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  • 1
    In: Clinical and Applied Thrombosis/Hemostasis, SAGE Publications, Vol. 16, No. 2 ( 2010-04), p. 161-169
    Abstract: One class of oligonucleotides with a high potential for use in medical applications is short nucleic acids, widely known as aptamers. Although several aptamers are already being used clinically, there are very few studies dealing with the impact aptamers have on the hemostatic system. In this study, we have performed a comprehensive evaluation of the hemostatic system including coagulation, platelets, complement, and inflammatory activation by using different aptamer concentrations and fresh human whole blood in a well-established flow model. We found that single-stranded aptamers did not have a negative influence on platelets, complement, or inflammation but were able to activate factor XII, kallikrein, and prothrombin in a concentration-dependent manner. Consequently, the influence of aptamers on the coagulation system should be taken into consideration before the use of any aptamer-based drugs in patients.
    Type of Medium: Online Resource
    ISSN: 1076-0296 , 1938-2723
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2010
    detail.hit.zdb_id: 2230591-9
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  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 2014
    In:  HAND Vol. 9, No. 4 ( 2014-12), p. 466-470
    In: HAND, SAGE Publications, Vol. 9, No. 4 ( 2014-12), p. 466-470
    Abstract: Flexor digitorum superficialis (FDS) arch is a site of compression in pronator syndrome yet little is known about its anatomic structure. The purpose of the study is to delineate the surgical anatomy of the FDS arch along with its relationship to the anterior interosseous nerve (AIN) takeoff. Methods Thirty-eight cadavers were dissected using a modified Henry's approach. The FDS arch was identified, and its distance to the antebrachial crease and medial and lateral epicondyle were measured. The FDS arch was divided in a sequential fashion until adequate decompression of the median nerve was achieved. The total length of the release was measured. The takeoff of the AIN was identified in relation to the FDS arch. Results Two types of the FDS arch were discovered, a distinct fibrous arch and an indistinct fibrous arch with vertical fibers blending into overlying fascia. Only 42 % of specimens had a distinct FDS arch averaging 1.69 cm in length. The majority of specimens had an indistinct arch, and of those, 77 % had overlying muscle, requiring an average release of 2.6 cm. The AIN branched at or distal to the FDS arch in 74 % of specimens, and only 8 % was found to have an ulnar-sided origin off the median nerve. Conclusions A longer surgical release is needed with indistinct FDS arches. Overlying muscle during dissection may be indicative of an indistinct arch. Dissection along the ulnar side of the median nerve can possibly decrease the chance of injury to the AIN during decompression.
    Type of Medium: Online Resource
    ISSN: 1558-9447 , 1558-9455
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2014
    detail.hit.zdb_id: 2316440-2
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  • 3
    Online Resource
    Online Resource
    SAGE Publications ; 2014
    In:  Experimental Biology and Medicine Vol. 239, No. 9 ( 2014-09), p. 1215-1224
    In: Experimental Biology and Medicine, SAGE Publications, Vol. 239, No. 9 ( 2014-09), p. 1215-1224
    Abstract: The tremendous cost of drug development is often attributed to the long time interval between identifying lead compounds in preclinical studies to assessing clinical efficacy in randomized clinical trials. Many candidate molecules show promise in cell culture or animal models, only to fail in late stage in human investigations. There is a need for novel technologies that allow investigators to quickly and reliably predict drug safety and efficacy. The advent of microtechnology has made it possible to integrate multiple microphysiologic organ systems into a single microfabricated chip. This review focuses on three-dimensional engineered skin, which has enjoyed a long history of uses both in clinical treatments of refractory ulcers and as a laboratory model. We discuss current biological and engineering challenges in construction of a robust bioengineered skin and provide a blueprint for its potential utility to model dermatologic disorders such as psoriasis or cutaneous drug reactions.
    Type of Medium: Online Resource
    ISSN: 1535-3702 , 1535-3699
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2014
    detail.hit.zdb_id: 2020856-X
    SSG: 12
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  • 4
    In: Nonprofit and Voluntary Sector Quarterly, SAGE Publications, Vol. 52, No. 1_suppl ( 2023-04), p. 12S-28S
    Type of Medium: Online Resource
    ISSN: 0899-7640 , 1552-7395
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2023
    detail.hit.zdb_id: 2029449-9
    SSG: 3,4
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 2016
    In:  Nonprofit and Voluntary Sector Quarterly Vol. 45, No. 5 ( 2016-10), p. 885-887
    In: Nonprofit and Voluntary Sector Quarterly, SAGE Publications, Vol. 45, No. 5 ( 2016-10), p. 885-887
    Type of Medium: Online Resource
    ISSN: 0899-7640 , 1552-7395
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2016
    detail.hit.zdb_id: 2029449-9
    SSG: 3,4
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  • 6
    Online Resource
    Online Resource
    SAGE Publications ; 2015
    In:  Journal of Child Neurology Vol. 30, No. 12 ( 2015-10), p. 1633-1639
    In: Journal of Child Neurology, SAGE Publications, Vol. 30, No. 12 ( 2015-10), p. 1633-1639
    Abstract: The preterm cerebellum is vulnerable to impaired development impacting long-term outcome. Preterm newborns ( 〈 32 weeks) underwent serial magnetic resonance imaging (MRI) scans. The association between parental education and cerebellar volume at each time point was assessed, adjusting for age at scan. In 26 infants, cerebellar volumes at term ( P = .001), but not birth ( P = .4), were associated with 2-year volumes. For 1 cm 3 smaller cerebellar volume (4% total volume) at term, the cerebellum was 3.18 cm 3 smaller (3% total volume) by 2 years. Maternal postsecondary education was not associated with cerebellar volume at term ( P = .16). Maternal postsecondary education was a significant confounder in the relationship between term and 2-year cerebellar volumes ( P = .016), with higher education associated with improved volumes by 2 years. Although preterm birth has been found to be associated with smaller cerebellar volumes at term, maternal postsecondary education is associated with improved growth detectable by 2 years.
    Type of Medium: Online Resource
    ISSN: 0883-0738 , 1708-8283
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2015
    detail.hit.zdb_id: 2068710-2
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  • 7
    Online Resource
    Online Resource
    SAGE Publications ; 2019
    In:  Nonprofit and Voluntary Sector Quarterly Vol. 48, No. 5 ( 2019-10), p. 907-909
    In: Nonprofit and Voluntary Sector Quarterly, SAGE Publications, Vol. 48, No. 5 ( 2019-10), p. 907-909
    Type of Medium: Online Resource
    ISSN: 0899-7640 , 1552-7395
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2019
    detail.hit.zdb_id: 2029449-9
    SSG: 3,4
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  • 8
    Online Resource
    Online Resource
    SAGE Publications ; 2020
    In:  Nonprofit and Voluntary Sector Quarterly Vol. 49, No. 6 ( 2020-12), p. 1117-1118
    In: Nonprofit and Voluntary Sector Quarterly, SAGE Publications, Vol. 49, No. 6 ( 2020-12), p. 1117-1118
    Type of Medium: Online Resource
    ISSN: 0899-7640 , 1552-7395
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2020
    detail.hit.zdb_id: 2029449-9
    SSG: 3,4
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  • 9
    In: Public Health Reports, SAGE Publications
    Abstract: To help achieve the initial goal of providing universal COVID-19 vaccine access to approximately 258 million adults in 62 US jurisdictions, the federal government launched the Federal Retail Pharmacy Program (FRPP) on February 11, 2021. We describe FRPP’s collaboration among the federal government, US jurisdictions, federal entity partners, and 21 national chain and independent pharmacy networks to provide large-scale access to COVID-19 vaccines, particularly in communities disproportionately affected by COVID-19 (eg, people aged ≥65 years, people from racial and ethnic minority groups). FRPP initially provided 10 000 vaccination sites for people to access COVID-19 vaccines, which was increased to 〉 35 000 vaccination sites by May 2021 and sustained through January 31, 2022. From February 11, 2021, through January 31, 2022, FRPP vaccination sites received 293 million doses and administered 219 million doses, representing 45% of all COVID-19 immunizations provided nationwide (38% of all first doses, 72% of all booster doses). This unprecedented public–private partnership allowed the federal government to rapidly adapt and scale up an equitable vaccination program to reach adults, later expanding access to vaccine-eligible children, during the COVID-19 pandemic. As the largest federal COVID-19 vaccination program, FRPP exemplifies how public–private partnerships can expand access to immunizations during a public health emergency. Pharmacies can help meet critical national public health goals by serving as convenient access points for sustained health services. Lessons learned from this effort—including the importance of strong coordination and communication, efficient reporting systems and data quality, and increasing access to and demand for vaccine, among others—may help improve future immunization programs and support health system resiliency, emphasizing community-level access and health equity during public health emergencies.
    Type of Medium: Online Resource
    ISSN: 0033-3549 , 1468-2877
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2023
    detail.hit.zdb_id: 2017700-8
    SSG: 20,1
    SSG: 27
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  • 10
    Online Resource
    Online Resource
    SAGE Publications ; 2017
    In:  Experimental Biology and Medicine Vol. 242, No. 17 ( 2017-11), p. 1657-1668
    In: Experimental Biology and Medicine, SAGE Publications, Vol. 242, No. 17 ( 2017-11), p. 1657-1668
    Abstract: Many diseases, as well as side effects of drugs, manifest themselves through skin symptoms. Skin is a complex tissue that hosts various specialized cell types and performs many roles including physical barrier, immune and sensory functions. Therefore, modeling skin in vitro presents technical challenges for tissue engineering. Since the first attempts at engineering human epidermis in 1970s, there has been a growing interest in generating full-thickness skin constructs mimicking physiological functions by incorporating various skin components, such as vasculature and melanocytes for pigmentation. Development of biomimetic in vitro human skin models with these physiological functions provides a new tool for drug discovery, disease modeling, regenerative medicine and basic research for skin biology. This goal, however, has long been delayed by the limited availability of different cell types, the challenges in establishing co-culture conditions, and the ability to recapitulate the 3D anatomy of the skin. Recent breakthroughs in induced pluripotent stem cell (iPSC) technology and microfabrication techniques such as 3D-printing have allowed for building more reliable and complex in vitro skin models for pharmaceutical screening. In this review, we focus on the current developments and prevailing challenges in generating skin constructs with vasculature, skin appendages such as hair follicles, pigmentation, immune response, innervation, and hypodermis. Furthermore, we discuss the promising advances that iPSC technology offers in order to generate in vitro models of genetic skin diseases, such as epidermolysis bullosa and psoriasis. We also discuss how future integration of the next generation human skin constructs onto microfluidic platforms along with other tissues could revolutionize the early stages of drug development by creating reliable evaluation of patient-specific effects of pharmaceutical agents. Impact statement Skin is a complex tissue that hosts various specialized cell types and performs many roles including barrier, immune, and sensory functions. For human-relevant drug testing, there has been a growing interest in building more physiological skin constructs by incorporating different skin components, such as vasculature, appendages, pigment, innervation, and adipose tissue. This paper provides an overview of the strategies to build complex human skin constructs that can faithfully recapitulate human skin and thus can be used in drug development targeting skin diseases. In particular, we discuss recent developments and remaining challenges in incorporating various skin components, availability of iPSC-derived skin cell types and in vitro skin disease models. In addition, we provide insights on the future integration of these complex skin models with other organs on microfluidic platforms as well as potential readout technologies for high-throughput drug screening.
    Type of Medium: Online Resource
    ISSN: 1535-3702 , 1535-3699
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2017
    detail.hit.zdb_id: 2020856-X
    SSG: 12
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