| Dendrosomal curcumin increases expression of the long non-coding RNA gene MEG3 via up-regulation of epi-miRs in hepatocellular cancer M Zamani, M Sadeghizadeh, M Behmanesh, F Najafi Phytomedicine 22 (10), 961-967, 2015 | 113 | 2015 |
| The protective and therapeutic effects of alpha-solanine on mice breast cancer M Mohsenikia, AM Alizadeh, S Khodayari, H Khodayari, A Karimi, ... European journal of pharmacology 718 (1-3), 1-9, 2013 | 110 | 2013 |
| Encapsulation of curcumin in diblock copolymer micelles for cancer therapy AM Alizadeh, M Sadeghizadeh, F Najafi, SK Ardestani, ... BioMed research international 2015, 2015 | 87 | 2015 |
| Dendrosomal nano-curcumin, the novel formulation to improve the anticancer properties of curcumin BM TAHMASEBI, MV ERFANI, E Babaei, F NAJAFI, M Zamani, M Shariati, ... PROGRESS IN BIOLOGICAL SCIENCES 5 (2), 143-158, 2015 | 58 | 2015 |
| A novel diblock of copolymer of (monomethoxy poly [ethylene glycol]-oleate) with a small hydrophobic fraction to make stable micelles/polymersomes for curcumin delivery to … V Erfani-Moghadam, A Nomani, M Zamani, Y Yazdani, F Najafi, ... International journal of nanomedicine, 5541-5554, 2014 | 47 | 2014 |
| Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with … EG Jones, N Mazaheri, R Maroofian, M Zamani, T Seifi, A Sedaghat, ... Scientific reports 9 (1), 9038, 2019 | 27 | 2019 |
| Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals K Saida, R Maroofian, T Sengoku, T Mitani, AT Pagnamenta, D Marafi, ... Genetics in Medicine 25 (1), 90-102, 2023 | 16 | 2023 |
| HOXC10 is significantly overexpressed in colorectal cancer M Enteghami, M Ghorbani, M Zamani, H Galehdari Biomedical reports 13 (3), 1-1, 2020 | 15 | 2020 |
| Dendrosomal curcumin upregulates expression of the long non-coding RNA gene MEG3 in U87MG glioblastoma cells M Zamani, M Sadeghizadeh, M Behmanesh Pathobiology Research 17 (3), 41-56, 2014 | 11 | 2014 |
| Identification of three novel mutations in the FANCA, FANCC, and ITGA2B genes by whole exome sequencing S Negahdari, M Zamani, T Seifi, S Sedighzadeh, N Mazaheri, J Zeighami, ... International journal of preventive medicine 11 (1), 117, 2020 | 4 | 2020 |
| Validity of chromosomal aneuploidies testing during pregnancy: a comparison of karyotype, interphase-FISH and QF-PCR techniques H Galehdari, M Barati, M Mahmoudi, N Shahbazian, S Masihi, M Zamani, ... Biomed Res 29 (10), 2164-8, 2018 | 4 | 2018 |
| An insight into detection pathways/biosensors of highly infectious coronaviruses M Entesari, M Zamani, M Heidarizadeh, R Moradi, F Khakdan, F Rafiei Molecular Biotechnology, 1-16, 2022 | 3 | 2022 |
| Frequent novel mutations are causative for maple syrup urine disease from Southwest Iran A Sedaghat, M Zamani, A Jahanshahi, SB Ghaderian, G Shariati, ... Meta Gene 16, 96-104, 2018 | 3 | 2018 |
| Novel homozygous missense mutation in RYR1 leads to severe congenital ptosis, ophthalmoplegia, and scoliosis in the absence of myopathy N Dilaver, N Mazaheri, R Maroofian, J Zeighami, T Seifi, M Zamani, ... Molecular Syndromology 9 (1), 25-29, 2017 | 3 | 2017 |
| PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss SE Redfield, P De-la-Torre, M Zamani, H Wang, H Khan, T Morris, ... Human Genetics, 1-19, 2024 | 2 | 2024 |
| Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54 TB Smith, A Rea, HB Thomas, K Thompson, M Oláhová, R Maroofian, ... European Journal of Human Genetics 31 (10), 1190-1194, 2023 | 2 | 2023 |
| Whole-exome sequencing application for genetic diagnosis of kidney diseases: A study from southwest of Iran M Zamani, T Seifi, S Sedighzadeh, S Negahdari, J Zeighami, A Sedaghat, ... Kidney360 2 (5), 873-877, 2021 | 2 | 2021 |
| ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations L Laugwitz, F Cheng, SC Collins, A Hustinx, N Navarro, S Welsch, H Cox, ... Brain, awae058, 2024 | 1 | 2024 |
| Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian families R Zabihi, M Zamani, M Aminzadeh, N Chamanrou, FZ Kiani, T Seifi, ... Frontiers in Genetics 15, 1343094, 2024 | 1 | 2024 |
| TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions H Almousa, SA Lewis, S Bakhtiari, SH Nordlie, A Pagnozzi, H Magee, ... Brain 147 (1), 311-324, 2024 | 1 | 2024 |
Majid Sadeghizadeh, PhDProfessor of Genetics, School of Biological Sciences, Tarbiat Modares University.Tehran/IranVerified email at modares.ac.ir
