Lita Duraine

发表

Elevated COUP-TFII expression in dopaminergic neurons accelerates the progression of Parkinson’s disease through mitochondrial dysfunction

D. Goldstein, M. Tsai, H. Bellen, 2020, PLoS genetics.

Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production

Ke Zhang, H. Bellen, V. Bayat, 2014, eLife.

Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.

Donna M. Martin, J. Rosenfeld, J. Lupski, 2016, American journal of human genetics.

NFIA regulates granule recruitment and exocytosis in the adult pancreas

Matthew C. Hill, S. Quake, P. MacDonald, 2019, bioRxiv.

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

Michael F. Wangler, J. Rosenfeld, A. Moser, 2020, Neuron.

The Retromer Complex Is Required for Rhodopsin Recycling and Its Loss Leads to Photoreceptor Degeneration

H. Bellen, V. Bayat, H. Sandoval, 2014, PLoS biology.

A Voltage-Gated Calcium Channel Regulates Lysosomal Fusion with Endosomes and Autophagosomes and Is Required for Neuronal Homeostasis

H. Bellen, H. Sandoval, M. Jaiswal, 2015, PLoS biology.

Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction.

J. Rosenfeld, F. Alkuraya, A. Afenjar, 2019, American journal of human genetics.

WAC Regulates mTOR Activity by Acting as an Adaptor for the TTT and Pontin/Reptin Complexes.

H. Bellen, H. Sandoval, Ke Zhang, 2016, Developmental cell.

Lysosomal nucleotide metabolism regulates ER proteostasis through mTOR signaling

D. Sabatini, Yong Yu, Meng C. Wang, 2020, bioRxiv.

Ari-1 Regulates Myonuclear Organization Together with Parkin and Is Associated with Aortic Aneurysms.

Michael F. Wangler, Nele A. Haelterman, D. Nickerson, 2018, Developmental cell.

cindr, the Drosophila Homolog of the CD2AP Alzheimer’s Disease Risk Gene, Is Required for Synaptic Transmission and Proteostasis

Benjamin R. Arenkiel, D. Bennett, J. Shulman, 2019, Cell reports.

Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration

Nele A. Haelterman, H. Bellen, M. Jaiswal, 2016, eLife.

Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes

J. Lupski, S. Ellard, W. Yoon, 2020, bioRxiv.

Crag Is a GEF for Rab11 Required for Rhodopsin Trafficking and Maintenance of Adult Photoreceptor Cells

H. Bellen, V. Bayat, H. Sandoval, 2012, PLoS biology.

Drosophila Neuroligin 2 is Required Presynaptically and Postsynaptically for Proper Synaptic Differentiation and Synaptic Transmission

H. Bellen, K. Venken, Kuchuan Chen, 2012, The Journal of Neuroscience.

Correction: The Retromer Complex Is Required for Rhodopsin Recycling and Its Loss Leads to Photoreceptor Degeneration

H. Bellen, V. Bayat, H. Sandoval, 2015, PLoS biology.

Pancreatic Cell Fate Determination Relies on Notch Ligand Trafficking by NFIA.

B. Arenkiel, Lesley S. Chaboub, B. Deneen, 2018, Cell reports.

The Krebs Cycle Enzyme Isocitrate Dehydrogenase 3A Couples Mitochondrial Metabolism to Synaptic Transmission.

H. Bellen, B. Ugur, Huan Bao, 2017, Cell reports.

A conserved role for AMP-activated protein kinase in NGLY1 deficiency

T. Cowan, A. Galeone, A. Pandey, 2020, PLoS genetics.

A TRPV Channel in Drosophila Motor Neurons Regulates Presynaptic Resting Ca2+ Levels, Synapse Growth, and Synaptic Transmission

H. Bellen, W. Yoon, T. Lloyd, 2014, Neuron.

A TRPV Channel in Drosophila Motor Neurons Regulates Presynaptic Resting Ca 2+ Levels,

H. Bellen, W. Yoon, T. Lloyd, 2014 .

Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration

Nele A. Haelterman, H. Bellen, M. Jaiswal, 2016, eLife.

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

Benjamin R. Arenkiel, J. Shulman, P. D. De Jager, 2019, SSRN Electronic Journal.

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

M. Wangler, Paul C. Marcogliese, Hyung-Lok Chung, 2020, Neuron.