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1.
A A Pract ; 15(8): e01510, 2021 Aug 23.
Article in English | MEDLINE | ID: mdl-34428776

ABSTRACT

Vertebral body tethering (VBT) is an innovative surgical technique used to treat juvenile and adolescent idiopathic scoliosis. The optimal anesthetic technique, including the preferred management of postoperative pain, is not known. In this case series, we describe 3 patients with adolescent idiopathic scoliosis who received either continuous erector spinae plane block (ESPB) catheters or intercostal liposomal bupivacaine for postoperative pain management after bilateral VBT via minithoracotomy.


Subject(s)
Analgesia , Nerve Block , Adolescent , Anesthesia, Local , Anesthetics, Local , Humans , Vertebral Body
3.
Dev Cell ; 47(3): 348-362.e7, 2018 11 05.
Article in English | MEDLINE | ID: mdl-30293838

ABSTRACT

Centromeric chromatin defines the site of kinetochore formation and ensures faithful chromosome segregation. Centromeric identity is epigenetically specified by the incorporation of CENP-A nucleosomes. DNA replication presents a challenge for inheritance of centromeric identity because nucleosomes are removed to allow for replication fork progression. Despite this challenge, CENP-A nucleosomes are stably retained through S phase. We used BioID to identify proteins transiently associated with CENP-A during DNA replication. We found that during S phase, HJURP transiently associates with centromeres and binds to pre-existing CENP-A, suggesting a distinct role for HJURP in CENP-A retention. We demonstrate that HJURP is required for centromeric nucleosome inheritance during S phase. HJURP co-purifies with the MCM2-7 helicase complex and, together with the MCM2 subunit, binds CENP-A simultaneously. Therefore, pre-existing CENP-A nucleosomes require an S phase function of the HJURP chaperone and interaction with MCM2 to ensure faithful inheritance of centromere identity through DNA replication.


Subject(s)
Centromere Protein A/metabolism , DNA-Binding Proteins/metabolism , Nucleosomes/metabolism , Centromere/metabolism , Centromere Protein A/genetics , Chromatin/metabolism , Chromatin Assembly and Disassembly/physiology , Chromosomal Proteins, Non-Histone/metabolism , Chromosome Segregation/physiology , DNA Replication , DNA-Binding Proteins/genetics , Epigenomics , HEK293 Cells , HeLa Cells , Histones/metabolism , Humans , Kinetochores/metabolism , Mitosis/physiology , Nucleosomes/genetics , S Phase
4.
J Grad Med Educ ; 9(1): 118-122, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28261406

ABSTRACT

BACKGROUND: There has been limited evaluation of tools for teaching social determinants of health (SDOH). OBJECTIVE: We evaluated a field trip as a tool for teaching SDOH to incoming medical interns. METHODS: Incoming interns from The George Washington University participated in a bus field trip of Washington, DC, guided by community partners. The field trip introduced trainees to local neighborhoods. Pre- and postactivity surveys developed by the authors were analyzed using a Wilcoxon signed rank test. Reflection responses were recorded and counted for recurrent themes. RESULTS: Incoming interns participated in 2015 (85 of 90, 94%) and in 2016 (96 of 116, 83%). Postactivity, basic knowledge of DC geographic health disparities increased, and a greater percentage of interns reported being at least somewhat comfortable understanding the neighborhoods from which their patients come (2015: 58% versus 89%, P < .0001; 2016: 65% versus 88%, P < .0001); identifying challenges to health care that affect low-income patients (2015: 74% versus 90%, P < .0023); describing community resources (2015: 29% versus 67%, P < .0001; 2016: 29% versus 50%, P < .0001); and referring patients to local community resources (2015: 25% versus 64%, P < .0001; 2016: 36% versus 52%, P < .0001). Interns reported that this experience improved their understanding of patients' background and local resources, and that they would change the way they practice. CONCLUSIONS: A bus field trip guided by community partners is a feasible way to increase residents' perception of their understanding of local disparities and comfort in addressing SDOH.


Subject(s)
Internship and Residency/methods , Social Determinants of Health , Attitude of Health Personnel , Cities , District of Columbia , Education, Medical, Graduate , Healthcare Disparities , Humans , Poverty , Social Welfare , Surveys and Questionnaires
5.
PLoS Genet ; 12(8): e1006302, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27579875

ABSTRACT

[This corrects the article DOI: 10.1371/journal.pgen.1003670.].

6.
Soc Sci Med ; 138: 136-43, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26093071

ABSTRACT

This paper examines the origins of consumerist discourse in health care from a communication perspective via a historical textual analysis of health writing in popular magazines from 1930 to 1949. The focus is on Consumers Union's Consumer Reports and the American Medical Association's lay health magazine, Hygeia. Findings from Consumer Reports show that the consumer movement of the 1930s-40s staunchly advocated for universal health insurance. Whereas consumer rights language nowadays tends towards individual choice and personal responsibility, consumerism in health care during that era articulated ideas about consumer citizenship, framing choice and responsibility in collectivist terms and health care as a social good. This paper also illuminates the limits and weaknesses of a central tenet in consumerism-freedom of choice-by analyzing stories in Hygeia about the doctor-patient relationship. A textual analysis finds that the AMA's justification in the 1930s-40s against socialized medicine, i.e., the freedom to choose a doctor, was in practice highly controlled by the medical profession. Findings show that long before the rhetoric of the "empowered consumer" became popular, some patients exercised some choice even in an era when physicians achieved total professional dominance. But these patients were few and tend to occupy the upper socioeconomic strata of US society. In reality choice was an illusion in a fee-for-service era when most American families could not afford the costs of medical care.


Subject(s)
Communication/history , Delivery of Health Care/history , National Health Insurance, United States/history , American Medical Association/history , Bibliometrics , Choice Behavior , History, 20th Century , Humans , Patient Rights/history , Personal Autonomy , Physician-Patient Relations , Power, Psychological , State Medicine/history , United States
7.
PLoS Genet ; 9(8): e1003670, 2013.
Article in English | MEDLINE | ID: mdl-23935535

ABSTRACT

Suppression of duplication-mediated gross chromosomal rearrangements (GCRs) is essential to maintain genome integrity in eukaryotes. Here we report that SUMO ligase Mms21 has a strong role in suppressing GCRs in Saccharomyces cerevisiae, while Siz1 and Siz2 have weaker and partially redundant roles. Understanding the functions of these enzymes has been hampered by a paucity of knowledge of their substrate specificity in vivo. Using a new quantitative SUMO-proteomics technology, we found that Siz1 and Siz2 redundantly control the abundances of most sumoylated substrates, while Mms21 more specifically regulates sumoylation of RNA polymerase-I and the SMC-family proteins. Interestingly, Esc2, a SUMO-like domain-containing protein, specifically promotes the accumulation of sumoylated Mms21-specific substrates and functions with Mms21 to suppress GCRs. On the other hand, the Slx5-Slx8 complex, a SUMO-targeted ubiquitin ligase, suppresses the accumulation of sumoylated Mms21-specific substrates. Thus, distinct SUMO ligases work in concert with Esc2 and Slx5-Slx8 to control substrate specificity and sumoylation homeostasis to prevent GCRs.


Subject(s)
Ligases/genetics , Nuclear Proteins/genetics , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae/genetics , Sumoylation/genetics , Ubiquitin-Protein Ligases/genetics , Cell Cycle Proteins , Gene Duplication , Genome, Fungal , Genomic Instability , Nuclear Proteins/metabolism , SUMO-1 Protein/metabolism , Saccharomyces cerevisiae/enzymology , Saccharomyces cerevisiae Proteins/metabolism , Substrate Specificity , Ubiquitin-Protein Ligases/metabolism
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