نتایج جستجو برای: spinobulbar muscular atrophy

تعداد نتایج: 69863  

Journal: :international journal of pediatrics 0
farah ashrafzadeh professor of pediatric neurology ward, faculty of medicine, mashhad university of medical sciences, mashhad, iran. ariane sadr-nabavi assistant professor of human genetic, faculty of medicine, mashhad university of medical sciences, mashhad, iran. nazanin asadian students research committee, faculty of medicine, mashhad university of medical sciences, mashhad, iran. javad akhondian professor of pediatric neurology ward, faculty of medicine, mashhad university of medical sciences, mashhad, iran. mehran beiraghi toosi assistant professor of pediatric neurology ward, faculty of medicine, mashhad university of medical sciences, mashhad, iran.

spinal muscular atrophy (sma) is a genetic disorder which affect nervous system and is characterized with progressive distal motor neuron weakness. the survival motor neuron (smn) protein level reduces in patients with sma. two different genes code survival motor neuron protein in human genome. skeletal and intercostal muscles denervation lead to weakness, hypotony, hyporeflexia, respiratory fa...

Ariane Sadr-Nabavi Farah Ashrafzadeh, Javad Akhondian, Mehran Beiraghi Toosi, Nazanin Asadian

Spinal muscular atrophy (SMA) is a genetic disorder which affect nervous system and is characterized with progressive distal motor neuron weakness. The survival motor neuron (SMN) protein level reduces in patients with SMA. Two different genes code survival motor neuron protein in human genome. Skeletal and intercostal muscles denervation lead to weakness, hypotony, hyporeflexia, respiratory fa...

Journal: :The Journal of clinical investigation 2015
Jason P Chua Satya L Reddy Zhigang Yu Elisa Giorgetti Heather L Montie Sarmistha Mukherjee Jake Higgins Richard C McEachin Diane M Robins Diane E Merry Jorge A Iñiguez-Lluhí Andrew P Lieberman

Expansion of the polyglutamine (polyQ) tract within the androgen receptor (AR) causes neuromuscular degeneration in individuals with spinobulbar muscular atrophy (SBMA). PolyQ AR has diminished transcriptional function and exhibits ligand-dependent proteotoxicity, features that have both been implicated in SBMA; however, the extent to which altered AR transcriptional function contributes to pat...

Journal: :Journal of neurophysiology 2002
L B Wilson D Andrew A D Craig

Spinal lamina I neurons are selectively activated by small-diameter somatic afferents, and they project to brain stem sites that are critical for homeostatic control. Because small-diameter afferent activity evoked by contraction of skeletal muscle reflexly elicits exercise-related cardiorespiratory activation, we tested whether spinobulbar lamina I cells respond to muscle contraction. Spinobul...

Journal: :Human mutation 2004
Bruce Gottlieb Lenore K Beitel Jian Hui Wu Mark Trifiro

The current version of the androgen receptor (AR) gene mutations database is described. The total number of reported mutations has risen from 374 to 605, and the number of AR-interacting proteins described has increased from 23 to 70, both over the past 3 years. A 3D model of the AR ligand-binding domain (AR LBD) has been added to give a better understanding of gene structure-function relations...

Journal: :Human molecular genetics 2002
Natasha J Caplen J Paul Taylor Victoria S Statham Fumiaki Tanaka Andrew Fire Richard A Morgan

RNA interference (RNAi) is a mechanism that appears to control unwanted gene expression in a wide range of species. In Drosophila, RNAi is most effectively induced by double-stranded RNAs (dsRNAs) of over approximately 80 nucleotides (nt) and in mammalian cells an RNAi-like inhibition of gene expression has been shown to be mediated by dsRNAs of approximately 21-23 nt. To test if RNAi can be us...

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