DNA-SYNTHESIS

[1] NUCLEOSIDE 3'-PHOSPHOTRIESTERS AS KEY INTERMEDIATES FOR OLIGORIBONUCLEOTIDE SYNTHESIS .3. IMPROVED PREPARATION OF NUCLEOSIDE 3'-PHOSPHOTRIESTERS, THEIR H-1 NMR CHARACTERIZATION AND NEW CONDITIONS FOR REMOVAL OF 2-CYANOETHYL GROUP [J]. NUCLEIC ACIDS RESEARCH, 1976, 3 (12) : 3397 - 3408

[2] CHEMICAL SYNTHESIS OF ANTICODON LOOP OF AN EUKARYOTIC INITIATOR TRANSFER-RNA CONTAINING HYPERMODIFIED NUCLEOSIDE N-6-N-THREONYLCARBONY-ADENOSINE-T6A-1 [J]. NUCLEIC ACIDS RESEARCH, 1978, 5 (06) : 1889 - 1905

[3] ADAMIAK RW, 1977, TETRAHEDRON LETT, P1431

[4] DEOXYOLIGONUCLEOTIDE SYNTHESIS USING A NEW PHOSPHATE PROTECTING GROUP [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (06) : 2020 - 2021

[5] STUDIES ON POLYNUCLEOTIDES .143. RAPID AND CONVENIENT METHOD FOR SYNTHESIS OF DEOXYRIBOOLIGONUCLEOTIDES CARRYING 5'-PHOSPHATE END GROUPS USING A NEW PROTECTING GROUP [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (05) : 1065 - 1072

[6] STUDIES ON THE CHEMICAL NATURE OF THE SUBSTANCE INDUCING TRANSFORMATION OF PNEUMOCOCCAL TYPES INDUCTION OF TRANSFORMATION BY A DESOXYRIBONUCLEIC ACID FRACTION ISOLATED FROM PNEUMOCOCCUS TYPE III [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1944, 79 (02) : 137 - 158

[7] BAHL CP, 1978, BIOCHEM BIOPH RES CO, V81, P695, DOI 10.1016/0006-291X(78)91408-0

[8] STUDIES ON LACTOSE OPERON .2. CHEMICAL AND ENZYMATIC-SYNTHESIS OF LACTOSE OPERATOR OF ESCHERICHIA-COLI AND ITS BINDING TO LACTOSE REPRESSOR [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (01) : 91 - 94

[9] BAHL CP, 1976, GENE, V1, P76

[10] BERLIN YA, 1973, TETRAHEDRON LETT, P1353

[1] NUCLEOSIDE 3'-PHOSPHOTRIESTERS AS KEY INTERMEDIATES FOR OLIGORIBONUCLEOTIDE SYNTHESIS .3. IMPROVED PREPARATION OF NUCLEOSIDE 3'-PHOSPHOTRIESTERS, THEIR H-1 NMR CHARACTERIZATION AND NEW CONDITIONS FOR REMOVAL OF 2-CYANOETHYL GROUP [J]. NUCLEIC ACIDS RESEARCH, 1976, 3 (12) : 3397 - 3408

[2] CHEMICAL SYNTHESIS OF ANTICODON LOOP OF AN EUKARYOTIC INITIATOR TRANSFER-RNA CONTAINING HYPERMODIFIED NUCLEOSIDE N-6-N-THREONYLCARBONY-ADENOSINE-T6A-1 [J]. NUCLEIC ACIDS RESEARCH, 1978, 5 (06) : 1889 - 1905

[3] ADAMIAK RW, 1977, TETRAHEDRON LETT, P1431

[4] DEOXYOLIGONUCLEOTIDE SYNTHESIS USING A NEW PHOSPHATE PROTECTING GROUP [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (06) : 2020 - 2021

[5] STUDIES ON POLYNUCLEOTIDES .143. RAPID AND CONVENIENT METHOD FOR SYNTHESIS OF DEOXYRIBOOLIGONUCLEOTIDES CARRYING 5'-PHOSPHATE END GROUPS USING A NEW PROTECTING GROUP [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (05) : 1065 - 1072

[6] STUDIES ON THE CHEMICAL NATURE OF THE SUBSTANCE INDUCING TRANSFORMATION OF PNEUMOCOCCAL TYPES INDUCTION OF TRANSFORMATION BY A DESOXYRIBONUCLEIC ACID FRACTION ISOLATED FROM PNEUMOCOCCUS TYPE III [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1944, 79 (02) : 137 - 158

[7] BAHL CP, 1978, BIOCHEM BIOPH RES CO, V81, P695, DOI 10.1016/0006-291X(78)91408-0

[8] STUDIES ON LACTOSE OPERON .2. CHEMICAL AND ENZYMATIC-SYNTHESIS OF LACTOSE OPERATOR OF ESCHERICHIA-COLI AND ITS BINDING TO LACTOSE REPRESSOR [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (01) : 91 - 94

[9] BAHL CP, 1976, GENE, V1, P76

[10] BERLIN YA, 1973, TETRAHEDRON LETT, P1353