مقالات 2020

 Whole Exome Sequencing Reveals a Novel Damaging Mutation in Human Fibroblast Activation Protein in a Family With Esophageal Squamous Cell Carcinoma

Fatemeh Fardi Golyan 1, Morteza Moghaddassian 2, Mohammad Mahdi Forghanifard 3, Samaneh Talebi 1, Moein Farshchian 4, Reihaneh Alsadat Mahmoudian 1, Mohammad Reza Abbaszadegan.. J Gastrointest Cancer. 2020 Mar;51(1):179-188.

 .Role of Extra Cellular Proteins in Gastric Cancer Progression and Metastasis: An Update

Mohammad Reza Abbaszadegan , Majid Mojarrad , Meysam Moghbeli . Genes Environ. 2020 May 15;42:18. 

Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran. Ali Yousefian 1, Saeed Shokoohi-Rad 1, Mohammad Reza Abbaszadegan 2, Dorsa Morshedi Rad 3, Selma Zargari 2, Saman Milanizadeh 2, Negar Morovatdar 4, Ramin Daneshvar .. J Ophthalmic Vis Res.2020 Feb 2;15(1):45-52.

TWIST1 upregulates matrix metalloproteinase (MMP) genes family in esophageal squamous carcinoma cells

Ardalan Khales, S., Abbaszadegan, M.R., Majd, A., Forghanifard, M.M.

Ts polymorphisms are associated with epigenetic silencing of CDKN2A gene in esophageal squamous cell carcinoma

Forghanifard, M.M.a, Aarabi, A.b, Nasiri Aghdam, M.c, Memar, B.d, Hasanzadeh Khayat, M.e, Dadkhah, E.f, Abbaszadegan, M.R.

Integration analysis of long non-coding RNA (lncRNA) role in tumorigenesis of colon adenocarcinoma

Poursheikhani, A.a,b, Abbaszadegan, M.R.a,b,c, Nokhandani, N.d, Kerachian, M.A.

MAML1 promotes ESCC aggressiveness through upregulation of EMT marker TWIST1

Forghanifard, M.M.a, Azaraz, S.b, Ardalan Khales, S.b, Morshedi Rad, D.b, Abbaszadegan, M.R.

Whole-exome sequencing of familial esophageal squamous cell carcinoma identified rare pathogenic variants in new predisposition genes

Golyan, F.F.a, , Druley, T.E., Abbaszadegan, M.R.

Molecular Aspects of Co-morbidities in COVID-19 Infection

Farzaneh Pouya 1 2, Zeynab Imani Saber 3, Mohammad Amin Kerachian . Arch Bone Jt Surg. 2020 Apr;8(Suppl1):226-230 

Differential microRNAs Expression in Acute Graft-Versus-Host Disease as Potential Diagnostic Biomarkers. Mohammad Amin Kerachian. Bone Marrow Transplant. 2020 May 13.

Crosstalk between DNA methylation and gene expression in colorectal cancer, a potential plasma biomarker for tracing this tumor

Kerachian, M.A, Javadmanesh, A.c,d, Azghandi, M.c,d, Mojtabanezhad Shariatpanahi, A.c, Yassi, M.c, Shams Davodly, E.c, Talebi, A.a,b, Khadangi, F.e, Soltani, G.f, Hayatbakhsh, A.f, Ghaffarzadegan, K.g   

Role of aldo-keto reductase family 1 member B1 (AKR1B1) in the cancer process and its therapeutic potential

Khayami, R., Hashemi, S., Kerachian, M.A. 

Integration analysis of long non-coding RNA (lncRNA) role in tumorigenesis of colon adenocarcinoma

Poursheikhani, A.a,b, Abbaszadegan, M.R., Nokhandani, N.d, Kerachian, M.A., 

Expression of tumor pyruvate kinase M2 isoform in plasma and stool of patients with colorectal cancer or adenomatous polyps

Rigi, F., Jannatabad, A., Izanloo, A., Roshanravan, R.a, Hashemian, H.R., Kerachian, M.A.,

The effect of adrenocorticotropic hormone on alpha-2-macroglobulin in osteoblasts derived from human mesenchymal stem cells

Sadeghi, F.a,b, Vahednia, E.c, Naderi Meshkin, H.d, Kerachian, M.A.a,

Selective capture of plasma cell-free tumor DNA on magnetic beads: a sensitive and versatile tool for liquid biopsy

Kerachian, M.A., Azghandi, M.c,d, Javadmanesh, A.c,d, Ghaffarzadegan, K.e,f, Mozaffari-Jovin, S.

Genetic and molecular determinants of prostate cancer among Iranian patients: An updat

Ghayour-Mobarhan, M.a, Ferns, G.A.b, Moghbeli, M.

Genetic and Molecular Biology of Multiple Sclerosis Among Iranian Patients: An Overview

Moghbeli, M.

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

Neuray, C.a,b, Maroofian, R.a, Scala, M.a,c,d, Sultan, T.e, Pai, G.S.f, Mojarrad, M.g,h,i, Khashab, H.E.j,k, deHoll, L.f, Yue, W.l, Alsaif, H.S.m, Zanetti, M.N.n, Bello, O.n, Person, R.o, Eslahi, A.g,m, Khazaei, Z.i, Feizabadi, M.H.g, Efthymiou, S.a, El-Bassyouni, H.T.p, Soliman, D.R.q, Tekes, S.r, Ozer, L.s, Baltaci, V.t, Khan, S.u, Beetz, C.u, Amr, K.S.v, Salpietro, V.a,

Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

Schneeberger, P.E.a, Kortüm, F.a, Korenke, G.C.b, Alawi, M.c, Santer, R.d, Woidy, M.d, Buhas, D.e,f, Fox, S.e,f, Juusola, J.g, Alfadhel, M.h,i,j, Webb, B.D.k,l,m, Coci, E.G.n,o, Abou Jamra, R.p, Siekmeyer, M.q, Biskup, S.r, Heller, C.r, Maier, E.M.s, Javaher-Haghighi, P.t, Bedeschi, M.F.u, Ajmone, P.F.v, Iascone, M.w, Peeters, H.x, Ballon, K.y, Jaeken, J.z, Rodríguez Alonso, A.aa, Palomares-Bralo, M.ab, Santos-Simarro, F.ab, Meuwissen, M.E.C.ac, Beysen, D.ad, Kooy, R.F.ae, Houlden, H.af, Murphy, D.af, Doosti, M.ag, Karimiani, E.G.ag,ah, Mojarrad, M

The worldwide frequency of MYO15A gene mutations in patients with non-syndromic hearing loss: A meta-analysis. Farjami, M., Assadi, R., Javan, F., Alimardani, M, Eslami, S.e,f,Derakhshan, S.M.g,h,i, Eslahi, A.a,b, Mojarrad, M.

NR1H4-related Progressive Familial Intrahepatic Cholestasis 5: Further Evidence for Rapidly Progressive Liver Failure

Himes, R.W., Mojarrad, M., Eslahi, A., Finegold, M., Maroofian, R.g, Moore, D

RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability

Scala, M.a,b,c, Mojarrad, M.d,e,f, Riazuddin, S.g, Brigatti, K.W.h, Ammous, Z.i, Cohen, J.S.j, Hosny, H.k, Usmani, M.A.g, Shahzad, M.l, Riazuddin, S.l,m, Stanley, V.n, Eslahi, A.d,o, Person, R.E.p, Elbendary,

Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

 Perenthaler, E.a, Nikoncuk, A.a, Yousefi, S.a, Berdowski, W.M.a, Alsagob, M.b, Capo, I.c, van der Linde, H.C.a, van den Berg, P.a, Jacobs, E.H.a, Putar, D.a, Ghazvini, M.d, Aronica, E.e,f, van IJcken, W.F.J.g, de Valk, W.G.a, Medici-van den Herik, E.h, van Slegtenhorst, M.a, Brick, L.i, Kozenko, M.i, Kohler, J.N.j, Bernstein, J.A.k, Monaghan, K.G.l, Begtrup, A.l, Torene, R.l, Al Futaisi, A.m, Al Murshedi, F.n, Mani, R.m, Al Azri, F.o, Kamsteeg, E.-J.p, Mojarrad, M., Eslahi, A.q,t, Khazaei, Z.s,

Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing Loss

Farjami, M.a,b, Fathi, M.a,b, Ghasemi, M.M.c, Rajati, M.d, Eslahi, A.a,b, Alimardani, M.a,b, Mojarrad, M.a,

Common therapeutic advances for Duchenne muscular dystrophy (DMD) case presentation

Salmaninejad, A.a,bEmail Author, Jafari Abarghan, Y.b, Bozorg Qomi, S.b, Bayat, H., Yousefi, M.f, Azhdari, S.g, Talebi, S.b, Mojarrad, M.

Developmental regulation and lateralisation of the α7 and α4 subunits of nicotinic acetylcholine receptors in developing rat hippocampus

Baradaran, R.a, Khoshdel-Sarkarizi, H.a, Kargozar, S.b, Hami, J.c, Mohammadipour, A.a, Sadr-Nabavi, A.d,e, Peyvandi Karizbodagh, M.a, Kheradmand, H.f, Haghir, H.

Intellectual disability; an example of not relying on karyotype or array comparative genomic hybridization alone

Khadivi zand, F.b, Shariati, M.a, Sabeti Aghabozorgi, A.b, Saberi, S.c, Khatib Astaneh, H.a, Ahmadzadeh, A.a, Samie, Z.a, Ansari, P.a, Sadr-Nabavi, A., Jafarzadeh-Esfehani, R.

The relation between CYP2C9 gene polymorphism and warfarin dosing in an Iranian population

Abtahi, S.a, Rostami, D.b, Ajilain, N.c, Zafari, T.c, Esfehani, R.J.d,e, Poursheikhani, A.d,e, Soudyab, M.d,e, Pahlavani, N, Sadr-Nabavi, A.