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DNA Fingerprinting of Tetraploid Cherry Germplasm Using Simple Sequence Repeats

Journal of the American Society for Horticultural Science, 2001-03, Vol.126 (2), p.205-209

2001

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Microsatellite Markers Differentiate Eight Giessen Cherry Rootstocks

HortScience, 2002-02, Vol.37 (1), p.191-193

2002

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Analysis of Sweet Cherry (Prunus avium L.) Cultivars Using SSR and AFLP Markers

Journal of the American Society for Horticultural Science, 2003-11, Vol.128 (6), p.904-909

2003

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Detection of genetic diversity among populations of sweet cherry (Prunus avium L.) by AFLPs

The journal of horticultural science & biotechnology, 2001, Vol.76 (3), p.362-367

2001

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CULTIVAR IDENTIFICATION IN SWEET CHERRY (Prunus avium L.) USING AFLP AND MICROSATELLITE MARKERS

Acta horticulturae, 2000 (538), p.505-510

2000

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Optimizing the Expression of Human Dopamine Receptors in Escherichia coli

International journal of molecular sciences, 2021-08, Vol.22 (16), p.8647

2021

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Identification of potent nontoxic poly(ADP-ribose) polymerase-1 inhibitors: Chemopotentiation and pharmacological studies

Clinical cancer research, 2003-07, Vol.9 (7), p.2711-2718

2003

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Super in vitro synergy between inhibitors of dihydrofolate reductase and inhibitors of other folate-requiring enzymes: The critical role of polyglutamylation

Cancer research (Chicago, Ill.), 1998-07, Vol.58 (14), p.3036-3050

1998

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AG337, a novel lipophilic thymidylate synthase inhibitor : in vitro and in vivo preclinical studies

Cancer chemotherapy and pharmacology, 1996, Vol.37 (6), p.509-517

1996

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Identification of the major lesion from the reaction of an acridine targeted aniline mustard with DNA as an adenine N1 adduct

Chemical research in toxicology, 1994-01, Vol.7 (1), p.41-46

1994

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Protein Structure-Based Design, Synthesis, and Biological Evaluation of 5-Thia-2,6-diamino-4(3H)-oxopyrimidines: Potent Inhibitors of Glycinamide Ribonucleotide Transformylase with Potent Cell Growth Inhibition

Journal of medicinal chemistry, 1997-08, Vol.40 (16), p.2502-2524

1997

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Purine and pyrimidine nucleotide patterns of normal, differentiating, and regenerating liver and of hepatomas in rats

Cancer research (Chicago, Ill.), 1980-04, Vol.40 (4), p.1286-1291

1980

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In Vivo and In Vitro Evaluations of 5-[4-(Substituted Aryl)-1- Piperazinyl]-6-Alkyl-2,4-Pyrimidinediamines as Antitumor Agents

Montreal, Canada, June 15–20, 1986, 2019, Vol.8, p.69-72

2019

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Synthesis and biological evaluation of -n[4-(2-trans-[([2,6-diamino-4(3H)-oxopyrimidin-5-yl]methyl)thio]cyclobutyl)benzoyl] -l-glutamic acid a novel 5-thiapyrimidinone inhibitor of dihydrofolate reductase

Journal of heterocyclic chemistry, 1995-09, Vol.32 (5), p.1493-1498

1995

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ChemInform Abstract: Synthesis and Biological Evaluation of N-(4-(2-trans-(((2,6-Diamino-4( 3H)-oxopyrimidin-5-yl)methyl)thio)cyclobutyl)benzoyl)-L-glutamic Acid ( I), a Novel 5-Thiapyrimidinone Inhibitor of Dihydrofolate Reductase

ChemInform, 1996-03, Vol.27 (13), p.no-no

1996

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ChemInform Abstract: Protein Structure-Based Design, Synthesis, and Biological Evaluation of 5-Thia-2,6-diamino-4(3H)-oxopyrimidines: Potent Inhibitors of Glycinamide Ribonucleotide Transformylase with Potent Cell Growth Inhibition

ChemInform, 1997-11, Vol.28 (48), p.no-no

1997

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DNA Fingerprinting of Tetraploid Cherry Germplasm Using Simple Sequence Repeats

Microsatellite Markers Differentiate Eight Giessen Cherry Rootstocks

Analysis of Sweet Cherry (Prunus avium L.) Cultivars Using SSR and AFLP Markers

Detection of genetic diversity among populations of sweet cherry (Prunus avium L.) by AFLPs

CULTIVAR IDENTIFICATION IN SWEET CHERRY (Prunus avium L.) USING AFLP AND MICROSATELLITE MARKERS

Optimizing the Expression of Human Dopamine Receptors in Escherichia coli

Identification of potent nontoxic poly(ADP-ribose) polymerase-1 inhibitors: Chemopotentiation and pharmacological studies

Super in vitro synergy between inhibitors of dihydrofolate reductase and inhibitors of other folate-requiring enzymes: The critical role of polyglutamylation

AG337, a novel lipophilic thymidylate synthase inhibitor : in vitro and in vivo preclinical studies

Identification of the major lesion from the reaction of an acridine targeted aniline mustard with DNA as an adenine N1 adduct

Protein Structure-Based Design, Synthesis, and Biological Evaluation of 5-Thia-2,6-diamino-4(3H)-oxopyrimidines: Potent Inhibitors of Glycinamide Ribonucleotide Transformylase with Potent Cell Growth Inhibition

Purine and pyrimidine nucleotide patterns of normal, differentiating, and regenerating liver and of hepatomas in rats

In Vivo and In Vitro Evaluations of 5-[4-(Substituted Aryl)-1- Piperazinyl]-6-Alkyl-2,4-Pyrimidinediamines as Antitumor Agents

Synthesis and biological evaluation of -n[4-(2-trans-[([2,6-diamino-4(3H)-oxopyrimidin-5-yl]methyl)thio]cyclobutyl)benzoyl] -l-glutamic acid a novel 5-thiapyrimidinone inhibitor of dihydrofolate reductase

ChemInform Abstract: Synthesis and Biological Evaluation of N-(4-(2-trans-(((2,6-Diamino-4( 3H)-oxopyrimidin-5-yl)methyl)thio)cyclobutyl)benzoyl)-L-glutamic Acid ( I), a Novel 5-Thiapyrimidinone Inhibitor of Dihydrofolate Reductase

ChemInform Abstract: Protein Structure-Based Design, Synthesis, and Biological Evaluation of 5-Thia-2,6-diamino-4(3H)-oxopyrimidines: Potent Inhibitors of Glycinamide Ribonucleotide Transformylase with Potent Cell Growth Inhibition

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