N. Ngoc

发表

JAK2 rs10974944 is associated with both V617F‐positive and negative myeloproliferative neoplasms in a Vietnamese population: A potential genetic marker

N. Xuan, N. Vuong, N. Ngoc, 2022, Molecular genetics & genomic medicine.

Detection of a Novel Mutation on the Gene ESCO2 in a Pediatric Patient with Syndactyly

N. Duong, N. V. Hai, Le Thi Van Anh, 2020 .

Association of PSORS1C3, CARD14 and TLR4 genotypes and haplotypes with psoriasis susceptibility

N. T. Lien, N. Xuan, N. Hoang, 2022, Genetics and molecular biology.

Biochip for Real-Time Monitoring of Hepatitis B Virus (HBV) by Combined Loop-Mediated Isothermal Amplification and Solution-Phase Electrochemical Detection

Bui Quang Tien, Nguyen Thy Ngoc, Nguyen Thai Loc, 2017, Journal of Electronic Materials.

Genetics and Molecular Biology

N. Hoang, V. X. Nghia, Bui Kieu Trang, 2022 .

Prevalence of CYLD mutations in Vietnamese patients with polycythemia vera.

N. Xuan, Nguyen Giang, N. Vuong, 2022, Advances in clinical and experimental medicine : official organ Wroclaw Medical University.

Study on genetic variations of the D-loop region in three Vietnamese ethnic groups Kinh, Lolo and Lahu

N. Duong, N. V. Hai, N. V. Phong, 2020 .

CYLD stimulates macrophage phagocytosis of leukemic cells through STAT1 signalling in acute myeloid leukemia

N. Xuan, N. X. Canh, Nguyen Giang, 2023, PloS one.

Identification of novel missense mutations associated with non-syndromic syndactyly in two vietnamese trios by whole exome sequencing.

N. Duong, L. Huong, N. V. Hai, 2020 .

The Prevalence of JAK2 Exon 12 Mutations in Vietnamese Patients with JAK2 V617F-Negative Polycythemia Vera: Frequent or Rare?

N. Xuan, N. Ngoc, Nguyen Thuy Linh, 2022, Human Heredity.

The Prevalence of JAK2 Exon 12 Mutations in Vietnamese Patients with JAK2 V617F-Negative Polycythemia Vera: Frequent or Rare?

N. Xuan, N. Ngoc, Nguyen Thuy Linh, 2022, Human Heredity.