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The origin and functional heterogeneity of pericytes in glioblastoma (GBM) remain unclear. This study identifies tumor‐originated pericytes (T‐PCs) and normal‐originated pericytes as two distinctive populations in human GBM using single‐cell RNA‐sequencing.
Cuiying Chu +16 more
wiley +1 more source
Soybean Auxin Transporter PIN3 Regulates Nitrate Acquisition to Improve Nitrogen Use and Seed Traits
Xu et al. discovers that switching off auxin transporters in soybean, PIN3a and PIN3b, disrupts auxin flow; this triggers ARF‐STF3/4 signal cascade to activate the nitrate importer NPF2.13 and soil nitrogen acquisition. Multi‐year field trials show edited soybeans maintain yield with higher oil content, offering a potential genetic route to improve ...
Huifang Xu +16 more
wiley +1 more source
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Reverse transcription-polymerase chain reaction.
Cold Spring Harbor Protocols, 2014Reverse transcription coupled to the polymerase chain reaction (RT–PCR) is commonly used to detect the presence of mRNAs, pre-mRNAs, or other types of RNA such as noncoding RNAs. The method involves using a primer annealed to the RNA of interest. For mRNA, the primer is usually a synthetic oligo(dT)15–18, a random hexamer mixture (dN)6, or a synthetic ...
D. Rio
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Reverse Transcription Polymerase Chain Reaction
Neuroscience Methods, 2019The polymerase chain reaction (PCR) technique was developed to amplify, with high efficiency, double-stranded or single-stranded deoxyribonucleic acid (DNA) sequences. Amplification of individual Ribonucleic acid (RNA) molecules can also be accomplished with PCR when coupled with reverse transcription (RT) of RNA into a complementary DNA (cDNA) copy. A
M. Vidovic
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Quantification of RNA by Real-Time Reverse Transcription-Polymerase Chain Reaction (RT-PCR).
Cold Spring Harbor Protocols, 2018This protocol describes a real-time reverse transcription-polymerase chain reaction (RT-PCR) assay using a two-enzyme, two-tube approach, carried out using either SYBR Green I or TaqMan chemistries.
Michael R Green, J. Sambrook
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Quantification of RNA damage by reverse transcription polymerase chain reactions
Analytical Biochemistry, 2006RNA damages, such as those generated by nucleic acid-modifying agents, occur randomly in RNA and present challenging problems to organisms. It has been unclear how RNA function would be affected by many forms of RNA damage and how cells are protected against the damage.
Xin, Gong, Rui, Tao, Zhongwei, Li
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cDNA Equalization for Reverse Transcription-Polymerase Chain Reaction Quantitation
Analytical Biochemistry, 1993Reverse transcription coupled with the polymerase chain reaction has been increasingly utilized to study gene expression. However, most previously published quantitative techniques are limited by accurate initial RNA quantitation and do not account well for the relative efficiency of reverse transcription.
J, Kolls +3 more
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Analysis of Gene Expression: Reverse Transcription-Polymerase Chain Reaction
2003Numerous techniques have been developed to measure gene expression in tissues and cells. These include coupled reverse transcription and polymerase chain reaction amplification (RT-PCR), Northern blot (see Chapter 20 ), in situ hybridization (see Chapter 21 ), RNase protection assays, dot blots, and S1 nuclease assays.
el-B, Haddad, J, Rousell
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