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DESCRIPTION (provided by applicant): Influences of androgen on human neural-behavioral development will be evaluated by studying psychological outcomes in individuals with congenital adrenal hyperplasia (CAH: an autosomal recessive disorder causing increased adrenal androgen production beginning prenatally), as well as by relating normal variability in the prenatal hormone environment to postnatal behavior. 128 children with CAH (4-10 years) will be compared to 128 of their unaffected relatives in the same age range and to 128 demographically matched controls in regard to gender identity, gender constancy, social/cognitive processes involved in the acqusition of gender role behavior, and sex-typical toy, activity and playmate preferences. For 171 additional participants from the general population (who do not have CAH), testosterone in amniotic fluid will be related to postnatal behavior at the ages of 4 1/2, 5 1/2, and 6 1/2 years. Assessments of these children will be conducted using the same measures used to study individuals with CAH. Data will be collected by observation, interview and questionnaire, and cross-sectional and longitudinal approaches will be used. Hypotheses to be tested include: 1. Girls with CAH experience reduced feminine gender identity or are at increased risk for gender identity disorder; 2. High levels of androgen promote male-typical behavioral development in normal as well as abnormal situations; 3. Individual differences in gender role behavior are mediated by alterations in gender identity or in social/cognitive processes related to gender identity; 4. Alterations in gender identity in girls with CAH diminsh with age. The research will add to basic knowledge about the role of androgens in the development of human behavior, and will clarify the relevance to humans of animal models, where gonadal hormones have been found to influence basic processes of neural development and survival. In addition, the research will provide information on psychosexual outcomes in individuals with CAH, information which should prove relevant to other intersex conditions as well, and to other situations where fetuses are exposed to hormone-altering substances (e.g., "fertility" or contraceptive drugs, alcohol, cocaine, stress, environmental toxins). Finally, the research will further basic scientific understanding of the roles of hormones and social/cognitive processes in childrens acquisition of gender role behavior.
期刊论文(35)
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DOI: 10.1016/j.yhbeh.2011.02.007
发表时间: 2011-04
期刊: HORMONES AND BEHAVIOR
影响因子: 3.5
作者: [Pasterski, Vickie, Geffner, Mitchell E., Brain, Caroline, Hindmarsh, Peter, Brook, Charles, Hines, Melissa]
通讯作者: Hines, Melissa
Prenatal androgen exposure and children's gender-typed behavior and toy and playmate preferences.
产前雄激素暴露以及儿童性别类型的行为以及玩具和玩伴的偏好。
DOI: 10.1016/j.yhbeh.2020.104889
发表时间: 2021-01
期刊: Hormones and behavior
影响因子: 3.5
作者: [Spencer D, Pasterski V, Neufeld SAS, Glover V, O'Connor TG, Hindmarsh PC, Hughes IA, Acerini CL, Hines M]
通讯作者: Hines M
DOI: 10.1016/j.yhbeh.2017.09.012
发表时间: 2017-11
期刊: Hormones and behavior
影响因子: 3.5
作者: [Spencer D, Pasterski V, Neufeld S, Glover V, O'Connor TG, Hindmarsh PC, Hughes IA, Acerini CL, Hines M]
通讯作者: Hines M
Abnormal sexual development and psychosexual issues.
性发育异常和性心理问题。
DOI: 10.1016/s0950-351x(98)80563-6
发表时间: 1998
期刊: Bailliere's clinical endocrinology and metabolism.
影响因子: --
作者: [Hines,M]
通讯作者: Hines,M
15
    Brain and behavior in individuals with intersex conditions
    • 批准号:
      9706914
    • 项目类别:
    • 资助金额:
      $33.87万
    • 财政年份:
      2015
    • 负责人:
      Melissa Hines
    • 依托单位:
    Brain and behavior in individuals with intersex conditions
    • 批准号:
      9540059
    • 项目类别:
    • 资助金额:
      $38.07万
    • 财政年份:
      2015
    • 负责人:
      Melissa Hines
    • 依托单位:
    Brain and behavior in individuals with intersex conditions
    • 批准号:
      9285813
    • 项目类别:
    • 资助金额:
      $38.0万
    • 财政年份:
      2015
    • 负责人:
      Melissa Hines
    • 依托单位:
    HORMONAL INFLUENCES ON NEURAL-BEHAVIORAL DEVELOPMENT
    国内基金
    海外基金
    补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
    靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
    • 批准号:
      JCZRQN202500010
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
    • 依托单位:
    对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
    • 批准号:
      2025JJ70209
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
      雷芬芳
    • 依托单位:
    AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
    • 批准号:
      --
    • 项目类别:
      面上项目
    • 资助金额:
      --
    • 批准年份:
      2024
    • 负责人:
      万荣
    • 依托单位: