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Mol Biol Rep. 2021 Jun;48(6):5339-5345.

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

Arezou Karamzade, Meisam Babaei, Mohammad Saberi, Neda Golchin, Aysun Khalil Nejad Sani Banaei, Yeganeh Eshaghkhani, Zahra Golchehre, Mohammad Keramatipour

2021

Iran J Public Health. 2021 Aug;50(8):1697-1704.

Article

Increased Mitochondrial DNA Copy Number and Oxidative Damage in Patients with Hashimoto's Thyroiditis

Fatemeh Esfahanian, Mojgan Mirabdolhagh Hazaveh, Laya Hooshmand Garehbagh, Kowsar Falahati, Mitra Ataei, Mohammad Hossein Sanati, Zohreh Jadali

2021

J Med Case Rep. 2021 May 4;15(1):263.

Reports

A novel stop codon mutation in exon 5 (c.639G>A) of the cadherin-1 gene in a Vietnamese man with hereditary diffuse gastric cancer: a case report

Dzung Ngoc Thi Dang, Huong Thanh Thi Nguyen, Hoa Dieu Ngo, Bac Manh Tran, Anh Duc Vu, Huy Quang Dang, Van Thanh Ta

2021

Genomics. 2021 Jul;113(4):2645-2655.

Article

Exome sequencing reveals novel rare variants in Iranian familial multiple sclerosis: The importance of POLD2 in the disease pathogenesis

Zahra Salehi, Mohammad Keramatipour, Saeed Talebi, Seyed Shahriar Arab, Abdorreza Naser Moghadasi, Mohammad Ali Sahraian, Maryam Izad

2021

Anim Biotechnol. 2021 Aug;32(4):507-518.

Article

Documentation of extensive genetic diversity in the Ovar- DRB1 gene in native Turkish sheep

Veysel Bay, Murat Keleş, Ramazan Aymaz, Ecem Hatipoğlu, Yasemin Öner, Yalçın Yaman

2021

Genes (Basel). 2021 Oct 14;12(10):1622.

Article

Association of CYP26C1 Promoter Hypomethylation with Small Vessel Occlusion in Korean Subjects

Eun-Ji Lee, Myung-Sunny Kim, Nam-Hui Yim, Min Ho Cha

2021

Biotechnol J. 2021 May;16(5):e2000351.

Article

Comprehensive characterization of dihydrofolate reductase-mediated gene amplification for the establishment of recombinant human embryonic kidney 293 cells producing monoclonal antibodies

Sang Yoon Lee, Minhye Baek, Gyun Min Lee

2021

Rep Biochem Mol Biol. 2021 Jul;10(2):280-287.

Article

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

Yeganeh Eshaghkhani, Arezoo Mohamadifar, Mostafa Asadollahi, Mahdieh Taghizadeh, Arezou Karamzade, Mohammad Saberi, Parisa Nourmohammadi, Zahra Golchehre, Ahmad Amin, Mohammad Keramatipour

2021

Clin Exp Otorhinolaryngol. 2021 Nov;14(4):399-406.

Article

Genetic Variants and Clinical Phenotypes in Korean Patients With Hereditary Hemorrhagic Telangiectasia

Bo-Gyeong Kim, Joo-Hyun Jung, Mi-Jung Kim, Eun-Hye Moon, Jae-Hwan Oh, Jung-Woo Park, Heung-Eog Cha, Ju-Hyun Kim, Yoon-Jae Kim, Jun-Won Chung, Ki-Baik Hahm, Hong-Ryul Jin, Yong-Ju Jang, Sung Wan Kim, Seung-Kyu Chung, Dae-Woo Kim, Young Jae Lee, Seon-Tae Kim

2021

J Transl Med. 2021 Aug 16;19(1):350.

Article

Association of serum 25-OH-vitamin D level with FTO and IRX3 genes expression in obese and overweight boys with different FTO rs9930506 genotypes

Maryam Gholamalizadeh, Saeid Doaei, Zohreh Mokhtari, Vahideh Jalili, Fatemeh Bourbour, Saeed Omidi, Kamal Ebrahimi, Naser Kalantari, Sheyda Abdi, Ghasem Azizi Tabesh, Mohammad Naimi Joubani, Esmaeil Roohbakhsh, Seyed Alireza Mosavi Jarrahi

2021