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Representing the locations of places so that we can use them as landmarks is critical to our ability to navigate through large-scale spaces-a process referred to as "map-based navigation." While many neuroimaging studies in adults have revealed that this ability involves the retrosplenial complex (RSC)-a scene-selective region in the medial parietal cortex-nothing is known about how this cortical system develops. So, does it develop only late in childhood, as generally assumed from some behavioral studies? Or is it, perhaps counterintuitively, present in the first few years of life? To test this question, using functional magnetic resonance imaging (fMRI) multivoxel pattern analysis and a virtual town paradigm, we investigated the representation of location information in the RSC of 5-y-olds. We found that i) the RSC in 5-y-olds already represents the locations of particular buildings in the town (e.g., the ice cream store by the mountain versus by the lake), but not their category membership (e.g., ice cream store, regardless of location), and ii) this neural representation is correlated with their performance on a location task. Using multidimensional scaling, we also found that the neural representation of the buildings in RSC reflects the actual layout of the virtual town. Finally, the parahippocampal place area-a scene-selective region implicated in scene categorization, not map-based navigation-did not represent location information, but instead category information, the exact opposite of RSC. Taken together, these findings reveal the early development of navigationally relevant location information in RSC and thus the early origins of map-based navigation.
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http://dx.doi.org/10.1073/pnas.2503569122 | DOI Listing |
J Am Soc Nephrol
September 2025
Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Background: Genetic modifiers are believed to play an important role in the onset and severity of polycystic kidney disease (PKD), but identifying these modifiers has been challenging due to the lack of effective methodologies.
Methods: We generated zebrafish mutants of IFT140, a skeletal ciliopathy gene and newly identified autosomal dominant PKD (ADPKD) gene, to examine skeletal development and kidney cyst formation in larval and juvenile mutants. Additionally, we utilized ift140 crispants, generated through efficient microhomology-mediated end joining (MMEJ)-based genome editing, to compare phenotypes with mutants and conduct a pilot genetic modifier screen.
JCI Insight
September 2025
Edinburgh Medical School: Biomedical Sciences & Euan MacDonald Centre for M, University of Edinburgh, Edinburgh, United Kingdom.
Spinal muscular atrophy (SMA) is a neuromuscular disease caused by low levels of SMN protein. Several therapeutic approaches boosting SMN are approved for human patients, delivering remarkable improvements in lifespan and symptoms. However, emerging phenotypes, including neurodevelopmental comorbidities, are being reported in some treated SMA patients, indicative of alterations in brain development.
View Article and Find Full Text PDFClin J Am Soc Nephrol
September 2025
University College London Great Ormond Street Hospital for Children and Institute of Child Health, London, UK.
Background: Experience with icodextrin use in children on long-term peritoneal dialysis is limited. We describe international icodextrin prescription practices and their impact on clinical outcomes: ultrafiltration, blood pressure control, residual kidney function (RKF), technique and patient survival.
Methods: We included patients under 21 years enrolled in the International Pediatric Peritoneal Dialysis Network (IPPN) between 2007 and 2024, on automated PD with a daytime dwell.
JAMA Netw Open
September 2025
Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Importance: Exposure to inflammation from chorioamnionitis places the fetus at higher risk of premature birth and may increase the risk of neurodevelopmental impairments, though the evidence for the latter is mixed.
Objective: To evaluate whether moderate to severe histologic chorioamnionitis (HCA) is directly associated with adverse motor performance, independent of the indirect mediating effects of premature birth.
Design, Setting, And Participants: This prospective, population-based cohort study recruited participants between September 16, 2016, and November 19, 2019, from referral and nonreferral neonatal intensive care units of 5 southwestern Ohio hospitals.
Purpose: The purpose of this document is to review current methods for cervical ripening and to summarize the effectiveness of these approaches based on appropriately conducted outcomes-based research. This document focuses on cervical ripening in individuals with term, singleton, vertex pregnancies with membranes intact, because this is the population in whom most studies were conducted. For more information on recommended timing of delivery based on maternal, fetal, and obstetric conditions and on labor management, refer to: American College of Obstetricians and Gynecologists (ACOG) Committee Opinion No.
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