Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
about
Antitumor activity of a pyrrole-imidazole polyamideBinding studies of a large antiviral polyamide to a natural HPV sequence.Controlling gene networks and cell fate with precision-targeted DNA-binding proteins and small-molecule-based genome readers.Guiding the design of synthetic DNA-binding molecules with massively parallel sequencing.Synthesis of cyclic Py-Im polyamide libraries.Fluorescent probes for nucleic Acid visualization in fixed and live cells.Characterization and solubilization of pyrrole-imidazole polyamide aggregatesSingle-dose pharmacokinetic and toxicity analysis of pyrrole-imidazole polyamides in mice.Gene expression changes in a tumor xenograft by a pyrrole-imidazole polyamide.Animal toxicity of hairpin pyrrole-imidazole polyamides varies with the turn unit.Programmable DNA-binding small molecules.Complex of the herpes simplex virus type 1 origin binding protein UL9 with DNA as a platform for the design of a new type of antiviral drugs.Crosstalk of the Androgen Receptor with Transcriptional Collaborators: Potential Therapeutic Targets for Castration-Resistant Prostate CancerModulation of topoisomerase IIα expression and chemosensitivity through targeted inhibition of NF-Y:DNA binding by a diamino p-anisyl-benzimidazole (Hx) polyamide.A synthetic DNA-binding inhibitor of SOX2 guides human induced pluripotent stem cells to differentiate into mesoderm.What is the antiviral potential of pyrrole-imidazole polyamides?Reprogramming cell fate with artificial transcription factors.Chemical modification of a synthetic small molecule boosts its biological efficacy against pluripotency genes in mouse fibroblasts.The past and presence of gene targeting: from chemicals and DNA via proteins to RNA.
P2860
Q24628320-496503A3-8FE5-4B8B-9B33-E21B60DF4364Q33717554-5240CBEB-58DA-4A70-B367-B65ADF1876B1Q34381076-939C317A-6289-406C-B0C1-1F83C9C0976EQ34421960-52494054-5449-4AD5-AD71-E0F8F42A0641Q34459196-52E3DD24-FDF5-4C0A-BA81-A057DDB4C238Q35066396-968CA894-F833-45FF-83C6-7B6387B22A09Q36031605-3946D352-256F-4955-AAC8-BEE5CBDBBC37Q36275422-1972B283-A648-4A31-8543-5B4998938C62Q36342812-175BAF69-15A7-4459-BC32-9556B8ED7E4AQ37210876-9BF77FB1-6F41-4412-B7AC-1D129284481DQ38105825-0D4A1ECD-544A-4CF4-96C5-27AA8B6FE55AQ38313901-DE579274-0AEF-4052-9F2B-276CABF81F38Q39164084-59D717A7-8772-4DEC-B5A7-956DB0D91FF5Q42806236-5E0FF25E-C0B7-4862-B431-614DC37938C0Q47766729-C05C5E9A-077B-41BA-95A5-4197EBD5117CQ48345023-C6A17F3E-A27C-4136-9BFC-FBF79758049AQ49497409-2ACE3095-3FC4-4668-9B3E-187653B65859Q51067185-8D9D0379-D16B-4356-BD74-DBAF23688DC5Q52431809-32127339-2647-48EB-860F-4A223542BB24
P2860
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
@ast
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
@en
type
label
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
@ast
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
@en
prefLabel
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
@ast
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
@en
P2860
P356
P1476
Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.
@en
P2093
David C Montgomery
P2860
P304
P356
10.1093/NAR/GKR970
P407
P577
2011-11-12T00:00:00Z