نتایج جستجو برای: prph

تعداد نتایج: 157  

Journal: :Folia neuropathologica 2008
Angel Fernandez-Flores

BACKGROUND Cutaneous anaesthesia in necrobiosis lipoidica (NL) has been attributed to the destruction of nerve fibres by the inflammatory process. In the 1980s, one study demonstrated a decrease in S100 positive neural fibres as proof of this. Thermalgic information is mainly dependent on small fibres, either myelinated or unmyelinated, and S100 protein is expressed by Schwann cells. OBJECTIV...

Journal: :Brain research 2000
I Nir R Haque P M Iuvone

Dopamine metabolism was studied in dystrophic retinal degeneration slow (rds) mice which carry a mutation in the rds/peripherin gene. RDS mutations in humans cause several forms of retinal degeneration. Dopamine synthesis and utilization were analyzed at various time points in the diurnal cycle in homozygous rds/rds retinas which lack photoreceptor outer segments and heterozygous rds/+ retinas ...

Journal: :Molecular biology of the cell 2003
Brian T Helfand Melissa G Mendez Jason Pugh Claude Delsert Robert D Goldman

To date, the functions of most neural intermediate filament (IF) proteins have remained elusive. Peripherin is a type III intermediate filament (IF) protein that is expressed in developing and in differentiated neurons of the peripheral and enteric nervous systems. It is also the major IF protein expressed in PC12 cells, a widely used model for studies of peripheral neurons. Dramatic increases ...

Journal: :The Journal of Cell Biology 1991
P D Kouklis T Papamarcaki A Merdes S D Georgatos

To identify sites of self-association in type III intermediate filament (IF) proteins, we have taken an "anti-idiotypic antibody" approach. A mAb (anti-Ct), recognizing a similar feature near the end of the rod domain of vimentin, desmin, and peripherin (epsilon site or epsilon epitope), was characterized. Anti-idiotypic antibodies, generated by immunizing rabbits with purified anti-Ct, recogni...

2014
Haner Daher Abdel Belaïd Vincent Poulain D'Andecy

RÉSUMÉ. Cet article propose une approche de segmentation supervisée de flux de documents. L'approche traite le flux de documents comme une suite de paires de pages et étudie la relation qui existe entre elles pour déceler une continuité de documents ou une rupture. Dans un premier temps, des descripteurs sont extraits des pages et une approche est proposée pour fusionner ces descripteurs en un ...

2018
Teppei Noda Steven J. Meas Jumpei Nogami Yutaka Amemiya Ryutaro Uchi Yasuyuki Ohkawa Koji Nishimura Alain Dabdoub

Primary auditory neurons (PANs) play a critical role in hearing by transmitting sound information from the inner ear to the brain. Their progressive degeneration is associated with excessive noise, disease and aging. The loss of PANs leads to permanent hearing impairment since they are incapable of regenerating. Spiral ganglion non-neuronal cells (SGNNCs), comprised mainly of glia, are resident...

2012
Christin Klenke Sebastian Janowski Daniela Borck Darius Widera Jörg Ebmeyer Jörn Kalinowski Anke Leichtle Ralf Hofestädt Tahwinder Upile Christian Kaltschmidt Barbara Kaltschmidt Holger Sudhoff

BACKGROUND Cholesteatoma is a gradually expanding destructive epithelial lesion within the middle ear. It can cause extensive local tissue destruction in the temporal bone and can initially lead to the development of conductive hearing loss via ossicular erosion. As the disease progresses, sensorineural hearing loss, vertigo or facial palsy may occur. Cholesteatoma may promote the spread of inf...

Journal: :Vision Research 2002
B. Chang N. L. Hawes R. E. Hurd M. T. Davisson S. Nusinowitz J. R. Heckenlively

The Jackson Laboratory, having the world's largest collection of mouse mutant stocks and genetically diverse inbred strains, is an ideal place to look for genetically determined eye variations and disorders. Through ophthalmoscopy, electroretinography and histology, we have discovered disorders affecting all aspects of the eye including the lid, cornea, iris, lens and retina, resulting in corne...

Journal: :Genome research 2017
Michael J Keogh Wei Wei Ian Wilson Jon Coxhead Sarah Ryan Sara Rollinson Helen Griffin Marzena Kurzawa-Akanbi Mauro Santibanez-Koref Kevin Talbot Martin R Turner Chris-Anne McKenzie Claire Troakes Johannes Attems Colin Smith Safa Al Sarraj Chris M Morris Olaf Ansorge Stuart Pickering-Brown James W Ironside Patrick F Chinnery

Given the central role of genetic factors in the pathogenesis of common neurodegenerative disorders, it is critical that mechanistic studies in human tissue are interpreted in a genetically enlightened context. To address this, we performed exome sequencing and copy number variant analysis on 1511 frozen human brains with a diagnosis of Alzheimer's disease (AD, n = 289), frontotemporal dementia...

Journal: :The British journal of ophthalmology 2005
P J Francis D W Schultz A M Gregory M B Schain R Barra J Majewski J Ott T Acott R G Weleber M L Klein

BACKGROUND The pattern dystrophies (PD) represent a clinically heterogeneous family of inherited macular diseases frequently caused by mutations in the peripherin/RDS gene. Most previous studies have detailed the clinical findings in single families, making it difficult to derive data from which progression and visual outcome can be generalised. METHODS Families were ascertained and clinicall...

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