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  1. 2741
    “…Here we show that offspring sex can be affected by the incubation temperature its father experiences years earlier. We incubated eggs of an Australian lizard with temperature-dependent sex determination under three thermal regimes; some eggs were given an aromatase inhibitor to produce sons at temperatures that usually produce only daughters. …”
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    Transgenerational sex determination: the embryonic environment experienced by a male affects offspring sex ratio
  2. 2742
    “…The method is based on real-time PCR and allele-specific hybridization probes, followed by fluorescent melting curve analysis to expose a change in melting temperature (T(m)). Ninety-two mother-father-child triads (n=276) from preeclamptic pregnancies were genotyped for three haplotype-tagging single nucleotide polymorphisms (htSNPs) in REN. …”
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    Rapid Genotyping of the Human Renin (REN) Gene by the LightCycler® Instrument: Identification of Unexpected Nucleotide Substitutions within the Selected Hybridization Probe Area
  3. 2743
    “…The subjects were 17 couples, 1 father and 9 mothers, and 24 couples who had at least one healthy child formed the control group. …”
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    Micronucleated lymphocytes in parents of Down syndrome children
  4. 2744
    “…Epidemiological studies suggest that a father’s diet can influence offspring health. A proposed mechanism for paternal transmission of environmental information is via the sperm epigenome. …”
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    Low paternal dietary folate alters the mouse sperm epigenome and is associated with negative pregnancy outcomes
  5. 2745
    “…We examined the effect of father’s age at birth on offspring intelligence, head circumference and personality traits. …”
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    The Effect of Paternal Age on Offspring Intelligence and Personality when Controlling for Parental Trait Levels
  6. 2746
    “…We compare this material with various languages (once) spoken in the region, showing that four attested Carabayo forms (a first person singular prefix and words for ‘warm’, ‘father’, and ‘boy’) display striking similarities with Yurí and at least 13 Carabayo forms display clear correspondences with contemporary Tikuna. …”
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    Evidence for the Identification of Carabayo, the Language of an Uncontacted People of the Colombian Amazon, as Belonging to the Tikuna-Yurí Linguistic Family
  7. 2747
    “…Background: A family case report of cleidocranial dysplasia (CCD) with varied manifestations from father to three siblings is presented. CCD ( MIM # 119600) is a rare autosomal dominant skeletal dysplasia caused by CBAF1 gene ( OMIM 600211) with a wide range of variability. …”
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    Cleidocranial Dysplasia: Case Report of Three Siblings
  8. 2748
    “…Sequencing of the fibrinogen genes revealed a γ375Arg → Trp mutation (fibrinogen Aguadilla) in the child and in her father. In conclusion, when confronted with chronic hepatitis of unknown origin, one should check the plasma fibrinogen level and look carefully for the presence of hepatocellular intracytoplasmic globular inclusions to exclude hepatic fibrinogen storage disease.…”
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    Hepatic Fibrinogen Storage Disease Due to the Fibrinogen γ375 Arg → Trp Mutation “Fibrinogen Aguadilla” is present in Arabs
  9. 2749
    por Emmott, Emily H., Mace, Ruth
    Publicado 2014
    “…Here, we build on previous studies by investigating whether the effects of stepfather presence on child outcomes are driven by differences in maternal and partner (i.e., father or stepfather) direct investments. We use data from the Avon Longitudinal Study of Parents and Children to explore stepfather effects on children’s educational achievement and behavioural difficulties at age 7. …”
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    Direct investment by stepfathers can mitigate effects on educational outcomes but does not improve behavioural difficulties
  10. 2750
    “…Kola nut use was associated with lower age group, poor school attendance, polygamous background, low education of mother, high education of father and the description of mother as being too permissive. …”
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    Prevalence and associated risk factors of Kola nut chewing among secondary school students in Osogbo, Nigeria
  11. 2751
    “…We report a male patient with developmental delay carrying an interstitial 4p16.3 deletion of 287 kb, disclosed by oligo array-CGH and inherited from his father with a similar but milder phenotype. This deletion is distal to the Wolf-Hirschhorn syndrome critical regions, but includes the FGFRL1 gene proposed to be a plausible candidate for part of the craniofacial characteristics of Wolf-Hirschhorn syndrome patients. …”
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    Interstitial 287 kb deletion of 4p16.3 including FGFRL1 gene associated with language impairment and overgrowth
  12. 2752
    por Stortelder, Frans
    Publicado 2014
    “…Variations of sexual identity development are present in all cultures, as well as in many animal species. Freud – founding father of psychoanalysis – believed that all men have an inherited, bisexual disposition, and that many varieties of love and desire are experienced as alternative pathways to intimacy. …”
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    Varieties of male-sexual-identity development in clinical practice: a neuropsychoanalytic model
  13. 2753
    “…RESULTS: At the baseline (2005), female gender, internet use, maternal education, physical activity and father’s education were associated with mental health (p<0.05). …”
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    Mental Health Changes and Its Predictors in Adolescents using the Path Analytic Model: A 7-Year Observational Study
  14. 2754
    “…RESULTS: Here we describe a patient with epilepsy, mental retardation, developmental disorders, and dysmorphic features, who inherited a deletion of 16p13.11 and a triplication of 19p13.3 from his father and mother, respectively. The mother presented mild mental retardation and language delay too. …”
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    Concomitant deletion of chromosome 16p13.11 and triplication of chromosome 19p13.3 in a child with developmental disorders, intellectual disability, and epilepsy
  15. 2755
    por Perrard, Adrien, Loope, Kevin J.
    Publicado 2015
    “…Here, we show that the father’s genotype has a direct effect on wing morphology in colonies of social wasps. …”
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    Patriline Differences Reveal Genetic Influence on Forewing Size and Shape in a Yellowjacket Wasp (Hymenoptera: Vespidae: Vespula flavopilosa Jacobson, 1978)
  16. 2756
    “…Furthermore, social variables were important covariates of adolescent gambling; significant associations were found for family and friends’ approval of gambling, parental monitoring, father’s level of education, and having relatives or friends with a history of a gambling disorder. …”
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    Prevalence and Correlates of Problem Gambling in a Representative Sample of Norwegian 17-Year-Olds
  17. 2757
    “…In 70% of the cases the sSMC is de novo, in 20% it is inherited from the mother, and in 10% it is inherited from the father. An sSMC can be causative for specific syndromes such as Emanuel, Pallister-Killian, or cat eye syndromes. …”
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    Small supernumerary marker chromosomes and their correlation with specific syndromes
  18. 2758
    por Salehzadeh, Farhad, Fathi, Afshin
    Publicado 2015
    “…CASE REPORT: Here we report a child with complex allele mutations E148Q/V726A/R761H, whilst, whose mother showed E148Q/V726A and his father had R761H/wt in analysis. The severity of the disease and genotype-phenotype correlation of patient showed no significant differences with his mother and other patients with the same two mutations, V726A/R761H, E148Q/V726A, and E148Q/R761H. …”
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    Patient with FMF and Triple MEFV Gene Mutations
  19. 2759
    “…An application of the new approach to mother, father, and child reports of impulsivity, frustration tolerance, and externalizing problems (N = 454) is presented. …”
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    Analyzing Statistical Mediation with Multiple Informants: A New Approach with an Application in Clinical Psychology
  20. 2760
    “…These mutations are inherited from their normal father. CONCLUSION: Despite apparent recessive pattern of inheritance a dominant gene (here BRCA2) can be involved in pathogenesis of hereditary breast cancer which can be explained by incomplete penetrance of BRCA2 mutations.…”
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    Double Heterozygosity of BRCA2 and STK11 in Familial Breast Cancer Detected by Exome Sequencing
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