نتایج جستجو برای: rara positive apl

تعداد نتایج: 662831  

Journal: :Blood 2002
Qi Zhu Ji-Wang Zhang Hai-Qing Zhu Yu-Lei Shen Maria Flexor Pei-Ming Jia Yun Yu Xun Cai Samuel Waxman Michel Lanotte Sai-Juan Chen Zhu Chen Jian-Hua Tong

Acute promyelocytic leukemia (APL) is characterized by the specific chromosome translocation t(15;17) with promyelocytic leukemia-retinoic acid receptor-alpha (PML-RARA) fusion gene and the ability to undergo terminal differentiation as an effect of all-trans retinoic acid (ATRA). Recently, arsenic trioxide (As(2)O(3)) has been identified as an alternative therapy in patients with both ATRA-sen...

Journal: :Molecular and cellular biology 2003
Vernon T Phan David B Shultz Bao-Tran H Truong Timothy J Blake Anna L Brown Thomas J Gonda Michelle M Le Beau Scott C Kogan

We utilized a mouse model of acute promyelocytic leukemia (APL) to investigate how aberrant activation of cytokine signaling pathways interacts with chimeric transcription factors to generate acute myeloid leukemia. Expression in mice of the APL-associated fusion, PML-RARA, initially has only modest effects on myelopoiesis. Whereas treatment of control animals with interleukin-3 (IL-3) resulted...

2001
Luca Mologni Edoardo Marchesi Peter E. Nielsen Carlo Gambacorti-Passerini

The fusion protein promyelocytic leukemia (PML)/retinoic acid receptor (RAR)a is tightly linked to the pathogenesis of acute promyelocytic leukemia (APL); hence, it represents a tumor-associated, transformationrelated molecule. In this study, three anti-PML adamantyl-conjugated peptide nucleic acid (PNA) oligomers previously described as in vitro inhibitors of PML/RARa translation were combined...

2015
Yanli He Ping Wang Kaiwei Liang Xiangjun Chen Wen Du Juan Li Yanjie Hu Yan Bai Wei Liu Xiaoqing Li Runming Jin Min Zhang Jine Zheng Martin Staege.

Acute promyelocytic leukemia (APL) is a specific malignant hematological disorder with a diagnostic hallmark of chromosome translocation t(15;17)(q22;q21). As a very rare secondary cytogenetic aberration in pediatric APL, ider(17q) (q10)t(15;17) was suggested to be a poor prognostic factor based on previous case reports.Here, we report a pediatric APL case with a rare karyotype of ider(17)(q10)...

Journal: :Cell reports 2016
Jessica N Nichol Matthew D Galbraith Claudia L Kleinman Joaquín M Espinosa Wilson H Miller

Perturbation in the transcriptional control of genes driving differentiation is an established paradigm whereby oncogenic fusion proteins promote leukemia. From a retinoic acid (RA)-sensitive acute promyelocytic leukemia (APL) cell line, we derived an RA-resistant clone characterized by a block in transcription initiation, despite maintaining wild-type PML/RARA expression. We uncovered an aberr...

2017
Jae-Ho Yoon Hee-Je Kim Dae-Hun Kwak Sung-Soo Park Young-Woo Jeon Sung-Eun Lee Byung-Sik Cho Ki-Seong Eom Yoo-Jin Kim Seok Lee Chang-Ki Min Seok-Goo Cho Dong-Wook Kim Jong Wook Lee Woo-Sung Min

Wilms' tumor gene 1 (WT1) expression is a well-known predictor for relapse in acute myeloid leukemia. We monitored WT1 decrement along the treatment course to identify its significant role as a marker for residual disease in acute promyelocytic leukemia (APL) and tried to suggest its significance for relapse prediction. In this single center retrospective study, we serially measured PML-RARa an...

Journal: :Blood 2010
Jun Imagawa Yuka Harada Takeshi Shimomura Hideo Tanaka Yoshiko Okikawa Hideo Hyodo Akiro Kimura Hironori Harada

Acute promyelocytic leukemia (APL) is a highly curable disease with excellent complete remission and long-term survival rates. However, the development of therapy-related myeloid neoplasms (t-MN) is being reported with increasing frequency in patients successfully treated for APL. We attempted to clarify the different clinical features and hematologic findings between t-MN and relapse cases, an...

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