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Ring Autosomes: Some Unexpected Findings

Balkan journal of medical genetics, 2012-12, Vol.15 (2), p.35-46

2012

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A new case of tetrasomy X in a 8 years old girl

Acta endocrinologica (Bucharest, Romania : 2005), 2012-12, Vol.8 (4), p.627-632

Plaiasu, V

2012

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Sexual Ambiguity Associated with "in utero" Antiretroviral Exposure

Acta endocrinologica (Bucharest, Romania : 2005), 2011-10, Vol.7 (4), p.551-560

Cristea, Cosmina

2011

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Selective targeting of the stress chaperome as a therapeutic strategy

Trends in pharmacological sciences (Regular ed.), 2014-11, Vol.35 (11), p.592-603

2014

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A Hyperactive Signalosome in Acute Myeloid Leukemia Drives Addiction to a Tumor-Specific Hsp90 Species

Cell reports (Cambridge), 2015-12, Vol.13 (10), p.2159-2173

2015

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Heat shock protein 90 inhibitors in the treatment of cancer: current status and future directions

Expert opinion on investigational drugs, 2014-05, Vol.23 (5), p.611-628

2014

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Chemical tools for epichaperome-mediated interactome dysfunctions of the central nervous system

Nature communications, 2021-08, Vol.12 (1), p.4669-4669, Article 4669

2021

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Structure–Activity Relationship in a Purine-Scaffold Compound Series with Selectivity for the Endoplasmic Reticulum Hsp90 Paralog Grp94

Journal of medicinal chemistry, 2015-05, Vol.58 (9), p.3922-3943

2015

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Experimental and Structural Testing Module to Analyze Paralogue-Specificity and Affinity in the Hsp90 Inhibitors Series

Journal of medicinal chemistry, 2013-09, Vol.56 (17), p.6803-6818

2013

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Synthesis and assessment of catechol diether compounds as inhibitors of trypanosomal phosphodiesterase B1 (TbrPDEB1)

Bioorganic & medicinal chemistry letters, 2013-11, Vol.23 (21), p.5971-5974

2013

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Pharmacological Validation of Trypanosoma brucei Phosphodiesterases B1 and B2 as Druggable Targets for African Sleeping Sickness

Journal of medicinal chemistry, 2011-12, Vol.54 (23), p.8188-8194

2011

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Affinity Purification Probes of Potential Use To Investigate the Endogenous Hsp70 Interactome in Cancer

ACS chemical biology, 2014-08, Vol.9 (8), p.1698-1705

2014

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Repurposing Human PDE4 Inhibitors for Neglected Tropical Diseases. Evaluation of Analogs of the Human PDE4 Inhibitor GSK-256066 as Inhibitors of PDEB1 of Trypanosoma brucei

Chemical biology & drug design, 2015-05, Vol.85 (5), p.549-564

2015

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Synthesis and evaluation of human phosphodiesterases (PDE) 5 inhibitor analogs as trypanosomal PDE inhibitors. Part 1. Sildenafil analogs

Bioorganic & medicinal chemistry letters, 2012-04, Vol.22 (7), p.2579-2581

2012

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Synthesis and evaluation of human phosphodiesterases (PDE) 5 inhibitor analogs as trypanosomal PDE inhibitors. Part 2. Tadalafil analogs

Bioorganic & medicinal chemistry letters, 2012-04, Vol.22 (7), p.2582-2584

2012

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Repurposing Human PDE 4 Inhibitors for Neglected Tropical Diseases. Evaluation of Analogs of the Human PDE 4 Inhibitor GSK ‐256066 as Inhibitors of PDEB 1 of Trypanosoma brucei

Chemical biology & drug design, 2015-05, Vol.85 (5), p.549-564

2015

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Synthesis and evaluation of human phosphodiesterases (PDE) 5 inhibitor analogs as trypanosomal PDE inhibitors. 1. Sildenafil analogs

Bioorganic & medicinal chemistry letters, 2012-02, Vol.22 (7), p.2579-2581

2012

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Les « îles » d’Henri Queffélec

Ochiana, Florin

2001

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Ring Autosomes: Some Unexpected Findings

A new case of tetrasomy X in a 8 years old girl

Sexual Ambiguity Associated with "in utero" Antiretroviral Exposure

Selective targeting of the stress chaperome as a therapeutic strategy

A Hyperactive Signalosome in Acute Myeloid Leukemia Drives Addiction to a Tumor-Specific Hsp90 Species

Heat shock protein 90 inhibitors in the treatment of cancer: current status and future directions

Chemical tools for epichaperome-mediated interactome dysfunctions of the central nervous system

Structure–Activity Relationship in a Purine-Scaffold Compound Series with Selectivity for the Endoplasmic Reticulum Hsp90 Paralog Grp94

Experimental and Structural Testing Module to Analyze Paralogue-Specificity and Affinity in the Hsp90 Inhibitors Series

Synthesis and assessment of catechol diether compounds as inhibitors of trypanosomal phosphodiesterase B1 (TbrPDEB1)

Pharmacological Validation of Trypanosoma brucei Phosphodiesterases B1 and B2 as Druggable Targets for African Sleeping Sickness

Affinity Purification Probes of Potential Use To Investigate the Endogenous Hsp70 Interactome in Cancer

Repurposing Human PDE4 Inhibitors for Neglected Tropical Diseases. Evaluation of Analogs of the Human PDE4 Inhibitor GSK-256066 as Inhibitors of PDEB1 of Trypanosoma brucei

Synthesis and evaluation of human phosphodiesterases (PDE) 5 inhibitor analogs as trypanosomal PDE inhibitors. Part 1. Sildenafil analogs

Synthesis and evaluation of human phosphodiesterases (PDE) 5 inhibitor analogs as trypanosomal PDE inhibitors. Part 2. Tadalafil analogs

Repurposing Human PDE 4 Inhibitors for Neglected Tropical Diseases. Evaluation of Analogs of the Human PDE 4 Inhibitor GSK ‐256066 as Inhibitors of PDEB 1 of Trypanosoma brucei

Synthesis and evaluation of human phosphodiesterases (PDE) 5 inhibitor analogs as trypanosomal PDE inhibitors. 1. Sildenafil analogs

Les « îles » d’Henri Queffélec

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