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

S 129 2017-09-05

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

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

1832-1846 2017-12-18

Nasibeh Roozbeh, Farzaneh Banihashemi, Mitra Mehraban, Fatemeh Abdi

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

1693-1704 2017-10-16

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

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

757-769 2016-08-30

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

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

S67 2017-09-05

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

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

S33 2017-09-05

Van Thanh Ta

A novel KIF11 missense mutation causing Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR): A case report and literature review

6532-6547 2024-06-30

Samira Asadollahi, Fatemeh Sefid, Masoumeh Askari, Seyed Ahmad Mohammadi, Hamid Reza Jahantigh, Mahtab Ordooei

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

4809-4817 2021-12-31

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

Simple-Virilizing Congenital adrenal hyperplasia sustained by five mutations on the CYP21A2 gene

6583-6591 2024-07-31

Gloria Agrimonti, Giorgia Spaggiari, Soara Menabò, Silvia Vezzani, Elisa Magnani, Andrea Frasoldati, Antonio R.M. Granata, Daniele Santi

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

S 131 2017-09-05

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

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

3739-3743 2020-05-25

Rozhgar A. Khailany, Naser Gilani, Mehmet Ozaslan, Muhamad Safdar, Ihsan Al-Shamari, Belan O. Kanabe, Khandakar A. S. M. Saadat, Javad Homayounvash, Amir Monfaredan, Mustafa S. Al-Attar, Ahmet Arslan

Mutational variants of KRAS gene versus Wild-type KRAS in the survival outcomes of Vietnamese colon cancer stage II-III

6723-6729 2024-09-30

Hoang Minh Cuong, Nguyen Thuan Loi, Tran Bao Ngoc, Vu Hong Thang

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

5326-5331 2022-10-29

Vuong Van Dang, Dung Hoang Nguyen, Si Van Nguyen

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

3962-3970 2020-09-30

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

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

5771-5782 2023-07-31

Niti Yashvardhini, Deepak Kumar Jha, Parimal Kumar Khan, Amit Kumar, Kumar Pranay

Evaluation of UHRF1 and P16INK4A expression levels in newly diagnosed AML patients

2658-2663 2018-09-27

Vahid Amiri, Mohamadhossein Mohammadi, Mohammad Reza Khosravi Farsani, Arshia Gharehbaghian, Abbas Hajifathali, Zaher Khazaei, Mehdi Allahbakhshian Farsani

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

5717-5725 2023-06-30

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

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

S68 2017-09-05

Hong-Quan Duong

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

2651-2657 2018-09-24

Titilope M. Dokunmu, Grace I. Olasehinde, David O. Oladejo, Cynthia U. Adjekukor, Adesola E. Akinbohun, Olabode A. Onileere, Chisom J. Eze, Grace S. Jir

Association study between polymorphisms within MPPED2 (rs12797813), MTR (rs61739582), ACTN2 (rs6656267) and LPO (rs7209537) genes and susceptibility to dental caries: a case-control study

6592-6602 2024-07-31

Shakiba Akbarian, Shiva Daneshmehr, Yasin Nazari, Sepehr Kobravi, Asal Fetrati, Mahmood Rezvani Amin, Bagher Biglak, Farzaneh Alizadeh

Biomedical Research and Therapy

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

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

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

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

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

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

A novel KIF11 missense mutation causing Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR): A case report and literature review

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

Simple-Virilizing Congenital adrenal hyperplasia sustained by five mutations on the CYP21A2 gene

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

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

Mutational variants of KRAS gene versus Wild-type KRAS in the survival outcomes of Vietnamese colon cancer stage II-III

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

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

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

Evaluation of UHRF1 and P16INK4A expression levels in newly diagnosed AML patients

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

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

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

Association study between polymorphisms within MPPED2 (rs12797813), MTR (rs61739582), ACTN2 (rs6656267) and LPO (rs7209537) genes and susceptibility to dental caries: a case-control study

Study of the association of Trp64Arg mutation of beta three adrenergic receptor with obesity in Saudi population

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

In vitro and in vivo biocompatibility of Ti-6Al-4V titanium alloy and UHMWPE polymer for total hip replacement

Association between SORT1/CELSR2/PSRC1 rs646776 polymorphism and statin-affected plasma lipid levels

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Search Results

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

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

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

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

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

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

A novel KIF11 missense mutation causing Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR): A case report and literature review

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

Simple-Virilizing Congenital adrenal hyperplasia sustained by five mutations on the CYP21A2 gene

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

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

Mutational variants of KRAS gene versus Wild-type KRAS in the survival outcomes of Vietnamese colon cancer stage II-III

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

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

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

Evaluation of UHRF1 and P16INK4A expression levels in newly diagnosed AML patients

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

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

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

Association study between polymorphisms within MPPED2 (rs12797813), MTR (rs61739582), ACTN2 (rs6656267) and LPO (rs7209537) genes and susceptibility to dental caries: a case-control study

Study of the association of Trp64Arg mutation of beta three adrenergic receptor with obesity in Saudi population

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

In vitro and in vivo biocompatibility of Ti-6Al-4V titanium alloy and UHMWPE polymer for total hip replacement

Association between SORT1/CELSR2/PSRC1 rs646776 polymorphism and statin-affected plasma lipid levels