Author details

Full Name

Jamie L Marshall

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36865221	FALCON systematically interrogates free fatty acid biology and identifies a novel mediator of lipotoxicity.	bioRxiv	2023
37337297	The effect of background noise and its removal on the analysis of single-cell expression data.	Genome Biol	2023
37075753	FALCON systematically interrogates free fatty acid biology and identifies a novel mediator of lipotoxicity.	Cell Metab	2023
34861215	Single-Cell Transcriptomics Reveal Disrupted Kidney Filter Cell-Cell Interactions after Early and Selective Podocyte Injury.	American Journal of Pathology	2022
35372810	High-resolution Slide-seqV2 spatial transcriptomics enables discovery of disease-specific cell neighborhoods and pathways.	iScience	2022
35549429	Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function.	Science	2022
35069263	Principles of Spatial Transcriptomics Analysis: A Practical Walk-Through in Kidney Tissue.	Frontiers in Physiology	2021
33859401	Compressed sensing for highly efficient imaging transcriptomics.	Nat Biotechnol	2021
33444290	Targeting a Braf/Mapk pathway rescues podocyte lipid peroxidation in CoQ-deficiency kidney disease.	J Clin Invest	2021
33977140	WGS and RNA Studies Diagnose Noncoding <i>DMD</i> Variants in Males With High Creatine Kinase.	Neurol Genet	2021
33288904	Highly sensitive spatial transcriptomics at near-cellular resolution with Slide-seqV2.	Nature Biotechnology	2021
33432327	Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease.	Human Molecular Genetics	2021
33294858	A High-Content Screen for Mucin-1-Reducing Compounds Identifies Fostamatinib as a Candidate for Rapid Repurposing for Acute Lung Injury.	Cell Rep Med	2020
31844291	Efficient, continuous mutagenesis in human cells using a pseudo-random DNA editor.	Nature Biotechnology	2020
32341542	Disease-associated astrocytes in Alzheimer's disease and aging.	Nat Neurosci	2020
33376219	HyPR-seq: Single-cell quantification of chosen RNAs via hybridization and sequencing of DNA probes.	Proc Natl Acad Sci U S A	2020
32637960	A High Content Screen for Mucin-1-Reducing Compounds Identifies Fostamatinib as a Candidate for Rapid Repurposing for Acute Lung Injury during the COVID-19 pandemic.	bioRxiv	2020
30895940	A recurrent COL6A1 pseudoexon insertion causes muscular dystrophy and is effectively targeted by splice-correction therapies.	JCI Insight	2019
31784515	Single cell census of human kidney organoids shows reproducibility and diminished off-target cells after transplantation.	Nat Commun	2019
31039133	Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy.	JCI insight	2019
29691892	Congenital Titinopathy: Comprehensive characterization and pathogenic insights.	Ann Neurol	2018
29517003	Corrigendum: Landscape of X chromosome inactivation across human tissues.	Nature	2018
29022598	Landscape of X chromosome inactivation across human tissues.	Nature	2017
28424332	Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.	Sci Transl Med	2017
27676442	Reversal of neurobehavioral social deficits in dystrophic mice using inhibitors of phosphodiesterases PDE5A and PDE9A.	Transl Psychiatry	2016
27236198	Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx.	Glycobiology	2016
26791950	Quantifying prion disease penetrance using large population control cohorts.	Sci Transl Med	2016
27798107	High levels of sarcospan are well tolerated and act as a sarcolemmal stabilizer to address skeletal muscle and pulmonary dysfunction in DMD.	Human Molecular Genetics	2016
26702077	Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy.	Journal of the American Heart Association	2015
25504048	Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and Î±7 integrin.	Human Molecular Genetics	2015
26582133	Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype.	Cell	2015
24789910	MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms.	J Clin Invest	2014
23282144	Sarcospan: a small protein with large potential for Duchenne muscular dystrophy.	Skeletal Muscle	2013
23601082	The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy.		2013
22570487	High throughput screening for compounds that alter muscle cell glycosylation identifies new role for N-glycans in regulating sarcolemmal protein abundance and laminin binding.	J Biol Chem	2012
22798625	Dystrophin and utrophin expression require sarcospan: loss of Î±7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice.	Human Molecular Genetics	2012
22734004	Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration.	Journal of Cell Biology	2012
18981229	Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex.	Journal of Cell Biology	2008
17720911	Genomewide clonal analysis of lethal mutations in the Drosophila melanogaster eye: comparison of the X chromosome and autosomes.	Genetics	2007
16849596	An efficient genetic screen in Drosophila to identify nuclear-encoded genes with mitochondrial function.	Genetics	2006
15719063	Discovery-based science education: functional genomic dissection in Drosophila by undergraduate researchers.	PLoS Biol	2005