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(2014), Volume 2, Issue 10, 725-733
(2014), Volume 2, Issue 10, 725-733

... 2 diabetes mellitus with male to female ratio30/19 and group (2), which included 22 normal subjects with male to female ratio 7/15 table (1&2) . The mean age of patients group was 46.3+8.1 years versus 43+ 5 years in control group table (3) .There was a significant increase in serum level (FBS, AST, ...
Quick Overview of Bioinformatics - What's New?
Quick Overview of Bioinformatics - What's New?

... B. Bloom (1995) A microbial minimalist. Nature 378:236 ...
Quick Overview of Bioinformatics
Quick Overview of Bioinformatics

... B. Bloom (1995) A microbial minimalist. Nature 378:236 ...
Chapter 1
Chapter 1

... biological complexity. Remember: this book is living in the age of the Central Dogma in understanding life, post-genomic era will certainly tell us a more complex but I hope a clear story of life. ...
Ayurveda and Drug Standardization
Ayurveda and Drug Standardization

... Ayurvedic classic has described dravya to be the nucleus of Ayurvedic pharmacy. To sum up. ...
HEREDITARY DISEASES phenylketonuria
HEREDITARY DISEASES phenylketonuria

... medical care they usually die at the age of 30 ...
Constitutional Mismatch Repair Deficiency Syndrome
Constitutional Mismatch Repair Deficiency Syndrome

... anxious, or angry. Parents who pass on MMR mutations to one or more of their children can feel guilty. Some people with MMR mutations could have trouble getting disability coverage, life insurance or long-term care insurance in some states. More information about genetic discrimination can be found ...
Practice guidelines for the Interpretation and Reporting of
Practice guidelines for the Interpretation and Reporting of

... ensure that all patients are offered the same quality of care. 4.1 Mutation databases including LSDBs. LSDBs are an essential means of recording all variation within a gene. The most successful databases contain accurate (curated), clearly referenced data naming variants at the DNA, RNA and protein ...
The Genetic Code: Yesterday, Today, and Tomorrow
The Genetic Code: Yesterday, Today, and Tomorrow

... particular amino acid at the 3’-end, and uses an anticodon (complementary to the triplet codon) to load the amino acid at a ribosomal site in response to the correct codon (Figure 1). Such codon– anticodon pairing allows proteins to be correctly synthesized according to the genetic information store ...
Cancer Cachexia: an update on the aetiology and management
Cancer Cachexia: an update on the aetiology and management

... high mortality • Thromboembolic events were increased with MA (RR 1.84 95%CI 1.07-3.18) however, this is a group that experience a high rate of thromboembolic events particularly if on chemotherapy ...
1 Transmission of genetic variation: conjugation Transmission of
1 Transmission of genetic variation: conjugation Transmission of

... bacterium's DNA. Since there was transfer of some donor chromosomal DNA but usually not a complete F+ plasmid, the recipient bacterium usually remains F- ...
Your Pomeranian`s Personalised Genetic Information Book
Your Pomeranian`s Personalised Genetic Information Book

... There is no such thing as a “good outdoor dog”. Pomeranian puppies need to learn how to behave around different animals and people from a young age. This is called socialisation, and it is essential to prevent your puppy growing up to have problems with nervousness and aggression… ...
Application of Ethical Theories to Human Genome Sequencing
Application of Ethical Theories to Human Genome Sequencing

... their brains to understand some natural laws and life processes. So, this is not wrong according to divine command theory; and this is ethically right thing according to the natural law theory. Moreover, the playing God argument rests on rather vague premises (divine commands), which change in their ...
Lecture 3. Mitochodrial pathology
Lecture 3. Mitochodrial pathology

... Every 30 minutes a child is born who will develop a mitochondrial disease by age 10. UMDF, 2009 ...
here
here

... available at the Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine.   The assistant professor will be responsible for overseeing a project on nonsyndromic hearing impairment (NSHI). This large ongoing study has over 1,000 families with NSHI tha ...
Predicting drug-target interaction in cancers using homology
Predicting drug-target interaction in cancers using homology

... response to drugs. Our aim was towards the understanding of the possible role of structural variations in breast cancer drug metabolising gene such as MTHFR that closely interact with the neoplastic drugs viz. Cyclophosphamide, 5-Fluorouracil, Methotrexate and others. We investigated the polymorphis ...
Stephen J. Freeland and Melissa Ilardo – Language Evolution in
Stephen J. Freeland and Melissa Ilardo – Language Evolution in

... codons (and the nucleotides of which they are composed) are, in the modern system, symbolic signifiers for the amino acids they encode. By the late 1950’s, this much was known (Hoagland, Stephenson, Scott, Hecht & Zamecnik, 1958), and the concept of a truly symbolic code is important to much of what ...
Familial juvenile hyperuricemic nephropathy: Detection of mutations
Familial juvenile hyperuricemic nephropathy: Detection of mutations

... and chronic renal failure. More than 50 families in various ethnic groups have been described since Duncan and Dixon first noted the disease in 1960 [1]. Affected family members show the impairment of urate excretion before puberty and usually develop hyperuricemia and gout after adolescence [2]. Re ...
PDT Treatment
PDT Treatment

... levels (B) of PhGPx are present in parental (wt), vector control (neo) and transfectants (P-1 to P-4). The lipid-derived radical adducts (C) of DMPO were observed using electron paramagnetic resonance spin trapping. Cells with low PhGPx activity produced higher levels of radicals. PhGPx ...
ASX and Media release
ASX and Media release

... The Peter MacCallum Cancer Centre is Australia’s only public hospital solely dedicated to cancer and one of an elite group of hospitals worldwide to have its own integrated cancer research program and laboratories. It treats more cancer patients each year than any other hospital in Australia and its ...
1 fructose intolerance
1 fructose intolerance

... technique (PCR) followed by hybridization with allele-specific oligonucleotides (ASOs). • While this test is relatively harmless and effective, the screen does not monitor >95% of HFI mutations (many are unkown and require further research ), and is not considered diagnostic. – in other words, a neg ...
Project Title: Genetic diversity and structure in the Whiskey Mountain
Project Title: Genetic diversity and structure in the Whiskey Mountain

... from other herds, but not they are not enough to determine herd substructure within Whiskey. From this research, we will provide a written and oral report to WGFD and Wyoming WSF and outreach materials on the Whiskey herd to the National Bighorn Sheep Center in Dubois, WY. Alignment with Wild Sheep ...
Genetic engineering : DNA sequencing By: Dr. Hanaa Farhan
Genetic engineering : DNA sequencing By: Dr. Hanaa Farhan

... organisms and the primary means of obtaining DNA sequence was so-called reverse genetics in which the amino acid sequence of the gene product of interest is backtranslated into a nucleotide sequence based upon the appropriate codons. Given the degeneracy of the genetic code, this process can be tric ...
Bio 251 07 TLN Genet..
Bio 251 07 TLN Genet..

... complementary base pairing ...
My following published symmetrical table for genetic codes
My following published symmetrical table for genetic codes

... tamic acid (Glu/E). For the formation of proteins in living organism cells, it is found that each amino acid can be specified by either a minimum of one codon or up to a maximum of six possible codons. In other words, different codons specify the different number of amino acids. A table for genetic c ...
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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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