Results 81 to 90 of about 153,813 (237)

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

Sociedad Rioplatense de Genética

open access: yes, 1951
Fil: Sociedad Rioplatense de ...
Sociedad Rioplatense de Genética
core  

It Takes Two to Tango: A Pluralist Account for Building Comprehensive Explanations in Human Evolution

open access: yesAmerican Anthropologist, EarlyView.
ABSTRACT The evolutionary study of human dispersal is a key topic in biological anthropology. However, recent research has revealed inconsistencies between molecular and anatomical data across different timescales and geographic regions. Despite increased interdisciplinary dialogue, these discordances are rarely analyzed in depth or interpreted for ...
Lumila Paula Menéndez, Sophie Veigl
wiley   +1 more source

Estudio de las deleciones de los genes GSTM1 y GSTT1 y del polimorfismo Ile105Val del gen GSTP1 en pacientes con enfermedad ósea de Paget

open access: yesRevista de Osteoporosis y Metabolismo Mineral, 2014
Fundamento: La enfermedad ósea de Paget (EOP) es un trastorno focal del hueso con aumento el número, tamaño y actividad de los osteoclastos. Algunos datos epidemiológicos apoyan la teoría de su relación con agentes ambientales tóxicos o infecciosos.
Usategui-Martín R   +12 more
doaj  

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

BIOMEDICINA GENÉTICA CLÍNICA Plano de Ensino 2016.1

open access: yes, 2016
Genética Humana e Médica; estudo de casos clínicos tipos de herança genética e grupos de patologias; doenças genéticas mais comuns; aspectos genéticos do Câncer; aspectos da Genética ...
CLÍNICA, GENÉTICA
core  

Morphology of Guard Hairs in Amazonian Marsupials: Intergeneric Variation, Habitat and Habit Association in a Phylogenetic Framework of the Order Didelphimorphia

open access: yesActa Zoologica, EarlyView.
ABSTRACT The cuticle and medulla of guard hairs exhibit distinct morphological patterns among mammalian species. To investigate this variability in marsupials from the Brazilian Amazon, we analysed guard hairs from nine Didelphimorphia species and incorporated data from an additional 25 didelphid species.
Matheus M. Bitencourt   +4 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

Geometric Morphometrics Reveal Body Shape Variation in Freshwater Shrimps of the Genus Macrobrachium Lacking a Mandibular Palp (Formerly Pseudopalaemon Sollaud, 1911) (Decapoda: Palaemonidae)

open access: yesActa Zoologica, EarlyView.
ABSTRACT Shape variation in the cephalothorax of Macrobrachium species without mandibular palp using geometric morphometrics was used as a tool to support species differentiation and propose new diagnostic characters for taxonomic identification.
Thaís Arrais Mota   +4 more
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  

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