Search Results - "Ta, Dat Thanh"

Comparative FISH analysis of Senna tora tandem repeats revealed insights into the chromosome dynamics in Senna by Ta, Thanh Dat, Waminal, Nomar Espinosa, Nguyen, Thi Hong, Pellerin, Remnyl Joyce, Kim, Hyun Hee

“…Background DNA tandem repeats (TRs) are often abundant and occupy discrete regions in eukaryotic genomes. These TRs often cause or generate chromosomal…”
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Comparative triple-color FISH mapping in eleven Senna species using rDNA and telomeric repeat probes by Nguyen, Thi Hong, Waminal, Nomar Espinosa, Lee, Do Sin, Pellerin, Remnyl Joyce, Ta, Thanh Dat, Campomayor, Nicole Bon, Kang, Byung Yong, Kim, Hyun Hee

“…Senna is a diverse and paraphyletic genus in the subfamily Caesalpinioideae (Fabaceae Lindl.) comprising various species of industrial and medicinal value. To…”
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Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease by Chung Tran, Nam, Lien, Nguyen Thi Kim, Ta, Thanh Dat, Nguyen, Van Hung, Tran, Huy Thinh, Van Tung, Nguyen, Xuan, Nguyen Thi, Huy Hoang, Nguyen, Tran, Van Khanh

“…Background: Limb-girdle muscular dystrophy (LGMD) is a group of inherited neuromuscular disorders characterized by atrophy and weakness in the shoulders and…”
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Correlation of Epstein-Barr virus copy numbers, MICA expression and rs2596542 variant in nasopharyngeal carcinoma tumour by Ta, Thanh Dat, Nguyen, Thanh Binh, Van, Khanh Tran, Le, Manh Thuong, Hai, Long Ha Le, Nguyen, Hoang Viet

“…Major histocompatibility complex class I chain-related A (MICA) is a tumour antigen that is greatly expressed on the surfaces of human malignancies and…”
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Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam by Ngo, Thi Thao, Tran, Thinh Huy, Ta, Thanh Dat, Le, Thi Phuong, Nguyen, Phuoc Dung, Tran, Mai Anh, Bui, The-Hung, Ta, Thanh Van, Tran, Van Khanh

“…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder and is caused by G6PD gene mutations. To date, more than 400 variants in…”
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A case of response to combination treatment with autologous immunotherapy and bevacizumab in advanced non-small cell lung cancer by Nguyen, Thuy Mau Thi, Van Tran, Khanh, Ta, Van Thanh, Tran, Linh Mai, Tran, Chi Khanh, Trinh, Huy Le, Ta, Dat Thanh, Nguyen, Binh Thanh, Tran, Thinh Huy

“…Natural killer (NK) cells have developed as a potent tool in cancer immunotherapy. Especially, patients who have failed in the first-line or maintenance…”
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Acromesomelic dysplasia Maroteaux‐type in patients from Vietnam by Tran, Thinh Huy, Cao, My Ha, Luong, Long Hoang, Le, Phuong Thi, Vu, Dung Chi, Ta, Thanh Dat, Bui, The‐Hung, Nguyen, Duc Hinh, Van Ta, Thanh, Tran, Van Khanh

“…Acromesomelic dysplasias are rare skeletal disorders leading to severe short stature and abnormal skeletal morphology. Acromesomelic dysplasia Maroteaux‐type…”
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Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report by Tran, Nam‐Chung, Nguyen, Tuan Anh, Ta, Thanh Dat, Tran, Thinh Huy, Nguyen, Phuoc‐Dung, Vu, Chi Dung, Nguyen, Van‐Hung, Bui, The‐Hung, Ta, Thanh Van, Tran, Van Khanh

“…Limb‐girdle muscular dystrophy‐type 2C (LGMD2C) is caused by mutations in the SGCG gene. Here, we report a case of a 26‐year‐old male who had inactive walking…”
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In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome by Pham, Hung Manh, Nguyen, Duy Phuong, Ta, Thanh Dat, Le, Thi Phuong, Phan, Phong Hai, Trinh, Hoai An, Tran, Tuan Viet, Luong, Thi Lan Anh, Nguyen, Ha Minh, Bui, The‐Hung, Tran, Thinh Huy, Ta, Thanh Van, Tran, Van‐Khanh

“…Background Brugada syndrome (BrS) is a rare genetic disease that causes sudden cardiac death (SCD) and arrhythmia. SCN5A pathogenic variants (about 30% of…”
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Mutation spectrum of retinoblastoma patients in Vietnam by Linh, Dao Nguyen Ha, Van Huy, Nguyen, Nguyen, Phuoc-Dung, Le Thi, Phuong, Tuan, Hoang Anh, Van Nguyen, Trong, Tran, Thu Ha, Tran, Hai Anh, Ta, Thanh Dat, Pham, Tuan L A, Bui, The-Hung, Tran, Thinh Huy, Van Ta, Thanh, Tran, Van-Khanh

“…Retinoblastoma (RB), an intraocular malignancy commonly diagnosed in children, is mostly caused by inactivating mutations of both alleles of the RB1 gene…”
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Primary congenital glaucoma in Vietnam: analysis and identification of novel CYP1B1 variants by Tran, Ha Thu, Tran, Huy Thinh, Luong, Long Hoang, Nguyen, Tung Son, Nguyen, Hoai Quy, Vu, Thanh Thi, Ta, Thanh Dat, Dao, Thi Mai Anh, Bui, The-Hung, Ta, Thanh Van, Tran, Van Khanh

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