Mizuho Mimoto

TitleAssociate Physician
InstitutionUniversity of California San Diego
Address9500 Gilman Drive #0912
La Jolla CA 92093
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    1. Çatli G, Fujisawa H, Kirbiyik Ö, Mimoto M, Gençpinar P, Özdemir TR, Dündar BN, Dumitrescu AM. A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy. Thyroid. 2018 Aug 02. PMID: 29882503.
      View in: PubMed
    2. Mimoto M, Karaca A, Scherberg N, Dumitrescu AM, Refetoff S. Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid Tests. Thyroid. 2018 Jun; 28(6):811-814. PMID: 29676214.
      View in: PubMed
    3. Mimoto M, Oyler JL, Davis AM. Evaluation and Treatment of Hirsutism in Premenopausal Women. JAMA. 2018 Apr 17; 319(15):1613-1614. PMID: 29522641.
      View in: PubMed
    4. Mimoto M, Nadal A, Sargis RM. Polluted Pathways: Mechanisms of Metabolic Disruption by Endocrine Disrupting Chemicals. Curr Environ Health Rep. 2017 06; 4(2):208-222. PMID: 28432637.
      View in: PubMed
    5. Green YS, Kwon S, Mimoto M, Xie Y, Christian JL. Tril targets Smad7 for degradation to allow hematopoietic specification in Xenopus embryos. Development. 2016 11 01; 143(21):4016-4026. PMID: 27633996.
      View in: PubMed
    6. Mimoto M, Kwon S, Green YS, Goldman D, Christian JL. GATA2 regulates Wnt signaling to promote primitive red blood cell fate. Dev Biol. 2015 Nov 01; 407(1):1-11. PMID: 26365900; PMCID: PMC4641806 [Available on 11/01/16].
    7. Mimoto M, Christian JL. Friend of GATA (FOG) interacts with the nucleosome remodeling and deacetylase complex (NuRD) to support primitive erythropoiesis in Xenopus laevis. PLoS One. 2012; 7(1):e29882. PMID: 22235346; PMCID: PMC3250481.
    8. Mimoto M, Christian JL. Manipulation of gene function in Xenopus laevis. Methods Mol Biol. 2011; 770:55-75. PMID: 21805261; PMCID: PMC3911881.
    9. Loomes KM, Stevens SA, O'Brien ML, Gonzalez DM, Ryan MJ, Segalov M, Dormans NJ, Mimoto M, Gibson JD, Sewell W, Schaffer AA, Nah HD, Rappaport EF, Pratt SC, Dunwoodie SL, Kusumi K. Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects. Dev Dyn. 2007 Oct; 236(10):2943-51. PMID: 17849441.
      View in: PubMed
    10. Kusumi K, Mimoto M, Covello KL, Beddington RS, Krumlauf R, Dunwoodie SL. Dll3 pudgy mutation differentially disrupts dynamic expression of somite genes. Genesis. 2004 Jun; 39(2):115-21. PMID: 15170697.
      View in: PubMed
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