Results 41 to 50 of about 1,717 (223)
Immunohistochemical analysis of P53 protein in odontogenic cysts
Saudi Dental Journal, 2010 The p53 is a well-known tumor suppressor gene, the mutations of which are closely related to the decreased differentiation of cells. Findings of studies on immunohistochemical P53 expression in odontogenic cysts are controversial.
Essam Taher M.A. Gaballah +1 more
doaj +1 more source
Clinical Oral Implants Research, Volume 36, Issue 9, Page 1035-1052, September 2025.ABSTRACT Objectives This study aimed to investigate implant outcomes in patients with head and neck cancer undergoing radiotherapy or chemotherapy by incorporating the latest research findings. Methods The present review was conducted to update the focused question: What is the survival rate of implants placed in patients with head and neck cancer ...
Shengchi Fan +5 more
wiley +1 more source
Multiple keratocysts of the mandible in association with Gorlin-Goltz syndrome: A rare case report
Contemporary Clinical Dentistry, 2014 Nevoid basal cell carcinoma syndrome is a syndrome with wide variety of manifestations ranging from oral lesions to skeletal deformities. It calls for due responsibility of maxillofacial surgeon to diagnose the syndrome because very often they are the ...
Gayithri Harish Kulkarni +4 more
doaj +1 more source
BCL2, IRS1, AKT3, PTEN, and HIF1A expression levels in non‐small cell lung cancer patients
Malignancy 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]
Journal 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
Rapidly Expanding Odontogenic Myxoma: An Entity With Diagnostic Challenges—A Case Report
Case 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
Journal 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
Radicular (periapical) cyst causing exophthalmos in a dog
Veterinary 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
Journal 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
American 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