About: How neutral are synonymous codon mutations?

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article published in 1995

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в липні 1995 (uk) im Juli 1995 veröffentlichter wissenschaftlicher Artikel (de) article published in 1995 (en)
publication date	wds:Q57398305-D0FB34BB-A5AB-49BD-B2BD-1C2541D39AD7
publication date	1995-07-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57398305-A24A289D-6852-45DD-9861-2F980DF28980
language of work or name	English
exact match	wds:Q57398305-FDA62A9D-9991-4D7A-8FF7-C6B15585049F
exact match	https://scigraph.springernature.com/pub.10.1038/ng0795-259
cites work	wds:Q57398305-03B36B73-3C84-4303-9CEB-0637B9E41271 wds:Q57398305-0D2A70A8-B46C-4C84-B779-48F101843EA9 wds:Q57398305-96CC15D9-D684-4E0C-A395-E807214FB384 wds:Q57398305-DBC75349-4B9F-4F35-B919-5957BCA316D4 wds:Q57398305-E42DE3BB-4028-4A53-8239-50908FC25F4F wds:Q57398305-E7B129E1-AB68-44F8-AB49-8116D28C136F wds:Q57398305-ECCFAC8A-BE6F-4C66-8F94-CD0886EEC72A
cites work	Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2 Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A Illegitimate transcription: transcription of any gene in any cell type Effect on splicing of a silent FGFR2 mutation in Crouzon syndrome
author name string	wds:Q57398305-8DA76492-8D2F-4315-B34D-958637B0CA70
author name string	Isabella Richard
rdfs:label	How neutral are synonymous codon mutations? (en) How neutral are synonymous codon mutations? (nl)
skos:prefLabel	How neutral are synonymous codon mutations? (en) How neutral are synonymous codon mutations? (nl)
name	How neutral are synonymous codon mutations? (en) How neutral are synonymous codon mutations? (nl)
author	wds:Q57398305-B4A61C00-76DA-4FAD-8D12-8217E06A78C7
author	Jacques S Beckmann
title	wds:Q57398305-6C4EFC09-1F3A-44CD-9392-8EE4804946E3
title	How neutral are synonymous codon mutations? (en)
page(s)	wds:Q57398305-EF368CC1-E86A-4A7C-832A-F8D0D9282EF7
page(s)	259-259
instance of	wds:Q57398305-60425B36-0266-4AC6-B618-92F03FA507C5
instance of	scholarly article
PubMed ID	wds:Q57398305-CF90B4B7-C308-4871-B080-40D4A2613921
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7670461
PubMed ID	7670461
published in	wds:Q57398305-6D6766FE-7577-4EBE-8B75-E4FC37ADDE1D
published in	Nature Genetics
issue	wds:Q57398305-6B62FC82-B337-4F86-80D1-F224010C4F25
volume	wds:Q57398305-16B7AE6C-8F25-4574-BC05-D4A526BD2643
issue	3
volume	10
DOI	wds:Q57398305-D953D8DB-7F71-43DF-ACAD-463F1C8ACCBE
DOI	http://dx.doi.org/10.1038/NG0795-259
DOI	10.1038/NG0795-259
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57398305
is cites work of	Association of two silent polymorphisms of platelet glycoprotein Ia/IIa receptor with risk of myocardial infarction: a case-control study. Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution. Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease Automated splicing mutation analysis by information theory. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion Calpainopathy-a survey of mutations and polymorphisms Molecular diagnosis in LGMD2A: mutation analysis or protein testing? Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Role in tumorigenesis of silent mutations in the TP53 gene. A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype Advances in molecular marker techniques and their applications in plant sciences Low incidence of BRCA2 mutations in breast carcinoma and other cancers A silent mutation, C924T (G308G), in the L1CAM gene results in X linked hydrocephalus (HSAS). Genetic contributions to preterm birth: implications from epidemiological and genetic association studies Screening breast cancer patients for ATM mutations and polymorphisms by using denaturing high-performance liquid chromatography Nucleotide variation at the Gpdh locus in the genus Drosophila Acute intermittent porphyria caused by defective splicing of porphobilinogen deaminase RNA: a synonymous codon mutation at -22 bp from the 5' splice site causes skipping of exon 3. A synonymous mutation in the CFTR gene causes aberrant splicing in an italian patient affected by a mild form of cystic fibrosis. The Réunion paradox and the digenic model Mutations in PAX1 may be associated with Klippel-Feil syndrome. Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins Molecular analysis of the androgen-receptor gene in a family with receptor-positive partial androgen insensitivity: an unusual type of intronic mutation Diagnostic protein expression in human muscle biopsies X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. Calpain-3 mutations in Turkey Genomic profile of the plants with pharmaceutical value. A paradigm for single nucleotide polymorphism analysis: the case of the acetylcholinesterase gene Expression Changes Confirm Genomic Variants Predicted to Result in Allele-Specific, Alternative mRNA Splicing Molecular markers and cotton genetic improvement: current status and future prospects. Molecular and functional characterization of the BMPR2 gene in Pulmonary Arterial Hypertension
is cites work of	wds:Q29616531-06451248-F687-4283-8FD9-F58689A8CD4D wds:Q42589339-4DBE901E-1C5D-4BF5-B797-A64AFA5D4359 wds:Q50534959-A7FFB5FF-C871-4460-9362-E62225BAD0BF wds:Q34381064-D1533D1B-E909-4769-864E-FC92974D5EC9 wds:Q33967394-62D9E331-FC55-4BD5-AF72-E1B9E5BC057F wds:Q33680815-7DACF02B-8DE6-49E1-83FB-79CC09D5474E wds:Q37126070-1F9E9B1F-AE2E-45B8-84EA-14F007D296DF wds:Q90640119-C33DE19A-1463-4431-AC01-79E4850A6FA6 wds:Q33891334-9C0E7B3C-6C65-40BA-A6E8-A11F8DE89960 wds:Q35250011-A90BCAB8-88D1-4D23-ABCF-115009A1B323 wds:Q46597044-1E197A67-59DF-4826-A896-7E6099E7CC82 wds:Q24524120-2371BD5C-DCEB-4E9C-83A9-F430AEBA65D3 wds:Q37075960-3282FDA8-340B-4F03-BF49-0E03DDC9F602 wds:Q28295097-02FA5D8F-1C62-4FC2-88AB-CD6FE0DBF9DE wds:Q42036972-56FA1E82-7577-4892-B4F4-E98C2AEA6BEC

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