Item talk:Q167215

From geokb
Revision as of 21:17, 12 September 2024 by Sky (talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

{

 "OpenAlex": {
   "cited_by_count": 1956195,
   "created_date": "2024-01-23",
   "description": "This cluster of papers focuses on the genetics, classification, treatment, and epidemiology of gliomas, particularly glioblastoma and medulloblastoma. It covers topics such as the molecular pathways, mutations (e.g., IDH), treatment strategies (e.g., temozolomide, radiotherapy), and the use of immunotherapy in neuro-oncology.",
   "display_name": "Gliomas",
   "domain": {
     "id": "https://openalex.org/domains/4",
     "display_name": "Health Sciences"
   },
   "field": {
     "id": "https://openalex.org/fields/27",
     "display_name": "Medicine"
   },
   "id": "https://openalex.org/T10129",
   "ids": {
     "openalex": "https://openalex.org/T10129",
     "wikipedia": "https://en.wikipedia.org/wiki/Glioma"
   },
   "keywords": [
     "Glioblastoma",
     "Temozolomide",
     "IDH Mutation",
     "Radiotherapy",
     "Molecular Classification",
     "MGMT Promoter Methylation",
     "Medulloblastoma",
     "Brain Tumor Epidemiology",
     "Immunotherapy",
     "Neuro-Oncology"
   ],
   "siblings": [
     {
       "id": "https://openalex.org/T13738",
       "display_name": "CHARGE Syndrome and Related Genetic Disorders"
     },
     {
       "id": "https://openalex.org/T12199",
       "display_name": "Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia"
     },
     {
       "id": "https://openalex.org/T12400",
       "display_name": "Gene Therapy for Spinal Muscular Atrophy"
     },
     {
       "id": "https://openalex.org/T10554",
       "display_name": "Genetic and Clinical Aspects of Hemoglobin Disorders"
     },
     {
       "id": "https://openalex.org/T11157",
       "display_name": "Genomic Aberrations and Treatment of Chronic Lymphocytic Leukemia"
     },
     {
       "id": "https://openalex.org/T11917",
       "display_name": "Hereditary Angioedema: Molecular Mechanisms and Clinical Management"
     },
     {
       "id": "https://openalex.org/T11628",
       "display_name": "Molecular Pathogenesis of Myeloproliferative Disorders"
     },
     {
       "id": "https://openalex.org/T10176",
       "display_name": "Multipotent Mesenchymal Stem Cells"
     }
   ],
   "subfield": {
     "id": "https://openalex.org/subfields/2716",
     "display_name": "Genetics"
   },
   "updated_date": "2024-08-19T06:02:54.686710",
   "works_count": 116478,
   "oa_id": "T10129"
 }

}