A distinct set of brain areas process prosody–the melody of speech

Human speech carries information beyond the words themselves: pitch, loudness, duration, and pauses–jointly referred to as ‘prosody’–emphasize critical words, help group words into phrases, and convey emotional and other socially-relevant information. Using a novel fMRI paradigm, we identify a set of prosody-responsive brain areas and then richly characterize them across 8 experiments (25 experimental conditions; […]

Auditory representations of words during silent visual reading

Silent visual reading is accompanied by the phenomenological experience of an inner voice. However, the temporal dynamics and functional role of the underlying neural representations remain unclear. Here, we recorded electroencephalography (EEG) data while humans read naturalistic narratives, and applied computational modelling to isolate time-resolved auditory from visual and semantic representations. Our results revealed robust […]

Identifying left and right hemispheres using functional connectivity

Many studies have analyzed what organizational features distinguish the left and right hemispheres of the human brain, with most differences typically being found in language areas. In this analysis, we test whether supervised learning can categorize an unseen hemisphere as right or left based on functional connectivity. Using data from the Human Connectome Project, we […]

Striatal pathology in Spinocerebellar Ataxia Type 1 mice: A comparative study with Huntingtons disease

Spinocerebellar ataxia type 1 (SCA1) and Huntingtons disease (HD), are motor diseases caused by CAG expansions in ATXN1 and HTT, where SCA1 shows prominent cerebellar neurodegeneration and HD shows prominent striatal neurodegeneration, particularly in the Medium Spiny Neurons (MSNs). Since human and mouse studies demonstrate progressive striatal vulnerability in SCA1, we examined age-dependent molecular, cellular […]

Pharmacological inhibition of MCL-1 disrupts mitochondrial cristae and depletes the human neural progenitor cell pool

Myeloid Cell Leukemia-1 (MCL-1) is an anti-apoptotic protein that is crucial for early neurodevelopment. Loss of MCL-1 results in embryonic lethal neurodevelopmental defects that cannot be rescued by other anti-apoptotic proteins of the BCL-2 family. Here, we find a non-apoptotic role for MCL-1 in sustaining mitochondrial cristae integrity, fatty acid oxidation (FAO), and neural progenitor […]

Contextual associations impact visual search across multiple processing stages

Growing evidence indicates that visual search is influenced not only by perceptual but also by semantic information. Among such semantic influences, categorical effects have been extensively studied. By contrast, the influence of contextual associations, that is, how objects commonly co-occur within specific scene contexts, remains less understood. Here, we orthogonally manipulated contextual and categorical relationships […]

Nucleophagy removes cytotoxic trapped PARP1

Poly (ADP-Ribose) Polymerase inhibitors (PARPi) induce cytotoxicity in homologous recombination repair (HRR)-deficient cancers by causing PARP1 to become trapped on chromatin, resulting in irreparable replication-associated DNA damage. Although increased clearance of trapped PARP1 from chromatin reduces the sensitivity of cancer cells to PARPi, details surrounding this process remain unclear. PARPi exposure is known to cause […]

Nucleophagy removes cytotoxic trapped PARP1

Poly (ADP-Ribose) Polymerase inhibitors (PARPi) induce cytotoxicity in homologous recombination repair (HRR)-deficient cancers by causing PARP1 to become trapped on chromatin, resulting in irreparable replication-associated DNA damage. Although increased clearance of trapped PARP1 from chromatin reduces the sensitivity of cancer cells to PARPi, details surrounding this process remain unclear. PARPi exposure is known to cause […]

WRN helicase regulates mitophagy by resolving an intricate nexus of G-quadruplexes-R loops-ATG7 pre-mRNA maturation in cancer

Werner syndrome (WS) is a progeroid and cancer-predisposition disorder caused by loss of the Werner RECQ helicase-exonuclease (WRN), a key genome-maintenance enzyme essential for replication-stress signalling and DNA-repair. WS patients also develop metabolic abnormalities, including fatty-liver and diabetes, suggesting a link between WRN-deficiency and mitochondrial-dysfunction. WRN is frequently epigenetically silenced in cancers, yet its precise […]

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