Search

Your search keyword '"V. Miroshnikova"' showing total 14 results
Start Over Author "V. Miroshnikova" Topic internal medicine
14 results on '"V. Miroshnikova"'

1. Case report of late-onset olivopontocerebellar atrophy

Author

Olga V. Kurushina, Polina S. Krivonozhkina, Valentina V. Miroshnikova, and Natalia A. Chernaya

Subjects
olivopontocerebellar atrophy, spinocerebellar ataxia, parkinsonism, cerebellar ataxia, case report, Internal medicine, RC31-1245
Abstract

Background. Olivopontocerebellar atrophy (OPCA) is a rare neurodegenerative disorder characterized by the continuously progressive course that combines the signs of cerebellar ataxia, parkinsonism, pyramidal syndrome, choreoathetosis, dementia, oculomotor dysfunction, affected peripheral nerves, and autonomic failure. Differential diagnosis is hampered by late onset of the disease in adulthood and older age, low prevalence in the population, non-specific nature, and slowly emerging symptoms. The paper investigates the clinical case of olivopontocerebellar atrophy that has been extremely difficult to verify. Aim. To attract attention of physicians of different specialties, primarily neurologists, psychiatrists, general practitioners, on the issue of rare neurodegenerative disorders, which are extremely difficult to verify in adulthood and older age. Methods. Medical history of female patient М., 68 years, who stayed at psychotherapy department. Assessment of the whole body, mental, and neurological status. Results. Considering the complaints of the patient and her relatives, the data of psychological and psychiatric assessment, neurological status, brain MRI, and no response to treatment with neurological and psychotherapeutic drugs, the following probable clinical diagnosis was established: “Congenital spinocerebellar ataxia of unspecified type (olivopontocerebellar atrophy)”. Conclusion. Early diagnosis of the OPCA clinical manifestations is extremely difficult, especially in elderly individuals, since the disorder occurs under the guise of age-related vascular changes in the brain matter and manifests itself in focal symptoms and mental function impairment. The history of the signs of prominent cognitive decline and multiple focal symptoms in the elderly patient, who is not excessive drinker and has no malignant hypertension or severe atherosclerosis, as well as any other background disease, requires exclusion of the disease vascular or degenerative origin. In the reported case, the combination of cerebellar ataxia and dementia constituted the core of clinical manifestations of the neurodegenerative process confirmed by brain imaging to exclude the conversion disorder.

Published
2023
Full Text
View/download PDF

2. Epicardial and subcutenious adipose tissue adiponectin gene expression in coronary artery disease patients

Author

S. N. Pchelina, O V Galkina, O. Berkovich, A A Panteleeva, V V Miroshnikova, O D Belyaeva, E A Polyakova, S. Nifontov, D A Kolodina, Elena Baranova, I A Pobozheva, and N D Razgildina

Subjects
medicine.medical_specialty, Adipose tissue, 030209 endocrinology & metabolism, Coronary Artery Disease, 030204 cardiovascular system & hematology, ADIPOQ Gene, Coronary artery disease, 03 medical and health sciences, 0302 clinical medicine, Blood serum, Internal medicine, Gene expression, medicine, Humans, cardiovascular diseases, Coronary atherosclerosis, Adiponectin, business.industry, medicine.disease, Endocrinology, Adipose Tissue, Bypass surgery, Cardiology and Cardiovascular Medicine, business, Pericardium
Abstract

AimTo determine the expression of adiponectin gene (ADIPOQ) and the content of high-molecular-weight adiponectin (HMWA) in epicardial (EAT) and subcutaneous adipose tissue (SCAT) in patients with ischemic heart disease (IHD).Material and methodsPaired samples of EAT and SCAT and blood serum were withdrawn from patients with IHD after bypass surgery and 16 subjects without IHD (comparison group). Matrix RNA (mRNA) level was measured using real-time polymerase chain reaction. HMWA levels in EAT and SCAT were evaluated by Western blotting. Serum adiponectin concentration was measured immunoenzymatically. For all patients, echocardiography was performed to measure the EAT thickness; coronarography was performed to determine severity of coronary atherosclerosis.ResultsSerum adiponectin concentration was lower in IHD patients than in the comparison group (pConclusionThe decreased serum concentration of antiatherogenic adiponectin and the reduced expression of ADIPOQ gene in SCAT (mRNA, HMWA) are associated with IHD.

Published
2020

3. ABCA1 and ABCG1 DNA methylation in epicardial adipose tissue of patients with coronary artery disease

Author

O. Berkovich, E A Polyakova, Natalia D Razgildina, A A Panteleeva, V. V. Miroshnikova, A.V. Markov, Irina A. Pobozheva, Elena Baranova, M.S. Nazarenko, V. P. Puzyrev, Olga Belyaeva, and S.N. Pchelina

Subjects
Adult, Male, medicine.medical_specialty, Coronary Artery Disease, Gastroenterology, Coronary artery disease, chemistry.chemical_compound, Peripheral Arterial Disease, Internal medicine, Carotid artery disease, Epicardial adipose tissue, medicine, Diseases of the circulatory (Cardiovascular) system, Humans, cardiovascular diseases, Obesity, Promoter Regions, Genetic, ATP Binding Cassette Transporter, Subfamily G, Member 1, Aged, Hypertriglyceridemia, DNA methylation, Cholesterol, business.industry, Reverse cholesterol transport, Middle Aged, medicine.disease, ABCA1 and ABCG1 transporters, medicine.anatomical_structure, Real-time polymerase chain reaction, chemistry, Adipose Tissue, Gene Expression Regulation, RC666-701, lipids (amino acids, peptides, and proteins), CpG Islands, Female, Cardiology and Cardiovascular Medicine, business, Pericardium, Artery, ATP Binding Cassette Transporter 1, Research Article
Abstract

Background Recent studies have focused on the potential role of epicardial adipose tissue (EAT) in the development of coronary artery disease (CAD). ABCA1 and ABCG1 transporters regulate cell cholesterol content and reverse cholesterol transport. We aimed to determine whether DNA methylation and mRNA levels of the ABCA1 and ABCG1 genes in EAT and subcutaneous adipose tissue (SAT) were associated with CAD. Methods Paired EAT and SAT samples were collected from 82 patients undergoing elective cardiac surgery either for coronary artery bypass grafting (CAD group, N = 66) or valve surgery (NCAD group, N = 16). ABCA1 and ABCG1 mRNA levels in EAT and SAT samples were analyzed using real time polymerase chain reaction, ABCA1 protein levels in EAT samples were assessed by western blotting. ABCA1 and ABCG1 DNA methylation analysis was performed in 24 samples from the CAD group and 9 samples from the NCAD group via pyrosequencing. Results DNA methylation levels in the ABCA1 promoter and ABCG1 cg27243685 and cg06500161 CpG sites were higher in EAT samples from patients with CAD compared with NCAD (21.92% vs 10.81%, p = 0.003; 71.51% vs 68.42%, p = 0.024; 46.11% vs 37.79%, p = 0.016, respectively). In patients with CAD, ABCA1 and ABCG1 DNA methylation levels were higher in EAT than in SAT samples (p ABCA1 mRNA levels in EAT samples were reduced in the subgroup of patients with CAD and concomitant carotid artery disease or peripheral artery disease compared with the NCAD group (p = 0.024). ABCA1 protein levels in EAT samples tended to be lower in CAD patients than in the NCAD group (p = 0.053). DNA methylation levels at the ABCG1 cg27243685 site positively correlated with plasma triglyceride concentration (r = 0.510, p = 0.008), body mass index (r = 0.556, p = 0.013) and waist-to-hip ratio (r = 0.504, p = 0.012) in SAT samples. Conclusion CAD is associated with ABCA1 and ABCG1 DNA hypermethylation in EAT. CAD with concomitant carotid artery disease or peripheral artery disease is accompanied by decreased ABCA1 gene expression in EAT. DNA methylation levels at the ABCG1 cg27243685 locus in SAT are associated with hypertriglyceridemia and obesity.

Published
2020

5. Regulation of ABCA1 and ABCG1 transporter gene expression in the intraabdominal adipose tissue

Author

E P Demina, T.S. Usenko, J He, I A Semenova, A A Panteleeva, V. V. Miroshnikova, S.N. Pchelina, A E Neimark, Olga Belyaeva, Elena Baranova, M. A. Nikolaev, E. Bazhenova, and O. Berkovich

Subjects
0301 basic medicine, medicine.medical_specialty, biology, Cholesterol, Clinical Biochemistry, Adipose tissue, Biochemistry, 03 medical and health sciences, chemistry.chemical_compound, 030104 developmental biology, Endocrinology, ABCG1, chemistry, Adipogenesis, ABCA1, Internal medicine, Gene expression, biology.protein, medicine, Molecular Medicine, lipids (amino acids, peptides, and proteins), Gene, Transcription factor
Abstract

Tissue specific expression of genes encoding the cholesterol transporters ABCA1 and ABCG1 as well as genes encoding the most important transcriptional regulators of adipogenesis (LXRα, LXRβ, PPARγ and RORα) has been investigated in intraabdominal adipose tissue (IAT) samples from obese patients and patients without overweight. A direct correlation between the content of ABCA1 and ABCG1 proteins and the RORα protein level (r = 0.480, p < 0.05; r = 0.435, p < 0.05, respectively) suggests involvement of the transcription factor RORα in the regulation of ABCA1 and ABCG1 protein levels in IAT. ABCA1 and ABCG1 gene expression positively correlated with such obesity indicators as body mass index (BMI) (r = 0.522, p = 0.004; r = 0.594, p = 0.001, respectively) and waist circumference (r = 0.403, p = 0.033; r = 0.474, p = 0.013, respectively). The development of obesity is also associated with decreased IAT levels of RORα and LXRβ mRNA (p = 0.016 and p = 0.002, respectively). This suggest that the nuclear factor RORα can play a significant role in the regulation of cholesterol metabolism and control IAT expression of ABCA1 and ABCG1 genes, while the level of IAT LXRβ gene expression may be an important factor associated with the development of obesity.

Published
2016

6. Reduction of the level of LXRβ mRNA and PPARγ mRNA in macrophages stimulated with a macrophage colony-stimulating factor in patients with atherosclerosis

Author

Ye. P. Demina, A. L. Schvartzman, N. V. Mayorov, V. V. Miroshnikova, and V. V. Davydenko

Subjects
Macrophage colony-stimulating factor, medicine.medical_specialty, Messenger RNA, Reverse cholesterol transport, Lipid metabolism, Biology, law.invention, Endocrinology, Nuclear receptor, law, Internal medicine, Immunology, Genetics, medicine, Macrophage, Animal Science and Zoology, Agronomy and Crop Science, Gene, Polymerase chain reaction
Abstract

Nuclear receptors LXRα/β and PPARγ play an important role in the regulation of lipid metabolism and reverse cholesterol transport. However, the effect of the expression of LXRα/β and PPARγ genes in macrophages on the development of atherosclerosis remains poorly studied. We determined the levels of LXRα mRNA, LXRβ mRNA, and PPARγ mRNA by a real-time polymerase chain reaction in macrophages cultivated for 5 days with macrophage colony-stimulating factor (M-CSF). The levels of LXRβ mRNA and PPARγ mRNA were lower in patients with coronary artery stenosis than in the control group, p < 0.001. The groups did not differ in the content of LXRα mRNA (p = 0.17). We suggest that the level of expression of LXRβ and PPARγ genes in macrophages may be a significant factor associated with the development of atherosclerosis.

Published
2015

7. The expression of ABCG1 transporter gene in peripheral blood mononuclear cells of patients with atherosclerosis

Author

A. G. Vinogradov, V. V. Miroshnikova, A. D. Denisenko, N. V. Mayorov, V. V. Davydenko, P. S. Kurjanov, V. N. Vavilov, A. L. Schwarzman, and E. P. Demina

Subjects
medicine.medical_specialty, Messenger RNA, biology, Cholesterol, Reverse cholesterol transport, Cell Biology, Peripheral blood mononuclear cell, chemistry.chemical_compound, Endocrinology, chemistry, ABCG1, Internal medicine, Blood plasma, Immunology, medicine, biology.protein, Macrophage, lipids (amino acids, peptides, and proteins), Artery occlusion
Abstract

The antiatherogenic role of high-density lipoproteins (HDL) was demonstrated by numerous experimental, clinical and epidemiological studies. The mechanism underlying the antiatherogenic potential of HDL is based on their involvement in reverse cholesterol transport (RCT) from peripheral tissues into the liver. Transmembrane transporter ABCG1 is a key RCT protein. Its function is to remove cholesterol from cells and transfer it to HDL. The role of ABCG1 transporter in the development of atherosclerosis in humans remains unexplored. The goal of our study was to investigate the expression of ABCG1 gene in patients with atherosclerosis. Real-time PCR was applied to study ABCG1 mRNA content in leukocytes, monocytes, and macrophages activated with macrophage colony-stimulating factor (M-CSF) from patients with atherosclerosis and healthy people. The amount of ABCG1 protein in monocytes and macrophages of patients and healthy donors was assayed by immunoblotting. It was found that the level of ABCG1 mRNA (p < 0.001) and ABCG1 protein (p < 0.05) was lower in macrophages of patients with atherosclerosis. The level of ABCG1 mRNA in monocytes of patients with artery occlusion was lower than in patients with features of lesser stenosis and the control group (p < 0.05). No correlation was found between ABCG1 gene expression and total and HDL cholesterol levels in the blood plasma. It can be concluded that reduced ABCG1 gene expression in monocytes and macrophages may be critical for the atherosclerosis progression.

Published
2014

8. Reducing of LXRβ and PPARγ mRNA in M-CSF stimulated macrophages in patients with levels atherosclerosis

Author

V. V. Miroshnikova, Nikolay Vladimirovich Mayorov, Vladimir Valentinovich Davydenko, Alexander L`vovich Schwarzman, and Yekaterina Petrovna Demina

Subjects
medicine.medical_specialty, lcsh:QH426-470, pparγ gene, lxrα/β genes, Biology, Biochemistry, Internal medicine, Genetics, medicine, Macrophage, In patient, Gene, Genetics (clinical), Ecology, Evolution, Behavior and Systematics, Messenger RNA, Ecology, Reverse cholesterol transport, Lipid metabolism, macrophages, lcsh:Genetics, Real-time polymerase chain reaction, Endocrinology, Nuclear receptor, Immunology, artery stenosis, atherosclerosis
Abstract

Nuclear receptors LXRα/β and PPARγ play an important role in lipid metabolism and reverse cholesterol transport. However, the influence of LXRα/β and PPARγ mRNA levels in macrophages on atherosclerosis remains unexplored. Using real time PCR, we determined LXRα mRNA, LXRβ mRNA and PPARγ mRNA levels in macrophages cultured for 5 days with macrophage colony-stimulating factor (M-CSF). Levels of LXRβ mRNA and PPARγ mRNA in patients with arterial stenosis were reduced when compared with the control group, p 0.001. LXRa gene mRNA level in macrophages was not changed in the study groups, (p = 0.17). Thus, our study shows that the LXRβ and PPARγ genes expression levels in macrophages may be significant factors associated with the development of atherosclerosis.

Published
2014

9. ABCA1 mRNA and protein levels in M-CSF-activated macrophages from patients with arterial stenosis

Author

V. V. Miroshnikova, A. L. Schwarzman, V. V. Davydenko, E. P. Demina, and N. V. Majorov

Subjects
medicine.medical_specialty, Messenger RNA, Cholesterol, Arterial stenosis, Reverse cholesterol transport, nutritional and metabolic diseases, hemic and immune systems, Transporter, Cell Biology, Biology, Peripheral, chemistry.chemical_compound, Endocrinology, chemistry, Internal medicine, ABCA1, Immunology, polycyclic compounds, medicine, biology.protein, Macrophage, lipids (amino acids, peptides, and proteins), cardiovascular diseases
Abstract

ABCA1 transporter is one of the key factors defining the level of antiatherogenic HDL in plasma. It is involved in cholesterol removal from peripheral tissues by reverse cholesterol transport. However, the influence of ABCA1 mRNA and ABCA1 protein levels in macrophages on atherosclerosis remains unexplored. Using real-time PCR, we determined the ABCA1 mRNA level in macrophages cultured for 5 days with macrophage colony-stimulating factor (M-CSF). The ABCA1 mRNA level in macrophages from patients with arterial stenosis was increased compared to the control group, p = 0.04. Western-blot assayed ABCA1 protein content in macrophages from patients was significantly lower than in the control group, p = 0.01. Our results suggest that ABCA1 mRNA and ABCA1 protein levels in macrophages may be important factors in the development of atherosclerosis.

Published
2013

10. Poster session 2

Author

J. M. Perez-Pomares, A. Ruiz-Villalba, A. Ziogas, J. C. Segovia, M. Ehrbar, R. Munoz-Chapuli, A. De La Rosa, J. N. Dominguez, L. Hove-Madsen, B. Sankova, D. Sedmera, D. Franco, A. Aranega Jimenez, G. Babaeva, N. Chizh, S. Galchenko, B. Sandomirsky, M. Schwarzl, S. Seiler, P. Steendijk, S. Huber, H. Maechler, M. Truschnig-Wilders, B. Pieske, H. Post, S. Simrick, R. Kreutzer, C. Rao, C. M. Terracciano, P. Kirchhof, L. Fabritz, T. Brand, M. Theveniau-Ruissy, P. Parisot, A. Francou, E. Saint-Michel, K. Mesbah, R. G. Kelly, H.-T. Wu, S.-S. Sie, C.-Y. Chen, T.-C. Kuan, C. S. Lin, Z. Ismailoglu, M. Guven, A. Yakici, Y. Ata, S. Ozcan, E. Yildirim, Z. Ongen, V. Miroshnikova, E. Demina, T. Rodygina, P. Kurjanov, A. Denisenko, A. Schwarzman, A. Rubanenko, Y. Shchukin, A. Germanov, M. Goldbergova, J. Parenica, J. Lipkova, N. Pavek, P. Kala, M. Poloczek, A. Vasku, I. Parenicova, J. Spinar, C. Gambacciani, E. Chiavacci, M. Evangelista, N. Vesentini, C. Kusmic, L. Pitto, A. Chernova, S. U. Y. Nikulina, D. A. Arvanitis, I. Mourouzis, C. Pantos, E. G. Kranias, D. V. Cokkinos, D. Sanoudou, T. E. Vladimirskaya, I. A. Shved, S. G. Kryvorot, I. M. Schirmer, A. Appukuttan, L. Pott, K. Jaquet, Y. Ladilov, C. R. Archer, M. D. Bootman, H. L. Roderick, A. Fusco, D. Sorriento, G. Santulli, B. Trimarco, G. Iaccarino, M. Hagenmueller, J. Riffel, E. Bernhold, H. A. Katus, S. E. Hardt, A. Maqsood, M. Zi, S. Prehar, L. Neyses, S. Ray, D. Oceandy, N. Khatami, P. Wadowski, V. Wagh, J. Hescheler, A. Sachinidis, W. Mohl, B. Chaudhry, D. Burns, D. J. Henderson, N. A. M. Bax, M. H. Van Marion, B. Shah, M. J. Goumans, C. V. C. Bouten, D. W. J. Van Der Schaft, A. A. M. Van Oorschot, S. Maas, J. Braun, J. Van Tuyn, A. A. F. De Vries, A. C. Gittenberger-De Groot, S. Bageghni, M. J. Drinkhill, T. F. C. Batten, J. F. X. Ainscough, B. Onate, G. Vilahur, R. Ferrer-Lorente, J. Ybarra, A. Diez-Caballero, C. Ballesta-Lopez, F. Moscatiello, J. Herrero, L. Badimon, E. Martin-Rendon, D. M. Clifford, S. A. Fisher, S. J. Brusnkill, C. Doree, A. Mathur, M. Clarke, S. M. Watt, R. Hernandez-Vera, D. Kavanagh, A. I. Yemm, J. Frampton, N. Kalia, Y. Terajima, T. Shimizu, S. Tsuruyama, H. Ishii, H. Sekine, N. Hagiwara, T. Okano, K. R. Vrijsen, S. A. J. Chamuleau, J. P. G. Sluijter, P. F. M. Doevendans, R. Madonna, S. Delli Pizzi, L. Di Donato, A. Mariotti, L. Di Carlo, E. D'ugo, M. A. Teberino, A. Merla, A. T, R. De Caterina, L. Kolker, N. N. Ali, K. Maclellan, M. Moore, J. Wheeler, S. E. Harding, R. A. Fleck, J. M. Rowlinson, N. Kraenkel, R. Ascione, P. Madeddu, J. F. O'sullivan, A. L. Leblond, G. Kelly, A. H. S. Kumar, P. Metharom, C. K. Buneker, N. Alizadeh-Vikali, B. G. Hynes, R. O'connor, N. M. Caplice, M. Noseda, A. J. De Smith, T. Leja, P. H. Rao, F. Al-Beidh, M. S. Abreu Pavia, A. I. Blakemore, M. D. Schneider, K. Stathopoulou, F. Cuello, E. Ehler, R. S. Haworth, M. Avkiran, H. Morawietz, C. Eickholt, H. Langbein, M. Brux, C. Goettsch, W. Goettsch, A. Arsov, C. Brunssen, L. Mazilu, I. R. Parepa, A. I. Suceveanu, A. P. Suceveanu, F. S. De Man, C. Guignabert, L. Tu, M. L. Handoko, I. Schalij, E. Fadel, P. E. Postmus, A. Vonk-Noordegraaf, M. Humbert, S. Eddahibi, C. Del Giudice, A. Anastasio, L. Fazal, F. Azibani, N. Bihry, R. Merval, E. Polidano, J.-L. Samuel, C. Delcayre, Y. Zhang, Y. M. Mi, L. L. Ren, Y. P. Cheng, R. Guo, Y. Liu, Y. N. Jiang, A. D. Kokkinos, P. Tretjakovs, A. Jurka, I. Bormane, I. Mikelsone, D. Reihmane, K. Elksne, G. Krievina, J. Verbovenko, G. Bahs, N. Lopez-Andres, A. Rousseau, L. Calvier, R. Akhtar, C. Labat, K. Cruickshank, J. Diez, F. Zannad, P. Lacolley, P. Rossignol, K. Hamesch, P. Subramanian, X. Li, A. Thiemann, K. Heyll, K. Dembowsky, E. Chevalier, C. Weber, A. Schober, L. Yang, G. Kim, B. Gardner, J. Earley, M. Hofmann-Bowman, C.-F. Cheng, W.-S. Lian, H. Lin, N. J. Jinjolia, G. A. Abuladze, S. H. T. Tvalchrelidze, I. Khamnagadaev, M. Shkolnikova, L. Kokov, I. Miklashevich, I. Drozdov, I. Ilyich, B. O. Bingen, S. F. A. Askar, D. L. Ypey, A. Van Der Laarse, M. J. Schalij, D. A. Pijnappels, C. H. Roney, F. S. Ng, R. A. Chowdhury, E. T. Y. Chang, P. M. Patel, A. R. Lyon, J. H. Siggers, N. S. Peters, A. Obergrussberger, S. Stoelzle, A. Bruggemann, C. Haarmann, M. George, N. Fertig, D. Moreira, A. Souza, P. Valente, J. Kornej, C. Reihardt, J. Kosiuk, A. Arya, G. Hindricks, V. Adams, D. Husser, A. Bollmann, P. Camelliti, J. Dudhia, P. Dias, J. Cartledge, D. J. Connolly, M. Nobles, S. Sebastian, A. Tinker, A. Opel, H. Daimi, A. Haj Khelil, J. Be Chibani, A. Barana, I. Amoros, M. Gonzalez De La Fuente, R. Caballero, A. Aranega, A. Kelly, O. Bernus, O. J. Kemi, R. C. Myles, I. A. Ghouri, F. L. Burton, G. L. Smith, M. Del Lungo, L. Sartiani, V. Spinelli, M. Baruscotti, D. Difrancesco, A. Mugelli, E. Cerbai, A. M. Thomas, Q. Aziz, T. Khambra, J. M. A. Addlestone, E. J. Cartwright, R. Wilkinson, W. Song, S. Marston, A. Jacquet, N. M. Mougenot, A. J. Lipskaia, E. R. Paalberends, K. Stam, S. J. Van Dijk, M. Van Slegtenhorst, C. Dos Remedios, F. J. Ten Cate, M. Michels, H. W. M. Niessen, G. J. M. Stienen, J. Van Der Velden, M. I. Read, A. A. Andreianova, J. C. Harrison, C. S. Goulton, D. S. Kerr, I. A. Sammut, M. Wallner, D. Von Lewinski, D. Kindsvater, M. Saes, I. Morano, A. Muegge, B. Buyandelger, S. Kostin, S. Gunkel, J. Vouffo, K. Ng, J. Chen, M. Eilers, R. Isaacson, H. Milting, R. Knoell, M.-E. Cattin, C. Crocini, S. Schlossarek, S. Maron, A. Hansen, T. Eschenhagen, L. Carrier, G. Bonne, R. Coppini, C. Ferrantini, I. Olivotto, L. Belardinelli, C. Poggesi, M. C. Leung, A. E. Messer, O. Copeland, S. B. Marston, A. M. Mills, T. Collins, P. O'gara, T. Thum, K. Regalla, K. T. Macleod, T. Prodromakis, U. Chaudhry, A. Darzi, M. H. Yacoub, T. Athanasiou, A. Bogdanova, A. Makhro, M. Hoydal, T. O. Stolen, A. B. Johnssen, M. Alves, D. Catalucci, G. Condorelli, L. G. Koch, S. L. Britton, U. Wisloff, V. Bito, P. Claus, K. Vermeulen, C. Huysmans, R. Ventura-Clapier, K. R. Sipido, M. N. Seliuk, A. P. Burlaka, E. P. Sidorik, N. V. Khaitovych, M. M. Kozachok, V. S. Potaskalova, R. B. Driesen, D. T. Galan, D. De Paulis, T. Arnoux, S. Schaller, R. M. Pruss, D. M. Poitz, A. Augstein, R. C. Braun-Dullaeus, A. Schmeisser, R. H. Strasser, P. Micova, P. Balkova, M. Hlavackova, J. Zurmanova, D. Kasparova, F. Kolar, J. Neckar, F. Novak, O. Novakova, S. Pollard, M. Babba, A. Hussain, R. James, H. Maddock, A. S. Alshehri, G. F. Baxter, B. Dietel, R. Altendorf, W. G. Daniel, R. Kollmar, C. D. Garlichs, R. Sirohi, N. Roberts, D. Lawrence, A. Sheikh, S. Kolvekar, J. Yap, M. Arend, G. Walkinshaw, D. J. Hausenloy, D. M. Yellon, A. Posa, R. Szabo, Z. Szalai, P. Szablics, M. A. Berko, K. Orban, Z. S. Murlasits, L. Balogh, C. Varga, H. C. Ku, M. J. Su, R.-M. Chreih, C. Ginghina, D. Deleanu, A. L. B. J. Ferreira, A. Belal, M. A. Ali, X. Fan, A. Holt, R. Campbell, R. Schulz, C. Bonanad, V. Bodi, J. Sanchis, J. M. Morales, V. Marrachelli, J. Nunez, M. J. Forteza, F. Chaustre, C. Gomez, F. J. Chorro, T. Csont, V. Fekete, Z. Murlasits, E. Aypar, P. Bencsik, M. Sarkozy, Z. V. Varga, P. Ferdinandy, G. D. Duerr, M. Zoerlein, D. Dewald, B. Mesenholl, P. Schneider, A. Ghanem, S. Rittling, A. Welz, O. Dewald, E. Becker, C. Peigney, C. Bouleti, A. Galaup, C. Monnot, B. Ghaleh, S. Germain, A. Timmermans, A. Ginion, C. De Meester, K. Sakamoto, J.-L. Vanoverschelde, S. Horman, C. Beauloye, L. Bertrand, N. Maroz-Vadalazhskaya, E. Drozd, L. Kukharenko, I. Russkich, D. Krachak, Y. Seljun, Y. Ostrovski, A.-C. Martin, B. Le Bonniec, T. Lecompte, B. Dizier, J. Emmerich, A.-M. Fischer, C.-M. Samama, A. Godier, S. Mogensen, E. M. Furchtbauer, C. Aalkjaer, W. L. Choong, A. Jovanovic, F. Khan, J. M. Daniel, J. M. Dutzmann, R. Widmer-Teske, D. Guenduez, D. Sedding, M. M. Castro, J. J. C. Cena, W. J. C. Cho, G. G. Goobie, M. P. W. Walsh, R. S. Schulz, J. Dutzmann, K. T. Preissner, W. Sones, M. Kotlikoff, K. Serizawa, K. Yogo, K. Aizawa, M. Hirata, Y. Tashiro, N. Ishizuka, A. Varela, M. Katsiboulas, D. Tousoulis, T. G. Papaioannou, S. Vaina, C. H. Davos, C. Piperi, C. Stefanadis, E. K. Basdra, A. G. Papavassiliou, C. Hermenegildo, M. Lazaro-Franco, A. Sobrino, C. Bueno-Beti, N. Martinez-Gil, T. Walther, C. Peiro, C. F. Sanchez-Ferrer, S. Novella, M. Ciccarelli, A. Franco, G. W. Dorn, P. Cseplo, O. Torok, Z. S. Springo, Z. Vamos, D. Kosa, J. Hamar, A. Koller, K. J. Bubb, A. Ahluwalia, E. L. Stepien, A. Gruca, J. Grzybowska, J. Goralska, A. Dembinska-Kiec, J. Stolinski, L. Partyka, H. Zhang, D. Sweeney, G. N. Thomas, P. V. Fish, D. P. Taggart, S. Cioffi, M. Bilio, S. Martucciello, E. Illingworth, A. Caporali, S. Shantikumar, M. Marchetti, F. Martelli, C. Emanueli, M. Meloni, A. Al Haj Zen, G. Sala-Newby, S. Del Turco, C. Saponaro, B. Dario, S. Sartini, A. Menciassi, P. Dario, C. La Motta, G. Basta, V. Santiemma, C. Bertone, F. Rossi, E. Michelon, M. J. Bianco, A. Castelli, D. I. Shin, K. B. Seung, S. M. Seo, H. J. Park, P. J. Kim, S. H. Baek, Y. S. Choi, S. H. Her, D. B. Kim, J. M. Lee, C. S. Park, S. Rocchiccioli, A. Cecchettini, G. Pelosi, L. Citti, O. Parodi, M. G. Trivella, D. Michel-Monigadon, F. Burger, S. Dunoyer-Geindre, G. Pelli, B. Cravatt, S. Steffens, A. Didangelos, U. Mayr, X. Yin, C. Stegemann, J. Shalhoub, A. H. Davies, C. Monaco, M. Mayr, S. Lypovetska, S. Grytsenko, I. U. Njerve, A. A. Pettersen, T. B. Opstad, V. Bratseth, H. Arnesen, I. Seljeflot, I. E. Dumitriu, P. Baruah, R. F. Antunes, J. C. Kaski, I. Trapero, I. Benet, C. Alguero, F. J. Chaustre, A. Mangold, S. Puthenkalam, K. Distelmaier, C. Adlbrecht, I. M. Lang, T. Koizumi, I. Inoue, N. Komiyama, S. Nishimura, O. N. Korneeva, O. M. Drapkina, L. Fornai, A. Angelini, A. Kiss, F. Giskes, G. Eijkel, M. Fedrigo, M. L. Valente, G. Thiene, R. M. A. Heeren, T. Padro, L. Casani, R. Suades, B. Bertoni, R. Carminati, V. Carlini, L. Pettinari, C. Martinelli, N. Gagliano, G. Noppe, P. Buchlin, N. Marquet, N. Baeyens, N. Morel, A. Baysa, J. Sagave, C. P. Dahl, L. Gullestad, A. Carpi, F. Di Lisa, M. Giorgio, J. Vaage, G. Valen, E. Vafiadaki, V. Papalouka, G. Terzis, K. Spengos, P. Manta, C. Gales, G. Genet, E. Dague, O. Cazorla, B. Payre, C. Mias, A. Ouille, A. Lacampagne, A. Pathak, J. M. Senard, M. Abonnenc, P. Da Costa Martins, S. Srivastava, M. Gautel, L. De Windt, L. Comelli, C. Lande, N. Ucciferri, L. Ikonen, H. Vuorenpaa, K. Kujala, J.-R. Sarkanen, T. Heinonen, T. Ylikomi, K. Aalto-Setala, H. Capros, N. Sprincean, N. Usurelu, V. Egorov, N. Stratu, V. Matchkov, E. Bouzinova, N. Moeller-Nielsen, O. Wiborg, P. S. Gutierrez, R. Aparecida-Silva, L. F. Borges, L. F. P. Moreira, R. R. Dias, J. Kalil, N. A. G. Stolf, W. Zhou, K. Suntharalingam, N. Brand, R. Vilar Compte, L. Ying, K. Bicknell, A. Dannoura, P. Dash, G. Brooks, I. Tsimafeyeu, Y. Tishova, N. Wynn, I. P. Oyeyipo, L. A. Olatunji, L. Maegdefessel, J. Azuma, R. Toh, U. Raaz, D. R. Merk, A. Deng, J. M. Spin, P. S. Tsao, L. Tedeschi, M. Taranta, I. Naldi, S. Grimaldi, C. Cinti, M. Bousquenaud, F. Maskali, S. Poussier, P. Y. Marie, H. Boutley, G. Karcher, D. R. Wagner, Y. Devaux, I. Torre, S. Psilodimitrakopoulos, I. Iruretagoiena, A. Gonzalez-Tendero, D. Artigas, P. Loza-Alvarez, E. Gratacos, I. Amat-Roldan, L. Murray, D. M. Carberry, P. Dunton, M. J. Miles, M.-S. Suleiman, K. Kanesalingam, R. Taylor, C. N. Mc Collum, A. Parniczky, M. Solymar, A. Porpaczy, A. Miseta, Z. S. Lenkey, S. Szabados, A. Cziraki, J. Garai, I. Myloslavska, S. M. Menazza, M. C. Canton, F. D. L. Di Lisa, S. H. V. Oliveira, C. A. S. Morais, M. R. Miranda, T. T. Oliveira, M. R. A. Lamego, L. M. Lima, N. S. Goncharova, A. V. Naymushin, A. V. Kazimli, O. M. Moiseeva, M. G. Carvalho, A. P. Sabino, A. P. L. Mota, M. O. Sousa, A. Niessner, B. Richter, P. J. Hohensinner, K. Rychli, G. Zorn, R. Berger, D. Moertl, R. Pacher, J. Wojta, M. Huelsmann, G. Kukharchik, N. Nesterova, A. Pavlova, L. Gaykovaya, N. Krapivka, I. Konstantinova, L. Sichinava, S. Prapa, K. P. Mccarthy, P. J. Kilner, X. Y. Xu, M. R. Johnson, S. Y. Ho, M. A. Gatzoulis, E. G. Stoupel, R. Garcia, D. Merino, C. Montalvo, M. A. Hurle, J. F. Nistal, A. V. Villar, A. Perez-Moreno, R. Gilabert, and E. Ros

Subjects
medicine.medical_specialty, Endocrinology, Physiology, Activator (genetics), Chemistry, Physiology (medical), Internal medicine, medicine, AMPK, Myocyte, Long-term potentiation, Metabolism, Cardiology and Cardiovascular Medicine
Published
2012

11. Association of polymorphisms in apolipoprotein A-I gene with plasma lipid profile in population of Saint-Petersburg

Author

A. L. Schwarzman, A. A. Panteleeva, S. N. Pchelina, and V. V. Miroshnikova

Subjects
apoa1 gene, Medicine (General), medicine.medical_specialty, Apolipoprotein B, apolipoprotein a-i, education, Population, chemistry.chemical_compound, R5-920, аполипопротеин а-i, Internal medicine, APOA1 Gene, Plasma lipids, medicine, Saint petersburg, Allele, Gene, education.field_of_study, biology, Cholesterol, ген apoa1, Endocrinology, chemistry, атеросклероз, липопротеины высокой плотности, biology.protein, lipids (amino acids, peptides, and proteins), high density lipoproteins, atherosclerosis
Abstract

Apolipoprotein A-I is a key structure protein of antiatherogenic high density lipoproteins (HDL). The aim of the study was to investigate the relationship between (-75)G/A and 83C/T polymorphic variants of apolipoprotein A-I gene (APOA1) and the plasma lipid profile in the population of Saint-Petersburg. Allele T83 of APOA1 gene was found to be associated with the reduced risk of atherosclerosis development among Saint-Petersburg inhabitants. The study demonstrates that allele T83 of APOA1 gene is associated with higher plasma HDL cholesterol levels (p

Published
2014

12. Polymorphism of dopamine transporter gene DAT1 and individual variability of defense cardiac response in humans

Author

L. I. Aftanas, E. A. Gromova, P. V. Miroshnikova, K. V. Loktev, and V. V. Gafarov

Subjects
Cardiac response, Electrophoresis, Male, medicine.medical_specialty, Blood Pressure, Polymerase Chain Reaction, General Biochemistry, Genetics and Molecular Biology, Cardiovascular Physiological Phenomena, Tandem repeat polymorphism, Polymorphism (computer science), Stress, Physiological, Internal medicine, Genotype, medicine, Humans, Allele, Gene, Serotonin transporter, Dopamine transporter, Aged, Serotonin Plasma Membrane Transport Proteins, Dopamine Plasma Membrane Transport Proteins, Polymorphism, Genetic, biology, General Medicine, Middle Aged, Endocrinology, Acoustic Stimulation, Tandem Repeat Sequences, biology.protein, Stress, Psychological
Abstract

We evaluated association of BP stress-reactivity on the model of cardiac defense response in 45-70-year-old men with variable number of tandem repeat polymorphism in genes encoding dopamine transporter protein (DAT1) and serotonin transporter protein (5-HTTLPR). It was found that individuals carrying long allele variant (l) of DAT1 gene (l/l: allele l homozygotes) in the genotype in comparison with short variant (s) carriers (heterozygous genotype l/s) demonstrate hyperreactive profi les of cardiovascular stress reactivity characterized by a signifi cant increase in the amplitude and duration of long-latency BP components in cardiac defensive response.

Published
2012

Catalog

Books, media, physical & digital resources
See catalog results