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Year Number of Results
2012 2
2013 1
2014 1
2015 1
2016 5
2017 7
2018 3
2019 6
2020 4
2024 0

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23 results

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Page 1
A fresh look at the male-specific region of the human Y chromosome.
Jangravi Z, Alikhani M, Arefnezhad B, Sharifi Tabar M, Taleahmad S, Karamzadeh R, Jadaliha M, Mousavi SA, Ahmadi Rastegar D, Parsamatin P, Vakilian H, Mirshahvaladi S, Sabbaghian M, Mohseni Meybodi A, Mirzaei M, Shahhoseini M, Ebrahimi M, Piryaei A, Moosavi-Movahedi AA, Haynes PA, Goodchild AK, Nasr-Esfahani MH, Jabbari E, Baharvand H, Sedighi Gilani MA, Gourabi H, Salekdeh GH. Jangravi Z, et al. Among authors: karamzadeh r. J Proteome Res. 2013 Jan 4;12(1):6-22. doi: 10.1021/pr300864k. Epub 2012 Dec 20. J Proteome Res. 2013. PMID: 23253012 Review.
Identification of a missense variant in CLDN2 in obstructive azoospermia.
Askari M, Karamzadeh R, Ansari-Pour N, Karimi-Jafari MH, Almadani N, Sadighi Gilani MA, Gourabi H, Vosough Taghi Dizaj A, Mohseni Meybodi A, Sadeghi M, Bashamboo A, McElreavey K, Totonchi M. Askari M, et al. Among authors: karamzadeh r. J Hum Genet. 2019 Oct;64(10):1023-1032. doi: 10.1038/s10038-019-0642-0. Epub 2019 Jul 18. J Hum Genet. 2019. PMID: 31320686
Human closed and open apex premolar teeth express different toll-like receptor.
Jafari R, Karamzadeh R, Pesaran Hajabbas F, Sayyadizadeh F, Chekini Z, Aghajanpour S, Shakeri L, Nazarimoghaddam K, Aflatoonian R. Jafari R, et al. Among authors: karamzadeh r. Mol Genet Genomic Med. 2020 Jul;8(7):e1268. doi: 10.1002/mgg3.1268. Epub 2020 May 13. Mol Genet Genomic Med. 2020. PMID: 32400961 Free PMC article.
Type 1 Diabetes Mellitus: Cellular and Molecular Pathophysiology at A Glance.
Saberzadeh-Ardestani B, Karamzadeh R, Basiri M, Hajizadeh-Saffar E, Farhadi A, Shapiro AMJ, Tahamtani Y, Baharvand H. Saberzadeh-Ardestani B, et al. Among authors: karamzadeh r. Cell J. 2018 Oct;20(3):294-301. doi: 10.22074/cellj.2018.5513. Epub 2018 May 15. Cell J. 2018. PMID: 29845781 Free PMC article.
Temporal activation of LRH-1 and RAR-γ in human pluripotent stem cells induces a functional naïve-like state.
Taei A, Kiani T, Taghizadeh Z, Moradi S, Samadian A, Mollamohammadi S, Sharifi-Zarchi A, Guenther S, Akhlaghpour A, Asgari Abibeiglou B, Najar-Asl M, Karamzadeh R, Khalooghi K, Braun T, Hassani SN, Baharvand H. Taei A, et al. Among authors: karamzadeh r. EMBO Rep. 2020 Oct 5;21(10):e47533. doi: 10.15252/embr.201847533. Epub 2020 Aug 16. EMBO Rep. 2020. PMID: 33252195 Free PMC article.
A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma.
Youssefian L, Vahidnezhad H, Saeidian AH, Mahmoudi H, Karamzadeh R, Kariminejad A, Huang J, Li L, Jannace TF, Fortina P, Zeinali S, White TW, Uitto J. Youssefian L, et al. Among authors: karamzadeh r. Hum Mutat. 2019 Feb;40(2):217-229. doi: 10.1002/humu.23686. Epub 2018 Dec 1. Hum Mutat. 2019. PMID: 30431684 Free PMC article.
Quantitative proteomic analysis of human testis reveals system-wide molecular and cellular pathways associated with non-obstructive azoospermia.
Alikhani M, Mirzaei M, Sabbaghian M, Parsamatin P, Karamzadeh R, Adib S, Sodeifi N, Gilani MAS, Zabet-Moghaddam M, Parker L, Wu Y, Gupta V, Haynes PA, Gourabi H, Baharvand H, Salekdeh GH. Alikhani M, et al. Among authors: karamzadeh r. J Proteomics. 2017 Jun 6;162:141-154. doi: 10.1016/j.jprot.2017.02.007. Epub 2017 Feb 15. J Proteomics. 2017. PMID: 28213128
23 results