Harvard Catalyst Profiles

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Yaser Heshmati, Ph.D.


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Harada T, Heshmati Y, Kalfon J, Perez MW, Xavier Ferrucio J, Ewers J, Hubbell Engler B, Kossenkov A, Ellegast JM, Yi JS, Bowker A, Zhu Q, Eagle K, Liu T, Kai Y, Dempster JM, Kugener G, Wickramasinghe J, Herbert ZT, Li CH, Vrabic Koren J, Weinstock DM, Paralkar VR, Nabet B, Lin CY, Dharia NV, Stegmaier K, Orkin SH, Pimkin M. A distinct core regulatory module enforces oncogene expression in KMT2A-rearranged leukemia. Genes Dev. 2022 Mar 01; 36(5-6):368-389. PMID: 35301220.
    Citations:    Fields:    Translation:Humans
  2. Sanjiv K, Calderón-Montaño JM, Pham TM, Erkers T, Tsuber V, Almlöf I, Höglund A, Heshmati Y, Seashore-Ludlow B, Nagesh Danda A, Gad H, Wiita E, Göktürk C, Rasti A, Friedrich S, Centio A, Estruch M, Våtsveen TK, Struyf N, Visnes T, Scobie M, Koolmeister T, Henriksson M, Wallner O, Sandvall T, Lehmann S, Theilgaard-Mönch K, Garnett MJ, Östling P, Walfridsson J, Helleday T, Warpman Berglund U. MTH1 Inhibitor TH1579 Induces Oxidative DNA Damage and Mitotic Arrest in Acute Myeloid Leukemia. Cancer Res. 2021 11 15; 81(22):5733-5744. PMID: 34593524.
    Citations: 1     Fields:    Translation:HumansAnimalsCells
  3. Atta H, Gheinani AH, Wacker A, Heshmati Y, Bigger-Allen A, Lambrinos G, Gao Y, Bielenberg DR, Adam RM. A Single Cell Dissociation Approach for Molecular Analysis of Urinary Bladder in the Mouse Following Spinal Cord Injury. J Vis Exp. 2020 06 17; (160). PMID: 32628176.
    Citations:    Fields:    Translation:AnimalsCells
  4. Heshmati Y, Kharazi S, Türköz G, Chang D, Kamali Dolatabadi E, Boström J, Krstic A, Boukoura T, Wagner E, Kadri N, Månsson R, Altun M, Qian H, Walfridsson J. The histone chaperone NAP1L3 is required for haematopoietic stem cell maintenance and differentiation. Sci Rep. 2018 07 25; 8(1):11202. PMID: 30046127.
    Citations: 3     Fields:    Translation:HumansAnimalsCells
  5. Xiao P, Sandhow L, Heshmati Y, Kondo M, Bouderlique T, Dolinska M, Johansson AS, Sigvardsson M, Ekblom M, Walfridsson J, Qian H. Distinct roles of mesenchymal stem and progenitor cells during the development of acute myeloid leukemia in mice. Blood Adv. 2018 06 26; 2(12):1480-1494. PMID: 29945938.
    Citations: 7     Fields:    Translation:AnimalsCells
  6. Heshmati Y, Türköz G, Harisankar A, Kharazi S, Boström J, Dolatabadi EK, Krstic A, Chang D, Månsson R, Altun M, Qian H, Walfridsson J. The chromatin-remodeling factor CHD4 is required for maintenance of childhood acute myeloid leukemia. Haematologica. 2018 07; 103(7):1169-1181. PMID: 29599201.
    Citations: 7     Fields:    Translation:HumansCells
  7. Herold N, Rudd SG, Ljungblad L, Sanjiv K, Myrberg IH, Paulin CB, Heshmati Y, Hagenkort A, Kutzner J, Page BD, Calderón-Montaño JM, Loseva O, Jemth AS, Bulli L, Axelsson H, Tesi B, Valerie NC, Höglund A, Bladh J, Wiita E, Sundin M, Uhlin M, Rassidakis G, Heyman M, Tamm KP, Warpman-Berglund U, Walfridsson J, Lehmann S, Grandér D, Lundbäck T, Kogner P, Henter JI, Helleday T, Schaller T. Targeting SAMHD1 with the Vpx protein to improve cytarabine therapy for hematological malignancies. Nat Med. 2017 Feb; 23(2):256-263. PMID: 28067901.
    Citations: 43     Fields:    Translation:HumansAnimals
  8. Rezazadeh M, Khorrami A, Yeghaneh T, Talebi M, Kiani SJ, Heshmati Y, Gharesouran J. Genetic Factors Affecting Late-Onset Alzheimer's Disease Susceptibility. Neuromolecular Med. 2016 Mar; 18(1):37-49. PMID: 26553058.
    Citations: 8     Fields:    Translation:Humans
  9. Sadeghi B, Heshmati Y, Khoein B, Kaipe H, Uzunel M, Walfridsson J, Ringdén O. Xeno-immunosuppressive properties of human decidual stromal cells in mouse models of alloreactivity in vitro and in vivo. Cytotherapy. 2015 Dec; 17(12):1732-45. PMID: 26481415.
    Citations: 8     Fields:    Translation:HumansAnimalsCells
  10. Rafati M, Seyyedaboutorabi E, Ghadirzadeh MR, Heshmati Y, Adibi H, Keihanidoust Z, Eshraghian MR, Javadi GR, Dastan J, Mosavi-Jarrahi A, Hoseini A, Purhoseini M, Ghaffari SR. "Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes. Mol Cytogenet. 2012 Jan 29; 5(1):9. PMID: 22283845.
    Citations: 3     
  11. Rafati M, Ghadirzadeh MR, Heshmati Y, Adibi H, Keihanidoust Z, Eshraghian MR, Dastan J, Hoseini A, Purhoseini M, Ghaffari SR. "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements. Mol Cytogenet. 2012 Jan 19; 5(1):4. PMID: 22260313.
    Citations: 3     
  12. Zarif Yeganeh M, Mirabzadeh A, Khorram Khorshid HR, Kamali K, Heshmati Y, Gozalpour E, Veissy K, Olad Nabi M, Najmabadi H, Ohadi M. Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 05; 153B(1):347-9. PMID: 19475601.
    Citations: 6     Fields:    Translation:Humans
  13. Heshmati Y, Mirabzadeh A, Feizzade G, Gilanipour M, Etminan MR, Khoram Khorshid HR, Kamali K, Fakhri M, Moghimi N, Najmabadi H, Ohadi M. A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin-1 gene and risk of Alzheimer's disease; extra-short alleles and accumulated allele homozygosity. Am J Med Genet B Neuropsychiatr Genet. 2009 Mar 05; 150B(2):248-53. PMID: 18561140.
    Citations: 5     Fields:    Translation:HumansCells
  14. Moheb LA, Tzschach A, Garshasbi M, Kahrizi K, Darvish H, Heshmati Y, Kordi A, Najmabadi H, Ropers HH, Kuss AW. Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome. Eur J Hum Genet. 2008 Feb; 16(2):270-3. PMID: 18043714.
    Citations: 28     Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.