953 resultados para Laitinen, Lea: Kieliopillistuminen
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Summary: Parenting styles and parents' psychosocial functioning
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Tutkimus on osa Jyväskylän yliopistossa toteutettua Emootion ja käyttäytymisen säätelyn (EMO) tutkimusta, joka kuuluu Ihmisen kehitys ja sen riskitekijät -huippututkimusohjelmaan.
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Artikkelissa kuvataan, miten perustutkimuksen tuloksista voi saada lähtökohtia ajankohtaisten ongelmien ennalta ehkäisyyn tähtäävälle työlle. Lähtökohtana on Lapsesta aikuiseksi -tutkimus.
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Summary: Work-family interface : a measure for identifying negative and positive spillover between work and family
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Abstract: Security borders in a world of changing threats
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Obesity is globally prevalent and highly heritable, but its underlying genetic factors remain largely elusive. To identify genetic loci for obesity susceptibility, we examined associations between body mass index and ∼ 2.8 million SNPs in up to 123,865 individuals with targeted follow up of 42 SNPs in up to 125,931 additional individuals. We confirmed 14 known obesity susceptibility loci and identified 18 new loci associated with body mass index (P < 5 × 10⁻⁸), one of which includes a copy number variant near GPRC5B. Some loci (at MC4R, POMC, SH2B1 and BDNF) map near key hypothalamic regulators of energy balance, and one of these loci is near GIPR, an incretin receptor. Furthermore, genes in other newly associated loci may provide new insights into human body weight regulation.
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Summary: Neuroticism and jealousy as factors weakening the quality of a relationship
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Carcinoembryonic antigen (CEA) was purified from primary tumour or from hepatic metastases obtained from ten cases of carcinoma of the colon. In nine cases the blood group antigens A, B, Lea or Leb were detected in CEA preparations by the binding of 125I-labelled CEA by blood group antibodies. The extent of binding appeared to preclude simple contamination of CEA preparations by blood group glycoprotein. In all cases the blood group antigens detected were consistent with the patients' known blood groups. Blood group I and i activities were not detected. It is concluded that the determinants of A, B and Lewis antigens and of CEA share the same glycoprotein carrier molecules.