Context of deletions and insertions in human coding sequences.
about
SIMPROT: using an empirically determined indel distribution in simulations of protein evolution.DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indelsGenetic analysis of West Nile virus isolates from an outbreak in Idaho, United States, 2006-2007Single nucleotide polymorphism analysis of Korean native chickens using next generation sequencing data.A macaque's-eye view of human insertions and deletions: differences in mechanisms.The nucleotide composition of microsatellites impacts both replication fidelity and mismatch repair in human colorectal cellsNew words in human mutagenesis.Next-generation sequencing of colorectal cancers in chinese: identification of a recurrent frame-shift and gain-of-function Indel mutation in the TFDP1 geneEffects of PON polymorphisms and haplotypes on molecular phenotype in Mexican-American mothers and children.Genome wide analysis reveals single nucleotide polymorphisms associated with fatness and putative novel copy number variants in three pig breeds.On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited diseaseExploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromasThe genomic landscape of short insertion and deletion polymorphisms in the chicken (Gallus gallus) Genome: a high frequency of deletions in tandem duplicates.EvalMSA: A Program to Evaluate Multiple Sequence Alignments and Detect Outliers.Sequence context affects the rate of short insertions and deletions in flies and primates.The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.A versatile microsatellite instability reporter system in human cells.Ride the wavelet: A multiscale analysis of genomic contexts flanking small insertions and deletions.Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates.Strong heterogeneity in mutation rate causes misleading hallmarks of natural selection on indel mutations in the human genome.Measurements of spontaneous rates of mutations in the recent past and the near future.Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease.Spontaneous Chloroplast Mutants Mostly Occur by Replication Slippage and Show a Biased Pattern in the Plastome of Oenothera.Absence of keratins 8 and 18 in rodent epithelial cell lines associates with keratin gene mutation and DNA methylation: Cell line selective effects on cell invasion.Using the Neandertal genome to study the evolution of small insertions and deletions in modern humans.Local sequence determinants of two in-frame triplet deletion/duplication hotspots in the RHD/RHCE genes.Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.A Role for Non-B DNA Forming Sequences in Mediating Microlesions Causing Human Inherited Disease.CpG/CpNpG motifs in the coding region are preferred sites for mutagenesis in the breast cancer susceptibility genes.Comparative analysis of germline and somatic microlesion mutational spectra in 17 human tumor suppressor genes.Mutational signatures and mutable motifs in cancer genomes.
P2860
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P2860
Context of deletions and insertions in human coding sequences.
description
2004 nî lūn-bûn
@nan
2004 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
name
Context of deletions and insertions in human coding sequences.
@ast
Context of deletions and insertions in human coding sequences.
@en
Context of deletions and insertions in human coding sequences.
@nl
type
label
Context of deletions and insertions in human coding sequences.
@ast
Context of deletions and insertions in human coding sequences.
@en
Context of deletions and insertions in human coding sequences.
@nl
prefLabel
Context of deletions and insertions in human coding sequences.
@ast
Context of deletions and insertions in human coding sequences.
@en
Context of deletions and insertions in human coding sequences.
@nl
P356
P1433
P1476
Context of deletions and insertions in human coding sequences
@en
P2093
Alexey S Kondrashov
P2860
P304
P356
10.1002/HUMU.10312
P577
2004-02-01T00:00:00Z