez, Santiago R Torres-Martinez, Joseph Heitman, Soo Chan Lee
Publikováno v:
PLoS Pathogens, Vol 7, Iss 6, p e1002086 (2011)
Mucor circinelloides is a zygomycete fungus and an emerging opportunistic pathogen in immunocompromised patients, especially transplant recipients and in some cases otherwise healthy individuals. We have discovered a novel example of size dimorphism
Externí odkaz:
https://doaj.org/article/c1f2c4e53c0342ca8add07659717b7ba
Publikováno v:
Haematologica, Vol 105, Iss 3 (2020)
Externí odkaz:
https://doaj.org/article/d651a6a0d8ad4132a3e7c999ead11700
Autor:
Brian J. Abraham, Denes Hnisz, Abraham S. Weintraub, Nicholas Kwiatkowski, Charles H. Li, Zhaodong Li, Nina Weichert-Leahey, Sunniyat Rahman, Yu Liu, Julia Etchin, Benshang Li, Shuhong Shen, Tong Ihn Lee, Jinghui Zhang, A. Thomas Look, Marc R. Mansour, Richard A. Young
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
Sequencing initiatives have detected multiple types of mutations in cancer. Here the authors, analysing enhancer-targeting sequence data, show that small insertions in transcriptional enhancers are frequently found near oncogenes, and demonstrate how
Externí odkaz:
https://doaj.org/article/83aabc930e7b4c009b32aff780ab64f2
Autor:
Taku Harada, Yaser Heshmati, Jérémie Kalfon, Monika W. Perez, Juliana Xavier Ferrucio, Jazmin Ewers, Benjamin Hubbell Engler, Andrew Kossenkov, Jana M. Ellegast, Joanna S. Yi, Allyson Bowker, Qian Zhu, Kenneth Eagle, Tianxin Liu, Yan Kai, Joshua M. Dempster, Guillaume Kugener, Jayamanna Wickramasinghe, Zachary T. Herbert, Charles H. Li, Jošt Vrabič Koren, David M. Weinstock, Vikram R. Paralkar, Behnam Nabet, Charles Y. Lin, Neekesh V. Dharia, Kimberly Stegmaier, Stuart H. Orkin, Maxim Pimkin
Publikováno v:
Genes & Development. 36:368-389
Acute myeloid leukemia with KMT2A (MLL) rearrangements is characterized by specific patterns of gene expression and enhancer architecture, implying unique core transcriptional regulatory circuitry. Here, we identified the transcription factors MEF2D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b4d7a78af1a17e0bab960f57503beb
https://doi.org/10.1101/gad.349284.121
https://doi.org/10.1101/gad.349284.121
Autor:
Junming Qian, Xiaonan Guan, Bing Xie, Chuanyun Xu, Jacqueline Niu, Xin Tang, Charles H. Li, Henry M. Colecraft, Rudolf Jaenisch, X. Shawn Liu
Publikováno v:
Science Translational Medicine. 15
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by loss-of-function heterozygous mutations of methyl CpG-binding protein 2 ( MECP2 ) on the X chromosome in young females. Reactivation of the silent wild-type MECP2 allele from th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ad0527b4f368a98876470a73923c3c9
https://doi.org/10.1126/scitranslmed.add4666
https://doi.org/10.1126/scitranslmed.add4666
Autor:
Junming Qian, Xiaonan Guan, Bing Xie, Chuanyun Xu, Jacqueline Niu, Xin Tang, Charles H. Li, Henry M. Colecraft, Rudolf Jaenisch, X. Shawn Liu
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by loss-of-function heterozygous mutations of Methyl CpG-binding Protein 2 (MECP2) on the X chromosome in girls. Reactivation of the silent wild-typeMECP2allele from the inactive X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3a84fbb4500b7cc7b4be1bc9f2967f6
https://doi.org/10.1101/2022.11.30.518560
https://doi.org/10.1101/2022.11.30.518560
Publikováno v:
Frontiers in Human Neuroscience, Vol 12 (2018)
Perceiving and producing vocal sounds are important functions of the auditory-motor system and are fundamental to communication. Prior studies have identified a network of brain regions involved in pitch production, specifically pitch matching. Here
Externí odkaz:
https://doaj.org/article/0fe41e9a339c4275bb4070de940f68c8
Autor:
Arup K. Chakraborty, John Mantiega, Anthony A. Hyman, Ann Boija, Mrityunjoy Kar, Patrick M. McCall, Jesse M. Platt, Charles H. Li, Mengyang Fan, Victoria E. Clark, Tong Lee, Alessandra Dall’Agnese, Jonathan E. Henninger, Krishna Shrinivas, Ido Sagi, Phillip A. Sharp, Dylan J. Taatjes, Tim-Michael Decker, Tinghu Zhang, Jing-Ke Weng, Eliot L. Coffey, Lena K. Afeyan, Alicia V. Zamudio, Nathanael S. Gray, Benjamin R. Sabari, Isaac A. Klein, Richard A. Young, Nancy M. Hannett, Young-Tae Chang, Ozgur Oksuz, Yang Guo, Susana Wilson Hawken
Publikováno v:
Cancer Research. 81:GS3-10
The molecules of the cell are compartmentalized into membrane- and non-membrane-bound organelles. Many non-membrane-bound organelles are phase-separated biomolecular condensates with distinct physicochemical properties that can absorb and concentrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::813421c57b00b902403b00605df75237
https://doi.org/10.1158/1538-7445.sabcs20-gs3-10
https://doi.org/10.1158/1538-7445.sabcs20-gs3-10
Autor:
Xin Tang, Gary LeRoy, Alicia V. Zamudio, Alessandra Dall’Agnese, Richard A. Young, Emile Wogram, Jurian Schuijers, Nancy M. Hannett, Jonathan E. Henninger, Tenzin Lungjangwa, Tong Ihn Lee, Jesse M. Platt, Eliot L. Coffey, Ozgur Oksuz, X. Shawn Liu, Styliani Markoulaki, Charles H. Li, Lena K. Afeyan, Rudolf Jaenisch, Devon S. Svoboda
Publikováno v:
Nature
Methyl CpG binding protein 2 (MeCP2) is a key component of constitutive heterochromatin, which is crucial for chromosome maintenance and transcriptional silencing1–3. Mutations in the MECP2 gene cause the progressive neurodevelopmental disorder Ret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f51fc72bdd6c60ff1b8c95fcbf6cd08
https://doi.org/10.1038/s41586-020-2574-4
https://doi.org/10.1038/s41586-020-2574-4