Add to ORKGIn this mini-review, we provide an overview of phenylethanolamine-N-methyl transferase (Pnmt)-derived cardiomyocytes (PdCMs), a recently discovered cardiomyocyte subpopulation. We discuss their anatomical localization, physiological characteristics, possible function, and future perspectives. Their unique distribution in the heart, electrical activity, Ca2+ transient properties, and potential role in localized adrenergic signaling are discussed
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Our group recently described a distinctive, novel class of Pnmt+ cell-derived cardiomyocytes (PdCMs...
In the present study, channelrhodopsin 2 (ChR2) was specifically introduced into murine cells expres...
In the present study, channelrhodopsin 2 (ChR2) was specifically introduced into murine cells expres...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Phenylethanolamine N-methyltransferase (Pnmt) is the enzyme that N-methylates norepinephrine to prod...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Our group recently described a distinctive, novel class of Pnmt+ cell-derived cardiomyocytes (PdCMs...
In the present study, channelrhodopsin 2 (ChR2) was specifically introduced into murine cells expres...
In the present study, channelrhodopsin 2 (ChR2) was specifically introduced into murine cells expres...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Elucidating the function of specific cell types in a highly complex multicellular system such as the...
Phenylethanolamine N-methyltransferase (Pnmt) is the enzyme that N-methylates norepinephrine to prod...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...
Myotonic Dystrophy type 1 (DM1) is a multisystemic disease, autosomal dominant, caused by a CTG repe...