Sentences with phrase «of embryonal»

Epidermoid and dermoid cysts result from inclusion of epithelial components of embryonal tissue at the time of closure of the neural tube.
But the average age of embryonal rhabdomyosarcoma is 8.2 years.
It is possible that the Oct4 expression patterns that we observe is due to failure of one or more of these processes in the complex, abnormal milieu of this embryonal carcinoma cell line during differentiation.
DATE: April 2 TIME: 3:35 p.m. LOCATION: Room 144, Level 1, Washington Convention Center TITLE: Non-myogenic origin of embryonal rhabdomyosarcoma ABSTRACT: 1036
As Gurwitsch hypothesized: «The place of the embryonal formative process is a field, the boundaries of which, in general, do not coincide with those of the embryo but surpass them.»
About 60 percent of rhabdomyosarcoma patients have tumors of the embryonal subtype, and about 25 percent have the alveolar subtype.

Not exact matches

When researchers screened a library of more than 200 drugs and related compounds for activity against embryonal subtype tumor cells from three patients, the most promising results involved drugs that increased oxidative stress in tumor cells.
Abstract Neuroblastoma is an embryonal neoplasm arising from the peripheral nervous system that accounts for 15 % of cancer deaths in childhood.
Nearly 150 years ago, Julius Cohnheim first proposed the CSC hypothesis (also called the «embryonal - rest theory») that suggested the presence of embryonic - like cancerous cell remnants in adult tissues that can develop into cancer in a non-spontaneous way (1).
Research led by Mark Hatley, MD, PhD, of St. Jude Oncology, has shown that certain embryonal rhabdomyosarcoma tumors arise from early endothelial cells instead.
Pineal region tumors: This group of tumors includes germ cell tumors, germinomas, non-germinomatous germ cell tumors, embryonal cell tumor, yolk sac tumors, teratomas (immature vs. mature), pinealoblastomas, and pineocytomas.
Beckwith - Wiedemann syndrome (BWS) is a disorder of prenatal overgrowth and affected patients frequently have embryonal malignancies such as Wilms» tumor (WT).
In vivo imaging of tumor - propagating cells, regional tumor heterogeneity, and dynamic cell movements in embryonal rhabdomyosarcoma.
Manjila S, Ray A, Hu Y, Cai DX, Cohen ML, Cohen AR: Embryonal tumor with abundant neuropil and true rosettes (ETANTR): two illustrative cases and review of the literature.
In another case a 4 - month old dog was affected with embryonal rhabdomyosarcoma of the trachea.
They typically lie close to embryonal lines of closure.
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