Global Analysis in Nonobstructive Azoospermic Testis Identifies miRNAs Critical to Spermatogenesis.

Autor: Piryaei, Fahimeh¹ (AUTHOR), Mozdarani, Hossein¹ (AUTHOR), Sadighi Gilani, Mohammad Ali² (AUTHOR), Rajender, Singh^3,4 (AUTHOR), Finelli, Renata⁵ (AUTHOR), Darestanifarahani, Mahsa⁶ (AUTHOR), Sarli, Abdolazim¹ (AUTHOR), Mehta, Poonam^3,4 (AUTHOR), Agarwal, Ashok⁷ (AUTHOR)

Publikováno v: Andrologia. 5/10/2023, p1-13. 13p.

Two New Variants in FYCO1 Are Responsible for Autosomal Recessive Congenital Cataract in Iranian Population.

Autor: Shirzadeh, Ebrahim¹ dreshirzad@yahoo.com, Piryaei, Fahimeh², Naddaf, Hanieh³, Barabadi, Zahra^4,5 z.barabadi@umsha.ac.ir

Publikováno v: Cell Journal (Yakhteh). Sep2022, Vol. 24 Issue 9, p546-551. 6p.

Investigation of the Mitochondrial ATPase 6/8 and tRNA^Lys Genes Mutations in Autism.

Autor: Piryaei, Fahimeh¹, Houshmand, Massoud^1,2 massoudh@nigeb.ac.ir, Aryani, Omid², Dadgar, Sepideh², Soheili, Zahra-Soheila³

Publikováno v: Cell Journal (Yakhteh). Summer2012, Vol. 14 Issue 2, p98-101. 4p. 1 Chart.

Homozygosity for Robertsonian Translocation (14q;15q) in a Newborn with a Familial History of Recurrent Abortion and Newborns Affected by Hepatosplenomegaly: A Case Report.

Autor: Sahraeean S; Dr. F. Nabipour Pathobiology laboratory, Kerman, Iran., Jebelli A; Department of Biological Sciences, Faculty of Basic Sciences, Higher Education Institute of Rab-Rashid, Tabriz, Iran., Shahbazi Z; Molecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran., Piryaei F; Research Center for Molecular Medicine, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Publikováno v: Journal of reproduction & infertility [J Reprod Infertil] 2023 Oct-Dec; Vol. 24 (4), pp. 301-305.