Bayesian inference of molecular kinetic parameters from astrocyte calcium imaging data

Bayesian inference of molecular kinetic parameters from astrocyte calcium imaging data

Model-based Bayesian inference from high-content data obtained on live specimens is a burgeoning field with demonstrated applications to neuroscience. In parallel, computer vision methods for extracting the calcium signaling information from imaging data have advanced in application to neuronal phys...

Full description

Bibliographic Details
Main Authors:	Ivan V. Maly, Wilma A. Hofmann
Format:	Article
Language:	English
Published:	Elsevier 2022-01-01
Series:	MethodsX
Subjects:	Schizophrenia 22q11.2 deletion syndrome Glia Model-based inference Li-Rinzel model Calcium dynamics
Online Access:	http://www.sciencedirect.com/science/article/pii/S2215016122002059

Similar Items

Consequences of 22q11.2 Microdeletion on the Genome, Individual and Population Levels
by: Małgorzata Karbarz
Published: (2020-08-01)

Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies
by: Paula Sandrin-Garcia, et al.
Published: (2007-01-01)

A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
by: Arisa Tsurue, et al.
Published: (2023-06-01)

Characterization and prediction of clinical pathways of vulnerability to psychosis through graph signal processing
by: Corrado Sandini, et al.
Published: (2021-09-01)

Schizophrenia patients and 22q11.2 deletion syndrome adolescents at risk express the same deviant patterns of resting state EEG microstates: A candidate endophenotype of schizophrenia
by: Miralena I. Tomescu, et al.
Published: (2015-09-01)

Hypoparathyroidism concomitant with macrothrombocytopenia in an elderly woman with 22q11.2 deletion syndrome
by: Hsiu-Chien Yang, et al.
Published: (2018-10-01)

Palatoschisis, Schizophrenia and Hypocalcaemia: Phenotypic Expression of 22q11.2 Deletion Syndrome (DiGeorge Syndrome) in an Adult
by: Melissa Elise van der Meijs, et al.
Published: (2021-04-01)

Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
by: Jente Verbesselt, et al.
Published: (2023-03-01)

The impact of social cognition deficits on real life functioning in 22q11.2 deletion syndrome: A comparative study with a large population of patients with schizophrenia
by: T. Accinni, et al.
Published: (2021-04-01)

Treatment of 22q11.2 deletion syndrome-associated schizophrenia with comorbid anxiety and panic disorder
by: Candace B. Borders, et al.
Published: (2017-10-01)

Genotypic and phenotypic variability of 22q11.2 microdeletions – an institutional experience
by: Gabrielle C. Manno, et al.
Published: (2021-12-01)

Recurrent convulsions, hypocalcemia, and hypoparathyroidism related to delayed diagnosis of 22q11.2 deletion syndrome in a middle‐aged man
by: Tomoya Okazaki, et al.
Published: (2016-10-01)

Parent-Reported Social-Communicative Skills of Children with 22q11.2 Copy Number Variants and Siblings
by: Jente Verbesselt, et al.
Published: (2022-10-01)

The Unique Experience of a New Multidisciplinary Program for 22q Deletion and Duplication Syndromes in a Community Hospital in Florida: A Reaffirmation That Multidisciplinary Care Is Essential for Best Outcomes in These Patients
by: Zaimary Meneses, et al.
Published: (2022-10-01)

Differential resting-state patterns across networks are spatially associated with Comt and Trmt2a gene expression patterns in a mouse model of 22q11.2 deletion
by: Natalia Gass, et al.
Published: (2021-11-01)

Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years’ experience in Catalonia (Spain)
by: Andrea Martin‐Nalda, et al.
Published: (2019-12-01)

Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
by: Yen-Ni Chen, et al.
Published: (2016-02-01)

Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders
by: Ryo Saito, et al.
Published: (2021-04-01)

Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome
by: Kathryn L. McCabe, et al.
Published: (2019-12-01)

Prenatal diagnosis of rearrangements in the fetal 22q11.2 region
by: Suping Li, et al.
Published: (2020-07-01)

Contribution of Mitochondrial DNA Heteroplasmy to the Congenital Cardiac and Palatal Phenotypic Variability in Maternally Transmitted 22q11.2 Deletion Syndrome
by: Boris Rebolledo-Jaramillo, et al.
Published: (2021-01-01)

The 22q11.2 Low Copy Repeats
by: Lisanne Vervoort, et al.
Published: (2022-11-01)

A Case of Bernard-Soulier Syndrome Associated with 22q11.2 Deletion Syndrome
by: Oh Cheol Kwon, et al.
Published: (2023-10-01)

Relationship between high trait anxiety in 22q11.2 deletion syndrome and the difficulties in medical, welfare, and educational services
by: Naomi Nakajima, et al.
Published: (2023-03-01)

The genetic landscape of polymicrogyria
by: Jesmy James, et al.
Published: (2022-01-01)

Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
by: Yu-Ling Kuo, et al.
Published: (2014-06-01)

A case report of a Chinese patient with 22q11.2 deletion accompanied with EOPD, severe dystonia and hypocalcemia
by: Zheng-Xiang Hu, et al.
Published: (2019-01-01)

Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome
by: Hidenori Tabata, et al.
Published: (2023-04-01)

22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis
by: Steven de Reuver, et al.
Published: (2021-10-01)

22q11.2 deletion (DiGeorge) syndrome: a mother’s open letter
by: Antonio Baldini, et al.
Published: (2011-07-01)

FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME
by: I. A. Tuzankina, et al.
Published: (2017-01-01)

Optometry in adults with microdeletion 22q11.2: The eye as a window to the brain
by: Emma N.M.M. von Scheibler, et al.
Published: (2023-12-01)

Tonsillectomy in Children with 22q11.2 Deletion Syndrome
by: Jill M. Arganbright, et al.
Published: (2022-11-01)

Structural Cerebellar Abnormalities and Parkinsonism in Patients with 22q11.2 Deletion Syndrome
by: Claudia Piervincenzi, et al.
Published: (2022-11-01)

The Relationships between Dopaminergic, Glutamatergic, and Cognitive Functioning in 22q11.2 Deletion Syndrome: A Cross-Sectional, Multimodal <sup>1</sup>H-MRS and <sup>18</sup>F-Fallypride PET Study
by: Carmen F. M. van Hooijdonk, et al.
Published: (2022-09-01)

A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome
by: Steven Pastor, et al.
Published: (2022-09-01)

Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms
by: Nicholas A Donnelly, et al.
Published: (2022-08-01)

Familial 22q11.2 deletion syndrome with autosomal dominant inheritance
by: Bahar Gokturk, et al.
Published: (2016-06-01)

Self-Reported Speech Problems in Adolescents and Young Adults with 22q11.2 Deletion Syndrome: A Cross-Sectional Cohort Study
by: Nicole E Spruijt, et al.
Published: (2014-09-01)

DiGeorge Syndrome: a not so rare disease
by: Angela BF Fomin, et al.
Published: (2010-01-01)