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retinoblastoma Meaning in Bengali



রেটিনার কোষ ম্যালিগন্যান্ট চাক্ষুষ টিউমার; সাধারণত জীবনের তৃতীয় বছর আগে ঘটে; আদিম ছোট বৃত্তাকার রেটিনার কোষ দ্বারা গঠিত

Noun:

রেটিনোব্ল্যাস্টোমা,





retinoblastoma's Usage Examples:

The retinoblastoma protein (protein name abbreviated pRb; gene name abbreviated Rb, RB or RB1) is a tumor suppressor protein that is dysfunctional in several.


or bilateral retinoblastoma.


When retinoblastoma patients present with pinealoblastoma this is characterized as "trilateral retinoblastoma".


several other proteins, to retinoblastoma protein which regulates cell proliferation.


Examples are nephroblastoma, medulloblastoma, and retinoblastoma.


the retinoblastoma tumor suppressor protein.


Alfred Knudson, a pediatrician and cancer geneticist, proposed that in order to develop retinoblastoma, two.


It binds directly, with several other proteins, to retinoblastoma protein (pRB) which regulates cell proliferation.


present in retina is retinoblastoma.


Retinoblastoma is a rare cancer of the retina, caused by the mutation of both copies of retinoblastoma genes (RB1).


proliferation through it close interaction with retinoblastoma protein (Rb), a master cell cycle regulator.


cases of retinoblastoma, a tumor of the retina that occurs both as an inherited disease and sporadically.


He noted that inherited retinoblastoma occurs.


ubiquitin ligase and has been shown to target cell-cycle regulators such as retinoblastoma protein (pRb).


known for pioneering the use of chemotherapy in the treatment of the retinoblastoma form of cancer.


cancer During this transition, G1 cyclin D-Cdk4/6 dimer phosphorylates retinoblastoma releasing transcription factor E2F, which then drives the transition.


This gene aligns with an internal intron of the retinoblastoma susceptibility gene in the reverse orientation.


Trilateral retinoblastoma is a malignant midline primitive neuroectodermal tumor occurring in patients with inherited uni- or bilateral retinoblastoma.



retinoblastoma's Meaning':

malignant ocular tumor of retinal cells; usually occurs before the third year of life; composed of primitive small round retinal cells

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