Year |
Citation |
Score |
2020 |
Kumar P, Caruthers MH. DNA Analogues Modified at the Nonlinking Positions of Phosphorus. Accounts of Chemical Research. PMID 32885957 DOI: 10.1021/acs.accounts.0c00078 |
0.425 |
|
2020 |
Langner HK, Jastrzebska K, Caruthers MH. Synthesis and Characterization of Thiophosphoramidate Morpholino Oligonucleotides and Chimeras. Journal of the American Chemical Society. PMID 32866014 DOI: 10.1021/jacs.0c04335 |
0.392 |
|
2019 |
Krishna H, Jastrzebska K, Caruthers M. Exploring site-specific activation of bis-N,N'-dialkylaminophosphordiamidites and the synthesis of morpholinophosphoramidate oligonucleotides. Febs Letters. 593: 1459-1467. PMID 31206627 DOI: 10.1002/1873-3468.13492 |
0.373 |
|
2019 |
Paul S, Caruthers MH. Retraction of "Synthesis of Phosphorodiamidate Morpholino Oligonucleotides and Their Chimeras Using Phosphoramidite Chemistry". Journal of the American Chemical Society. PMID 31144801 DOI: 10.1021/jacs.7b04308 |
0.303 |
|
2017 |
Paul S, Roy S, Monfregola L, Shang S, Shoemaker R, Caruthers MH. Correction to "Oxidative Substitution of Boranephosphonate Diesters as a Route to Post-synthetically Modified DNA". Journal of the American Chemical Society. PMID 28915019 DOI: 10.1021/Jacs.7B08410 |
0.771 |
|
2017 |
Roy S, Olesiak M, Shang S, Caruthers MH. Correction to "Silver Nanoassemblies Constructed from Boranephosphonate DNA". Journal of the American Chemical Society. PMID 28902993 DOI: 10.1021/Jacs.7B08409 |
0.759 |
|
2017 |
Vejlegaard K, Paul S, Kosbar T, Wengel J, Caruthers MH. Oligodeoxynucleotides containing 2'-amino-LNA nucleotides as constrained morpholino phosphoramidate and phosphorodiamidate monomers. Bioorganic & Medicinal Chemistry Letters. PMID 28552336 DOI: 10.1016/j.bmcl.2017.05.023 |
0.323 |
|
2017 |
Roy S, Paul S, Roy M, Kundu R, Monfregola L, Caruthers MH. Corrections to "Pyridinium Boranephosphonate Modified DNA Oligonucleotides". The Journal of Organic Chemistry. PMID 28467068 DOI: 10.1021/Acs.Joc.7B01022 |
0.732 |
|
2017 |
Roy S, Paul S, Roy M, Kundu R, Monfregola L, Caruthers MH. Pyridinium Boranephosphonate Modified DNA Oligonucleotides. The Journal of Organic Chemistry. PMID 28099007 DOI: 10.1021/Acs.Joc.6B02599 |
0.766 |
|
2016 |
Shang S, Monfregola L, Caruthers MH. Peptide-substituted oligonucleotide synthesis and non-toxic, passive cell delivery. Signal Transduction and Targeted Therapy. 1: 16019. PMID 29263901 DOI: 10.1038/sigtrans.2016.19 |
0.725 |
|
2016 |
Paul S, Caruthers MH. Synthesis of Phosphorodiamidate Morpholino Oligonucleotides and Their Chimeras Using Phosphoramidite Chemistry. Journal of the American Chemical Society. 138: 15663-15672. PMID 27934012 DOI: 10.1021/jacs.6b08854 |
0.416 |
|
2015 |
Paul S, Roy S, Monfregola L, Shang S, Shoemaker R, Caruthers MH. Correction to "Oxidative Substitution of Boranephosphonate Diesters as a Route to Post-synthetically Modified DNA". Journal of the American Chemical Society. 137: 10016. PMID 26196959 DOI: 10.1021/jacs.5b04071 |
0.771 |
|
2015 |
Russell C, Roy S, Ganguly S, Qian X, Caruthers MH, Nilsson M. Formation of Silver Nanostructures by Rolling Circle Amplification Using Boranephosphonate-Modified Nucleotides. Analytical Chemistry. 87: 6660-6. PMID 26059318 DOI: 10.1021/Acs.Analchem.5B00783 |
0.395 |
|
2015 |
Paul S, Roy S, Monfregola L, Shang S, Shoemaker R, Caruthers MH. Oxidative substitution of boranephosphonate diesters as a route to post-synthetically modified DNA. Journal of the American Chemical Society. 137: 3253-64. PMID 25679520 DOI: 10.1021/Ja511145H |
0.794 |
|
2014 |
Caruthers MH. Robert Letsinger: the father of synthetic DNA chemistry. Proceedings of the National Academy of Sciences of the United States of America. 111: 18098-9. PMID 25422449 DOI: 10.1073/pnas.1420277111 |
0.387 |
|
2013 |
Roy S, Caruthers M. Synthesis of DNA/RNA and their analogs via phosphoramidite and H-phosphonate chemistries Molecules. 18: 14268-14284. PMID 24252996 DOI: 10.3390/Molecules181114268 |
0.471 |
|
2013 |
Roy S, Olesiak M, Shang S, Caruthers MH. Silver nanoassemblies constructed from boranephosphonate DNA. Journal of the American Chemical Society. 135: 6234-41. PMID 23557435 DOI: 10.1021/Ja400898S |
0.763 |
|
2013 |
Caruthers MH. The chemical synthesis of DNA/RNA: our gift to science. The Journal of Biological Chemistry. 288: 1420-7. PMID 23223445 DOI: 10.1074/jbc.X112.442855 |
0.39 |
|
2012 |
Krishna H, Caruthers MH. Alkynyl phosphonate DNA: a versatile "click"able backbone for DNA-based biological applications. Journal of the American Chemical Society. 134: 11618-31. PMID 22612466 DOI: 10.1021/ja3026714 |
0.375 |
|
2012 |
Threlfall RN, Torres AG, Krivenko A, Gait MJ, Caruthers MH. Synthesis and biological activity of phosphonoacetate- and thiophosphonoacetate-modified 2'-O-methyl oligoribonucleotides. Organic & Biomolecular Chemistry. 10: 746-54. PMID 22124653 DOI: 10.1039/c1ob06614e |
0.331 |
|
2011 |
Dellinger DJ, Timár Z, Myerson J, Sierzchala AB, Turner J, Ferreira F, Kupihár Z, Dellinger G, Hill KW, Powell JA, Sampson JR, Caruthers MH. Streamlined process for the chemical synthesis of RNA using 2'-O-thionocarbamate-protected nucleoside phosphoramidites in the solid phase. Journal of the American Chemical Society. 133: 11540-56. PMID 21688829 DOI: 10.1021/Ja201561Z |
0.349 |
|
2011 |
Krishna H, Caruthers MH. Solid-phase synthesis, thermal denaturation studies, nuclease resistance, and cellular uptake of (oligodeoxyribonucleoside)methylborane phosphine-DNA chimeras. Journal of the American Chemical Society. 133: 9844-54. PMID 21585202 DOI: 10.1021/ja201314q |
0.408 |
|
2011 |
Caruthers MH. A brief review of DNA and RNA chemical synthesis. Biochemical Society Transactions. 39: 575-80. PMID 21428942 DOI: 10.1042/BST0390575 |
0.373 |
|
2011 |
Olesiak M, Krivenko A, Krishna H, Caruthers MH. Synthesis and biological activity of borane phosphonate DNA Phosphorus, Sulfur and Silicon and the Related Elements. 186: 921-932. DOI: 10.1080/10426507.2010.538456 |
0.418 |
|
2010 |
LeProust EM, Peck BJ, Spirin K, McCuen HB, Moore B, Namsaraev E, Caruthers MH. Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process. Nucleic Acids Research. 38: 2522-40. PMID 20308161 DOI: 10.1093/nar/gkq163 |
0.357 |
|
2010 |
SEEBERGER PH, CARUTHERS MH. ChemInform Abstract: Modified Oligodeoxynucleotides as Antisense Therapeutics Cheminform. 29: no-no. DOI: 10.1002/chin.199831312 |
0.37 |
|
2010 |
SEEBERGER PH, JORGENSEN PN, BANKAITIS-DAVIS DM, BEATON G, CARUTHERS MH. ChemInform Abstract: Nucleotide Chemistry. Part 46. 5′-Dithiophosphoryl Deoxyoligonucleotides: Synthesis and Biological Studies. Cheminform. 28: no-no. DOI: 10.1002/chin.199707253 |
0.471 |
|
2010 |
WIESLER WT, CARUTHERS MH. ChemInform Abstract: Nucleotide Chemistry. Part 42. Synthesis of Phosphorodithioate DNA via Sulfur-Linked, Base-Labile Protecting Groups. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199645258 |
0.405 |
|
2010 |
SEEBERGER PH, CARUTHERS MH. ChemInform Abstract: Oxidative Formation of Phosphorodithioates via H-Phosphonodithioates. Cheminform. 26: no-no. DOI: 10.1002/chin.199523165 |
0.401 |
|
2010 |
CARUTHERS MH. ChemInform Abstract: Synthesis of DNA, RNA, and Biochemically Interesting Analogs Cheminform. 22: no-no. DOI: 10.1002/chin.199105330 |
0.432 |
|
2007 |
Yamada CM, Dellinger DJ, Caruthers MH. Synthesis and biological activity of phosphonocarboxylate DNA. Nucleosides, Nucleotides & Nucleic Acids. 26: 539-46. PMID 18066852 DOI: 10.1080/15257770701489896 |
0.806 |
|
2006 |
McCuen HB, Noé MS, Sierzchala AB, Higson AP, Caruthers MH. Synthesis of mixed sequence borane phosphonate DNA. Journal of the American Chemical Society. 128: 8138-9. PMID 16787069 DOI: 10.1021/Ja061757E |
0.327 |
|
2006 |
Yamada CM, Dellinger DJ, Caruthers MH. Synthesis and biochemical evaluation of phosphonoformate oligodeoxyribonucleotides. Journal of the American Chemical Society. 128: 5251-61. PMID 16608361 DOI: 10.1021/Ja060112B |
0.785 |
|
2005 |
Dellinger DJ, Betley JR, Wyrzykiewicz TK, Caruthers MH. Synthesis of DNA using a new two-step cycle. Methods in Molecular Biology (Clifton, N.J.). 288: 1-16. PMID 15333894 |
0.324 |
|
2005 |
Caruthers MH. New methods for synthesizing DNA, RNA, and phosphonates Chimia. 59: 39-42. |
0.388 |
|
2004 |
Dellinger DJ, Yamada CM, Caruthers MH. Oligodeoxyribonucleotide analogs functionalized with phosphonoacetate and thiophosphonoacetate diesters. Current Protocols in Nucleic Acid Chemistry / Edited by Serge L. Beaucage ... [Et Al.]. Unit 4.24. PMID 18428930 DOI: 10.1002/0471142700.Nc0424S18 |
0.811 |
|
2003 |
Sierzchala AB, Dellinger DJ, Betley JR, Wyrzykiewicz TK, Yamada CM, Caruthers MH. Solid-phase oligodeoxynucleotide synthesis: a two-step cycle using peroxy anion deprotection. Journal of the American Chemical Society. 125: 13427-41. PMID 14583038 DOI: 10.1021/Ja030376N |
0.773 |
|
2003 |
Sheehan D, Lunstad B, Yamada CM, Stell BG, Caruthers MH, Dellinger DJ. Biochemical properties of phosphonoacetate and thiophosphonoacetate oligodeoxyribonucleotides. Nucleic Acids Research. 31: 4109-18. PMID 12853628 DOI: 10.1093/Nar/Gkg439 |
0.66 |
|
2003 |
Dellinger DJ, Sheehan DM, Christensen NK, Lindberg JG, Caruthers MH. Solid-phase chemical synthesis of phosphonoacetate and thiophosphonoacetate oligodeoxynucleotides. Journal of the American Chemical Society. 125: 940-50. PMID 12537492 DOI: 10.1021/ja027983f |
0.357 |
|
2002 |
Jenkins KE, Higson AP, Seeberger PH, Caruthers MH. Solid-phase synthesis and biochemical studies of O-boranophosphopeptides and O-dithiophosphopeptides. Journal of the American Chemical Society. 124: 6584-93. PMID 12047178 DOI: 10.1021/Ja0126576 |
0.448 |
|
2002 |
Brummel HA, Caruthers MH. Chemical synthesis of an oligodeoxythymidylate containing boranephosphate and phosphate linkages Tetrahedron Letters. 43: 749-751. DOI: 10.1016/S0040-4039(01)02278-X |
0.777 |
|
1999 |
Seeberger PH, Caruthers MH, Bankaitis-Davis D, Beaton G. Synthesis of phosphorodithioate DNA by the H-phosphonothioate method Tetrahedron. 55: 5759-5772. DOI: 10.1016/S0040-4020(99)00241-0 |
0.559 |
|
1998 |
Higson AP, Sierzchala A, Brummel H, Zhao Z, Caruthers MH. Synthesis of an oligothymidylate containing boranophosphate linkages Tetrahedron Letters. 39: 3899-3902. DOI: 10.1016/S0040-4039(98)00687-X |
0.787 |
|
1996 |
Wiesler WT, Caruthers MH. Synthesis of Phosphorodithioate DNA via Sulfur-Linked, Base-Labile Protecting Groups(1). The Journal of Organic Chemistry. 61: 4272-4281. PMID 11667326 DOI: 10.1021/jo960274y |
0.43 |
|
1996 |
Cummins L, Graff D, Beaton G, Marshall WS, Caruthers MH. Biochemical and physicochemical properties of phosphorodithioate DNA. Biochemistry. 35: 8734-41. PMID 8679636 DOI: 10.1021/bi960318x |
0.456 |
|
1996 |
Seeberger PH, Jorgensen PN, Bankaitis-Davis DM, Beaton G, Caruthers MH. 5'-Dithiophosphoryl deoxyoligonucleotides: Synthesis and biological studies Journal of the American Chemical Society. 118: 9562-9566. DOI: 10.1021/Ja961189A |
0.468 |
|
1996 |
Zhao Z, Caruthers MH. Synthesis and preliminary biochemical studies with 5'-deoxy-5'-methylidyne phosphonate linked thymidine oligonucleotides Tetrahedron Letters. 37: 6239-6242. DOI: 10.1016/0040-4039(96)01380-9 |
0.321 |
|
1996 |
Greef CH, Seeberger PH, Caruthers MH, Beaton G, Bankaitis-Davis D. Synthesis of phosphorodithioate RNA by the H-phosphonothioate method Tetrahedron Letters. 37: 4451-4454. DOI: 10.1016/0040-4039(96)00882-9 |
0.477 |
|
1995 |
Seeberger PH, Yau E, Caruthers MH. 2'-deoxynucleoside dithiophosphates: Synthesis and biological studies Journal of the American Chemical Society. 117: 1472-1478. DOI: 10.1021/Ja00110A002 |
0.448 |
|
1995 |
Seeberger PH, Caruthers MH. Oxidative formation of phosphorodithioates via H-phosphonodithioates Tetrahedron Letters. 36: 695-698. DOI: 10.1016/0040-4039(94)02355-F |
0.428 |
|
1993 |
Piccirilli JA, Vyle JS, Caruthers MH, Cech TR. Metal ion catalysis in the Tetrahymena ribozyme reaction. Nature. 361: 85-8. PMID 8421499 DOI: 10.1038/361085A0 |
0.68 |
|
1993 |
Wiesler WT, Marshall WS, Caruthers MH. Synthesis and purification of phosphorodithioate DNA. Methods in Molecular Biology (Clifton, N.J.). 20: 191-206. PMID 8242137 DOI: 10.1385/0-89603-281-7:191 |
0.415 |
|
1991 |
Caruthers MH, Beaton G, Cummins L, Graff D, Hall M, Marshall WS, Sasmor H, Wiesler W. Synthesis and biological studies with dithioate DNA. Nucleic Acids Symposium Series. 91-4. PMID 1726757 |
0.414 |
|
1991 |
Caruthers MH, Beaton G, Cummins L, Graff D, Ma YX, Marshall WS, Sasmor H, Norris P, Yau EK. Synthesis and biochemical studies of dithioate DNA. Ciba Foundation Symposium. 158: 158-66; discussion 1. PMID 1718668 |
0.409 |
|
1991 |
Caruthers MH, Beaton G, Cummins L, Dellinger D, Graff D, Ma - YX, Marshall WS, Sasmor H, Shankland P, Van Wu J, Yau EK. Chemical and biochemical studies with dithioate DNA Nucleosides and Nucleotides. 10: 47-59. DOI: 10.1080/07328319108046435 |
0.36 |
|
1991 |
Beaton G, Brill WKD, Grandas A, Ma YX, Nielsen J, Yau E, Caruthers MH. Synthesis of oligonucleotide phosphorodithioates Tetrahedron. 47: 2377-2388. DOI: 10.1016/S0040-4020(01)81775-0 |
0.635 |
|
1991 |
Caruthers MH. Chemical synthesis of DNA and DNA analogues Accounts of Chemical Research. 24: 278-284. |
0.412 |
|
1989 |
Caruthers MH. Chemical synthesis of DNA Journal of Chemical Education. 66: 577. DOI: 10.1021/ED066P577 |
0.417 |
|
1989 |
Grandas A, Marshall WS, Nielsen J, Caruthers MH. Synthesis of deoxycytidine oligomers containing phosphorodithioate linkages Tetrahedron Letters. 30: 543-546. DOI: 10.1016/S0040-4039(00)95248-1 |
0.566 |
|
1988 |
Nielsen J, Caruthers MH. Directed Arbuzov-type reactions of 2-cyano-1,1-dimethylethyl deoxynucleoside phosphites. Journal of the American Chemical Society. 110: 6275-6. PMID 22148829 DOI: 10.1021/Ja00226A069 |
0.434 |
|
1988 |
Brill WKD, Nielsen J, Caruthers MH. Synthesis of dinucleoside phosphorodithioates via thioamidites Tetrahedron Letters. 29: 5517-5520. DOI: 10.1016/S0040-4039(00)80801-1 |
0.62 |
|
1988 |
Nielsen J, Brill WKD, Caruthers MH. Synthesis and characterization of dinucleoside phosphorodithioates Tetrahedron Letters. 29: 2911-2914. DOI: 10.1016/0040-4039(88)85045-7 |
0.537 |
|
1988 |
CARUTHERS MH. ChemInform Abstract: DNA Synthesis for Nonchemists: The Phosphoramidite Method on Silica Supports Cheminform. 19. DOI: 10.1002/CHIN.198829349 |
0.375 |
|
1987 |
Dubendorff JW, deHaseth PL, Rosendahl MS, Caruthers MH. DNA functional groups required for formation of open complexes between Escherichia coli RNA polymerase and the lambda PR promoter. Identification via base analog substitutions. The Journal of Biological Chemistry. 262: 892-8. PMID 2948952 |
0.315 |
|
1986 |
Kierzek R, Kopp DW, Edmonds M, Caruthers MH. Chemical synthesis of branched RNA. Nucleic Acids Research. 14: 4751-64. PMID 2425338 DOI: 10.1093/Nar/14.12.4751 |
0.301 |
|
1985 |
Caruthers MH. Gene synthesis machines: DNA chemistry and its uses. Science (New York, N.Y.). 230: 281-5. PMID 3863253 |
0.419 |
|
1983 |
deHaseth PL, Goldman RA, Cech CL, Caruthers MH. Chemical synthesis and biochemical reactivity of bacteriophage lambda PR promoter. Nucleic Acids Research. 11: 773-87. PMID 6300767 |
0.416 |
|
1982 |
Nick H, Arndt K, Boschelli F, Jarema MA, Lillis M, Sadler J, Caruthers M, Lu P. lac repressor-lac operator interaction: NMR observations. Proceedings of the National Academy of Sciences of the United States of America. 79: 218-22. PMID 7043455 DOI: 10.1073/Pnas.79.2.218 |
0.317 |
|
1982 |
Lillis M, Nick H, Lu P, Sadler J, Caruthers MH. Iac operon operator DNA: isolation and trimming for NMR spectroscopy. Analytical Biochemistry. 120: 52-8. PMID 6283934 DOI: 10.1016/0003-2697(82)90316-5 |
0.363 |
|
1976 |
Agarwal KL, Caruthers MH, Büchi H, van de Sande JH, Khorana HG. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 6. Synthesis of the deoxyribopolynucleotide segments corresponding to the nucleotide sequence 100-126. The Journal of Biological Chemistry. 251: 624-33. PMID 765331 |
0.41 |
|
1976 |
Jay E, Cashion PJ, Fridkin M, Ramamoorthy B, Agarwal KL, Caruthers MH, Khorana HG. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 5. Synthesis of the deoxyribopolynucleotide segments representing the nucleotide sequence 71-103. The Journal of Biological Chemistry. 251: 609-23. PMID 765330 |
0.38 |
|
1976 |
Agarwal KL, Caruthers MH, Fridkin M, Kumar A, van de Sande JH, Khorana HG. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 4. Synthesis of deoxyribopolynucleotide segments corresponding to the nucleotide sequence 47-78. The Journal of Biological Chemistry. 251: 599-608. PMID 765329 |
0.401 |
|
1976 |
van de Sande JH, Caruthers MH, Kumar A, Khorana HG. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 2. Chemical synthesis of the deoxypolynucleotide segments corresponding to the nucleotide sequence 1-31. The Journal of Biological Chemistry. 251: 571-86. PMID 765328 |
0.408 |
|
1976 |
Khorana HG, Agarwal KL, Besmer P, Büchi H, Caruthers MH, Cashion PJ, Fridkin M, Jay E, Kleppe K, Kleppe R, Kumar A, Loewen PC, Miller RC, Minamoto K, Panet A, et al. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 1. General introduction. The Journal of Biological Chemistry. 251: 565-70. PMID 765327 |
0.573 |
|
1976 |
Kleppe R, Sekiya T, Loewen PC, Kleppe K, Agarwal KL, Büchi H, Besmer P, Caruthers MH, Cashion PJ, Fridkin M, Jay E, Kumar A, Miller RC, Minamoto K, Panet A, et al. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 11. Enzymatic joining to form the total DNA duplex. The Journal of Biological Chemistry. 251: 667-75. PMID 175058 |
0.508 |
|
1976 |
Caruthers MH, Kleppe R, Kleppe K, Khorana HG. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 10. Enzymatic joining of chemically synthesized segments to form the DNA duplex corresponding to the nucleotide sequence 86-126. The Journal of Biological Chemistry. 251: 658-66. PMID 175057 |
0.514 |
|
1976 |
Minamoto K, Caruthers MH, Ramamoorthy B, van de Sande JH, Sidorova N, Khorana HG. Total synthesis of the structural gene for the precursor of a tyrosine suppressor transfer RNA from Escherichia coli. 3. Synthesis of deoxyribopolynucleotide segments corresponding to the nucleotide sequence 27-51. The Journal of Biological Chemistry. 251: 587-98. PMID 175056 |
0.419 |
|
1975 |
Powers GJ, Jones RL, Randall GA, Caruthers MH, van de Sande JH, Khorana HG. Optimal strategies for the chemical and enzymatic synthesis of bihelical deoxyribonucleic acids. Journal of the American Chemical Society. 97: 875-84. PMID 1133373 |
0.429 |
|
1972 |
Besmer P, Miller RC, Caruthers MH, Kumar A, Minamoto K, Van de Sande JH, Sidarova N, Khorana HG. Studies on polynucleotides. CXVII. Hybridization of polydeoxynucleotides with tyrosine transfer RNA sequences to the r-strand of phi80psu + 3 DNA. Journal of Molecular Biology. 72: 503-22. PMID 4660319 |
0.526 |
|
1972 |
Caruthers MH, Kleppe K, Van de Sande JH, Sgaramella V, Agarwal KL, Büchi H, Gupta NK, Kumar A, Otsuka E, RajBhandary UL, Terao T, Weber H, Yamada T, Khorana HG. CXV. Total synthesis of the structural gene for an alanine transfer RNA from yeast. Enzymic joining to form the total DNA duplex. Journal of Molecular Biology. 72: 475-92. PMID 4571087 DOI: 10.1016/0022-2836(72)90158-1 |
0.451 |
|
1972 |
Van de Sande JH, Caruthers MH, Sgaramella V, Yamada T, Khorana HG. CXIV. Total synthesis of the structural gene for an alanine transfer RNA from yeast. Enzymic joining of the chemically synthesized segments to form the DNA duplex corresponding to nucleotide sequence 46 to 77. Journal of Molecular Biology. 72: 457-74. PMID 4571086 |
0.565 |
|
1972 |
Caruthers MH, Khorana HG. CXI. Total synthesis of the structural gene for an alanine transfer ribonucleic acid from yeast. Synthesis of a dodecadeoxynucleotide and a heptadeoxynucleotide corresponding to the nucleotide sequence 66 to 77. Journal of Molecular Biology. 72: 407-26. PMID 4571083 |
0.455 |
|
1972 |
Caruthers MH, Van de Sande JH, Khorana HG. CX. Total synthesis of the structural gene for an alanine transfer ribonucleic acid from yeast. Synthesis of three decadeoxynucleotides corresponding to the nucleotide sequence 51 to 70. Journal of Molecular Biology. 72: 375-405. PMID 4571082 |
0.455 |
|
1972 |
Khorana HG, Agarwal KL, Büchi H, Caruthers MH, Gupta NK, Kleppe K, Kumar A, Otsuka E, RajBhandary UL, Van de Sande JH, Sgaramella V, Terao T, Weber H, Yamada T. Studies on polynucleotides. 103. Total synthesis of the structural gene for an alanine transfer ribonucleic acid from yeast. Journal of Molecular Biology. 72: 209-17. PMID 4571075 DOI: 10.1016/0022-2836(72)90146-5 |
0.536 |
|
1970 |
Agarwal KL, Büchi H, Caruthers MH, Gupta N, Khorana HG, Kleppe K, Kumar A, Ohtsuka E, Rajbhandary UL, Van de Sande JH, Sgaramella V, Weber H, Yamada T. Total synthesis of the gene for an alanine transfer ribonucleic acid from yeast. Nature. 227: 27-34. PMID 5422620 DOI: 10.1038/227027a0 |
0.422 |
|
1970 |
AGARWAL KL, BUECHI H, CARUTHERS MH, GUPTA N, KHORANA HG, KLEPPE K, KUMAR A, OHTSUKA E, RAJBHANDARY UL, VAN DE SANDE JH, SGARAMELLA V, WEBER H, YAMADA T. ChemInform Abstract: TOTALSYNTH. DES GENS FUER EINE ALANIN-TRANSFER-RIBONUCLEINSAEURE AUS HEFE Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197039343 |
0.352 |
|
1968 |
Khorana HG, Büchi H, Caruthers MH, Chang SH, Gupta NK, Kumar A, Ohtsuka E, Sgaramella V, Weber H. Progress in the total synthesis of the gene for ala-tRNA. Cold Spring Harbor Symposia On Quantitative Biology. 33: 35-44. PMID 5254575 |
0.421 |
|
1967 |
Letsinger RL, Caruthers MH, Miller PS, Ogilvie KK. Oligonucleotide syntheses utilizing beta-benzoylpropionyl, a blocking group with a trigger for selective cleavage. Journal of the American Chemical Society. 89: 7146-7. PMID 6064358 DOI: 10.1021/Ja01002A074 |
0.665 |
|
1967 |
Letsinger RL, Caruthers MH, Jerina DM. Reactions of nucleosides on polymer supports. Synthesis of thymidylylthymidylylthymidine. Biochemistry. 6: 1379-88. PMID 6036831 DOI: 10.1021/Bi00857A021 |
0.579 |
|
Show low-probability matches. |