Results 241 to 250 of about 131,495 (261)
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Carbon nanofiber-based multiplexed immunosensor for the detection of survival motor neuron 1, cystic fibrosis transmembrane conductance regulator and Duchenne Muscular Dystrophy proteins

Biosensors and Bioelectronics, 2018
Simultaneous and point-of-care detection of multiple protein biomarkers has significant impact on patient care. Spinal Muscular Atrophy (SMA), Cystic Fibrosis (CF) and Duchenne Muscular Dystrophy (DMD) are well known progressive hereditary disorders associated with increased morbidity as well as mortality.
Shimaa, Eissa   +7 more
openaire   +2 more sources

Molecular docking and dynamics simulation studies to identify the phytochemicals as lead molecules against the survival motor neuron 1 (SMN1) protein of spinal muscular atrophy

Medicinal Plants - International Journal of Phytomedicines and Related Industries
AbstractSpinal Muscular Atrophy is an autosomal recessive neuromuscular disorder resulting from deletions or mutations in the survival motor neuron (SMN1) gene. Loss of lower motor neurons (anterior horn cells) in the brainstem and spinal cord nuclei is a characteristic of SMA, which causes gradual symmetrical muscular weakening and atrophy. Currently,
Pankaj Bagga   +3 more
openaire   +1 more source

Health insurance status and cancer stage at diagnosis and survival in the United States

Ca-A Cancer Journal for Clinicians, 2022
Jingxuan Zhao   +2 more
exaly  

A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein

Cell Reports, 2021
Nikki M Mccormack   +2 more
exaly  

Progression and survival of patients with motor neuron disease relative to their fecal microbiota

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2020
Shyuan T Ngo   +2 more
exaly  

Neurotrophins promote motor neuron survival and are present in embryonic limb bud

Nature, 1993
William Camu   +2 more
exaly  

The frontotemporal dementia-motor neuron disease continuum

Lancet, The, 2016
Glenda Halliday   +2 more
exaly  

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