日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Partial Monosomy 21q Due to De Novo t(15;21)(q26.3;q22.11): A Case Report with Clinical and Molecular Findings

由新生t(15;21)(q26.3;q22.11)引起的21q部分单体:一例临床和分子学发现的病例报告

Nojehdeh, Somayeh Takrim; Fattahi, Tannaz; Arish, Sara; Mokabber, Haleh; Nobakht, Ramiz; Davarnia, Sana; Davarnia, Behzad

Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran

揭示听力损失的遗传图谱:伊朗阿尔达比勒阿塞拜疆家庭的综合研究

Mohseni, Marzieh; Ashrafi, Farzane Zare; Abbaspour Rodbaneh, Ehsan; Mokabber, Haleh; Vafaei, Maryam; Nobakht, Ramiz; Keshavarzi, Fatemeh; Arzhangi, Sanaz; Arish, Sara; Azar, Zahra Nematollahi; Kahrizi, Kimia; Najmabadi, Hossein; Davarnia, Behzad

Molecular Analysis of the HGD Gene in 9 Families With Alkaptonuric Ochronosis in Iran and Identification of Two Novel Variants

对伊朗9个患有尿黑酸症家族的HGD基因进行分子分析,并鉴定出两个新的变异体

Azami, Ahad; Jahanpanah, Mohammad; Marani, Yousef Imani; Mokhtari, Diana; Mokaber, Haleh; Davarnia, Behzad

A novel variant in ASNS gene responsible for syndromic intellectual disability and microcephaly: Case report and literature review

ASNS基因中一种导致综合征性智力障碍和小头畸形的新型变异:病例报告及文献综述

Jahanpanah, Mohammad; Mokhtari, Diana; Mokaber, Haleh; Arish, Sara; Ahmadabadi, Farzad; Davarnia, Behzad

Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes

对常染色体隐性共济失调患者进行基因检测,并鉴定出SQSTM1和SYNE1基因中的两个新变异。

Mokhtari, Diana; Jahanpanah, Mohammad; Jabbari, Nasim; Azari, Hamed; Davarnia, Sana; Mokaber, Haleh; Arish, Sara; Molatefi, Rasol; Abbasi, Vahid; Davarnia, Behzad

Immunogenic Potential of the Mediterranean Fever Gene in Patients with Coronavirus Disease: A Cross-Sectional Study

地中海热基因在冠状病毒病患者中的免疫原性:一项横断面研究

Salehzadeh, Farhad; Pourfarzi, Farhad; Molatefi, Rasool; Davarnia, Behzad; Shahbazfar, Ehsan; Ahmadabadi, Farzad

A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran

伊朗一例新型β-地中海贫血合并HbG-Coushatta复合杂合子病例报告

Soozangar, Narges; Abbaspour, Ehsan; Mokaber, Haleh; Nematollahi, Zahra; Davarnia, Behzad

Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients

伊朗大量患者中鸟嘌呤核苷酸交换因子基因变异的表型和基因型谱

Meysam Mosallaei, Naeim Ehtesham, Maryam Beheshtian, Shahrouz Khoshbakht, Behzad Davarnia, Kimia Kahrizi, Hossein Najmabadi

Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran

外显子组测序在伊朗听力损失遗传图谱的界定和新基因发现中的应用

Mohseni, Marzieh; Babanejad, Mojgan; Booth, Kevin T; Jamali, Payman; Jalalvand, Khadijeh; Davarnia, Behzad; Ardalani, Fariba; Khoshaeen, Atefeh; Arzhangi, Sanaz; Ghodratpour, Fatemeh; Beheshtian, Maryam; Jahanshad, Faezeh; Otukesh, Hasan; Bahrami, Fatemeh; Seifati, Seyed Morteza; Bazazzadegan, Niloofar; Habibi, Farkhonde; Behravan, Hanieh; Mirzaei, Sepide; Keshavarzi, Fatemeh; Nikzat, Nooshin; Mehrjoo, Zohreh; Thiele, Holger; Nothnagel, Michael; Azaiez, Hela; Smith, Richard J; Kahrizi, Kimia; Najmabadi, Hossein

TNF-induced necroptosis and PARP-1-mediated necrosis represent distinct routes to programmed necrotic cell death

TNF 诱导的坏死性凋亡和 PARP-1 介导的坏死代表程序性坏死性细胞死亡的不同途径

Justyna Sosna, Susann Voigt, Sabine Mathieu, Arne Lange, Lutz Thon, Parvin Davarnia, Thomas Herdegen, Andreas Linkermann, Andrea Rittger, Francis Ka-Ming Chan, Dieter Kabelitz, Stefan Schütze, Dieter Adam