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ID: 1048 A novel nonsense mutation in the CYP21A2 gene of a Vietnamese patient with congenital adrenal hyperplasia

Vu Chi Dung, Ngoc Lan Nguyen, Huy Hoang Nguyen, Thi Kim Lien Nguyen, Thinh Huy Tran, Thanh Van Ta, Van Khanh Tran

S 129 | published: 2017-09-05

The prevalence of KRAS mutation in colorectal cancer patients in Iranian population: A systematic review and meta-analysis study

Mehrdad Payandeh, Nasrin Amirifard, Masoud Sadeghi, Babak Shazad, Negin Farshchian, Edris Sadeghi, Malihe Dayani

1693-1704 | published: 2017-10-16

Immunological and mutational analysis of SARS-CoV-2 structural proteins from Asian countries

Deepak Kumar Jha, Niti Yashvardhini, Amit Kumar

4367-4381 | published: 2021-05-31

Optimizing a multiplex high resolution melting curve to diagnose G6PD deficiency based on viangchan and canton mutations

Nghia Le Tri, Giang Thanh Nguyen-Dien, Anh Thi Lan Dang, Ngoc Tran Bao, Hien Tran Tinh, Hue Thi Nguyen

757-769 | published: 2016-08-30

Prevalence of TECTA and GJB2 mutations in Asian children with nonsyndromic hearing loss: A meta-analysis

Phuong Thu Vu Hoang, Quang An Lam, Minh Xuan Ngo, Anh Thu Ha Nguyen, Thanh Vu Nguyen, Chung Thuy Tran Phan

5717-5725 | published: 2023-06-30

ID: 2036 Next-generation sequencing to evaluate frequency of BCR-ABL1 kinase domain Imatinib-resistance mutations

Chinh Q. Duong, Trang T. Nguyen, Lam V. Nguyen, Huy Q. Pham, Hien T. T. Trinh, Hoang C. Tran, Tuong Q. Le, Thanh H. Nguyen, Hai N. Truong, Tri A. Nguyen, Cuong Nguyen

S67 | published: 2017-09-05

Potential role of Factor V Leiden mutation in adverse pregnancy outcomes: An updated systematic review

Nasibeh Roozbeh, Farzaneh Banihashemi, Mitra Mehraban, Fatemeh Abdi

1832-1846 | published: 2017-12-18

ID3021 Acquired resistance to with EGFR tyrosine kinase inhibitors by the EGFR T790M mutation in non-small cell lung cancer

Van Thanh Ta

S33 | published: 2017-09-05

Prevalence of GJB2 and TECTA gene mutations in children with non-syndromic hearing loss visiting an Otorhino-laryngology Hospital in Ho Chi Minh City, Viet Nam

Phuong Thu Vu Hoang, Minh Xuan Ngo, Quang Minh Le Tran, Thanh Vinh Nguyen, Hong Giang Do, Thanh Vu Nguyen, Anh Thu Ha Nguyen, Thu Hang Do Thi, Dieu Hien Huynh Thi, Chung Thuy Tran Phan

5523-5529 | published: 2023-01-31

ID: 1036 FAM134B, a new player in human colorectal cancer pathogenesis

Farhadul Islam, Vinod Gopalan, Alfred K-Y Lam

S 113-114 | published: 2017-09-05

The APC gene rs41115 polymorphism is associated with survival in Iranian colorectal cancer patients

Sousan Mir Najd Gerami, Mohammad Hossein Somi, Leila Vahedi, Faris Farassati, Roya Dolatkhah

3962-3970 | published: 2020-09-30

Genetic variations in the Orf7a protein of SARS-CoV-2 and its possible role in vaccine development

Niti Yashvardhini, Deepak Kumar Jha, Amit Kumar, Kumar Sayrav, Manjush Gaurav

4497-4504 | published: 2021-08-28

Identification of a novel de novo deletion mutation of desmin in a neonate with desminopathy

Nguyen Thi Huynh Nga, Bui Chi Bao, Nguyen Vuong Thao Vy, Nguyen Manh Cong, Nguyen Minh Hiep

4809-4817 | published: 2021-12-31

ID: 1051 Telomerase activity, telomere length and P53 mutation detection on cellular senescence of Human Amnion Mesenchymal Stem Cells (HAMCs)

Fiona Macniesia Thomas, Vijay Kumar, Siti Fatimah Simat, Helen Benedict Lasimbang

S 131 | published: 2017-09-05

Influence of loop permutation on immunostimulatory activities of CpG oligodeoxynucleotides forming monomeric guanine-quadruplex structures

Anh Thi Tram Tu, Kazuaki Hoshi, Tomohiko Yamazaki

5410-5417 | published: 2022-11-30

Comprehensive diagnostic approach and real-life treatment strategy in a Vietnamese pedigree with familial protein S deficiency

Vuong Van Dang, Dung Hoang Nguyen, Si Van Nguyen

5326-5331 | published: 2022-10-29

Polymorphisms of endothelial nitric oxide synthase and hypoxia-inducible factor 1 alpha genes play a role in susceptibility to coronary artery disease

Ali Asghar Kiani, Vahide Heydari Nazarabad, Kolsoum Ahmadi, Khatereh Anbari, Babak Baharvand Ahmadi

2688-2696 | published: 2018-09-29

1 - 25 of 32 items 1 2 > >>

ID: 1048 A novel nonsense mutation in the CYP21A2 gene of a Vietnamese patient with congenital adrenal hyperplasia

The prevalence of KRAS mutation in colorectal cancer patients in Iranian population: A systematic review and meta-analysis study

Immunological and mutational analysis of SARS-CoV-2 structural proteins from Asian countries

Optimizing a multiplex high resolution melting curve to diagnose G6PD deficiency based on viangchan and canton mutations

Prevalence of TECTA and GJB2 mutations in Asian children with nonsyndromic hearing loss: A meta-analysis

ID: 2036 Next-generation sequencing to evaluate frequency of BCR-ABL1 kinase domain Imatinib-resistance mutations

Potential role of Factor V Leiden mutation in adverse pregnancy outcomes: An updated systematic review

ID3021 Acquired resistance to with EGFR tyrosine kinase inhibitors by the EGFR T790M mutation in non-small cell lung cancer

Prevalence of GJB2 and TECTA gene mutations in children with non-syndromic hearing loss visiting an Otorhino-laryngology Hospital in Ho Chi Minh City, Viet Nam

ID: 1036 FAM134B, a new player in human colorectal cancer pathogenesis

The APC gene rs41115 polymorphism is associated with survival in Iranian colorectal cancer patients

Genetic variations in the Orf7a protein of SARS-CoV-2 and its possible role in vaccine development

Identification of a novel de novo deletion mutation of desmin in a neonate with desminopathy

ID: 1051 Telomerase activity, telomere length and P53 mutation detection on cellular senescence of Human Amnion Mesenchymal Stem Cells (HAMCs)

Influence of loop permutation on immunostimulatory activities of CpG oligodeoxynucleotides forming monomeric guanine-quadruplex structures

Recent findings on molecular alterations in IDH1, TP53, and CASP9 in gliomagenesis

Structural genomics and immunoinformatics analyses of non-structural protein 6 (NSP6) and its probable role in autophagy

Association of a point mutation (m.9176T>G) of the MT-ATP6 gene with Leigh syndrome: A case report

Evaluation of Plasmodium falciparum K13 gene polymorphism and susceptibility to dihydroartemisinin in an endemic area

Pachyonychia Congenita Type PC-K6a: The first report in the Vietnamese population

Comprehensive diagnostic approach and real-life treatment strategy in a Vietnamese pedigree with familial protein S deficiency

ID:2037 Molecular mechanisms underlying resistance to MEK1/2 inhibitor in BRAF-mutated colorectal cancer

Art of using maintenance therapy in a patient with metastatic colon cancer harboring RAS-wt/BRAF V600E

A case of a long course of Oslerâ€“Weberâ€“Rendu disease in a 65-year-old patient

Polymorphisms of endothelial nitric oxide synthase and hypoxia-inducible factor 1 alpha genes play a role in susceptibility to coronary artery disease