Reza Vazifehmand

发表

MicroRNA Based Therapy and Osteoporosis: A Review of a Novel Therapeutic Agent from Diagnosis to Treatment

Nahid Davoodian, F. Niknam, Dhuha Saeed Ali, 2018 .

A large family with spinocerebellar ataxia type 6 in Iran: a clinical and genetic study.

H. Shimazaki, Y. Takiyama, I. Nakano, 2008, Archives of Iranian medicine.

Detection of BTNL2 Gene Mutation (rs2076530 Allele) in Iranian Sarcoidosis Patients: A clinical and Genetic Study

H. K. Khorshid, S. Saber, Reza Vazifehmand, 2017 .

The evaluation expression of non-coding RNAs in response to HSV-G47∆ oncolytic virus infection in glioblastoma multiforme cancer stem cells

Z. Sekawi, J. Stanslas, M. Shafa, 2022, Journal of NeuroVirology.

Identification of a Rare Mutation Causing Hereditary Tyrosinemia Type 1 in an Iranian Child Compound with Dextrocardia Phenotype

Dhuha Saeed Ali, Reza Vazifehmand, Seyed Abbas Ghasemi Ahangarkolaee, 2016 .

Tailoring drug co-delivery nanosystem for mitigating U-87 stem cells drug resistance

Z. Sekawi, M. J. Masarudin, A. Syahir, 2021, Drug Delivery and Translational Research.

Analysis of serum circulating MicroRNAs level in Malaysian patients with gestational diabetes mellitus

H. Kamyab, S. Zain, S. Omar, 2022, Scientific Reports.

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

Wei Chen, S. Lenzner, H. Ropers, 2007, Human Genetics.

A novel ABCB11 mutation in an Iranian girl with progressive familial intrahepatic cholestasis

S. Saber, Reza Vazifehmand, I. Bagherizadeh, 2013, Indian Journal of Human Genetics.

Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnostics

P. Harris, S. Rossetti, H. K. Khorshid, 2013, BMC Nephrology.

Tailoring drug co-delivery nanosystem for mitigating U-87 stem cells drug resistance

Z. Sekawi, M. J. Masarudin, A. Syahir, 2021, Drug Delivery and Translational Research.

Two Novel Somatic Mutations in Exon 15 of the Adenomatous Polyposis Coli Gene in Iranian Familial Adenomatousis Polyposis Coli Patients

H. K. Khorshid, S. Saber, Reza Vazifehmand, 2016 .

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

S. Lenzner, H. Ropers, F. Rüschendorf, 2006, Human Genetics.

Analysis of serum circulating MicroRNAs level in Malaysian patients with gestational diabetes mellitus

H. Kamyab, S. Zain, S. Omar, 2022, Scientific Reports.

Modulating Wnt/β-Catenin Signaling Pathway on U251 and T98G Glioblastoma Cell Lines Using a Combination of Paclitaxel and Temozolomide, A Molecular Docking Simulations and Gene Expression Study.

Reza Vazifehmand, S. M. Maddah, S. Jamalpour, 2023, Chemical & pharmaceutical bulletin.