Homa Majd • UCSF Profiles

Homa Majd, PhD

Title(s)	Postdoctoral Scholar, Cellular Molecular Pharmacology
School	School of Medicine
Address	600 16th Street, #S576 San Francisco CA 94158
Phone	--
ORCID	0000-0002-2048-1839
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Biography

Education and Training

University of Cambridge	PhD	2016	Biological Sciences
University of Tehran	BSc	2012	Biotechnology

Bibliographic

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. to make corrections and additions.

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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.

A call for a unified and multimodal definition of cellular identity in the enteric nervous system. bioRxiv. 2024 Feb 05. Majd H, Cesiulis A, Samuel RM, Richter MN, Elder N, Guyer RA, Hao MM, Stamp LA, Goldstein AM, Fattahi F. PMID: 38293133; PMCID: PMC10827084.

View in: PubMed Mentions:
Modeling enteric glia development, physiology and disease using human pluripotent stem cells. Neurosci Lett. 2023 08 10; 811:137334. Scantlen MD, Majd H, Fattahi F. PMID: 37315730.

View in: PubMed Mentions: 1 Fields:
Neu Neurology
Translation:Humans Cells
Deriving Schwann cells from hPSCs enables disease modeling and drug discovery for diabetic peripheral neuropathy. Cell Stem Cell. 2023 05 04; 30(5):632-647.e10. Majd H, Amin S, Ghazizadeh Z, Cesiulis A, Arroyo E, Lankford K, Majd A, Farahvashi S, Chemel AK, Okoye M, Scantlen MD, Tchieu J, Calder EL, Le Rouzic V, Shibata B, Arab A, Goodarzi H, Pasternak G, Kocsis JD, Chen S, Studer L, Fattahi F. PMID: 37146583; PMCID: PMC10249419.

View in: PubMed Mentions: 3 Fields:
Cel Cell Biology
Translation:Humans Animals Cells
Generation of Schwann cell derived melanocytes from hPSCs identifies pro-metastatic factors in melanoma. bioRxiv. 2023 Mar 07. Samuel RM, Navickas A, Maynard A, Gaylord EA, Garcia K, Bhat S, Majd H, Richter MN, Elder N, Le D, Nguyen P, Shibata B, Llabata ML, Selleri L, Laird DJ, Darmanis S, Goodarzi H, Fattahi F. PMID: 36945537; PMCID: PMC10028814.

View in: PubMed Mentions:
Androgens increase excitement in brain organoid research. Cell Stem Cell. 2022 04 07; 29(4):495-497. Samuel RM, Majd H, Richter MN, Fattahi F. PMID: 35395183.

View in: PubMed Mentions: Fields:
Cel Cell Biology
Translation:Humans Cells
Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men. Cell Stem Cell. 2020 12 03; 27(6):876-889.e12. Samuel RM, Majd H, Richter MN, Ghazizadeh Z, Zekavat SM, Navickas A, Ramirez JT, Asgharian H, Simoneau CR, Bonser LR, Koh KD, Garcia-Knight M, Tassetto M, Sunshine S, Farahvashi S, Kalantari A, Liu W, Andino R, Zhao H, Natarajan P, Erle DJ, Ott M, Goodarzi H, Fattahi F. PMID: 33232663; PMCID: PMC7670929.

View in: PubMed Mentions: 135 Fields:
Cel Cell Biology
Translation:Humans Animals Cells
Androgen Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men. bioRxiv. 2020 May 15. Ghazizadeh Z, Majd H, Richter M, Samuel R, Zekavat SM, Asgharian H, Farahvashi S, Kalantari A, Ramirez J, Zhao H, Natarajan P, Goodarzi H, Fattahi F. PMID: 32511360; PMCID: PMC7263488.

View in: PubMed Mentions:
BCAA catabolism in brown fat controls energy homeostasis through SLC25A44. Nature. 2019 08; 572(7771):614-619. 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. PMID: 31435015; PMCID: PMC6715529.

View in: PubMed Mentions: 175 Fields:
Sci Science
Translation:Humans Animals Cells
Screening of candidate substrates and coupling ions of transporters by thermostability shift assays. Elife. 2018 10 15; 7. Majd H, King MS, Palmer SM, Smith AC, Elbourne LD, Paulsen IT, Sharples D, Henderson PJ, Kunji ER. PMID: 30320551; PMCID: PMC6211832.

View in: PubMed Mentions: 27 Fields:
Bio Biology
Translation:Humans Animals Cells
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. Majd H, King MS, Smith AC, Kunji ERS. PMID: 29031613.

View in: PubMed Mentions: 18 Fields:
Bio Biochemistry Bio Biophysics Met Metabolism
Translation:Humans Cells
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. 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. PMID: 27912046; PMCID: PMC5142113.

View in: PubMed Mentions: 14 Fields:
Gen Genetics
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. Kunji ER, Aleksandrova A, King MS, Majd H, Ashton VL, Cerson E, Springett R, Kibalchenko M, Tavoulari S, Crichton PG, Ruprecht JJ. PMID: 27713079.

View in: PubMed Mentions: 1 Fields:
Bio Biochemistry Bio Biophysics
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. 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. PMID: 27693233; PMCID: PMC5065686.

View in: PubMed Mentions: 50 Fields:
Gen Genetics
Translation:Humans Cells
The transport mechanism of the mitochondrial ADP/ATP carrier. Biochim Biophys Acta. 2016 10; 1863(10):2379-93. Kunji ER, Aleksandrova A, King MS, Majd H, Ashton VL, Cerson E, Springett R, Kibalchenko M, Tavoulari S, Crichton PG, Ruprecht JJ. PMID: 27001633.

View in: PubMed Mentions: 72 Fields:
Bio Biochemistry Bio Biophysics
Translation:Humans Animals Cells
The mitochondrial dicarboxylate and 2-oxoglutarate carriers do not transport glutathione. FEBS Lett. 2015 Feb 27; 589(5):621-8. Booty LM, King MS, Thangaratnarajah C, Majd H, James AM, Kunji ER, Murphy MP. PMID: 25637873; PMCID: PMC4332691.

View in: PubMed Mentions: 29 Fields:
Bio Biochemistry
Translation:Cells