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ElMallah, Mai
One or more keywords matched the following items that are connected to ElMallah, Mai
Item TypeName
Concept Mice, Inbred mdx
Concept Mice, Knockout
Concept Mice
Concept Mice, Inbred C57BL
Concept Mice, Transgenic
Concept Mice, Mutant Strains
Academic Article Hypoglossal neuropathology and respiratory activity in pompe mice.
Academic Article Retrograde gene delivery to hypoglossal motoneurons using adeno-associated virus serotype 9.
Academic Article Intrapleural administration of AAV9 improves neural and cardiorespiratory function in Pompe disease.
Academic Article Sustained correction of motoneuron histopathology following intramuscular delivery of AAV in pompe mice.
Academic Article Peripheral nerve and neuromuscular junction pathology in Pompe disease.
Academic Article Stimulation of Respiratory Motor Output and Ventilation in a Murine Model of Pompe Disease by Ampakines.
Academic Article Therapeutic rAAVrh10 Mediated SOD1 Silencing in Adult SOD1(G93A) Mice and Nonhuman Primates.
Academic Article Power spectral analysis of hypoglossal nerve activity during intermittent hypoxia-induced long-term facilitation in mice.
Academic Article Adeno-associated virus-delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model.
Academic Article Neuropathology in respiratory-related motoneurons in young Pompe (Gaa(-/-)) mice.
Academic Article Restrictive Lung Disease in the Cu/Zn Superoxide-Dismutase 1 G93A Amyotrophic Lateral Sclerosis Mouse Model.
Academic Article Airway smooth muscle dysfunction in Pompe (Gaa-/- ) mice.
Academic Article Systemic Delivery of AAVB1-GAA Clears Glycogen and Prolongs Survival in a Mouse Model of Pompe Disease.
Academic Article Editing out five Serpina1 paralogs to create a mouse model of genetic emphysema.
Academic Article AAV9 gene replacement therapy for respiratory insufficiency in very-long chain acyl-CoA dehydrogenase deficiency.
Academic Article Comparisons of Infant and Adult Mice Reveal Age Effects for Liver Depot Gene Therapy in Pompe Disease.
Academic Article Intralingual and Intrapleural AAV Gene Therapy Prolongs Survival in a SOD1 ALS Mouse Model.
Academic Article The Respiratory Phenotype of Pompe Disease Mouse Models.
Academic Article Intralingual Administration of AAVrh10-miRSOD1 Improves Respiratory But Not Swallowing Function in a Superoxide Dismutase-1 Mouse Model of Amyotrophic Lateral Sclerosis.
Academic Article Motor axonopathies in a mouse model of Duchenne muscular dystrophy.
Academic Article Respiratory pathology in the Optn-/- mouse model of Amyotrophic Lateral Sclerosis.
Academic Article Corrigendum to "Respiratory pathology in the optn-/- mouse model of amyotrophic lateral sclerosis" [Respir. Physiol. Neurobiol. 282 (2020) 103525].
Academic Article Genetic deletion of the Tas2r143/Tas2r135/Tas2r126 cluster reveals that TAS2Rs may not mediate bitter tastant-induced bronchodilation.
Academic Article Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3Mashl/+, Mouse Model of Alternating Hemiplegia of Childhood.
Academic Article Glycogen accumulation in smooth muscle of a Pompe disease mouse model.
Academic Article Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7.
Concept Mice, 129 Strain
Academic Article What's new and what's next for gene therapy in Pompe disease?
Academic Article Cross-species evolution of a highly potent AAV variant for therapeutic gene transfer and genome editing.
Academic Article X-linked SBMA model mice display relevant non-neurological phenotypes and their expression of mutant androgen receptor protein in motor neurons is not required for neuromuscular disease.
Academic Article Respiratory characterization of a humanized Duchenne muscular dystrophy mouse model.
Academic Article Respiratory neuropathology in spinocerebellar ataxia type 7.
Academic Article Respiratory pathology in the TDP-43 transgenic mouse model of amyotrophic lateral sclerosis.
Academic Article Progressive central cardiorespiratory rate downregulation and intensifying epilepsy lead to sudden unexpected death in epilepsy in mouse model of the most common human ATP1A3 mutation.
Academic Article Respiratory pathology in the mdx/utrn -/- mouse: A murine model for Duchenne Muscular Dystrophy (DMD).
Academic Article GAA replacement improves respiratory muscle, neural, and alveolar pathology in the pompe mouse.
Academic Article Neuromuscular junction transcriptome analysis of spinal and bulbar muscular atrophy mice implicates sarcomere gene expression and calcium flux dysregulation in disease pathogenesis.
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