Gotowa bibliografia na temat „Cardiovascular system – Diseases – Genetic aspects”
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Artykuły w czasopismach na temat "Cardiovascular system – Diseases – Genetic aspects"
Tatour, Yasmin, i Tamar Ben-Yosef. "Syndromic Inherited Retinal Diseases: Genetic, Clinical and Diagnostic Aspects". Diagnostics 10, nr 10 (2.10.2020): 779. http://dx.doi.org/10.3390/diagnostics10100779.
Pełny tekst źródłaKireeva, Victoria Vladimirovna, Svetlana Aleksandrovna Lepekhova, Lyubov Nazirovna Mansurova i Saryuna Chingisovna Dugarova. "EPIGENETIC AND MOLECULAR AND GENETIC ASPECTS OF OBESITY AS A RISK FACTOR OF CARDIOVASCULAR CATASTROPHES". EurasianUnionScientists 5, nr 7(76) (20.08.2020): 39–44. http://dx.doi.org/10.31618/esu.2413-9335.2020.5.76.926.
Pełny tekst źródłaSychev, Dmitry A., Igor N. Sychev, Karin B. Mirzaev, Eric I. Rytkin, Dmitriy V. Ivashchenko, Irina V. Bure i Vitaliy A. Otdelenov. "Clinical pharmacology technologies for personalization of cardiovascular diseases drug treatment: focus on direct oral anticoagulants". Annals of the Russian academy of medical sciences 74, nr 5 (4.12.2019): 299–306. http://dx.doi.org/10.15690/vramn1214.
Pełny tekst źródłaJones, Elizabeth A. V., Ferdinand le Noble i Anne Eichmann. "What Determines Blood Vessel Structure? Genetic Prespecification vs. Hemodynamics". Physiology 21, nr 6 (grudzień 2006): 388–95. http://dx.doi.org/10.1152/physiol.00020.2006.
Pełny tekst źródłaSaveleva, N. N., I. I. Sokolova, S. I. German i T. V. Tomilina. "SOME ASPECTS OF THE EATIOLOGY OF PARODONTUS DISEASES. (LITERATURE REVIEW)". Ukrainian Dental Almanac, nr 2 (25.06.2018): 54–59. http://dx.doi.org/10.31718/2409-0255.2.2018.13.
Pełny tekst źródłaFajemiroye, James Oluwagbamigbe, Luiz Carlos da Cunha, Roberto Saavedra-Rodríguez, Karla Lima Rodrigues, Lara Marques Naves, Aline Andrade Mourão, Elaine Fernanda da Silva i in. "Aging-Induced Biological Changes and Cardiovascular Diseases". BioMed Research International 2018 (10.06.2018): 1–14. http://dx.doi.org/10.1155/2018/7156435.
Pełny tekst źródłaMacit, Melahat S., i Nilüfer Acar-Tek. "Current Perspectives for Diabetes and Allostatic Load: The Role of Nutrition". Current Nutrition & Food Science 15, nr 7 (12.11.2019): 646–52. http://dx.doi.org/10.2174/1573401314666180620164859.
Pełny tekst źródłaDemidov, O. N., A. V. Shakula, G. V. Gulevatiy i A. V. Sobolev. "Role of clonal gemopoeisis in development of individual approaches for early diagnostics, treatment and rehabilitation of patients with cardio-vascular diseases". Bulletin of Restorative Medicine 97, nr 3 (28.06.2020): 45–49. http://dx.doi.org/10.38025/2078-1962-2020-97-3-45-49.
Pełny tekst źródłaMotta, Benedetta M., Peter P. Pramstaller, Andrew A. Hicks i Alessandra Rossini. "The Impact of CRISPR/Cas9 Technology on Cardiac Research: From Disease Modelling to Therapeutic Approaches". Stem Cells International 2017 (2017): 1–13. http://dx.doi.org/10.1155/2017/8960236.
Pełny tekst źródłaCai, Wanwan, Wanbang Zhou, Zhe Han, Junrong Lei, Jian Zhuang, Ping Zhu, Xiushan Wu i Wuzhou Yuan. "Master regulator genes and their impact on major diseases". PeerJ 8 (6.10.2020): e9952. http://dx.doi.org/10.7717/peerj.9952.
Pełny tekst źródłaRozprawy doktorskie na temat "Cardiovascular system – Diseases – Genetic aspects"
McCaskie, Pamela Ann. "Multiple-imputation approaches to haplotypic analysis of population-based data with applications to cardiovascular disease". University of Western Australia. School of Population Health, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0160.
Pełny tekst źródłaWilder, Steven P. "Computational analysis of susceptibility genes for diabetes and cardiovascular diseases in animal models". Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670109.
Pełny tekst źródłaThomas, Saralene Iona. "Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness". Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51777.
Pełny tekst źródłaPretorius, Jakobus. "Investigation of the relationship between genetic and environmental risk factors associated with obesity and insulin resistance in South African patients with non-alcoholic fatty liver disease(NAFLD)". Thesis, Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/71689.
Pełny tekst źródłaIncludes bibliography
ENGLISH ABSTRACT: Non-alcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disease in the world. The disease spectrum of NAFLD extends from steatosis (types 1,2) to non-alcoholic steatohepatitis (NASH) with inflammation (types 3,4). The aims of the study were 1) to analytically validate high-throughput real time polymerase chain reaction (RT-PCR) assays for three selected single nucleotide polymorphisms (SNPs), FTO rs9939609 (intron 1 T>A), TNF-α rs1800629 (-308 G>A) and PPARγ rs1801282 (Pro12Ala, 34 C>G), and 2) to perform genotype-phenotype association studies in relation to biochemical abnormalities, disease severity and age of onset. A total of 119 patients with fatty liver identified on ultrasound, including 88 histologically confirmed NAFLD patients, and 166 control individuals were genotyped for the three selected SNPs. RT-PCR validated against direct sequencing as the gold standard was used for detection of genetic variation. All three SNPs were in Hardy Weinberg equilibrium in the study population, except for a deviation in genotype distribution detected for PPARγ rs1801282 in the NAFLD patient subgroup (p<0.001). After adjustment for age and gender, the risk-associated FTO rs9939609 A-allele was detected at a significantly higher frequency in the Caucasian compared with Coloured patients (p=0.005). The opposite was detected for the risk-associated TNF-α rs1800629 A-allele, which occurred at a significantly higher frequency in the Coloured compared with Caucasian NAFLD patients (p=0.034). The onset of fatty liver disease symptoms was on average 5 years younger in the presence of each risk-associated TNF-α rs1800629 A-allele (p=0.028). When considered in the context of an inferred genotype risk score ranging from 0-6, disease onset occurred on average 3 years earlier (p=0.008) in the presence of each risk-associated FTO A-allele, TNF-α A-allele or PPARγ C-allele. After adjustment for age, gender and race, no differences in genotype distribution or allele frequencies were observed between histologically confirmed NAFLD (types 1,2) and NASH (types 3,4) patients, while the minor allele frequency for the TNF-α rs1800629 was significantly higher in the total NAFLD (types 1-4) (p=0.047) as well as NASH subgroup (NAFLD types 3,4) (p=0.030) compared with obese patients without a histologically confirmed NAFLD diagnosis. A significant correlation was furthermore observed between the number of TNF-α rs1800629 A-alleles and increasing CRP levels (p=0.029), with a favourable reduced effect in the presence of low- to moderate alcohol intake. The average waist circumference of physically active NAFLD patients was 12% lower than in physically inactive patients (p=0.004). In view of the results presented in this study, the inclusion of the selected SNPs, and in particular the pro-inflammatory TNF-α rs1800629 polymorphism, may be considered as part of a comprehensive cardiovascular risk evaluation of NAFLD patients. Ultimately, early detection of patients with fatty liver disease symptoms and effective intervention based on the underlying disease mechanism may prevent progression from NAFLD to NASH, shown to be an independent risk factor for cardiovascular diseases.
AFRIKAANSE OPSOMMING: Nie-alkoholiese lewervervetting (NALV) is die mees algemene kroniese lewersiekte in die wêreld. Die siektespektrum van NALV strek van steatose (vervette lewer tipes 1,2) tot steatohepatitis met inflammasie (NASH tipes 3,4). Die doel van die studie was 1) om analities die hoë omset polimerase kettingreaksie (RT-PKR) metode te valideer vir die geselekteerde enkel nukleotied polimorfismes (ENPs) FTO rs9939609 (intron 1 T>A), TNF-α rs1800629 (-308 G>A) en PPARγ rs1801282 (Pro12Ala, 34 C>G), en 2) om genotipe-fenotipe assosiasie studies uit te voer ten opsigte van relevante biochemiese abnormaliteite, graad van die siekte en aanvangsouderdom. ’n Totaal van 119 pasiënte met vervette lewers is geïdentifiseer met behulp van ultraklank, insluited 88 histologies-bevestigde NALV pasiënte, en 166 kontrole individue. Hierdie pasiënte is gegenotipeer vir die 3 geselekteerde ENP’s. RT-PKR gevalideer met direkte DNA volgorde bepaling as die goue standaard, is gebruik vir opsporing van genetiese variasie. Al die ENP’s was in Hardy Weinberg ekwilibrium in die studie populasie, behalwe vir ’n afwyking in genotipe verspreiding waargeneem vir PPARγ in die NALV subgroep (p<0.001). Nadat aanpassings gemaak is vir ouderdom en geslag, is die risiko-geassosieerde FTO rs9939609 A-alleel waargeneem teen ’n betekenisvol hoër frekwensie in die Kaukasiese pasiënte in vergelyking met Kleurling pasiënte (p=0.005). Die teenoorgestelde is waargeneem vir die risiko-geassosieerde TNF-α rs1800629 A-alleel wat voorgekom het teen ’n betekenisvol hoër frekwensie in die Kleurling NALV pasiënte, in vergelyking met Kaukasiese NALV pasiënte (p=0.034). Die aanvang van NALV was gemiddeld 5 jaar vroeër in die teenwoordigheid van elke risiko-geassosieerde TNF-α rs1800629 A-alleel (p=0.028). Met inagneming van ’n genotipe risiko telling tussen 0–6, het aanvang van siekte gemiddeld 3 jaar vroeër voorgekom (p=0.008) in die teenwoordigheid van elke toenemende risiko-geassosieerde FTO A-alleel, TNF-α A-alleel en PPARγ C-alleel. Nadat aanpassings gemaak is vir ouderdom, geslag en ras, is geen verskille waargeneem in genotipe verspreiding of alleel frekwensies tussen histologies bevestigde NALV (tipes 1,2) en NASH (tipes 3,4) pasiënte nie, terwyl die minor alleel telling vir die TNF-α rs1800629 betekenisvol hoër was in die totale NALV (tipes 1–4) (p=0.047) asook die NASH subgroep (NALV tipes 3,4) (p=0.03) in vergelyking met vetsugtige pasiënte sonder ’n histologies bevestigde diagnose. ‘n Statisties beteknisvolle korrelasie is verder waargeneem tussen die aantal TNF-α rs1800629 A-allele en toenemende CRP vlakke (p=0.029), met n gunstige verlaagde effek in die teenwoordigheid van lae alcohol gebruik. Die gemiddelde middellyf-omtrek van fisies aktiewe NALV pasiënte was 12% minder as fisies onaktiewe pasiente (p=0.004). Na aanleiding van die resultate van hierdie studie behoort insluiting van geselekteerde ENP’s, en in besonder die pro-inflammatoriese TNF-α rs1800629 polimorfisme, as deel van ’n omvattende kardiovaskulere risiko evaluasie oorweeg te word. Aan die einde van die dag mag vroeë identifikasie van NALV pasiente en effektieve intervensie gebasseer op die onderliggende siekte meganisme, vordering tot NASH verhoed wat getoon is om ’n onafhanklike risiko faktor vir kardiovaskulêre siekte te wees.
Stellenbosch University. Faculty of Medicine and Health Sciences. Dept. of Pathology
Chan, Hiu-ting, i 陳曉庭. "The effect of diet intake on vascular function and therapeutic effect of cardiovascular medicine in patients with cardiovascular disease". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hub.hku.hk/bib/B50434342.
Pełny tekst źródłapublished_or_final_version
Medicine
Doctoral
Doctor of Philosophy
Chow, Wai-sum, i 周瑋琛. "A systematic review on the role of chocolate in the prevention of cardiovascular diseases". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B47560198.
Pełny tekst źródłapublished_or_final_version
Community Medicine
Master
Master of Public Health
Ng, Kuen-to, i 伍權韜. "The gender difference and association between social position and cardiovascular risk factors in Hong Kong". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2007. http://hub.hku.hk/bib/B45012775.
Pełny tekst źródłaChen, Hua, i 陳華. "Relationship between psychological status and vascular function in subjects with and without cardiovascular diseases". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2008. http://hub.hku.hk/bib/B41290409.
Pełny tekst źródłaCai, Wenjun, i 蔡文珺. "A review of the association between occasional and moderate alcohol consumption and cardiovascular disease". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/206907.
Pełny tekst źródłapublished_or_final_version
Public Health
Master
Master of Public Health
Henning, Andrea L. "Monitoring Monocyte Oxldl Phagocytosis As a Cardiovascular Disease Risk Factor Following a High-fat Meal". Thesis, University of North Texas, 2014. https://digital.library.unt.edu/ark:/67531/metadc700101/.
Pełny tekst źródłaKsiążki na temat "Cardiovascular system – Diseases – Genetic aspects"
Genes and cardiovascular function. New York: Springer, 2011.
Znajdź pełny tekst źródłaSinagra, Gianfranco, F. Camerini i Luisa Mestroni. Genetic cardiomyopathies: A clinical approach. Milan: Springer, 2013.
Znajdź pełny tekst źródłaKåre, Berg, i Nora Audrey Hart 1936-, red. Cardiovascular diseases: Genetics, epidemiology, and prevention. New York: Oxford University Press, 1991.
Znajdź pełny tekst źródłaMolecular cardiology for the cardiologists. Boston: Kluwer Academic Publisher, 1995.
Znajdź pełny tekst źródłaBaars, H. F. Clinical Cardiogenetics. London: Springer-Verlag London Limited, 2011.
Znajdź pełny tekst źródłaA, Doevendans Pieter, i Kääb Stefan 1963-, red. Cardiovascular genomics: New pathophysiological concepts : proceedings of the 2001 European Science Foundation Workshop in Maastricht. Boston: Kluwer Academic Publishers, 2002.
Znajdź pełny tekst źródłaCardiovascular genomics: Methods and protocols. New York, N.Y: Humana Press, 2009.
Znajdź pełny tekst źródłaCardiovascular disease in racial and ethnic minorities. Totowa, N.J: Humana, 2009.
Znajdź pełny tekst źródłaMolecular cardiology for the cardiologist. Wyd. 2. Boston: Kluwer Academic, 1998.
Znajdź pełny tekst źródłaDhalla, Naranjan S. Molecular defects in cardiovascular disease. Redaktor Ošt̕ádal Bohuslav. New York: Springer, 2011.
Znajdź pełny tekst źródłaCzęści książek na temat "Cardiovascular system – Diseases – Genetic aspects"
Benetos, Athanase, Abraham Aviv, Patrick Lacolley, Michel E. Safar i Véronique Regnault. "Genetic and Cellular Aspects of Arterial Stiffness". W Blood Pressure and Arterial Wall Mechanics in Cardiovascular Diseases, 83–94. London: Springer London, 2014. http://dx.doi.org/10.1007/978-1-4471-5198-2_8.
Pełny tekst źródłaGirolami, Jean-Pierre, Nelly Blaes, Nadine Bouby i François Alhenc-Gelas. "Genetic Manipulation and Genetic Variation of the Kallikrein-Kinin System: Impact on Cardiovascular and Renal Diseases". W Recent Developments in the Regulation of Kinins, 145–96. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-06683-7_6.
Pełny tekst źródłaBredella, Miriam A., i Bruno C. Vande Berg. "Metabolic-Endocrine". W IDKD Springer Series, 169–82. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-71281-5_12.
Pełny tekst źródła"Renin-Angiotensin System and Cardiovascular Physiology". W New Aspects of the Renin Angiotensin System in Cardiovascular and Renal Diseases, redaktorzy Maria Cláudia Irigoyen, Kátia De Angelis, Ivana Cinthya de Moraes da Silva, Silvia Lacchini, Janaina Barcellos Ferreira, Kátia Bilhar Scapini i Fernanda Marciano Consolim-Colombo, 45–78. BENTHAM SCIENCE PUBLISHERS, 2016. http://dx.doi.org/10.2174/9781681083131116010006.
Pełny tekst źródła"Renin Receptors in Cardiovascular and Renal Diseases". W New Aspects of the Renin Angiotensin System in Cardiovascular and Renal Diseases, redaktor A. H. Jan Danser, 217–31. BENTHAM SCIENCE PUBLISHERS, 2016. http://dx.doi.org/10.2174/9781681083131116010014.
Pełny tekst źródła"Renin Angiotensin System: Old System with New Different Components". W New Aspects of the Renin Angiotensin System in Cardiovascular and Renal Diseases, redaktorzy Danielle Yuri Arita, Rosana Inácio dos Reis, Bruno Sevá Pessôa i Dulce Elena Casarini, 3–14. BENTHAM SCIENCE PUBLISHERS, 2016. http://dx.doi.org/10.2174/9781681083131116010004.
Pełny tekst źródła"Cardiac Intracellular Renin-Angiotensin System". W New Aspects of the Renin Angiotensin System in Cardiovascular and Renal Diseases, redaktorzy Rajesh Kumar, Kenneth M. Baker, Wen Chen, Larissa Miranda Pereira, Candice M. Thomas i Qian Chen Yong, 79–91. BENTHAM SCIENCE PUBLISHERS, 2016. http://dx.doi.org/10.2174/9781681083131116010007.
Pełny tekst źródła"Exercise and Renin Angiotensin System". W New Aspects of the Renin Angiotensin System in Cardiovascular and Renal Diseases, redaktorzy Tatiana Sousa Cunha, Kleiton Augusto Santos Silva, Andrea Sanches, Sebastiao Donato Silva Jr., Vanessa Oliveira, Lilia Firoozmand, Fernanda Klein Marcondes i Lisete C. Michelini, 275–321. BENTHAM SCIENCE PUBLISHERS, 2016. http://dx.doi.org/10.2174/9781681083131116010017.
Pełny tekst źródła"ACE Gene “Dosage” and Cardiovascular and Renal Disease". W New Aspects of the Renin Angiotensin System in Cardiovascular and Renal Diseases, redaktorzy José Geraldo Mill, Alexandre Costa Pereira, Rebeca Caldeira Machado, Ludimila Forechi, Marcelo Perim Baldo i José Eduardo Krieger, 175–93. BENTHAM SCIENCE PUBLISHERS, 2016. http://dx.doi.org/10.2174/9781681083131116010012.
Pełny tekst źródłaRaghavapanicker Sanal Kumar, Valsalayam, Shiv Kumar Choudhary, Pradeep Kumar Radhakrishnan, Rajaghatta Sundararam Bharath, Nichith Chandrasekaran, Vigneshwaran Sankar, Ajith Sukumaran i Charlie Oommen. "Internal Flow Choking in Cardiovascular System: A Radical Theory in the Risk Assessment of Asymptomatic Cardiovascular Diseases". W Cardiac Diseases - Novel Aspects of Cardiac Risk, Cardiorenal Pathology and Cardiac Interventions. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96987.
Pełny tekst źródłaStreszczenia konferencji na temat "Cardiovascular system – Diseases – Genetic aspects"
Rastgar Agah, Mobin, Kaveh Laksari, Kurosh Darvish i Alexander Rachev. "Buckling of Porcine Aorta Under Static and Dynamic Loading". W ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80931.
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