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1.
Nature ; 592(7853): 195-204, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33828315

RESUMEN

The move from reading to writing the human genome offers new opportunities to improve human health. The United States National Institutes of Health (NIH) Somatic Cell Genome Editing (SCGE) Consortium aims to accelerate the development of safer and more-effective methods to edit the genomes of disease-relevant somatic cells in patients, even in tissues that are difficult to reach. Here we discuss the consortium's plans to develop and benchmark approaches to induce and measure genome modifications, and to define downstream functional consequences of genome editing within human cells. Central to this effort is a rigorous and innovative approach that requires validation of the technology through third-party testing in small and large animals. New genome editors, delivery technologies and methods for tracking edited cells in vivo, as well as newly developed animal models and human biological systems, will be assembled-along with validated datasets-into an SCGE Toolkit, which will be disseminated widely to the biomedical research community. We visualize this toolkit-and the knowledge generated by its applications-as a means to accelerate the clinical development of new therapies for a wide range of conditions.


Asunto(s)
Células/metabolismo , Edición Génica/métodos , Genoma Humano/genética , National Institutes of Health (U.S.)/organización & administración , Animales , Terapia Genética , Objetivos , Humanos , Estados Unidos
2.
Nature ; 574(7777): 187-192, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31597973

RESUMEN

Transformative technologies are enabling the construction of three-dimensional maps of tissues with unprecedented spatial and molecular resolution. Over the next seven years, the NIH Common Fund Human Biomolecular Atlas Program (HuBMAP) intends to develop a widely accessible framework for comprehensively mapping the human body at single-cell resolution by supporting technology development, data acquisition, and detailed spatial mapping. HuBMAP will integrate its efforts with other funding agencies, programs, consortia, and the biomedical research community at large towards the shared vision of a comprehensive, accessible three-dimensional molecular and cellular atlas of the human body, in health and under various disease conditions.


Asunto(s)
Atlas como Asunto , Investigación Biomédica/organización & administración , Cooperación Internacional , Modelos Anatómicos , National Institutes of Health (U.S.)/organización & administración , Análisis de la Célula Individual , Envejecimiento , Femenino , Salud , Humanos , Masculino , Biología Molecular/organización & administración , Especificidad de Órganos , Estados Unidos
4.
Nature ; 569(7758): 641-648, 2019 05.
Artículo en Inglés | MEDLINE | ID: mdl-31142853

RESUMEN

The NIH Human Microbiome Project (HMP) has been carried out over ten years and two phases to provide resources, methods, and discoveries that link interactions between humans and their microbiomes to health-related outcomes. The recently completed second phase, the Integrative Human Microbiome Project, comprised studies of dynamic changes in the microbiome and host under three conditions: pregnancy and preterm birth; inflammatory bowel diseases; and stressors that affect individuals with prediabetes. The associated research begins to elucidate mechanisms of host-microbiome interactions under these conditions, provides unique data resources (at the HMP Data Coordination Center), and represents a paradigm for future multi-omic studies of the human microbiome.


Asunto(s)
Recien Nacido Prematuro , Enfermedades Inflamatorias del Intestino/microbiología , Microbiota , National Institutes of Health (U.S.)/organización & administración , Estado Prediabético/microbiología , Investigación/organización & administración , Dieta , Femenino , Microbioma Gastrointestinal/fisiología , Interacciones Microbiota-Huesped/fisiología , Humanos , Recién Nacido , Infecciones/complicaciones , Infecciones/microbiología , Microbiota/fisiología , Estado Prediabético/complicaciones , Embarazo , Factores de Tiempo , Estados Unidos , Vagina/microbiología
10.
Nature ; 603(7899): 25-27, 2022 03.
Artículo en Inglés | MEDLINE | ID: mdl-35233098

Asunto(s)
Antivirales/uso terapéutico , Tratamiento Farmacológico de COVID-19 , Ensayos Clínicos como Asunto , Reposicionamiento de Medicamentos , Interacciones Huésped-Patógeno/efectos de los fármacos , SARS-CoV-2/efectos de los fármacos , Adenosina Monofosfato/administración & dosificación , Adenosina Monofosfato/análogos & derivados , Adenosina Monofosfato/uso terapéutico , Administración Oral , Alanina/administración & dosificación , Alanina/análogos & derivados , Alanina/uso terapéutico , Animales , Antiinflamatorios/administración & dosificación , Antiinflamatorios/uso terapéutico , Anticuerpos Monoclonales/administración & dosificación , Anticuerpos Monoclonales/uso terapéutico , Anticuerpos Neutralizantes/administración & dosificación , Anticuerpos Neutralizantes/economía , Anticuerpos Neutralizantes/uso terapéutico , Antivirales/administración & dosificación , Antivirales/farmacología , COVID-19/economía , COVID-19/inmunología , COVID-19/mortalidad , COVID-19/virología , Vacunas contra la COVID-19 , Citidina/análogos & derivados , Citidina/uso terapéutico , Depsipéptidos/farmacología , Depsipéptidos/uso terapéutico , Dexametasona/administración & dosificación , Dexametasona/uso terapéutico , Combinación de Medicamentos , Sinergismo Farmacológico , Ésteres/farmacología , Ésteres/uso terapéutico , Guanidinas/farmacología , Guanidinas/uso terapéutico , Hospitalización , Humanos , Hidroxilaminas/uso terapéutico , Internacionalidad , Lactamas/uso terapéutico , Leucina/uso terapéutico , Ratones , National Institutes of Health (U.S.)/organización & administración , Nitrilos/uso terapéutico , Factor 1 de Elongación Peptídica/antagonistas & inhibidores , Péptidos Cíclicos/farmacología , Péptidos Cíclicos/uso terapéutico , Prolina/uso terapéutico , Inhibidores de Proteasas/farmacología , Inhibidores de Proteasas/uso terapéutico , ARN Polimerasa Dependiente del ARN/antagonistas & inhibidores
11.
FASEB J ; 35(11): e21973, 2021 11.
Artículo en Inglés | MEDLINE | ID: mdl-34624149

RESUMEN

Contemporary science has become increasingly multi-disciplinary and team-based, resulting in unprecedented growth in biomedical innovation and technology over the last several decades. Collaborative research efforts have enabled investigators to respond to the demands of an increasingly complex 21st century landscape, including pressing scientific challenges such as the COVID-19 pandemic. A major contributing factor to the success of team science is the mobilization of core facilities and shared research resources (SRRs), the scientific instrumentation and expertise that exist within research organizations that enable widespread access to advanced technologies for trainees, faculty, and staff. For over 40 years, SRRs have played a key role in accelerating biomedical research discoveries, yet a national strategy that addresses how to leverage these resources to enhance team science and achieve shared scientific goals is noticeably absent. We believe a national strategy for biomedical SRRs-led by the National Institutes of Health-is crucial to advance key national initiatives, enable long-term research efficiency, and provide a solid foundation for the next generation of scientists.


Asunto(s)
Investigación Biomédica/organización & administración , COVID-19 , Colaboración Intersectorial , National Institutes of Health (U.S.)/organización & administración , Pandemias , SARS-CoV-2 , Academias e Institutos/organización & administración , Movilidad Laboral , Congresos como Asunto , Humanos , Políticas , Evaluación de Programas y Proyectos de Salud , Apoyo a la Investigación como Asunto , Sociedades Científicas/organización & administración , Participación de los Interesados , Estados Unidos , Universidades/organización & administración
15.
FASEB J ; 34(3): 3570-3582, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-31960495

RESUMEN

Biomedical research training has undergone considerable change over the past several years. At its core, the goal of graduate and postdoctoral training is to provide individuals with the skills and knowledge to become outstanding scientists and expand knowledge through the scientific method. Historically, graduate school training has focused on preparation for academic positions. Increasingly, however, a shift toward preparation for a wider range of career options has emerged. This is largely because most biomedical PhD graduates do not become Principal Investigators in academic laboratories. Here we describe an National Institutes of Health Common Fund program with the major goal of culture change for biomedical research training and training that prepares individuals for a broader expanse of careers in the biomedical research enterprise. These "Broadening Experiences in Scientific Training" (BEST) awards, issued in 2012 and 2013, provided support to institutions to develop innovative approaches to achieving these goals, as a complement to traditional training. Awardees were tasked with catalyzing change at their institutions and sharing best practices across the training community. Awardees were required to participate in a cross-site evaluation that assessed the impact of BEST activities on three main areas: (a) trainee confidence and knowledge to make career decisions, (b) influence of this added activity on time in training, and (c) ability of the institutions to sustain activities deemed to be beneficial. Here we present the fundamental approach to the BEST program and early evaluative data.


Asunto(s)
National Institutes of Health (U.S.)/organización & administración , Investigación Biomédica/educación , Humanos , Investigadores/educación , Estados Unidos
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