Zahra Golchehre

发表

An introduction to expression and regulation of cancer/testis antigens (CTAs): review article

Arash Salmaninejad, A. Shakoori, E. Taghizadeh, 2018 .

Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy.

M. Keramatipour, A. Amin, Y. Eshaghkhani, 2021, Reports of biochemistry & molecular biology.

The frequency of human leukocyte antigen-DRB1 alleles, using sequence-based genotyping in 68 parents-child trios study in Iranian subjects

Arash Salmaninejad, M. Keramatipour, D. Sayer, 2016 .

Cernunnos defect in an Iranian patient with T− B+ NK + severe combined immunodeficiency: A case report and review of the literature

Z. Chavoshzadeh, M. Jamee, S. Sharafian, 2022, Molecular genetics & genomic medicine.

Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum

M. Keramatipour, N. Golchin, Y. Eshaghkhani, 2021, Molecular Biology Reports.

Cancer/Testis Antigens: Expression, Regulation, Tumor Invasion, and Use in Immunotherapy of Cancers

Arash Salmaninejad, M. Zamani, N. Rezaei, 2016, Immunological investigations.

First report of Klein-Waardenburg Syndrome in Iran and a novel pathogenic splice site variant in PAX3 gene.

M. Keramatipour, S. Tabatabaie, Arezou Karamzade, 2018, International journal of pediatric otorhinolaryngology.

CRB1-Related Leber Congenital Amaurosis: Reporting Novel Pathogenic Variants and a Brief Review on Mutations Spectrum

M. Keramatipour, Y. Eshaghkhani, Arezou Karamzade, 2019, Iranian biomedical journal.

Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families

M. Alaei, M. Keramatipour, Daniz Kooshavar, 2022, Iranian journal of child neurology.

A Novel Mutation in SNX10 Gene Causes Malignant Infantile Osteopetrosis

M. Keramatipour, A. Hamidieh, A. Rezamand, 2017, Avicenna journal of medical biotechnology.

Alterations of KRAS Exon 2 Codon 12/13 Mutation Status in Prostatic Adenocarcinoma; Bioinformatics Aspects

Arash Salmaninejad, M. Zamani, A. Shakoori, 2016 .

A rare immunological disease, caspase 8 deficiency: case report and literature review

M. Keramatipour, A. Karimi, M. Jamee, 2023, Allergy, Asthma & Clinical Immunology.

Integrative genomic and transcriptomic analysis reveals genetic alterations associated with the early progression of follicular lymphoma

Z. Chavoshzadeh, Xianhuo Wang, B. Meng, 2023, British journal of haematology.

Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature

J. Sayer, M. Keramatipour, M. Jamee, 2023, CEN Case Reports.

A Novel Mutation in the OXCT1 Gene Causing Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Deficiency Starting with Neurologic Manifestations

M. Keramatipour, S. Talebi, R. Hosseini, 2023, Iranian journal of child neurology.

Integrative genomic and transcriptomic analysis reveals genetic alterations associated with the early progression of follicular lymphoma.

Z. Chavoshzadeh, Xianhuo Wang, B. Meng, 2023, British Journal of Haematology.

Molecular Characterization of KRAS, BRAF, and EGFR Genes in Cases with Prostatic Adenocarcinoma; Reporting Bioinformatics Description and Recurrent Mutations.

M. Nowroozi, Arash Salmaninejad, M. Zamani, 2015, Clinical laboratory.

Cancer/Testis Antigens: Expression, Regulation, Tumor Invasion, and Use in Immunotherapy of Cancers

Arash Salmaninejad, M. Zamani, N. Rezaei, 2016, Immunological investigations.

A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature

M. Keramatipour, Y. Eshaghkhani, Arezou Karamzade, 2023, Journal of Genetics.