Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Dmitry Goryunov"'
Autor:
Amy K. Kim, Selena Y. Lin, Surbhi Jain, Yixiao Cui, Terence Gade, Fwu-Shan Shieh, Max Chao, John Shieh, Jonathan Cheng, James P. Hamilton, Hie-Won Hann, Dmitry Goryunov, Zhili Wang, Ying-Hsiu Su
Cell-free DNA (cfDNA) from blood has become a promising analyte for cancer genetic liquid biopsy. Urinary cfDNA has been shown to contain mutations associated with non-genitourologic cancers including hepatocellular carcinoma (HCC). In this study, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afdcd7d236b30cb36f4e7e697dcf783a
https://doi.org/10.1101/2021.12.03.21266943
https://doi.org/10.1101/2021.12.03.21266943
Autor:
Selena Y. Lin, James P. Hamilton, Hie-Won L. Hann, Fwu-Shan Shieh, John Caleb Shieh, Yixiao Cui, Jonathan Cheng, Amy K. Kim, Ying-Hsiu Su, Max Chao, Dmitry Goryunov, Terence P. Gade, Surbhi Jain
Publikováno v:
Cancer Research. 81:544-544
BACKGROUND: Cell-free DNA (cfDNA) from blood has become a promising analyte for cancer diagnostics. However, because blood contains high concentrations of proteins and enzyme inhibitors, plasma cfDNA quality can be variable. Urinary cfDNA has been sh
Autor:
Dmitry, Goryunov, Ronald K H, Liem
Publikováno v:
Methods in enzymology. 569
The cytoskeleton of most eukaryotic cells is composed of three principal filamentous components: actin filaments, microtubules (MTs), and intermediate filaments. It is a highly dynamic system that plays crucial roles in a wide range of cellular proce
Autor:
Ronald K.H. Liem, Dmitry Goryunov
The cytoskeleton of most eukaryotic cells is composed of three principal filamentous components: actin filaments, microtubules (MTs), and intermediate filaments. It is a highly dynamic system that plays crucial roles in a wide range of cellular proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8a805c7238dbf16912d41b9d1325ed4
https://doi.org/10.1016/bs.mie.2015.05.022
https://doi.org/10.1016/bs.mie.2015.05.022
Publikováno v:
Molecular and Cellular Neuroscience. 44:1-14
The microtubule-actin crosslinking factor 1 (MACF1) is a ubiquitous cytoskeletal linker protein with multiple spliced isoforms expressed in different tissues. The MACF1a isoform contains microtubule and actin binding regions and is expressed at high
Publikováno v:
Journal of Neurochemistry. 104:1536-1552
Charcot-Marie-Tooth disease (CMT) is an inherited peripheral neuropathy that has been linked to mutations in multiple genes. Mutations in the neurofilament light (NFL) chain gene lead to the CMT2E form whereas mutations in the myotubularin-related pr
Autor:
Ronald K.H. Liem, Dmitry Goryunov, Adijat Adebola, Julius J. Jefferson, Conrad L. Leung, Anne Messer
Publikováno v:
Brain Research. 1140:179-187
Dystonia musculorum (dt) is an inherited autosomal recessive neuropathy in mice. Homozygous animals display primarily sensory neurodegeneration resulting in a severe loss of coordination. Several dt strains exist, including spontaneous mutants dt-Alb
Autor:
Noemi Cabrera‐Poch, Dmitry Goryunov, Leonidas Stefanis, Ronald K.H. Liem, Miguel A. Lopez-Toledano, Kristy R. Brown, Raul Perez-Olle
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Neurofilament light gene mutations have been linked to a subset of patients with Charcot-Marie-Tooth disease, the most common inherited motor and sensory neuropathy. We have previously shown that Charcot-Marie-Tooth-linked mutant neurofilament light
Autor:
Ronald K.H. Liem, Dmitry Goryunov
Publikováno v:
Journal of Clinical Investigation. 117:590-592
A primary pathologic component of Alzheimer’s disease (AD) is the formation of neurofibrillary tangles composed of hyperphosphorylated tau (p-tau). Expediting the removal of these p-tau species may be a relevant therapeutic strategy. Here we report
Publikováno v:
Journal of neurochemistry. 104(6)
Charcot-Marie-Tooth disease (CMT) is an inherited peripheral neuropathy that has been linked to mutations in multiple genes. Mutations in the neurofilament light (NFL) chain gene lead to the CMT2E form whereas mutations in the myotubularin-related pr