نتایج جستجو برای: atrophy

تعداد نتایج: 36500  

Journal: :Journal of applied physiology 2010
Robert D Hyldahl Kevin S O'Fallon Lawrence M Schwartz Priscilla M Clarkson

Skeletal muscle atrophy is a significant health problem that results in decreased muscle size and function and has been associated with increases in oxidative stress. The molecular mechanisms that regulate muscle atrophy, however, are largely unknown. The metallothioneins (MT), a family of genes with antioxidant properties, have been found to be consistently upregulated during muscle atrophy, a...

Journal: :American journal of physiology. Endocrinology and metabolism 2014
Daniel K Fox Scott M Ebert Kale S Bongers Michael C Dyle Steven A Bullard Jason M Dierdorff Steven D Kunkel Christopher M Adams

Immobilization causes skeletal muscle atrophy via complex signaling pathways that are not well understood. To better understand these pathways, we investigated the roles of p53 and ATF4, two transcription factors that mediate adaptations to a variety of cellular stresses. Using mouse models, we demonstrate that 3 days of muscle immobilization induces muscle atrophy and increases expression of p...

Golfeshan Atefe Namazi Nastaran Saghi Bita

Gyrate atrophy (GA) is a rare, progressive metabolic choroid and retinal degeneration that results from a deficiency of the pyridoxal phosphate-dependent mitochondrial matrix enzyme ornithine aminotransferase. Here, we report the case of a 40-yearold woman who presented with a gradual decline in visual acuity since puberty, along with a history of high myopia and cataract surgery. She was admit...

Journal: :Archives of Iranian medicine 2007
Iman Salahshourifar Yousef Shafeghati Zahra Golkar Hossein Najmabadi

BACKGROUND Spinal muscular atrophy is an autosomal recessive disorder characterized by degeneration of anterior horn cells in the spinal cord leading to progressive muscular weakness and atrophy. The spinal muscular atrophy candidate interval genes including survival motor neuron, the responsible gene in spinal muscular atrophy phenotype expression, neuronal apoptosis inhibitory protein, and P4...

Journal: :Brain : a journal of neurology 2012
Emily C Oates Stephen Reddel Michael L Rodriguez Luke C Gandolfo Melanie Bahlo Simon H Hawke Shireen R Lamandé Nigel F Clarke Kathryn N North

Autosomal dominant congenital spinal muscular atrophy is characterized by predominantly lower limb weakness and wasting, and congenital or early-onset contractures of the hip, knee and ankle. Mutations in TRPV4, encoding a cation channel, have recently been identified in one large dominant congenital spinal muscular atrophy kindred, but the genetic basis of dominant congenital spinal muscular a...

Journal: :Neurorehabilitation and neural repair 2011
Christoph Globas Judith M Lam Weihong Zhang Anuar Imanbayev Benjamin Hertler Clemens Becker Jill Whitall Sandy McCombe-Waller Susumu Mori Daniel F Hanley Andreas R Luft

OBJECTIVE Stroke survivors with motor deficits often have pyramidal tract atrophy caused by degeneration of corticospinal fibers. The authors hypothesized that the degree of atrophy correlates with severity of motor impairment in patients with chronic stroke and predicts the response to rehabilitation training. METHODS They performed a post hoc analysis of 42 hemiparetic patients (>6 months) ...

Journal: :The American journal of surgical pathology 2006
Angelo M De Marzo Elizabeth A Platz Jonathan I Epstein Tehmina Ali Anthanase Billis Teresa Y Chan Liang Cheng Milton Datta Lars Egevad Dilek Ertoy-Baydar Xavier Farre Samson W Fine Kenneth A Iczkowski Michael Ittmann Beatrice S Knudsen Massimo Loda Antonio Lopez-Beltran Cristina Magi-Galluzzi Gregor Mikuz Roldolfo Montironi Eli Pikarsky Galina Pizov Mark A Rubin Hema Samaratunga Thomas Sebo Isabel A Sesterhenn Rajal B Shah Sabina Signoretti Jeffery Simko George Thomas Patricia Troncoso Toyonori T Tsuzuki Geert J van Leenders Ximing J Yang Ming Zhou William D Figg Ashraful Hoque M S Lucia

Focal atrophy is extremely common in prostate specimens. Although there are distinct histologic variants, the terminology is currently nonstandardized and no formal classification has been tested for interobserver reliability. This lack of standardization hampers the ability to study the biologic and clinical significance of these lesions. After informal and formal meetings by a number of the a...

Journal: :Pakistan Journal of Medical and Health Sciences 2023

Parry Romberg syndrome (PRS), also referred to as progressive hemifacial atrophy, facial hemiatrophy, or idiopathic was first described by C and M Romberg.1 It manifests in the two decades morphologically normal-born individuals. commonly affects one more dermatomes trigeminal nerve territory. has an early onset of ophthalmic neurological involvement a variable maxillo-facial cardiac involvemen...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید