Results 91 to 100 of about 22,167,058 (263)

Fortalecimientos del centro nacional de tecnología agropecuaria y forestal.

open access: yes, 2013
Centro Nacional de Tecnología Agropecuaria y Forestal "Enrique Álvarez Córdova" (CENTA), es una institución autónoma de Derecho Público, de carácter científico y técnico con autonomía en lo administrativo, económico y técnico.
Consejo Nacional de Ciencia y Tecnología (CONACYT)
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CONACYT informa, septiembre-diciembre de 2010. [PDF]

open access: yes, 2010
En el Boletín de septiembre a diciembre del año 2010, Identifica los documentos impresos disponibles del CONACYT en este periodo y las temáticas son: Los Indicadores de ciencia y tecnología, Ponencia de divulgación en áreas temáticas de ciencia ...
Consejo Nacional de Ciencia y Tecnología (CONACYT)
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First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%–5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature.
Gabriela Roldão Correia‐Costa   +4 more
wiley   +1 more source

Memoria de labores 2009. [PDF]

open access: yes, 2009
La memoria de labores 2009 ha desarrollado acciones conducentes a promover la investigación científica por medio del CONACYT y ayuda de otras instituciones privadas. Principalmente se destaca el apoyo del Programa Iberoamericano para el programa de la
Consejo Nacional de Ciencia y Tecnología (CONACYT)
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A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Van Maldergem syndrome (VMLDS) is an ultra‐rare autosomal recessive disorder characterized by craniofacial dysmorphism, intellectual disability, hypotonia, skeletal anomalies, and feeding difficulties. It is caused by biallelic variants in DCHS1 or FAT4 genes.
Gabriela Roldão Correia‐Costa   +4 more
wiley   +1 more source

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

CONACYT informa, enero-abril de 2013. [PDF]

open access: yes, 2009
El Boletín del CONACYT de enero-abril de 2013, se enfoca principalmente en la difusión de la ciencia, tecnología e innovación de El Salvador y en este documento aborda los siguientes temas: 1.presentación de la Ley de Desarrollo Científico y Tecnológico,
Consejo Nacional de Ciencia y Tecnología (CONACYT)
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Genetic Variants of Na+,K+‐ATPase Associated With Neurological Disorders: A Systematic Review

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Neurological disorders encompass a wide range of severe symptoms and manifestations, many of which are associated with genetic variants that affect ionic homeostasis. Na+,K+‐ATPase, a transmembrane enzyme responsible for maintaining electrochemical gradients in cells, plays a crucial role in neuronal excitability and brain function.
Giovana Kummer da Rosa   +3 more
wiley   +1 more source

CONACYT informa, septiembre-diciembre de 2009. [PDF]

open access: yes, 2009
El Boletín de septiembre a diciembre del año 2009, identifica los siguientes contenidos: capacitación a investigadores en el uso y manejo de nuevas tecnologías agrícolas, difusión de indicadores de recursos humanos en ciencia y tecnología 1999-2007 ...
Consejo Nacional de Ciencia y Tecnología (CONACYT)
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Methacrylated Gelatin and Graphene Oxide Hybrid Hydrogels Composed‐Bioinks for 3D Tissue Engineering

open access: yesAdvanced NanoBiomed Research, EarlyView.
Bioinks made from hydrogels, such as methacrylated gelatin (GelMA), serve as the base material for bioprinted tissues, offering versatility and biocompatibility for a range of applications. Additional components however are still needed to improve functionality and mechanical stability of hydrogels. One of these components is graphene oxide (GO), added
Wanessa S. Mota   +10 more
wiley   +1 more source

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