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OpenAlex topic

Renal and related cancers

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 2,621 works 19 author topics

Works

2,621 works

  1. Pten dependence distinguishes haematopoietic stem cells from leukaemia-initiating cells 2006
    OpenAlex top 1% OpenAlex 100.0%

    No abstract yet.

  2. The International Society of Urological Pathology ISUP Vancouver Classification of Renal Neoplasia 2013
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 100.0%

    The classification working group of the International Society of Urological Pathology consensus conference on renal neoplasia was in charge of making recommendations regarding additions and changes to the current World Health Organization Classification of Renal Tumors (2004). Members of the group performed an exhaust…

  3. The International Society of Urological Pathology ISUP Grading System for Renal Cell Carcinoma and Other Prognostic Parameters 2013
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.8%

    The International Society of Urological Pathology 2012 Consensus Conference made recommendations regarding classification, prognostic factors, staging, and immunohistochemical and molecular assessment of adult renal tumors. Issues relating to prognostic factors were coordinated by a workgroup who identified tumor morp…

  4. Whole-exome sequencing of neoplastic cysts of the pancreas reveals recurrent mutations in components of ubiquitin-dependent pathways 2011
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.7%

    More than 2% of adults harbor a pancreatic cyst, a subset of which progresses to invasive lesions with lethal consequences. To assess the genomic landscapes of neoplastic cysts of the pancreas, we determined the exomic sequences of DNA from the neoplastic epithelium of eight surgically resected cysts of each of the ma…

  5. Nephrotic Syndrome in the First Year of Life Two Thirds of Cases Are Caused by Mutations in 4 Genes NPHS1 NPHS2 WT1 and LAMB2 2007
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.2%

    OBJECTIVES: Mutations in each of the NPHS1, NPHS2, WT1, and LAMB2 genes have been implicated in nephrotic syndrome, manifesting in the first year of life. The relative frequency of causative mutations in these genes in children with nephrotic syndrome manifesting in the first year of life is unknown. Therefore, we ana…

  6. TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum 2011
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.7%

    No abstract yet.

  7. Building consensus on definition and nomenclature of hepatic, pancreatic, and biliary organoids 2021
    OpenAlex top 1% OpenAlex 99.8%

    No abstract yet.

  8. Multipotent mesenchymal stem cells reduce interstitial fibrosis but do not delay progression of chronic kidney disease in collagen4A3-deficient mice 2006
    OpenAlex top 10% OpenAlex 97.8%

    No abstract yet.

  9. Mixed Epithelial and Stromal Tumor of the Kidney 2000
    YÖKSİS SJR Q1 JCR Q1 OpenAlex 84.9%

    We describe the clinicopathologic features of 12 patients with a distinctive tumor of the kidney characterized by a mixture of epithelial and stromal elements that form solid and cystic growth patterns. Similar tumors were reported previously in the literature under various names, including adult mesoblastic nephroma.…

  10. Understanding follicle growth in vivo 2010
    OpenAlex top 1% OpenAlex 99.0%

    Ovarian reserve is determined by the number of primordial follicles in the ovary. Quiescent primordial follicles are activated for growth and pass through stages of development before they reach the antral stage. Then a cohort of antral follicles is recruited for further growth, dominance and ovulation under the cycli…

  11. Conformal Radiation Therapy for Pediatric Ependymoma, Chemotherapy for Incompletely Resected Ependymoma, and Observation for Completely Resected, Supratentorial Ependymoma 2019
    OpenAlex top 1% OpenAlex 99.3%

    PURPOSE The Children’s Oncology Group trial ACNS0121 estimated event-free survival (EFS) and overall survival for children with intracranial ependymoma treated with surgery, radiation therapy, and—selectively—with chemotherapy. Treatment was administered according to tumor location, histologic grade, and extent of res…

  12. Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease 2010
    YÖKSİS OpenAlex top 10% OpenAlex 95.8%

    The histiocytoses are a heterogeneous group of disorders characterised by an excessive number of histiocytes. In most cases the pathophysiology is unclear and treatment is nonspecific. Faisalabad histiocytosis (FHC) (MIM 602782) has been classed as an autosomal recessively inherited form of histiocytosis with similari…

Academicians

19 academicians