Carol C Gregorio (Carol Gregorio)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Topics

Binding Protein

Intellectual Disability

Top Venues

Communications biology

Science advances

NPJ Regenerative medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Catalina Vasilescu, Mert Colpan, Tiina H Ojala, Tuula Manninen, Aino Mutka, Kaisa Ylänen, Otto Rahkonen, Tuija Poutanen, Laura Martelius, Reena Kumari, Helena Hinterding, Virginia Brilhante, Simo Ojanen, Pekka Lappalainen, Juha Koskenvuo, Christopher J Carroll, Velia M Fowler, Carol C Gregorio, Anu Suomalainen
Recessive TMOD1 mutation causes childhood cardiomyopathy. Communications biology 7 (1) (2024)
Catalina Vasilescu, Mert Colpan, Tiina H Ojala, Tuula Manninen, Aino Mutka, Kaisa Ylänen, Otto Rahkonen, Tuija Poutanen, Laura Martelius, Reena Kumari, Helena Hinterding, Virginia Brilhante, Simo Ojanen, Pekka Lappalainen, Juha Koskenvuo, Christopher J Carroll, Velia M Fowler, Carol C Gregorio, Anu Suomalainen
Recessive TMOD1 mutation causes childhood cardiomyopathy. Communications biology 7 (1) (2024)
Jessika B Iwanski, Christopher T Pappas, Rachel M Mayfield, Gerrie P Farman, Rebecca Ahrens-Nicklas, Jared M Churko, Carol C Gregorio
Leiomodin 2 neonatal dilated cardiomyopathy mutation results in altered actin gene signatures and cardiomyocyte dysfunction. NPJ Regenerative medicine 9 (1) (2024)
Tania M Larrinaga, Gerrie P Farman, Rachel M Mayfield, Michaela Yuen, Rebecca C Ahrens-Nicklas, Sandra T Cooper, Christopher T Pappas, Carol C Gregorio
Lmod2 is necessary for effective skeletal muscle contraction. Science advances 10 (11) (2024)
Tania M Larrinaga, Gerrie P Farman, Rachel M Mayfield, Michaela Yuen, Rebecca C Ahrens-Nicklas, Sandra T Cooper, Christopher T Pappas, Carol C Gregorio
Lmod2 is necessary for effective skeletal muscle contraction. Science advances 10 (11) (2024)
Catalina Vasilescu, Mert Colpan, Tiina H Ojala, Tuula Manninen, Aino Mutka, Kaisa Ylänen, Otto Rahkonen, Tuija Poutanen, Laura Martelius, Reena Kumari, Helena Hinterding, Virginia Brilhante, Simo Ojanen, Pekka Lappalainen, Juha Koskenvuo, Christopher J Carroll, Velia M Fowler, Carol C Gregorio, Anu Suomalainen
Recessive TMOD1 mutation causes childhood cardiomyopathy. Communications biology 7 (1) (2024)
Catalina Vasilescu, Mert Colpan, Tiina H Ojala, Tuula Manninen, Aino Mutka, Kaisa Ylänen, Otto Rahkonen, Tuija Poutanen, Laura Martelius, Reena Kumari, Helena Hinterding, Virginia Brilhante, Simo Ojanen, Pekka Lappalainen, Juha Koskenvuo, Christopher J Carroll, Velia M Fowler, Carol C Gregorio, Anu Suomalainen
Recessive TMOD1 mutation causes childhood cardiomyopathy. Communications biology 7 (1) (2024)
Tania M Larrinaga, Gerrie P Farman, Rachel M Mayfield, Michaela Yuen, Rebecca C Ahrens-Nicklas, Sandra T Cooper, Christopher T Pappas, Carol C Gregorio
Lmod2 is necessary for effective skeletal muscle contraction. Science advances 10 (11) (2024)
Christopher T Pappas, Rachel M Mayfield, Ava E Dickerson, Lei Mi-Mi, Carol C Gregorio
Human disease-causing mutations result in loss of leiomodin 2 through nonsense-mediated mRNA decay. PLoS genetics 20 (5) (2024)
Christopher T Pappas, Rachel M Mayfield, Ava E Dickerson, Lei Mi-Mi, Carol C Gregorio
Human disease-causing mutations result in loss of leiomodin 2 through nonsense-mediated mRNA decay. PLoS genetics 20 (5) (2024)
Christopher T Pappas, Rachel M Mayfield, Ava E Dickerson, Lei Mi-Mi, Carol C Gregorio
Human disease-causing mutations result in loss of leiomodin 2 through nonsense-mediated mRNA decay. PLoS genetics 20 (5) (2024)
Catalina Vasilescu, Mert Colpan, Tiina H Ojala, Tuula Manninen, Aino Mutka, Kaisa Ylänen, Otto Rahkonen, Tuija Poutanen, Laura Martelius, Reena Kumari, Helena Hinterding, Virginia Brilhante, Simo Ojanen, Pekka Lappalainen, Juha Koskenvuo, Christopher J Carroll, Velia M Fowler, Carol C Gregorio, Anu Suomalainen
Recessive TMOD1 mutation causes childhood cardiomyopathy. Communications biology 7 (1) (2024)
Christopher T Pappas, Rachel M Mayfield, Ava E Dickerson, Lei Mi-Mi, Carol C Gregorio
Human disease-causing mutations result in loss of leiomodin 2 through nonsense-mediated mRNA decay. PLoS genetics 20 (5) (2024)
Mert Colpan, Jessika B Iwanski, Carol C Gregorio
CAP2 is a regulator of actin pointed end dynamics and myofibrillogenesis in cardiac muscle. Communications biology 4 (1) (2021)
Balázs Kiss, Jochen Gohlke, Paola Tonino, Zaynab Hourani, Justin Kolb, Joshua G Strom, Olga Alekhina, John Edward Smith, Coen Ottenheijm, Carol C Gregorio, Henk L Granzier
Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle. Science advances 6 (46) (2020)
Rebecca C Ahrens-Nicklas, Christopher T Pappas, Gerrie P Farman, Rachel M Mayfield, Tania M Larrinaga, Livija Medne, Alyssa Ritter, Ian D Krantz, Chaya N Murali, Kimberly Yee Lin, Justin H Berger, Sabrina W Yum, Chrystalle Katte Carreon, Carol C Gregorio
Disruption of cardiac thin filament assembly arising from a mutation in LMOD2: A novel mechanism of neonatal dilated cardiomyopathy. Science advances 5 (9) (2019)