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1.
Soc Sci Res ; 96: 102539, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33867010

RESUMO

Separation from a spouse or cohabiting partner is associated with a high likelihood of moving, even over long distances. In this paper, we use longitudinal data from the Panel Study of Income Dynamics for the United States to analyze the role of non-resident family in the migration of separated people immediately after and in the years following union dissolution. We explore both migration in general and return migration among separated people, drawing comparisons to married and never-married people. We find that having parents, children, or siblings living close by substantially deters migration, especially among separated people. We also find marked positive effects of having family members in the county where the respondent grew up on the likelihood of returning there. Separated people are especially likely to return, compared to others, if they have parents in their county of origin. Furthermore, a lack of an effect of years of education on migration, and a negative effect of this variable on return migration, suggest that migration after separation is less related to human-capital considerations than other types of migration.


Assuntos
Divórcio , Emigração e Imigração , Criança , Humanos , Casamento , Fatores Socioeconômicos , Estados Unidos
2.
J Neurotrauma ; 37(1): 66-79, 2020 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-31256709

RESUMO

Traumatic brain injury (TBI) can lead to life-changing neurological deficits, which reflect the fast-evolving secondary injury post-trauma. There is a need for acute protective interventions, and the aim of this study was to explore in an experimental TBI model the neuroprotective potential of a single bolus of a neuroactive omega-3 fatty acid, docosahexaenoic acid (DHA), administered in a time window feasible for emergency services. Adult mice received a controlled cortical impact injury (CCI) and neurological impairment was assessed with the modified Neurological Severity Score (mNSS) up to 28 days post-injury. DHA (500 nmol/kg) or saline were injected intravenously at 30 min post-injury. The lipid mediator profile was assessed in the injured hemisphere at 3 h post-CCI. After completion of behavioral tests and lesion assessment using magnetic resonance imaging, over 7 days or 28 days post-TBI, the tissue was analyzed by immunohistochemistry. The single DHA bolus significantly reduced the injury-induced neurological deficit and increased pro-resolving mediators in the injured brain. DHA significantly reduced lesion size, the microglia and astrocytic reaction, and oxidation, and decreased the accumulation of beta-amyloid precursor protein (APP), indicating a reduced axonal injury at 7 days post-TBI. DHA reduced the neurofilament light levels in plasma at 28 days. Therefore, an acute single bolus of DHA post-TBI, in a time window relevant for acute emergency intervention, can induce a long-lasting and significant improvement in neurological outcome, and this is accompanied by a marked upregulation of neuroprotective mediators, including the DHA-derived resolvins and protectins.


Assuntos
Lesões Encefálicas Traumáticas/patologia , Encéfalo/efeitos dos fármacos , Ácidos Docosa-Hexaenoicos/farmacologia , Fármacos Neuroprotetores/farmacologia , Recuperação de Função Fisiológica/efeitos dos fármacos , Animais , Encéfalo/patologia , Metabolismo dos Lipídeos/efeitos dos fármacos , Camundongos
3.
Commun Biol ; 2: 478, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31886416

RESUMO

Hibernation in sciurid rodents is a dynamic phenotype timed by a circannual clock. When housed in an animal facility, 13-lined ground squirrels exhibit variation in seasonal onset of hibernation, which is not explained by environmental or biological factors. We hypothesized that genetic factors instead drive variation in timing. After increasing genome contiguity, here, we employ a genotype-by-sequencing approach to characterize genetic variation in 153 ground squirrels. Combined with datalogger records (n = 72), we estimate high heritability (61-100%) for hibernation onset. Applying a genome-wide scan with 46,996 variants, we identify 2 loci significantly (p < 7.14 × 10-6), and 12 loci suggestively (p < 2.13 × 10-4), associated with onset. At the most significant locus, whole-genome resequencing reveals a putative causal variant in the promoter of FAM204A. Expression quantitative trait loci (eQTL) analyses further reveal gene associations for 8/14 loci. Our results highlight the power of applying genetic mapping to hibernation and present new insight into genetics driving its onset.


Assuntos
Variação Genética , Hibernação/genética , Sciuridae/fisiologia , Estações do Ano , Animais , Feminino , Loci Gênicos , Genética Populacional , Genoma , Genômica/métodos , Geografia , Padrões de Herança , Masculino , Polimorfismo de Nucleotídeo Único
4.
Eur J Popul ; 34(4): 463-489, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30310246

RESUMO

Using detailed geocoded microdata from the British Household Panel Survey and longitudinal random-effects models, we analyse the determinants and trajectories of geographical distances between separated parents. Findings of particular note include the following: (1) post-separation linked lives, proximities and spatial constraints are characterised by important gender asymmetries; (2) the formation of new post-separation family ties (i.e. new partners and children) by fathers is linked to moves over longer distances away from the ex-partner than for mothers; (3) the distribution of pre-separation childcare responsibilities is relevant for determining post-separation proximity between parents; and (4) most variation in the distance between ex-partners occurs in the immediate period following separation (approximately the first year), suggesting that the initial conditions around separation can have long-lasting implications for the types of family life, ties and contact experienced in the years after separation.

5.
PLoS One ; 13(5): e0196325, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29715266

RESUMO

We analyzed 391 samples from 12 Argentinian populations from the Center-West, East and North-West regions with the Illumina Human Exome Beadchip v1.0 (HumanExome-12v1-A). We did Principal Components analysis to infer patterns of populational divergence and migrations. We identified proportions and patterns of European, African and Native American ancestry and found a correlation between distance to Buenos Aires and proportion of Native American ancestry, where the highest proportion corresponds to the Northernmost populations, which is also the furthest from the Argentinian capital. Most of the European sources are from a South European origin, matching historical records, and we see two different Native American components, one that spreads all over Argentina and another specifically Andean. The highest percentages of African ancestry were in the Center West of Argentina, where the old trade routes took the slaves from Buenos Aires to Chile and Peru. Subcontinentaly, sources of this African component are represented by both West Africa and groups influenced by the Bantu expansion, the second slightly higher than the first, unlike North America and the Caribbean, where the main source is West Africa. This is reasonable, considering that a large proportion of the ships arriving at the Southern Hemisphere came from Mozambique, Loango and Angola.


Assuntos
Dinâmica Populacional , Argentina , Exoma/genética , Genótipo , Geografia , Humanos
6.
Geogr Rev ; 108(4): 503-522, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-32494088

RESUMO

Wilbur Zelinsky's 1971 paper in Geographical Review entitled the "Hypothesis of the Mobility Transition" was both forward-looking and offered innovative ideas regarding human geographic mobility. One of the most interesting aspects of the paper was a set of predictions for mobility in a "future superadvanced society". Many of these predictions have now come to pass, including a general decline in international and internal migration and residential change, the increasing regulation of migration - especially internally, and the possibility that the widespread adoption of information and communication technologies has impacted human geographic mobility. Hence, this essay looks at the mobility transition not as an obsolete frame of reference but as a prescient, pliable, and adaptable framework which not only informs the study of human geographic mobility today but also, perhaps, even into the future.

7.
Eur J Popul ; 34(4): 689, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-30976257

RESUMO

[This corrects the article DOI: 10.1007/s10680-017-9437-1.].

8.
Cell ; 171(2): 427-439.e21, 2017 Oct 05.
Artigo em Inglês | MEDLINE | ID: mdl-28985565

RESUMO

Parrot feathers contain red, orange, and yellow polyene pigments called psittacofulvins. Budgerigars are parrots that have been extensively bred for plumage traits during the last century, but the underlying genes are unknown. Here we use genome-wide association mapping and gene-expression analysis to map the Mendelian blue locus, which abolishes yellow pigmentation in the budgerigar. We find that the blue trait maps to a single amino acid substitution (R644W) in an uncharacterized polyketide synthase (MuPKS). When we expressed MuPKS heterologously in yeast, yellow pigments accumulated. Mass spectrometry confirmed that these yellow pigments match those found in feathers. The R644W substitution abolished MuPKS activity. Furthermore, gene-expression data from feathers of different bird species suggest that parrots acquired their colors through regulatory changes that drive high expression of MuPKS in feather epithelia. Our data also help formulate biochemical models that may explain natural color variation in parrots. VIDEO ABSTRACT.


Assuntos
Proteínas Aviárias/genética , Plumas/fisiologia , Melopsittacus/genética , Pigmentos Biológicos/biossíntese , Polienos/metabolismo , Policetídeo Sintases/genética , Sequência de Aminoácidos , Animais , Proteínas Aviárias/metabolismo , Plumas/anatomia & histologia , Plumas/química , Expressão Gênica , Genoma , Estudo de Associação Genômica Ampla , Melopsittacus/anatomia & histologia , Melopsittacus/fisiologia , Pigmentação , Policetídeo Sintases/metabolismo , Polimorfismo de Nucleotídeo Único , Regeneração , Alinhamento de Sequência
9.
PLoS Genet ; 12(2): e1005631, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26828719

RESUMO

Reduced representation sequencing methods such as genotyping-by-sequencing (GBS) enable low-cost measurement of genetic variation without the need for a reference genome assembly. These methods are widely used in genetic mapping and population genetics studies, especially with non-model organisms. Variant calling error rates, however, are higher in GBS than in standard sequencing, in particular due to restriction site polymorphisms, and few computational tools exist that specifically model and correct these errors. We developed a statistical method to remove errors caused by restriction site polymorphisms, implemented in the software package GBStools. We evaluated it in several simulated data sets, varying in number of samples, mean coverage and population mutation rate, and in two empirical human data sets (N = 8 and N = 63 samples). In our simulations, GBStools improved genotype accuracy more than commonly used filters such as Hardy-Weinberg equilibrium p-values. GBStools is most effective at removing genotype errors in data sets over 100 samples when coverage is 40X or higher, and the improvement is most pronounced in species with high genomic diversity. We also demonstrate the utility of GBS and GBStools for human population genetic inference in Argentine populations and reveal widely varying individual ancestry proportions and an excess of singletons, consistent with recent population growth.


Assuntos
Alelos , Técnicas de Genotipagem , Sequenciamento de Nucleotídeos em Larga Escala/métodos , Software , Estatística como Assunto , Genética Populacional , Humanos , Polimorfismo de Nucleotídeo Único/genética
10.
G3 (Bethesda) ; 4(9): 1681-7, 2014 Jul 16.
Artigo em Inglês | MEDLINE | ID: mdl-25031181

RESUMO

Next-generation DNA sequencing (NGS) produces vast amounts of DNA sequence data, but it is not specifically designed to generate data suitable for genetic mapping. Recently developed DNA library preparation methods for NGS have helped solve this problem, however, by combining the use of reduced representation libraries with DNA sample barcoding to generate genome-wide genotype data from a common set of genetic markers across a large number of samples. Here we use such a method, called genotyping-by-sequencing (GBS), to produce a data set for genetic mapping in an F1 population of apples (Malus × domestica) segregating for skin color. We show that GBS produces a relatively large, but extremely sparse, genotype matrix: over 270,000 SNPs were discovered but most SNPs have too much missing data across samples to be useful for genetic mapping. After filtering for genotype quality and missing data, only 6% of the 85 million DNA sequence reads contributed to useful genotype calls. Despite this limitation, using existing software and a set of simple heuristics, we generated a final genotype matrix containing 3967 SNPs from 89 DNA samples from a single lane of Illumina HiSeq and used it to create a saturated genetic linkage map and to identify a known QTL underlying apple skin color. We therefore demonstrate that GBS is a cost-effective method for generating genome-wide SNP data suitable for genetic mapping in a highly diverse and heterozygous agricultural species. We anticipate future improvements to the GBS analysis pipeline presented here that will enhance the utility of next-generation DNA sequence data for the purposes of genetic mapping across diverse species.


Assuntos
Mapeamento Cromossômico/métodos , DNA de Plantas/genética , Malus/genética , Análise de Sequência de DNA/métodos , Cor , Frutas , Ligação Genética , Genoma de Planta , Polimorfismo de Nucleotídeo Único , Locos de Características Quantitativas
11.
Plant Cell ; 24(2): 536-50, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22327740

RESUMO

The lipid-derived hormone jasmonoyl-L-Ile (JA-Ile) initiates large-scale changes in gene expression by stabilizing the interaction of JASMONATE ZIM domain (JAZ) repressors with the F-box protein CORONATINE INSENSITIVE1 (COI1), which results in JAZ degradation by the ubiquitin-proteasome pathway. Recent structural studies show that the JAZ1 degradation signal (degron) includes a short conserved LPIAR motif that seals JA-Ile in its binding pocket at the COI1-JAZ interface. Here, we show that Arabidopsis thaliana JAZ8 lacks this motif and thus is unable to associate strongly with COI1 in the presence of JA-Ile. As a consequence, JAZ8 is stabilized against jasmonate (JA)-mediated degradation and, when ectopically expressed in Arabidopsis, represses JA-regulated growth and defense responses. These findings indicate that sequence variation in a hypervariable region of the degron affects JAZ stability and JA-regulated physiological responses. We also show that JAZ8-mediated repression depends on an LxLxL-type EAR (for ERF-associated amphiphilic repression) motif at the JAZ8 N terminus that binds the corepressor TOPLESS and represses transcriptional activation. JAZ8-mediated repression does not require the ZIM domain, which, in other JAZ proteins, recruits TOPLESS through the EAR motif-containing adaptor protein NINJA. These findings show that EAR repression domains in a subgroup of JAZ proteins repress gene expression through direct recruitment of corepressors to cognate transcription factors.


Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis/genética , Ciclopentanos/metabolismo , Oxilipinas/metabolismo , Proteínas Repressoras/metabolismo , Sequência de Aminoácidos , Arabidopsis/metabolismo , Proteínas de Arabidopsis/genética , Regulação da Expressão Gênica de Plantas , Dados de Sequência Molecular , Mutagênese Sítio-Dirigida , Plantas Geneticamente Modificadas/genética , Plantas Geneticamente Modificadas/metabolismo , Domínios e Motivos de Interação entre Proteínas , Proteínas Repressoras/genética , Transcrição Gênica
12.
Mol Syst Biol ; 7: 532, 2011 Sep 27.
Artigo em Inglês | MEDLINE | ID: mdl-21952135

RESUMO

The heterotrimeric G-protein complex is minimally composed of Gα, Gß, and Gγ subunits. In the classic scenario, the G-protein complex is the nexus in signaling from the plasma membrane, where the heterotrimeric G-protein associates with heptahelical G-protein-coupled receptors (GPCRs), to cytoplasmic target proteins called effectors. Although a number of effectors are known in metazoans and fungi, none of these are predicted to exist in their canonical forms in plants. To identify ab initio plant G-protein effectors and scaffold proteins, we screened a set of proteins from the G-protein complex using two-hybrid complementation in yeast. After deep and exhaustive interrogation, we detected 544 interactions between 434 proteins, of which 68 highly interconnected proteins form the core G-protein interactome. Within this core, over half of the interactions comprising two-thirds of the nodes were retested and validated as genuine in planta. Co-expression analysis in combination with phenotyping of loss-of-function mutations in a set of core interactome genes revealed a novel role for G-proteins in regulating cell wall modification.


Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis , Parede Celular , Proteínas de Ligação ao GTP/metabolismo , Glicômica , Proteômica , Receptores Acoplados a Proteínas G/metabolismo , Transdução de Sinais/genética , Arabidopsis/genética , Arabidopsis/crescimento & desenvolvimento , Arabidopsis/metabolismo , Proteínas de Arabidopsis/genética , Membrana Celular/genética , Membrana Celular/metabolismo , Parede Celular/genética , Parede Celular/metabolismo , Bases de Dados Genéticas , Proteínas de Ligação ao GTP/genética , Regulação da Expressão Gênica de Plantas , Redes Reguladoras de Genes , Teste de Complementação Genética , Genótipo , Imunoprecipitação , Morfogênese/genética , Fenótipo , Mapeamento de Interação de Proteínas , Receptores Acoplados a Proteínas G/genética , Técnicas do Sistema de Duplo-Híbrido
13.
Proc Natl Acad Sci U S A ; 108(22): 9298-303, 2011 May 31.
Artigo em Inglês | MEDLINE | ID: mdl-21576464

RESUMO

The phytohormone jasmonoyl-L-isoleucine (JA-Ile) signals through the COI1-JAZ coreceptor complex to control key aspects of plant growth, development, and immune function. Despite detailed knowledge of the JA-Ile biosynthetic pathway, little is known about the genetic basis of JA-Ile catabolism and inactivation. Here, we report the identification of a wound- and jasmonate-responsive gene from Arabidopsis that encodes a cytochrome P450 (CYP94B3) involved in JA-Ile turnover. Metabolite analysis of wounded leaves showed that loss of CYP94B3 function in cyp94b3 mutants causes hyperaccumulation of JA-Ile and concomitant reduction in 12-hydroxy-JA-Ile (12OH-JA-Ile) content, whereas overexpression of this enzyme results in severe depletion of JA-Ile and corresponding changes in 12OH-JA-Ile levels. In vitro studies showed that heterologously expressed CYP94B3 converts JA-Ile to 12OH-JA-Ile, and that 12OH-JA-Ile is less effective than JA-Ile in promoting the formation of COI1-JAZ receptor complexes. CYP94B3-overexpressing plants displayed phenotypes indicative of JA-Ile deficiency, including defects in male fertility, resistance to jasmonate-induced growth inhibition, and susceptibility to insect attack. Increased accumulation of JA-Ile in wounded cyp94b3 leaves was associated with enhanced expression of jasmonate-responsive genes. These results demonstrate that CYP94B3 exerts negative feedback control on JA-Ile levels and performs a key role in attenuation of jasmonate responses.


Assuntos
Arabidopsis/metabolismo , Ciclopentanos/farmacologia , Sistema Enzimático do Citocromo P-450/metabolismo , Isoleucina/análogos & derivados , Reguladores de Crescimento de Plantas/metabolismo , Animais , Ciclopentanos/metabolismo , Ácidos Graxos/metabolismo , Regulação Enzimológica da Expressão Gênica , Isoleucina/farmacologia , Metabolismo , Oxigenases de Função Mista/metabolismo , Modelos Genéticos , Oxilipinas/metabolismo , Fenótipo , Proteínas de Plantas/metabolismo , Transdução de Sinais , Spodoptera
14.
Plant J ; 63(4): 613-22, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20525008

RESUMO

Jasmonates (JAs) are fatty acid-derived signaling compounds that control diverse aspects of plant growth, development and immunity. The F-box protein COI1 functions both as a receptor for jasmonoyl-l-isoleucine (JA-Ile) and as the component of an E3-ubiquitin ligase complex (SCF(COI1) ) that targets JAZ transcriptional regulators for degradation. A key feature of JAZ proteins is the C-terminal Jas motif that mediates the JA-Ile-dependent interaction with COI1. Here, we show that most JAZ genes from evolutionarily diverse plants contain a conserved intron that splits the Jas motif into 20 N-terminal and seven C-terminal (X(5) PY) amino acid submotifs. In most members of the Arabidopsis JAZ family, alternative splicing events involving retention of this intron generate proteins that are truncated before the X(5) PY sequence. In vitro pull-down and yeast two-hybrid assays indicate that these splice variants have reduced capacity to form stable complexes with COI1 in the presence of the bioactive stereoisomer of the hormone (3R,7S)-JA-Ile. cDNA overexpression studies showed that some, but not all, truncated splice variants are dominant repressors of JA signaling. We also show that strong constitutive expression of an intron-containing JAZ10 genomic clone is sufficient to repress JA responses. These findings provide evidence for functional differences between JAZ isoforms, and establish a direct link between the alternative splicing of JAZ pre-mRNA and the dominant repression of JA signal output. We propose that production of dominant JAZ repressors by alternative splicing reduces the negative consequences associated with inappropriate or hyperactivation of the JA response pathway.


Assuntos
Processamento Alternativo , Proteínas de Arabidopsis/genética , Ciclopentanos/farmacologia , Oxilipinas/farmacologia , Motivos de Aminoácidos/genética , Sequência de Aminoácidos , Proteínas de Arabidopsis/metabolismo , Ciclopentanos/química , Íntrons/genética , Isoleucina/análogos & derivados , Isoleucina/química , Isoleucina/farmacologia , Dados de Sequência Molecular , Estrutura Molecular , Mutação , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Oxilipinas/química , Reguladores de Crescimento de Plantas/farmacologia , Raízes de Plantas/genética , Raízes de Plantas/metabolismo , Plantas/genética , Plantas Geneticamente Modificadas , Ligação Proteica/efeitos dos fármacos , Proteínas Repressoras/genética , Proteínas Repressoras/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Plântula/genética , Plântula/metabolismo , Homologia de Sequência de Aminoácidos , Transdução de Sinais , Estereoisomerismo , Técnicas do Sistema de Duplo-Híbrido
15.
Demography ; 46(1): 147-67, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19348113

RESUMO

This article uses longitudinal data for the United States and Great Britain to examine the impact of residential mobility and childbirth on the earnings of women, their family earnings, and the related division of earnings by gender. This project is the first to compare explicitly the impact of childbirth and family migration on women's earnings, and it extends prior cross-sectional and longitudinal studies on isolated countries by providing a direct contrast between two major industrialized nations, using comparable measures. The results indicate that families respond in similar ways in both countries to migration and childbirth. In response to both migration and childbirth, women's earnings fall at the time of the event and recover slowly afterward, but the magnitude of the impact is roughly twice as large for childbirth as for migration. However; migration--but not the birth of a child--is also associated with a significant increase in total family earnings because of increased husbands' earnings. As a result, the effect of migration on the relative earnings of wives to husbands is similar to the effect of childbirth. These results suggest that family migration should be given consideration in the literature on the gender earnings gap.


Assuntos
Emigração e Imigração , Família , Renda/estatística & dados numéricos , Renda/tendências , Parto , Adulto , Comparação Transcultural , Feminino , Humanos , Recém-Nascido , Estudos Longitudinais , Masculino , Gravidez , Análise de Regressão , Fatores Sexuais , Reino Unido , Estados Unidos , Mulheres Trabalhadoras/estatística & dados numéricos
16.
Demography ; 45(1): 209-22, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18390300

RESUMO

This paper examines the effect of migration and residential mobility on union dissolution among married and cohabiting couples. Moving is a stressful life event, and a large, multidisciplinary literature has shown that family migration often benefits one partner (usually the man) more than the other Even so, no study to date has examined the possible impact of within-nation geographical mobility on union dissolution. We base our longitudinal analysis on retrospective event-history data from Austria. Our results show that couples who move frequently have a significantly higher risk of union dissolution, and we suggest a variety of mechanisms that may explain this.


Assuntos
Emigração e Imigração/estatística & dados numéricos , Estado Civil/estatística & dados numéricos , Dinâmica Populacional/estatística & dados numéricos , Adolescente , Adulto , Áustria , Canadá , Demografia , Emigração e Imigração/tendências , Europa (Continente) , Feminino , Geografia , Humanos , Masculino , Modelos Estatísticos , Nova Zelândia , Dinâmica Populacional/tendências , Estudos Retrospectivos , Risco , Estados Unidos
18.
Am J Orthopsychiatry ; 45(1): 4-17, 1975 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-1089360

RESUMO

It is hypothesized that interaction between infants may serve to facilitate their overall behavioral development, particularly if the environment is structured to maximize the developmental quality of the interaction. The developmental literature, which has largely ignorned the potential value of infant peer interaction is reviewed, and several lines of psychological theory and investigation are cited in support of the hypothesis. Development of a technology for enhancing infant interaction is proposed, and initial research questions are suggested.


Assuntos
Comportamento Infantil , Desenvolvimento Infantil , Grupo Associado , Fatores Etários , Agressão , Terapia Comportamental , Creches , Período Crítico Psicológico , Meio Ambiente , Humanos , Comportamento Imitativo , Lactente , Recém-Nascido , Relações Interpessoais , Jogos e Brinquedos , Teoria Psicológica , Comportamento Social , Transtornos do Comportamento Social/etiologia , Transtornos do Comportamento Social/terapia , Facilitação Social , Isolamento Social
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