About: [31] Detection and localization of single base changes by denaturing gradient gel electrophoresis

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article by Richard M. Myers et al published 1987 in Methods in Enzymology

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) наукова стаття, опублікована в 1987 (uk) im Januar 1987 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en 1987 (fr) article by Richard M. Myers et al published 1987 in Methods in Enzymology (en)
publication date	wds:Q56542213-D30693A3-4361-4662-B8C4-D2D811A31107
publication date	1987-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56542213-EF3A0AC5-3189-41A0-B82D-B29831A1C23F
language of work or name	English
author name string	wds:Q56542213-0B7F3E11-021E-4F32-8D55-EE09A962AAA6 wds:Q56542213-E3920DBE-7EB1-428B-B3CE-591B788CFE59
author name string	Richard M. Myers Leonard S. Lerman
rdfs:label	[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis (en) [31] Detection and localization of single base changes by denaturing gradient gel electrophoresis (nl)
skos:prefLabel	[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis (en) [31] Detection and localization of single base changes by denaturing gradient gel electrophoresis (nl)
name	[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis (en) [31] Detection and localization of single base changes by denaturing gradient gel electrophoresis (nl)
author	wds:Q56542213-5447CAF1-B193-4F7A-B09E-474795F322EB
author	Tom Maniatis
title	wds:Q56542213-252CBE08-9833-4A49-9EA2-DB5A05116423
title	[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis (en)
page(s)	wds:Q56542213-BA73741C-E98A-4576-B1FD-345180C43DD7
page(s)	501-527
instance of	wds:Q56542213-85CE6691-C808-4803-ABB1-D22514482F8C
instance of	scholarly article
published in	wds:Q56542213-63C4AF3E-239E-4C4A-8610-5CE6D84BE38B
published in	Methods in Enzymology
DOI	wds:Q56542213-B55CB33B-D771-4545-8F04-869C60E535E2
DOI	http://dx.doi.org/10.1016/0076-6879(87)55033-9
DOI	10.1016/0076-6879(87)55033-9
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56542213
is cites work of	Bipolar clamping improves the sensitivity of mutation detection by temperature gradient gel electrophoresis. Three novel mutations of the NF1 gene detected by temperature gradient gel electrophoresis of exons 5 and 8. Analysis of the NF1 gene by temperature gradient gel electrophoresis reveals a high incidence of mutations in exon 4b. A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophy How sensitive is PCR-SSCP? Mutation scanning methods for the analysis of parasite genes Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels Application of denaturing gradient gel electrophoresis (DGGE) to the analysis of microbial communities of subgingival plaque Nitrogen-fixing bacteria in Eucalyptus globulus plantations Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: comparison with denaturing gradient gel electrophoresis and nucleotide sequencing The rapid detection of unknown mutations in nucleic acids. Automated detection of point mutations using fluorescent sequence trace subtraction Induction by zinc of specific metallothionein isoforms in human monocytes Denaturing gradient gel electrophoresis (DGGE) approaches to study the diversity of ammonia-oxidizing bacteria Detecting single base substitutions, mismatches and bulges in DNA by temperature gradient gel electrophoresis and related methods Molecular analysis of the estrogen receptor alpha gene in men with coronary artery disease: association with disease status Variation on islands: major histocompatibility complex (Mhc) polymorphism in populations of the Australian bush rat. Variegate porphyria in Western Europe: identification of PPOX gene mutations in 104 families, extent of allelic heterogeneity, and absence of correlation between phenotype and type of mutation Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update DHR3, an ecdysone-inducible early-late gene encoding a Drosophila nuclear receptor, is required for embryogenesis Screening of follicle-stimulating hormone receptor gene in women with premature ovarian failure in southern Brazil and associations with phenotype Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia DNA probes: applications of the principles of nucleic acid hybridization Drosophila ecdysone receptor mutations reveal functional differences among receptor isoforms Development and application of DNA techniques for validating and improving pinniped diet estimates Monoallelic mutation analysis (MAMA) for identifying germline mutations Analysis of bacterial communities on historical glass by denaturing gradient gel electrophoresis of PCR-amplified gene fragments coding for 16S rRNA. Detection of point mutations by capillary electrophoresis in liquid polymers in temporal thermal gradients Detection of single DNA base mutations with mismatch repair enzymes Effects of chemical contaminants on genetic diversity in natural populations: implications for biomonitoring and ecotoxicology MHC diversity in two Acrocephalus species: the outbred Great reed warbler and the inbred Seychelles warbler Allelic polymorphisms in the transcriptional regulatory region of apolipoprotein E gene Assessing high-resolution melt curve analysis for accurate detection of gene variants in complex DNA fragments. Identification of the repressor subdomain within the signal reception module of the prokaryotic enhancer-binding protein XylR of Pseudomonas putida Streptococcal diversity in oral biofilms with respect to salivary function. Myoglobin intron variation in the Gouldian Finch Erythrura gouldiae assessed by temperature gradient gel electrophoresis. What's in that band? An overview of the analysis of DNA methylation in mammalian genomes A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasia The polymerase chain reaction in histopathology Detection of over 98% cystic fibrosis mutations in a Celtic population Detection of more than 94% cystic fibrosis mutations in a sample of Belgian population and identification of four novel mutations Characterization of genetic defects of hemophilia A in patients of Chinese origin Terminal investment induced by immune challenge and fitness traits associated with major histocompatibility complex in the house sparrow. Peutz-Jeghers syndrome: 78-year follow-up of the original family A one-step DGGE scanning method for detection of mutations in the K-, N-, and H-ras oncogenes: mutations at codons 12, 13 and 61 are rare in B-cell non-Hodgkin's lymphoma. Mutational spectrometry: means and ends. A comparison of fluorescent SSCP and denaturing HPLC for high throughput mutation scanning. Analysis of the dynamics of fungal communities in soil via fungal-specific PCR of soil DNA followed by denaturing gradient gel electrophoresis Analysis of mutations using PCR and denaturing gradient gel electrophoresis Use of polymerase chain reaction-based single strand conformational polymorphism and denaturing gradient gel electrophoresis methods for detection of sequence variation of ribosomal DNA of Trypanosoma cruzi Somatic hypermutation of immunoglobulin genes is linked to transcription initiation Tools for molecular genetic epidemiology: a comparison of MADGE methodology with other systems p21WAF1 Mutation Is Not a Predominant Alteration in Pediatric Bone Tumors PCR-based technology in veterinary parasitology. How useful are the genetic markers in attempts to understand and manage marine biodiversity? Comprehensive, rapid and sensitive detection of sequence variants of human mitochondrial tRNA genes Associations between malaria and MHC genes in a migratory songbird Nasopharyngeal lymphomas: further evidence for a natural killer cell origin. Genetic diagnosis of 21-hydroxylase deficiency: DGGE-based mutation scanning of CYP21 Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours Detection and characterization of a novel splice mutation in the LDL receptor intron 12 resulting in two different mutant mRNA variants Detection of clonal T-cell receptor gamma gene rearrangements in paraffin-embedded tissue by polymerase chain reaction and nonradioactive single-strand conformational polymorphism analysis Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.

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