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341
Heads or tails: L1 insertion-associated 5' homopolymeric sequences
Published 2010-02-01“…We identified loci using computational analyses of the human, chimpanzee, orangutan, rhesus macaque and marmoset genomes. Insertion site characteristics for all putative loci were experimentally verified.…”
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342
Modeling enamel matrix secretion in mammalian teeth.
Published 2019-05-01“…Simulations reveal how concave and convex dentine features have distinct effects on enamel surface, thereby explaining why the enamel surface is not a straightforward extrapolation of the dentine template. Human and orangutan molar simulations show that even subtle variation in dentine topography can be mapped to the enamel surface features. …”
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343
Sex-biased evolutionary forces shape genomic patterns of human diversity.
Published 2008-09-01“…We correct for differences in mutation rates between males and females by considering the ratio of within-human diversity to human-orangutan divergence. We find that relative levels of genetic variation are higher than expected on the X chromosome in all six human populations. …”
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344
A gradient of silent substitution rate in the human pseudoautosomal region.
Published 2004“…Here I report the analysis of substitution patterns and rates in 10 human, chimpanzee, gorilla, and orangutan genes across the p-PAR. Between species silent divergence in the p-PAR forms a gradient, increasing toward the telomere. …”
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345
Accurate sex identification of ancient elephant and other animal remains using low-coverage DNA shotgun sequencing data
Published 2020“…Such taxa include the domestic cat, sheep, goat, and horse; and non-domesticated animals such as the Sumatran orangutan, western lowland gorilla and meerkat.…”
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346
Quantifying interaction with robotic toys in pre-term and full-term infants
Published 2023-10-01“…Using a set of classification codes developed from the literature, we analyzed videos from 24 pre-term and full-term infants as they played with each of three robotic toys designed to elicit different types of interactions—a lion, an orangutan, and an elephant. We manually coded for frequency and duration of toy interactions such as kicking, grasping, touching, and gazing. …”
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347
Genetic characterization of nodular worm infections in Asian Apes
Published 2021-03-01“…To better understand which Oesophagostomum species infect Asian non-human primates and determine their phylogeny we analysed 55 faecal samples from 50 orangutan and 5 gibbon individuals from Borneo and Sumatra. …”
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348
The origin of the RB1 imprint.
Published 2013-01-01“…To examine the origin of the RB1 imprint, we compared the methylation patterns of the parental PPP1R26 gene and its retrocopies in different primates (human, chimpanzee, orangutan, rhesus macaque, marmoset and galago). Methylation analysis by deep bisulfite sequencing showed that PPP1R26 is methylated whereas the retrocopy in RB1 intron 2 is differentially methylated in all primates studied. …”
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349
Human and non-human primate genomes share hotspots of positive selection.
Published 2010-02-01“…To answer this question, we analysed heterozygous Single Nucleotide Polymorphisms (SNPs) in the genomes of single human, chimpanzee, orangutan, and macaque individuals using a new method aiming to identify selective sweeps genome-wide. …”
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350
Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion.
Published 2004-05-01“…Here we have isolated large genomic clones containing the complete ASPM gene, including promoter regions and introns, from chimpanzee, gorilla, orangutan, and rhesus macaque by transformation-associated recombination cloning in yeast. …”
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351
Co-evolution of primate SAMHD1 and lentivirus Vpx leads to the loss of the vpx gene in HIV-1 ancestor.
Published 2012-01-01“…We found evidence for positive selection of SAMHD1 in orangutan, gibbon, rhesus macaque, and marmoset, but not in human, chimpanzee and gorilla that are natural hosts of Vpx-negative HIV-1, SIVcpz and SIVgor, respectively, indicating that vpx drives the evolution of primate SAMHD1. …”
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352
Molecular Cloning, Sequence Identification and Tissue Expression Profile of Three Novel Sheep (Ovis aries) Genes - BCKDHA, NAGA and HEXA
Published 2009-01-01“…The sheep HEXA gene encodes a protein of 529 amino acids that has high homology with the hexosaminidase A(HEXA) of five species bovine (98%), human (84%), Bornean orangután (84%), rat (80%) and mouse (81%). Finally these three novel sheep genes were assigned to GenelDs: 100145857, 100145858 and 100145856. …”
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353
The distribution and persistence of primate species in disturbed and converted forest landscapes in Sabah, Malaysia: preliminary results
Published 2014“…Interestingly, however, the presence of eight species of primates within the heavily logged forest sampling sites, which included Bornean endemic species and species of high conservation concern, e.g. orangutan, proboscis monkey and Bornean gibbon, shows that even highly disturbed forests in Sabah are still valuable for primate conservation.…”
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354
Shared human-chimpanzee pattern of perinatal femoral shaft morphology and its implications for the evolution of hominin locomotor adaptations.
Published 2012-01-01“…Diaphyseal morphology in humans and chimpanzees exhibits several shared-derived features, despite substantial differences in locomotor adaptations. Orangutan and gorilla morphologies are largely similar, and likely represent the primitive hominoid state.…”
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355
Evolutionary appearance of Von Economo’s Neurons in the mammalian cerebral cortex
Published 2014-03-01“…<br/>VENs have been identified in humans, chimpanzee, bonobos, gorillas, orangutan and, more recently, in the macaque. Their distribution in great apes seems to correlate with human-like social cognitive abilities and self-awareness. …”
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356
Allelic lineages of the ficolin genes (FCNs) are passed from ancestral to descendant primates.
Published 2011-01-01“…The exons and intron-exon boundaries of the FCN1-3 genes were sequenced in the following primate species: chimpanzee, gorilla, orangutan, rhesus macaque, cynomolgus macaque, baboon and common marmoset. …”
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357
Strongyloides infections among human and non-human host in indonesia: a systematic review
Published 2023-05-01“…Strongyloides infected some animal group hosts, such as pigs, ruminants (beef cattle, swamp buffalo, sheep, and goat), rodents, nonhuman primates (orangutan, lutung (Trachypithecus auratus), and long-tailed macaque), and others (rabbit, snake, and chicken) in different regions. …”
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358
Retrocopy contributions to the evolution of the human genome
Published 2008-10-01“…In addition to their presence in human, several of the gene candidates also had potentially viable ORFs in chimpanzee, orangutan, and rhesus macaque, underscoring their potential of function.…”
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359
Genome sequencing and application of Taiwanese macaque Macaca cyclopis
Published 2023-07-01“…Genome-based phylogenetic study using the assembled M. cyclopis genome together with genomes of four other macaque species, human, orangutan and chimpanzee showed similar result as previously reported. …”
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360
Hydrological and economic effects of oil palm cultivation in Indonesian peatlands
Published 2016-06-01“…For the economic analysis, we analyzed four ecosystem services: oil palm production, jelutung production, carbon sequestration, and orangutan habitat. This study shows that after 100 years, in the oil palm scenario, about 67% of peat in the study area will be subject to regular flooding. …”
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