R
Ramin Ghahremanzadeh
Researcher at Avicenna Research Institute
Publications - 90
Citations - 2072
Ramin Ghahremanzadeh is an academic researcher from Avicenna Research Institute. The author has contributed to research in topics: Indoline & Catalysis. The author has an hindex of 24, co-authored 89 publications receiving 1796 citations. Previous affiliations of Ramin Ghahremanzadeh include Islamic Azad University & Shahid Beheshti University.
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Composition of the Essential Oils of Ferula szowitsiana DC., Artedia squamata L. and Rhabdosciadium petiolare Boiss. & Hausskn.ex Boiss. Three Umbelliferae Herbs Growing Wild in Iran
TL;DR: Water-distilled essential oils from the aerial parts of Ferula szowitsiana DC and Artedia squamata L. and Rhabdosciadium petiolare Boiss.
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Placenta-specific1 (PLAC1) is a potential target for antibody-drug conjugate-based prostate cancer immunotherapy.
Mohammad-Reza Nejadmoghaddam,Mohammad-Reza Nejadmoghaddam,Amir-Hassan Zarnani,Ramin Ghahremanzadeh,Roya Ghods,Jafar Mahmoudian,Maryam Yousefi,Mahboobeh Nazari,Mohammad Hossein Ghahremani,Maryam Abolhasani,Ali Anissian,Morteza Mahmoudi,Rassoul Dinarvand +12 more
TL;DR: This work generated and evaluated an anti-placenta-specific1 (PLAC1)-based antibody drug conjugate (ADC) for targeted immunotherapy of PCa and induced apoptosis in human primary prostate cancer cells and prostate cell lines.
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Simple and Catalyst-Free Synthesis of Oxoindolin-3-yl Phosphonates
TL;DR: An efficient, simple, and catalyst-free synthesis of dialkyl or diaryl 3-(dicyanomethyl)-2-oxoindolin-3-ylphosphonates by the reaction of Dialkyl/Diaryl phosphites and oxoINDolin- 3-ylidenemalononitriles under solvent-free conditions is reported.
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Reduced graphene oxide: osteogenic potential for bone tissue engineering
TL;DR: Reducing the Col-GO scaffolds can effectively activate the differentiation of hBM-MSCs into osteoblasts after 14 days, even without the addition of an osteogenic differentiation medium, highlighting that GO and its reduced form have considerable potential as bone substitutes for orthopaedic and dental applications.
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Clean Synthesis and Antibacterial Activities of Spiro[pyrimido[4,5- b ]quinoline-5,5′-pyrrolo[2,3- d ]pyrimidine]-pentaones
TL;DR: A simple, clean and efficient method for the synthesis of spiro[pyrimido[4,5-b]quinoline-5,5'-pyrrolo[2,3-d]pyrimidine]-pentaone derivatives by condensation reaction of 6-amino-uracils and isatins in aqueous media is reported.