Faculty

Institution

Unit

Venue

Judith L. Campbell

Professor of Chemistry and Biology

California Institute of Technology

Affiliations

Division of Biology and Biological Engineering

Biology

Division of Chemistry and Chemical Engineering

Judith L. Campbell is currently serving as a Biology Professor of Chemistry and Biology at California Institute of Technology.

Honors

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Experiences

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Education

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Judith L. Campbell

California Institute of Technology

Professor of Chemistry and Biology

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molecular biology genetics biochemistry cell biology yeast molecular genetics dna replication dna repair genome biology gene expression biological chemistry structural biology protein science genomics molecular and cellular biology nucleic acids replication molecular cell biology rna biology biochemical sciences mutagenesis saccharomyces cerevisiae cell cycle structural molecular biology chromosome biology biochemical genetics cellular enzymology protein genetics protein purification gene characterization enzyme inhibition biomolecular interactions gene regulation molecular microbiology cellular biochemistry microbial genetics gene function molecular regulation dna analysis fungal genetics molecular science protein biosynthesis integrative biology cellular biology transcription regulation genome instability cancer genetics molecular substrates yeast cells okazaki fragment processing dna polymerase ii mammalian biology biochemical interaction gene editing cloning protein function cytogenetics molecular research cell regulation epigenetic changes dna end resection dna replication genes eukaryotic dna polymerases chromosomal replication dna polymerases okazaki fragment flaps genome stability plasmid copy number eukaryotic dna replication fragment processing protein stitchery dna polymerase epsilon biopolymers cell death aging cell experimental gerontology plo biology genomic stability

Notable Scholarly Works

Notable Federal Grants

Collaborators

Error-Prone, Stress-Induced 3′ Flap–Based Okazaki Fragment Maturation Supports Cell Survival. Science (2021)

Haitao SunZhaoning LuAmanpreet SinghYajing ZhouEric ZhengMian ZhouJinhui WangXiwei WuZunsong HuZhaohui GuJudith L. CampbellLi ZhengBinghui Shen

developmental biologytissue engineeringcell survivalcancer biologycell biologyregenerative medicinedna repairmolecular biologystress (biology)

Characterization of the Dimeric Cmg/Pre-Initiation Complex and Its Transition Into Dna Replication Forks. Cellular and Molecular Life Sciences (2019)

Lu LiuYue ZhangJingjing ZhangJian-Hua WangQinhong CaoZhen LiJudith L. CampbellMeng-Qiu DongHuiqiang Lou

dna replication forksgeneticscellular biologycell biologycell and molecular biologymolecular biology

Multiple Roles of Dna2 Nuclease/Helicase in Dna Metabolism, Genome Stability and Human Diseases. Nucleic Acids Research (2019)

Li ZhengYuan MengJudith L CampbellBinghui Shen

epigeneticsgeneticsmolecular geneticsdna metabolismmolecular biologygenome stabilityhuman diseases

Rad51 and Mitotic Function of Mus81 Are Essential for Recovery From Low-Dose of Camptothecin in the Absence of the Wrn Exonuclease. Nucleic Acids Research (2019)

Francesca Antonella AielloAnita PalmaEva MalacariaLi ZhengJudith L CampbellBinghui ShenAnnapaola FranchittoPietro Pichierri

geneticswrn exonucleaseradiation oncologynucleic acidsmitotic functionrna biologydna repairmolecular biologygene therapy

Flexibly-Oriented Double Cdc45-MCM-Gins Intermediates During Eukaryotic Replicative Helicase Maturation. bioRxiv (Cold Spring Harbor Laboratory) (2018)

Lu LiuYue ZhangJingjing ZhangJian-Hua WangQinhong CaoZhen LiJudith L. CampbellMeng-Qiu DongHuiqiang Lou

molecular biologybiochemistrygeneticsstructural biology

Mutations in the Non-Catalytic Subunit Dpb2 of Dna Polymerase Epsilon Affect the Nrm1 Branch of the Dna Replication Checkpoint. PLoS Genetics (2017)

Michał DmowskiJustyna RudzkaJudith L. CampbellPiotr JonczykIwona J. Fijałkowska

epigeneticsgeneticsdna replicationmolecular geneticsenzymesdna polymerase epsilongenomicsbiochemistrymutagenesisgenome biologymolecular biologydna replication checkpointcancer genetics

Polθ Helicase: Drive or Reverse. Nature Structural & Molecular Biology (2017)

Judith L CampbellHongzhi Li

polth helicasecell biologystructural molecular biologyprotein structurebiochemistrymolecular biologystructural biology

The Dna Pol ϵ Stimulatory Activity of Mrc1 is Modulated by Phosphorylation. Cell Cycle (2017)

Zhong-Xin ZhangJingjing ZhangQinhong CaoJudith L. CampbellHuiqiang Lou

epigeneticsgeneticscell biologycell cycledna repairmolecular biology

Cell-Cycle-Regulated Interaction Between Mcm10 and Double Hexameric Mcm2-7 is Required for Helicase Splitting and Activation During S Phase. Cell Reports (2015)

Yun QuanYisui XiaLu LiuJiamin CuiZhen LiQinhong CaoXiaojiang S. ChenJudith L. CampbellHuiqiang Lou

developmental biologycell-cycle-regulated interactioncell biologycell cyclemembrane biologymolecular biologyhelicase splitting

Preventing Over-Resection by Dna2 Helicase/Nuclease Suppresses Repair Defects in Fanconi Anemia Cells. Cell Cycle (2014)

Kenneth K KaranjaEu Han LeeEric A HendricksonJudith L Campbell

geneticsdna replicationmolecular and cellular biologynucleic acidschromatin remodelinggenome instabilitycell biologymolecular cell biologyexcessive resectionbiological chemistrydna repairmolecular biologygfp reporter

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Judith L. Campbell

Professor of Chemistry and Biology

California Institute of Technology

Affiliations

Division of Biology and Biological Engineering

Biology

Division of Chemistry and Chemical Engineering

Judith L. Campbell is currently serving as a Biology Professor of Chemistry and Biology at California Institute of Technology.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Judith L. Campbell

California Institute of Technology

Professor of Chemistry and Biology

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Error-Prone, Stress-Induced 3′ Flap–Based Okazaki Fragment Maturation Supports Cell Survival. Science (2021)

Haitao SunZhaoning LuAmanpreet SinghYajing ZhouEric ZhengMian ZhouJinhui WangXiwei WuZunsong HuZhaohui GuJudith L. CampbellLi ZhengBinghui Shen

developmental biologytissue engineeringcell survivalcancer biologycell biologyregenerative medicinedna repairmolecular biologystress (biology)

Characterization of the Dimeric Cmg/Pre-Initiation Complex and Its Transition Into Dna Replication Forks. Cellular and Molecular Life Sciences (2019)

Lu LiuYue ZhangJingjing ZhangJian-Hua WangQinhong CaoZhen LiJudith L. CampbellMeng-Qiu DongHuiqiang Lou

dna replication forksgeneticscellular biologycell biologycell and molecular biologymolecular biology

Multiple Roles of Dna2 Nuclease/Helicase in Dna Metabolism, Genome Stability and Human Diseases. Nucleic Acids Research (2019)

Li ZhengYuan MengJudith L CampbellBinghui Shen

epigeneticsgeneticsmolecular geneticsdna metabolismmolecular biologygenome stabilityhuman diseases

Rad51 and Mitotic Function of Mus81 Are Essential for Recovery From Low-Dose of Camptothecin in the Absence of the Wrn Exonuclease. Nucleic Acids Research (2019)

Francesca Antonella AielloAnita PalmaEva MalacariaLi ZhengJudith L CampbellBinghui ShenAnnapaola FranchittoPietro Pichierri

geneticswrn exonucleaseradiation oncologynucleic acidsmitotic functionrna biologydna repairmolecular biologygene therapy

Flexibly-Oriented Double Cdc45-MCM-Gins Intermediates During Eukaryotic Replicative Helicase Maturation. bioRxiv (Cold Spring Harbor Laboratory) (2018)

Lu LiuYue ZhangJingjing ZhangJian-Hua WangQinhong CaoZhen LiJudith L. CampbellMeng-Qiu DongHuiqiang Lou

molecular biologybiochemistrygeneticsstructural biology

Mutations in the Non-Catalytic Subunit Dpb2 of Dna Polymerase Epsilon Affect the Nrm1 Branch of the Dna Replication Checkpoint. PLoS Genetics (2017)

Michał DmowskiJustyna RudzkaJudith L. CampbellPiotr JonczykIwona J. Fijałkowska

epigeneticsgeneticsdna replicationmolecular geneticsenzymesdna polymerase epsilongenomicsbiochemistrymutagenesisgenome biologymolecular biologydna replication checkpointcancer genetics

Polθ Helicase: Drive or Reverse. Nature Structural & Molecular Biology (2017)

Judith L CampbellHongzhi Li

polth helicasecell biologystructural molecular biologyprotein structurebiochemistrymolecular biologystructural biology

The Dna Pol ϵ Stimulatory Activity of Mrc1 is Modulated by Phosphorylation. Cell Cycle (2017)

Zhong-Xin ZhangJingjing ZhangQinhong CaoJudith L. CampbellHuiqiang Lou

epigeneticsgeneticscell biologycell cycledna repairmolecular biology

Cell-Cycle-Regulated Interaction Between Mcm10 and Double Hexameric Mcm2-7 is Required for Helicase Splitting and Activation During S Phase. Cell Reports (2015)

Yun QuanYisui XiaLu LiuJiamin CuiZhen LiQinhong CaoXiaojiang S. ChenJudith L. CampbellHuiqiang Lou

developmental biologycell-cycle-regulated interactioncell biologycell cyclemembrane biologymolecular biologyhelicase splitting

Preventing Over-Resection by Dna2 Helicase/Nuclease Suppresses Repair Defects in Fanconi Anemia Cells. Cell Cycle (2014)

Kenneth K KaranjaEu Han LeeEric A HendricksonJudith L Campbell

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Similar Faculty Members

Jasper Rine

Institution

University of California, Berkeley

epigenetic mechanisms

chromatin remodeling

Gregory Verdine

Institution

Harvard University

therapeutic modalities

peptide

Susan L Forsburg

Institution

University of Southern California

dna replication

systems biology

Jeremy Thorner

Institution

University of California, Berkeley

signaling pathway

phosphoinositide-dependent signaling

Graham C. Walker

Institution

Massachusetts Institute of Technology

molecular biology

mutagenesis

Kelley Moremen

Institution

University of Georgia

glycan trimming enzymes

glycosylation

James Wohlschlegel

Institution

University of California, Los Angeles

molecular informatics

bioinformatics

Nancy Kleckner

Institution

Harvard University

developmental biology

super-resolution time-lapse microscopy

Gerald R. Fink

Institution

Massachusetts Institute of Technology

yeast

fungal ecology

James Haber

Institution

Brandeis University

genome instability

recombination dynamic