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Vili K Stoyanova

Showing results (1-10 of 8) with videos related to

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Folia Medica|October 30, 2012
Epigenetic aspects in schizophrenia etiology and pathogenesisNikolay T Popov, Vili K Stoyanova, Nadezhda P Madzhirova, et al.
Folia Medica|October 3, 2015
Autism Spectrum Disorder - A Complex Genetic DisorderHristo Y Ivanov, Vili K Stoyanova, Nikolay T Popov, et al.
Biomarker Research|August 22, 2020
Application of pharmacogenetics in oncologyNelly N Miteva-Marcheva, Hristo Y Ivanov, Dimitar K Dimitrov, et al.
Folia Medica|March 6, 2023
Analysis and evaluation of correlation between DNA polymorphism in the genes MTHFR, PAI-1 and serum creatinine, creatinine clearance and albumin/creatinine ratio in morning urine of patients with type 2 diabetes mellitus and diabetic nephropathyDimitar Nikolov, Vili K Stoyanova, Ludmila Vladimirova-Kitova, et al.
Folia Medica|April 12, 2005
A reproducible model of cardiac hypertrophy in rats. Problems and obstacles we facedVili K Stoyanova, Evghenii D Ghenev, Ivan B Yanev, et al.
Folia Medica|March 21, 2006
Time course and progression of pressure overload-induced cardiac hypertrophy in ratsVili K Stoyanova, Nikolai Z Zhelev, Ivan B Yanev, et al.
Folia Medica|June 13, 2019
Mutations Associated with Imatinib Mesylate Resistance - ReviewAlexandar J Linev, Hristo J Ivanov, Ivan G Zhelyazkov, et al.
Molecular Genetics and Metabolism|August 4, 2014
Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma childrenIvan S Ivanov, Dimitar N Azmanov, Mariya B Ivanova, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Folia Medica|October 30, 2012
Epigenetic aspects in schizophrenia etiology and pathogenesisNikolay T Popov, Vili K Stoyanova, Nadezhda P Madzhirova, et al.
Folia Medica|October 3, 2015
Autism Spectrum Disorder - A Complex Genetic DisorderHristo Y Ivanov, Vili K Stoyanova, Nikolay T Popov, et al.
Biomarker Research|August 22, 2020
Application of pharmacogenetics in oncologyNelly N Miteva-Marcheva, Hristo Y Ivanov, Dimitar K Dimitrov, et al.
Folia Medica|March 6, 2023
Analysis and evaluation of correlation between DNA polymorphism in the genes MTHFR, PAI-1 and serum creatinine, creatinine clearance and albumin/creatinine ratio in morning urine of patients with type 2 diabetes mellitus and diabetic nephropathyDimitar Nikolov, Vili K Stoyanova, Ludmila Vladimirova-Kitova, et al.
Folia Medica|April 12, 2005
A reproducible model of cardiac hypertrophy in rats. Problems and obstacles we facedVili K Stoyanova, Evghenii D Ghenev, Ivan B Yanev, et al.
Folia Medica|March 21, 2006
Time course and progression of pressure overload-induced cardiac hypertrophy in ratsVili K Stoyanova, Nikolai Z Zhelev, Ivan B Yanev, et al.
Folia Medica|June 13, 2019
Mutations Associated with Imatinib Mesylate Resistance - ReviewAlexandar J Linev, Hristo J Ivanov, Ivan G Zhelyazkov, et al.
Molecular Genetics and Metabolism|August 4, 2014
Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma childrenIvan S Ivanov, Dimitar N Azmanov, Mariya B Ivanova, et al.
Pageof 1