Search Results - "Moriwaki, Mika"

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  1. 1

    Chronic hypoxia disrupts T regulatory cell phenotype contributing to the emergence of exTreg-TH17 cells by Lantz, Benjamin J., Moriwaki, Mika, Oyebamiji, Olufunmilola M., Guo, Yan, Gonzalez Bosc, Laura

    Published in Frontiers in physiology (29-01-2024)
    “…The imbalance between pro-inflammatory T helper 17 (T H 17) cells and anti-inflammatory regulatory T cells (Tregs) has been implicated in multiple inflammatory…”
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    Journal Article
  2. 2

    PRL Mutation Causing Alactogenesis: Insights Into Prolactin Structure and Function Relationships by Moriwaki, Mika, Welt, Corrine K

    “…Abstract Context Isolated prolactin deficiency is a rare disorder manifesting as absence of puerperal lactation. We identified a 2-generation family with 3…”
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    Journal Article
  3. 3

    Chronic hypoxia disrupts memory T regulatory cell phenotype which contributes to the pathogenesis of pulmonary hypertension by Lantz, Benjamin, Moriwaki, Mika, Oyebamiji, Olufunmilola, Guo, Yan, Garcia, Selina, Gonzalez Bosc, Laura

    Published in Physiology (Bethesda, Md.) (01-05-2023)
    “…Abstract only Pulmonary hypertension (PH) caused by chronic hypoxia (CH) is a multifaceted disease most often caused by sleep apnea, prolonged high-altitude…”
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    Journal Article
  4. 4

    Heterozygous Eif4nif1 Stop Gain Mice Replicate the Primary Ovarian Insufficiency Phenotype by Moriwaki, Mika, Welt, Corrine Kolka

    Published in Journal of the Endocrine Society (03-05-2021)
    “…Abstract We identified a stop-gain mutation in eIF4ENIF1 in a family in which multiple women developed primary ovarian insufficiency (POI) at approximately age…”
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    Journal Article
  5. 5

    MON-434 Familial Alactogenesis Associated with a Prolactin Mutation by Moriwaki, Mika, Welt, Corrine

    Published in Journal of the Endocrine Society (30-04-2019)
    “…BACKGROUND: Isolated prolactin deficiency is a rare disorder manifesting as absence of puerperal lactation. We identified a family with multiple members who…”
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    Journal Article
  6. 6

    Chronic hypoxia disrupts T regulatory cell phenotype contributing to the emergence of exTreg-T H 17 cells by Lantz, Benjamin J, Moriwaki, Mika, Oyebamiji, Olufunmilola M, Guo, Yan, Gonzalez Bosc, Laura

    Published in Frontiers in physiology (2023)
    “…The imbalance between pro-inflammatory T helper 17 (T 17) cells and anti-inflammatory regulatory T cells (Tregs) has been implicated in multiple inflammatory…”
    Get full text
    Journal Article
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    Rapid, sensitive detection of bacteria in platelet samples with Fountain Flow Cytometry by Johnson, Paul, Moriwaki, Mika, Johnson, Joseph

    Published in Journal of clinical laboratory analysis (01-11-2017)
    “…Background There is a current need to develop a technique for bacterial screening of platelet donations that is more rapid, sensitive, and economical than…”
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  9. 9

    Primary Ovarian Insufficiency and Azoospermia in Carriers of a Homozygous PSMC3IP Stop Gain Mutation by Al-Agha, Abdulmoein Eid, Ahmed, Ihab Abdulhamed, Nuebel, Esther, Moriwaki, Mika, Moore, Barry, Peacock, Katherine A, Mosbruger, Tim, Neklason, Deborah W, Jorde, Lynn B, Yandell, Mark, Welt, Corrine K

    “…Abstract Context The etiology of primary ovarian insufficiency (POI) remains unknown in most cases. Objective We sought to identify the genes causing POI…”
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    OR31-06 Candidate Gene Variants in a Large Cohort of Women with Primary Ovarian Insufficiency by Gorsi, Bushra, Moriwaki, Mika, Moore, Marvin B, Rajkovic, Aleksandar, Nelson, Lawrence M, Yandell, Mark, Welt, Corrine Kolka

    Published in Journal of the Endocrine Society (08-05-2020)
    “…Abstract Primary ovarian insufficiency (POI) is highly heritable. The majority of cases have no known cause. We hypothesized that mutations in previously…”
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    Journal Article
  13. 13

    POLR2C Mutations Are Associated With Primary Ovarian Insufficiency in Women by Moriwaki, Mika, Moore, Barry, Mosbruger, Timothy, Neklason, Deborah W, Yandell, Mark, Jorde, Lynn B, Welt, Corrine K

    Published in Journal of the Endocrine Society (01-03-2017)
    “…Primary ovarian insufficiency (POI) results from a premature loss of oocytes, causing infertility and early menopause. The etiology of POI remains unknown in a…”
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    Journal Article
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    POLR2C Mutations Are Associated With Primary Ovarian Insufficiency in Women by Moriwaki, Mika, Moore, Barry, Mosbruger, Timothy, Neklason, Deborah W, Yandell, Mark, Jorde, Lynn B, Welt, Corrine K

    Published in Journal of the Endocrine Society (01-03-2017)
    “…Primary ovarian insufficiency (POI) results from a premature loss of oocytes, causing infertility and early menopause. The etiology of POI remains unknown in a…”
    Get full text
    Journal Article
  16. 16

    POLR2C Mutations Are Associated With Primary Ovarian Insufficiency in Women by Moriwaki, Mika, Moore, Barry, Mosbruger, Timothy, Neklason, Deborah W., Yandell, Mark, Jorde, Lynn B., Welt, Corrine K.

    Published in Journal of the Endocrine Society (07-02-2017)
    “…We demonstrate POLR2C , a heterozygous nonsense mutation in subunit C of RNA polymerase II associated with POI in a family previously thought to have an…”
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    Journal Article
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