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Family Structure

Family Structure: The organizational system of an individual family, including the relationships, roles, and dynamics between family members.
This encompasses the structure and composition of the family unit, such as the number, gender, and ages of family members, as well as the emotional and functional connections within the family.
Understanding family structure is crucial for researching topics related to child development, social dynamics, and intergenerational influences.
PubCompare.ai's AI-driven platform can help optimize your family structure research by locating the best protocols and products, comparing data from literature, preprints, and patents, and enhancing reproducibility through advanced tools and analyses.
Experence the power of data-driven decision making for your family structure studies.

Most cited protocols related to «Family Structure»

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Publication 2010
Cardiovascular System Dental Health Services Diet Disabled Persons Family Structure Food Hearing Aids Hearing Impairment Hispanic or Latino Hispanics Interviewers Latinos Lung Diseases Malignant Neoplasms Mental Recall Tinnitus
As HBSC is a school-based survey, data are collected through self-completion questionnaires administered in the classroom. The international standard questionnaire for each survey consists of three levels of questions which are used to create national survey instruments: core questions that each country is required to include to create the international dataset; optional packages of questions on specific topic areas from which countries can choose; and country-specific questions related to issues of national importance.
Survey questions cover a range of health indicators and health-related behaviours as well as the life circumstances of young people. Questions are subject to validation studies and piloting at national and international levels, with the outcomes of these studies often being published.7 –12 The core questions provide information on: demographic factors (e.g., age and state of maturation); social background (e.g., family structure and socio-economic status); social context (e.g., family, peer culture, school environment); health outcomes (e.g., self-rated health, injuries, overweight and obesity); health behaviours (e.g., eating and dieting, physical activity and weight reduction behaviour); and risk behaviours (e.g., smoking, alcohol use, cannabis use, sexual behaviour, bullying).13 Analysis of trends is possible as a number of these core items have remained the same since the study’s inception.
Publication 2009
Cannabis Family Structure Hemoglobin SC Disease Injuries Obesity
Metabolic profiling was done on fasting serum from participants of the German KORA F4 study (n=1,768) and the British TwinsUK study (n=1,052) using ultrahigh performance liquid-phase chromatography and gas chromatography separation coupled with tandem mass spectrometry 5 (link)-7 (link). We achieved highly efficient profiling (24 minutes/sample) with low median process variability (<12%) of more than 250 metabolites, covering over 60 biochemical pathways of human metabolism (Supplemental Table 1). Based on our previous observation that ratios between metabolite concentrations can strengthen the association signal and provide new information about possible metabolic pathways 4 (link),8 (link), we included all pairs of ratios between these metabolites in the genome-wide statistical analysis. To reduce the computational and data storage burden associated with meta-analyzing over 37,000 metabolites and ratios, we applied a staged approach for selection of promising association signals (Supplemental Figure 1). In the initial screening stage we assessed associations of approximately 600,000 genotyped SNPs with over 37,000 metabolic traits (concentrations and their ratios) by fitting linear models separately in both cohorts to log-transformed metabolic traits, adjusting for age, gender and family structure (Supplemental Figure 2 & Supplemental Table 2). Next, we selected all association signals having suggestive evidence for association with a metabolic trait in both cohorts (p<10−6 in both cohorts or p<10−3 in one and p<10−9 in the other). For each of these loci, we then re-assessed the amount of association signals through fixed-effects inverse variance meta-analysis of the two cohorts for all 37,000 available traits using imputed SNPs relative to HapMap2 data (see Online Methods for details). The SNP/trait combination yielding the smallest P-value in this meta-analysis was finally selected for each locus. To account for multiple testing we applied conservative Bonferroni correction leading to an adjusted threshold for genome-wide significance of p < 2.0×10−12.
Publication 2011
Family Structure Gas Chromatography Genome Homo sapiens Liquid Chromatography Metabolism Serum Tandem Mass Spectrometry
The database is built using MySQL Server 5.1.33 as back-end and the front-end is built using PHP, HTML, JavaScript, Open Flash Chart 2 and Perl. The database is hosted on Apache web server 2.2.11. Statistical software R version 2.9.1 (25 ) was used for development of the prediction server. JSmol viewer (http://wiki.jmol.org/index.php/JSmol) has been integrated for AMP structure visualization.
A brief description of the user interface of CAMPR3 is provided as follows.
Home: the home page provides information about various features of the database.
Databases: the data is divided into four databases which include sequence, structure, patents and the newly incorporated signature database.
Tools: the database includes the following tools for analysis. The AMP prediction tool has been developed in-house. Access to various tools relevant to sequence/structure analysis and available in public domain have also been provided in CAMPR3 for the benefit of the users.

AMP prediction: users can (i) predict AMPs (ii) predict antimicrobial region within peptides and (iii) rationally design AMPs by generating an exhaustive combinatorial library of sequences for a user-defined sequence and predict effect of single residue substitutions on antimicrobial activity using SVMs, RF and DA.

BLAST: users can use BLAST tool (26 (link)) to query protein sequence/s against various data sets of CAMPR3 which include the entire database, sequence, structure, patent, experimentally validated, predicted and predicted based on signature data sets to find homologous sequences, structures and other relevant information.

Clustal Omega: users can use Clustal Omega tool of EMBL-EBI to obtain multiple sequence alignment of peptides.

Vector Alignment Search Tool: users can identify similar protein structures and distant homologs that cannot be identified by sequence comparison using VAST of NCBI (27 (link)).

PRATT: users can generate AMP family-specific patterns using this tool from ExPASy.

ScanProsite: using this tool from Swiss Institute of Bioinformatics, users can (i) scan proteins against the PROSITE collection of PSSMs/patterns; (ii) scan patterns against protein sequence, structure or user defined database/s and (iii) scan user defined patterns against a set of protein sequences.

PHI-BLAST: users can use PHI-BLAST (28 (link)) to find AMPs similar to the query based on a family-specific pattern.

jackhmmer: users can iteratively search a protein sequence/structure database using a set of protein sequences/multiple sequence alignment/HMM as an input to find homologs using this tool from EMBL-EBI.

Search: basic and advanced search options are available for search of AMP families/sequences/structures and signatures.
Links: links to other online AMP databases are provided.
Statistics: information on CAMPR3 statistics can be viewed.
Help: detailed description and use of the various features and tools incorporated in the database is provided for the benefit of the users.
Publication 2015
Amino Acid Sequence Antimicrobial Peptide Cloning Vectors DNA Library Family Structure Homologous Sequences Microbicides Peptides Proteins protein S, human Public Domain Radionuclide Imaging Sequence Alignment SET protein, human Staphylococcal Protein A
This is a family-based study, recruiting participants and their relatives mainly through primary care. Recruitment of general practices is facilitated by Scottish Practices and Professionals Involved in Research (SPPIRe) [11 ]. Potential participants are identified from the registers of collaborating general practices via the Community Health Number, a unique identifying number allocated to every individual in Scotland who is registered with a general practitioner (GP), ie approximately 96% of the population. They are eligible to participate if they are aged between 35 and 55 years and have at least one first degree relative aged 18 years or over, and at least one full sibling group (the larger the better) in the participating family group.
An independent party, based in the NHS, generates a list of eligible people registered with each collaborating general practice, from the Scottish NHS register (known as the Community Health Index (CHI)). The names of all potential participants are screened by their GP, and individuals whom it might be inappropriate to approach (such as those with a serious or terminal illness, or those unable to consent) are excluded. Letters of invitation to eligible participants are generated on practice headed note-paper and signed by one of its GP Principals. These letters are dispatched by the independent party by post, with up to two reminders as required. This invitation is for agreement to discuss the study with family members with a view to possible participation. When the eligible person returns the tear-off slip agreeing to be contacted by the research team the individual's details are sent from the independent party to the study team.
In addition, targeted approaches in the Tayside area will be made to potentially eligible individuals whose details are held on the Walker Birth Cohort database [12 (link)]. This is a database of over 48,000 births in Dundee between 1952 and 1966, identified by CHI numbers, and therefore with current information about family structure and location. This provides the opportunity to approach individuals and their families simultaneously, with the ability to maximise the efficiency of recruitment by targeting larger local families in the first instance.
Upon receiving their permission, potential participants are contacted by a member of the research team to ensure that participants understand the study, that all demographics and details are accurate, and to discuss participation in the study with the relevant first degree relatives (including at least one sibling group). The names and contact details are requested of all first degree relatives who have verbally indicated, to the individual initially contacted, their willingness to be approached by the research team. These relatives are then also contacted by telephone by the study team. Each relative contacted is invited to discuss with and identify further first degree relatives, and so on, with the aim of creating a "snowball" sampling effect.
Similar methods of approaching and recruiting participants and their relatives have been successfully used in other studies in which several of the co-applicants have been closely involved. These include the British Genetics of Hypertension (BRIGHT) study [13 ] and "Family and population genetic studies in major mental illness" (D Blackwood et al). Although it is the main method of approach and recruitment, it will be augmented by a programme of communication and publicity about the study. Throughout this programme, individual families will be invited to volunteer directly for the study, by contacting the research team. They will be able to participate if the family includes at least one sibling pair.
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Publication 2006
ARID1A protein, human Birth Cohort Family Member Family Structure High Blood Pressures Laceration Mental Disorders Primary Health Care Voluntary Workers Walkers

Most recents protocols related to «Family Structure»

Sociodemographic characteristics, daily nursing variables, and maternal perceptions of infant hunger cues in EBF and FF groups were described by frequencies and percentages. In univariate analysis, bivariate associations between the feeding methods and the maternal perceptions of infant hunger cues, including maternal perceptions of the number of infant hunger cues, and early, active, late hunger cues, were evaluated using the chi-square test.
Logistic regression was used to examine the association between maternal perceptions to infant hunger cues and the sociodemographic variables, daily nursing variables, feeding methods measures in multivariate analysis. This regression employed four models, in which the dependent variables included the number of perceived hunger cues (Model A), hand sucking (Model B), moving head frantically from side to side (Model C), and crying (Model D), respectively. And nine multi-categorical variables, including infant’s birth weight, maternal age, father’s age, maternal education level, father’s education level, family structure, location, feeding interval, and feeding duration, were transformed into dummy variables in logistic analysis. Odds ratios (ORs) were presented as results for both bivariate associations and logistic regression model. All of the data preparation and statistical analyses were performed using the SPSS for Windows software program (version 25.0).
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Publication 2023
Birth Weight Family Structure Head Hunger Infant
Variables assessed in this study were obtained from self-report questionnaires designed by the study team, including general sociodemographic data, nursing-related variables, and variables of maternal perceptions of infant hunger cues.
Sociodemographic variables included infant gender, ethnicity, maternal age, maternal education level, family structure, and one-child status. Nursing-related variables included “whether the mother is the primary caregiver”, “whether the baby sleeps with mother”, feeding interval, and feeding duration.
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Publication 2023
Child Ethnicity Family Structure Hunger Infant Mothers Sleep

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Publication 2023
Child Chinese elder flower Family Structure Households
Demographic characteristics of students were collected through self-designed questionnaire including age, sex, BMI, serious disease in the past year (yes or no), family location (rural area, town, and city), and the only child in family (yes or no) of adolescents, paternal educational level and maternal educational level. It is well known that ACEs exposure is cumulative along with the age of children and there is sensitive and critical periods for the development of children [2 (link)], the ACEs exposure in different age of children may have different effects [23 (link)]. Physical health of children has been widely demonstrated to be closely associated with ACE exposure and psychology and behavior of children [2 (link), 3 (link), 44 (link)]. In addition, family structure has been identified as the factor associated with both the ACEs exposure and mental health of children [45 (link)]. Overall, all of above characteristics of students have been demonstrated to be closely associated with ACEs exposure and/or the physical and mental outcomes of children [2 (link), 3 (link), 44 (link)–46 (link)], which may confuse accurate associations between ACEs and interest outcomes. Therefore, these covariables were controlled in the adjusted models of statistical analysis. In addition, considering individual intrinsic attribute specificity that resilience was demonstrated to be an important factor against consequences of ACE exposure [47 (link)], resilience score of adolescents was, therefore, measured through Child Youth Resilience Measurement (CYRM-28). CYRM-28 is a 5-point Likert scale which contained 28 items with response options ranging from “not at all” to “a lot”and higher sum score of CYRM-28 represent higher resilience [48 (link)].
Publication 2023
Adolescent Child Child Development Children's Health Family Structure Mental Health N-(2-acetamido)-2-aminoethanesulfonic acid Only Child Physical Examination Student
Multidomain/Multilevel contextual variables assessed at kindergartens were used as predictors. We selected representative variables, instead of an exhaustive list, based on the social determinants framework for the purpose of exploration and feasibility demonstration. Children, their families, teachers, schools and care providers provided information on children’s cognitive, social, emotional, and physical development characteristics, as well as culture, immigration, home environment, parenting, home educational activities, school environment and quality, and neighborhood characteristics.
Child level predictors included measures on child learning, health, physical and socioemotional wellbeing, disability status, and social-process skills from direct child assessment, and parent and teacher report data. The kindergarten direct child assessment measured reading, mathematics, and science knowledge and skills, and executive function. Teachers reported on approaches to learning scale, providing information on how often their students exhibited a selected set of learning behaviors. The kindergarten questionnaires also asked teachers to indicate how often their children exhibited certain social skills and behaviors related to inhibitory control and attentional focusing. The parents-reported social scales consisted of four subscales, self-control, social interaction, sad/lonely, and impulsive/overactive behaviors. Parents also reported on approaches to learning scale. The parent interview reported on family structure, family literacy practices, parental involvement in school, care arrangements, household composition, family income, parent education level, culture/immigration, and other demographic indicators. Neighborhood level measures included measures of community support and community violence.
A complete list of predictors and their descriptions are presented in Supplement 1. Measures with less than 30% missingness were included in the predictive analysis, resulting in a total of 24 predictors. Continuous predictors were standardized to have mean 0 and variance of 1. Mean imputation was considered for missing continuous variables. An explicit class of missing was introduced for each categorical variable to maintain sample size in the predictive analysis.
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Publication 2023
Child Dietary Supplements Disabled Persons Emotions Executive Function Family Structure Households Impulsive Behavior Parent Physical Examination Psychological Inhibition Student

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More about "Family Structure"

Family structure refers to the organizational system and dynamics within an individual family unit.
This encompasses the composition, roles, and relationships between family members, as well as the emotional and functional connections that exist.
Understanding family structure is crucial for research related to child development, social dynamics, and intergenerational influences.
The structure of a family can vary in terms of the number, gender, and ages of its members.
It also encompasses the hierarchy, power dynamics, and communication patterns within the family.
Family structure analysis can provide insights into topics such as parenting styles, sibling dynamics, and the impact of divorce or remarriage.
Researchers studying family structure may utilize various statistical software tools, such as SAS 9.4, SPSS 25.0, Stata 15, or SPSS version 22.0.
These programs can help analyze data related to family composition, household characteristics, and interpersonal relationships.
Additionally, genetic analysis tools like the HumanOmniExpress BeadChip can be used to explore the role of genetics in family dynamics.
Optimizing family structure research can be achieved through the use of data-driven platforms like PubCompare.ai.
This AI-driven tool can help researchers locate the best protocols and products, compare data from literature, preprints, and patents, and enhance the reproducibility of their studies through advanced analyses.
By harnessing the power of data-driven decision making, researchers can gain a deeper understanding of the complex and multifaceted nature of family structure.