نتایج جستجو برای: سلول hek 293t

تعداد نتایج: 19597  

2014
JIANZHANG WANG JUN WANG CHANGPING CAI SHILI WANG SHUAI LIU SHUO SHI YIFAN ZHANG BIAO LI

Vectors that are capable of coexpressing two or more exogenous genes for in vitro and in vivo gene delivery are being increasingly studied. The aim of the present study was to explore the feasibility of using the pFastBac™ Dual vector, under the control of two cytomegalovirus (CMV) promoters with opposite directions, to coexpress enhanced green fluorescent protein (EGFP) and glial cell line-der...

Journal: :The Biochemical journal 2006
Mio Horii Hideki Shibata Ryota Kobayashi Keiichi Katoh Chiharu Yorikawa Jiro Yasuda Masatoshi Maki

All CHMPs (charged multivesicular body proteins) reported to date have common features: they all contain approx. 200 amino acid residues, have coiled-coil regions and have a biased distribution of charged residues (basic N-terminal and acidic C-terminal halves). Yeast orthologues of CHMPs, including an ESCRT-III component Snf7, are required for the sorting of cargo proteins to intraluminal vesi...

Journal: :The Journal of physiology 2005
Koichi Nakajo Yoshihiro Kubo

It is well established that stimulation of G(q)-coupled receptors such as the M1 muscarinic acetylcholine receptor inhibits KCNQ/M currents. While it is generally accepted that this muscarinic inhibition is mainly caused by the breakdown of PIP(2), the role of the subsequent activation of protein kinase C (PKC) is not well understood. By reconstituting M currents in Xenopus oocytes, we observed...

Journal: :Investigative ophthalmology & visual science 2011
José-Daniel Aroca-Aguilar Francisco Sánchez-Sánchez Sikha Ghosh Ana Fernández-Navarro Miguel Coca-Prados Julio Escribano

PURPOSE Myocilin is an extracellular glycoprotein with unknown function that is associated with glaucoma. Calpain II cleaves recombinant myocilin within the linker region of the protein, releasing the C-terminal olfactomedin domain from the N-terminal domain. The authors previously reported that myocilin interacts with the C-terminal region of hevin, a secretory glycoprotein belonging to the SP...

2016
Hui-Yung Song Huai-Chih Chiang Wei-Lien Tseng Ping Wu Chian-Shiu Chien Hsin-Bang Leu Yi-Ping Yang Mong-Lien Wang Yuh-Jyh Jong Chung-Hsuan Chen Wen-Chung Yu Shih-Hwa Chiou

The CRISPR/Cas9 Genome-editing system has revealed promising potential for generating gene mutation, deletion, and correction in human cells. Application of this powerful tool in Fabry disease (FD), however, still needs to be explored. Enzyme replacement therapy (ERT), a regular administration of recombinant human α Gal A (rhα-GLA), is a currently available and effective treatment to clear the ...

2013
Adriano Senatore Arnaud Monteil Jan van Minnen August B. Smit J. David Spafford

NALCN is a member of the family of ion channels with four homologous, repeat domains that include voltage-gated calcium and sodium channels. NALCN is a highly conserved gene from simple, extant multicellular organisms without nervous systems such as sponges and placozoans and mostly remains a single gene compared to the calcium and sodium channels which diversified into twenty genes in humans. ...

2009
Sabyasachi Halder Masanao Murakami Subhash C. Verma Pankaj Kumar Fuming Yi Erle S. Robertson

Epstein Barr virus (EBV) is closely associated with the development of a vast number of human cancers. To develop a system for monitoring early cellular and viral events associated with EBV infection a self-recombining BAC containing 172-kb of the Epstein Barr virus genome BAC-EBV designated as MD1 BAC (Chen et al., 2005, J.Virology) was used to introduce an expression cassette of green fluores...

2014
Neeta Adhikari Weihua Guan Brian Capaldo Aaron J. Mackey Marjorie Carlson Sundaram Ramakrishnan Dinesha Walek Manu Gupta Adam Mitchell Peter Eckman Ranjit John Euan Ashley Paul J. Barton Jennifer L. Hall

RATIONALE The rationale was to utilize a bioinformatics approach to identify miRNA binding sites in genes with single nucleotide mutations (SNPs) to discover pathways in heart failure (HF). OBJECTIVE The objective was to focus on the genes containing miRNA binding sites with miRNAs that were significantly altered in end-stage HF and in response to a left ventricular assist device (LVAD). ME...

2016
John D. Hulleman Annie Nguyen V.L. Ramprasad Sakthivel Murugan Ravi Gupta Avinash Mahindrakar Ravi Angara Chandrasekhar Sankurathri V. Vinod Mootha

PURPOSE To identify the causative mutation in two siblings from a consanguineous family in India with retinitis pigmentosa (RP) and polydactyly without other findings of Bardet-Biedl syndrome (BBS). We also performed functional characterization of the mutant protein to explore its role in this limited form of BBS. METHODS The siblings underwent a thorough ophthalmological examination, includi...

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