نتایج جستجو برای: wilms

تعداد نتایج: 3145  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2000
M A Ghanem T H Van der Kwast J C Den Hollander M K Sudaryo M H Oomen M A Noordzij M M Van den Heuvel S M Nassef R M Nijman G J Van Steenbrugge

Wilms' tumor is one of the most common solid tumors of children. The protein product of the tumor-suppressor gene, Wilms' tumor 1 (WT-1), binds to the same DNA sequences as the protein product of the early growth response 1 (EGR-1) gene. There is experimental evidence that EGR-1 is involved in controlling cell growth. The expression of both genes in Wilms' tumor was studied by others, mainly at...

Journal: :Journal of medical genetics 1994
C Moutou J Hochez A Chompret M F Tournade C Le Bihan J M Zucker J Lemerle C Bonaïti-Pellié

Wilms' tumour of the kidney is known to occur in Beckwith-Wiedemann syndrome. It has also been described in four cancer prone families displaying Li-Fraumeni syndrome but it is not usually considered to be part of this syndrome. In order to detect particular familial cancer aggregations associated with this tumour, we studied the cancer incidence and mortality among relatives of the 501 Wilms' ...

Journal: :Urology 2012
Blake W Palmer Yan Xiong Awet Gherezghiher David Buethe Adam Metwalli Dominic Frimberger Bradley P Kropp

A 7-year-old male with bilateral palpable testicular masses was found to have metastatic stage IV Wilms' tumors associated with both left renal and lung lesions. The patient was treated successfully with testicular-sparing bilateral partial orchiectomies, radical nephrectomy, chemotherapy, and radiation, with 8 years free of recurrence. This is the only reported case of bilateral testicular tum...

Journal: :Canadian journal of surgery. Journal canadien de chirurgie 2008
Jonathan I Izawa Mohammad Al-Omar Eric Winquist Larry Stitt George Rodrigues Steven Steele D Robert Siemens Patrick P Luke

OBJECTIVE To identify outcomes and prognostic variables that predict survival outcomes in adult Wilms tumour patients. METHODS We collected data on 128 patients with adult Wilms tumour treated between 1973 and 2006. Six cases from our 2 Canadian centres have not been previously reported. We collected data on the remaining 122 patients from published case reports or case series. Analyzed facto...

2007
Maureen A. Cooney Julie L. Daniels Julie A. Ross Norman E. Breslow Brad H. Pollock Andrew F. Olshan

BACKGROUND Previous epidemiologic studies have suggested that exposure to pesticides in utero and during early childhood may increase the risk for development of childhood cancer, including Wilms tumor, a childhood kidney tumor. OBJECTIVES In this analysis we evaluated the role of residential pesticide exposure in relation to the risk of Wilms tumor in children using data from a North America...

Journal: :Cancer research 2006
Rachael Natrajan Jorge S Reis-Filho Suzanne E Little Boo Messahel Marie-Anne Brundler Jeffrey S Dome Paul E Grundy Gordan M Vujanic Kathy Pritchard-Jones Chris Jones

Most Wilms' tumors are of low stage, favorable histology, and have a high likelihood of cure with current multimodal therapy. Despite this, there remains a group of patients whose tumors recur for whom intensive salvage regimens result in survival of only 50%. Fitting a Cox proportional hazards model to microarray-based comparative genomic hybridization (aCGH) data on 68 Wilms' tumor samples, w...

2005
Wenliang Li Patricia Kessler Herman Yeger Jennifer Alami Anthony E. Reeve Rosemary Heathcott Jane Skeen

Anaplastic histology and metastasis are each associated with higher relapse and mortality rates in Wilms tumor patients. However, not all anaplastic tumors relapse and some nonanaplastic tumors relapse unexpectedly. To identify more accurate early prognostic indicators, we analyzed expression of 4,900 cancer-related genes in 26 primary Wilms tumors. This analysis revealed that expression of a s...

Journal: :Cancer research 2005
Wenliang Li Patricia Kessler Herman Yeger Jennifer Alami Anthony E Reeve Rosemary Heathcott Jane Skeen Bryan R G Williams

Anaplastic histology and metastasis are each associated with higher relapse and mortality rates in Wilms tumor patients. However, not all anaplastic tumors relapse and some nonanaplastic tumors relapse unexpectedly. To identify more accurate early prognostic indicators, we analyzed expression of 4,900 cancer-related genes in 26 primary Wilms tumors. This analysis revealed that expression of a s...

Journal: :Genes & development 2015
Peter Hohenstein Kathy Pritchard-Jones Jocelyn Charlton

Wilms' tumor, or nephroblastoma, is the most common pediatric renal cancer. The tumors morphologically resemble embryonic kidneys with a disrupted architecture and are associated with undifferentiated metanephric precursors. Here, we discuss genetic and epigenetic findings in Wilms' tumor in the context of renal development. Many of the genes implicated in Wilms' tumorigenesis are involved in t...

2015
Elizabeth J Perlman Samantha Gadd Stefan T Arold Anand Radhakrishnan Daniela S Gerhard Lawrence Jennings Vicki Huff Jaime M Guidry Auvil Tanja M Davidsen Jeffrey S Dome Daoud Meerzaman Chih Hao Hsu Cu Nguyen James Anderson Yussanne Ma Andrew J Mungall Richard A Moore Marco A Marra Charles G Mullighan Jing Ma David A Wheeler Oliver A Hampton Julie M Gastier-Foster Nicole Ross Malcolm A Smith

Wilms tumour is an embryonal tumour of childhood that closely resembles the developing kidney. Genomic changes responsible for the development of the majority of Wilms tumours remain largely unknown. Here we identify recurrent mutations within Wilms tumours that involve the highly conserved YEATS domain of MLLT1 (ENL), a gene known to be involved in transcriptional elongation during early devel...

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