about
Sex-biased evolutionary forces shape genomic patterns of human diversityHigh-throughput sequencing of three Lemnoideae (duckweeds) chloroplast genomes from total DNAForces shaping the fastest evolving regions in the human genomeGenetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.Continued colonization of the human genome by mitochondrial DNADuplication and relocation of the functional DPY19L2 gene within low copy repeatsCalculating expected DNA remnants from ancient founding events in human population geneticsComplex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humansThe ups and downs of mutation frequencies during aging can account for the Apert syndrome paternal age effectDeterministic mutation rate variation in the human genomeAnalysis of genetic inheritance in a family quartet by whole-genome sequencingVariation in genome-wide mutation rates within and between human familiesAre rare variants responsible for susceptibility to complex diseases?Heterozygous mutations of OTX2 cause severe ocular malformationsGenomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees.Likelihood and Bayes estimation of ancestral population sizes in hominoids using data from multiple lociNucleotide variation at Msn and Alas2, two genes flanking the centromere of the X chromosome in humansA revised root for the human Y chromosomal phylogenetic tree: the origin of patrilineal diversity in AfricaA map of human genome variation from population-scale sequencingDirect measure of the de novo mutation rate in autism and schizophrenia cohortsEstimating the human mutation rate using autozygosity in a founder populationMobile elements reveal small population size in the ancient ancestors of Homo sapiensRate of de novo mutations and the importance of father's age to disease riskRates and fitness consequences of new mutations in humansThe amino-acid mutational spectrum of human genetic diseaseWhole-genome screening indicates a possible burst of formation of processed pseudogenes and Alu repeats by particular L1 subfamilies in ancestral primatesGene conversion homogenizes the CMT1A paralogous repeatsPAX6 mutations: genotype-phenotype correlationsGenomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineagesUncertainty principle of genetic information in a living cell.MAOA haplotypes associated with thrombocyte-MAO activity.Molecular Signatures of Natural Selection for Polymorphic Genes of the Human Dopaminergic and Serotonergic Systems: A ReviewInfluence of paternal preconception exposures on their offspring: through epigenetics to phenotypeFactors influencing the effect size distribution of adaptive substitutionsFifteen years of genomewide scans for selection: trends, lessons and unaddressed genetic sources of complicationThe human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and functionBreaking bad: The mutagenic effect of DNA repairEpigenetic inheritance: a contributor to species differentiation?Child development and molecular genetics: 14 years laterCreating diseases to understand what prevents them: genetic analysis of inflammation in the gastrointestinal tract
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Estimate of the mutation rate per nucleotide in humans
@ast
Estimate of the mutation rate per nucleotide in humans
@en
Estimate of the mutation rate per nucleotide in humans
@nl
type
label
Estimate of the mutation rate per nucleotide in humans
@ast
Estimate of the mutation rate per nucleotide in humans
@en
Estimate of the mutation rate per nucleotide in humans
@nl
prefLabel
Estimate of the mutation rate per nucleotide in humans
@ast
Estimate of the mutation rate per nucleotide in humans
@en
Estimate of the mutation rate per nucleotide in humans
@nl
P2860
P3181
P1433
P1476
Estimate of the mutation rate per nucleotide in humans
@en
P2093
Crowell SL
Nachman MW
P2860
P304
P3181
P407
P577
2000-09-01T00:00:00Z