Search for publications in the Transfection Database with Polyplus transfection reagents or for transfection conditions.

Over 6000 publications, 1000 cell lines and primary cells available.

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Found 5890 results :
Cell Linein vitro
in vivo
Delivered MoleculeReagentResults & Citations
HEK-293Tin vitroDNAjetPRIME
Sauvegarde, C. et al. (2016)

PLoS One 11, e0165898
Dynamic Pattern of HOXB9 Protein Localization during Oocyte Maturation and Early Embryonic Development in Mammals
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CS3BEin vitroDNAjetPRIME
Scheibye-Knudsen, M. et al. (2016)

Proc Natl Acad Sci U S A 113, 12502-12507
Cockayne syndrome group A and B proteins converge on transcription-linked resolution of non-B DNA
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BSR-T7in vitroDNAjetPRIME
Severin, C. et al. (2016)

J Virol ,
Releasing the genomic RNA sequestered in the mumps virus nucleocapsid
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HEK-293in vitromimic miRNAjetPRIME
Shahar, T. et al. (2016)

J Neurooncol ,
Expression level of miRNAs on chromosome 14q32.31 region correlates with tumor aggressiveness and survival of glioblastoma patients
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HEK-293in vitroDNAjetPRIME
Shen, Y. et al. (2016)

J Med Chem 59, 9124-9139
Discovery of a Potent, Selective, and Cell-Active Dual Inhibitor of Protein Arginine Methyltransferase 4 and Protein Arginine Methyltransferase 6
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HEK-293in vitroDNAjetPRIME
Sulaiman, A. A. et al. (2016)

PLoS Pathog 12, e1005991
A Trematode Parasite Derived Growth Factor Binds and Exerts Influences on Host Immune Functions via Host Cytokine Receptor Complexes
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HL-1, RAW 264.7in vitroDNAjetPEI-Macrophage, jetPRIME
Sun, Z. et al. (2016)

Basic Res Cardiol 111, 63
Cross-talk between macrophages and atrial myocytes in atrial fibrillation
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CHO, HEK-293Tin vitroDNAjetPRIME
Telley, L. et al. (2016)

Neuron 91, 1276-91
Dual Function of NRP1 in Axon Guidance and Subcellular Target Recognition in Cerebellum
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A549in vitroDNAjetPRIME
Thiele, C. et al. (2016)

Drug Deliv Transl Res ,
Biodegradable starch derivatives with tunable charge density-synthesis, characterization, and transfection efficiency
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COS-7in vitroDNAjetPRIME
Turro, E. et al. (2016)

Sci Transl Med 8, 328ra30
A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies
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