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Point mutation
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111	HGMD Professional Schema Overview The HGMD database comprises four schemata: hgmd_pro, hgmd_snp, hgmd_advanced and hgmd_phenbase. The schema relevant to users who want to access data in HGMD Professional is hgmd_pro, whi Add to Reading List Source URL: www.biobase-international.com Language: English - Date: 2014-07-01 12:37:21 Molecular biology DNA Evolutionary biology Point mutation Genetic code Single-nucleotide polymorphism Insertion Deletion Missense mutation Biology Genetics Mutation
112	HGMD® Professional[removed]Release date 28th September[removed]HGMD Introduction Citing HGMD If you refer to HGMD in any publication, please cite: Stenson et al (2008), The Human Gene Mutation Database (HGMD®): 2008 Upda Add to Reading List Source URL: portal.biobase-international.com Language: English - Date: 2013-01-15 12:18:20 Mutation Population genetics Evolutionary biology Single-nucleotide polymorphism Point mutation Human genome Penetrance Genetic code Genomes Project Biology Genetics Molecular biology
113	Mutation Research[removed]–119 Quantification of CD59− mutants in human–hamster hybrid (AL) cells by flow cytometry Hongning Zhou a,∗ , An Xu a , Joseph A. Gillispie a , Charles A. Waldren b , Tom K. Hei a Add to Reading List Source URL: www.raraf.org Language: English - Date: 2014-11-19 16:49:06 Cell biology CD59 Mutagen Flow cytometry Assay Antibody Point mutation Cytometry Biology Laboratory techniques Mutation
114	Blackwell Science, LtdOxford, UKMMIMolecular Microbiology0950-382XBlackwell Publishing Ltd, 2004? 2004553712723Original ArticleDirected evolution of LuxRC. H. Collins, F. H. Arnold and J. R. Leadbetter Molecular Microbi Add to Reading List Source URL: www.its.caltech.edu Language: English - Date: 2005-01-18 17:03:25 Cell signaling Lactones N-Acyl homoserine lactone Vibrionales Quorum sensing Vibrio fischeri Green fluorescent protein Site-directed mutagenesis Point mutation Biology Microbiology Amides
115	NeuroRx威: The Journal of the American Society for Experimental NeuroTherapeutics Genetics of Parkinson Disease Nathan Pankratz and Tatiana Foroud Department of Medical and Molecular Genetics, Indiana University School Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Genetics Health Parkin Alpha-synuclein Neurodegeneration Presenilin Chromosome 1 Point mutation Genetic disorder Biology Geriatrics Medicine
116	vol. 157, no. 5 the american naturalist may 2001 Add to Reading List Source URL: biology.mcgill.ca Language: English - Date: 2014-06-10 10:17:57 Population genetics Mutation Natural selection Evolution Fitness Genetic algorithm Complementation Genetics Point mutation Evolutionary biology Biology Philosophy of biology
117	Exercise-induced Pgc-1α Expression does not Lower mtDNA Point Mutation Levels but Downregulates Tyrosine hydroxylase Expression in the Striatum Zera Ong Raffles Institution (Junior College), Singapore, Singapore Under t Add to Reading List Source URL: www.cee.org Language: English - Date: 2012-12-20 11:28:38 Mitochondrial DNA Mitochondrial biogenesis POLG Mitochondrion Mutation Senescence FGF21 Human mitochondrial genetics Biology DNA Aging
118	Plant Mutation Reports, Vol. 3, No. 1, July[removed]Vol. 3, No. 1 July 2013 Add to Reading List Source URL: www-naweb.iaea.org Language: English - Date: 2013-08-27 04:04:26 Mutation Molecular biology Breeding Point mutation Microsatellite Mutagenesis Mutant Zinc finger nuclease Restriction fragment length polymorphism Biology Genetics Evolutionary biology
119	1. Introduction 1.1 Soon after the recognition of a new, fatal disease in UK cattle, it was realised that the disorder was one of a very unusual group of neurodegenerative diseases,1 the spongiform encephalopathies,2 whi Add to Reading List Source URL: webarchive.nationalarchives.gov.uk Language: English Chromosome Mutation Meiosis Point mutation Homologous chromosome Dominance Virino Y chromosome Nucleic acid sequence Biology Genetics Gene
120	Handbook Help Me Understand Genetics Mutations and Health Reprinted from Genetics Home Reference (http://ghr.nlm.nih.gov/) Add to Reading List Source URL: www.ghr.nlm.nih.gov Language: English Point mutation Insertion Frameshift mutation Genetic code Silent mutation Cystic fibrosis transmembrane conductance regulator Missense mutation Mutagen Nonsense mutation Biology Mutation Genetics

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