نتایج جستجو برای: dmd

تعداد نتایج: 4377  

Journal: :Journal of Neuromuscular Diseases 2020

Journal: :Science-Business eXchange 2008

Journal: :Pharmacy Today 2017

Journal: :Photonics 2023

A digital micromirror device (DMD) has a wide range of applications in holographic display, light field manipulation, etc., due to its high-speed refresh rates. In order precisely control the wavefront, influence array structure DMD requires careful analysis. Based on an accurate three-dimensional phase model DMD, we analyzed diffraction characteristics DMD. The was established by accurately de...

Journal: :Journal of cell science 1987
J A Pizzey J A Witkowski G E Jones

Cultured skin fibroblasts from patients with Duchenne muscular dystrophy (DMD) are more sensitive than normal cells to prolonged exposure to the ionophore monensin. In a cell spreading assay in which cells were preincubated with monensin and subsequently allowed to adhere to and spread on a glass substratum in serum-free medium for 100 min, the mean transformed cell area of normal and DMD cells...

2015
C.I. Morse J. Smith A. Denny J. Tweedale N.D. Searle

OBJECTIVES To describe muscle size and architecture of the gastrocnemius medialis (GM) muscle in eleven adult males with Duchenne Muscular Dystrophy (DMD, age 24.5±5.4 years), and a control group of eleven males without DMD (CTRL, age 22.1±0.9 years). METHODS GM anatomical cross sectional area (ACSA), volume (VOL), physiological cross sectional area (PCSA), fascicle length (Lf) and pennation ...

Journal: :Current gene therapy 2012
Virginia Arechavala-Gomeza Karen Anthony Jennifer Morgan Francesco Muntoni

Duchenne muscular dystrophy (DMD) is the most common childhood neuromuscular disorder. It is caused by mutations in the DMD gene that disrupt the open reading frame (ORF) preventing the production of functional dystrophin protein. The loss of dystrophin ultimately leads to the degeneration of muscle fibres, progressive weakness and premature death. Antisense oligonucleotides (AOs) targeted to s...

Journal: :Archives of disease in childhood 1984
M E Pembrey K E Davies R M Winter R G Elles R Williamson T A Fazzone C Walker

Seventy families with Duchenne muscular dystrophy (DMD) known to the Institute of Child Health fall into three categories with respect to potential linkage analysis with the X chromosome DNA markers RC8 and L1.28 that bridge the DMD gene. Families in which there is at least one obligatory female heterozygote (n = 13). Here 'prediction' and 'exclusion' of DMD gene transmission may be possible, t...

2015
Joe W. McGreevy Chady H. Hakim Mark A. McIntosh Dongsheng Duan

Duchenne muscular dystrophy (DMD) is a progressive muscle-wasting disorder. It is caused by loss-of-function mutations in the dystrophin gene. Currently, there is no cure. A highly promising therapeutic strategy is to replace or repair the defective dystrophin gene by gene therapy. Numerous animal models of DMD have been developed over the last 30 years, ranging from invertebrate to large mamma...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید