Results 61 to 70 of about 197,571 (210)

Regulación de los hallazgos secundarios e incidentales derivados del análisis genético: desde el ámbito clínico hasta el Espacio Europeo de Datos de Salud

open access: yesRevista de Bioética y Derecho
El desarrollo y disponibilidad de tecnologías ómicas de alto rendimiento, como la secuenciación completa del exoma (WES) y del genoma (WGS), suscitan nuevos retos ético-jurídicos.
Guillermo Lazcoz Moratinos   +2 more
doaj   +1 more source

Size, Spines, and Nests: What Drives Variation in Death‐Feigning Behavior in Fungus‐Farming Ants?

open access: yesIntegrative Zoology, EarlyView.
We investigated death‐feigning (DF; thanatosis) in fungus‐farming ants, testing how stimulus intensity, morphology, and nest traits shape its occurrence and duration using generalized linear mixed models. Stronger stimuli increased both likelihood and duration, but most variation was structured across species, colonies, and individuals.
Danon Clemes Cardoso   +2 more
wiley   +1 more source

Neurogenetics in Peru, example of translational research

open access: yesRevista Peruana de Medicina Experimental y Salud Pública, 2015
Neurogenetics is an emerging discipline in Peru that links basic research with clinical practice. The Neurogenetics Research Center located in Lima, Peru is the only unit dedicated to the specialized care of neurogenetic diseases in the country. From the
Pilar Mazzetti   +6 more
doaj   +1 more source

Standardizing assessment of novel methods for ecological data collection

open access: yesMethods in Ecology and Evolution, EarlyView.
Abstract Methodological advances in ecology enable more efficient data collection, yet researchers need to clearly and consistently report the ways in which these methods benefit their own research within the context of their specific needs. Here, we advocate for greater standardization and transparency when assessing new ecological data collection ...
Maisie G. MacKnight, David A. W. Miller
wiley   +1 more source

Algunas consideraciones clínico-genéticas de la trombocitopenia con ausencia de radios Some clinical-genetic considerations of the thrombocytopenia with lack of radios

open access: yesRevista Cubana de Hematología, Inmunología y Hemoterapia, 2010
La trombocitopenia con ausencia de radios (TAR) es un síndrome genético poco frecuente caracterizado por ausencia bilateral de radios con presencia de ambos pulgares y trombocitopenia. Suelen estar presentes, además, malformaciones en miembros inferiores,
Dunia de la C. Castillo-González
doaj  

De plantas y hombres: cómo los genetistas se vincularon a la eugenesia en Brasil (un estudio de caso, 1929-1938)

open access: yesAsclepio: Revista de Historia de la Medicina y de la Ciencia, 2014
En el presente artículo pretendemos reflexionar sobre la trayectoria de Octávio Domingues (1897-1972) y Salvador Toledo Piza Jr. (1898-1988), dos genetistas de una escuela agrícola del Estado de São Paulo que se vincularon al principal propagador de la ...
Paula Arantes Botelho Briglia Habib   +1 more
doaj   +1 more source

Autosomal Dominant Hyper‐IgE Syndrome Patients Retain IL10‐Producing preTh17‐Cells That Are Activated by Opportunistic Pathogens and Support IgE Production

open access: yesAllergy, EarlyView.
IL‐10 producing CCR6+Th‐cells are central memory T‐cells that express ROR‐γt and differentiate to Th17‐cells via an autocrine loop of STAT3‐activating cytokines (preTh17). STAT3‐deficient AD‐HIES patients lack Th17‐ and Tfh17‐cells but retain preTh17‐ and Th1/17‐cells.
Giorgia Moschetti   +18 more
wiley   +1 more source

Genética cidadã no livro didático: análise de coleções de biologia integrantes do programa nacional do livro didático 2012 [PDF]

open access: yes, 2013
TCC(graduação) - Universidade Federal de Santa Catarina. Centro de Ciências Biológicas. Biologia.Este trabalho aborda a formação para a cidadania no conteúdo de Genética dos livros didáticos (LDs) de Biologia. A formação para a cidadania foi estabelecida
Pereira, Beatriz
core  

Clinical and molecular features of PRCD‐associated retinopathy

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose To describe the clinical and genetic characteristics of patients with biallelic disease‐causing variants in the PRCD (Progressive Rod‐Cone Degeneration) gene. Methods Multicentre, retrospective cohort study of 19 patients from 13 families across nine reference centres in six countries.
Vasil Kostin   +30 more
wiley   +1 more source

Producción científica española en el área de Genética

open access: yesRevista Española de Documentación Científica, 1996
Con este estudio bibliométrico se ha intentado conocer la situación que ocupa la investigación española en Genética biomédica a nivel internacional, así como dentro del contexto nacional.
Carmen Martín Moreno   +1 more
doaj   +1 more source

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