Results 51 to 60 of about 3,305 (180)
Biomolecules, 2017 Transfer RNAs (tRNAs) harbor a subset of post‐transcriptional modifications required for structural stability or decoding function. N6‐threonylcarbamoyladenosine (t6A) is a universally conserved modification found at position 37 in tRNA that pair A ...
Diego Rojas‐Benítez +2 more
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Systematic Entomology, Volume 51, Issue 1, January‐March 2026.A subgeneric classification is proposed for Triepeolus—the second‐largest genus of cleptoparasitic apid bees in the world—and its sister genus Epeolus, with support from a newly presented dated phylogeny. Phylogenomic analysis based on ultraconserved elements revealed strong support for the monophyly of Triepeolus, which diverged from Epeolus sometime ...
Thomas M. Onuferko +2 more
wiley +1 more source
Sexagesimal scale for mapping human genome Escala sexagesimal para mapear el genoma humano
Revista Chilena de Historia Natural, 2001 In a previous work I designed a diagram of the human genome based on a circular ideogram of the haploid set of chromosomes, using a low resolution scale of Megabase units.
RICARDO CRUZ-COKE
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Revista FAMECOS, 2008 Como parte das tantas indagações que alimentamos sobre nossa identidade, este artigo lança/resgata mais um ponto de vista sobre a questão da identidade gaúcha. Ancorado em referências que têm contribuído para este tema, faz-se uma análise crítica a partir da argumentação que a identidade é construída sobre imagens, sobre representações que desejamos ...
openaire +2 more sources
International Journal of Microbiology, Volume 2026, Issue 1, 2026.Introduction Type 2 diabetes mellitus (T2DM) is known to increase the risk of Alzheimer’s disease (AD), but the role of the gut microbiota in this relationship is not fully understood. This study investigated the gut microbiota profiles of adults with T2DM, adults with AD, both conditions (AD–T2DM), and healthy controls to identify patterns associated ...
Alexis M. Rodríguez-Rosas +11 more
wiley +1 more source
Journal of Neurodevelopmental Disorders, 2019 Background Phelan-McDermid syndrome (PMS) is a rare genetic disorder characterized by global developmental delay, intellectual disability (ID), autism spectrum disorder (ASD), and mild dysmorphisms associated with several comorbidities caused by SHANK3 ...
Claudia Ismania Samogy-Costa +12 more
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Exonic Variation and Its Clinical Impact in 7221 Old Order Amish
American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.ABSTRACT The Amish of Lancaster County, PA has been the focus of genetic studies for many years due to its demographic history and unique genetic makeup that includes a historical bottleneck event and subsequent genetic drift, resulting in a marked decrease in genetic diversity and increased frequency of some variants that have substantially shaped the
Braxton D. Mitchell +21 more
wiley +1 more source
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects
BMC Medical Genetics, 2018 Background Mutations in the SLC26A4 gene are associated with Pendred syndrome and autosomal recessive non-syndromic deafness (DFNB4). Both disorders have similar audiologic characteristics: bilateral hearing loss, often severe or profound, which may be ...
Renata Watanabe Nonose +5 more
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Revista de la Facultad de Odontología, 2023 CRISPR has gained a lot of attention recently as a result of a debate among scientists about the possibility of genetically modifying the human germ line and the ethical implications of doing so. However, CRISPR is not just a method for editing the genomes of embryonic cells, as the public discussion might have implied; is a powerful, efficient, and ...
openaire +1 more source
Revista Chilena de Historia Natural, 2003 Genome data analysis indicates that the major evolutionary transitions have been driven by substantial increases in genomic complexity. These increases, accounting for novelty in evolution, have proceeded mainly by gene duplication.
MILTON GALLARDO
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