Faculty

Institution

Unit

Venue

Carol C. Gregorio

Professor Emerita

University of Arizona

Affiliations

College of Science

Molecular and Cellular Biology

Carol C. Gregorio is currently serving as a College Of Science Professor Emerita at University of Arizona.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Carol C. Gregorio

University of Arizona

Professor Emerita

You can click a keyword to filter the displayed items

cell biology molecular biology physiology structural biology cellular physiology cardiology genetics membrane biology protein science molecular physiology gene expression molecular and cellular biology cardiac muscle molecular cell biology cellular biology cardiomyopathy cardiovascular research mammalian biology vascular biology cell biomechanics protein function muscle function skeletal muscle cell and molecular biology cell physiology protein structure biomechanics structural molecular biology cell motility liver physiology circulatory physiology cellular biochemistry cardiovascular physiology animal physiology biological chemistry tissue development protein assembly biomolecular interactions developmental genetics protein transport genome biology cell research cell biophysics functional modification thin filaments cardiac myocytes developmental science cell regulation embryonic development gene function experimental biology cell adhesion cardiovascular function structural heart disease cellular structure rna biology thin filament assembly heart development striated muscle novel mechanism brain circulation molecular regulation receptor (biochemistry) human sciences fragmentation effect gene regulation actin dynamics complete gene sequence linking system muscle cytoarchitecture intricate web titin kinase domain potential regulators myofibrillar elastic diversity elastic spring region structural basis muscular dystrophies

Notable Scholarly Works

Notable Federal Grants

Collaborators

Discovery of a Fourth Actin-Binding Site on Leiomodin-2. Biophysical Journal (2024)

Madison LittleGarry E. SmithMason SummersAlan Palma GuillenCarol GregorioVitold E. GalkinAlla S. Kostyukova

molecular biophysicsbiophysicscell biology

Human Disease-Causing Mutations Result in Loss of Leiomodin 2 Through Nonsense-Mediated Mrna Decay. PLoS Genetics (2024)

Christopher T. PappasRachel M. MayfieldAva E. DickersonLei Mi-MiCarol C. Gregorio

genomicscancer geneticsnonsense-mediated mrna decaygeneticscancer genomicshuman disease-causing mutationsmolecular biologyepigeneticsrna biologyhuman genetics

Leiomodin-2 Inhibits Actomyosin Interactions and Perturbs the Structure of the Thin Filament. Biophysical Journal (2024)

Cristina M. RisiJennifer AthertonTyler NguyenHoward D. WhiteCarol GregorioAlla S. KostyukovaVitold E. Galkin

biomolecular interactionsbiophysicspharmacologyprotein structurethin filamentstructural molecular biologystructural biologyneuroscience

Leiomodin 2 Neonatal Dilated Cardiomyopathy Mutation Results in Altered Actin Gene Signatures and Cardiomyocyte Dysfunction. npj Regenerative Medicine (2024)

JB IwanskiCT PappasRM MayfieldGP FarmanR Ahrens-Nicklas...

cardiologymedicinecardiomyocyte dysfunctionregenerative medicinecardiovascular researchgeneticsmolecular biologyregeneration (biology)disease physiologycardiomyopathycardiac pathologiescardiovascular disease

Lmod2 is Necessary for Effective Skeletal Muscle Contraction. Science Advances (2024)

TM LarrinagaGP FarmanRM MayfieldM YuenRC Ahrens-Nicklas...

physiologyrehabilitationmusculoskeletal scienceskeletal muscleexercise physiologyhuman movementscience advancehealth sciences

Lmod2 is Necessary for Effective Skeletal Muscle Contraction.. Sci Adv (2024)

physiologycellular physiologyapplied physiologymuscle functionskeletal muscleneuromuscular medicinemusculoskeletal disordersmolecular physiologybiomechanicsorthopaedic research

PHILAMENT: A Filament Tracking Program to Quickly and Accurately Analyze in Vitro Motility Assays. Biophysical Reports (2024)

RM BowserGP FarmanCC Gregorio

medicinebiophysicsbioanalysisbiomedical engineeringexperimental biophysics

Recessive Tmod1 Mutation Causes Childhood Cardiomyopathy. Communications Biology (2024)

Catalina VasilescuMert ColpanTiina H. OjalaTuula ManninenAino MutkaKaisa YlänenOtto RahkonenTuija PoutanenLaura MarteliusReena KumariHelena HinterdingVirginia BrilhanteSimo OjanenPekka LappalainenJuha KoskenvuoChristopher J. CarrollVelia M. FowlerCarol C. GregorioAnu Suomalainen

childhood cardiomyopathygene expressionearly childhood developmentgenetic factorschild developmentgeneticsdevelopmental geneticscardiomyopathycommunication researchmolecular biologymolecular geneticsepigeneticspediatricshuman geneticsgenetic disorders

A Nemaline Myopathy-Linked Mutation Inhibits the Actin-Regulatory Functions of Tropomodulin and Leiomodin.. Proc Natl Acad Sci U S A (2023)

cellular physiologycytoskeletoncell motilitysystems biologycell signalingmolecular and cellular biologymolecular cell biologyactin-regulatory functionsnemaline myopathy-linked mutationsignal transductioncellular biochemistrycell biology

A Nemaline Myopathy–Linked Mutation Inhibits the Actin-Regulatory Functions of Tropomodulin and Leiomodin. Proceedings of the National Academy of Sciences (2023)

Lauren E. SchultzMert ColpanGarry E. SmithRachel M. MayfieldTania M. LarrinagaAlla S. KostyukovaCarol C. Gregorio

immunologygene expressiongeneticsactin-regulatory functionsmolecular biologynemaline myopathy-linked mutation

1
2
3
4
5
13
10 / page

Carol C. Gregorio

Professor Emerita

University of Arizona

Affiliations

College of Science

Molecular and Cellular Biology

Carol C. Gregorio is currently serving as a College Of Science Professor Emerita at University of Arizona.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Carol C. Gregorio

University of Arizona

Professor Emerita

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Discovery of a Fourth Actin-Binding Site on Leiomodin-2. Biophysical Journal (2024)

Madison LittleGarry E. SmithMason SummersAlan Palma GuillenCarol GregorioVitold E. GalkinAlla S. Kostyukova

molecular biophysicsbiophysicscell biology

Human Disease-Causing Mutations Result in Loss of Leiomodin 2 Through Nonsense-Mediated Mrna Decay. PLoS Genetics (2024)

Christopher T. PappasRachel M. MayfieldAva E. DickersonLei Mi-MiCarol C. Gregorio

genomicscancer geneticsnonsense-mediated mrna decaygeneticscancer genomicshuman disease-causing mutationsmolecular biologyepigeneticsrna biologyhuman genetics

Leiomodin-2 Inhibits Actomyosin Interactions and Perturbs the Structure of the Thin Filament. Biophysical Journal (2024)

Cristina M. RisiJennifer AthertonTyler NguyenHoward D. WhiteCarol GregorioAlla S. KostyukovaVitold E. Galkin

biomolecular interactionsbiophysicspharmacologyprotein structurethin filamentstructural molecular biologystructural biologyneuroscience

Leiomodin 2 Neonatal Dilated Cardiomyopathy Mutation Results in Altered Actin Gene Signatures and Cardiomyocyte Dysfunction. npj Regenerative Medicine (2024)

JB IwanskiCT PappasRM MayfieldGP FarmanR Ahrens-Nicklas...

Lmod2 is Necessary for Effective Skeletal Muscle Contraction. Science Advances (2024)

TM LarrinagaGP FarmanRM MayfieldM YuenRC Ahrens-Nicklas...

physiologyrehabilitationmusculoskeletal scienceskeletal muscleexercise physiologyhuman movementscience advancehealth sciences

Lmod2 is Necessary for Effective Skeletal Muscle Contraction.. Sci Adv (2024)

physiologycellular physiologyapplied physiologymuscle functionskeletal muscleneuromuscular medicinemusculoskeletal disordersmolecular physiologybiomechanicsorthopaedic research

PHILAMENT: A Filament Tracking Program to Quickly and Accurately Analyze in Vitro Motility Assays. Biophysical Reports (2024)

RM BowserGP FarmanCC Gregorio

medicinebiophysicsbioanalysisbiomedical engineeringexperimental biophysics

Recessive Tmod1 Mutation Causes Childhood Cardiomyopathy. Communications Biology (2024)

A Nemaline Myopathy-Linked Mutation Inhibits the Actin-Regulatory Functions of Tropomodulin and Leiomodin.. Proc Natl Acad Sci U S A (2023)

A Nemaline Myopathy–Linked Mutation Inhibits the Actin-Regulatory Functions of Tropomodulin and Leiomodin. Proceedings of the National Academy of Sciences (2023)

Lauren E. SchultzMert ColpanGarry E. SmithRachel M. MayfieldTania M. LarrinagaAlla S. KostyukovaCarol C. Gregorio

immunologygene expressiongeneticsactin-regulatory functionsmolecular biologynemaline myopathy-linked mutation

1
2
3
4
5
13
10 / page

Similar Faculty Members

Jian-Ping Jin

Institution

University of Illinois Chicago

developmental biology

muscle cell motility

Robert J. Schwartz

Institution

University of Houston

cellular differentiation

stem cell

Leslie Leinwand

Institution

University of Colorado Boulder

molecular biology

cardiology

Jian-Ping Jin

Institution

Wayne State University

mechanical tension regulation

protein structure-function relationships

Sakthivel Sadayappan

Institution

University of Arizona

medical genetics

disease gene identification

R John Solaro

Institution

University of Illinois Chicago

electrophysiology

cellular physiology

Thomas C. Irving

Institution

Illinois Institute of Technology

muscle function

cellular physiology

Colin G. Nichols

Institution

Washington University in St. Louis

membrane transport

electrophysiology

Ju Chen

Institution

University of California, San Diego

naxos disease

pathology

William T. Pu

Institution

Harvard University

cardiology

genetics

Similar Faculty Members

Jian-Ping Jin

Institution

University of Illinois Chicago

developmental biology

muscle cell motility

Robert J. Schwartz

Institution

University of Houston

cellular differentiation

stem cell

Leslie Leinwand

Institution

University of Colorado Boulder

molecular biology

cardiology

Jian-Ping Jin

Institution

Wayne State University

mechanical tension regulation

protein structure-function relationships

Sakthivel Sadayappan

Institution

University of Arizona

medical genetics

disease gene identification

R John Solaro

Institution

University of Illinois Chicago

electrophysiology

cellular physiology

Thomas C. Irving

Institution

Illinois Institute of Technology

muscle function

cellular physiology

Colin G. Nichols

Institution

Washington University in St. Louis

membrane transport

electrophysiology

Ju Chen

Institution

University of California, San Diego

naxos disease

pathology

William T. Pu

Institution

Harvard University

cardiology

genetics