Identification of novel genes involved in spinal muscular atrophy using high density microarrays

Identification of novel genes involved in spinal muscular atrophy using high density microarrays

Manylion Llyfryddiaeth
Prif Awduron:	Anderson, K, Potter, A, Ponting, C, Davies, K
Fformat:	Conference item
Cyhoeddwyd:	2002

Eitemau Tebyg

Spinal muscular atrophy.
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Cyhoeddwyd: (2001)

Protein expression changes in spinal muscular atrophy revealed with a novel antibody array technology.
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Cyhoeddwyd: (2003)

Chapter 16 Spinal Muscular Atrophy
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Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit.
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Spinal muscular atrophy at the crossroads of basic science and therapy.
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Spinal muscular atrophy at the crossroads of basic science and therapy
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Spinal Muscular Atrophy
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Spinal muscular atrophy
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Modelling of spinal muscular atrophy in D-melanogaster and C-elegans
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Chapter 7 Spinal muscular atrophies and hereditary motor neuropathies.
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Spinal Muscular Atrophy and Arthrogryposis
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Rehabilitation in spinal muscular atrophy
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Rehabilitation in spinal muscular atrophy
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Gene therapy for spinal muscular atrophy: timing is key
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MOLECULAR ANALYSIS OF CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY
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Development and Translation of Therapies for Spinal Muscular Atrophy
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Splice-switching therapy for spinal muscular atrophy.
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Spinal Muscular Atrophy Diagnosed by Newborn Screening
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Recent developments in the treatment of Duchenne muscular dystrophy and spinal muscular atrophy
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Spinal muscular atrophies reveal motor neuron vulnerability to defects in ribonucleoprotein handling.
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Modeling spinal muscular atrophy in Drosophila.
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Reviews of spinal muscular atrophy in Taiwan
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Genetics of Juvenile Spinal Muscular Atrophy
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Euglycemic Ketoacidosis in Spinal Muscular Atrophy
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Spinal Muscular Atrophy With Myoclonic Epilepsy
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Editorial: Advances in spinal muscular atrophy
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Advances in spinal muscular atrophy therapeutics
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The Neurobiology of Childhood Spinal Muscular Atrophy
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Modeling spinal muscular atrophy in Drosophila.
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Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype
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Commentary: Current Status of Gene Therapy for Spinal Muscular Atrophy
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Spinal muscular atrophy: disease mechanisms and therapeutic approaches
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Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders.
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Nusinersen and spinal muscular atrophies: Where are we in 2020?
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Analysis of the survival of motor neuron (SMN1) gene mutations in Spinal Muscular Atrophy through models
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Therapeutic strategies for spinal muscular atrophy: SMN and beyond
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Therapeutic strategies for spinal muscular atrophy: SMN and beyond
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High-throughput screening reveals novel mutations in spinal muscular atrophy patients
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Newborn Screening for Spinal Muscular Atrophy: Variations in Practice and Early Management of Infants with Spinal Muscular Atrophy in the United States
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Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy
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