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Pesquisa : I01.409.418.750.600.650.496.450 [Categoria DeCS]
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[PMID]:27146411
[Au] Autor:Wood JD
[Ad] Endereço:Department of Physiology and Cell Biology, College of Medicine,, The Ohio State University, 305D Hamilton Hall, 1645 Neil Avenue, Columbus, OH, 43210-1218, USA. Jackie.Wood@osumc.edu.
[Ti] Título:GRG Profiles: Jackie D. Wood.
[So] Source:Dig Dis Sci;61(7):1793-802, 2016 07.
[Is] ISSN:1573-2568
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Pesquisa Biomédica/educação
Doenças do Sistema Digestório
Pessoal de Laboratório/educação
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)
[Mh] Termos MeSH secundário: Pesquisa Biomédica/métodos
Pesquisa Biomédica/tendências
Seres Humanos
Pessoal de Laboratório/tendências
Tutoria/métodos
Tutoria/tendências
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)/tendências
Estados Unidos
[Pt] Tipo de publicação:EDITORIAL
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171027
[Lr] Data última revisão:
171027
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:160506
[St] Status:MEDLINE
[do] DOI:10.1007/s10620-016-4182-6


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[PMID]:26507906
[Au] Autor:Irvin VL; Kaplan RM
[Ad] Endereço:College of Public Health and Human Sciences, School of Social & Behavioral Health Sciences, Oregon State University, 457 Waldo Hall, Corvallis, OR, 97331, USA. Veronica.irvin@oregonstate.edu.
[Ti] Título:Effect Sizes and Primary Outcomes in Large-Budget, Cardiovascular-Related Behavioral Randomized Controlled Trials Funded by NIH Since 1980.
[So] Source:Ann Behav Med;50(1):130-46, 2016 Feb.
[Is] ISSN:1532-4796
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:PURPOSE: We reviewed large-budget, National Institutes of Health (NIH)-supported randomized controlled trials (RCTs) with behavioral interventions to assess (1) publication rates, (2) trial registration, (3) use of objective measures, (4) significant behavior and physiological change, and (5) effect sizes. METHODS: We identified large-budget grants (>$500,000/year) funded by NIH (National Heart Lung and Blood Institute (NHLBI) or National Institute of Diabetes & Digestive and Kidney Diseases (NIDDK)) for cardiovascular disease (dates January 1, 1980 to December 31, 2012). Among 106 grants that potentially met inclusion criteria, 20 studies were not published and 48 publications were excluded, leaving 38 publications for analysis. ClinicalTrials.gov abstracts were used to determine whether outcome measures had been pre-specified. RESULTS: Three fourths of trials were registered in ClinicalTrials.gov and all published pre-specified outcomes. Twenty-six trials reported a behavioral outcome with 81 % reporting significant improvements for the target behavior. Thirty-two trials reported a physiological outcome. All were objectively measured, and 81 % reported significant benefit. Seventeen trials reported morbidity outcomes, and seven reported a significant benefit. Nine trials assessed mortality, and all were null for this outcome. CONCLUSIONS: Behavioral trials complied with trial registration standards. Most reported a physiological benefit, but few documented morbidity or mortality benefits.
[Mh] Termos MeSH primário: Doenças Cardiovasculares/terapia
National Heart, Lung, and Blood Institute (U.S.)/economia
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)/economia
Psicoterapia
Ensaios Clínicos Controlados Aleatórios como Assunto/economia
Ensaios Clínicos Controlados Aleatórios como Assunto/estatística & dados numéricos
Apoio à Pesquisa como Assunto/estatística & dados numéricos
[Mh] Termos MeSH secundário: Feminino
Seres Humanos
Masculino
Ensaios Clínicos Controlados Aleatórios como Assunto/normas
Resultado do Tratamento
Estados Unidos
[Pt] Tipo de publicação:JOURNAL ARTICLE; META-ANALYSIS; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, N.I.H., INTRAMURAL
[Em] Mês de entrada:1610
[Cu] Atualização por classe:170220
[Lr] Data última revisão:
170220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:151029
[St] Status:MEDLINE
[do] DOI:10.1007/s12160-015-9739-7


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[PMID]:26465948
[Au] Autor:Kelly KA; Hollingsworth MA; Brand RE; Liu CH; Singh VK; Srivastava S; Wasan AD; Yadav D; Andersen DK
[Ad] Endereço:From the *Department of Biomedical Engineering, University of Virginia, Charlottesville, VA; †Eppley Cancer Institute, University of Nebraska School of Medicine, Omaha, NE; ‡Division of Gastroenterology, Hepatology and Nutrition, Departments of Medicine and Anesthesiology and Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA; §Office of Cancer Nanotechnology Research and the Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, MD; ∥Division of Gastroenterology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD; ¶Cancer Biomarkers Research Group, Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, MD; and #Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
[Ti] Título:Advances in Biomedical Imaging, Bioengineering, and Related Technologies for the Development of Biomarkers of Pancreatic Disease: Summary of a National Institute of Diabetes and Digestive and Kidney Diseases and National Institute of Biomedical Imaging and Bioengineering Workshop.
[So] Source:Pancreas;44(8):1185-94, 2015 Nov.
[Is] ISSN:1536-4828
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:A workshop sponsored by the National Institute of Diabetes and Digestive and Kidney Diseases and the National Institute of Biomedical Imaging and Bioengineering focused on research gaps and opportunities in the development of new biomarkers of pancreatic disease. The session was held on July 22, 2015, and structured into 6 sessions: 1) Introduction and Overview; 2) Keynote Address; 3) New Approaches to the Diagnosis of Chronic Pancreatitis; 4) Biomarkers of Pain and Inflammation; 5) New Approaches to the Detection of Pancreatic Cancer; and 6) Shed Exosomes, Shed Cells, and Shed Proteins. Recent advances in the fields of pancreatic imaging, functional markers of pancreatic disease, proteomics, molecular and cellular imaging, and detection of circulating cancer cells and exosomes were reviewed. Knowledge gaps and research needs were highlighted. The development of new methods for the noninvasive determination of pancreatic pathology; the use of cellular markers of pancreatic function, inflammation, pain, and malignancy; and the refinement of methods to identify cells and cellular constituents of pancreatic cancer were discussed. The further refinement of sophisticated technical methods and the need for clinical studies to validate these new approaches in large-scale studies of patients at risk for the development of pancreatic disease were repeatedly emphasized.
[Mh] Termos MeSH primário: Bioengenharia/métodos
Biomarcadores/análise
Diagnóstico por Imagem/métodos
Pancreatopatias/diagnóstico
[Mh] Termos MeSH secundário: Bioengenharia/tendências
Diagnóstico por Imagem/tendências
Seres Humanos
National Institute of Biomedical Imaging and Bioengineering (U.S.)
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)
Pancreatopatias/terapia
Neoplasias Pancreáticas/diagnóstico
Neoplasias Pancreáticas/terapia
Pancreatite Crônica/diagnóstico
Pancreatite Crônica/terapia
Estados Unidos
[Pt] Tipo de publicação:CONGRESSES
[Nm] Nome de substância:
0 (Biomarkers)
[Em] Mês de entrada:1608
[Cu] Atualização por classe:170220
[Lr] Data última revisão:
170220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:151015
[St] Status:MEDLINE
[do] DOI:10.1097/MPA.0000000000000552


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[PMID]:26393351
[Au] Autor:Whetzel PL; Grethe JS; Banks DE; Martone ME
[Ad] Endereço:Center for Research in Biological Systems, University of California, San Diego, San Diego, California, United States of America.
[Ti] Título:The NIDDK Information Network: A Community Portal for Finding Data, Materials, and Tools for Researchers Studying Diabetes, Digestive, and Kidney Diseases.
[So] Source:PLoS One;10(9):e0136206, 2015.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The NIDDK Information Network (dkNET; http://dknet.org) was launched to serve the needs of basic and clinical investigators in metabolic, digestive and kidney disease by facilitating access to research resources that advance the mission of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). By research resources, we mean the multitude of data, software tools, materials, services, projects and organizations available to researchers in the public domain. Most of these are accessed via web-accessible databases or web portals, each developed, designed and maintained by numerous different projects, organizations and individuals. While many of the large government funded databases, maintained by agencies such as European Bioinformatics Institute and the National Center for Biotechnology Information, are well known to researchers, many more that have been developed by and for the biomedical research community are unknown or underutilized. At least part of the problem is the nature of dynamic databases, which are considered part of the "hidden" web, that is, content that is not easily accessed by search engines. dkNET was created specifically to address the challenge of connecting researchers to research resources via these types of community databases and web portals. dkNET functions as a "search engine for data", searching across millions of database records contained in hundreds of biomedical databases developed and maintained by independent projects around the world. A primary focus of dkNET are centers and projects specifically created to provide high quality data and resources to NIDDK researchers. Through the novel data ingest process used in dkNET, additional data sources can easily be incorporated, allowing it to scale with the growth of digital data and the needs of the dkNET community. Here, we provide an overview of the dkNET portal and its functions. We show how dkNET can be used to address a variety of use cases that involve searching for research resources.
[Mh] Termos MeSH primário: Diabetes Mellitus/patologia
Doenças do Sistema Digestório/patologia
Serviços de Informação
Nefropatias/patologia
[Mh] Termos MeSH secundário: Animais
Bases de Dados Factuais
Seres Humanos
Modelos Animais
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)
Pesquisa
Ferramenta de Busca
Estados Unidos
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL
[Em] Mês de entrada:1606
[Cu] Atualização por classe:170220
[Lr] Data última revisão:
170220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:150923
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0136206


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[PMID]:26040640
[Au] Autor:Sanghvi A; Redman LM; Martin CK; Ravussin E; Hall KD
[Ad] Endereço:National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD; and.
[Ti] Título:Validation of an inexpensive and accurate mathematical method to measure long-term changes in free-living energy intake.
[So] Source:Am J Clin Nutr;102(2):353-8, 2015 Aug.
[Is] ISSN:1938-3207
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Accurate measurement of free-living energy intake (EI) over long periods is imperative for understanding obesity and its treatment. Unfortunately, traditional methods rely on self-report and are notoriously inaccurate. Although EI can be indirectly estimated by the intake-balance method, this technique is prohibitively labor-intensive and expensive, requiring repeated measures of energy expenditure via doubly labeled water (DLW) along with multiple dual-energy X-ray absorptiometry (DXA) scans to measure changes in body energy stores. OBJECTIVE: Our objective was to validate a mathematical method to measure long-term changes in free-living energy intake. DESIGN: We measured body weight and EI changes (ΔEI) over 4 time intervals by using the intake-balance method in 140 individuals who underwent 2 y of caloric restriction as part of the Comprehensive Assessment of Long-term Effects of Reducing Intake of Energy study. We compared the ΔEI values calculated by using DLW/DXA with those obtained by using a mathematical model of human metabolism whose only inputs were the initial demographic information and repeated body weight data. RESULTS: The mean ΔEI values calculated by the model were within 40 kcal/d of the DLW/DXA method throughout the 2-y study. For individual subjects, the overall root mean square deviation between the model and DLW/DXA method was 215 kcal/d, and most of the model-calculated ΔEI values were within 132 kcal/d of the DLW/DXA method. CONCLUSIONS: Accurate and inexpensive estimates of ΔEI that are comparable to the DLW/DXA method can be obtained by using a mathematical model and repeated body weight measurements.
[Mh] Termos MeSH primário: Dieta Redutora
Ingestão de Energia
Modelos Biológicos
Avaliação Nutricional
Sobrepeso/dietoterapia
Perda de Peso
[Mh] Termos MeSH secundário: Adulto
Algoritmos
Índice de Massa Corporal
Peso Corporal
Restrição Calórica
Metabolismo Energético
Feminino
Seres Humanos
Masculino
Meia-Idade
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)
Sobrepeso/metabolismo
Reprodutibilidade dos Testes
Estados Unidos
Adulto Jovem
[Pt] Tipo de publicação:CLINICAL TRIAL; JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; VALIDATION STUDIES
[Em] Mês de entrada:1510
[Cu] Atualização por classe:170222
[Lr] Data última revisão:
170222
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:150605
[Cl] Clinical Trial:ClinicalTrial
[St] Status:MEDLINE
[do] DOI:10.3945/ajcn.115.111070


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[PMID]:25775180
[Au] Autor:Lumeng JC; Taveras EM; Birch L; Yanovski SZ
[Ad] Endereço:Division of Child Behavioral Health, Department of Pediatrics, University of Michigan, Ann Arbor2Department of Environmental Health Sciences, School of Public Health, University of Michigan, Ann Arbor3Center for Human Growth and Development, University of.
[Ti] Título:Prevention of obesity in infancy and early childhood: a National Institutes of Health workshop.
[So] Source:JAMA Pediatr;169(5):484-90, 2015 May.
[Is] ISSN:2168-6211
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Addressing the childhood obesity epidemic continues to be a challenge. Given that once obesity develops it is likely to persist, there has been an increasing focus on prevention at earlier stages of the life course. Research to develop and implement effective prevention and intervention strategies in the first 2 years after birth has been limited. In fall 2013, the National Institute of Diabetes and Digestive and Kidney Diseases convened a multidisciplinary workshop to summarize the current state of knowledge regarding the prevention of infant and early childhood obesity and to identify research gaps and opportunities. The questions addressed included (1) "What is known regarding risk for excess weight gain in infancy and early childhood?" (2) "What is known regarding interventions that are promising or have been shown to be efficacious?" and (3) "What are the challenges and opportunities in implementing and evaluating behavioral interventions for parents and other caregivers and their young children?"
[Mh] Termos MeSH primário: Obesidade Pediátrica/prevenção & controle
[Mh] Termos MeSH secundário: Pré-Escolar
Educação
Seres Humanos
Lactente
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)
Estados Unidos
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL
[Em] Mês de entrada:1507
[Cu] Atualização por classe:150826
[Lr] Data última revisão:
150826
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:150317
[St] Status:MEDLINE
[do] DOI:10.1001/jamapediatrics.2014.3554


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[PMID]:25770083
[Au] Autor:Grey MJ; James SP; Rodgers GP
[Ad] Endereço:Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.
[Ti] Título:NIDDK Programs and Emerging Opportunities for Digestive Diseases Research.
[So] Source:Gastroenterology;148(5):868-76, 2015 May.
[Is] ISSN:1528-0012
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Pesquisa Biomédica/economia
Doenças do Sistema Digestório
Gastroenterologia/economia
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)/economia
Apoio à Pesquisa como Assunto/economia
[Mh] Termos MeSH secundário: Doenças do Sistema Digestório/diagnóstico
Doenças do Sistema Digestório/fisiopatologia
Doenças do Sistema Digestório/terapia
Seres Humanos
Revisão da Pesquisa por Pares
Estados Unidos
[Pt] Tipo de publicação:EDITORIAL
[Em] Mês de entrada:1506
[Cu] Atualização por classe:150424
[Lr] Data última revisão:
150424
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:150315
[St] Status:MEDLINE


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[PMID]:25673806
[Au] Autor:Hill WG
[Ad] Endereço:Nephrology Division, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts whill@bidmc.harvard.edu.
[Ti] Título:New impetus for innovation in benign urology.
[So] Source:Am J Physiol Renal Physiol;308(8):F797-8, 2015 Apr 15.
[Is] ISSN:1522-1466
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Pesquisa Biomédica/tendências
Difusão de Inovações
Motivação
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)/tendências
Pesquisadores/tendências
Apoio à Pesquisa como Assunto/tendências
Doenças Urológicas
Urologia/tendências
[Mh] Termos MeSH secundário: Animais
Pesquisa Biomédica/economia
Prioridades em Saúde/tendências
Seres Humanos
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)/economia
Pesquisadores/economia
Apoio à Pesquisa como Assunto/economia
Estados Unidos
Doenças Urológicas/diagnóstico
Doenças Urológicas/fisiopatologia
Doenças Urológicas/terapia
Urologia/economia
[Pt] Tipo de publicação:EDITORIAL
[Em] Mês de entrada:1506
[Cu] Atualização por classe:150416
[Lr] Data última revisão:
150416
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:150213
[St] Status:MEDLINE
[do] DOI:10.1152/ajprenal.00021.2015


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[PMID]:25533002
[Au] Autor:Bharucha AE; Dunivan G; Goode PS; Lukacz ES; Markland AD; Matthews CA; Mott L; Rogers RG; Zinsmeister AR; Whitehead WE; Rao SS; Hamilton FA
[Ad] Endereço:Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.
[Ti] Título:Epidemiology, pathophysiology, and classification of fecal incontinence: state of the science summary for the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) workshop.
[So] Source:Am J Gastroenterol;110(1):127-36, 2015 Jan.
[Is] ISSN:1572-0241
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:In August 2013, the National Institutes of Health sponsored a conference to address major gaps in our understanding of the epidemiology, pathophysiology, and management of fecal incontinence (FI) and to identify topics for future clinical research. This article is the first of a two-part summary of those proceedings. FI is a common symptom, with a prevalence that ranges from 7 to 15% in community-dwelling men and women, but it is often underreported, as providers seldom screen for FI and patients do not volunteer the symptom, even though the symptoms can have a devastating impact on the quality of life. Rough estimates suggest that FI is associated with a substantial economic burden, particularly in patients who require surgical therapy. Bowel disturbances, particularly diarrhea, the symptom of rectal urgency, and burden of chronic illness are the strongest independent risk factors for FI in the community. Smoking, obesity, and inappropriate cholecystectomy are emerging, potentially modifiable risk factors. Other risk factors for FI include advanced age, female gender, disease burden (comorbidity count, diabetes), anal sphincter trauma (obstetrical injury, prior surgery), and decreased physical activity. Neurological disorders, inflammatory bowel disease, and pelvic floor anatomical disturbances (rectal prolapse) are also associated with FI. The pathophysiological mechanisms responsible for FI include diarrhea, anal and pelvic floor weakness, reduced rectal compliance, and reduced or increased rectal sensation; many patients have multifaceted anorectal dysfunctions. The type (urge, passive or combined), etiology (anorectal disturbance, bowel symptoms, or both), and severity of FI provide the basis for classifying FI; these domains can be integrated to comprehensively characterize the symptom. Several validated scales for classifying symptom severity and its impact on the quality of life are available. Symptom severity scales should incorporate the frequency, volume, consistency, and nature (urge or passive) of stool leakage. Despite the basic understanding of FI, there are still major knowledge gaps in disease epidemiology and pathogenesis, necessitating future clinical research in FI.
[Mh] Termos MeSH primário: Incontinência Fecal/classificação
Incontinência Fecal/epidemiologia
Incontinência Fecal/fisiopatologia
[Mh] Termos MeSH secundário: Canal Anal/fisiopatologia
Educação
Incontinência Fecal/etiologia
Feminino
Seres Humanos
Masculino
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)
Diafragma da Pelve/fisiopatologia
Prevalência
Qualidade de Vida
Fatores de Risco
Índice de Gravidade de Doença
Estados Unidos
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, U.S. GOV'T, P.H.S.
[Em] Mês de entrada:1503
[Cu] Atualização por classe:170714
[Lr] Data última revisão:
170714
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:141224
[St] Status:MEDLINE
[do] DOI:10.1038/ajg.2014.396


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[PMID]:25376765
[Au] Autor:Rasooly RS; Akolkar B; Spain LM; Guill MH; Del Vecchio CT; Carroll LE
[Ad] Endereço:Division of Kidney, Urologic and Hematologic Diseases, and rebekah.rasooly@nih.gov.
[Ti] Título:The National Institute of Diabetes and Digestive and Kidney Diseases Central Repositories: a valuable resource for nephrology research.
[So] Source:Clin J Am Soc Nephrol;10(4):710-5, 2015 Apr 07.
[Is] ISSN:1555-905X
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Central Repositories, part of the National Institutes of Health (NIH), are an important resource available to researchers and the general public. The Central Repositories house samples, genetic data, phenotypic data, and study documentation from >100 NIDDK-funded clinical studies, in areas such as diabetes, digestive disease, and liver disease research. The Central Repositories also have an exceptionally rich collection of studies related to kidney disease, including the Modification of Diet in Renal Disease landmark study and recent data from the Chronic Renal Insufficiency Cohort and CKD in Children Cohort studies. The data are carefully curated and linked to the samples from the study. The NIDDK is working to make the materials and data accessible to researchers. The Data Repositories continue to improve flexible online searching tools that help researchers identify the samples or data of interest, and NIDDK has created several different paths to access the data and samples, including some funding initiatives. Over the past several years, the Central Repositories have seen steadily increasing interest and use of the stored materials. NIDDK plans to make more collections available and do more outreach and education about use of the datasets to the nephrology research community in the future to enhance the value of this resource.
[Mh] Termos MeSH primário: Pesquisa Biomédica/métodos
Bases de Dados Factuais
National Institute of Diabetes and Digestive and Kidney Diseases (U.S.)
Nefrologia/métodos
[Mh] Termos MeSH secundário: Acesso à Informação
Comportamento Cooperativo
Mineração de Dados
Seres Humanos
Disseminação de Informação
Comunicação Interdisciplinar
Cooperação Internacional
Estados Unidos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1601
[Cu] Atualização por classe:160407
[Lr] Data última revisão:
160407
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:141108
[St] Status:MEDLINE
[do] DOI:10.2215/CJN.06570714



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