Results 41 to 50 of about 55,390 (242)
Integrative analysis identifies candidate tumor microenvironment and intracellular signaling pathways that define tumor heterogeneity in NF1 [PDF]
Neurofibromatosis type 1 (NF1) is a monogenic syndrome that gives rise to numerous symptoms including cognitive impairment, skeletal abnormalities, and growth of benign nerve sheath tumors.
Allaway, Robert J +11 more
core +2 more sources
Ameloblastoma is one of the most common benign odontogenic tumors of the jaw. It is generally categorized into: solid (multicystic), unicystic, and peripheral. Unicystic ameloblastoma is a single cystic cavity presenting ameloblastomatous differentiation
Kailash Chandra Dash +3 more
doaj +1 more source
Loss of the PTCH1 tumor suppressor defines a new subset of plexiform fibromyxoma. [PDF]
BackgroundPlexiform fibromyxoma (PF) is a rare gastric tumor often confused with gastrointestinal stromal tumor. These so-called "benign" tumors often present with upper GI bleeding and gastric outlet obstruction.
Banerjee, Sudeep +9 more
core +1 more source
Dendritic and axonal targeting patterns of a genetically-specified class of retinal ganglion cells that participate in image-forming circuits. [PDF]
BackgroundThere are numerous functional types of retinal ganglion cells (RGCs), each participating in circuits that encode a specific aspect of the visual scene.
Feldheim, David A +6 more
core +2 more sources
ABSTRACT Objectives Retrograde trans‐synaptic degeneration (rTSD) from posterior visual pathway lesions in multiple sclerosis (MS) is characterized by hemi‐macular ganglion cell‐inner plexiform layer (GCIPL) thinning and contralateral visual field loss.
Abdul Jaber Tayem +17 more
wiley +1 more source
Granular Cell Transformation in Plexiform Ameloblastoma: Case Report and Literature Review [PDF]
Ameloblastoma is the most common odontogenic tumor, primarily occurring in the posterior mandible. It is a slow-growing yet locally invasive epithelial tumor that generally follows a benign course.
Aravindan S +5 more
doaj +1 more source
A case report of a 4-year-old girl with neurofibromatosis type 1
Neurofibromatosis type 1 is a rare genetic disorder, which is a benign nerve tumor resulting from aberrant growth of the cells of nerve sheath. NF1 patients were associated with multisystem involvement, characterized by neurofibroma, of which 50% were ...
Mengying Peng, Yuqing Zhang, Qiong Zhou
doaj +1 more source
Gender dimorphism and age of onset in malignant peripheral nerve sheath tumor preclinical models and human patients. [PDF]
BackgroundGender-based differences in disease onset in murine models of malignant peripheral nerve sheath tumor (MPNST) and in patients with Neurofibromatosis type-1-(NF-1)-associated or spontaneous MPNST has not been well studied.MethodsForty-three ...
Dry, Sarah M +10 more
core +2 more sources
A zebrafish model carrying an identical human RHO S334X allele reveals two independent genetic layers shaping retinitis pigmentosa (RP) severity: a protective 3‐bp cis‐regulatory insertion that attenuates transgene expression, and a dominant trans‐acting modifier that restores a severe phenotype.
Cong Cui +9 more
wiley +1 more source
Prevalence of ameloblastoma: A three-year retrospective study
Context: This study intends to assess the data on the prevalence and types of ameloblastoma reported in the Outpatient Department retrospectively, so that the distribution of ameloblastomas among this geographic area can be reported.
Ramesh Tatapudi +3 more
doaj +1 more source

