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Homa Majd, PhD

Title(s)Postdoctoral Scholar, Regeneration Medicine
SchoolSchool of Medicine
Emailhoma.majd@ucsf.edu
ORCID ORCID Icon0000-0002-2048-1839 Additional info
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    Collapse Biography 
    Collapse Education and Training
    University of CambridgePhD2016Biological Sciences
    University of TehranBSc2012Biotechnology

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Yoneshiro T, Wang Q, Tajima K, Matsushita M, Maki H, Igarashi K, Dai Z, White PJ, McGarrah RW, Ilkayeva OR, Deleye Y, Oguri Y, Kuroda M, Ikeda K, Li H, Ueno A, Ohishi M, Ishikawa T, Kim K, Chen Y, Sponton CH, Pradhan RN, Majd H, Greiner VJ, Yoneshiro M, Brown Z, Chondronikola M, Takahashi H, Goto T, Kawada T, Sidossis L, Szoka FC, McManus MT, Saito M, Soga T, Kajimura S. BCAA catabolism in brown fat controls energy homeostasis through SLC25A44. Nature. 2019 08; 572(7771):614-619. PMID: 31435015.
      View in: PubMed
    2. Majd H, King MS, Palmer SM, Smith AC, Elbourne LD, Paulsen IT, Sharples D, Henderson PJ, Kunji ER. Screening of candidate substrates and coupling ions of transporters by thermostability shift assays. Elife. 2018 10 15; 7. PMID: 30320551.
      View in: PubMed
    3. Majd H, King MS, Smith AC, Kunji ERS. Pathogenic mutations of the human mitochondrial citrate carrier SLC25A1 lead to impaired citrate export required for lipid, dolichol, ubiquinone and sterol synthesis. Biochim Biophys Acta Bioenerg. 2018 Jan; 1859(1):1-7. PMID: 29031613.
      View in: PubMed
    4. Thompson K, Majd H, Dallabona C, Reinson K, King MS, Alston CL, He L, Lodi T, Jones SA, Fattal-Valevski A, Fraenkel ND, Saada A, Haham A, Isohanni P, Vara R, Barbosa IA, Simpson MA, Deshpande C, Puusepp S, Bonnen PE, Rodenburg RJ, Suomalainen A, Õunap K, Elpeleg O, Ferrero I, McFarland R, Kunji ERS, Taylor RW. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. Am J Hum Genet. 2016 12 01; 99(6):1405. PMID: 27912046.
      View in: PubMed
    5. Kunji ER, Aleksandrova A, King MS, Majd H, Ashton VL, Cerson E, Springett R, Kibalchenko M, Tavoulari S, Crichton PG, Ruprecht JJ. Corrigendum to "The transport mechanism of the mitochondrial ADP/ATP carrier" [Biochim. Biophys. Acta 1863/10 (2016) 2379-2393]. Biochim Biophys Acta. 2016 12; 1863(12):3169. PMID: 27713079.
      View in: PubMed
    6. Thompson K, Majd H, Dallabona C, Reinson K, King MS, Alston CL, He L, Lodi T, Jones SA, Fattal-Valevski A, Fraenkel ND, Saada A, Haham A, Isohanni P, Vara R, Barbosa IA, Simpson MA, Deshpande C, Puusepp S, Bonnen PE, Rodenburg RJ, Suomalainen A, Õunap K, Elpeleg O, Ferrero I, McFarland R, Kunji ER, Taylor RW. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. Am J Hum Genet. 2016 10 06; 99(4):860-876. PMID: 27693233.
      View in: PubMed
    7. Kunji ER, Aleksandrova A, King MS, Majd H, Ashton VL, Cerson E, Springett R, Kibalchenko M, Tavoulari S, Crichton PG, Ruprecht JJ. The transport mechanism of the mitochondrial ADP/ATP carrier. Biochim Biophys Acta. 2016 10; 1863(10):2379-93. PMID: 27001633.
      View in: PubMed
    8. Booty LM, King MS, Thangaratnarajah C, Majd H, James AM, Kunji ER, Murphy MP. The mitochondrial dicarboxylate and 2-oxoglutarate carriers do not transport glutathione. FEBS Lett. 2015 Feb 27; 589(5):621-8. PMID: 25637873.
      View in: PubMed