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Human Development

Human Development: The process of physical, mental, emotional, and social growth and change that occurs throughout the human lifespan.
This encompasses the development of cognitive, language, motor, and social-emotional capabilities.
Key stages include prenatal, childhood, adolescence, and adulthood.
Reasearchers leverage advanced techniques, such as PubCompare.ai's AI-powered insights, to optimize research protocols and accelerate discoveries that enhance human potential and wellbeing.

Most cited protocols related to «Human Development»

A full description of the materials and methods is available in the supplementary materials. Briefly, we precisely dissected multiple brain regions (HIP, STR, AMY, cerebellum, thalamus, and 11 neocortical areas) in more than 60 postmortem human brains ranging in age from 5 PCW to 64 PY. We then applied bulk tissue RNA-seq, scRNA-seq and snRNA-seq, smRNA-seq, DNA methylation assay, or ChIP-seq to generate multimodal datasets, often from the same brain. After applying stringent quality control checks and independent analysis of each dataset, we performed integrated analyses to gain insights into human brain development, function, and disease.
Publication 2018
Autopsy Biological Assay Brain Cerebellum Chromatin Immunoprecipitation Sequencing Dietary Fiber DNA Methylation Homo sapiens Human Development Multimodal Imaging RNA-Seq Single-Cell RNA-Seq Small Nuclear RNA Thalamus Tissues
We invited authors of eligible datasets to contribute de-identified primary data. Two investigators independently extracted country, recruitment setting (non-medical, primary care, inpatient specialty, outpatient specialty), and diagnostic interview from published reports, with disagreements resolved by consensus. We categorized countries as “very high,” “high,” or “low-medium” development on the basis of the United Nations’ human development index.26 Participant level data included age, sex, major depression status, current mental health diagnosis or treatment, and PHQ-9 scores. In two primary studies, multiple recruitment settings were included, so recruitment setting was coded at the participant level. When datasets included statistical weights to reflect sampling procedures, we used the weights provided. For studies in which sampling procedures merited weighting but the original study did not weight, we constructed weights by using inverse selection probabilities. Weighting occurred, for instance, when a diagnostic interview was administered to all participants with positive screens and a random subset of participants with negative screens.
We converted individual participant data to a standard format and synthesized them into a single dataset with study level data. We compared published participant characteristics and diagnostic accuracy results with results from raw datasets and resolved any discrepancies in consultation with the original investigators.
Two investigators assessed risk of bias of included studies independently, on the basis of the primary publications, using the Quality Assessment of Diagnostic Accuracy Studies-2 tool (supplementary methods B).27 (link) Discrepancies were resolved by consensus.
Publication 2019
Diagnosis Human Development Inpatient Major Depressive Disorder Mental Health Outpatients Primary Health Care Tests, Diagnostic
Sixteen regions of the macaque brain spanning from early prenatal to adulthood were dissected using the same standardized protocol used for human specimens and described in the accompanying study by Li et al ((33 ); see also (32 )). The macaque brain regions and developmental timepoints matched human brain regions and timepoints analyzed in the study by Li et al ((33 )). The sampled homologous brain regions were identified using anatomical landmarks provided in the macaque brain atlas (74 ). An overview of dissected brain regions is provided in fig. S1. Translating Time model (38 (link)) was used to identify equivalent timepoints between macaque and human prenatal development. The list of macaque brains used in this study and relevant metadata are provided in tables S12. Macaque studies were carried out in accordance with a protocol approved by Yale University’s Committee on Animal Research and NIH guidelines.
We performed tissue-level RNA extraction and sequencing of all 16 regions, single-cell RNA-Seq of dorsolateral prefrontal cortex [DFC], hippocampus [HIP], amygdala [AMY], striatum [STR], mediodorsal nucleus of the thalamus [MD], and cerebellar cortex [CBC] of mid-fetal macaque, and single-nucleus RNA-Seq of DFC of adult macaque. Single cell/nucleus sample processing was done with 10X Genomics and sequencing was done with Illumina platforms.
For tissue-level analysis, we generated annotation of human-macaque orthologs using the XSAnno pipeline, and matched the developmental age of human and macaque samples based on their respective transcriptome using our algorithm TranscriptomeAge. We also developed TempShift, a method based on Gaussian process model, to reveal the inter-regional differences, inter-species divergence, and genes with heterotopic and heterochronic expression. We also queried differentially expressed genes for enrichment in transcription factor binding sites using findMotifs.pl, and analyzed inter-species differential exon usage using the R package DEXSeq.
The single cell/nucleus data was first analysed by cellranger for decoding, alignment, quality filtering, and UMI counting. After that, data was further analyzed with Seurat according to its guidelines, and cell types were clustered for classification with SpecScore.R. In order to perform direct comparisons between human and macaque at the single-cell level, we focused on the homologous genes between these species and aligned monkey and human cells together to further analyze inter-species divergence of homologous cell types (fig. S47). We used MetageneBicorPlot function to examine the correlation of neuronal and glial cell subtypes, and we employed the correlation analysis to detect the correspondence of excitatory neuron and interneuron subtypes. Finally, we did functional enrichment of disease-associated genes in both tissue-level and single-cell datasets.
Publication 2018
Adult Allogeneic Cells Amygdaloid Body Anatomic Landmarks Binding Sites Brain Cell Nucleus Cells Cortex, Cerebellar Dorsolateral Prefrontal Cortex Ectopic Tissue Exons Fetus Genes Hereditary Diseases Homo sapiens Human Development Interneurons Macaca Monkeys Neuroglia Neurons Nucleus Solitarius RNA-Seq Seahorses Single-Cell RNA-Seq Strains Striatum, Corpus Thalamic Nuclei Tissues Transcription Factor Transcriptome
Twenty-five hundred adults, ages 25-45, were enrolled in METS between January 2010 and September 2011 and have had energy expenditure, dietary intake, body weight and composition, and biomarkers of obesity and diabetes measured at baseline. The participants will all be followed over the subsequent 24 months to assess change in body weight, composition, and diabetes and CVD risk. Five hundred participants, 50% of whom are female, were enrolled in each of five study sites: rural Ghana, urban South Africa, Seychelles, urban Jamaica and suburban United States (Chicago area). The populations sampled are of African descent and provide a range of body sizes, i.e., the mean BMIs of adults from the study sites vary from a low of about 24 kg/m2 in rural Nkwantakese (Ghana) to a high of 31 kg/m2 in suburban Maywood (USA). The study sites also represent a range of social and economic development as defined by the UN Human Development Index (HDI) 2010: Ghana is defined as a low HDI country, South Africa as middle HDI, Jamaica and Seychelles as high HDI and the US as a very high HDI country [28 ].
The in-country study sites include the town of Nkwantakese in the Afigya-Kwabre District of the Ashanti Region of Ghana and its surrounding villages. The town is situated to the southwest of Agona Ashanti the District Capital, and is about 20km from Kumasi with a population of approximately 17,000. Khayelitsha is the 3rd largest township in South Africa and is adjacent to the city of Cape Town. The population is about 500,000 with 80 percent of the residents living in temporary housing and 40 percent unemployed. The study site in Jamaica is in Kingston, the capital and largest city with a population of 651,880. In Seychelles, individuals have been recruited from the main island of the archipelago, Mahé, which includes approximately 75,000 inhabitants for a surface of 155 km2. Mahé can be qualified as semi-urban and its economy is mainly driven by tourism, industrial fishing and services. Seychelles is located approximately 1,600 km east of Kenya in the Indian Ocean, and approximately 2,000 km north of the island of Mauritius, and has a total population of about 87,000. Maywood, in the US, is an African-American working class community adjacent to the western border of Chicago, Illinois, with a population of approximately 24,903 people. The research clinic is on the campus of Stritch School of Medicine, Loyola University, within walking distance of most neighborhoods and is well known to local residents. The coordinating center for METS is also located in Maywood, IL at Loyola University.
We excluded individuals with obvious infectious diseases (including active malaria), pregnant or lactating women, and HIV positive individuals. Any individual that has a condition preventing them from engaging in normal physical activities, such as severe osteo'- or rheumatoid arthritis, lower extremity disability, was also excluded from METS. Population-based surveys have been previously carried out in each of the sites, thus investigators from each site decided upon the best means of recruiting a representative sample from their respective communities. In Nkwantakese, Ghana, a simple random sample was generated for the age-range of the study from the population census for Nkwantakese and its surrounding villages. In both Seychelles and South Africa sex- and age-stratified random samples were generated from their respective national censuses. In Kingston, Jamaica, districts were randomly sampled; beginning from a fixed point in each district (e.g., the north-west corner), and door-to-door recruitment took place. Similarly, in Maywood, IL, USA, all city blocks in the community were randomized and door-to-door recruitment was conducted.
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Publication 2011
Adult African American Biological Markers Body Size Body Weight Communicable Diseases Diabetes Mellitus Disabled Persons Energy Metabolism Females HIV Seropositivity Human Body Human Development Lower Extremity Malaria Negroid Races Obesity Rheumatoid Arthritis Woman
In this Article, we built on GBD 201351 (link) concepts by improving the interpretability of sociodemographic status and characterising and describing this relationship in more detail for years of life lost due to premature mortality (YLLs), as well as highlighting changes in age-standardised death rates, population age structure, and YLL rates. We have made two important changes to the GBD 2013 computation. First, we have used only lag-dependent income per capita, average educational attainment in the population over age 15 years, and the total fertility rate. We excluded the mean age of the population because it is directly affected by death rates. Second, we have applied the methods used to compute the Human Development Index to generate an interpretable scale, resulting in the Socio-demographic Index (SDI).52 The Human Development Index method weights each component equally and rescales each component on a zero-to-one scale with zero being the lowest value observed in the time period 1980 to 2015 and 1 being the highest value observed. The final composite SDI value is the geometric mean of each of the components. The SDI ranges from 0·060 in Mozambique in 1987 to 0·978 in Washington, DC, USA, in 2015. The correlation of the SDI with the sociodemographic status principal component analysis used in GBD 2013 was 0·982. The very high correlation is because the principal component analysis yields weights that are nearly equal across components. The advantage of the index is that 1 can be interpreted as the level of SDI at which a geography has the highest observed log income per capita and educational attainment and lowest fertility rate. We tested whether alternative lags of the components of SDI would provide a better predictor of outcomes such as life expectancy and age-specific probabilities of death. Using lag distributed income per capita, educational attainment, and the total fertility rate in the current year was the most predictive of these mortality outcomes (methods appendix p 286).
To report on aggregate results, we divided geographies into SDI quintiles in 2015. Quintile cutoffs were based on the entire distribution of geography–years from 1980 to 2015, excluding populations smaller than 1 million. Figure 9 shows a map of the SDI level in 2015 categorised into five groups including subnational geographies. Because SDI includes educational attainment and the total fertility rate, some countries which have very high income, such as Saudi Arabia, are classified in the second quintile of SDI because of lower educational attainment and higher fertility rates.53
To capture the average relationships for each age–sex–cause group, we used spline regression of death rates on SDI (methods appendix pp 285–86). To ensure a coherent set of estimated death rates for Levels 1, 2, and 3 in the GBD cause hierarchy for each level of SDI, the Level 2 death rates were rescaled such that for each age–sex–cause bin, the sum of Level 2 death rates equalled the Level 1 death rate. This procedure was repeated for Level 3 and Level 2 causes. These rates were used as the expected death rates by age–sex–cause and SDI. Various summary measures have been computed on the basis of the age–sex–cause-specific predictions based on SDI, including age-standardised death rates, age-standardised YLL rates, and life expectancy at birth.
To further characterise how patterns of crude death rates and death numbers change with SDI, we have computed the average population age structure associated with each SDI level. These population age structures have then been used to estimate how crude death rates and death numbers by cause are expected to change with rising SDI.
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Publication 2016
Age Groups Birth Head Human Development Prognosis

Most recents protocols related to «Human Development»

Example 7

The development of fully human monoclonal antibodies directed against human IL-17RA was carried out using Abgenix (now Amgen Fremont Inc.) XenoMouse® technology (U.S. Pat. Nos. 6,114,598; 6,162,963; 6,833,268; 7,049,426; 7,064,244, which are incorporated herein by reference in their entirety; Green et al, 1994, Nature Genetics 7:13-21; Mendez et al., 1997, Nature Genetics 15:146-156; Green and Jakobovitis, 1998, J. Ex. Med. 188:483-495)). TABLE 4 shows the portions of the IL-17RA protein used as an immunogen and cell lines used to generate and screen anti-IL-17RA antibodies.

TABLE 4
ReagentDescription
IL-17RA.FcHuman IL-17RA extracellular domain with a
C-terminal human Fc domain. Expressed in a
stable CHO cell line.
IL-17RA-FLAG-polyHisHuman IL-17RA extracellular domain with a
(SEQ ID NO: 431)C-terminal FLAG-polyHis tag. Expressed by
transient transfection in COS PKB cells.
IL-17RA CHO cellsHuman IL-17RA full-length expressed on the
surface of CHO cells.

IgG2 XenoMouse® mice were immunized/boosted with IL-17RA-Fc (group 1) and IL-17RA-FLAG-polyHis (group 2). Serum titers were monitored by ELISA and mice with the best titers were fused to generate hybridomas. The resulting polyclonal supernatants were screened for binding to IL-17RA by ELISA, and the positive supernatants were screened for binding to IL-17RA CHO cells by FMAT. Positive supernatants were subjected to additional screening. IgG2 XenoMouse® mice were immunized with the following immunogens: IL-17RA-Fc (group 3) and IL-17RA-FLAG-pHis (group 4) and were tested following additional immunizations.

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Patent 2024
Anti-Antibodies Antigens Binding Proteins Cell Lines CHO Cells COS Cells Enzyme-Linked Immunosorbent Assay GPI protein, human Homo sapiens Human Development Hybridomas IgG2 IL17RA protein, human Immunization Monoclonal Antibodies Mus Natural Childbirth Proteins Serum Transfection Transients
Five socioeconomic indicators were included as SSDH: (1) Community Human Development Index (CHDI), (2) urban/rural location of the district, (3) school type, (4) caregiver’s education, and (5) family income (see Table 1).
CHDI is a local adjustment indicator created by the Chilean office of the United Nations Development Program [24 ]. CHDI estimates district-level development conceptualized as social advantage in the country and allows comparison between districts. Interpretation of this indicator is national; it cannot be used to compare across countries. To define location as urban or rural, we used the Chilean National Statistics Institute (INE) criteria, which defines a rural community as less than 1,000 inhabitants, or with less than 50% of the population working in secondary or tertiary occupational activities. School type is defined by the Chilean Ministry of Education as public, private subsidized (partially subsidized by the government), and private paid (not subsidized by the government).
Formal caregiver/parents’ education level was categorized as: primary (up to 8 years), secondary (8 to 12 years), and post-secondary (more than 12 years). Family income at the examination was considered as an ordinal variable of six categories, with the lowest category at the Chilean monthly minimum salary CLP $225,000 (approximately USD $300), and each category increasing in increments of CLP $500,000 (approximately USD $700).
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Publication 2023
Homo sapiens Human Development Parent Program Development Rural Communities

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Publication 2023
COVID 19 Head Households Human Development Infection Light Medical Devices Range of Motion, Articular
The following formula, which is like that used by the United Nations Development Programme (UNDP) in calculations of the Human Development Index [53 ], the Health Development Governance Index [54 ], Malawi NHRS Index [21 (link)], African NHRS Barometer [22 , 23 ], and EDCTP African Participating States NHRS Barometer, was used to calculate all indices for the 17 individual sub-functions: NHRSsub-functionindex=Actualxiscore-MinimumxiscoreMaximumxiscore-Minimumxiscore where xi is the i.th sub-function, such as existence of a national research ethics review committee (NEC)
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Publication 2023
Human Development Negroid Races Program Development
Using each of the domain specific variables, we first created sub-indices j {j = 1, 2, 3, 4} using the following formula for each district d in country c {c = Bangladesh, India, Pakistan}: SubIndexc,d,j=Xc,d,j-minXc,d,jmaxXc,d,j-minXc,d,j
Xc,d,j is the sub-national domain specific value, while minXc,d,j and maxXc,d,j are the country-domain specific minimum and maximum values of the variable at the district (sub-national) level. After generating sub-indices for each domain-district-country, we use simple arithmetic mean to generate the composite CR-Index for each district in each country, following the human development index (HDI) construction method of the UNDP for wide acceptability25 . Formally, CRIndexc,d=j=1nSubIndexc,d,jn
Here n is the number of domains. We used arithmetic mean, given some sub-indexes generated zero value (for example, some districts did not have any reported international migration, resulting in a score of zero for that sub-index). The process of CR-Index construction normalizes the variables based on the minimum and maximum variation of each variable across sub-nations for each country.
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Publication 2023
Human Development

Top products related to «Human Development»

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The ELISA development kit is a laboratory tool designed for the development and optimization of enzyme-linked immunosorbent assays (ELISA). The kit provides the necessary components, including microtiter plates, antibodies, and reagents, to facilitate the custom design and testing of ELISA protocols. The core function of this product is to enable researchers to establish and refine ELISA-based detection and quantification methods for various analytes.
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Bovine serum albumin (BSA) is a common laboratory reagent derived from bovine blood plasma. It is a protein that serves as a stabilizer and blocking agent in various biochemical and immunological applications. BSA is widely used to maintain the activity and solubility of enzymes, proteins, and other biomolecules in experimental settings.
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More about "Human Development"

Human Development encompasses the physical, mental, emotional, and social growth and changes that occur throughout the lifespan.
This encompasses the development of cognitive, language, motor, and social-emotional capabilities, spanning from prenatal to adulthood stages.
Researchers leverage advanced techniques, such as PubCompare.ai's AI-powered insights, to optimize research protocols and accelerate discoveries that enhance human potential and wellbeing.
Key aspects of human development research include the use of various ELISA (Enzyme-Linked Immunosorbent Assay) development kits, such as the Human Duoset ELISA, Human Granzyme B ELISA, ABTS ELISA, Human VEGF ELISA, and Human IL-6 ELISA.
These kits help researchers measure and analyze important biomarkers and cytokines involved in different stages of human growth and development.
Additionally, the use of Bovine Serum Albumin (BSA) and DuoSet ELISA kits are common in these studies, providing crucial tools for researchers to better understand the complexities of human development.
By leveraging the power of AI-driven insights from PubCompare.ai, researchers can optimize their research protocols, leading to faster discoveries and advancements in the field of human development.
This approach helps to elevate research and propel our understanding of how humans grow and thrive throughout their lives.
Through the integration of cutting-edge technologies and robust experimental methods, the field of human development research continues to evolve, unlocking new possibilities for enhancing human potential and wellbeing.