Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
2014 2
2018 2
2019 1
2020 2
2021 2
2022 4
2023 4
2024 16
2025 8

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

37 results

Results by year

Filters applied: . Clear all
Page 1
Evaluation of the efficacy of mesenchymal stem cells derived conditioned medium in the treatment of striae distensae: a double blind randomized clinical trial.
Behrangi E, Feizollahi M, Zare S, Goodarzi A, Ghasemi MR, Sadeghzadeh-Bazargan A, Dehghani A, Nouri M, Zeinali R, Roohaninasab M, Nilforoushzadeh MA. Behrangi E, et al. Among authors: ghasemi mr. Stem Cell Res Ther. 2024 Mar 5;15(1):62. doi: 10.1186/s13287-024-03675-7. Stem Cell Res Ther. 2024. PMID: 38439103 Free PMC article. Clinical Trial.
Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review.
Ghasemi MR, Tehrani Fateh S, Moeinafshar A, Sadeghi H, Karimzadeh P, Mirfakhraie R, Rezaei M, Hashemi-Gorji F, Rezvani Kashani M, Fazeli Bavandpour F, Bagheri S, Moghimi P, Rostami M, Madannejad R, Roudgari H, Miryounesi M. Ghasemi MR, et al. BMC Med Genomics. 2024 Feb 13;17(1):51. doi: 10.1186/s12920-024-01810-0. BMC Med Genomics. 2024. PMID: 38347586 Free PMC article.
Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG).
Ghasemi MR, Fateh ST, Ben-Mahmoud A, Gupta V, Stühn LG, Lesca G, Chatron N, Platzer K, Edery P, Sadeghi H, Isidor B, Cogné B, Schulz HL, Krauspe-Stübecke I, Periyasamy R, Nampoothiri S, Mirfakhraie R, Alijanpour S, Syrbe S, Pfeifer U, Spranger S, Grundmann-Hauser K, Haack TB, Papadopoulou MT, da Silva Gonçalves T, Panagiotakaki E, Arzimanoglou A, Tonekaboni SH, Rossi M, Korenke GC, Lacassie Y, Jang MH, Layman LC, Miryounesi M, Kim HG. Ghasemi MR, et al. Am J Med Genet A. 2025 May;197(5):e63963. doi: 10.1002/ajmg.a.63963. Epub 2024 Dec 20. Am J Med Genet A. 2025. PMID: 39707601
Correlated downregulation of VDR and CYP3A4 in colorectal cancer.
Sadeghi H, Hashemnia V, Nazemalhosseini-Mojarad E, Ghasemi MR, Mirfakhraie R. Sadeghi H, et al. Among authors: ghasemi mr. Mol Biol Rep. 2023 Feb;50(2):1385-1391. doi: 10.1007/s11033-022-08141-2. Epub 2022 Dec 5. Mol Biol Rep. 2023. PMID: 36469261
CREB-binding protein (CREBBP) and preeclampsia: a new promising target gene.
Sadeghi H, Esmkhani S, Pirjani R, Amin-Beidokhti M, Gholami M, Azizi Tabesh G, Ghasemi MR, Gachkar L, Mirfakhraie R. Sadeghi H, et al. Among authors: ghasemi mr. Mol Biol Rep. 2021 Mar;48(3):2117-2122. doi: 10.1007/s11033-021-06215-1. Epub 2021 Feb 24. Mol Biol Rep. 2021. PMID: 33625689
37 results