Search Results - "Ostermaier, K"
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Functional map of arrestin-1 at single amino acid resolution
Published in Proceedings of the National Academy of Sciences - PNAS (04-02-2014)“…Arrestins function as adapter proteins that mediate G protein-coupled receptor (GPCR) desensitization, internalization, and additional rounds of signaling…”
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2
RNA polymerase I-specific subunits promote polymerase clustering to enhance the rRNA gene transcription cycle
Published in The Journal of cell biology (24-01-2011)“…RNA polymerase I (Pol I) produces large ribosomal RNAs (rRNAs). In this study, we show that the Rpa49 and Rpa34 Pol I subunits, which do not have counterparts…”
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3
AAscan, PCRdesign and MutantChecker: a suite of programs for primer design and sequence analysis for high-throughput scanning mutagenesis
Published in PloS one (2013)“…Scanning mutagenesis is a powerful protein engineering technique used to study protein structure-function relationship, map binding sites and design more…”
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Immunodeficiency in Down Syndrome: Revisiting Recurrent Infections in the Post-Pneumococcal Vaccination Era
Published in Journal of allergy and clinical immunology (01-02-2011)“…Frequency of RI was significantly associated with history of allergic rhinitis/asthma (odds ratio [OR]:15.8 [95% confidence interval [CI]:4.3-58.5]), GERD…”
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A Road Map for Academic Developmental-Behavioral Pediatric Practices to Increase Access
Published in Journal of developmental and behavioral pediatrics (01-12-2022)“…There are currently at least 19 million children and adolescents in the United States with disorders of development (learning disorders,…”
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Incidence of Celiac Disease in Down Syndrome: A Longitudinal, Population-Based Birth Cohort Study
Published in Clinical pediatrics (01-10-2020)“…American Academy of Pediatrics (AAP) guidelines for children with Down syndrome (DS) include assessment for celiac disease (CD), although data to support this…”
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Insights into congenital stationary night blindness based on the structure of G90D rhodopsin
Published in EMBO reports (01-06-2013)“…We present active‐state structures of the G protein‐coupled receptor (GPCRs) rhodopsin carrying the disease‐causing mutation G90D. Mutations of G90 cause…”
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Immobilization of arrestin-3 on different biosensor platforms for evaluating GPCR binding
Published in Physical chemistry chemical physics : PCCP (28-10-2020)“…G protein-coupled receptors (GPCRs) are a large and ubiquitous family of membrane receptors of great pharmacological interest. Cell-based assays are the…”
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Functional map of arrestin binding to phosphorylated opsin, with and without agonist
Published in Scientific reports (28-06-2016)“…Arrestins desensitize G protein-coupled receptors (GPCRs) and act as mediators of signalling. Here we investigated the interactions of arrestin-1 with two…”
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Molecular mechanism of phosphorylation-dependent arrestin activation
Published in Current opinion in structural biology (01-12-2014)“…•Novel structures provide insight into the arrestin activation mechanism.•Arrestins are pre-activated by a C-tail exchange mechanism.•Functional data for…”
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Arrestin-1 engineering facilitates complex stabilization with native rhodopsin
Published in Scientific reports (24-01-2019)“…Arrestin-1 desensitizes the activated and phosphorylated photoreceptor rhodopsin by forming transient rhodopsin−arrestin-1 complexes that eventually decay to…”
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Constitutively active rhodopsin mutants causing night blindness are effectively phosphorylated by GRKs but differ in arrestin-1 binding
Published in Cellular signalling (01-11-2013)“…The effects of activating mutations associated with night blindness on the stoichiometry of rhodopsin interactions with G protein-coupled receptor kinase 1…”
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Teaching Pediatric Residents to Assess for Autism Spectrum Disorders
Published in Academic pediatrics (01-08-2016)Get full text
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Association of copper-zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele
Published in Birth defects research. A Clinical and molecular teratology (01-10-2012)“…BACKGROUND A common and severe neural tube defect (NTD) phenotype, myelomeningocele (MM), results from the defective closure of the caudal end of the neural…”
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Association of folate receptor (folr1, folr2, folr3) and reduced folate carrier (slc19a1) genes with meningomyelocele
Published in Birth defects research. A Clinical and molecular teratology (01-08-2010)“…Background Meningomyelocele (MM) results from lack of closure of the neural tube during embryologic development. Periconceptional folic acid supplementation is…”
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Corrigendum: Functional map of arrestin binding to phosphorylated opsin, with and without agonist
Published in Scientific reports (22-07-2016)Get full text
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Association of retinoic acid receptor genes with meningomyelocele
Published in Birth defects research. A Clinical and molecular teratology (01-01-2011)“…BACKGROUND Neural tube defects (NTDs) occur in as many as 0.5–2 per 1000 live births in the United States. One of the most common and severe neural tube…”
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Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals
Published in Birth defects research. A Clinical and molecular teratology (01-10-2008)“…BACKGROUND: Meningomyelocele (MM) is a common human birth defect. MM is a disorder of neural development caused by contributions from genes and environmental…”
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A Road Map for Academic Developmental-Behavioral Pediatric Practices to Increase Access
Published in Journal of developmental and behavioral pediatrics (27-09-2022)Get full text
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Correction: Corrigendum: Functional map of arrestin binding to phosphorylated opsin, with and without agonist
Published in Scientific reports (22-07-2016)“…Scientific Reports 6: Article number: 28686; published online: 28 June 2016; updated: 22 July 2016 In this Article, Martin K. Ostermaier is incorrectly listed…”
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