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A STUDY OF THE CONSTRUCT VALIDITY OF BARRON'S EGO STRENGTH SCALE WITH A STATE MENTAL HOSPITAL POPULATION

HAWKINSON, JOHN RUSSELL

1961

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Prematurity associated with cervicitis and vaginitis during pregnancy

American journal of obstetrics and gynecology, 1966-04, Vol.94 (7), p.898-902

1966

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CONTRIBUTIONS OF PSYCHOLOGY TO PSYCHIATRY

The American journal of psychiatry, 1956-03, Vol.112 (9), p.741-a-742

1956

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Tricaine Used to Separate Phase‐I Striped Bass with Uninflated Gas Bladders from Normal Fish

The Progressive fish-culturist, 1992-04, Vol.54 (2), p.133-135

1992

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Development of allosteric and selective CDK2 inhibitors for contraception with negative cooperativity to cyclin binding

Nature communications, 2023-06, Vol.14 (1), p.3213-3213, Article 3213

2023

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Placental polyp. Report of 3 cases

Obstetrics and gynecology (New York. 1953), 1963-07, Vol.22, p.25

1963

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Screening through Lead Optimization of High Affinity, Allosteric Cyclin-Dependent Kinase 2 (CDK2) Inhibitors as Male Contraceptives That Reduce Sperm Counts in Mice

Journal of medicinal chemistry, 2023-02, Vol.66 (3), p.1928-1940

2023

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FBNTI, a DOR-Selective Antagonist That Allosterically Activates MOR within a MOR–DOR Heteromer

Biochemistry (Easton), 2021-05, Vol.60 (18), p.1413-1419

2021

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7‑Methylation of Chenodeoxycholic Acid Derivatives Yields a Substantial Increase in TGR5 Receptor Potency

Journal of medicinal chemistry, 2019-07, Vol.62 (14), p.6824-6830

2019

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Electrophysiological ventricular substrate of stroke: a prospective cohort study in the Atherosclerosis Risk in Communities (ARIC) study

BMJ open, 2021-09, Vol.11 (9), p.e048542-e048542

2021

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WHERE TO LOOK FOR MONEY — A FINANCIAL CLINIC FOR LAWYERS

The Business lawyer, 1960-11, Vol.16 (1), p.257-289

1960

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Development of WEE2 kinase inhibitors as novel non-hormonal female contraceptives that target meiosis

Biology of reproduction, 2020-08, Vol.103 (2), p.368-377

2020

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Potent Pyrimidine and Pyrrolopyrimidine Inhibitors of Testis‐Specific Serine/Threonine Kinase 2 (TSSK2)

ChemMedChem, 2017-11, Vol.12 (22), p.1857-1865

2017

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Potent Pyrimidine and Pyrrolopyrimidine Inhibitors of Testis-Specific Serine/Threonine Kinase2 (TSSK2)

ChemMedChem, 2017-11, Vol.12 (22), p.1857

2017

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III. The Inside Story

Psychiatric services (Washington, D.C.), 1966-02, Vol.17 (2), p.44-48

1966

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First in Human Phase I Trial of 852A, a Novel Systemic Toll-like Receptor 7 Agonist, to Activate Innate Immune Responses in Patients with Advanced Cancer

Clinical cancer research, 2007-12, Vol.13 (23), p.7119-7125

2007

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The anti-parasitic agent suramin and several of its analogues are inhibitors of the DNA binding protein Mcm10

Open biology, 2019-08, Vol.9 (8), p.190117

2019

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Quantifying the Selectivity of Protein–Protein and Small Molecule Interactions with Fluorinated Tandem Bromodomain Reader Proteins

ACS chemical biology, 2020-11, Vol.15 (11), p.3038-3049

2020

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Where to Look for Money — A Financial Clinic for Lawyers

The Business lawyer, 1960-01, Vol.15 (2), p.439-466

1960

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2018: 135

Journal of surgical orthopaedic advances, 2018, Vol.27 (2)

2018

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Recombinant production of enzymatically active male contraceptive drug target hTSSK2 - Localization of the TSKS domain phosphorylated by TSSK2

Protein expression and purification, 2016-05, Vol.121, p.88-96

2016

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Synthesis and SAR of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones related to licostinel (Acea 1021) as NMDA/glycine site antagonists

Bioorganic & medicinal chemistry, 2003-04, Vol.11 (8), p.1769-1780

2003

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Structure−Activity Relationships of Alkyl- and Alkoxy-Substituted 1,4-Dihydroquinoxaline-2,3-diones: Potent and Systemically Active Antagonists for the Glycine Site of the NMDA Receptor

Journal of medicinal chemistry, 1997-02, Vol.40 (5), p.730-738

1997

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Synthesis of N-Substituted 4-(4-Hydroxyphenyl)piperidines, 4-(4-Hydroxybenzyl)piperidines, and (±)-3-(4-Hydroxyphenyl)pyrrolidines: Selective Antagonists at the 1a/2B NMDA Receptor Subtype

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.984-994

2000

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Synthesis and Structure−Activity Relationships of 1,2,3,4-Tetrahydroquinoline-2,3,4-trione 3-Oximes: Novel and Highly Potent Antagonists for NMDA Receptor Glycine Site

Journal of medicinal chemistry, 1996-08, Vol.39 (17), p.3248-3255

1996

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A STUDY OF THE CONSTRUCT VALIDITY OF BARRON'S EGO STRENGTH SCALE WITH A STATE MENTAL HOSPITAL POPULATION

Prematurity associated with cervicitis and vaginitis during pregnancy

CONTRIBUTIONS OF PSYCHOLOGY TO PSYCHIATRY

Tricaine Used to Separate Phase‐I Striped Bass with Uninflated Gas Bladders from Normal Fish

Development of allosteric and selective CDK2 inhibitors for contraception with negative cooperativity to cyclin binding

Placental polyp. Report of 3 cases

Screening through Lead Optimization of High Affinity, Allosteric Cyclin-Dependent Kinase 2 (CDK2) Inhibitors as Male Contraceptives That Reduce Sperm Counts in Mice

FBNTI, a DOR-Selective Antagonist That Allosterically Activates MOR within a MOR–DOR Heteromer

7‑Methylation of Chenodeoxycholic Acid Derivatives Yields a Substantial Increase in TGR5 Receptor Potency

Electrophysiological ventricular substrate of stroke: a prospective cohort study in the Atherosclerosis Risk in Communities (ARIC) study

WHERE TO LOOK FOR MONEY — A FINANCIAL CLINIC FOR LAWYERS

Development of WEE2 kinase inhibitors as novel non-hormonal female contraceptives that target meiosis

Potent Pyrimidine and Pyrrolopyrimidine Inhibitors of Testis‐Specific Serine/Threonine Kinase 2 (TSSK2)

Potent Pyrimidine and Pyrrolopyrimidine Inhibitors of Testis-Specific Serine/Threonine Kinase2 (TSSK2)

III. The Inside Story

First in Human Phase I Trial of 852A, a Novel Systemic Toll-like Receptor 7 Agonist, to Activate Innate Immune Responses in Patients with Advanced Cancer

The anti-parasitic agent suramin and several of its analogues are inhibitors of the DNA binding protein Mcm10

Quantifying the Selectivity of Protein–Protein and Small Molecule Interactions with Fluorinated Tandem Bromodomain Reader Proteins

Where to Look for Money — A Financial Clinic for Lawyers

2018: 135

Recombinant production of enzymatically active male contraceptive drug target hTSSK2 - Localization of the TSKS domain phosphorylated by TSSK2

Synthesis and SAR of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones related to licostinel (Acea 1021) as NMDA/glycine site antagonists

Structure−Activity Relationships of Alkyl- and Alkoxy-Substituted 1,4-Dihydroquinoxaline-2,3-diones: Potent and Systemically Active Antagonists for the Glycine Site of the NMDA Receptor

Synthesis of N-Substituted 4-(4-Hydroxyphenyl)piperidines, 4-(4-Hydroxybenzyl)piperidines, and (±)-3-(4-Hydroxyphenyl)pyrrolidines: Selective Antagonists at the 1a/2B NMDA Receptor Subtype

Synthesis and Structure−Activity Relationships of 1,2,3,4-Tetrahydroquinoline-2,3,4-trione 3-Oximes: Novel and Highly Potent Antagonists for NMDA Receptor Glycine Site

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