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Lions Club Genome Project
Lions Club Genome Project

... help with the future development of prevention and treatment strategies for cancers of childhood, and other cancers.” Whole genome sequencing examines the entire genome and its more than 20,000 genes. In the Lions Kids Cancer Genome Project, whole genome sequencing will be carried out on tumour DNA ...
Harvard Medical School
Harvard Medical School

... Required sub-internships, Required Clinical Electives, Unspecified Electives, Comprehensive Exam ...
Lecture: Hereditary Ovarian Cancer
Lecture: Hereditary Ovarian Cancer

... • In addition to BRCA1 or BRCA2 mutations, there are other hereditary ovarian cancer conditions such as Lynch Syndrome and inherited mutations in the genes: BRIP1, RAD51C and RAD51D • We have not yet identified the hereditary cause of ovarian cancer in over 20% of all families with a suspected inher ...
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ASSESS

... 60 year old patient with myopia, family history of glaucoma, and cardiovascular disease. Patient wants to know what tests should be done? Question of Diagnosis ...
Medicine "Lactobacterin" is a microbial mass of antagonistically
Medicine "Lactobacterin" is a microbial mass of antagonistically

... Lactic acid bacteria (Lactobacilli) are the microorganisms which are the main part of the normal human intestinal micro flora. They have saccharolytic type of metabolism [1,2]. They have good antagonistic activity against pathogenic microorganisms [3]. Lactobacilli are used not only in medicine, as ...
PINCC`s Program - Dana-Farber Cancer Institute
PINCC`s Program - Dana-Farber Cancer Institute

... I, Jean Talbert, have been asked to disclose any significant relationships with commercial entities that are either providing financial support for this program or whose products or services are mentioned during my presentation. I have no relationships to disclose. ...
Variant types of Haemoglobinopathies
Variant types of Haemoglobinopathies

... Genetic defects of Hb are the most common genetic disorders worldwide. ...
Genetic and molecular determinants of human ageing and longevity
Genetic and molecular determinants of human ageing and longevity

... genes composing DNA repair, pro/antioxidant and insulin/IGF-1 signaling pathways with human longevity and ageing (e.g. disease prevalence, physical and cognitive abilities)  Longitudinal study: 1651 individuals of The Danish 1905 birth cohort ...
STANYSintro2005
STANYSintro2005

... biological data (genomes, proteins, other databases) students learn biology as a dynamic process of interpreting complex data  students can reproduce current scientific work & ask new questions ...
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Slide 1

... Our study of HH approach with Illumina 550k SNP genotype data from a series of monogentic disease projects demonstrates that HH method is very efficient and effective in identifying disease linked regions. Based on the idea of homozygosity haplotype, we developed a new approach for the genome-wide s ...
Baby, don`t stop! - Alexander Mankin Lab
Baby, don`t stop! - Alexander Mankin Lab

... factors could be viewed as potential targets for drugs that would allow the cell to synthesize a full-length protein from a gene with a mutant stop codon. On the downside, such approaches are expected to be effective only against a small fraction of deleterious mutations. The effects of some genetic ...
Concepts of Biology
Concepts of Biology

... Biotechnology is the use of artificial methods to modify the genetic material of living organisms or cells to produce novel compounds or to perform new functions. Biotechnology has been used for improving livestock and crops since the beginning of agriculture through selective breeding. Since the di ...
Human Karyotyping Activity
Human Karyotyping Activity

... click on Biology, Schedule, and go to the date – there is a link there!!) http://www.biology.arizona.edu/human_bio/activities/karyotyping/karyotyping.html 1. Read the introduction and answer the following questions. A. What is a karyotype? ...
Asian Journal of Multidisciplinary Studies
Asian Journal of Multidisciplinary Studies

... Abstract: -genetics is of increasing importance in health care, as more is now known about the basic facts of inheritance. This article written introduces the general principles of genetics and its practical application in nursing and links these to real examples to allow nurses to apply this knowle ...
Genetic engineering - Fiji National University | E
Genetic engineering - Fiji National University | E

... embryos screened for the allele. Embryos that do not carry the allele could be used.  Genetic diseases can be found and treated more effectively. If some genetic diseases are diagnosed when a child is very young, treatments can be given which prevent some or all of the symptoms of the disease. PKU ...
Genetic Research Lesson 8
Genetic Research Lesson 8

... Science was something that I was always excited about. I have one foot in anthropology as an anthropological geneticist; therefore I’m not strictly limited to a laboratory, but can go into the field for my work reconstructing the history of human populations and their origins based on population gen ...
The use of genetic markers
The use of genetic markers

... To prevent genetic drift overriding natural selection as the main evolutionary process ...
Test Info Sheet
Test Info Sheet

... corresponding intron/exon boundaries. If clinically indicated, for patients who have a single mutation identified after full sequencing of all three genes, or when otherwise appropriate, GeneDx will perform reflex deletion/duplication testing (ExonArrayDx) of the appropriate gene at no additional ch ...
Eshelman School of Pharmacy pharmacy.unc.edu ROBERT A
Eshelman School of Pharmacy pharmacy.unc.edu ROBERT A

... The UNC Eshelman School of Pharmacy offers graduate curricula leading to the master of science in pharmaceutical sciences with a specialization in health-system pharmacy administration, and doctor of philosophy in pharmaceutical sciences with concentrations in one of four research areas: chemical b ...
Lecture 5
Lecture 5

... The ENCODE consortium's major findings include : 1) the majority of DNA in the human genome is transcribed into functional molecules RNA, and that these transcripts extensively overlap one another. This broad pattern of transcription challenges the long-standing view that the human genome consists o ...
Food to chew on
Food to chew on

... Guava and its leaves contain quercetin, which is used to treat allergies via its positive actions on IgE. ...
(NEU1) gene in two patients of sialidosis in India
(NEU1) gene in two patients of sialidosis in India

... protein/ cathepsin A) and/or beta- galactosidase to form a catalytically active high molecular weight complex and mutations in this site can result in disruption of this multi-enzyme complex11,12. However, this R294C mutation like the R294S mutation, most likely does not render the enzyme completely ...
Compounding 101
Compounding 101

... Introduction to the “Art of Compounding”  Assisting Pharmacy Technicians to understand individual needs of clients with special pharmacy requirements.  Learn prescription compounding practices. ...
Metabolic Genetic Disease Screening Program Pamphlet
Metabolic Genetic Disease Screening Program Pamphlet

... Precise diagnosis can help in predicting a clinical course and prognosis, as well as potentially identifying a specific treatment beyond supportive care. Once identified, biochemical and molecular tests can be developed to screen animals at risk for disease, and carriers with the goal of controlling ...
Mapping Mutations in the HIV RNA
Mapping Mutations in the HIV RNA

... What’s the explanation for this? Correlation analysis reveals that in clade B, D30N is highly correlated with other resistance Mutations. In clade C it’s not. One assumption can be that the Clade B structure can influence the connections between resistance mutations. ...
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Personalized medicine

Personalized medicine or PM is a medical model that proposes the customization of healthcare - with medical decisions, practices, and/or products being tailored to the individual patient. In this model, diagnostic testing is often employed for selecting appropriate and optimal therapies based on the context of a patient’s genetic content or other molecular or cellular analysis. The use of genetic information has played a major role in certain aspects of personalized medicine (e.g. pharmacogenomics), and the term was first coined in the context of genetics, though it has since broadened to encompass all sorts of personalization measures.
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