Results 51 to 60 of about 55,390 (242)

Identification of a synaptic vesicle-specific membrane protein with a wide distribution in neuronal and neurosecretory tissue. [PDF]

open access: yes, 1981
Two different monoclonal antibodies, characterized initially as binding synaptic terminal regions of rat brain, bind a 65,000-dalton protein, which is exposed on the outer surface of brain synaptic vesicles. Immunocytochemical experiments at the electron
Matthew, WD, Reichardt, LF, Tsavaler, L
core   +2 more sources

GHRHR Deficiency Enhances Retinal Ganglion Cell Survival and Visual Functions in Experimental Glaucoma by Inhibiting Ferroptosis

open access: yesAdvanced Science, EarlyView.
Glaucoma, a major cause of blindness, involves retinal ganglion cell (RGC) degeneration. This study shows growth hormone‐releasing hormone receptor (GHRHR) deficiency preserves RGC survival and restores vision, unlike activation which only aids survival.
Yan Tong   +24 more
wiley   +1 more source

Isolated plexiform neurofibroma over left palm: A case report and review of literature

open access: yesIndian Journal of Dermatology, 2013
Plexiform neurofibroma is common over the branches of trigeminal and cervical nerves over the face. Plexiform neurofibroma over palm is rare and affects the individuals with fine motor functions of hand.
Mohan H Kudur, Manjunath Hulmani
doaj   +1 more source

Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography. [PDF]

open access: yes, 2020
Changes in retinal vasculature and ocular circulation may play an important role in the glaucoma development and progression. We evaluated the vertical asymmetry across the temporal raphe of the deep retinal layer vessel density, using swept-source ...
Araie, Makoto   +6 more
core  

Long-term rearrangement of retinal structures in a novel mutation of X-linked retinoschisis [PDF]

open access: yes, 2017
The aim of the present study was to report a novel mutation in the retinoschisin 1 (RS1) gene in a Caucasian family affected by X-linked juvenile retinoschisis (XLRS) and to describe the long-term modification of retinal structure.
Colavito, Davide   +7 more
core   +1 more source

Composition‐Aware Cross‐Sectional Integration for Spatial Transcriptomics

open access: yesAdvanced Intelligent Discovery, EarlyView.
Multi‐section spatial transcriptomics demands coherent cell‐type deconvolution, domain detection, and batch correction, yet existing pipelines treat these tasks separately. FUSION unifies them within a composition‐aware latent framework, modeling reads as cell‐type–specific topics and clustering in embedding space.
Qishi Dong   +5 more
wiley   +1 more source

Arteriovenous malformation underlying a plexiform neurofibroma: An unusual presentation

open access: yesIndian Dermatology Online Journal, 2017
Vascular abnormalities associated with neurofibromatosis type 1 are well described in the literature, however, arteriovenous malformation is a very rare finding in neurofibromatosis type 1.
Zaheer Abbas, Sepideh Khani, Javad Zare
doaj   +1 more source

Immunohistochemical detection of nerve growth factor (NGF) in follicular and plexiform ameloblastoma – A novel study

open access: yesJournal of Pharmacy and Bioallied Sciences, 2020
Background: Ameloblastoma is the second most common odontogenic tumor that holds a unique position among benign tumors due to its locally destructive and invasive nature.
Thuckanickenpalayam Ragunathan Yoithapprabhunath   +5 more
doaj   +1 more source

Plexiform fibrohistiocytic tumor

open access: yesIndian Journal of Pathology and Microbiology, 2008
Plexiform fibrohistiocytic tumor is an uncommon mesenchymal tumor that can cause difficulty in diagnosis and surgical management. On clinical and histologic examination, these tumors can potentially be misdiagnosed as sebaceous/epidermal cysts. We report a case of plexiform fibrohistiocytic tumor in a young female, which on initial clinical evaluation ...
Thirumala Seshadri   +2 more
openaire   +3 more sources

Genetically engineered minipigs model the major clinical features of human neurofibromatosis type 1. [PDF]

open access: yes, 2018
Neurofibromatosis Type 1 (NF1) is a genetic disease caused by mutations in Neurofibromin 1 (NF1). NF1 patients present with a variety of clinical manifestations and are predisposed to cancer development.
Carlson, Daniel F   +21 more
core   +2 more sources

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