Results 21 to 30 of about 2,755,315 (290)

Alterations in the diversity, composition and function of the gut microbiota in Uyghur individuals with sarcopenia

open access: yesExperimental Gerontology
Background: Research on the gut microbiota has emerged as a new direction for understanding pathophysiologic changes in diseases associated with aging, such as sarcopenia.
Qiuxi Zhang   +7 more
doaj   +1 more source

Professionnalisme et rugby de haut niveau : approche anthropobiologique

open access: yesBulletins et Mémoires de la Société d’Anthropologie de Paris, 2006
Until recently rugby has traditionally represented the regions and has been an outstanding example of amateur sport. Its recent change to professionalism, mainly imposed by the media and business lobbies, has resulted in profound changes in the ...
Frédéric Bauduer   +2 more
doaj   +1 more source

Palaeoproteomic Deconvolution of Physical and Genetic Collagen Mixtures

open access: yesAdvanced Science, EarlyView.
ClassiCOL_v2 uses a novel “peptide patching” framework that treats any collagen sample as a patchwork of peptide sequences derived from phylogenetically related species. This allows the algorithm to simultaneously resolve two previously intractable problems: multi‐species samples and/or database deficiencies.
Ian Engels   +12 more
wiley   +1 more source

Characterization of gut microbiota in the Uyghur osteopenia population

open access: yesScientific Reports
The objectives of this study were to investigate the composition of gut microbiota and its relationship with bone loss in the Uyghur osteopenia population, identify potential disease-related taxa and collect information for the prevention and treatment ...
Kunchen Teng   +7 more
doaj   +1 more source

Związek filozofii Karla Jaspersa z klasyczną antropologią filozoficzną XX wieku

open access: yesAnaliza i Egzystencja, 2015
The main objective of this paper is to reconstruct Jaspers’ views on philosophical anthropology of the early twentieth century. The text can be divided into three parts.
Maciej Urbanek
doaj   +1 more source

UBE3A Dosage Imbalance as a Molecular Framework Linking Angelman Syndrome and Dup15q‐Associated Autism Phenotypes

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT UBE3A is a dosage‐sensitive HECT E3 ubiquitin ligase whose neuronal expression is shaped by genomic imprinting at the 15q11.2‐q13 locus. Opposite directions of UBE3A dosage imbalance contribute to distinct neurodevelopmental phenotypes: loss of maternal UBE3A underlies Angelman syndrome, whereas maternally derived 15q11.2‐q13 copy‐number gains,
Ruslan Kurmashev
wiley   +1 more source

Variation of Human Hairiness: A Possible Adaptation to Solar Radiation and Melanin

open access: yesAnthropological Review, 2014
Many theories have been advanced to explain human hairlessness, however, there is no consensus. This study of 76 males observed that skin reflectance measuring skin colouration and melanin pigmentation correlated with hair size and follicle density ...
Dhugga Amrita   +2 more
doaj   +1 more source

Genomic Insight Into the Population Admixture History of Tungusic-Speaking Manchu People in Northeast China

open access: yesFrontiers in Genetics, 2021
Manchu is the third-largest ethnic minority in China and has the largest population size among the Tungusic-speaking groups. However, the genetic origin and admixture history of the Manchu people are far from clear due to the sparse sampling and a ...
Xianpeng Zhang   +15 more
doaj   +1 more source

British Association for Biological Anthropology and Osteoarchaeology: Equality, Diversity and Inclusion Race Equality Review [PDF]

open access: yes, 2021
Racism continues to be widespread, subtle and often ignored or selectively attended to within organisations. This review sought to evaluate the British Association for Biological Anthropology and Osteoarchaeology (BABAO)’s existing race equality ...
Hullock, K. M.   +8 more
core  

Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos   +11 more
wiley   +1 more source

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