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Research Topic : premature death
Field of Research : Reproduction
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Reproduction (16)
Cell Development, Proliferation and Death (4)
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  • Researchers (8)
  • Funded Activities (16)
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  • Funded Activity

    Androgen Receptor Activity In Normal And Abnormal Human Ovarian Function

    Funder
    National Health and Medical Research Council
    Funding Amount
    $416,696.00
    Summary
    Androgens are hormones normally associated with men, but women also produce androgens and they are essential for normal female health and reproduction. Imbalances in female androgen activity could account for approximately 50% of female infertility, but exactly how androgens behave in women is not well understood. Making too much androgen is the most common hormonal problem experienced by women in their reproductive years, and it affects the ovary in a way that can cause infertility. Women with .... Androgens are hormones normally associated with men, but women also produce androgens and they are essential for normal female health and reproduction. Imbalances in female androgen activity could account for approximately 50% of female infertility, but exactly how androgens behave in women is not well understood. Making too much androgen is the most common hormonal problem experienced by women in their reproductive years, and it affects the ovary in a way that can cause infertility. Women with this problem have polycystic ovary syndrome (PCOS). Gaining weight increases the chance of having problems with fertility and increases the risk of diabetes and heart problems in women with PCOS. The cause of PCOS is unknown, but it can occur in families, which indicates that some genetic factor is involved. On the other hand, the concept that some women do not produce enough androgen is only beginning to emerge and remains a controversial topic among medical experts. Part of the problem with this notion is that normal female androgen levels are very difficult to measure accurately, so no one can say for certain how much is too little. A recent scientific study in female mice indicates that poor androgen action causes infertility early in life because the ovary is ageing too quickly. A similar thing could possibly occur in women, but this has never been scientifically explored. However, we have some early evidence that shows abnormally low androgen levels in infertile women with signs of early aging in the ovary. Our study aims to understand the role that androgens play in normal and abnormal ovarian function. A large part of this study involves investigation of the androgen receptor, a molecule that controls what androgens can do inside body organs. We think that abnormal activity of this receptor will be involved in ovarian diseases that cause infertility in women. This understanding may lead to new means of diagnosing and treating infertility in women.
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    Funded Activity

    The Role Of Hormones In The Control Of Uterine Activity At Birth

    Funder
    National Health and Medical Research Council
    Funding Amount
    $115,282.00
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    Funded Activity

    Computer Program To Predict Premature Birth

    Funder
    National Health and Medical Research Council
    Funding Amount
    $388,000.00
    Summary
    Preterm birth is a major cause of neonatal death and cerebral palsy. This grant will provide proof-of-concept that a computer program can be developed to predict a pregnant woman�s risk of preterm birth. There is a large market (4M US and 8M Europe), there are no competing technologies. This is a unique collaboration between Biomedical Engineering and an Australian centre with an international reputation in preterm birth, assisted by a pathology company.
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    Funded Activity

    Understanding Immune Tolerance In Pregnancy To Discover A New Intervention For The Treatment Of Pre-eclampsia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $492,202.00
    Summary
    Pre-eclampsia is a common complication of pregnancy. Women who develop pre-eclampsia experience high blood pressure, swelling and lose protein in the urine. There is no treatment for pre-eclampsia other than delivery of the baby. Pre-eclampsia has risks for the mother and the baby. This research will discover whether generalised inflammation in the mother is a cause of pre-eclampsia and will evaluate the role of a novel treatment for its potential to prevent this life threatening condition.
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    Funded Activity

    Premature Labour Induced By Vaginal Microorganisms

    Funder
    National Health and Medical Research Council
    Funding Amount
    $94,941.00
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    Funded Activity

    Prevention Of Preterm Labour

    Funder
    National Health and Medical Research Council
    Funding Amount
    $272,033.00
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    Funded Activity

    Androgen Receptor Mechanims In Female Reproductive Physiology

    Funder
    National Health and Medical Research Council
    Funding Amount
    $539,773.00
    Summary
    Infertility occurs in one in six Australian couples with 50% attributable to females, thus, enhancing our understanding of ovarian and uterine function is of great importance. This project tests the proposal that androgens (steroid hormones) play a major role in regulating female reproductive physiology through their interaction with the androgen receptor. We have developed novel mouse models which we will use to determine the roles of androgens in regulating female reproductive function.
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    Funded Activity

    Mechanisms Of Escape From Progesterone-induced Suppression: Role In Normal And Preterm Birth

    Funder
    National Health and Medical Research Council
    Funding Amount
    $547,970.00
    Summary
    Prematurity caused by preterm birth is the leading cause of death and disease among newborns in Australia. Here we will define how the length of pregnancy is determined by the opposing actions of progesterone, which maintains pregnancy, and prostaglandins, which induce labour. We will demonstrate the mechanism by which the actions of the two hormones are balanced in normal pregnancy and disrupted in preterm labour. We will show that preterm birth can be prevented by correcting the disorder.
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    Funded Activity

    Discriminating The Roles Of Inhibin A And B In Reproductive Systems

    Funder
    National Health and Medical Research Council
    Funding Amount
    $312,576.00
    Summary
    Inhibin A and B are essential for the regulation of fertility based on their dual inhibitory actions on follicle stimulating hormone secretion by the pituitary and egg and sperm production in the gonads. An understanding of the mechanisms involved in inhibin A and B actions will: (1) identify novel biomarkers for the diagnosis of reproductive disorders (2) enhance the management of reproductive disorders (3) identify targets for the development of therapeutic means of modulating fertility
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    Funded Activity

    Discovery Projects - Grant ID: DP160100647

    Funder
    Australian Research Council
    Funding Amount
    $398,000.00
    Summary
    A novel microtubule severing protein involved in male germ cell biology. The project aims to better understand the cellular and biochemical mechanisms underlying a key component of male fertility. Microtubules are a fundamental component of all cells. A mechanism that is increasingly recognised as essential for microtubules regulation is severing. It has been discovered that an uncharacterised microtubule severing protein, KATNAL2, has a key role in male germ cell development. This project aims .... A novel microtubule severing protein involved in male germ cell biology. The project aims to better understand the cellular and biochemical mechanisms underlying a key component of male fertility. Microtubules are a fundamental component of all cells. A mechanism that is increasingly recognised as essential for microtubules regulation is severing. It has been discovered that an uncharacterised microtubule severing protein, KATNAL2, has a key role in male germ cell development. This project aims to define the mechanisms underlying KATNAL2 function in the male germ line. It is expected that these data will generate a comprehensive picture of KATNAL2 function and provide foundation data of relevance across multiple species and tissues. In the longer term, it may also reveal a rational strategy for fertility enhancement or suppression.
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    Showing 1-10 of 16 Funded Activites

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