Faculty

Institution

Unit

Venue

Stefanie Kaech Petrie

Oregon Health & Science University

Affiliations

Biostatistics Shared Resources

Institute Of Knight Cancer

OHSU School of Medicine

Cancer Early Detection Advanced Research Center (Cedar)

Department Of Cell, Developmental And Cancer Biology

Department Of Pediatrics

Division Of Oncological Sciences

Center Of Cancer Early Detection Advanced Research (Cedar)

Institute Of Knight Cancer

Center Of Knight Cancer

Department of Medicine

Division Of Hematology/Medical Oncology

Department Of Pediatrics

Division Of Neurology

Flow Cytometry Shared Resource

Institute Of Knight Cancer

Cancer Early Detection Advanced Research Center (Cedar)

Institute Of Knight Cancer

Division Of Oncological Sciences

Institute Of Knight Cancer

Department Of Cell, Developmental And Cancer Biology

Institute Of Knight Cancer

Division Of Hematology/Medical Oncology

Institute Of Knight Cancer Insitute

Institute Of University Knight Cancer

Jungers Center For Neurosciences Research

OHSU Knight Cancer Institute

Oregon Health & Science University

NoneStefanie Kaech Petrie is currently serving as a Biostatistics Shared Resources faculty at Oregon Health & Science University.

Honors

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Experiences

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Education

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Stefanie Kaech Petrie

Oregon Health & Science University

You can click a keyword to filter the displayed items

neuroscience cell biology neurons cellular physiology molecular biology cellular biochemistry molecular cell biology neurophysiology cytoskeleton molecular neuroscience cellular neurobiology developmental biology developmental neurobiology protein science molecular neurobiology cell signaling developmental cell molecular neurodegeneration intracellular trafficking membrane proteins membrane biology proteome research developmental cognitive neuroscience biomedical imaging protein transport neural science drug targets hippocampal neurons biological macromolecules future medicinal chemistry enzyme inhibition neuropsychopharmacology neurotransmission nuclear organization molecular regulation brain imaging cerebral organoids neurodynamics mechanisms of action rational drug design resistance profile structural modeling nucleic acids molecular physiology pharmacological research endocytic pathway proteinlipid interaction cell regulation brain science membrane transport organelle dynamics secretory pathway neurochemistry molecular pathways precision macromolecule gene editing protein biosynthesis crispr rna processing protein phosphorylation signaling pathways cellular regulatory mechanism mitochondrial function polarized transport posttranslational modifications axonal surface synaptic plasticity axonal extension growth cone motility axon specification selective microtubule-based transport axon formation nuclear envelope cultured hippocampal neurons reversible labeling crispr-based designer

Notable Scholarly Works

Notable Federal Grants

Collaborators

Smap3-Id for Identification of Endogenous Protein–Protein Interactions Reveals Regulation of Mitochondrial Activity by Lamins. JACS Au (2025)

molecular and cellular biologyproteomicsprotein sciencemitochondrial activitycell signalingcell biologybiochemistrycell metabolismcytoskeletonmolecular cell biologyautophagymolecular biologymitochondrial functionmitophagycellular biochemistryproteome research

Abstract 5780: Simultaneous Targeting Existing Proteins and Nascent Proteins for Synergistic Anticancer Activity. Cancer Research (2024)

tumor targetingdrug targetingprotein scienceanti-cancer agentsdrug targetscell biologyabstract 5780molecular cancersynergistic anticancer activitynascent proteinsprotein engineeringmolecular biologytherapeutic targetsdrug discoverycancer cells

Nanotubules and Cellular Communication in Trabecular Meshwork Cells. Methods in molecular biology (2024)

biophysicsmatrix biologycell biomechanicscellular physiologybiomedical engineeringcytoskeletontrabecular meshwork cells

Cg -Slenp: A Chemical Genetics Strategy to Selectively Label Existing Proteins and Newly Synthesized Proteins. JACS Au (2024)

protein geneticsnewly synthesized proteinsproteomicsprotein sciencebiomolecular structuredirected evolutionstructural biologyprotein designbiochemistrychemical biologyprotein engineeringmolecular biologybiological chemistryprotein structurechemical genetics strategystructural molecular biologybiomolecular engineeringproteome research

Large-Scale Recording of Neuronal Activity in Freely-Moving Mice at Cellular Resolution. Nature Communications (2023)

neural scienceneural circuitsmolecular neurodegenerationsystems neurosciencelarge-scale recordingneuronsfreely-moving micecellular physiologyneuroscienceneuropsychopharmacologyneurophysiologybiomedical engineeringneurodynamicscellular resolution

Supplementary Data From Resistance Profile and Structural Modeling of Next-Generation Ros1 Tyrosine Kinase Inhibitors. (2023)

future medicinal chemistrysupplementary datadrug targetsbiochemistryrational drug designdrug resistanceresistance profileprotein structuresystems biologyenzyme inhibitionstructural modelingdrug discoverymechanisms of action

A Clickable Photoaffinity Probe of Betulinic Acid Identifies Tropomyosin as a Target. Acta Pharmaceutica Sinica B (2021)

Pedro Martín-AcostaQianli MengJohn KlimekAshok P. ReddyLarry DavidStefanie Kaech PetrieBingbing X. LiXiangshu Xiao

clickable photoaffinity probepeptide sciencebiochemistrybioactive compoundspharmacologydrug metabolismdrug discoverypharmacological research

High-Fidelity, Efficient, and Reversible Labeling of Endogenous Proteins Using Crispr-Based Designer Exon Insertion. eLife (2021)

Haining ZhongCesar C CeballosCrystian I MassengillMichael A MuniakLei MaMaozhen QinStefanie Kaech PetrieTianyi Mao

biological macromoleculesproteomicsrna processingsynthetic biologyprotein engineeringmolecular engineeringreversible labelingcrispr-based designercrisprmolecular biologyprotein biosynthesisgene editingprotein designsystems biologyproteome researchendogenous proteinsprotein scienceprecision macromoleculebiomolecular engineering

Resistance Profile and Structural Modeling of Next-Generation Ros1 Tyrosine Kinase Inhibitors. Molecular Cancer Therapeutics (2021)

future medicinal chemistrydrug targetsbiochemistryrational drug designdrug resistanceresistance profilepharmacologydrug discoveryenzyme inhibitionstructural modelingmechanisms of action

Deletion of Stim1 in Hypothalamic Arcuate Nucleus Kiss1 Neurons Potentiates Synchronous Gcamp Activity and Protects Against Diet-Induced Obesity. bioRxiv (Cold Spring Harbor Laboratory) (2020)

metabolic syndromeenergy homeostasisphysiologymetabolic regulationneuronsaddiction biologyneuropsychopharmacologyneuroscienceneuroendocrine mechanismssynchronous gcamp activitydiet-induced obesityobesityappetite controlobesity medicine

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Stefanie Kaech Petrie

Oregon Health & Science University

Affiliations

Biostatistics Shared Resources

Institute Of Knight Cancer

OHSU School of Medicine

Cancer Early Detection Advanced Research Center (Cedar)

Department Of Cell, Developmental And Cancer Biology

Department Of Pediatrics

Division Of Oncological Sciences

Center Of Cancer Early Detection Advanced Research (Cedar)

Institute Of Knight Cancer

Center Of Knight Cancer

Department of Medicine

Division Of Hematology/Medical Oncology

Department Of Pediatrics

Division Of Neurology

Flow Cytometry Shared Resource

Institute Of Knight Cancer

Cancer Early Detection Advanced Research Center (Cedar)

Institute Of Knight Cancer

Division Of Oncological Sciences

Institute Of Knight Cancer

Department Of Cell, Developmental And Cancer Biology

Institute Of Knight Cancer

Division Of Hematology/Medical Oncology

Institute Of Knight Cancer Insitute

Institute Of University Knight Cancer

Jungers Center For Neurosciences Research

OHSU Knight Cancer Institute

Oregon Health & Science University

NoneStefanie Kaech Petrie is currently serving as a Biostatistics Shared Resources faculty at Oregon Health & Science University.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Stefanie Kaech Petrie

Oregon Health & Science University

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Smap3-Id for Identification of Endogenous Protein–Protein Interactions Reveals Regulation of Mitochondrial Activity by Lamins. JACS Au (2025)

Abstract 5780: Simultaneous Targeting Existing Proteins and Nascent Proteins for Synergistic Anticancer Activity. Cancer Research (2024)

Nanotubules and Cellular Communication in Trabecular Meshwork Cells. Methods in molecular biology (2024)

biophysicsmatrix biologycell biomechanicscellular physiologybiomedical engineeringcytoskeletontrabecular meshwork cells

Cg -Slenp: A Chemical Genetics Strategy to Selectively Label Existing Proteins and Newly Synthesized Proteins. JACS Au (2024)

Large-Scale Recording of Neuronal Activity in Freely-Moving Mice at Cellular Resolution. Nature Communications (2023)

Supplementary Data From Resistance Profile and Structural Modeling of Next-Generation Ros1 Tyrosine Kinase Inhibitors. (2023)

A Clickable Photoaffinity Probe of Betulinic Acid Identifies Tropomyosin as a Target. Acta Pharmaceutica Sinica B (2021)

Pedro Martín-AcostaQianli MengJohn KlimekAshok P. ReddyLarry DavidStefanie Kaech PetrieBingbing X. LiXiangshu Xiao

clickable photoaffinity probepeptide sciencebiochemistrybioactive compoundspharmacologydrug metabolismdrug discoverypharmacological research

High-Fidelity, Efficient, and Reversible Labeling of Endogenous Proteins Using Crispr-Based Designer Exon Insertion. eLife (2021)

Haining ZhongCesar C CeballosCrystian I MassengillMichael A MuniakLei MaMaozhen QinStefanie Kaech PetrieTianyi Mao

Resistance Profile and Structural Modeling of Next-Generation Ros1 Tyrosine Kinase Inhibitors. Molecular Cancer Therapeutics (2021)

future medicinal chemistrydrug targetsbiochemistryrational drug designdrug resistanceresistance profilepharmacologydrug discoveryenzyme inhibitionstructural modelingmechanisms of action

Deletion of Stim1 in Hypothalamic Arcuate Nucleus Kiss1 Neurons Potentiates Synchronous Gcamp Activity and Protects Against Diet-Induced Obesity. bioRxiv (Cold Spring Harbor Laboratory) (2020)

1
2
3
10 / page