13.6 Some human genetic research can be conducted without the need for genetic information that can be related to specific persons or communities. For example, research on molecular processes can explore genetic processes and the production of enzymes or proteins. Similarly, research can use anonymous population data to examine patterns of human inheritance of disease or conditions.. 13.7 Unless otherwise indicated, this Report uses human genetic research to refer to any research that uses genetic samples or genetic information, whether or not those samples or information are identified, potentially identifiable, or de-identified.[5] Such research must involve human genetics and does not include the use of human tissue samples in order to study, for example, the genetics of infectious agents such as viruses.. 13.8 When discussing the protection of privacy interests in genetic samples and information, the chapters focus on human genetic research that needs to use or will develop information that ...
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The objective of the proposed study is to describe cultural congruence, including diversity, awareness, sensitivity, and competence in people conducting human genetics research in developing countries, as well as to explore challenges and opportunities to improve cultural congruence. Human genetics research is becoming more common in developing countries, as researchers take advantage of differences in environment and population diversity. However, when research is conducted with individuals living in developing countries, there is a chance that culture will lead to misunderstandings between investigators and participants and consequently ineffective research. The proposed study uses a cross-sectional semi-structured qualitative interview design. Thirty to forty-five participants will be recruited. Participants will be researchers with experience in conducting genetics research in developing countries, who will have had direct contact with the participants in their research studies. These ...
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The following are the current most viewed articles on Wikipedia within Wikipedias Top genetics research organizations: All category. Think of it as a Whats Hot list for Top genetics research organizations: All. More info ». This is a beta release and so the figures may be a day or two out of date. Wed love to get your thoughts. ...
23andMes mission has always been to help people access, understand, and benefit from the human genome. Everyone should gain from the scientific insights we learn through research. That means people of all ethnicities. But that hasnt happened because research - not just 23andMe research - but all biomedical and genetic research has been hampered by a lack of diversity.. A recently article published in the journal Nature found that less than three percent of the genome wide association studies published involve people of African Ancestry. And its not just African Americans who are being left out. More than 80 percent of biomedical research is focused on people of European ancestry. There are very real repercussions when research is limited to just one group.. For example, a lack of diversity in research could lead to misdiagnosis. A recent study by researchers at Harvard looked specifically at how a gene mutation was misclassified among African American patients indicating that they were at ...
Paris, 3 November 2006 Scientists have known for years that complex diseases, such as cancer, heart disease, stroke, and diabetes, arise from a combination of lifestyle, environmental, genetic and random factors. Large-scale study of populations may contribute significantly to sciences understanding of the complex multi-factorial basis of disease and to improvements in prevention, detection, diagnosis, treatment and cure. As a result of developments in biotechnology and bioinformatics, the opportunity to store and analyse increasingly large amounts of genetic data have rendered possible the creation of large-scale population databases. Genetic research, involving the use of such databases containing human genetic and genomic data, information, and biological samples, is thus becoming increasingly feasible. More recently, the databases being developed include data, information and biological samples from whole populations. Large-scale population databases which contain a significantly broader ...
TY - JOUR. T1 - Electronic medical records for genetic research. T2 - Results of the eMERGE consortium. AU - Kho, Abel N.. AU - Pacheco, Jennifer A.. AU - Peissig, Peggy L.. AU - Rasmussen, Luke. AU - Newton, Katherine M.. AU - Weston, Noah. AU - Crane, Paul K.. AU - Pathak, Jyotishman. AU - Chute, Christopher G.. AU - Bielinski, Suzette J. AU - Kullo, Iftikhar Jan. AU - Li, Rongling. AU - Manolio, Teri A.. AU - Chisholm, Rex L.. AU - Denny, Joshua C.. PY - 2011/4/20. Y1 - 2011/4/20. N2 - Clinical data in electronic medical records (EMRs) are a potential source of longitudinal clinical data for research. The Electronic Medical Records and Genomics Network (eMERGE) investigates whether data captured through routine clinical care using EMRs can identify disease phenotypes with sufficient positive and negative predictive values for use in genome-wide association studies (GWAS). Using data from five different sets of EMRs, we have identified five disease phenotypes with positive predictive values of ...
Free Online Library: Genetic research: who is at risk for alcoholism?(Report) by Alcohol Research & Health; Health, general Adoption Alcoholism Genetic aspects Risk factors Anopheles DNA Enzymes Enzymology Genomics Quantitative genetics
Read chapter PROSPECTS FOR FUTURE HUMAN GENETIC RESEARCH: This volume contains commissioned reviews of research on biological influences on violent or agg...
Genetic issues are of great importance to human life. We have compiled an extensive list of genetic research paper topics for you to choose from.
Search from 60 top Genetic Research pictures and royalty-free images from iStock. Find high-quality stock photos that you wont find anywhere else.
Genetic research focusing on the soil nematode C. elegans has generated fundamental new insights into the way in which these tiny worms age. During the ageing process, the activity of the worms genes gradually becomes more ...
Read chapter Front Matter: Population surveys traditionally collect information from respondents about their circumstances, behaviors, attitudes, and othe...
Issues in returning individual results from genome research using population-based banked specimens, with a focus on the National Health and Nutrition Examination Survey : workshop summary (0-309-30704-X, 978-0-309-30704-8) Guidelines for Returning Individual Results From Genome Research Using Population-Based Banked Specimens (Workshop) ...
BACKGROUND: Genetic research has potential benefits for improving health, such as identifying molecular characteristics of a disease, understanding disease prevalence and treatment, and developing treatments tailored to patients based on individual genetic characteristics of their disease. Indigenous people are often targeted for genetic research because genes are easier to study in communities that practice endogamy. Therefore, populations perceived to be more homogenous, such as Indigenous peoples, are ideal for genetic studies. While Indigenous communities remain the focal point of many genomic studies, some result in harm and unethical practice. Unfortunately, the harms of poorly formulated and unethical research involving Indigenous people have created barriers to participation that prevent critical and lifesaving research. These harms have led a number of Indigenous communities to develop guidelines for engaging with researchers to assist in safely bridging the gap between genetic research and
The Psychosocial Cancer Genetics Research Group conducts psychosocial and genetic counselling research in the area of inherited cancer and cancer genomics
The purpose of ClinSeq is to pilot large-scale medical sequencing (LSMS) in a clinical. research setting. By sequencing a person s exome or genome and returning relevant and. individual results to that person, we will begin investigating some of the technical, medical,. and genetic counseling issues that accompany the implementation of LSMS in the clinical. setting. Specifically, we seek to develop technologic and procedural infrastructures to. facilitate this type of research and demonstrate that it is feasible to sequence and interpret. large amounts of genomic sequence data and return individual results to subjects.. A cohort of ~1,500 individuals selected from the surrounding general population will be. evaluated at the NIH Clinical Center for a common set of cardiovascular phenotypic. features, including, but not limited to, coronary artery calcification, lipid profiles, and blood. pressure. Participants will be selected to fall within a spectrum of coronary artery. calcification from ...
Disclaimer: Nothing contained on this Site is intended to provide health care advice. Should you have any health care-related questions, please call or see your physician or other health care provider. Consult your physician or healthcare provider before beginning the Hallelujah Diet as you would any other weight loss or weight maintenance program. Individual results may vary. Testimonials appearing on this website are received in various forms via a variety of submission methods. The testimonials reflect the real life experiences of individuals who used our products and/or services. However, individual results may vary. We do not claim, nor should the reader assume, that any individual experience recounted is typical or representative of what any other consumer might experience. Testimonials are not necessarily representative of what anyone else using our products and/or services may experience ...
Disclaimer: Nothing contained on this Site is intended to provide health care advice. Should you have any health care-related questions, please call or see your physician or other health care provider. Consult your physician or healthcare provider before beginning the Hallelujah Diet as you would any other weight loss or weight maintenance program. Individual results may vary. Testimonials appearing on this website are received in various forms via a variety of submission methods. The testimonials reflect the real life experiences of individuals who used our products and/or services. However, individual results may vary. We do not claim, nor should the reader assume, that any individual experience recounted is typical or representative of what any other consumer might experience. Testimonials are not necessarily representative of what anyone else using our products and/or services may experience ...
The content/images on this website are not a guarantee of individual results. Individual results may vary. The information provided on this site is for general informational purposes only, and does not replace the need for a formal consultation with a plastic and reconstructive surgeon before undergoing a surgical procedure or skin care treatment.. ...
The content/images on this website are not a guarantee of individual results. Individual results may vary. The information provided on this site is for general informational purposes only, and does not replace the need for a formal consultation with a plastic and reconstructive surgeon before undergoing a surgical procedure or skin care treatment.. ...
Now that genome-wide association studies (GWAS) are dominating the landscape of genetic research on neuropsychiatric syndromes, investigators are being faced with complexity on an unprecedented scale. It is now clear that phenomics, the systematic study of phenotypes on a genome-wide scale, comprise …
Story posted December 16, 2003. James M. Wilkins 04 of Medina, Ohio, is one of 44 leading young Americans to be awarded Marshall Scholarships to study at a university in the United Kingdom next year.. After his Bowdoin graduation in May, Wilkins will begin a two-year program toward a master of science research degree at Oxford University, conducting genetic research on osteoarthritis (OA), and working with Dr. John Loughlin. (Wilkins describes his upcoming research below.). In the future, Wilkins plans to pursue a combined M.D./Ph.D. degree, focusing his Ph.D. work on genetic studies of musculoskeletal diseases, and finish a residency in orthopedic surgery.. As a medical scientist, I want to conduct significant research leading to more efficient treatments and more appropriate therapeutic interventions for patients with a particular musculoskeletal disease, said Wilkins. I want to be able to effectively treat patients in the clinic by addressing the physical manifestations of their genetic ...
Deborah Zoe Laufer's Informed Consent officially opens Aug. 18 at the Duke on 42nd Street, following previews that began Aug. 4. The play examines the many possibilities of genetics research and begs the question: If we could know everything about our genetic make-up, including potentially life-threatening diseases, would we chose to do so?
RGautier writes Wired News has published that Scientists have successfully modified the AIDS-causing HIV in such a way that it can attack metasticized melanoma (cancer cells). The impact of genetic research on cancer research is in and of itself amazing. To mix this with the strategy of using one...
Much of the genetic research on Alzheimers centers on amyloid-beta, a key component of brain plaques that build up in the brains of people with the disease. In the new study, the scientists identified several genes linked to the tau protein, which is found in the tangles that develop in the brain as Alzheimers progresses and patients develop dementia. The findings may help provide targets for a different class of drugs that could be used for treatment.. The researchers reported their findings online April 4 in the journal Neuron.. We measured the tau protein in the cerebrospinal fluid and identified several genes that are related to high levels of tau and also affect risk for Alzheimers disease, said senior investigator Alison M. Goate, DPhil, the Samuel and Mae S. Ludwig Professor of Genetics in Psychiatry. As far as were aware, three of these genes have no effect on amyloid-beta, suggesting that they are operating through a completely different pathway.. A fourth gene in the mix, APOE, ...
New genetic research on ancient bones reveals that a prehistoric population of hunters migrated into the high Arctic of North America and Greenland and survived for 4,000 years in almost complete isolation from the rest of humanity. Then, about 700 years ago, they vanished - either victims of genocide or simply out-competed by a new population of hunters with more advanced technology, the research indicates. This is the tale of the Dorset culture. They were
British scientists are to map 100,000 complete DNA code sequences in a project that will make the country a world leader in genetic research on cancer and rare diseases, the Prime Minister said.
Review the latest Genetics research at Sutter Healths world-class research institutes. See current studies, clinical trials, publications and more.
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DESCRIPTION (provided by applicant): Pre mortem tests of Alzheimers disease (AD) pathology are increasingly popular in research on cognitive aging and AD. Due to concerns that information from such tests may be misunderstood, psychologically harmful, and of unclear clinical significance, results of pre mortem tests of AD pathology have typically been withheld from research participants. However, as the reliability and potential clinical significance of test like brain amyloid imaging have become clear, there is a pressing need to revisit the practice of unilaterally withholding such information from research participants and identify responsible approaches to communicating individual results. Amyloid imaging results may be particularly relevant to mild cognitive impairment (MCI), a population for whom a growing body of evidence suggests that such testing may provide valuable prognostic and planning information, despite the unavailability of interventions to alter ones clinical course. Our ...
14.27 Consultations and submissions highlighted the continuing convergence of public and private research. Many private sector organisations receive public funding and there is increasing collaboration through public and private partnerships-collaboration recommended and encouraged by the Wills Report.[28]. 14.28 Investment in research by private commercial interests is likely to have at least two relevant consequences. First, institutions conducting privately funded research may not be dependent on remaining eligible for public research funding. Second, the commercial interests of researchers and research organisations may lead to conflicts of interest that can compromise the validity and safety of research.. 14.29 In 2001, the House of Representatives Standing Committee on Legal and Constitutional Affairs reported on its inquiry into the scientific, ethical and regulatory aspects of human cloning and stem cell research. The Standing Committee observed that: ...
While human genetic research promises to deliver a range of health benefits to the population, genetic research that takes place in Indigenous communities has proven controversial. Indigenous peoples
The dietary information provided by Vital Mend is not intended to diagnose, treat, or cure any illness or to provide medical advice. We are not medical doctors and we do not prescribe medication. As with any weight loss program, individual results may vary. If you have any questions about the relationship between nutrition and supplements, we recommend that you seek advice of a qualified and licensed health practitioner. Our opinions are based on literature and research by a variety of medical doctors, naturopathic physicians, biochemists, and other professional researchers. Homeopathic supplements are not approved by the FDA for weight loss, individual results may vary. All of our products are manufactured in an FDA licensed and approved laboratory. We adhere to strict GMP (Good Manufacturing Practice) standards. You are encouraged to make your health care decisions based on your own research and the advice of a qualified health care professional. Side effects to homeopathic supplements could ...
Individual results from the use of this product may vary due to management, environment, genetics, health and sanitation differences. Therefore, Hi-Pro Feeds LP does not warrant or guarantee individual results.. ...
This is a 55-year-old lady who is seeing some of the classic signs of aging when people get in their 50s. She is noticing some looseness in the neck. She has loss of volume in the face, especially around the lower cheek area. She has loose skin along the jawline and loose skin in the face just lateral to the mouth.. Just simply a face and neck lift will not rejuvenate her face as much as we were able to do by tightening the skin as well as adding fat to the face area. Fat was added under the eyelid. Also, it was added to the lateral face area and the area just under the corners of the mouth. As you can see, the face is much more youthful now because the volume has been restored in the face. As people age, not only does the skin get loose and sag but also they lose volume in certain places of the face. The volume is restored with fat grafting. The fat grafting is a long lasting procedure unlike fillers like Juvéderm and Restylane. Once the fat is injected into the deficient areas and the blood ...
The content/images on this website are not a guarantee of individual results. Individual results may vary. The information provided on this site is for general informational purposes only, and does not replace the need for a formal consultation with a plastic and reconstructive surgeon before undergoing a surgical procedure or skin care treatment.. ...
Decoding the genome of the camel ScienceDaily (May 28, 2013) By sequencing the genome of a Bactrian camel, researchers have made a significant contribution to population genetic research on camels. The study has laid the foundation for future scientific work on these enigmatic desert animals. A blood sample from a single Bactrian camel with the evocative name of Mozart provided the genetic raw material for the work.. Story Source. The above story is based on materials provided by Veterinärmedizinische Universität Wien.. Pour en savoir plus (ScienceDaily) ...
For a long time, anthropological and genetic research on the Neolithic revolution in Europe was mainly concentrated on the mechanism of agricultural dispersal over different parts of the continent. Recently, attention has shifted towards population processes that occurred after the arrival of the first farmers, transforming the genetically very distinctive early Neolithic Linear Pottery Culture (LBK) and Mesolithic forager populations into present-day Central Europeans. The latest studies indicate that significant changes in this respect took place within the post-Linear Pottery cultures of the Early and Middle Neolithic which were a bridge between the allochthonous LBK and the first indigenous Neolithic culture of north-central Europe-the Funnel Beaker culture (TRB). The paper presents data on mtDNA haplotypes of a Middle Neolithic population dated to 4700/4600-4100/4000 BC belonging to the Brześć Kujawski Group of the Lengyel culture (BKG) from the Kuyavia region in north-central Poland. BKG ...
For a long time, anthropological and genetic research on the Neolithic revolution in Europe was mainly concentrated on the mechanism of agricultural dispersal over different parts of the continent. Recently, attention has shifted towards population processes that occurred after the arrival of the first farmers, transforming the genetically very distinctive early Neolithic Linear Pottery Culture (LBK) and Mesolithic forager populations into present-day Central Europeans. The latest studies indicate that significant changes in this respect took place within the post-Linear Pottery cultures of the Early and Middle Neolithic which were a bridge between the allochthonous LBK and the first indigenous Neolithic culture of north-central Europe-the Funnel Beaker culture (TRB). The paper presents data on mtDNA haplotypes of a Middle Neolithic population dated to 4700/4600-4100/4000 BC belonging to the Brześć Kujawski Group of the Lengyel culture (BKG) from the Kuyavia region in north-central Poland. BKG ...
For a long time, anthropological and genetic research on the Neolithic revolution in Europe was mainly concentrated on the mechanism of agricultural dispersal over different parts of the continent. Recently, attention has shifted towards population processes that occurred after the arrival of the first farmers, transforming the genetically very distinctive early Neolithic Linear Pottery Culture (LBK) and Mesolithic forager populations into present-day Central Europeans. The latest studies indicate that significant changes in this respect took place within the post-Linear Pottery cultures of the Early and Middle Neolithic which were a bridge between the allochthonous LBK and the first indigenous Neolithic culture of north-central Europe-the Funnel Beaker culture (TRB). The paper presents data on mtDNA haplotypes of a Middle Neolithic population dated to 4700/4600-4100/4000 BC belonging to the Brześć Kujawski Group of the Lengyel culture (BKG) from the Kuyavia region in north-central Poland. BKG ...
The West of England NHS Genomic Medicine Centre (WEGMC) has started work on analysing the results of the 100,000 Genomes Project which could lead to more knowledge about underlying causes of conditions or new future treatments.. Just under 1,500 patients with rare diseases have consented to be part of the project through the WEGMC, with a further 200 patients with cancer also consenting since the centre was set up at the end of 2015.. Around 500 of these patients have consented to be part of the project in the last six months, as the centre continues to go from strength to strength.. Catherine Carpenter-Clawson, programme manager for the WEGMC, said: Its been a really busy year. Weve got up and running and are now able to consent patients with certain types of cancer and rare diseases from across the west of England.. Im looking forward to the future as we move towards genome sequencing being provided as standard care for people with certain types of cancer and rare diseases.. One of the ...
Incidental findings arise when clinically relevant genetic information about a research participant or patient is identified outside the scope of the original research objective or diagnostic test being performed
Whole genome and whole exome sequencing (WGS and WES) are performed on each 2.500 and 2.600 genomes. This can be used as population-based reference for deriving extended genetic information from all GSA genotypes in the biobank by imputation. In the past few years, we increased our focus on translating genetic research results to improve public health. A nationwide technical infrastructure (X-road) for the secure electronic exchange of medical data has also been established and is maintained by the state. This allows creating the disease (or life!) trajectories on all sample donors from the birth in the Estonian Biobank, where all contacts with the medical systems incl. ICD-10 diagnoses, prescriptions, lab data and electronic medical records are included. Using our WGS and WES data, we have demonstrated that this genetics first approach discovers many previously carriers of familiar hypercholesterolemia. Over 50% of these diagnosed patients received consequentially adapted medical treatment. ...
Slide set: The Pathway to Genomic Medicine. Richard Gibbs, PhD, explains genomic medicine and its role in and relationship to genetic research, and outlines how cutting-edge technologies and the study of genetics in human and in different species is transforming our understanding and treatment of human disease. This slide set accompanies the presentation, The Pathway to Genomic Medicine.
Slide set: The Pathway to Genomic Medicine. Richard Gibbs, PhD, explains genomic medicine and its role in and relationship to genetic research, and outlines how cutting-edge technologies and the study of genetics in human and in different species is transforming our understanding and treatment of human disease. This slide set accompanies the presentation, The Pathway to Genomic Medicine.
|i|Aims:|/i| The objective was to evaluate childrens opinions about their participation in a large research project. |i|Methods:|/i| Polish children between 6 and 14 years of
In 1998 there were only 30-40 red squirrels remaining on Anglesey. These formed a single isolated population in the eastern part of Pentraeth forest.. A comparative analysis of hair samples taken from the forest population and material collected from island specimens living within broadleaved woodland sites on Anglesey twenty years ago showed that the island has lost much of the genetic diversity which was once present. By the late 1990s only a single haplotype (in simple terms one female bloodline) remained and was shared by all the animals in the Pentraeth forest population.. Download the BBC News Report on Welsh red squirrel genetics. Download the Conservation Genetics Paper (2005). This historical research also revealed that there were several red squirrel bloodlines that were unique Wales. These genetic types have, to date, not been found anywhere else in the UK, but in 2011, studies revealed that an animal imported from the European mainland had a similar bloodline.. The red squirrel ...
The Scandinavian island’s unique combination of genetic homogeneity, genealogical tradition, and high participation in research make it a prime location for discovery and validation of drug targets.
In a new study on children with severe forms of epilepsy, researchers have found the genetic copying mistake that causes the severe epilepsy in children can be found in their parents who do not have epilepsy
Welcome to the Peking University home page, English version. Students, Faculty, Staff, and the general public can use this site to find information on campus news, services, events, and resources posted on the campus web.
Detect genetic variations e.g., single nucleotide polymorphisms, or perform genetic quantification, short DNA sequencing or CpG site quantification
Detect genetic variations e.g., single nucleotide polymorphisms, or perform genetic quantification, short DNA sequencing or CpG site quantification
Detect genetic variations e.g., single nucleotide polymorphisms, or perform genetic quantification, short DNA sequencing or CpG site quantification
In eMERGE Phase I (September 2007 - July 2011), each participating institution led studies of the relationship between genetic variation and at least two common human traits among the network participants. Sites also explored the ethical and social issues associated with large-scale genomic research.. The Northwestern eMERGE team led the implementation of diabetes, asthma, lipids and several other phenotype algorithms. During Phase I, investigators successfully analyzed genome-wide association study (GWAS) data to discover new and validate known genetic associations with type II diabetes and height in African-Americans. The NUgene Project biobank, Northwesterns hospital-based biorepository, served as the source of DNA samples and data used for the eMERGE studies. The Northwestern team also led studies on the public perception of participation in genetic research and data sharing of genomic research results and the understanding of IRB professionals of data sharing for genomic research. In Phase ...
As first Director of the MGH Center for Human Genetic Research, Dr. Gusella pioneered the genetic research cycle paradigm to conceptualize genetics research from basic science to genotype-driven modeling, based on associations with human disease and translation into diagnostics, treatments, and prevention strategies. He has led numerous national and international research consortia with broad impact on human disease. In 1983, Dr. Gusella and colleagues published a seminal study that used recombinant DNA technology to link DNA markers to the mutation causing Huntington disease (HD). Over the following years, he and his colleagues cloned the HD gene, located its stretch of repeated DNA, showed that the size of that stretch is correlated with age of disease onset and age of death, described how it causes disease, and identified genetic factors that affect how quickly symptoms develop. Dr. Gusellas lab and collaborators have mapped and identified the genes associated with many other neurological ...
BMC Bioinformatics 8:411.. 14 Karvanen J., Kulathinal S., Gasbarra D. (2009) Optimal designs to select individuals for genotyping conditional on observed binary or survival outcomes and non-genetic covariates Computational Statistics and Data Analysis 53 1782-1793.. 15 Kulathinal S., Gasbarra D., Kinra S., Ebrahim S. & Sillanpää M.J. (2008).Estimation of additive genetic and environmental sources of quantitative trait variation using data on married couples and their siblings Genetics Research 90 269-279.. 16 Pirinen, M., Kulathinal, S., Gasbarra, D. & Sillanpää M. (2008). Estimating population haplotype frequencies from pooled DNA samples using PHASE algorithm Genetic Research 90 6 :525-40.. 17 Gasbarra D, Pirinen M, Sillanpää, MJ & Arjas E. (2009)Bayesian quantitative trait locus mapping based on reconstruction of recent genetic histories Genetics 183 709-721.. 18. Gasbarra D. Esko Valkeila & Lioudmila Vostrikova (2006).Enlargement of filtration and additional information in pricing ...
Available Open Access under CC-BY-NC licence The Avon Longitudinal Study of Parents and Children (ALSPAC), also known as Children of the 90s, is a world-leading birth cohort study that uniquely enrolled participants in utero and obtained genetic material from a geographic population. It instigated the innovative but controversial ALSPAC Ethics and Law Committee. This book describes in detail the early work of this Committee, from establishing the core ethical principles necessary to protect participants, to the evolution of policies concerning confidentiality and anonymity, consent, non-intervention and disclosure of individual results, data access and security. Quotes from interviews with early members of the Committee reflect not only on its pioneering work but also on the unusual style and inspirational leadership of the first Chair, Professor Michael Furmston. This will be of interest to those involved in other cohort studies in understanding the evolution of ethical policies as ALSPAC ...
The dietary information provided by Your HCG is not intended to diagnose, treat, or cure any illness or to provide medical advice. We are not medical doctors and we do not prescribe medication. As with any weight loss program, individual results may vary. If you have any questions about the relationship between nutrition and supplements, we recommend that you seek advice of a qualified and licensed health practitioner. Our opinions are based on literature and research by a variety of medical doctors, naturopathic physicians, biochemists, and other professional researchers. HCG drops and the HCG diet is not approved by the FDA for weight loss. Your HCG is manufactured in an FDA licensed and approved laboratory for safety. You are encouraged to make your health care decisions based on your own research and the advice of a qualified health care professional. ...
Because both defensive compounds come from the same parent molecule, the researchers suspected that feeding by one group of insects, such as chewing caterpillars, might affect the plants ability to fight off another group, like aphids.. To test this idea, the researchers grew corn seedlings of a common variety, called B73, and exposed some to caterpillars. They then seeded them with aphids and counted the number of offspring that the aphids produced on pristine plants, compared to previously nibbled ones. The aphids consistently produced more offspring on corn that had been pre-chewed by caterpillars.. But, when the researcher tested other corn varieties, individual results would vary. They repeated the experiment with 17 different lines of corn from around the world. Like B73, some varieties supported more aphid offspring after a caterpillar feeding, while the pre-feeding reduced the number of aphids or had no effect on other varieties.. The variation they saw is likely due to the evolutionary ...
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Products on this website are not for sale to persons under the age of 18. Products should be used as directed on the label or by your health professional. Not recommended for pregnant or nursing women. Consult with a physician before use if you have a serious medical condition or use prescription medications. All trademarks and copyrights are property of their respective owners and are not affiliated with nor do they endorse a specific product. These statements have not been evaluated by the FDA. Products sold here are not intended to diagnose, treat, cure or prevent any disease. Individual results will vary. By using this site you agree to follow the Privacy Policy and all Terms & Conditions published on this site. Void Where Prohibited By Law.. ...
Disclaimer: Products, services, information and other content provided on this website, is for informational purposes only and is not a substitute for medical advice from a health care professional and is not intended to diagnose, treat, cure or prevent any disease. This website does not recommend self-management of health issues or concerns. You should always consult your doctor or other qualified healthcare professional with any questions you may have regarding a medical condition. Customer reviews only reflect individual experiences and are strictly their own personal views made in their own personal capacity and are not intended as a substitute medical advise. Always read the label of any supplements or natural health products you purchase and use only as directed. Individual results may vary.. ...