Auswahl der wissenschaftlichen Literatur zum Thema „Genetic risk factor“
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Zeitschriftenartikel zum Thema "Genetic risk factor"
Koch, Linda. „Genetic T2DM risk factor found“. Nature Reviews Endocrinology 10, Nr. 3 (14.01.2014): 128. http://dx.doi.org/10.1038/nrendo.2013.273.
Der volle Inhalt der QuelleReitsma, Pieter H. „Genetic Risk Factors of Thrombosis.“ Blood 114, Nr. 22 (20.11.2009): SCI—43—SCI—43. http://dx.doi.org/10.1182/blood.v114.22.sci-43.sci-43.
Der volle Inhalt der QuelleSokolova, I. V., D. A. Mustafina, A. G. Sadertdinova, A. N. Zagitova, D. A. Khusnullin, L. G. Sadertdinova und N. A. Mescheryakov. „GENETIC RISK FACTOR FOR IDIOPATHIC SCOLIOSIS“. International Journal of Applied and Fundamental Research (Международный журнал прикладных и фундаментальных исследований), Nr. 1 2023 (2023): 25–29. http://dx.doi.org/10.17513/mjpfi.13501.
Der volle Inhalt der QuelleOhishi, Mitsuru, Kenshi Fujii, Takazo Minamino, Jitsuo Higaki, Atsushi Kamitani, Hiromi Rakugi, Yi Zhao, Hiroshi Mikami, Tetsuro Miki und Toshio Ogihara. „A potent genetic risk factor for restenosis“. Nature Genetics 5, Nr. 4 (Dezember 1993): 324–25. http://dx.doi.org/10.1038/ng1293-324.
Der volle Inhalt der QuelleSenior, Kathryn. „New genetic risk factor for sporadic PD“. Nature Reviews Neurology 5, Nr. 7 (Juli 2009): 354. http://dx.doi.org/10.1038/nrneurol.2009.79.
Der volle Inhalt der QuelleBertina, Rogier M. „Factor V Leiden and other coagulation factor mutations affecting thrombotic risk“. Clinical Chemistry 43, Nr. 9 (01.09.1997): 1678–83. http://dx.doi.org/10.1093/clinchem/43.9.1678.
Der volle Inhalt der QuelleCushman, Mary. „Inherited Risk Factors for Venous Thrombosis“. Hematology 2005, Nr. 1 (01.01.2005): 452–57. http://dx.doi.org/10.1182/asheducation-2005.1.452.
Der volle Inhalt der QuelleCheekurthy, Alice Jayapradha. „Predisposition of Obesity through Genetic and Non-Genetic Risk Factors“. Journal of Endocrinology Research 2, Nr. 2 (06.02.2021): 27. http://dx.doi.org/10.30564/jer.v2i2.2767.
Der volle Inhalt der QuelleSchwab, Manfred, Andreas Claas und Larissa Savelyeva. „BRCA2: a genetic risk factor for breast cancer“. Cancer Letters 175, Nr. 1 (Januar 2002): 1–8. http://dx.doi.org/10.1016/s0304-3835(01)00752-2.
Der volle Inhalt der QuelleEVANS, JEFF. „Major Genetic Risk Factor Is Discovered for Parkinson's“. Clinical Psychiatry News 38, Nr. 2 (Februar 2010): 33. http://dx.doi.org/10.1016/s0270-6644(10)70097-7.
Der volle Inhalt der QuelleDissertationen zum Thema "Genetic risk factor"
Ruth, Katherine Sarah. „Identification of genetic and non-genetic factors contributing to female reproductive ageing“. Thesis, University of Exeter, 2015. http://hdl.handle.net/10871/19189.
Der volle Inhalt der QuelleChen, Hong [Verfasser]. „Plasminogen is a genetic risk factor of periodontitis / Hong Chen“. Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2018. http://d-nb.info/1196803110/34.
Der volle Inhalt der QuellePerdigão, Catarina. „The impact of the genetic risk factor BIN1 to Alzheimer’s disease development“. Doctoral thesis, Universidade Nova de Lisboa. Instituto de Tecnologia Quimica e Biológica António Xavier, 2021. http://hdl.handle.net/10362/132008.
Der volle Inhalt der QuelleN/A
Caglayan, Safak [Verfasser]. „SORLA/SORL1 as genetic risk factor in Alzheimer disease / Safak Caglayan“. Berlin : Freie Universität Berlin, 2013. http://d-nb.info/1043480935/34.
Der volle Inhalt der QuelleNewsome, Jamie. „Resilience and Vulnerability in Adolescents at Risk for Delinquency: A Behavioral Genetic Study of Differential Response to Risk“. University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367937532.
Der volle Inhalt der QuelleMutize, Tinashe. „DNA methylation : a risk factor for type 2 diabetes mellitus“. Thesis, Cape Peninsula University of Technology, 2016. http://hdl.handle.net/20.500.11838/2388.
Der volle Inhalt der QuelleThe early detection of individuals who are at risk of developing type 2 diabetes mellitus (T2DM) would decrease the morbidity and mortality associated with this disease. DNA methylation, the most widely studied epigenetic mechanism, offers unique opportunities in this regard. Aberrant DNA methylation is associated with disease pathogenesis and is observed during the asymptomatic stage of disease. DNA methylation has therefore attracted increasing attention as a potential biomarker for identifying individuals who have an increased risk of developing T2DM. The identification of high risk biomarkers for T2DM could facilitate risk stratification and lifestyle interventions, which could ultimately lead to better ways to prevent, manage and control the T2DM epidemic that is rampant worldwide. The aim of the study was to investigate global DNA methylation as a potential risk factor for T2DM by studying the association between the global DNA methylation levels and hyperglycaemic states. A cross-sectional, quantitative study design, involving 564 individuals of mixed ancestry descent, residing in Bellville South, South Africa was used. Participants were classified as normal, pre-diabetic (impaired fasting glucose (IFG) and/or impaired glucose tolerance (IGT)) or diabetic (screen detected diabetic and known diabetics) according to WHO criteria of 1998. DNA was extracted from whole blood using the salt extraction method. The percentage global DNA methylation was measured by an enzyme-linked immunosorbent assay (ELISA). The association between global DNA methylation and hyperglycaemia, as well as other biochemical markers of T2DM was tested in a robust linear regression analysis adjusted for age, gender and smoking.
Kirin, Mirna. „Genetic analysis of retinal traits“. Thesis, University of Edinburgh, 2014. http://hdl.handle.net/1842/9619.
Der volle Inhalt der QuelleMahlman, M. (Mari). „Genetic background and antenatal risk factors of bronchopulmonary dysplasia“. Doctoral thesis, Oulun yliopisto, 2018. http://urn.fi/urn:isbn:9789526219530.
Der volle Inhalt der QuelleTiivistelmä Ennenaikaisen syntymän ja keskoslasten hoidon kehittymisen myötä yhä useammat huomattavan epäkypsinä syntyneet lapset jäävät henkiin. Samalla erityisesti juuri näitä lapsia uhkaavien sairauksien esiintyvyys on pysynyt korkeana. Bronkopulmonaalinen dysplasia (BPD, keskosen krooninen keuhkosairaus) on yksi näistä sairauksista. BPD:n molekyylitasoinen tautimekanismi on vielä osin tuntematon, eikä BPD:tä tehokkaasti estävää tai siitä parantavaa hoitoa ole. Myös BPD riskin arvioiminen vastasyntyneen keskoslapsen kohdalla on vaikeaa. BPD on huomattavan perinnöllinen tauti. BPD:lle altistavista geeneistä on kuitenkin vasta vähän tietoa. Tämän tutkimuksen tavoitteena oli lisätä tietoa BPD:n tautimekanismista tutkimalla BPD:lle altistavia geenejä. Lisäksi tutkimuksessa tarkasteltiin BPD:n esiintyvyyttä ja syntymää edeltäviä riskitekijöitä erityisesti kaksosten osalta. Ehdokasgeenitutkimuksessa verisuonten endoteelikasvutekijää koodaava geeni ei assosioitunut toistuvasti BPD:hen. Kit ligandia koodaava geeni sen sijaan assosioitui. Koko genomin assosiaatiotutkimuksessa C-reaktiivista proteiinia (CRP) koodaavan geenin lähistöltä löydettiin BPD:hen mahdollisesti assosioituva alue. Lisäksi ensimmäisen viikon CRP-arvojen osoitettiin ennakoivan myöhemmin kehittyvää BPD:tä. BPD-riskin todettiin olevan matalampi kaksi- kuin yksisikiöisistä raskauksista syntyneillä lapsilla. Tutkimuksen tulokset lisäävät tietoa BPD:n perinnöllisyydestä ja sitä kautta BPD:n tautimekanismista. Tutkimus toi myös uutta tietoa BPD:n riskitekijöistä parantaen vastasyntyneen keskoslapsen BPD-riskin arviota
Bayoumy, Nervana M. K. „Genetic analysis of plasma von Willebrand factor antigen levels as a risk factor for arterial and venous thrombosis“. Thesis, University of Aberdeen, 2006. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU223247.
Der volle Inhalt der QuellePolasek, Ozren. „Investigating the role of human genome-wide heterozygosity as a health risk factor“. Thesis, University of Edinburgh, 2009. http://hdl.handle.net/1842/4799.
Der volle Inhalt der QuelleBücher zum Thema "Genetic risk factor"
Petrakis, Peter L. Alcoholism, and inherited disease. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Alcohol Abuse and Alcoholism, 1985.
Den vollen Inhalt der Quelle findenYoung, Ian D. Introduction to risk calculation in genetic counselling. Oxford: Oxford University Press, 1991.
Den vollen Inhalt der Quelle findenJ, Alberts Mark, Hrsg. Genetics of cerebrovascular disease. Armonk, NY: Futura Pub. Co., 1999.
Den vollen Inhalt der Quelle findenUri, Goldbourt, De Faire Ulf und Berg Kåre, Hrsg. Genetic factors in coronary heart disease. Dordrecht: Kluwer Academic, 1994.
Den vollen Inhalt der Quelle findenOffit, Kenneth. Clinical cancer genetics: Risk counseling and management. New York: Wiley-Liss, 1998.
Den vollen Inhalt der Quelle findenKåre, Berg, Hrsg. Genetic approaches of coronary heart disease and hypertension. Berlin: Springer-Verlag, 1991.
Den vollen Inhalt der Quelle findenGarte, Seymour J. Genetic susceptibility to cancer. Boston: Kluwer Academic, 1998.
Den vollen Inhalt der Quelle findenSymposium on Phenotypic Variation in Populations: Relevance to Risk Assessment (1986 Brookhaven National Laboratory). Phenotypic variation in populations: Relevance to risk assessment. New York: Plenum Press, 1988.
Den vollen Inhalt der Quelle findenA, Levin Morris, und Strauss Harlee S, Hrsg. Risk assessment in genetic engineering. New York: McGraw-Hill, 1991.
Den vollen Inhalt der Quelle findenYoung, Ian D. Introduction to risk calculation in genetic counseling. 2. Aufl. Oxford [England]: Oxford University Press, 1999.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Genetic risk factor"
Waldinger, Marcel D. „Risks Factors in Premature Ejaculation: The Genetic Risk Factor“. In Premature Ejaculation, 111–23. Milano: Springer Milan, 2012. http://dx.doi.org/10.1007/978-88-470-2646-9_9.
Der volle Inhalt der QuelleAstermark, Jan. „Genetic and Environmental Risk Factors for Factor VIII Inhibitor Development“. In Textbook of Hemophilia, 48–52. Oxford, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118398258.ch6.
Der volle Inhalt der QuelleBerg, Kåre. „Lp(a) Lipoprotein: A Monogenic Risk Factor for Cardiovascular Disease“. In Genetic factors in coronary heart disease, 275–87. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1130-0_18.
Der volle Inhalt der QuelleFriedlander, Yechiel. „Familial Clustering of Coronary Heart Disease: A Review of its Significance and Role as a Risk Factor for the Disease“. In Genetic factors in coronary heart disease, 37–53. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1130-0_3.
Der volle Inhalt der QuelleGonchar, Alexander, Maxim Ameliyanovich, Kristina Zhur, Irma Mosse und Konstantin Mosse. „Molecular-Genetic Analysis of Genetic Predisposition to Myocardial Infarction and Comparison of Risk Factor Population Rates in Different Countries“. In Radiobiology and Environmental Security, 111–25. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1939-2_11.
Der volle Inhalt der QuellePoirier, Judes. „Apolipoprotein E4: From synaptic remodeling to genetic risk factor in both familial and sporadic Alzheimer’s disease“. In Alzheimer: 100 Years and Beyond, 289–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-37652-1_37.
Der volle Inhalt der QuelleZheng, Wei. „Genetic Polymorphisms in the Transforming Growth Factor-β Signaling Pathways and Breast Cancer Risk and Survival“. In Methods in Molecular Biology, 265–77. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-492-0_11.
Der volle Inhalt der QuelleThiriet, Marc. „Genetic Risk Factors“. In Biomathematical and Biomechanical Modeling of the Circulatory and Ventilatory Systems, 595–676. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-89315-0_7.
Der volle Inhalt der QuelleKronenberg, Florian. „Lipoprotein(a)“. In Prevention and Treatment of Atherosclerosis, 201–32. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/164_2021_504.
Der volle Inhalt der QuelleThimm, F., und G. Fleckenstein-Grün. „Potentiation of the Age-Dependent Ca Uptake into Coronary Arteries of Rats by the Risk Factor Genetic Hypertension“. In Advances in Experimental Medicine and Biology, 489–93. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0333-6_62.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Genetic risk factor"
Kulkarni, S., X. Zhou, M. Nesline, C. Murekeyisoni, N. Watroba, M. Berry, W. Davis, C. Ambrosone und Y. Zheng. „Genetic Susceptibility as a Possible Risk Factor for Breast Cancer.“ In Abstracts: Thirty-Second Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 10‐13, 2009; San Antonio, TX. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-09-6067.
Der volle Inhalt der QuelleMOTSINGER, ALISON A., BRIAN S. DONAHUE, NANCY J. BROWN, DAN M. RODEN und MARYLYN D. RITCHIE. „RISK FACTOR INTERACTIONS AND GENETIC EFFECTS ASSOCIATED WITH POST-OPERATIVE ATRIAL FIBRILLATION“. In Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812701626_0054.
Der volle Inhalt der QuelleDooper, Marten. „Nitric oxide synthase genetic variant is a risk factor for suicidal behaviour“. In 35th ECNP Congress, herausgegeben von Christina Dalla. Baarn, the Netherlands: Medicom Medical Publishers, 2022. http://dx.doi.org/10.55788/c63a9364.
Der volle Inhalt der QuelleFerreira, Nancy, Darley Ferreira und Thais Ferreira. „GENETIC EVALUATION OF MICROCALCIFICATIONS AS A PROGNOSTIC FACTOR“. In Abstracts from the Brazilian Breast Cancer Symposium - BBCS 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s2101.
Der volle Inhalt der QuelleSurniyantoro, H. N. E., und N. R. Hidayati. „Preliminary study in genetic polymorphism of hOGG1 and risk factor for thyroid cancer in Indonesia“. In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE AND SCHOOL ON PHYSICS IN MEDICINE AND BIOSYSTEM (ICSPMB): Physics Contribution in Medicine and Biomedical Applications. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0047941.
Der volle Inhalt der QuelleBatai, Ken, Ebony Shah und Rick A. Kittles. „Abstract B14: Population genetics analysis of prostate cancer GWAS SNPs to evaluate West African genetic ancestry as a risk factor“. In Abstracts: Sixth AACR Conference: The Science of Cancer Health Disparities; December 6–9, 2013; Atlanta, GA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7755.disp13-b14.
Der volle Inhalt der QuelleAllam, Ines, Aldjia Lamri, Sihem Oulacrouz, Mohamed Saidani und Reda Djidjik. „P85 The IRF5 (rs729302) polymorphism is a genetic risk factor for systemic lupus erythematosus in Algerian patients“. In 12th European Lupus Meeting. Lupus Foundation of America, 2020. http://dx.doi.org/10.1136/lupus-2020-eurolupus.130.
Der volle Inhalt der QuelleAnghel, Lucretia, Dumitru Ursu, Simona Mitincu Caramfil, Cristina Stefanescu, Stefana Maria Moisa, Anamaria Ciubara und Liliana Baroiu. „THE LINK BETWEEN LIPIDIC PROFILE, DEPRESSION AND CARDIOVASCULAR DISEASE“. In The European Conference of Psychiatry and Mental Health "Galatia". Archiv Euromedica, 2023. http://dx.doi.org/10.35630/2022/12/psy.ro.17.
Der volle Inhalt der QuelleSmyk, W., R. Hall, S. Weber, F. Grünhage, F. Lammert und M. Krawczyk. „Common genetic variant c.711A>T in the hepatobiliary phospholipid translocator ABCB4 as risk factor for liver fibrosis“. In 36. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0039-3402121.
Der volle Inhalt der QuelleFinlen Copeland, Catherine, Francine L. Kelly, Laurie D. Snyder und Scott M. Palmer. „Clinical And Genetic Predictors Of Pulmonary Aspergillus Infection, A Major Risk Factor For Bronchiolitis Obliterans Syndrome After Lung Transplantation“. In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a2570.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Genetic risk factor"
Gelmann, Edward P. Genetic Risk Factor for Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, Januar 2005. http://dx.doi.org/10.21236/ada434784.
Der volle Inhalt der QuelleGelmann, Edward P. Genetic Risk Factor for Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, Januar 2003. http://dx.doi.org/10.21236/ada414867.
Der volle Inhalt der QuelleCao, Xianling, Xuanyou Zhou, Naixin Xu, Songchang Chang und Chenming Xu. Association of IL-4 and IL-10 Polymorphisms with Preterm Birth Susceptibility: A Systematic Review and Meta-Analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, April 2022. http://dx.doi.org/10.37766/inplasy2022.4.0044.
Der volle Inhalt der QuelleGelmann, Edward P. Genetics Risk Factor for Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, Januar 2004. http://dx.doi.org/10.21236/ada422932.
Der volle Inhalt der QuelleSarma, Aruna. Genetic and Hormonal Risk Factors for Cancer in African American Men. Fort Belvoir, VA: Defense Technical Information Center, Mai 2006. http://dx.doi.org/10.21236/ada455088.
Der volle Inhalt der QuelleMack, Thomas M. Genetic Abnormalities in Breast Cancer Tumors and Relationships to Environmental and Genetic Risk Factors Using Twins. Fort Belvoir, VA: Defense Technical Information Center, Oktober 1995. http://dx.doi.org/10.21236/ada303152.
Der volle Inhalt der QuelleMack, Thomas M. Genetic Abnormalities in Breast Cancer Tumors and Relationships to environmental and Genetic Risk Factors Using Twins. Fort Belvoir, VA: Defense Technical Information Center, Oktober 1999. http://dx.doi.org/10.21236/ada393066.
Der volle Inhalt der QuelleSarma, Aruna V. Genetic and Hormonal Risk Factors for Prostate Cancer in African American Men. Fort Belvoir, VA: Defense Technical Information Center, Mai 2005. http://dx.doi.org/10.21236/ada442683.
Der volle Inhalt der QuelleEshed-Williams, Leor, und Daniel Zilberman. Genetic and cellular networks regulating cell fate at the shoot apical meristem. United States Department of Agriculture, Januar 2014. http://dx.doi.org/10.32747/2014.7699862.bard.
Der volle Inhalt der QuelleChejanovsky, Nor, Diana Cox-Foster, Victoria Soroker und Ron Ophir. Honeybee modulation of infection with the Israeli acute paralysis virus, in asymptomatic, acutely infected and CCD colonies. United States Department of Agriculture, Dezember 2013. http://dx.doi.org/10.32747/2013.7594392.bard.
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