نتایج جستجو برای: wilms tumor gene 1

تعداد نتایج: 3825016  

Journal: :Cancer research 2007
Elizabeth M Algar Luke St Heaps Artur Darmanian Vinod Dagar Dirk Prawitt Greg B Peters Felicity Collins

Loss of imprinting at insulin-like growth factor II (IGFII), in association with H19 silencing, has been described previously in a subgroup of Beckwith-Wiedemann syndrome (BWS) patients who have an elevated risk for Wilms' tumor. An equivalent somatic mutation occurs in sporadic Wilms' tumor. We describe a family with overgrowth in three generations and Wilms' tumor in two generations, with pat...

2016
Min-Ju Li Da-Xing Tang Shan Xu Yong Huang De-Hua Wu Jin-Hu Wang Can Lai Hong-Feng Tang Qiang Shu

From 2003 to 2013, 55 patients (median age 3.3 years; 29 males, 26 females) with unresectable, metastatic, or diffuse anaplastic histology (AH) Wilms tumor were treated with neoadjuvant transcatheter arterial chemoembolization (TACE) and systemic chemotherapy. Characteristics In: Wilms Tumor. Marry M. van den Heuvel-Eibrink (Editor) ISBN: 978-0-9944381-1-9; Doi: http://dx.doi.org/10.15586/codon...

2010
Hatice KOÇAK Gülay CEYLANER

The WAGR contiguous gene deletion syndrome is a combination of Wilms tumor, Aniridia, Genito-urinary abnormalities, and growth and mental Retardation which is invariably associated with an 11p13 deletion. This deletion included the PAX6 and WT1 genes as previously reported in typical WAGR patients. Ocular defects result from hemizygosity for the PAX6 gene. Urogenital and renal abnormalities and...

2017
Heloisa Cristina Caldas Fernando Henrique Lojudice Cinthia Dias Ida Maria Maximina Fernandes-Charpiot Maria Alice Sperto Ferreira Baptista Rosa Sayoko Kawasaki-Oyama Mari Cleide Sogayar Christina Maeda Takiya Mario Abbud-Filho

The therapeutic effect of induced pluripotent stem cells (iPSs) on the progression of chronic kidney disease (CKD) has not yet been demonstrated. In this study, we sought to assess whether treatment with iPSs retards progression of CKD when compared with bone marrow mesenchymal stem cells (BMSCs). Untreated 5/6 nephrectomized rats were compared with CKD animals receiving BMSCs or iPSs. Renal fu...

2016
O. H. Radhika Krishna Geetha Kayla Mohammed Abdul Aleem Ramani Malleboyina Ramesh Reddy Kota

Aim. Evaluate tumor proliferation marker (Ki67) and p53 tumor suppressor marker in Wilms tumor and correlate with histology, anaplasia, and staging. Design. Prospective, hospital based study conducted at a tertiary pediatric referral centre in south India. Setting. Wilms tumor is the most common childhood renal malignancy worldwide. Anaplasia on histology is associated with treatment resistance...

Ali Davati, Mehdi Abedini Mohammad Reza Jalali Nadoushan Seyed Mohammad Bagher AkhaviRad,

Background and Objective: Wilms’ tumor has been recognized as the most common primary malignancy of kidney at childhood, comprises 5-6% of tumors in this period, and manifests itself with various clinical symptoms. Since there have been no sufficient studies in this field in Iran, therefore, this study w...

2013
Hassan Errihani

Wilms’ tumor (nephroblastoma) is a malignant renal tumor that arises from abnormal proliferation of metanephric blastema without differentiation into glomeruli and tubules. It is the most common malignant kidney tumor in children and accounts for 6% of all childhood malignancies. Nephroblastoma is a very rare tumor in the adult age group. Only 3% off all Wilms’ tumors are diagnosed in age over ...

Journal: :international journal of hematology-oncology and stem cell research 0
shahla ansari department of hematology-oncology, ali asghar children's hospital, school of medicine, iran university of medical sciences, tehran, iran. ghasem miri-aliabad fellow, pediatric hematology-oncology, ali asghar children's hospital, school of medicine, iran university of medical sciences, tehran, iran. naser rakhshani department of pathology, ali asghar children's hospital, school of medicine, iran university of medical sciences, tehran, iran.

wilms' tumor (wt) is the most common primary renal tumor in children. common sites of metastases are lungs, liver and regional lymph nodes. testicular and paratesticular metastasis due to wt have been reported but it is extremely rare. we report a 33-month -old male with bilateral wt and metastasis to right spermatic cord.

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