Search Results - "Xinh, Phan Thi"

Down-regulated expression of NPM1 in IMS-M2 cell line by(-)-epigallocatechin-3-gallate by Chi, Hoang Thanh, Ly, Bui Thi Kim, Vu, Hoang Anh, Sato, Yuko, Dung, Phu Chi, Xinh, Phan Thi

“…Objective:To investigate the inhibited effect of epigallocatechin-3-gallate(EGCG)on the expression of NPM1 in IMS-M2 cells harboring the NPMl…”
Get full text

Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis by Xinh, Phan Thi, Chuong, Ho Quoc, Diem, Truong Pham Hong, Nguyen, Tuan Minh, Van, Nguyen Dinh, Mai Anh, Nguyen Hoang, Nghia, Huynh, Vu, Hoang Anh

“…Introduction The prevalence of gene mutations in hemophagocytic lymphohistiocytosis (HLH) varied between studies. Thus far, data on the genetic background of…”
Get full text

Possible Concomitant Aggressive NK Cell Leukemia and EBV-positive T-cell lymphoma; Using the online beta version of WHO-HAEM5 and videoconferencing software to make diagnoses accessible in an emerging economy by Dayton, Vanessa J, Hoang Thien, Dang, Xinh, Phan Thi, Arries, Cade, Sang, Nguyen Ngoc, Linh, Ngo Ngoc Ngan, Lien, Nguyen Phuong, Dung, Phu Chi

“…Abstract Background Using the World Health Organization Classification 5th edition (beta version online; WHO-HAEM5bv) in emerging economies is key to global…”
Get full text

Spectrum of mutations in the RB1 gene in Vietnamese patients with retinoblastoma by Kiet, Nguyen Cong, Khuong, Le Thai, Minh, Do Duc, Quan, Nguyen Huynh Minh, Xinh, Phan Thi, Trang, Nguyen Ngoc Chau, Luan, Nguyen Thanh, Khai, Nguyen Minh, Vu, Hoang Anh

“…Retinoblastoma (RB) is a rare childhood malignant disorder caused by the biallelic inactivation of the gene. Early diagnosis and identification of carriers of…”
Get full text

Real-time Quantitative Polymerase Chain Reaction Assay for Detecting 1p and 19q Codeletion in Glioma by Vo, Niem Van Thanh, Truong, Diem Dinh-Kieu, Xinh, Phan Thi, Vu, Hoang Anh

“…Abstract Background: Glioma is a type of tumor that occurs in the brain and spinal cord. Gliomas begin in the gluey supportive cells (glial cells) that…”
Get full text

The effects of NUDT15 and TPMT variants on mercaptopurine treatment in Vietnamese pediatric acute lymphoblastic leukemia patients by Nghia, Huynh, Than, Huynh Huu, Dong, Cao Van, Oanh, Tran Thi Kieu, Truc, Vo Thi Thanh, Ngan, Cai Thi Thu, Ngon, Huynh Thien, Binh, Nguyen Tan, Dung, Phu Chi, Anh Vu, Hoang, Xinh, Phan Thi

“…6-mercaptopurine (6-MP) plays a critical role in the treatment of pediatric acute lymphoblastic leukemia (ALL). NUDT15 and TPMT gene variants have been…”
Get full text

CD40LG mutations in Vietnamese patients with X‐linked hyper‐IgM syndrome; catastrophic anti‐phospholipid syndrome as a new complication by Phan, Anh Nguyen Lien, Pham, Thuy Thi Thanh, Phan, Xinh Thi, Huynh, Nghia, Nguyen, Tuan Minh, Cao, Cuc Tran Thu, Nguyen, Duong Thuy, Luong, Khanh Thi Xuan, Nguyen, Tam Thi Minh, Tran, Anh Ngoc Kim, Pham, Linh Thi Truc, Nguyen, Vy Vuong Thao, Swagemakers, Sigrid, Bui, Chi‐Bao, Van Hagen, Petrus Martinus

“…Background X‐linked hyper‐IgM syndrome (XHIGM) is a rare primary immunodeficiency caused by CD40 ligand defects. Methods We identified three patients with…”
Get full text

Green Tea Epigallocatechin Gallate Exhibits Anticancer Effect in Human Pancreatic Carcinoma Cells via the Inhibition of Both Focal Adhesion Kinase and Insulin-Like Growth Factor-I Receptor by Vu, Hoang Anh, Beppu, Yuuichi, Chi, Hoang Thanh, Sasaki, Kousuke, Yamamoto, Hideaki, Xinh, Phan Thi, Tanii, Takashi, Hara, Yukihiko, Watanabe, Toshiki, Sato, Yuko, Ohdomari, Iwao

“…The exact molecular mechanism by which epigallocatechin gallate (EGCG) suppresses human pancreatic cancer cell proliferation is unclear. We show here that…”
Get full text

Synergistic effect of all-trans retinoic acid in combination with protein kinase C 412 in FMS-like tyrosine kinase 3-mutated acute myeloid leukemia cells by CHI, HOANG THANH, LY, BUI THI KIM, VU, HOANG ANH, SATO, YUKO, DUNG, PHU CHI, XINH, PHAN THI

“…Acute myeloid leukemia (AML) is a heterogeneous disease. Numerous molecular abnormalities have been identified in AML and, amongst these, FMS-like tyrosine…”
Get full text

Spectrum of EGFR gene mutations in Vietnamese patients with non-small cell lung cancer by Vu, Hoang Anh, Xinh, Phan Thi, Ha, Hua Thi Ngoc, Hanh, Ngo Thi Tuyet, Bach, Nguyen Duc, Thao, Doan Thi Phuong, Dat, Ngo Quoc, Trung, Nguyen Sao

“…Aim Epidermal growth factor receptor (EGFR) mutational status is a crucial biomarker for prediction of response to tyrosine kinase inhibitors in patients with…”
Get full text

A recurrent duodenal gastrointestinal stromal tumor with a frameshift mutation resulting in a stop codon in KIT exon 13 by Vu, Hoang Anh, Xinh, Phan Thi, Kikushima, Makoto, Zhu, Yi, Tokuhara, Makoto, Tani, Masayoshi, Shimizu, Toshio, Saito, Kiyoshi, Tokunaga, Katsushi, Sato, Yuko

“…Gastrointestinal stromal tumors (GISTs) are a specific and rare subset of human gastrointestinal tract tumors. Most GISTs show gain‐of‐function mutations of…”
Get full text

Spectrum of HBB gene mutations among 696 β–thalassemia patients and carriers in Southern Vietnam by Xinh, Phan Thị, Chuong, Ho Quoc, Ha, Nguyen Thi Thanh, Tram, Huynh Duong Bich, Van Dong, Cao, Thanh, Le Vu Ha, Hoa, Nguyen Thi Hong, Nghia, Huynh, Binh, Nguyen Tan, Dung, Phu Chi, Vu, Hoang Anh

“…Background Thalassemias are common inherited blood disorders that have been extensively studied in Asia. Thus far, data on mutations of the HBB gene in…”
Get full text

Establishment and characterization of A novel Philadelphia-chromosome positive chronic myeloid leukemia cell line, TCC-S, expressing P210 and P190 BCR/ABL transcripts but missing normal ABL gene by Van, Phan Nguyen Thanh, Xinh, Phan Thi, Kano, Yasuhiko, Tokunaga, Katsushi, Sato, Yuko

“…A novel Philadelphia-chromosome positive (Ph+) cell line, TCC-S, has been established from a patient with Ph+ chronic myeloid leukemia (CML) in the blastic…”
Get full text

Spectrum of WAS gene mutations in Vietnamese patients with Wiskott-Aldrich syndrome by Chuong, Ho Quoc, Xinh, Phan Thi, Tram, Duong Bich, Ha, Nguyen Thi Thanh, Nguyen, Tuan Minh, Anh, Phan Nguyen Lien, Van, Nguyen Dinh, Anh, Nguyen Hoang Mai, Dung, Phu Chi, Nghia, Huynh, Vu, Hoang Anh

“…WAS gene mutational analysis is crucial to establish a definite diagnosis of Wiskott-Aldrich syndrome (WAS). Data on the genetic background of WAS in…”
Get full text

Cytogenetic Characteristics of de novo Acute Myeloid Leukemia in Southern Vietnam by Thao, Lai Thi Thanh, Ha, Chau Thuy, Ha, Nguyen Thi Thanh, Beaupha, Suzanne Monivong Cheanh, Nghia, Huynh, Tung, Tran Thanh, Son, Nguyen Truong, Binh, Nguyen Tan, Dung, Phu Chi, Vu, Hoang Anh, Xinh, Phan Thi

Get full text

Clinical and Hematological Relevance of JAK2V617F, CALR, and MPL Mutations in Vietnamese Patients with Essential Thrombocythemia by Vu, Hoang Anh, Thao, Tran Thi, Dong, Cao Van, Vuong, Nguyen Lam, Chuong, Ho Quoc, Van, Phan Nguyen Thanh, Nghia, Huynh, Binh, Nguyen Tan, Dung, Phu Chi, Xinh, Phan Thi

“…Background: The picture of Vietnamese patients with essential thrombocythemia (ET) remains mostly undetermined. Our study intended to determine the frequency…”
Get full text

ID:2035 Chromosomal abnormalities and treatment response in Multiple myeloma patients at Cho Ray hospital by Suzanne, Thanh Thanh, Le, Oanh Hoang, Phan, Xinh Thi, Tran, Tung Thanh, Nguyen, Cuong Kim, Phan, Thang Thanh, Huynh, Hoa Hong

“…Multiple myeloma (MM) is a malignant plasma cell, generating abnormal immunoglobulins in the blood and urin. From January 2012 to December 2014, we performed…”
Get full text

The juxtamembrane domain in ETV6/FLT3 is critical for PIM-1 up-regulation and cell proliferation by Vu, Hoang Anh, Xinh, Phan Thi, Kano, Yasuhiko, Tokunaga, Katsushi, Sato, Yuko

“…We recently reported that the ETV6/FLT3 fusion protein conferred interleukin-3-independent growth on Ba/F3 cells. The present study has been conducted to…”
Get full text

Activation of Nuclear Factor KappaB in ETV6/FLT3-Transformed Ba/F3 Cells Depends on the FLT3 Tyrosine 591 by Vu, Hoang Anh, Xinh, Phan Thi, Kano, Yasuhiko, Ishida, Takaomi, Watanabe, Toshiki, Tokunaga, Katsushi, Sato, Yuko

“…The FLT3 gene is one of the most frequently mutated genes in hematologic malignancies. Mutated FLT3 has been found to lead to strong constitutive activation of…”
Get full text

MEL1 at 1p36.3 Is Fused to Several Partner Genes Including HOXA9 Located at Different Chromosomal Bands from 3q21.3 in t(1;3)(p36.3;q21.3)-Leukemia by Xinh, Phan Thi, Anh, Hoang, Tanaka, Hideo, Fujisawa, Shin, Taketazu, Fumitoshi, Rowley, Janet D., Tokunaga, Katsushi, Sato, Yuko

“…In MDS/AML with t(1;3)(p36;q21), overexpression of MEL1 lacking PR domain (MEL1S) driven by the RPN1 promoter at 3q21.3 is reported to be closely associated…”
Get full text