Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Hung-Sang Tang"'
Autor:
Anh-Hoa Nguyen Pham, MD, PhD, Kim-Oanh Bui Thi, MD, Mai-Huong Nguyen Thi, MD, Diem-Ngoc Ngo, MD, Nakayuki Naritaka, MD, Hiroshi Nittono, MD, Hisamitsu Hayashi, MD, Trang Thi Dao, MD, Kim-Huong Thi Nguyen, MD, Hoai-Nghia Nguyen, PhD, Hoa Giang, PhD, Hung-Sang Tang, MD, Tat-Thanh Nguyen, MD, Dinh-Kiet Truong, PhD, Minh-Dien Tran, MD
Publikováno v:
Medicine, Vol 101, Iss 25, p e29476 (2022)
Abstract. Rationale:. Congenital bile acid synthesis defect (BASD) is a rare disease caused by mutations in the aldo-keto reductase 1D1 gene, which encodes the primary Δ4-3-oxosteroid 5β-reductase enzyme. Early disease diagnosis is critical for ear
Externí odkaz:
https://doaj.org/article/07ebe75c38304d43ba06851477b8609f
Autor:
Luu Hong Dang Nguyen, Ba Linh Tieu, Thi Thanh Nguyen, Nhung Phuong Ha, Giang Thi Huong Nguyen, Thi Hue Hanh Nguyen, Van Hoi Le, Vinh Quang Bui, Lan Hieu Nguyen, Nhu Hiep Pham, Thanh Hai Phan, Huu Thinh Nguyen, Van Song Tran, Chi Viet Bui, Van Kha Vo, Pham Thanh Nhan Nguyen, Ha Huu Phuoc Dang, Van Dung Pham, Van Thinh Cao, Ngoc Minh Phan, Van Tung Nguyen, Thi Le Quyen Le, Thi Lan-Anh Luong, Thi Kim Phuong Doan, Canh Duy Phan, Thanh Xuan Nguyen, Nguyen Tuong Pham, Bao Toan Nguyen, Thi Thu Thuy Pham, Huu Linh Le, Cong Thanh Truong, Thanh Xuan Jasmine, Minh Chi Le, Van Bau Phan, Quang Binh Truong, Thi Huong Ly Tran, Minh Thien Huynh, Tu Quy Tran, Si Tuan Nguyen, Vu Tran, Van Khanh Tran, Huu Nguyen Nguyen, Thi Van Phan, Thi Thanh-Thuy Do, Dinh Kiet Truong, Hoa Giang, Hoai-Nghia Nguyen, Minh-Duy Phan, Le Son Tran, Hung Sang Tang, Duy Sinh Nguyen
Publikováno v:
Future Science OA, Vol 10, Iss 1 (2024)
The emergence of multicancer early detection (MCED) tests holds promise for improving early cancer detection and public health outcomes. However, positive MCED test results require confirmation through recommended cancer diagnostic imaging modalities
Externí odkaz:
https://doaj.org/article/6eedeea161724379aaf8585e61ff0076
Autor:
Hai Xuan Tang, Y‐Thanh Lu, Thi Minh Thi Ha, Nhat‐Thang Tran, Doan Minh Dang, Son Xuan Ly, Thu Ha Thi Bui, Son Ta Vo, Minh Doan Thai, Vu Dinh Nguyen, Thong Van Nguyen, Linh Thuy Dinh, Lan‐Anh Thi Luong, Kim‐Phuong Doan, Kim Huong Thi Nguyen, Thanh‐Thuy Thi Do, Dinh‐Kiet Truong, Hoa Giang, Hoai‐Nghia Nguyen, Thu Huong Nhut Trinh, Hung Sang Tang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract Background De novo variations are a primary cause of Rett syndrome and Tubulinopathy, accounting for over 90% of cases. Some studies have identified and documented parental inheritance by mosaicism in these two disorders, albeit with limited
Externí odkaz:
https://doaj.org/article/19102d2952084acf94b9f1f48e3f6b86
Autor:
Van Thien Chi Nguyen, Trong Hieu Nguyen, Nhu Nhat Tan Doan, Thi Mong Quynh Pham, Giang Thi Huong Nguyen, Thanh Dat Nguyen, Thuy Thi Thu Tran, Duy Long Vo, Thanh Hai Phan, Thanh Xuan Jasmine, Van Chu Nguyen, Huu Thinh Nguyen, Trieu Vu Nguyen, Thi Hue Hanh Nguyen, Le Anh Khoa Huynh, Trung Hieu Tran, Quang Thong Dang, Thuy Nguyen Doan, Anh Minh Tran, Viet Hai Nguyen, Vu Tuan Anh Nguyen, Le Minh Quoc Ho, Quang Dat Tran, Thi Thu Thuy Pham, Tan Dat Ho, Bao Toan Nguyen, Thanh Nhan Vo Nguyen, Thanh Dang Nguyen, Dung Thai Bieu Phu, Boi Hoan Huu Phan, Thi Loan Vo, Thi Huong Thoang Nai, Thuy Trang Tran, My Hoang Truong, Ngan Chau Tran, Trung Kien Le, Thanh Huong Thi Tran, Minh Long Duong, Hoai Phuong Thi Bach, Van Vu Kim, The Anh Pham, Duc Huy Tran, Trinh Ngoc An Le, Truong Vinh Ngoc Pham, Minh Triet Le, Dac Ho Vo, Thi Minh Thu Tran, Minh Nguyen Nguyen, Thi Tuong Vi Van, Anh Nhu Nguyen, Thi Trang Tran, Vu Uyen Tran, Minh Phong Le, Thi Thanh Do, Thi Van Phan, Hong-Dang Luu Nguyen, Duy Sinh Nguyen, Van Thinh Cao, Thanh-Thuy Thi Do, Dinh Kiet Truong, Hung Sang Tang, Hoa Giang, Hoai-Nghia Nguyen, Minh-Duy Phan, Le Son Tran
Publikováno v:
eLife, Vol 12 (2023)
Despite their promise, circulating tumor DNA (ctDNA)-based assays for multi-cancer early detection face challenges in test performance, due mostly to the limited abundance of ctDNA and its inherent variability. To address these challenges, published
Externí odkaz:
https://doaj.org/article/c43c93b76df74ebbb83d778241a75b5d
Autor:
Tat‐Thanh Nguyen, Quang‐Thanh Le, Diem‐Tuyet Thi Hoang, Huu Du Nguyen, Thi Minh Thi Ha, My‐Nhi Ba Nguyen, Thanh‐Thuy Thi Ta, Nhat Thang Tran, Thu Huong Nhat Trinh, Kim Phuong Thi Doan, Duc Tam Lam, Son Tra Thi Tran, Thanh Xuan Nguyen, Hong‐Thinh Le, Van Tuan Ha, Manh Hoan Nguyen, Ba‐Liem Kim Le, My Linh Duong, Trung Ha Pham, Anh Tuan Tran, Xuan Lan Thi Phan, Thanh Liem Huynh, Lan‐Phuong Thi Nguyen, Thanh Binh Vo, Duy‐Khang Nguyen Le, Ngoc Nhu Thi Tran, Quynh Nhu Thi Tran, Yen‐Linh Thi Van, Bich‐Ngoc Thi Huynh, Thanh‐Phương Thi Nguyen, Trang Thi Dao, Lan Phuong Thi Nguyen, Truong‐Giang Vo, Thanh‐Thuy Thi Do, Dinh‐Kiet Truong, Hung Sang Tang, Minh‐Duy Phan, Hoai‐Nghia Nguyen, Hoa Giang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Background Several inherited metabolic diseases are underreported in Vietnam, namely glucose‐6‐phosphate dehydrogenase deficiency (G6PDd), phenylketonuria (PKU) and galactosemia (GAL). Whilst massively parallel sequencing (MPS) allows re
Externí odkaz:
https://doaj.org/article/037b4a2351ac4123ba7b778f1ae0fea6
Autor:
Thi Hue Hanh Nguyen, Y-Thanh Lu, Van Hoi Le, Vinh Quang Bui, Lan Hieu Nguyen, Nhu Hiep Pham, Thanh Hai Phan, Huu Thinh Nguyen, Van Song Tran, Chi Viet Bui, Van Kha Vo, Pham Thanh Nhan Nguyen, Ha Huu Phuoc Dang, Van Dung Pham, Van Thinh Cao, Thanh Dat Nguyen, Luu Hong Dang Nguyen, Ngoc Minh Phan, Trong Hieu Nguyen, Van Thien Chi Nguyen, Thi Mong Quynh Pham, Vu Uyen Tran, Minh Phong Le, Dac Ho Vo, Thi Minh Thu Tran, Minh Nguyen Nguyen, Thi Thanh Nguyen, Ba Linh Tieu, Huu Tam Phuc Nguyen, Dinh Yen An Truong, Chi Thuy Tien Cao, Van Tung Nguyen, Thi Le Quyen Le, Thi Lan Anh Luong, Thi Kim Phuong Doan, Thi Trang Dao, Canh Duy Phan, Thanh Xuan Nguyen, Nguyen Tuong Pham, Bao Toan Nguyen, Thi Thu Thuy Pham, Huu Linh Le, Cong Thanh Truong, Thanh Xuan Jasmine, Minh Chi Le, Van Bau Phan, Quang Binh Truong, Thi Huong Ly Tran, Minh Thien Huynh, Tu Quy Tran, Si Tuan Nguyen, Vu Tran, Van Khanh Tran, Huu Nguyen Nguyen, Duy Sinh Nguyen, Thi Quynh Tho Nguyen, Thi Van Phan, Thi Thanh-Thuy Do, Dinh-Kiet Truong, Hung Sang Tang, Minh Duy Phan, Hoa Giang, Hoai Nghia Nguyen, Le Son Tran
Publikováno v:
Cancer Investigation. 41:232-248
The SPOT-MAS assay “Screening for the Presence Of Tumor by Methylation And Size” detects the five most common cancers in Vietnam by evaluating circulating tumor DNA in the blood. Here, we validated its performance in a prospective multi-center cl
Autor:
Mai-Huong Thi Nguyen, Anh-Hoa Pham Nguyen, Diem-Ngoc Ngo, Phuong-Mai Thi Nguyen, Hung-Sang Tang, Hoa Giang, Y-Thanh Lu, Hoai-Nghia Nguyen, Minh-Dien Tran
Publikováno v:
Journal of Human Genetics. 68:305-312
Citrin deficiency (CD), a disorder caused by mutations in the SLC25A13 gene, may result in neonatal intrahepatic cholestasis. This study was purposely to explore the mutation spectrum of SLC25A13 gene in Vietnamese CD patients.The 292 unrelated CD pa
Autor:
Danh-Cuong Tran, Hong-Thuy Thi Dao, Hong-Dang Luu Nguyen, Duy-Anh Nguyen, Quang Thanh Le, Diem-Tuyet Thi Hoang, Nhat Thang Tran, Thi Minh Thi Ha, Thuy Linh Dinh, Canh Chuong Nguyen, Kim Phuong Thi Doan, Lan Anh Thi Luong, Ta Son Vo, Thu Huong Nhat Trinh, Van Thong Nguyen, Phuong-Anh Ngoc Vo, Yen-Nhi Nguyen, My-An Dinh, Minh Ngoc Phan, Phuoc-Loc Doan, Thanh-Thuy Thi Do, Quynh-Tho Thi Nguyen, Dinh-Kiet Truong, Hoai-Nghia Nguyen, Minh-Duy Phan, Hung-Sang Tang, Hoa Giang
Copy number variation (CNV) analysis is a powerful tool for discovering structural genomic variation. Still, no program uses this tool to analyze chromosomal aneuploidies in the Vietnamese population. Pregnant women attending routine prenatal checkup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fcb57f2891efecb7b3b9cc563d2e66b
https://doi.org/10.21203/rs.3.rs-2410361/v1
https://doi.org/10.21203/rs.3.rs-2410361/v1
Autor:
Tuan-Thanh Lam, Doan-Tu Nguyen, Quang Thanh Le, Duy-Anh Nguyen, Diem-Tuyet Thi Hoang, Huu Du Nguyen, Canh Chuong Nguyen, Kim Phuong Thi Doan, Nhat-Thang Tran, Thi Minh Thi Ha, Thu Huong Nhat Trinh, Van Thong Nguyen, Duc Tam Lam, Minh Tam Le, Xuan Thao Nguyen, Thu-Hang Thi Ho, Trung Hoanh Tran, Viet Thang Ho, Thanh Van Bui, Van Trong Nguyen, Phuoc Ba Hoang, Hoai Thanh Nguyen, Manh Hoan Nguyen, Thanh-Binh Vo, Duy-Khang Nguyen Le, Thao Ngoc Truong, Hong-Thuy Thi Dao, Phuong-Anh Ngoc Vo, Thien-Chi Van Nguyen, Ngoc-Nhu Thi Tran, Quynh-Nhu Thi Tran, Yen-Linh Thi Van, Thanh-Thanh Thi Nguyen, Bich-Ngoc Thi Huynh, Thanh-Phuong Thi Nguyen, Kim-Van Thi Tran, Cong-Trai Nguyen, Phuoc-Loc Doan, Thanh-Dat Nguyen, Thanh-Thuy Thi Do, Dinh-Kiet Truong, Hung Sang Tang, Ngoc-Phuong Thi Cao, Minh-Duy Phan, Hoa Giang, Hoai-Nghia Nguyen
Publikováno v:
Hemoglobin. 46(4)
Vietnam has a high thalassemia burden. We collected blood samples from 5880 pregnant Vietnamese women during prenatal health checks to assess thalassemia carrier frequency using combined gap-polymerase chain reaction (gap-PCR) and targeted next-gener
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