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Candidate biomarkers in exosome-like vesicles purified from rat and mouse urine samples

Proteomics. Clinical applications, 2010-04, Vol.4 (4), p.416-425

2010

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In vivo pharmacological characterisation of bilastine, a potent and selective histamine H1 receptor antagonist

Drugs in R&D, 2006, Vol.7 (4), p.219-231

2006

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Development of national logistics in support of the Serbian Air Force - long-term prospects / Развитие национальной логистики, поддерживающей Военно-воздушные силы Республики Сербия – долгосрочные перспективы / Razvoj nacionalne logistike u podršci Ratnom vazduhoplovstvu Vojske Srbije - dugoročne perspektive

Vojnotehnički glasnik, 2020-01, Vol.68 (1), p.107-130

Hatidža A. Beriša

2020

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Structural, conformational and pharmacological study of some amides derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9β-amine as potential analgesics

Journal of molecular structure, 1999-05, Vol.482-483, p.425-430

1999

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Synthesis, structural, conformational and pharmacological study of esters derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9α-ol as potential analgesics

Journal of physical organic chemistry, 1998-02, Vol.11 (2), p.125-132

1998

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Synthesis and Structural, Conformational, Biochemical, and Pharmacological Study of New Compounds Derived from Tropane-3-spiro-4’(5’)-imidazoline as Potential 5-HT3 Receptor Antagonists

Journal of pharmaceutical sciences, 1995-01, Vol.84 (1), p.101-106

1995

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Structural, conformational, biochemical, and pharmacological study of some amides derived from 3,7-dimethyl-3,7-diazabicyclo [3.3.1] nonan-9-amine as potential 5-HT3 receptor antagonists

Journal of molecular structure, 1995-12, Vol.372 (2-3), p.203-213

1995

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Impact of the current level in the development of the telecommunicationinformation system of the Serbian Armed Forces on the defense of the Republic of Serbia / Влияние достигнутого уровня развития информационной и телекоммуникационной систем Вооруженных сил Республики Сербия на военную оборону / Uticaj dostignutog stepena razvoja telekomunikaciono-informacionog sistema Vojske Srbije na odbranu Republike Srbije

Vojnotehnički glasnik, 2019-01, Vol.67 (1), p.131-158

2019

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Synthesis and histamine H1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

European journal of medicinal chemistry, 1996, Vol.31 (10), p.813-818

1996

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Synthesis and structural, conformational and pharmacological study of new esters derived from 3,7-dimethyl-3,7-diazabicyclo[3.3.1]nonan-9-ol

Journal of molecular structure, 1995, Vol.351, p.127-135

1995

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PREVENTIVE DIPLOMACY IN CONFLICT RESOLUTION

ALTERNATIVE, 2022, p.35-39

2022

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Challenges of the implementation of the concept of flexible use of airspace in the Republic of Serbia / Вызовы при внедрении концепции гибкого использования воздушного пространства в Республике Сербия / Izazovi implementacije koncepta fleksibilnog korišćenja vazdušnog prostora u Republici Srbiji

Vojnotehnički glasnik, 2019-04, Vol.67 (2), p.374-402

2019

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Structural, conformational, theoretical and pharmacological study of some amides derived from 3,7-dimethyl-9-[( N-substituted)-4-chlorobenzamido]3,7-diazabicyclo[3.3.1]nonane-9-carboxamide

Journal of molecular structure, 1995, Vol.351, p.137-146

1995

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Synthesis, structural, conformational and pharmacological study of new fentanyl derivatives of the camphidine system

Journal of heterocyclic chemistry, 1994-03, Vol.31 (2), p.313-318

1994

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Preclinical pharmacology of bilastine, a new selective histamine H1 receptor antagonist: receptor selectivity and in vitro antihistaminic activity

Drugs in R&D, 2005, Vol.6 (6), p.371-384

2005

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The defense-security and protective role of modern state in the function of state interests achievement

Tehnika (Beograd), 2017, Vol.72 (5), p.771-774

2017

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Application of the sustainability concept in the functioning of ecological security

Tehnika (Beograd), 2017, Vol.72 (5), p.765-770

2017

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Synthesis, and structural, conformational and pharmacological studies of new fentanyl derivatives of the norgranatane system

J. Chem. Soc., Perkin Trans. 2, 1992 (4), p.687-695

1992

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Resources scarcity: Cause of potential conflicts

Tehnika (Beograd), 2016, Vol.71 (2), p.338-344

2016

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New security challenges in view of environmental protection

Tehnika (Beograd), 2015, Vol.70 (4), p.727-734

2015

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Synthesis and structural, conformational, biochemical, and pharmacological study of new compounds derived from tropane-3-spiro4′(5′)-imidazoline as potential 5-HT3 receptor antagonists

Journal of pharmaceutical sciences, 1995-01, Vol.84 (1), p.101-106

1995

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Structural, conformational and pharmacological study of some esters derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9β-ol

Journal of molecular structure, 1995, Vol.351, p.119-125

1995

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Synthesis and histamine H(1)-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

European journal of medicinal chemistry, 1996, Vol.31 (10), p.813-818

1996

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Synthesis and histamine H 1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

European journal of medicinal chemistry, 1996, Vol.31 (10), p.813-818

1996

Volltextzugriff (PDF)

Structural, conformational, biochemical, and pharmacological study of some amides derived from 3,7-dimethyl-3,7-diazabicyclo [3.3.1] nonan-9-amine as potential 5-HT 3 receptor antagonists

Journal of molecular structure, 1995, Vol.372 (2), p.203-213

1995

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Candidate biomarkers in exosome-like vesicles purified from rat and mouse urine samples

In vivo pharmacological characterisation of bilastine, a potent and selective histamine H1 receptor antagonist

Structural, conformational and pharmacological study of some amides derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9β-amine as potential analgesics

Synthesis, structural, conformational and pharmacological study of esters derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9α-ol as potential analgesics

Synthesis and Structural, Conformational, Biochemical, and Pharmacological Study of New Compounds Derived from Tropane-3-spiro-4’(5’)-imidazoline as Potential 5-HT3 Receptor Antagonists

Structural, conformational, biochemical, and pharmacological study of some amides derived from 3,7-dimethyl-3,7-diazabicyclo [3.3.1] nonan-9-amine as potential 5-HT3 receptor antagonists

Synthesis and histamine H1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

Synthesis and structural, conformational and pharmacological study of new esters derived from 3,7-dimethyl-3,7-diazabicyclo[3.3.1]nonan-9-ol

PREVENTIVE DIPLOMACY IN CONFLICT RESOLUTION

Structural, conformational, theoretical and pharmacological study of some amides derived from 3,7-dimethyl-9-[( N-substituted)-4-chlorobenzamido]3,7-diazabicyclo[3.3.1]nonane-9-carboxamide

Synthesis, structural, conformational and pharmacological study of new fentanyl derivatives of the camphidine system

Preclinical pharmacology of bilastine, a new selective histamine H1 receptor antagonist: receptor selectivity and in vitro antihistaminic activity

The defense-security and protective role of modern state in the function of state interests achievement

Application of the sustainability concept in the functioning of ecological security

Synthesis, and structural, conformational and pharmacological studies of new fentanyl derivatives of the norgranatane system

Resources scarcity: Cause of potential conflicts

New security challenges in view of environmental protection

Synthesis and structural, conformational, biochemical, and pharmacological study of new compounds derived from tropane-3-spiro4′(5′)-imidazoline as potential 5-HT3 receptor antagonists

Structural, conformational and pharmacological study of some esters derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9β-ol

Synthesis and histamine H(1)-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

Synthesis and histamine H 1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

Structural, conformational, biochemical, and pharmacological study of some amides derived from 3,7-dimethyl-3,7-diazabicyclo [3.3.1] nonan-9-amine as potential 5-HT 3 receptor antagonists

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