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 Translation for 'retinoblastoma' from English to Russian
NOUN   retinoblastoma | retinoblastomas / retinoblastomata
мед.
ретинобластома {ж}
retinoblastoma <Rb>
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Translation for 'retinoblastoma' from English to Russian

retinoblastoma <Rb>
ретинобластома {ж}мед.
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Usage Examples English
  • In 1971, Knudson published the 2-hit hypothesis for mutation and cancer based on statistical analysis of inherited and sporadic cases of retinoblastoma.
  • FRK has been shown to interact with retinoblastoma protein.
  • PA2G4 has been shown to interact with ERBB3, retinoblastoma protein, and androgen receptor.
  • Hereditary retinoblastoma is related to mutations in the RB1 gene, which not only increase the probability of developing retinoblastoma to about 90%, but also increase the probabilities of developing other forms of cancer.
  • Knudson performed a statistical analysis on cases of retinoblastoma, a tumor of the retina that occurs both as an inherited disease and sporadically.

  • Robert Phillips and Andy Becker to set up a Retinoblastoma Group in Toronto.
  • Knudson for cases of retinoblastoma. Non-hereditary retinoblastoma involves two mutations, one on each allele.
  • She joined Great Ormond Street Hospital's haematology and oncology department in 2004, and continued seeing patients at the Royal London Hospital, where she directed the retinoblastoma unit.
  • Albert's research has focused on ocular tumors, particularly melanoma and retinoblastoma.
  • When Harbour joined Washington University in 1996, he undertook a three-year postdoctoral research training program in molecular oncology, which resulted in a first author publication in the journal "Cell" showing that the retinoblastoma protein is regulated by successive phosphorylation events.

  • The Dyson Lab studies the retinoblastoma protein.
  • He is best known for developing free software for smartphones that can detect eye cancer (retinoblastoma) and other eye disorders in children by searching the child's picture for "white eye" (leukocoria).
  • Human retinoblastoma is a well studied example of a cancer type where mitotic nondisjunction can contribute to malignant transformation: Mutations of the RB1 gene, which is located on chromosome 13 and encodes the tumor suppressor retinoblastoma protein, can be detected by cytogenetic analysis in many cases of retinoblastoma.
  • Almost half of children with retinoblastoma have a hereditary genetic defect associated with retinoblastoma.
  • Due to PFV’s close resemblance with retinoblastoma in particular, conclusively identifying PFV through advanced medical imaging is timely and crucial for an accurate diagnosis.

  • EBNA-3C can recruit a ubiquitin ligase and has been shown to target cell-cycle regulators such as retinoblastoma protein (pRb).
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Contains translations by TU Chemnitz and Mr Honey's Business Dictionary (German-English only).
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