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The Network
Grantees
The five labs funded this cycle and what each is working on right now. Reach out directly to explore a collaboration or shared reagents.

Wade Harper, PhD
Harvard Medical School
Autophagy & endolysosomal proteomics
Understanding FTD risk alleles through the lens of endolysosomal molecular profiles
Building molecular maps (proteomics, lipidomics, cryo-ET) of the endolysosomal system across FTD driver mutations (C9ORF72, GRN, MAPT, CHMP2B) to test whether they share a common molecular basis.

Florian Wilfling, PhD
Max Planck Institute for Biophysics
Lysosomal structural biology
Comparative lysosomal ultrastructure in FTD using cryo-electron tomography
Using cryo-ET and whole-cell volume imaging to compare lysosome architecture across FTD mutations in neurons versus microglia.

Tobias Walther, PhD
Sloan Kettering & Cornell
Lysosomal lipid metabolism
Granulin-deficient FTD: disease mechanisms and intervention strategies
Defining how progranulin (GRN) deficiency disrupts lysosomal lipid metabolism, and testing whether modulating sphingolipids can treat FTD/ALS.

Eric J. Huang, MD, PhD
Washington University in St. Louis
Neuroimmunology & microglia
TLR7 signaling in autoimmune dysfunction and neuroinflammation in FTD
Investigating how combined progranulin and C9orf72 loss drives TLR7-mediated immune dysfunction in B cells and microglia, and whether TLR7 inhibition is protective.

Joachim Herz, MD
UT Southwestern
Lysosomal protein sorting
Progranulin as a secretory-pathway scaffold for lysosomal protein sorting
Mapping progranulin's secretory-pathway interaction partners (SIMPL screen + cryo-EM) to explain how its loss selectively depletes lysosomal enzymes in FTD.