نتایج جستجو برای: in situ fusion

تعداد نتایج: 17003508  

2016
K. Takeuchi Y. Togashi Y. Kamihara T. Fukuyama H. Yoshioka A. Inoue H. Katsuki K. Kiura K. Nakagawa T. Seto M. Maemondo T. Hida M. Harada Y. Ohe N. Nogami N. Yamamoto M. Nishio T. Tamura

BACKGROUND Anaplastic lymphoma kinase (ALK) fusions need to be accurately and efficiently detected for ALK inhibitor therapy. Fluorescence in situ hybridization (FISH) remains the reference test. Although increasing data are supporting that ALK immunohistochemistry (IHC) is highly concordant with FISH, IHC screening needed to be clinically and prospectively validated. PATIENTS AND METHODS In ...

Journal: :Haematologica 1994
M Mancini M Nanni M Cedrone M R De Cuia M B Rondinelli F Malagnino G Alimena

We describe the application of fluorescence in situ hybridization (FISH) in a case of suspected chronic myelogenous leukemia (CML), cytogenetically characterized by a t(21;22) with no clear involvement of chromosome 9. The dual color FISH technique, performed using specific painting probes for chromosomes 9,21,22 and a BCR/ABL translocation probe, enabled us to confirm the diagnosis of CML by d...

2017
Tajana Tešan Tomić Josefin Olausson Annica Wilzén Magnus Sabel Katarina Truvé Helene Sjögren Sándor Dósa Magnus Tisell Birgitta Lannering Fredrik Enlund Tommy Martinsson Pierre Åman Frida Abel

Pilocytic astrocytoma (PA) is the most common pediatric brain tumor. A recurrent feature of PA is deregulation of the mitogen activated protein kinase (MAPK) pathway most often through KIAA1549-BRAF fusion, but also by other BRAF- or RAF1-gene fusions and point mutations (e.g. BRAFV600E). These features may serve as diagnostic and prognostic markers, and also facilitate development of targeted ...

Journal: :Genome research 2014
Anton Valouev Ziming Weng Robert T Sweeney Sushama Varma Quynh-Thu Le Christina Kong Arend Sidow Robert B West

We present the discovery of genes recurrently involved in structural variation in nasopharyngeal carcinoma (NPC) and the identification of a novel type of somatic structural variant. We identified the variants with high complexity mate-pair libraries and a novel computational algorithm specifically designed for tumor-normal comparisons, SMASH. SMASH combines signals from split reads and mate-pa...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2014
Jun Dong Li Xiao Lu Sheng Jun Xu Zhong-Quan Sun

TMPRSS2:ERG gene fusions in prostate cancer have a dominant prevalence of approximately 50.0%, but infomration is limited on differences among ethnic and geographical groups. Some studies focusing on Japanese and Korean patients reported a lower incidence. Investigations concerning Chinese revealed controversial results. We evaluated TMPRSS2:ERG, TMPRSS2:ETV1 and TMPRSS2:ETV4 fusions in more th...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید باهنر کرمان - دانشکده کشاورزی 1391

این مطالعه به منظور تعیین ترکیب شیمیایی، خصوصیات فیزیکی، قابلیت هضم، تجزیه پذیری و ارزش غذایی علوفه خشک روناس در مقایسه با علوفه خشک یونجه با استفاده از دو روش in situ و in vitro انجام شد. داده های جمع آوری شده در قالب طرح کاملا تصادفی تجزیه آماری شدند. در مطالعه حاضر تفاوت معنی داری بین علوفه های خشک روناس و یونجه از نظر ماده آلی، پروتئین خام، الیاف نامحلول در شوینده خنثی و عصاره اتری مشاهده گ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2009
Juan-Miguel Mosquera Rohit Mehra Meredith M Regan Sven Perner Elizabeth M Genega Gerri Bueti Rajal B Shah Sandra Gaston Scott A Tomlins John T Wei Michael C Kearney Laura A Johnson Jeffrey M Tang Arul M Chinnaiyan Mark A Rubin Martin G Sanda

PURPOSE Fusion of the TMPRSS2 prostate-specific gene with the ERG transcription factor is a putatively oncogenic gene rearrangement that is commonly found in prostate cancer tissue from men undergoing prostatectomy. However, the prevalence of the fusion was less common in samples of transurethral resection of the prostate from a Swedish cohort of patients with incidental prostate cancer followe...

Journal: :Cancer research 2002
Frederic G Barr Stephen J Qualman Michele H Macris Natalya Melnyk Elizabeth R Lawlor Donna M Strzelecki Timothy J Triche Julia A Bridge Poul H B Sorensen

Previous studies of the PAX3-FKHR and PAX7-FKHR gene fusions in alveolar rhabdomyosarcoma (ARMS) indicated that the corresponding fusiontranscripts are not detectable in 20% of ARMS cases. To investigate the genetic features of this ARMS subset, we identified 23 ARMS cases in which PAX3-FKHR and PAX7-FKHR transcripts were not detected by a standard sensitivity reverse transcription-PCR (RT-PCR)...

2018
Jasmina Topcagic Rebecca Feldman Anatole Ghazalpour Jeffrey Swensen Zoran Gatalica Semir Vranic

Olfactory neuroblastoma (ONB) is a rare, locally aggressive, malignant neoplasm originating in the olfactory epithelium in the nasal vault. The recurrence rate of ONB remains high and there are no specific treatment guidelines for recurrent/metastatic ONBs. This study retrospectively evaluated 23 ONB samples profiled at Caris Life Sciences (Phoenix, Arizona) using DNA sequencing (Sanger/NGS [Il...

Journal: :American journal of clinical pathology 2012
Tobias Klatte Berthold Streubel Friedrich Wrba Mesut Remzi Barbara Krammer Michela de Martino Matthias Waldert Michael Marberger Martin Susani Andrea Haitel

We studied the characteristics and prognosis of renal cell carcinoma (RCC) associated with Xp11.2 translocation and transcription factor E3 (TFE3) expression and determined the need for genetic analysis in routine diagnostics. Of 848 consecutive cases, 75 showed microscopic features suggestive of Xp11.2 translocation RCC or occurred in patients 40 years or younger. Of these cases, 17 (23%) show...

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