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Sensing of Alzheimer's Disease and Multiple Sclerosis Using Nano-Bio Interfaces.
Hajipour MJ, Ghasemi F, Aghaverdi H, Raoufi M, Linne U, Atyabi F, Nabipour I, Azhdarzadeh M, Derakhshankhah H, Lotfabadi A, Bargahi A, Alekhamis Z, Aghaie A, Hashemi E, Tafakhori A, Aghamollaii V, Mashhadi MM, Sheibani S, Vali H, Mahmoudi M. Hajipour MJ, et al. Among authors: tafakhori a. J Alzheimers Dis. 2017;59(4):1187-1202. doi: 10.3233/JAD-160206. J Alzheimers Dis. 2017. PMID: 28759965
PRDM12 Is Transcriptionally Active and Required for Nociceptor Function Throughout Life.
Kokotović T, Langeslag M, Lenartowicz EM, Manion J, Fell CW, Alehabib E, Tafakhori A, Darvish H, Bellefroid EJ, Neely GG, Kress M, Penninger JM, Nagy V. Kokotović T, et al. Among authors: tafakhori a. Front Mol Neurosci. 2021 Sep 27;14:720973. doi: 10.3389/fnmol.2021.720973. eCollection 2021. Front Mol Neurosci. 2021. PMID: 34646120 Free PMC article.
Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes.
Darvish H, Azcona LJ, Tafakhori A, Mesias R, Ahmadifard A, Sanchez E, Habibi A, Alehabib E, Johari AH, Emamalizadeh B, Jamali F, Chapi M, Jamshidi J, Kajiwara Y, Paisán-Ruiz C. Darvish H, et al. Among authors: tafakhori a. Sci Rep. 2020 Jan 22;10(1):968. doi: 10.1038/s41598-020-57929-4. Sci Rep. 2020. PMID: 31969655 Free PMC article.
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.
Wagner M, Osborn DPS, Gehweiler I, Nagel M, Ulmer U, Bakhtiari S, Amouri R, Boostani R, Hentati F, Hockley MM, Hölbling B, Schwarzmayr T, Karimiani EG, Kernstock C, Maroofian R, Müller-Felber W, Ozkan E, Padilla-Lopez S, Reich S, Reichbauer J, Darvish H, Shahmohammadibeni N, Tafakhori A, Vill K, Zuchner S, Kruer MC, Winkelmann J, Jamshidi Y, Schüle R. Wagner M, et al. Among authors: tafakhori a. Nat Commun. 2019 Oct 21;10(1):4790. doi: 10.1038/s41467-019-12620-9. Nat Commun. 2019. PMID: 31636353 Free PMC article.
159 results