Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure. - Wikidata - awgldk - TriplyDB

Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure.

Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure.

http://www.wikidata.org/entity/Q40406767

about

Determination of optimal sites of antisense oligonucleotide cleavage within TNFalpha mRNA.Polyamine-assisted rapid and clean cleavage of oligonucleotides from cis-diol bearing universal support Characterization of specific noncovalent complexes between guanidinium derivatives and single-stranded DNA by MALDI.Developmentally regulated initiation of DNA synthesis by telomerase: evidence for factor-assisted de novo telomere formation.Interactions of oligonucleotide analogs containing methylphosphonate internucleotide linkages and 2'-O-methylribonucleosides.Processing of nontelomeric 3' ends by telomerase: default template alignment and endonucleolytic cleavage.Design and calibration of a semi-synthetic DNA phasing assay.Application of oligonucleoside methylphosphonates in the studies on phosphodiester hydrolysis by Serratia endonuclease.Effects of phosphate neutralization on the shape of the AP-1 transcription factor binding site in duplex DNA.Role of asymmetric phosphate neutralization in DNA bending by PU.1.Antisense oligonucleotide containing an internal, non-nucleotide-based linker promote site-specific cleavage of RNA Charge neutralization and DNA bending by the Escherichia coli catabolite activator protein Solid-phase synthesis of oligo-2-pyrimidinone-2'-deoxyribonucleotides and oligo-2-pyrimidinone-2'-deoxyriboside methylphosphonates.Synthesis and thermodynamics of oligonucleotides containing chirally pure R(P) methylphosphonate linkages.Hydroquinone-O,O'-diacetic acid ('Q-linker') as a replacement for succinyl and oxalyl linker arms in solid phase oligonucleotide synthesis.Synthesis of 3H-labeled nucleoside-methyl[CT3]phosphonamidite and incorporation into methylphosphonate oligonucleotides for biodistribution and biostability studies.On the rapid deprotection of synthetic oligonucleotides and analogs.Synthesis of oligodeoxynucleoside methylphosphonates utilizing the tert-butylphenoxyacetyl group for exocyclic amine protection.The application of the AMB protective group in the solid-phase synthesis of methylphosphonate DNA analogues.The energetic contribution of induced electrostatic asymmetry to DNA bending by a site-specific protein.Chemical synthesis of RNA with site-specific methylphosphonate modifications.Analysis of oligonucleotides by ion-pairing hydrophilic interaction liquid chromatography/electrospray ionization mass spectrometry.

P2860

Q30704352-54E422C2-DA12-4004-B4D3-157CF32D80A9 Q30872898-4DE52C13-00FF-488E-A6F0-71511AA1C804 Q33232613-EECBF0B4-FA2D-4767-B95C-897C530E95B8 Q33886575-05B9A15D-24E8-4FEC-9B40-2E207B78B029 Q34889727-84835C96-B978-46DD-8AAE-DE41EEBE16F5 Q36560631-431A1AF1-459D-4578-9D4F-EC02DC038C91 Q38306261-F9635FF1-5599-434A-B068-9D9E4724E88B Q38318823-1EF196D4-2432-41D3-9EF2-EF03D74BD12A Q38336842-4B447A8A-486A-44EB-A3D3-922CBF3D5538 Q38340065-A4856D1F-8550-4BBA-A613-619F9B92E8E7 Q38361679-82A9A883-0014-4BE3-A19F-1301DAA03BCD Q39600784-F8D47B5A-AB3F-4A77-8305-D1CED8931F20 Q39716857-3FED4ED7-C603-4269-800A-0C7248ED75F1 Q39718205-366ECF37-4B50-4A40-8629-7613B8BFFC7D Q39721115-85B33D32-9359-4013-9FD0-1DADCC1464A0 Q40395758-2372C9B1-FB28-4BCA-AE16-C59CE4FBB37C Q40398633-0BE5ACB7-1C7A-43F4-9ED8-4C4C18A93AD1 Q40411143-A79CC4BD-A46C-4C01-A505-BF69A3C69E5C Q40519835-EE57FC0D-A103-45E9-9A8B-6185E4EC5250 Q42060631-8BB91B0D-4A4E-4496-A90B-5A3DB53CFAF5 Q42290462-1B55E0EA-4B58-44F8-A2C1-6BB56780EBAE Q48253481-58BE1CE0-FE9A-49DC-96CD-8BEBB6E24B8A

P2860

Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure.

http://www.wikidata.org/entity/Q40406767

description

1993 nî lūn-bûn

@nan

1993年の論文

@ja

1993年論文

@yue

1993年論文

@zh-hant

1993年論文

@zh-hk

1993年論文

@zh-mo

1993年論文

@zh-tw

1993年论文

@wuu

1993年论文

@zh

1993年论文

@zh-cn

name

Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure.

@en

type

label

Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure.

@en

prefLabel

Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure.

@en

P1433

Q40406767-2940CF82-BDBE-434B-91A3-025EA439DDD7

P1476

Q40406767-7F503140-67FF-4926-9FD3-EB1D91F31F44

P2093

Q40406767-03779989-CB81-41DA-890E-66F383708061

Q40406767-62198CB5-8DE3-4EB9-8FE1-7CE8FD559D65

Q40406767-8713BCE9-B501-4544-B8DC-4B054C27C4EC

Q40406767-A7318CBC-FECF-4BF8-BB87-EEF3E12C7ECB

Q40406767-F6618992-0192-4A5B-A2CE-787FAAC86063

P2860

Q40406767-182AA913-8576-4A91-960C-A60F93F0E075

Q40406767-25B7ACC0-8F60-46E4-B5E4-3330116CFF68

Q40406767-3742E5B5-EEE7-4C5A-AC57-39B53B6B0255

Q40406767-37DD91A1-B0D5-4CD5-B236-5436B2F2842C

Q40406767-4A4ED6A1-1671-46D9-9D27-2DCB60E8C0C5

Q40406767-4D999A34-3E03-468E-9E32-84593653E7E0

Q40406767-56C6A86A-C352-4176-81CA-568566AAD810

Q40406767-60875EB3-3795-4179-8F32-41424B50F667

Q40406767-AF9250A8-1B13-4DB4-86CF-2A86F24764E3

Q40406767-CD099BA6-ACA5-4458-B709-608B12FDFBF1

P304

Q40406767-8BF4CBE3-5C03-4B5A-950E-E7B3BDDF2DB4

P31

Q40406767-5B4BEBF7-012C-495C-9894-2C3DEB60A29E

P356

Q40406767-3C404750-F327-4EE4-8891-FBBC72F1F6E3

P433

Q40406767-2E0605CF-6158-4457-9528-1AEDBF9FFD96

P478

Q40406767-E03A0C14-4C07-40B0-A466-A5FF48CBDDA5

P577

Q40406767-BE563B62-BF49-42E0-8357-DE2412757FE1

P5875

Q40406767-309B6265-8190-4BC9-B2F8-252362FE9736

P698

Q40406767-0E0784DA-C4DD-47B3-91C6-A302C4A0EBF2

P932

Q40406767-088A83C4-94CC-40E8-A6E6-F7F9931DDDB7

P356

P1433

Nucleic Acids Research

P1476

Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure.

@en

P2093

K M Young

http://www.w3.org/2001/XMLSchema#string

L J Arnold

http://www.w3.org/2001/XMLSchema#string

M A Reynolds

http://www.w3.org/2001/XMLSchema#string

M M Vaghefi

http://www.w3.org/2001/XMLSchema#string

R I Hogrefe

http://www.w3.org/2001/XMLSchema#string

P2860

The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups

Inhibition of acquired immunodeficiency syndrome virus by oligodeoxynucleoside methylphosphonates

Site specificity of the inhibitory effects of oligo(nucleoside methylphosphonate)s complementary to the acceptor splice junction of herpes simplex virus type 1 immediate early mRNA 4

Oligonucleoside methylphosphonates as antisense reagents.

Antiviral effect of an oligo(nucleoside methylphosphonate) complementary to the splice junction of herpes simplex virus type 1 immediate early pre-mRNAs 4 and 5.

Preparation of oligodeoxyribonucleoside methylphosphonates on a polystyrene support.

Synthesis and enzymatic properties of deoxyribooligonucleotides containing methyl and phenylphosphonate linkages

Comparative hybrid arrest by tandem antisense oligodeoxyribonucleotides or oligodeoxyribonucleoside methylphosphonates in a cell-free system

Inhibition of human immunodeficiency virus by using an oligonucleoside methylphosphonate targeted to the tat-3 gene.

Antisense oligodeoxynucleotides as antiviral agents.

P304

2031-2038

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1093/NAR/21.9.2031

http://www.w3.org/2001/XMLSchema#string

P433

9

http://www.w3.org/2001/XMLSchema#string

P478

21

http://www.w3.org/2001/XMLSchema#string

P577

1993-05-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

14695862

http://www.w3.org/2001/XMLSchema#string

P698

8502543

http://www.w3.org/2001/XMLSchema#string

P932

309461

http://www.w3.org/2001/XMLSchema#string