Resume-aware faculty matching

Find professors who actually fit you

Review faculty evidence in public, then use the workspace to turn your background into a shortlist, outreach, and meeting prep.

Profile-awarePaper evidenceSix agents
Thomas Neufeld

Thomas Neufeld

· Professor

University of Minnesota · Cell Biology

Active 1991–2023

h-index52
Citations28.2k
Papers845 last 5y
Funding$3.8M

Academic metrics are sourced from OpenAlex and public funding records; values may differ from Google Scholar.

See your match with Thomas Neufeld — sign in to PhdFit.Sign in

About

Thomas Neufeld, PhD, is a professor affiliated with the Genetics, Cell Biology & Development department at the University of Minnesota Medical School. His professional profile is accessible through the university's website, indicating his role within the academic community. The information provided does not specify his research focus, background, or key contributions, but it confirms his position as a faculty member involved in genetics, cell biology, and development.

Research topics

  • Medicine
  • Genetics
  • Biology
  • Art
  • Pediatrics
  • Cell biology
  • Internal medicine
  • Philosophy
  • Gerontology
  • Theology

Selected publications

  • ULK1 induces autophagy by phosphorylating Beclin-1 and activating VPS34 lipid kinase

    Nature Cell Biology · 2013-05-19 · 1529 citations

    articleOpen access
  • Bafilomycin A1 disrupts autophagic flux by inhibiting both V-ATPase-dependent acidification and Ca-P60A/SERCA-dependent autophagosome-lysosome fusion

    Autophagy · 2015-07-09 · 789 citations

    articleOpen accessSenior authorCorresponding

    Autophagosome-lysosome fusion and autolysosome acidification constitute late steps in the autophagic process necessary to maintain functional autophagic flux and cellular homeostasis. Both of these steps are disrupted by the V-ATPase inhibitor bafilomycin A1, but the mechanisms potentially linking them are unclear. We recently revisited the role of lysosomal acidification in autophagosome-lysosome fusion, using an in vivo approach in Drosophila. By genetically depleting individual subunits of th…

  • Autophagosome–lysosome fusion is independent of V-ATPase-mediated acidification

    Nature Communications · 2015-05-11 · 432 citations

    articleOpen accessSenior author

    The ATP-dependent proton pump V-ATPase ensures low intralysosomal pH, which is essential for lysosomal hydrolase activity. Based on studies with the V-ATPase inhibitor BafilomycinA1, lysosomal acidification is also thought to be required for fusion with incoming vesicles from the autophagic and endocytic pathways. Here we show that loss of V-ATPase subunits in the Drosophila fat body causes an accumulation of non-functional lysosomes, leading to a block in autophagic flux. However, V-ATPase-defi…

  • Dietary sugar promotes systemic TOR activation in Drosophila through AKH-dependent selective secretion of Dilp3

    Nature Communications · 2015-04-17 · 187 citations

    articleOpen accessSenior author

    Secreted ligands of the insulin family promote cell growth and maintain sugar homeostasis. Insulin release is tightly regulated in response to dietary conditions, but how insulin-producing cells (IPCs) coordinate their responses to distinct nutrient signals is unclear. Here we show that regulation of insulin secretion in Drosophila larvae has been segregated into distinct branches—whereas amino acids promote the secretion of Drosophila insulin-like peptide 2 (Dilp2), circulating sugars promote t…

  • Membrane remodeling by the PX-BAR protein SNX18 promotes autophagosome formation

    The Journal of Cell Biology · 2013-07-22 · 178 citations

    articleOpen access

    The membrane remodeling events required for autophagosome biogenesis are still poorly understood. Because PX domain proteins mediate membrane remodeling and trafficking, we conducted an imaging-based siRNA screen for autophagosome formation targeting human PX proteins. The PX-BAR protein SNX18 was identified as a positive regulator of autophagosome formation, and its Drosophila melanogaster homologue SH3PX1 was found to be required for efficient autophagosome formation in the larval fat body. We…

Recent grants

Frequent coauthors

  • Elaine C.M. Silva-Zacarin

    21 shared
  • Anna Nogalska

    Broad Center

    20 shared
  • Wen H. Yu

    Wuhan University of Technology

    20 shared
  • Dieter Willbold

    Heinrich Heine University Düsseldorf

    19 shared
  • Gerald M. Rubin

    Howard Hughes Medical Institute

    19 shared
  • Xuejun Jiang

    18 shared
  • Frank C. Dorsey

    17 shared
  • Frank Lafont

    16 shared

Similar researchers at University of Minnesota

  • Resume-aware match score
  • Save to shortlist
  • AI-drafted outreach

See your match with Thomas Neufeld

PhdFit ranks faculty by your research interests, methods, and publications — grounded in their actual work, not templates.

  • Free to start
  • No credit card
  • 30-second signup