Pub Date : 2015-05-24DOI: 10.4172/2169-0111.1000119
M. Agy, Zaher Ehf
The application of DNA sequences of standardized genetic markers for the identification of eukaryotic organisms is known as DNA barcoding. Based on a recent study by a multinational and multilaboratory fungal barcoding consortium, the nuclear ribosomal internal transcribed spacer (ITS) has been selected as the DNA barcode for fungi. DNA barcoding shows tremendous promise for the organisms rapid identification at the species level. Recently, DNA barcodes are used for identification of fungal species in marine sediments.
{"title":"Why Nuclear Ribosomal Internal Transcribed Spacer (ITS) has been Selected asthe DNA Barcode for Fungi","authors":"M. Agy, Zaher Ehf","doi":"10.4172/2169-0111.1000119","DOIUrl":"https://doi.org/10.4172/2169-0111.1000119","url":null,"abstract":"The application of DNA sequences of standardized genetic markers for the identification of eukaryotic organisms is known as DNA barcoding. Based on a recent study by a multinational and multilaboratory fungal barcoding consortium, the nuclear ribosomal internal transcribed spacer (ITS) has been selected as the DNA barcode for fungi. DNA barcoding shows tremendous promise for the organisms rapid identification at the species level. Recently, DNA barcodes are used for identification of fungal species in marine sediments.","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"4 1","pages":"1-2"},"PeriodicalIF":0.0,"publicationDate":"2015-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000119","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70874810","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-03-15DOI: 10.4172/2169-0111.1000118
A. Chhabra
Immune system is developed in such a way that it can efficiently recognize, target and eliminate foreign pathogens effectively, but leave the host self-architecture intact. During the developmental process self-reactive high avidity immune effectors are deleted, and several other mechanisms are put in place to ensure that the self-reactive low avidity immune effectors cannot generate harmful autoimmune reactions. T cells are critical immune effectors of a protective antigen specific adaptive immune response. While engagement of the T cell receptor (TCR) critical for the development of antigen specific T cell response, development of effector function in T cells is fine tuned by positive factors, the co-stimulatory factors, and negative factors, the co-inhibitory receptors. While role of co- stimulation was initially considered critical for the generation of an optimum protective immune response, it is well established that the co-inhibitory molecules play equally essential role in this process. Approaches targeting co- inhibitory receptor mediated immune blockade mechanisms have recently been shown to produce remarkable protective responses in cancer patients. We will here take a brief account of the recent advances towards development of immune checkpoint blockade strategies in cancer immunotherapy.
{"title":"Cancer Immunotherapy: Targeting Checkpoint Blockade","authors":"A. Chhabra","doi":"10.4172/2169-0111.1000118","DOIUrl":"https://doi.org/10.4172/2169-0111.1000118","url":null,"abstract":"Immune system is developed in such a way that it can efficiently recognize, target and eliminate foreign pathogens effectively, but leave the host self-architecture intact. During the developmental process self-reactive high avidity immune effectors are deleted, and several other mechanisms are put in place to ensure that the self-reactive low avidity immune effectors cannot generate harmful autoimmune reactions. T cells are critical immune effectors of a protective antigen specific adaptive immune response. While engagement of the T cell receptor (TCR) critical for the development of antigen specific T cell response, development of effector function in T cells is fine tuned by positive factors, the co-stimulatory factors, and negative factors, the co-inhibitory receptors. While role of co- stimulation was initially considered critical for the generation of an optimum protective immune response, it is well established that the co-inhibitory molecules play equally essential role in this process. Approaches targeting co- inhibitory receptor mediated immune blockade mechanisms have recently been shown to produce remarkable protective responses in cancer patients. We will here take a brief account of the recent advances towards development of immune checkpoint blockade strategies in cancer immunotherapy.","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"2015 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2015-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70874737","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-02-13DOI: 10.4172/2169-0111.1000117
N. Zhong, Leilei Wang, Xiucui Luo, Jing Pan
Preterm Premature Rupture of the Fetal Membranes (PPROM) is a reproductive system disorder and a major cause of prematurity. Several major etiologic factors have been linked to PPROM, one of which is the weakness of the amniochorion Extra Cellular Matrix (ECM) caused by collagen degradation. With increasingly deeper research studies on the human genome, rapidly growing evidence has suggested that abnormally expressed non-coding RNAs (ncRNAs) are involved with multiple diseases. Among various ncRNAs, the long non-coding RNAs (lncRNAs) have attracted more attention and were found to correlate with various inflammation-related conditions or diseases. Recent studies demonstrated that lncRNAs might be involved in regulation of the ubiquitin proteasome system (UPS) in PPROM. The UPS is an ATP-dependent enzyme process that targets substrate proteins, tagged with an isopeptide chain composed of covalently linked molecules of ubiquitin, for degradation by the 26S proteasome, and deeply involved in the regulation of most basic cellular processes. Here, we reviewed the UPS system, the collagen in extracellular matrix (ECM), the PPROM as well as lncRNAs. We hypothesize that a novel pathogenic pathway of “infection/inflammation lncRNA, UPS, collagen, membrane rupture” for exploring the molecular pathogenesis of PPROM
{"title":"Long Non-Coding RNAs, Ubiquitin Proteasome System, CollagenDegradation and Preterm Premature Rupture of Membrane","authors":"N. Zhong, Leilei Wang, Xiucui Luo, Jing Pan","doi":"10.4172/2169-0111.1000117","DOIUrl":"https://doi.org/10.4172/2169-0111.1000117","url":null,"abstract":"Preterm Premature Rupture of the Fetal Membranes (PPROM) is a reproductive system disorder and a major cause of prematurity. Several major etiologic factors have been linked to PPROM, one of which is the weakness of the amniochorion Extra Cellular Matrix (ECM) caused by collagen degradation. With increasingly deeper research studies on the human genome, rapidly growing evidence has suggested that abnormally expressed non-coding RNAs (ncRNAs) are involved with multiple diseases. Among various ncRNAs, the long non-coding RNAs (lncRNAs) have attracted more attention and were found to correlate with various inflammation-related conditions or diseases. Recent studies demonstrated that lncRNAs might be involved in regulation of the ubiquitin proteasome system (UPS) in PPROM. The UPS is an ATP-dependent enzyme process that targets substrate proteins, tagged with an isopeptide chain composed of covalently linked molecules of ubiquitin, for degradation by the 26S proteasome, and deeply involved in the regulation of most basic cellular processes. Here, we reviewed the UPS system, the collagen in extracellular matrix (ECM), the PPROM as well as lncRNAs. We hypothesize that a novel pathogenic pathway of “infection/inflammation lncRNA, UPS, collagen, membrane rupture” for exploring the molecular pathogenesis of PPROM","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"2015 1","pages":"1-8"},"PeriodicalIF":0.0,"publicationDate":"2015-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000117","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70874614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-01-28DOI: 10.4172/2169-0111.1000E114
A. Mastinu
“On the Origin of Species” by Charles Darwin changed the biology theories and the biblical creationism was replaced by a new vision of the world. From this new perspective, also the theories by Lamarck were considered incorrect, because the adaptations achieved by animals during their life could not be transmitted hereditarily. Moreover, after fifty years, the data collected by Gregor Mendel induced biologists to introduce the concept of gene and hereditary characteristics, underestimating the role of the environment
{"title":"Epigenetics: The Revenge of Lamarck?","authors":"A. Mastinu","doi":"10.4172/2169-0111.1000E114","DOIUrl":"https://doi.org/10.4172/2169-0111.1000E114","url":null,"abstract":"“On the Origin of Species” by Charles Darwin changed the biology theories and the biblical creationism was replaced by a new vision of the world. From this new perspective, also the theories by Lamarck were considered incorrect, because the adaptations achieved by animals during their life could not be transmitted hereditarily. Moreover, after fifty years, the data collected by Gregor Mendel induced biologists to introduce the concept of gene and hereditary characteristics, underestimating the role of the environment","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"4 1","pages":"1-1"},"PeriodicalIF":0.0,"publicationDate":"2015-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000E114","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70877556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Adoptive transfer of antigen specific T-cells can lead to eradication of cancer and viral infections. The broad application of this approach has further been hampered by the limited availability of adequate numbers of T-cells for treatment in a timely manner. This has led to efforts for the development of efficient methods to generate large numbers of T-cells with specificity for tumor or viral antigens that can be harnessed for use in cancer therapy. Recent studies have demonstrated that during encounter with tumor antigen, the signals delivered to T-cells by professional antigen-presenting cells can affect T-cell programming and their subsequent therapeutic efficacy. This has stimulated efforts to develop artificial antigen-presenting cells that allow optimal control over the signals provided to T-cells. In this review, we will discuss the cellular artificial antigen-presenting cell systems and their use in T-cell adoptive immunotherapy for cancer and infections.
{"title":"Artificial Antigen Presenting Cells: An Off the Shelf Approach for Generation of Desirable T-Cell Populations for Broad Application of Adoptive Immunotherapy.","authors":"A N Hasan, A Selvakumar, R J O'Reilly","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Adoptive transfer of antigen specific T-cells can lead to eradication of cancer and viral infections. The broad application of this approach has further been hampered by the limited availability of adequate numbers of T-cells for treatment in a timely manner. This has led to efforts for the development of efficient methods to generate large numbers of T-cells with specificity for tumor or viral antigens that can be harnessed for use in cancer therapy. Recent studies have demonstrated that during encounter with tumor antigen, the signals delivered to T-cells by professional antigen-presenting cells can affect T-cell programming and their subsequent therapeutic efficacy. This has stimulated efforts to develop artificial antigen-presenting cells that allow optimal control over the signals provided to T-cells. In this review, we will discuss the cellular artificial antigen-presenting cell systems and their use in T-cell adoptive immunotherapy for cancer and infections.</p>","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"4 3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891142/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35999938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-11-05DOI: 10.4172/2169-0111.1000E113
Wenlong Tang, Ji-Gang Zhang, D. Lin
Wenlong Tang1*, Jigang Zhang2,3 and Dongdong Lin2,4 1Department of Electrical and Computer Engineering, University of Alabama, Tuscaloosa, AL, USA 2Center of Genomics and Bioinformatics, Tulane University, New Orleans, LA, USA 3Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, LA, USA 4Department of Biomedical Engineering, Tulane University, New Orleans, LA, USA *Corresponding author: Wenlong Tang, Department of Electrical and Computer Engineering, University of Alabama, Tuscaloosa, AL, 35487, USA, Tel: 504-988-1341; E-mail: wtang11@bama.ua.edu
{"title":"Pleiotropic Enrichment Analysis with Diverse Omics Data","authors":"Wenlong Tang, Ji-Gang Zhang, D. Lin","doi":"10.4172/2169-0111.1000E113","DOIUrl":"https://doi.org/10.4172/2169-0111.1000E113","url":null,"abstract":"Wenlong Tang1*, Jigang Zhang2,3 and Dongdong Lin2,4 1Department of Electrical and Computer Engineering, University of Alabama, Tuscaloosa, AL, USA 2Center of Genomics and Bioinformatics, Tulane University, New Orleans, LA, USA 3Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, LA, USA 4Department of Biomedical Engineering, Tulane University, New Orleans, LA, USA *Corresponding author: Wenlong Tang, Department of Electrical and Computer Engineering, University of Alabama, Tuscaloosa, AL, 35487, USA, Tel: 504-988-1341; E-mail: wtang11@bama.ua.edu","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"3 1","pages":"1-2"},"PeriodicalIF":0.0,"publicationDate":"2014-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000E113","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70877949","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-08-16DOI: 10.4172/2169-0111.1000E112
M. Conese
Regenerative medicine is a multidisciplinary field that aims to replace or regenerate human cells, tissues, or organs in order to restore or establish normal function. In this broad sense, this operational definition should include the ultimate goal of tissue (bio) engineering, i.e. ‘the manufacture of living functional tissues and organs suitable for transplantation in reasonable time scales’ [1]. The process of regenerating body parts can occur in vivo or ex vivo, and may require stem cells, natural or synthetic cell-supporting scaffold materials, bioactive molecules such as for example trophic factors, genetic manipulation, or combinations of all of the above [2]. The interest in embryonic stem cells has increasingly faded away when the possibility of obtaining pluripotent cells by reprogramming adult somatic cells was achieved. Induced Pluripotent Stem Cells (iPSCs) represents nowadays the most interesting source to be used in regenerative medicine, as, besides pluripotency, they are obtained from the very same patient whom they will administer to and should thus not give any immune reaction [3]. Regenerative medicine and tissue engineering have broad interest as to the application to different fields of general surgery, among which skin restoration, heart repair, bioengineering of vessels, kidney, gastroenteric and upper respiratory tracts [4]. The medical application in this field started up in 2006 when Atala and colleagues implanted in patients who need cystoplasty bladders engineered ex vivo from the seeding of autologous cells (urothelium and muscle cells) on collagen-polyglycolic acid scaffolds as artificial supporting biomaterial [5]. Another milestone was the manufacture of a trachea from human components. Macchiarini and colleagues transplanted the first tissue-engineered trachea, utilizing the patient’s own stem cells, into a 30-year old woman with end-stage bronchomalacia, with positive results about respiratory functional tests following the transplantation [6]. The trachea was denuded and reseeded with cells from the recipient, i.e. chondrocytes differentiated from hematopoietic stem/progenitor cells on the outer surface and epithelial cells obtained from the right bronchus on the inner surface. A 5-year follow-up reported the safety and efficacy of this procedure highlighting the function of the tissue-engineered trachea and, importantly, the well-being of the patient [7].
{"title":"Bioprinting: A Further Step to Effective Regenerative Medicine and Tissue Engineering","authors":"M. Conese","doi":"10.4172/2169-0111.1000E112","DOIUrl":"https://doi.org/10.4172/2169-0111.1000E112","url":null,"abstract":"Regenerative medicine is a multidisciplinary field that aims to replace or regenerate human cells, tissues, or organs in order to restore or establish normal function. In this broad sense, this operational definition should include the ultimate goal of tissue (bio) engineering, i.e. ‘the manufacture of living functional tissues and organs suitable for transplantation in reasonable time scales’ [1]. The process of regenerating body parts can occur in vivo or ex vivo, and may require stem cells, natural or synthetic cell-supporting scaffold materials, bioactive molecules such as for example trophic factors, genetic manipulation, or combinations of all of the above [2]. The interest in embryonic stem cells has increasingly faded away when the possibility of obtaining pluripotent cells by reprogramming adult somatic cells was achieved. Induced Pluripotent Stem Cells (iPSCs) represents nowadays the most interesting source to be used in regenerative medicine, as, besides pluripotency, they are obtained from the very same patient whom they will administer to and should thus not give any immune reaction [3]. Regenerative medicine and tissue engineering have broad interest as to the application to different fields of general surgery, among which skin restoration, heart repair, bioengineering of vessels, kidney, gastroenteric and upper respiratory tracts [4]. The medical application in this field started up in 2006 when Atala and colleagues implanted in patients who need cystoplasty bladders engineered ex vivo from the seeding of autologous cells (urothelium and muscle cells) on collagen-polyglycolic acid scaffolds as artificial supporting biomaterial [5]. Another milestone was the manufacture of a trachea from human components. Macchiarini and colleagues transplanted the first tissue-engineered trachea, utilizing the patient’s own stem cells, into a 30-year old woman with end-stage bronchomalacia, with positive results about respiratory functional tests following the transplantation [6]. The trachea was denuded and reseeded with cells from the recipient, i.e. chondrocytes differentiated from hematopoietic stem/progenitor cells on the outer surface and epithelial cells obtained from the right bronchus on the inner surface. A 5-year follow-up reported the safety and efficacy of this procedure highlighting the function of the tissue-engineered trachea and, importantly, the well-being of the patient [7].","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"2014 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2014-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000E112","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70877888","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-05-27DOI: 10.4172/2169-0111.1000E111
Yu-bin Deng, Ruirui Yang, Cai Xia Xu, XiuQuan Zhang
This article concluded our serial studies on the therapeutic protective effects of modified bone marrow stromal cells on central nervous injury. Hope this will provide a prelusion of transition of central nervous disease treatment from experimental treatment to the idea of clinical application.
{"title":"Modified Bone Marrow Stromal Cells Therapy for Central Nervous System Disorders","authors":"Yu-bin Deng, Ruirui Yang, Cai Xia Xu, XiuQuan Zhang","doi":"10.4172/2169-0111.1000E111","DOIUrl":"https://doi.org/10.4172/2169-0111.1000E111","url":null,"abstract":"This article concluded our serial studies on the therapeutic protective effects of modified bone marrow stromal cells on central nervous injury. Hope this will provide a prelusion of transition of central nervous disease treatment from experimental treatment to the idea of clinical application.","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"3 1","pages":"1-2"},"PeriodicalIF":0.0,"publicationDate":"2014-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000E111","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70877872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-03-28DOI: 10.4172/2169-0111.1000E110
Lurdes Jorge
In recent years there has been a growing interest in biological control of pests and diseases as a strategy for integrated pest management (IPM) of crop cultures. Species of the genus Trichoderma have been used as antagonists for the control of some of the most important phytopathogenic fungi (Fusarium oxysporum, Rhizoctonia solani, Botrytis cinerea, Sclerotinia sclerotiorum), resembling T. harzianum, T. viride, T. virens and T. atroviride the best options for biological control of plant diseases.
{"title":"Trichoderma Strains as Biocontrol Agents","authors":"Lurdes Jorge","doi":"10.4172/2169-0111.1000E110","DOIUrl":"https://doi.org/10.4172/2169-0111.1000E110","url":null,"abstract":"In recent years there has been a growing interest in biological control of pests and diseases as a strategy for integrated pest management (IPM) of crop cultures. Species of the genus Trichoderma have been used as antagonists for the control of some of the most important phytopathogenic fungi (Fusarium oxysporum, Rhizoctonia solani, Botrytis cinerea, Sclerotinia sclerotiorum), resembling T. harzianum, T. viride, T. virens and T. atroviride the best options for biological control of plant diseases.","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"3 1","pages":"1-1"},"PeriodicalIF":0.0,"publicationDate":"2014-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000E110","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70877294","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-02-12DOI: 10.4172/2169-0111.1000e109
H. Gül
Epidemiology is the most important and frequently used scientific basic tool for public health researchers. There are different definitions given for epidemiology, but it can be briefly defined as the process of detection, investigation, and analysis of the causes of diseases in the human populations [1]. It is a methodology, which preventive medicine use to control and prevent the diseases also to improve the health status of the public in general. It is known that there is a heredity role in the majority of common human diseases because of that a multidisciplinary approach is required for a full understanding of the etiology of diseases [2]. Many non-infectious chronic diseases (cancer, allergy, asthma, diabetes mellitus, obesity, occupational diseases, neurological diseases, mental diseases, cardiovascular diseases etc.) which are estimated that associated with genetic structure of the human are still being investigated in the worldwide [3,4]. Genetic epidemiology is fairly a new discipline that has to research very large different fields. Genetic epidemiology is the methodology that is used to investigate the frequency, distribution, and cause of disease, and to examine to what extent factors that play a role in diseases are genetic or environmental, and to reveal the genetic structureenvironment interaction dimension. The research methods used in genetic epidemiologic studies can be similar with the designs that are used in general epidemiology (clinical trials, case controls, cohort studies etc.) [5]. Day by day, the attention on genetic epidemiology has increased as the mechanisms of genetic risk factors on health are diagnosed and understood. In particular, well-organized populationbased molecular epidemiology studies and prospective cohort studies have an important role in understanding the interaction between genetics and the environment in multi-factorial human diseases.
{"title":"Epidemiology in Genetic Studies from the Public Health Perspective","authors":"H. Gül","doi":"10.4172/2169-0111.1000e109","DOIUrl":"https://doi.org/10.4172/2169-0111.1000e109","url":null,"abstract":"Epidemiology is the most important and frequently used scientific basic tool for public health researchers. There are different definitions given for epidemiology, but it can be briefly defined as the process of detection, investigation, and analysis of the causes of diseases in the human populations [1]. It is a methodology, which preventive medicine use to control and prevent the diseases also to improve the health status of the public in general. It is known that there is a heredity role in the majority of common human diseases because of that a multidisciplinary approach is required for a full understanding of the etiology of diseases [2]. Many non-infectious chronic diseases (cancer, allergy, asthma, diabetes mellitus, obesity, occupational diseases, neurological diseases, mental diseases, cardiovascular diseases etc.) which are estimated that associated with genetic structure of the human are still being investigated in the worldwide [3,4]. Genetic epidemiology is fairly a new discipline that has to research very large different fields. Genetic epidemiology is the methodology that is used to investigate the frequency, distribution, and cause of disease, and to examine to what extent factors that play a role in diseases are genetic or environmental, and to reveal the genetic structureenvironment interaction dimension. The research methods used in genetic epidemiologic studies can be similar with the designs that are used in general epidemiology (clinical trials, case controls, cohort studies etc.) [5]. Day by day, the attention on genetic epidemiology has increased as the mechanisms of genetic risk factors on health are diagnosed and understood. In particular, well-organized populationbased molecular epidemiology studies and prospective cohort studies have an important role in understanding the interaction between genetics and the environment in multi-factorial human diseases.","PeriodicalId":89733,"journal":{"name":"Advancements in genetic engineering","volume":"3 1","pages":"1-3"},"PeriodicalIF":0.0,"publicationDate":"2014-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2169-0111.1000e109","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70877196","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}