99

Breakthroughs
Sub Categories on Breakthroughs
Latest Articles
Emerging trends and challenges in the grouping of digital health technologies

Emerging trends and challenges in the grouping of digital health technologies

byiCube ProgrammeCredit: Natanael Melchor on UnsplashThe widespread adoption of Digital Health Technologies (DHTs) is now evolving, with a growing trend towards the integration of these technolo

Emerging trends and challenges in the grouping of digital health technologies

byiCube ProgrammeCredit: Natanael Melchor on UnsplashThe widespread adoption of Digital Health Technologies (DHTs) is now evolving, with a growing trend towards the integration of these technolo
The roles of genes and 3D genome folds in determining health

The roles of genes and 3D genome folds in determining health

by Carmen Rotte,Max Planck SocietyModel for the mechanism of chromatin domain formation in S. cerevisiae. Credit:Nature Genetics(2024). DOI:10.1038/s41588-023-01649-8Whether we stay

The roles of genes and 3D genome folds in determining health

by Carmen Rotte,Max Planck SocietyModel for the mechanism of chromatin domain formation in S. cerevisiae. Credit:Nature Genetics(2024). DOI:10.1038/s41588-023-01649-8Whether we stay
First health care device powered by body heat made possible by liquid based metals

First health care device powered by body heat made possible by liquid based metals

by Kaitlyn Landram,Carnegie Mellon University Mechanical EngineeringCredit: Carnegie Mellon Unviersity, College of EngineeringIn the age of technology everywhere, we are all too familiar with th

First health care device powered by body heat made possible by liquid based metals

by Kaitlyn Landram,Carnegie Mellon University Mechanical EngineeringCredit: Carnegie Mellon Unviersity, College of EngineeringIn the age of technology everywhere, we are all too familiar with th
Experimental compound extends life in amyotrophic lateral sclerosis mouse model

Experimental compound extends life in amyotrophic lateral sclerosis mouse model

FEBRUARY 6, 2024byUT Southwestern Medical CenterMAP4K interactome and the effect on RANGAP1 subcellular distribution.AWestern-blotting analysis of proteins after proximity labeling i

Experimental compound extends life in amyotrophic lateral sclerosis mouse model

FEBRUARY 6, 2024byUT Southwestern Medical CenterMAP4K interactome and the effect on RANGAP1 subcellular distribution.AWestern-blotting analysis of proteins after proximity labeling i
Study with over 11,000 individuals of African descent finds genetic variants linked to glaucoma

Study with over 11,000 individuals of African descent finds genetic variants linked to glaucoma

byCell PressDiscovery of known and previously undescribed loci from the discovery mega-analysis of African ancestry individuals. Credit: Cell/Verma et al.Glaucoma is the leading cause of irrever

Study with over 11,000 individuals of African descent finds genetic variants linked to glaucoma

byCell PressDiscovery of known and previously undescribed loci from the discovery mega-analysis of African ancestry individuals. Credit: Cell/Verma et al.Glaucoma is the leading cause of irrever
Study: PR55α-controlled PP2A inhibits p16 expression and blocks cellular senescence induction

Study: PR55α-controlled PP2A inhibits p16 expression and blocks cellular senescence induction

by Impact Journals LLCPR55α level is much lower in human normal tissue specimens of older individuals compared to younger individuals and inversely correlates with p16 levels. Human normal tissue spec

Study: PR55α-controlled PP2A inhibits p16 expression and blocks cellular senescence induction

by Impact Journals LLCPR55α level is much lower in human normal tissue specimens of older individuals compared to younger individuals and inversely correlates with p16 levels. Human normal tissue spec
Study identifies molecular mechanisms of rare neurodevelopmental disorder

Study identifies molecular mechanisms of rare neurodevelopmental disorder

by Melissa Rohman,Northwestern UniversityNeurons cultured for 65 days from healthy cells and those containing the PACS1 syndrome variant both have complex morphology and express neuronal microtu

Study identifies molecular mechanisms of rare neurodevelopmental disorder

by Melissa Rohman,Northwestern UniversityNeurons cultured for 65 days from healthy cells and those containing the PACS1 syndrome variant both have complex morphology and express neuronal microtu
Examining the potential of the common bovine as a potential therapeutic research model

Examining the potential of the common bovine as a potential therapeutic research model

by Tom Fleischman,Cornell UniversityGraphical Abstract. Credit:iScience(2024). DOI: 10.1016/j.isci.2024.108886Research involving animal models—for purposes such as developing new vac

Examining the potential of the common bovine as a potential therapeutic research model

by Tom Fleischman,Cornell UniversityGraphical Abstract. Credit:iScience(2024). DOI: 10.1016/j.isci.2024.108886Research involving animal models—for purposes such as developing new vac
Research uncovers mechanism behind stubborn memories

Research uncovers mechanism behind stubborn memories

BRAIN HEALTHMEDICAL SCIENCESMENTAL HEALTHNEUROSCIENCERESEARCH18 January 2024Researchers from the Medical Research Council Brain Network Dynamics Unit at the University of Oxford and the Nuffield Depar

Research uncovers mechanism behind stubborn memories

BRAIN HEALTHMEDICAL SCIENCESMENTAL HEALTHNEUROSCIENCERESEARCH18 January 2024Researchers from the Medical Research Council Brain Network Dynamics Unit at the University of Oxford and the Nuffield Depar
Researchers identify peptides produced by the proteasome that degrade damaged proteins

Researchers identify peptides produced by the proteasome that degrade damaged proteins

FEBRUARY 14, 2024by Carmen Rotte,Max Planck SocietyUsing innovative computer programs and biochemical experiments, researchers identified and quantified fragments that the cellular garbage dispo

Researchers identify peptides produced by the proteasome that degrade damaged proteins

FEBRUARY 14, 2024by Carmen Rotte,Max Planck SocietyUsing innovative computer programs and biochemical experiments, researchers identified and quantified fragments that the cellular garbage dispo
Researchers find genetic variant coding for tubulin protein that may be partially responsible for left-handedness

Researchers find genetic variant coding for tubulin protein that may be partially responsible for left-handedness

by Bob Yirka , Medical XpressExome-wide, gene-based association testing in 38,043 left-handed and 313,271 right-handed individuals, based on rare protein-altering variants. Top: the strict variant set

Researchers find genetic variant coding for tubulin protein that may be partially responsible for left-handedness

by Bob Yirka , Medical XpressExome-wide, gene-based association testing in 38,043 left-handed and 313,271 right-handed individuals, based on rare protein-altering variants. Top: the strict variant set
ABT199/Venetoclax synergism with thiotepa in acute myeloid leukemia (AML) cells

ABT199/Venetoclax synergism with thiotepa in acute myeloid leukemia (AML) cells

by Impact Journals LLCEffects of various drug combinations on molecular markers of apoptosis in patient-derived cell samples. Credit:Oncotarget(2024). DOI: 10.18632/oncotarget.28563A new r

ABT199/Venetoclax synergism with thiotepa in acute myeloid leukemia (AML) cells

by Impact Journals LLCEffects of various drug combinations on molecular markers of apoptosis in patient-derived cell samples. Credit:Oncotarget(2024). DOI: 10.18632/oncotarget.28563A new r