1. Genotype And Phenotype Definition definitions of genotype and phenotype Relationship the realtionship between genotype and phenotype http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

2. Definition Genotype and Phenotype Definition Return to Science at a Distance Biological Information Genotype and Phenotype http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

3. DNA Print Genomics Develop analytics and information resource products, including platforms for genotype pattern recognition for complex trait determination. Includes http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. Pigliucci's Evolutionary Ecology Lab A research lab focusing on genotypeenvironment interactions and constraints on natural selection http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

5. Genotype Phenotype PHENOTYPE AND GENOTYPE Definitions phenotype is the constellation of Genotype is also used to refer to the pair of alleles present at a http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

6. Roman Verostko, Algorithmic Art Roman Verostko, algorist, artist and historian presents archival quality works on paper created with original software using multipen plotters. Site http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

7. Linking Phenotype To Genotype that give clear examples of linking genotype with clinical conditions and the reverse process of using small molecules to probe genotype. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

8. THE CEPH GENOTYPE DATABASE Welcome to the CEPH Genotype database. All genotypes contributed to the CEPH database are available on the anonymous FTP server. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

9. Identification Of Genes Contributing To The Obese Yellow Avy Identification of genes contributing to the obese yellow Avy phenotype caloric restriction, genotype, diet x genotype interactions http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

10. Ana-Gen Technologies, Inc.-Contract Molecular Biology Services Contract molecular biology and genetic/genotype analysis services to pharmaceutical, research and clinical markets. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

11. Genotype And Phenotype Definition. definitions of genotype and phenotype. Geno. Relationship.the realtionship between genotype and phenotype http://www.brooklyn.cuny.edu/bc/ahp/BioInfo/SD.Geno.HP.html

Definition definitions of genotype and phenotype Relationship the realtionship between genotype and phenotype Genetic Trait an example of a genetic trait Flow of Information DNA to RNA to protein Genetic Code codons of bases for each amino acid Science at a Distance Definition Relationship Genetic Trait ... Biological Information Science at a Distance

12. Definition center, genotype and phenotype Definition genotype This is the internallycoded, inheritable information carried by all living organisms. http://www.brooklyn.cuny.edu/bc/ahp/BioInfo/GP/Definition.html

Genotype and Phenotype Definition ... the outward physical manifestation of internally coded, inheritable, information. There are two parts to this definition ... This is the "outward, physical manifestation" of the organism. These are the physical parts, the sum of the atoms, molecules, macromolecules, cells, structures, metabolism, energy utilization, tissues, organs, reflexes and behaviors; anything that is part of the observable structure, function or behavior of a living organism. This is the "internally coded, inheritable information" carried by all living organisms. This stored information is used as a "blueprint" or set of instructions for building and maintaining a living creature. These instructions are found within almost all cells (the "internal" part), they are written in a coded language (the genetic code), they are copied at the time of cell division or reproduction and are passed from one generation to the next ("inheritable"). These instructions are intimately involved with all aspects of the life of a cell or an organism. They control everything from the formation of protein macromolecules, to the regulation of metabolism and synthesis. Return to : Science at a Distance Biological Information Genotype and Phenotype Science at a Distance

13. Kilbourne/NY Medical College Influenza Archive An archive of influenza virus reassortants, mutants, and antisera, including a database of flu viruses and vaccines, with information about phenotype, genotype, special properties, and relevant published references. http://www.flu-archive.org

Kilbourne/New York Medical College Archive of Influenza Virus Reassortants, Mutants and Antisera Scope and Limitations The Basis Of Categorization Categories And Code Numbers Glossary And Key To Abbreviations ... Search the Antisera This Archive of Influenza Virus Reassortants, Mutants and Antisera is an Integral Part of the NIAID Repository of Reference Reagents and Resources for influenza Research . The viruses and antisera described herein are available upon application to the NIAID Repository, in which they are stored. Refer to http://www.bratonbiotech.com/braton11.htm for information on the basic NIAID Catalogue. The viruses and antisera described in the present archive are available upon application by e-mail to var username = "dringer"; var domain = "braton.biotech"; var tld = ".com"; document.write( build_email_link("dringer","braton.biotech",".com") ); or by phone to D.Ringer, (301-208-1777). The Archive includes 181 reassortants or mutants of influenza viruses prevalent during the period 1933-2000. These reassortants were produced or the mutants were discovered in the laboratory of E.D. Kilbourne during the past 43 years. A number of the reassortants were designed as high yield, commercially-used vaccine viruses under FDA/CBER sponsorship, and others were produced under a remarkable arrangement of shared funding by the major American influenza vaccine manufacturers. However, the majority of the viruses have been designed (and employed) as research reagents.

14. The Genotype/Phenotype Distinction The distinction that is made between genotype and phenotype is made necessary The distinction between genotype and phenotype was introduced by Wilhelm http://plato.stanford.edu/entries/genotype-phenotype/

version history HOW TO CITE THIS ENTRY Stanford Encyclopedia of Philosophy A ... Z This document uses XHTML/Unicode to format the display. If you think special symbols are not displaying correctly, see our guide Displaying Special Characters last substantive content change JAN The Encyclopedia Now Needs Your Support Please Read How You Can Help Keep the Encyclopedia Free The Genotype/Phenotype Distinction The distinction between phenotype and genotype is fundamental to the understanding of heredity and development of organisms. The genotype of an organism is the class to which that organism belongs as determined by the description of the actual physical material made up of DNA that was passed to the organism by its parents at the organism's conception. For sexually reproducing organisms that physical material consists of the DNA contributed to the fertilized egg by the sperm and egg of its two parents. For asexually reproducing organisms, for example bacteria, the inherited material is a direct copy of the DNA of its parent. The phenotype of an organism is the class to which that organism belongs as determined by the description of the physical and behavioral characteristics of the organism, for example its size and shape, its metabolic activities and its pattern of movement.

15. BioLogica, Genotype To Phenotype Web Lab This activity explores the relationship between genotype and phenotype, usingboth sexlinked and autosomal dominant and recessive traits. http://biologica.concord.org/webtest1/web_labs_genophenotype.htm

Dragon Genetics . This activity explores the relationship between genotype and phenotype, using both sex-linked and autosomal dominant and recessive traits. By manipulating alleles (genotype), you create corresponding changes in the dragon's physical appearance (phenotype).

16. Genotype --> Phenotype Classroom Booklet genotype phenotype Classroom Booklet set of these booklets so the studentscan have some idea how the various phenotypic characteristics appear. http://www.woodrow.org/teachers/bi/1997/makeface/genphnoblt.html

Print each of these out and then construct a classroom set of these booklets so the students can have some idea how the various phenotypic characteristics appear. The chromosomes are linked to Genome Data Base Title Page Hair Types Sex Determination ... Back to Student's Instructions and Materials

17. Genotype -> Phenotype Eye Color Column 1. Column 2. genotypes. Protein Phenotypes. FFBB. Dark brown Place your baby s genotype for eye color in the data table. http://www.woodrow.org/teachers/bi/1997/makeface/bookeyecol.html

Chromosomes #'s 11 and 12 contain Eye Color Genes: Darker eyes are produced in the presence of more active alleles. In this situation, the Capital letters (F or B) represent alleles which are active in depositing dark pigment. Lower case letters (f or b) represent alleles which deposit little pigment. To determine the color of the eyes, assume there are two gene pairs involved, one of which codes for depositing pigment in the front of the iris, and the other codes for depositing pigment in the back of the iris. Determine the genotype of the first pair (FF,Ff,ff). and the the second (BB,Bb,bb). If your genotype is in the first column then check your eye color in the second column. Column #1 Column #2 Genotypes Protein Phenotypes FFBB Dark brown FFBb Brown FFbb Brown FfBB Brown FfBb Dark Blue Ffbb Dark Blue ffBB Light Blue ffBb Light Blue ffbb Pale blue Place your baby's genotype for eye color in the data table. Back to Front Page Back to Teacher's Information Page Back to Student's Instructions and Materials

18. Clinical Trial: Turner Syndrome: Genotype And Phenotype Previous studies attempting to correlate genotype with phenotype in TS have been This study aims to correlate TS phenotypes and genotypes using advanced http://www.clinicaltrials.gov/ct/gui/show/NCT00006334

Home Search Browse Resources ... About Turner Syndrome: Genotype and Phenotype This study is currently recruiting patients. Verified by National Institutes of Health Clinical Center (CC) September 8, 2005 Sponsored by: National Institute of Child Health and Human Development (NICHD) Information provided by: National Institutes of Health Clinical Center (CC) ClinicalTrials.gov Identifier: Purpose This study will examine the clinical and genetic factors related to Turner syndrome, a disorder of the female sex chromosomes. Humans have 23 pairs of chromosomes-thin strands of DNA-in the nucleus of every cell, which contain genes that determine our hereditary makeup. One pair of chromosomes is the sex chromosomes, designated X and Y. Females normally have two X chromosomes; however, patients with Turner syndrome have only a single X chromosome or one normal and one defective X chromosome. This abnormality can cause medical problems such as a webbed neck, low-set ears, and heart or kidney defects. It can also cause short stature, lack of sexual development and improperly functioning ovaries. Adult women with Turner syndrome have an increased risk of high blood pressure, diabetes mellitus and osteoporosis. This study will try to identify the genes responsible for the specific medical problems associated with the disorder. Females 7 years of age and older with X chromosome defects may be eligible for this 3- to 5- day inpatient study at the National Institutes of Health Clinical Center in Bethesda, Maryland. Participants will have a comprehensive physical examination, including (with the patient's permission) photographs of abnormal physical findings to document characteristics of Turner syndrome. Patients will have their body measurements (height, weight, hip and waist) taken and blood drawn for clinical and research purposes. Patients will be given a "metabolic diet," with meals designed to contain specific amounts of salt and carbohydrate to allow accurate measurements of blood pressure and glucose (sugar) metabolism.

19. Clinical Trial: Study Of Genotype And Phenotype Expression In Congenital Nephrog Study of genotype and phenotype Expression in Congenital Nephrogenic DiabetesInsipidus. This study has been completed. http://www.clinicaltrials.gov/ct/show/NCT00004360

Home Search Browse Resources ... About Study of Genotype and Phenotype Expression in Congenital Nephrogenic Diabetes Insipidus This study has been completed. Sponsors and Collaborators: National Center for Research Resources (NCRR) Northwestern University Information provided by: Office of Rare Diseases (ORD) ClinicalTrials.gov Identifier: Purpose OBJECTIVES: I. Determine the relationship between genotype variations and clinical phenotype in patients with congenital nephrogenic diabetes insipidus. Condition Intervention Diabetes Insipidus, Nephrogenic Drug: chlorothiazide MedlinePlus related topics: Diabetes Insipidus Kidney Failure Study Type: Observational Study Design: Screening Further Study Details: Study start: September 1995 PROTOCOL OUTLINE: A detailed family history is obtained from all participants. Whenever possible, standard growth curves of affected children are obtained. Participants then undergo clinical studies of antidiuretic function. A standard fluid deprivation-vasopressin challenge is performed with timed measurements of osmolality, electrolytes, creatinine, and vasopressin. The next day, blood pressure, plasma cyclic AMP, GMP, von Willebrand Factor, Factor VIII, and urine osmolality are measured during a water load desamino-D-arginine vasopressin (dDAVP) infusion test. Participants with a confirmed diagnosis of congenital diabetes insipidus are then treated with chlorothiazide. Daily urine volume and osmolality are determined before and after therapy. Sodium and fluid are not restricted.

20. EHJ -- Sign In Page Bauce et al.6 report the first systematic analysis of genotype–phenotype correlationsin dominant ARVC. Their study population includes four families with http://www.eurheartj.org/cgi/content/full/26/16/1582

@import "/css/global.css"; @import "/css/article.css"; ABOUT US ACCESS SUBMISSIONS SUBSCRIBE ... Vol. No. ( ) Pp. 1582-1584 doi:10.1093/eurheartj/ehi343 Search Advanced Search Browse by Subject Browse All Stay Informed Select one Basic Research Behavioral and Social Science Issues Cardiology and Cardiovascular Diseases Cardiovascular Surgical Procedures Clinical Research Emergency Cardiovascular Treatment Pediatric and Congenital Heart Disease Preventive Medicine Risk Factors Stroke and Cerebrovascular Disorders Set up email and RSS alerts to keep up-to-date. Issues Current issue Previous issues Article collections Editor's choice (free access) Fast track articles Guidelines This item requires a subscription to European Heart Journal. Full Text Sen-Chowdhry et al. Eur Heart J. This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Request Permissions PubMed PubMed Citation Articles by Sen-Chowdhry, S.

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