Results 61 to 70 of about 3,144 (260)

BCL2, IRS1, AKT3, PTEN, and HIF1A expression levels in non‐small cell lung cancer patients

open access: yesMalignancy Spectrum, Volume 2, Issue 1, Page 37-45, March 2025.
Restoration of miR‐15/16, miR‐126, and miR‐128 in NSCLC might be therapeutic candidates to control cell proliferation and apoptosis. Abstract Background Lung cancer is the leading cause of cancer‐related deaths worldwide. MicroRNAs (miRNAs) are small noncoding molecules that play critical roles in cell proliferation, apoptosis, invasion, and metastasis,
Mahdi Mohammadi   +4 more
wiley   +1 more source

ارزیابی تراکم عروق خونی در کیست فولیکولار، تومورادنتوژنیک کراتوسیست و آملوبلاستوما [PDF]

open access: yesJournal of Mashhad Dental School, 2011
Introduction: Ameloblastoma is a benign epithelial odontogenic tumor that exhibits a more aggressive behavior than follicular cyst and keratocystic odontogenic tumor.
صفورا سیفی   +2 more
doaj  

Keratocystic odontogenic tumor overexpresses invadopodia-related proteins, suggesting invadopodia formation [PDF]

open access: yes, 2016
OBJECTIVE: Keratocystic odontogenic tumor (KOT) is an odontogenic neoplasm that shows aggressive clinical behavior and local invasiveness. Invadopodia are actin-rich cellular protrusions exhibiting proteolytic pericellular activity, thereby inducing ...
Brasil da Silva, W   +8 more
core   +1 more source

Rapidly Expanding Odontogenic Myxoma: An Entity With Diagnostic Challenges—A Case Report

open access: yesCase Reports in Dentistry, Volume 2025, Issue 1, 2025.
Odontogenic myxoma is a rare benign odontogenic tumor having locally aggressive behavior. It frequently affects the females in the second or third decade of life and commonly occurs in the mandibular posterior region as a slow‐growing lesion. The aggressive behavior is often seen in maxillary lesions.
Suwarna Dangore-Khasbage   +5 more
wiley   +1 more source

Unusual presentation of keratocystic odontogenic tumor: Two case reports

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2016
Keratocystic odontogenic tumor (KOT) is a common odontogenic cyst with aggressive behavior with a high recurrence rate. Features that predict recurrence of KOT are thin friable epithelium which is difficult to enucleate and presence of satellite cysts in
Sunitha Kesidi   +3 more
doaj   +1 more source

NCAM (CD56) Expression in keratin-producing odontogenic cysts: aberrant expression in KCOT [PDF]

open access: yes, 2015
Background: Keratin-producing odontogenic cysts (KPOCs) are a group of cystic lesions that are often aggressive, with high rates of recurrence and multifocality.
B Vera-Sirera   +36 more
core   +2 more sources

Radicular (periapical) cyst causing exophthalmos in a dog

open access: yesVeterinary Record Case Reports, Volume 12, Issue 4, December 2024.
Abstract A 10‐year‐old male neutered Bichon Frise presented for assessment of right unilateral exophthalmos. The ophthalmological assessment revealed signs of retrobulbar disease. Computed tomography of the head showed a cavitary, well‐defined, fluid‐filled structure, which displayed a strong peripheral rim of contrast enhancement, and was centred ...
Luis Alejandro Pérez López   +4 more
wiley   +1 more source

Multiple keratocystic odontogenic tumors in a non-syndromic minor patient: Report of an unusual case

open access: yesJournal of Orofacial Sciences, 2013
Keratocystic odontogenic tumor (KCOT) is developmental odontogenic cysts of epithelial origin known for their potentially aggressive behavior and significant rate of recurrences.
Shalu Rai   +4 more
doaj   +1 more source

Trans-nasal endoscopic and intra-oral combined approach for odontogenic cysts [PDF]

open access: yes, 2018
Maxillary cysts are a common finding in maxillofacial surgery, dentistry and otolaryngology. Treatment is surgical; a traditional approach includes Caldwell-Luc and other intra-oral approaches.
Albanese, M.   +7 more
core   +1 more source

Germline PTCH1: c.361_362insAlu alteration identified by comprehensive exome and RNA sequencing in a patient with Gorlin syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 194, Issue 10, October 2024.
Abstract Gorlin syndrome can be caused by pathogenic/likely pathogenic (P/LP) variants in the tumor suppressor gene PTCH1 (9q22.1‐q31), which encodes the receptor for the sonic hedgehog (SHH) ligand. We present a 12‐month‐old boy clinically diagnosed with Gorlin syndrome who was found to have significantly delayed development, palmar pitting, palmar ...
Aaron Y. Mochizuki   +4 more
wiley   +1 more source

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