Lita Duraine

Baylor College of Medicine - Howard Hughes Medical Institute

Houston, TX 77030

United States

SCHOLARLY PAPERS

2

DOWNLOADS

62

SSRN CITATIONS

0

CROSSREF CITATIONS

0

Scholarly Papers (2)

1.

Loss or Gain of Function Mutations in ACOX1 Cause Axonal Loss Via Different Mechanisms

NEURON-D-19-01325
Number of pages: 67 Posted: 29 Aug 2019
Baylor College of Medicine - Howard Hughes Medical Institute, Baylor College of Medicine - Department of Molecular and Human Genetics, Baylor College of Medicine - Department of Molecular and Human Genetics, Texas Children's Hospital - Jan and Dan Duncan Neurologic Research Institute, Baylor College of Medicine - Department of Molecular and Human Genetics, Baylor College of Medicine - Howard Hughes Medical Institute, Harvard University - Department of Psychology, Baylor College of Medicine - Department of Molecular and Human Genetics, Washington University in St. Louis - Division of Neuropathology, Washington University in St. Louis - Division of Neuropathology, Baylor College of Medicine - Department of Molecular and Human Genetics, Baylor College of Medicine - Department of Molecular and Human Genetics, Washington University in St. Louis - Division of Neuropathology, Baylor College of Medicine - Department of Molecular and Human Genetics, affiliation not provided to SSRN, Cincinnati Children's Hospital Medical Center - Division of Human Genetics, University of Cincinnati - Department of Pediatrics, Cincinnati Children's Hospital Medical Center - Division of Human Genetics, University of Cincinnati - Department of Pediatrics, University of Cincinnati - Department of Pediatrics, Baylor College of Medicine - Department of Molecular and Human Genetics, Johns Hopkins University - Division of Neurogenetics, Johns Hopkins University - Division of Neurogenetics, Seoul National University - Department of Biomedical Sciences, Washington University in St. Louis - Department of Neurology, Seoul National University - Department of Biomedical Sciences, Washington University in St. Louis - Department of Neurology, Baylor College of Medicine - Department of Molecular and Human Genetics, Seoul National University - Department of Pediatrics, Cincinnati Children's Hospital Medical Center - Division of Human Genetics, Seoul National University - Department of Pediatrics, University of Chicago - Section of Rheumatology and Baylor College of Medicine - Howard Hughes Medical Institute
Downloads 51 (388,259)

Abstract:

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Personalized medicine, Mitchell Disease, Lipid metabolism, Very long chain fatty acids, ROS, Peroxisome, Schwann cell, Bezafibrate, Wrapping glial, Drosophila, ACOX1 deficiency, Undiagnosed Disease Network, Rare disease

2.

Cindr, the Drosophila Homolog of the CD2AP Alzheimer's Disease Susceptibility Gene, is Required for Synaptic Transmission and Proteostasis

Number of pages: 75 Posted: 10 Jan 2019
Baylor University, College of Medicine, Department of Neurology, Baylor University, College of Medicine, Department of Neurology, Baylor University, College of Medicine, Department of Neurology, Rush University Medical Center - Rush Alzheimer’s Disease Center, Baylor University - Program in Developmental Biology, Baylor College of Medicine - Howard Hughes Medical Institute, Baylor University - Department of Molecular and Human Genetics, Pacific Northwest National Laboratory, Columbia University - Center for Translational and Systems Neuroimmunology, Rush University Medical Center - Rush Alzheimer’s Disease Center, Baylor University, College of Medicine, Howard Hughes Medical Institute, Texas Children’s Hospital - Jan and Dan Duncan Neurologic Research Institute and Baylor University, College of Medicine, Department of Neurology
Downloads 11 (580,984)

Abstract:

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calcium; PMCA; Synapsin; ubiquitin-proteasome system; Alzheimer’s Disease; 14-3-3; GWAS; neurofibrillary tangles; Tau; endocytosis; exocytosis; neuromuscular junction