نتایج جستجو برای: rara

تعداد نتایج: 1856  

Journal: :American journal of human genetics 1992
G Chenevix-Trench K Jones A C Green D L Duffy N G Martin

The first association study of cleft lip with or without cleft palate (CL/P), with candidate genes, found an association with the transforming growth-factor alpha (TGFA) locus. This finding has since been replicated, in whole or in part, in three independent studies. Here we extend our original analysis of the TGFA TaqI RFLP to two other TGFA RFLPs and seven other RFLPs at five candidate genes ...

Journal: :Journal of applied physiology 2002
David Gozal Evelyne Gozal Stephen R Reeves Andrew J Lipton

Gasping is a critically important mechanism for autoresuscitation and survival during extreme tissue hypoxia. Evidence of antecedent hypoxia in sudden infant death syndrome suggests that intermittently occurring hypoxic episodes may modify gasping and autoresuscitation. To examine this issue, an intermittent hypoxia (IH) profile consisting of alternating room air and 10% O(2)-balance N(2) every...

2014
Hiromichi Matsushita Takashi Yahata Yin Sheng Yoshihiko Nakamura Yukari Muguruma Hideyuki Matsuzawa Masayuki Tanaka Hideki Hayashi Tadayuki Sato Anar Damdinsuren Makoto Onizuka Mamoru Ito Hayato Miyachi Pier Paolo Pandolfi Kiyoshi Ando

Recent advances in cancer biology have revealed that many malignancies possess a hierarchal system, and leukemic stem cells (LSC) or leukemia-initiating cells (LIC) appear to be obligatory for disease progression. Acute promyelocytic leukemia (APL), a subtype of acute myeloid leukemia characterized by the formation of a PML-RARα fusion protein, leads to the accumulation of abnormal promyelocyte...

2017
Fatemeh Zahedipour Reza Ranjbaran Abbas Behzad Behbahani Khalil Tavakol Afshari Mohammad Ali Okhovat Gholamhossein Tamadon Sedigheh Sharifzadeh

BACKGROUND Acute Promyelocytic Leukemia (APL) is a subclass of acute myeloid leukemia. The chromosomal aberration in 95% of APL cases is t(15; 17) (q22; q21), which prevents cell differentiation. Characterization of the underlying molecular lesion is valuable in determining optimal treatment strategy. The goal of this study was to develop a new and powerful Flow- FISH technique to detect the lo...

Journal: :Blood 2003
Jastinder Sohal Vernon T Phan Philip V Chan Elizabeth M Davis Bhumi Patel Louise M Kelly Tinya J Abrams Anne Marie O'Farrell D Gary Gilliland Michelle M Le Beau Scott C Kogan

The PML-RAR alpha fusion protein is central to the pathogenesis of acute promyelocytic leukemia (APL). Expression of this protein in transgenic mice initiates myeloid leukemias with features of human APL, but only after a long latency (8.5 months in MRP8 PML-RARA mice). Thus, additional changes contribute to leukemic transformation. Activating mutations of the FLT3 receptor tyrosine kinase are ...

Journal: :The Journal of Cell Biology 1981
C A Vaccaro J S Brody

The ultrastructural characteristics of alveolar (ABM) and capillary (CBM) basement membranes in the adult rat lung have been defined using tannic acid fixation, ruthenium red staining, or incubation in guanidine HCl. ABM is dense and amorphous, has 3- to 5-nm filaments in the lamina rara externa (facing the alveolus) that run between the lamina densa and the basal cell surface of the epithelium...

2000
Francesco Grignani Mauro Valtieri Marco Gabbianelli Vania Gelmetti Rosanna Botta Luisella Luchetti Barbara Masella Ornella Morsilli Elvira Pelosi Paola Samoggia Pier Giuseppe Pelicci

The role of fusion proteins in acute myeloid leukemia (AML) is well recognized, but the leukemic target cell and the cellular mechanisms generating the AML phenotype are essentially unknown. To address this issue, an in vitro model to study the biologic activity of leukemogenic proteins was established. Highly purified human hematopoietic progenitor cells/stem cells (HPC/HSC) in bulk cells or s...

Journal: :JAMA 2011
John S Welch Peter Westervelt Li Ding David E Larson Jeffery M Klco Shashikant Kulkarni John Wallis Ken Chen Jacqueline E Payton Robert S Fulton Joelle Veizer Heather Schmidt Tammi L Vickery Sharon Heath Mark A Watson Michael H Tomasson Daniel C Link Timothy A Graubert John F DiPersio Elaine R Mardis Timothy J Ley Richard K Wilson

CONTEXT Whole-genome sequencing is becoming increasingly available for research purposes, but it has not yet been routinely used for clinical diagnosis. OBJECTIVE To determine whether whole-genome sequencing can identify cryptic, actionable mutations in a clinically relevant time frame. DESIGN, SETTING, AND PATIENT We were referred a difficult diagnostic case of acute promyelocytic leukemia...

Journal: :Iranian biomedical journal 2012
Marjan Yaghmaie Kamran Alimoghaddam Hossein Mozdarani Ardeshir Ghavamzadeh Marjan Hajhashemi Mozaffar Aznab Seyed H Ghaffari

BACKGROUND The secondary genetic changes other than the promyelocytic leukemia-retinoic acid receptor (PML-RARA) fusion gene may contribute to the acute promyelocytic leukemogenesis. Chromosomal alterations and mutation of FLT3 (FMS-like tyrosine kinase 3) tyrosine kinase receptor are the frequent genetic alterations in acute myeloid leukemia. However, the prognostic significance of FLT3 mutati...

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