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11-β-hydroxysterols as possible endogenous stimulators of mitochondrial biogenesis as inferred from epicatechin molecular mimicry

Pharmacological research, 2020-01, Vol.151, p.104540-104540, Article 104540

2020

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Synthesis and evaluation of pyrrolotriazine based molecules as PI3 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (16), p.3142-3146

2015

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Discovery of Novel and Orally Bioavailable Inhibitors of PI3 Kinase Based on Indazole Substituted Morpholino-Triazines

ACS medicinal chemistry letters, 2015-12, Vol.6 (12), p.1190-1194

2015

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The GB/SA Continuum Model for Solvation. A Fast Analytical Method for the Calculation of Approximate Born Radii

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 1997-04, Vol.101 (16), p.3005-3014

1997

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Two classes of p38α MAP kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (23), p.5274-5279

2005

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Abstract 4515: SPR965: an oral PI3K/ mTOR C1/C2 inhibitor for the treatment of solid tumors

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.4515-4515

2014

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West African Food Systems and Changing Consumer Demands

West African Papers, 2016

2016

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Two classes of p38alpha MAP kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (23), p.5274-5279

2005

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Exploring the Role of Bromine at C(10) of (+)-4-[2-[4-(8-Chloro-3,10-dibromo- 6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11(R)-yl)-1-piperidinyl]-2- oxoethyl]-1-piperidinecarboxamide (Sch-66336): The Discovery of Indolocycloheptapyridine Inhibitors of Farnesyl Protein Transferase

Journal of medicinal chemistry, 2002-08, Vol.45 (18), p.3854-3864

2002

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Enantioselective Hosts for Neutral Derivatives of Amino Acids

Israel journal of chemistry, 1992, Vol.32 (1), p.41-45

1992

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Exploring the role of bromine at C(10) of (+)-4-[2-[4-(8-chloro-3,10-dibromo-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyr idin-11(R)-yl)-1-piperidinyl]-2-oxoethyl]-1-piperidinecarboxamide (Sch-66336): The discovery of indolocycloheptapyridine inhibitors of farnesyl protein transferase

Journal of medicinal chemistry, 2002, Vol.45 (18), p.3854-3864

2002

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The N 4 nitrogen of pirenzepine is responsible for selective binding of the M1 subtype human muscarinic receptor

Bioorganic & medicinal chemistry letters, 1996-04, Vol.6 (7), p.785-788

1996

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The N4 nitrogen of pirenzepine is responsible for selective binding of the M1 subtype human muscarinic receptor

Bioorganic & medicinal chemistry letters, 1996-04, Vol.6 (7), p.785-788

1996

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I. Design and synthesis of peptide binding macrocyclic molecules. II. Design and implementation of a continuum solvent model appropriate for molecular mechanics calculations

Hollinger, Frank Peter

1993

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A DETERMINATION OF THE ORBIT OF PLANETOID 115 THYRA

CLUTZ, FRANK HOLLINGER

1897

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2018 Update of the EULAR recommendations for the management of large vessel vasculitis

Annals of the rheumatic diseases, 2020-01, Vol.79 (1), p.19-30

2020

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Heavy ion linac as a high current proton beam injector

Physical review special topics. PRST-AB. Accelerators and beams, 2015-05, Vol.18 (5), p.050102, Article 050102

2015

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Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials

Neurology, 2017-10, Vol.89 (18), p.1915-1922

2017

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The new genus Pulvinora (Lecanoraceae) for species of the ‘Lecanora pringlei’ group, including the new species Pulvinora stereothallina

The Bryologist, 2021-05, Vol.124 (2)

2021

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Long-term mortality and morbidity of transfusion-associated non-A, non-B, and type C hepatitis: A National Heart, Lung, and Blood Institute collaborative study

Hepatology (Baltimore, Md.), 2001-02, Vol.33 (2), p.455-463

2001

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Long-Term Mortality after Transfusion-Associated Non-A, Non-B Hepatitis

The New England journal of medicine, 1992-12, Vol.327 (27), p.1906-1911

1992

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Modeling acclimation of photosynthesis to temperature in evergreen conifer forests

The New phytologist, 2010-10, Vol.188 (1), p.175-186

2010

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Comparative proteomics of a model MCF10A-KRasG12V cell line reveals a distinct molecular signature of the KRasG12V cell surface

Oncotarget, 2016-12, Vol.7 (52), p.86948-86971

2016

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A scalable, fully automated process for construction of sequence-ready barcoded libraries for 454

Genome biology, 2010-02, Vol.11 (2), p.R15-R15, Article R15

2010

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11-β-hydroxysterols as possible endogenous stimulators of mitochondrial biogenesis as inferred from epicatechin molecular mimicry

Synthesis and evaluation of pyrrolotriazine based molecules as PI3 kinase inhibitors

Discovery of Novel and Orally Bioavailable Inhibitors of PI3 Kinase Based on Indazole Substituted Morpholino-Triazines

The GB/SA Continuum Model for Solvation. A Fast Analytical Method for the Calculation of Approximate Born Radii

Two classes of p38α MAP kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes

Abstract 4515: SPR965: an oral PI3K/ mTOR C1/C2 inhibitor for the treatment of solid tumors

West African Food Systems and Changing Consumer Demands

Two classes of p38alpha MAP kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes

Exploring the Role of Bromine at C(10) of (+)-4-[2-[4-(8-Chloro-3,10-dibromo- 6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11(R)-yl)-1-piperidinyl]-2- oxoethyl]-1-piperidinecarboxamide (Sch-66336): The Discovery of Indolocycloheptapyridine Inhibitors of Farnesyl Protein Transferase

Enantioselective Hosts for Neutral Derivatives of Amino Acids

Exploring the role of bromine at C(10) of (+)-4-[2-[4-(8-chloro-3,10-dibromo-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyr idin-11(R)-yl)-1-piperidinyl]-2-oxoethyl]-1-piperidinecarboxamide (Sch-66336): The discovery of indolocycloheptapyridine inhibitors of farnesyl protein transferase

The N 4 nitrogen of pirenzepine is responsible for selective binding of the M1 subtype human muscarinic receptor

The N4 nitrogen of pirenzepine is responsible for selective binding of the M1 subtype human muscarinic receptor

I. Design and synthesis of peptide binding macrocyclic molecules. II. Design and implementation of a continuum solvent model appropriate for molecular mechanics calculations

A DETERMINATION OF THE ORBIT OF PLANETOID 115 THYRA

2018 Update of the EULAR recommendations for the management of large vessel vasculitis

Heavy ion linac as a high current proton beam injector

Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials

The new genus Pulvinora (Lecanoraceae) for species of the ‘Lecanora pringlei’ group, including the new species Pulvinora stereothallina

Phenology of Photosynthesis in Winter‐Dormant Temperate and Boreal Forests: Long‐Term Observations From Flux Towers and Quantitative Evaluation of Phenology Models

Long-term mortality and morbidity of transfusion-associated non-A, non-B, and type C hepatitis: A National Heart, Lung, and Blood Institute collaborative study

Long-Term Mortality after Transfusion-Associated Non-A, Non-B Hepatitis

Modeling acclimation of photosynthesis to temperature in evergreen conifer forests

Comparative proteomics of a model MCF10A-KRasG12V cell line reveals a distinct molecular signature of the KRasG12V cell surface

A scalable, fully automated process for construction of sequence-ready barcoded libraries for 454

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