Results 101 to 110 of about 559,485 (280)

Elucidating the Molecular Basis in a Cohort of Patients With Combined Bleeding Tendencies and Joint Hypermobility Manifestations

open access: yesHaemophilia, EarlyView.
ABSTRACT Background In patients with unexplained bleeding and normal haemostatic parameters, heritable disorders of connective tissue (HDCT) may be an underlying cause due to vascular fragility, as observed in Ehlers–Danlos syndrome (EDS) or Marfan syndrome (MS). This study aims to investigate the molecular profile of patients with joint hypermobility (
Perla Bandini   +11 more
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  

Microlitiasis alveolar pulmonar: presentación de un caso

open access: yesAnales de la Facultad de Medicina, 2018
La microlitiasis alveolar pulmonar es una enfermedad rara cuya principal característica es la acumulación de sales de calcio dentro del alvéolo pulmonar, esto debido a la presencia de una mutación genética autosómica recesiva.
Jose G. Somocurcio V.   +6 more
doaj   +1 more source

Seasonal dynamics in terrestrial insect communities after the impact of the Brumadinho tailings dam disaster

open access: yesInsect Conservation and Diversity, EarlyView.
Despite severe habitat loss, insect species richness, seasonal fluctuations in richness and temporal β‐diversity did not differ significantly among forests adjacent to the mudflow and reference sites. We found higher wet‐season species richness for ants, bees, butterflies and dung beetles, while termites showed no seasonal change; β‐diversity was ...
Frederico Neves   +11 more
wiley   +1 more source

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

Efecto de dos estrategias de agrupación de padres fantasmas en la evaluación genética de rasgos de crecimiento en el ganado Braunvieh mexicano

open access: gold, 2021
Luís Antonio Saavedra-Jiménez   +5 more
openalex   +2 more sources

Overexpression of SPARC obliterates the in vivo tumorigenicity of human hepatocellular carcinoma cells [PDF]

open access: yes, 2010
Hepatocellular carcinoma (HCC) is the sixth most common cancer and the third leading cause of cancer-related death worldwide. Current treatments are extremely disappointing.
Alaniz, Laura Daniela   +8 more
core   +1 more source

Genetic Parameter Estimation for Pregnancy Loss and Their Association With Reproductive and Growth Traits in Brahman Cattle Under Extensive Tropical Conditions

open access: yesJournal of Animal Breeding and Genetics, EarlyView.
ABSTRACT This study estimated genetic parameters for pregnancy loss (PL) in Brahman cattle and evaluated the genetic correlation of PL with growth and reproductive traits using both the pedigree relationship matrix (A) and pedigree plus genomic relationship matrix (H). Data were collected from two herds in Bolivia, focusing on three age groups: heifers,
Daniel Cardona‐Cifuentes   +7 more
wiley   +1 more source

Epistasis in Modifying Genes: Key Factor to Differentiate Clinical Subtypes in Neurodevelopmental Disorders

open access: yesRevista Finlay
Neurodevelopmental disorders group conditions in which the growth and development of the brain is altered. This can damage both the neurocognitive and behavioral spheres such as the development of language, emotions, behavior, self-control, learning and ...
José Ignacio Lao Villadóniga
doaj  

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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