Author Index

E

  • Eisazaei, Sepideh Analysis of Expression Profiles of GLI3A, LATS2 and MOB1A genes in Patients with Congenital hypothyroidism [Volume 3, Issue 1, 2022, Pages 21-26]

G

  • Ghaderi Nejad, Nazanin The relationship between FXIII Val34Leu and PAI-1 4G/5G gene polymorphisms and recurrent miscarriage in women from Golestan province [Volume 3, Issue 1, 2022, Pages 7-12]

K

  • Keikha, Mohammad Mehdi Breast Cancer Detection Using Deep Multilayer Neural Networks [Volume 3, Issue 1, 2022, Pages 27-34]
  • Kordi Tamandani, Dor-Mohammad Analysis of Expression Profiles of GLI3A, LATS2 and MOB1A genes in Patients with Congenital hypothyroidism [Volume 3, Issue 1, 2022, Pages 21-26]
  • Kordi-Tamandani, Dor Mohammad The relationship between FXIII Val34Leu and PAI-1 4G/5G gene polymorphisms and recurrent miscarriage in women from Golestan province [Volume 3, Issue 1, 2022, Pages 7-12]
  • Kord Tamandani, Yahya Breast Cancer Detection Using Deep Multilayer Neural Networks [Volume 3, Issue 1, 2022, Pages 27-34]

M

  • Mansour Samaei, Nader The relationship between FXIII Val34Leu and PAI-1 4G/5G gene polymorphisms and recurrent miscarriage in women from Golestan province [Volume 3, Issue 1, 2022, Pages 7-12]

N

  • Nakhaee-Moghadam, Maryam Analysis of Expression Profiles of GLI3A, LATS2 and MOB1A genes in Patients with Congenital hypothyroidism [Volume 3, Issue 1, 2022, Pages 21-26]
  • Nouripure, Sadaf Insect-Bacteria interaction: identification of some of the bacterial proteins in the gut of Nezara viridula [Volume 3, Issue 1, 2022, Pages 13-19]

R

  • Rafiee Komachali, sajjad Retinitis pigmentosa: A Case Report with Thr17Arg as a Novel Mutation in RHO Gene. [Volume 3, Issue 1, 2022, Pages 1-6]

S

  • Saadati, Mohammad Insect-Bacteria interaction: identification of some of the bacterial proteins in the gut of Nezara viridula [Volume 3, Issue 1, 2022, Pages 13-19]
  • Salehi, Mansoor Retinitis pigmentosa: A Case Report with Thr17Arg as a Novel Mutation in RHO Gene. [Volume 3, Issue 1, 2022, Pages 1-6]
  • Siahpoosh, Zakieh Retinitis pigmentosa: A Case Report with Thr17Arg as a Novel Mutation in RHO Gene. [Volume 3, Issue 1, 2022, Pages 1-6]