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  1. Article ; Online: Clinical Outcomes of Single-Stage Revision Anterior Cruciate Ligament Reconstruction Using a Fast-Setting Bone Graft Substitute.

    Rogers, Joseph D / Adsit, Matthew H / Serbin, Philip A / Worcester, Katherine S / Firoved, Amanda B / Bonner, Kevin F

    The journal of knee surgery

    2023  

    Abstract: Revision anterior cruciate ligament reconstruction (ACLR) can be achieved in a single-stage or two-stage approach. Single-stage revisions have several advantages, including one less operation, decreased cost, and a quicker recovery for patients. Revision ...

    Abstract Revision anterior cruciate ligament reconstruction (ACLR) can be achieved in a single-stage or two-stage approach. Single-stage revisions have several advantages, including one less operation, decreased cost, and a quicker recovery for patients. Revision ACLR can be complicated by malpositioned or dilated bone tunnels, which makes a single-stage revision more challenging or sometimes necessitates a two-stage approach. The use of fast-setting bone graft substitutes (BGS) has been described in recent literature as a strategy to potentially help address this problem in the setting of single-stage revision ACLR. The aim of this study was to evaluate patient-reported clinical outcomes of patients who have undergone single-stage revision ACLR using fast-setting BGS to address prior malpositioned or dilated tunnels. A retrospective review was conducted of the first nine consecutive patients who had undergone single-stage revision ACLR using a fast-setting BGS by a single surgeon between May 2017 and February 2020 with a minimum of 2-year follow-up. Patient-reported clinical outcomes, including the International Knee Documentation Committee (IKDC) questionnaire, the Tegner Lysholm Knee Scoring Scale, patient satisfaction questions, and the need for additional surgery were evaluated for this group between 26 and 49 months postoperative. Of the nine patients eligible for inclusion, eight patients (88.9%) were evaluated, and one was lost to follow-up. At an average follow-up of 37.9 months (range: 27.8-55.7), the mean postoperative IKDC score was 75.0 ± 11.3, and the mean postoperative Tegner Lysholm Knee Score was 83.0 ± 17.6. None of the patients required additional revision surgery or experienced construct failure at the time of follow-up. Seven of eight respondents (87.5%) had their preoperative expectations met with the surgery, and 100% of patients stated they would have the surgery again. Single-stage revision ACLR using fast-setting BGS showed overall positive clinical outcomes for this pilot group of patients at a minimum 2-year follow-up. In select revision scenarios, these materials may be a valuable option to allow the filling of defects without compromising fixation or clinical outcomes.
    Language English
    Publishing date 2023-12-04
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 2075354-8
    ISSN 1938-2480 ; 1538-8506 ; 0899-7403
    ISSN (online) 1938-2480
    ISSN 1538-8506 ; 0899-7403
    DOI 10.1055/s-0043-1777053
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Repair of spinal cord injury with neuronal relays: From fetal grafts to neural stem cells.

    Bonner, Joseph F / Steward, Oswald

    Brain research

    2015  Volume 1619, Page(s) 115–123

    Abstract: Spinal cord injury (SCI) disrupts the long axonal tracts of the spinal cord leading to devastating loss of function. Cell transplantation in the injured spinal cord has the potential to lead to recovery after SCI via a variety of mechanisms. One such ... ...

    Abstract Spinal cord injury (SCI) disrupts the long axonal tracts of the spinal cord leading to devastating loss of function. Cell transplantation in the injured spinal cord has the potential to lead to recovery after SCI via a variety of mechanisms. One such strategy is the formation of neuronal relays between injured long tract axons and denervated neurons. The idea of creating a neuronal relay was first proposed over 25 years ago when fetal tissue was first successfully transplanted into the injured rodent spinal cord. Advances in labeling of grafted cells and the development of neural stem cell culturing techniques have improved the ability to create and refine such relays. Several recent studies have examined the ability to create a novel neuronal circuit between injured axons and denervated targets. This approach is an alternative to long-distance regeneration of damaged axons that may provide a meaningful degree of recovery without direct recreation of lost pathways. This brief review will examine the contribution of fetal grafting to current advances in neuronal grafting. Of particular interest will be the ability of transplanted neurons derived from fetal grafts, neural precursor cells and neural stem cells to reconnect long distance motor and sensory pathways of the injured spinal cord. This article is part of a Special Issue entitled SI: Spinal cord injury.
    MeSH term(s) Animals ; Axons/physiology ; Graft Survival ; Humans ; Neural Stem Cells/physiology ; Neural Stem Cells/transplantation ; Neurons/physiology ; Spinal Cord Injuries/physiopathology ; Spinal Cord Injuries/surgery ; Synaptic Transmission
    Language English
    Publishing date 2015-09-04
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1200-2
    ISSN 1872-6240 ; 0006-8993
    ISSN (online) 1872-6240
    ISSN 0006-8993
    DOI 10.1016/j.brainres.2015.01.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Clinical Outcomes of Single-Stage Revision Anterior Cruciate Ligament Reconstruction Using a Fast-Setting Bone Graft Substitute

    Rogers, Joseph D. / Adsit, Matthew H. / Serbin, Philip A. / Worcester, Katherine S. / Firoved, Amanda B. / Bonner, Kevin F.

    The Journal of Knee Surgery

    2023  

    Abstract: Revision anterior cruciate ligament reconstruction (ACLR) can be achieved in a single-stage or two-stage approach. Single-stage revisions have several advantages, including one less operation, decreased cost, and a quicker recovery for patients. Revision ...

    Abstract Revision anterior cruciate ligament reconstruction (ACLR) can be achieved in a single-stage or two-stage approach. Single-stage revisions have several advantages, including one less operation, decreased cost, and a quicker recovery for patients. Revision ACLR can be complicated by malpositioned or dilated bone tunnels, which makes a single-stage revision more challenging or sometimes necessitates a two-stage approach. The use of fast-setting bone graft substitutes (BGS) has been described in recent literature as a strategy to potentially help address this problem in the setting of single-stage revision ACLR. The aim of this study was to evaluate patient-reported clinical outcomes of patients who have undergone single-stage revision ACLR using fast-setting BGS to address prior malpositioned or dilated tunnels. A retrospective review was conducted of the first nine consecutive patients who had undergone single-stage revision ACLR using a fast-setting BGS by a single surgeon between May 2017 and February 2020 with a minimum of 2-year follow-up. Patient-reported clinical outcomes, including the International Knee Documentation Committee (IKDC) questionnaire, the Tegner Lysholm Knee Scoring Scale, patient satisfaction questions, and the need for additional surgery were evaluated for this group between 26 and 49 months postoperative. Of the nine patients eligible for inclusion, eight patients (88.9%) were evaluated, and one was lost to follow-up. At an average follow-up of 37.9 months (range: 27.8–55.7), the mean postoperative IKDC score was 75.0 ± 11.3, and the mean postoperative Tegner Lysholm Knee Score was 83.0 ± 17.6. None of the patients required additional revision surgery or experienced construct failure at the time of follow-up. Seven of eight respondents (87.5%) had their preoperative expectations met with the surgery, and 100% of patients stated they would have the surgery again. Single-stage revision ACLR using fast-setting BGS showed overall positive clinical outcomes for this pilot group of patients at a minimum 2-year follow-up. In select revision scenarios, these materials may be a valuable option to allow the filling of defects without compromising fixation or clinical outcomes.
    Keywords ACL reconstruction ; bone graft substitutes ; revision ACLR ; grafting ACL tunnels
    Language English
    Publishing date 2023-12-04
    Publisher Thieme Medical Publishers, Inc.
    Publishing place Stuttgart ; New York
    Document type Article
    ZDB-ID 2075354-8
    ISSN 1938-2480 ; 1538-8506 ; 0899-7403
    ISSN (online) 1938-2480
    ISSN 1538-8506 ; 0899-7403
    DOI 10.1055/s-0043-1777053
    Database Thieme publisher's database

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  4. Article ; Online: Preparation of neural stem cells and progenitors: neuronal production and grafting applications.

    Bonner, Joseph F / Haas, Christopher J / Fischer, Itzhak

    Methods in molecular biology (Clifton, N.J.)

    2013  Volume 1078, Page(s) 65–88

    Abstract: Neural stem cells (NSC) are not only a valuable tool for the study of neural development and function, but an integral component in the development of transplantation strategies for neural disease. NSC can be used to study how neurons acquire distinct ... ...

    Abstract Neural stem cells (NSC) are not only a valuable tool for the study of neural development and function, but an integral component in the development of transplantation strategies for neural disease. NSC can be used to study how neurons acquire distinct phenotypes and how the reciprocal interactions between neurons and glia in the developing nervous system shape the structure and function of the central nervous system (CNS). In addition, neurons prepared from NSC can be used to elucidate the molecular basis of neurological disorders as well as potential treatments. Although NSC can be derived from different species and many sources, including embryonic stem cells, induced pluripotent stem cells, adult CNS, and direct reprogramming of non-neural cells, isolating primary NSC directly from rat fetal tissue is the most common technique for preparation and study of neurons with a wealth of data available for comparison. Regardless of the source material, similar techniques are used to maintain NSC in culture and to differentiate NSC toward mature neural lineages. This chapter will describe specific methods for isolating multipotent NSC and neural precursor cells (NPC) from embryonic rat CNS tissue (mostly spinal cord). In particular, NPC can be separated into neuronal and glial restricted precursors (NRP and GRP, respectively) and used to reliably produce neurons or glial cells both in vitro and following transplantation into the adult CNS. This chapter will describe in detail the methods required for the isolation, propagation, storage, and differentiation of NSC and NPC isolated from rat spinal cords for subsequent in vitro or in vivo studies.
    MeSH term(s) Animals ; Cell Culture Techniques/methods ; Cell Differentiation/drug effects ; Cell Lineage/drug effects ; Cell Separation/methods ; Chick Embryo ; Collagenases/pharmacology ; Cryopreservation ; Culture Media/chemistry ; Fibronectins/pharmacology ; Immunohistochemistry ; Laminin/pharmacology ; Neural Stem Cells/cytology ; Neural Stem Cells/transplantation ; Neuroepithelial Cells/cytology ; Neurons/cytology ; Polylysine/pharmacology ; Rats ; Spinal Cord/cytology ; Stem Cell Transplantation
    Chemical Substances Culture Media ; Fibronectins ; Laminin ; Polylysine (25104-18-1) ; Collagenases (EC 3.4.24.-) ; collagenase 1 (EC 3.4.24.-)
    Language English
    Publishing date 2013
    Publishing country United States
    Document type Journal Article
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-62703-640-5_7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Characterization of ectopic colonies that form in widespread areas of the nervous system with neural stem cell transplants into the site of a severe spinal cord injury.

    Steward, Oswald / Sharp, Kelli G / Yee, Kelly Matsudaira / Hatch, Maya N / Bonner, Joseph F

    The Journal of neuroscience : the official journal of the Society for Neuroscience

    2014  Volume 34, Issue 42, Page(s) 14013–14021

    Abstract: We reported previously the formation of ectopic colonies in widespread areas of the nervous system after transplantation of fetal neural stem cells (NSCs) into spinal cord transection sites. Here, we characterize the incidence, distribution, and cellular ...

    Abstract We reported previously the formation of ectopic colonies in widespread areas of the nervous system after transplantation of fetal neural stem cells (NSCs) into spinal cord transection sites. Here, we characterize the incidence, distribution, and cellular composition of the colonies. NSCs harvested from E14 spinal cords from rats that express GFP were treated with a growth factor cocktail and grafted into the site of a complete spinal cord transection. Two months after transplant, spinal cord and brain tissue were analyzed histologically. Ectopic colonies were found at long distances from the transplant in the central canal of the spinal cord, the surface of the brainstem and spinal cord, and in the fourth ventricle. Colonies were present in 50% of the rats, and most rats had multiple colonies. Axons extended from the colonies into the host CNS. Colonies were strongly positive for nestin, a marker for neural precursors, and contained NeuN-positive cells with processes resembling dendrites, GFAP-positive astrocytes, APC/CC1-positive oligodendrocytes, and Ki-67-positive cells, indicating ongoing proliferation. Stereological analyses revealed an estimated 21,818 cells in a colony in the fourth ventricle, of which 1005 (5%) were Ki-67 positive. Immunostaining for synaptic markers (synaptophysin and VGluT-1) revealed large numbers of synaptophysin-positive puncta within the colonies but fewer VGluT-1 puncta. Continuing expansion of NSC-derived cell masses in confined spaces in the spinal cord and brain could produce symptoms attributable to compression of nearby tissue. It remains to be determined whether other cell types with self-renewing potential can also form colonies.
    MeSH term(s) Animals ; Choristoma ; Female ; Nervous System/pathology ; Neural Stem Cells/transplantation ; Pregnancy ; Rats ; Rats, Inbred F344 ; Severity of Illness Index ; Spinal Cord Injuries/pathology ; Spinal Cord Injuries/therapy ; Stem Cell Transplantation/methods
    Language English
    Publishing date 2014-10-16
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 604637-x
    ISSN 1529-2401 ; 0270-6474
    ISSN (online) 1529-2401
    ISSN 0270-6474
    DOI 10.1523/JNEUROSCI.3066-14.2014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Developing international open science collaborations: Funder reflections on the Open Science Prize.

    Kittrie, Elizabeth / Atienza, Audie A / Kiley, Robert / Carr, David / MacFarlane, Aki / Pai, Vinay / Couch, Jennifer / Bajkowski, Jared / Bonner, Joseph F / Mietchen, Daniel / Bourne, Philip E

    PLoS biology

    2017  Volume 15, Issue 8, Page(s) e2002617

    Abstract: The Open Science Prize was established with the following objectives: first, to encourage the crowdsourcing of open data to make breakthroughs that are of biomedical significance; second, to illustrate that funders can indeed work together when ... ...

    Abstract The Open Science Prize was established with the following objectives: first, to encourage the crowdsourcing of open data to make breakthroughs that are of biomedical significance; second, to illustrate that funders can indeed work together when scientific interests are aligned; and finally, to encourage international collaboration between investigators with the intent of achieving important innovations that would not be possible otherwise. The process for running the competition and the successes and challenges that arose are presented.
    MeSH term(s) Awards and Prizes ; Crowdsourcing ; Internationality
    Keywords covid19
    Language English
    Publishing date 2017-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2126776-5
    ISSN 1545-7885 ; 1544-9173
    ISSN (online) 1545-7885
    ISSN 1544-9173
    DOI 10.1371/journal.pbio.2002617
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Heterozygote advantage at HLA class I and II loci and reduced risk of colorectal cancer.

    Tsai, Ya-Yu / Qu, Chenxu / Bonner, Joseph D / Sanz-Pamplona, Rebeca / Lindsey, Sidney S / Melas, Marilena / McDonnell, Kevin J / Idos, Gregory E / Walker, Christopher P / Tsang, Kevin K / Da Silva, Diane M / Moratalla-Navarro, Ferran / Maoz, Asaf / Rennert, Hedy S / Kast, W Martin / Greenson, Joel K / Moreno, Victor / Rennert, Gad / Gruber, Stephen B /
    Schmit, Stephanie L

    Frontiers in immunology

    2023  Volume 14, Page(s) 1268117

    Abstract: Objective: Reduced diversity at Human Leukocyte Antigen (HLA) loci may adversely affect the host's ability to recognize tumor neoantigens and subsequently increase disease burden. We hypothesized that increased heterozygosity at HLA loci is associated ... ...

    Abstract Objective: Reduced diversity at Human Leukocyte Antigen (HLA) loci may adversely affect the host's ability to recognize tumor neoantigens and subsequently increase disease burden. We hypothesized that increased heterozygosity at HLA loci is associated with a reduced risk of developing colorectal cancer (CRC).
    Methods: We imputed HLA class I and II four-digit alleles using genotype data from a population-based study of 5,406 cases and 4,635 controls from the Molecular Epidemiology of Colorectal Cancer Study (MECC). Heterozygosity at each HLA locus and the number of heterozygous genotypes at HLA class -I (
    Results: Individuals with all heterozygous genotypes at all three class I genes had a reduced odds of CRC (OR: 0.74; 95% CI: 0.56-0.97,
    Conclusion: Our findings support a heterozygote advantage for the HLA class-I and -II loci, indicating an important role for HLA genetic variability in the etiology of CRC.
    MeSH term(s) Humans ; Heterozygote ; Gene Frequency ; Histocompatibility Antigens Class I/genetics ; Histocompatibility Antigens Class II/genetics ; HLA Antigens ; Colorectal Neoplasms/genetics ; Receptors, Antigen, T-Cell/genetics
    Chemical Substances Histocompatibility Antigens Class I ; Histocompatibility Antigens Class II ; HLA Antigens ; Receptors, Antigen, T-Cell
    Language English
    Publishing date 2023-10-24
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1268117
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Travel history among persons infected with SARS-CoV-2 variants of concern in the United States, December 2020-February 2021.

    Dunajcik, Alicia / Haire, Kambria / Thomas, Jennifer D / Moriarty, Leah F / Springer, Yuri / Villanueva, Julie M / MacNeil, Adam / Silk, Benjamin / Nemhauser, Jeffrey B / Byrkit, Ramona / Taylor, Melanie / Queen, Krista / Tong, Suxiang / Lee, Justin / Batra, Dhwani / Paden, Clinton / Henderson, Tiffany / Kunkes, Audrey / Ojo, Mojisola /
    Firestone, Melanie / Martin Webb, Lindsey / Freeland, Melissa / Brown, Catherine M / Williams, Thelonious / Allen, Krisandra / Kauerauf, Judy / Wilson, Erica / Jain, Seema / McDonald, Eric / Silver, Elana / Stous, Sarah / Wadford, Debra / Radcliffe, Rachel / Marriott, Chandra / Owes, Jennifer P / Bart, Stephen M / Sosa, Lynn E / Oakeson, Kelly / Wodniak, Natalie / Shaffner, Julia / Brown, Quanta / Westergaard, Ryan / Salinas, Andrea / Hallyburton, Sara / Ogale, Yasmin / Offutt-Powell, Tabatha / Bonner, Kimberly / Tubach, Sheri / Van Houten, Clay / Hughes, Victoria / Reeb, Valerie / Galeazzi, Chris / Khuntia, Shreya / McGee, Sasha / Hicks, Joseph T / Dinesh Patel, Dimple / Krueger, Anna / Hughes, Scott / Jeanty, Fabiana / Wang, Jade C / Lee, Ellen H / Assanah-Deane, Tracey / Tompkins, Megan / Dougherty, Kendra / Naqvi, Ozair / Donahue, Matthew / Frederick, Justin / Abdalhamid, Baha / Powers, Ann M / Anderson, Mark

    PLOS global public health

    2023  Volume 3, Issue 3, Page(s) e0001252

    Abstract: The first three SARS-CoV-2 phylogenetic lineages classified as variants of concern (VOCs) in the United States (U.S.) from December 15, 2020 to February 28, 2021, Alpha (B.1.1.7), Beta (B.1.351), and Gamma (P.1) lineages, were initially detected ... ...

    Abstract The first three SARS-CoV-2 phylogenetic lineages classified as variants of concern (VOCs) in the United States (U.S.) from December 15, 2020 to February 28, 2021, Alpha (B.1.1.7), Beta (B.1.351), and Gamma (P.1) lineages, were initially detected internationally. This investigation examined available travel history of coronavirus disease 2019 (COVID-19) cases reported in the U.S. in whom laboratory testing showed one of these initial VOCs. Travel history, demographics, and health outcomes for a convenience sample of persons infected with a SARS-CoV-2 VOC from December 15, 2020 through February 28, 2021 were provided by 35 state and city health departments, and proportion reporting travel was calculated. Of 1,761 confirmed VOC cases analyzed, 1,368 had available data on travel history. Of those with data on travel history, 1,168 (85%) reported no travel preceding laboratory confirmation of SARS-CoV-2 and only 105 (8%) reported international travel during the 30 days preceding a positive SARS-CoV-2 test or symptom onset. International travel was reported by 92/1,304 (7%) of persons infected with the Alpha variant, 7/55 (22%) with Beta, and 5/9 (56%) with Gamma. Of the first three SARS-CoV-2 lineages designated as VOCs in the U.S., international travel was common only among the few Gamma cases. Most persons infected with Alpha and Beta variant reported no travel history, therefore, community transmission of these VOCs was likely common in the U.S. by March 2021. These findings underscore the importance of global surveillance using whole genome sequencing to detect and inform mitigation strategies for emerging SARS-CoV-2 VOCs.
    Language English
    Publishing date 2023-03-29
    Publishing country United States
    Document type Journal Article
    ISSN 2767-3375
    ISSN (online) 2767-3375
    DOI 10.1371/journal.pgph.0001252
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Promoting directional axon growth from neural progenitors grafted into the injured spinal cord.

    Bonner, Joseph F / Blesch, Armin / Neuhuber, Birgit / Fischer, Itzhak

    Journal of neuroscience research

    2009  Volume 88, Issue 6, Page(s) 1182–1192

    Abstract: Spinal cord injury (SCI) is a devastating condition characterized by disruption of axonal connections, failure of axonal regeneration, and loss of motor and sensory function. The therapeutic promise of neural stem cells has been focused on cell ... ...

    Abstract Spinal cord injury (SCI) is a devastating condition characterized by disruption of axonal connections, failure of axonal regeneration, and loss of motor and sensory function. The therapeutic promise of neural stem cells has been focused on cell replacement, but many obstacles remain in obtaining neuronal integration following transplantation into the injured CNS. This study investigated the neurotransmitter identity and axonal growth potential of neural progenitors following grafting into adult rats with a dorsal column lesion. We found that using a combination of neuronal and glial restricted progenitors (NRP and GRP) produced graft-derived glutamatergic and GABAergic neurons within the injury site, with minimal axonal extension. Administration of brain-derived neurotrophic factor (BDNF) with the graft promoted modest axonal growth from grafted cells. In contrast, injecting a lentiviral vector expressing BDNF rostral into the injured area generated a neurotrophin gradient and promoted directional growth of axons for up to 9 mm. Animals injected with BDNF lentivirus (at 2.5 and 5.0 mm) showed significantly more axons and significantly longer axons than control animals injected with GFP lentivirus. However, only the 5.0-mm-BDNF group showed a preference for extension in the rostral direction. We concluded that NRP/GRP grafts can be used to produce excitatory and inhibitory neurons, and neurotrophin gradients can guide axonal growth from graft-derived neurons toward putative targets. Together they can serve as a building block for neuronal cell replacement of local circuits and formation of neuronal relays.
    MeSH term(s) Aging ; Animals ; Axons/physiology ; Brain-Derived Neurotrophic Factor/genetics ; Brain-Derived Neurotrophic Factor/metabolism ; Cell Enlargement ; Female ; Genetic Vectors/therapeutic use ; Glutamic Acid/metabolism ; Lentivirus/genetics ; Nerve Regeneration/physiology ; Neuroglia/physiology ; Neuroglia/transplantation ; Neurons/cytology ; Neurons/physiology ; Neurons/transplantation ; Rats ; Rats, Inbred F344 ; Rats, Sprague-Dawley ; Spinal Cord Injuries/physiopathology ; Spinal Cord Injuries/surgery ; Spinal Cord Injuries/therapy ; Stem Cell Transplantation ; Stem Cells/cytology ; Stem Cells/physiology ; gamma-Aminobutyric Acid/metabolism
    Chemical Substances Brain-Derived Neurotrophic Factor ; Glutamic Acid (3KX376GY7L) ; gamma-Aminobutyric Acid (56-12-2)
    Language English
    Publishing date 2009-11-12
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 195324-2
    ISSN 1097-4547 ; 0360-4012
    ISSN (online) 1097-4547
    ISSN 0360-4012
    DOI 10.1002/jnr.22288
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Developing international open science collaborations

    Elizabeth Kittrie / Audie A Atienza / Robert Kiley / David Carr / Aki MacFarlane / Vinay Pai / Jennifer Couch / Jared Bajkowski / Joseph F Bonner / Daniel Mietchen / Philip E Bourne

    PLoS Biology, Vol 15, Iss 8, p e

    Funder reflections on the Open Science Prize.

    2017  Volume 2002617

    Abstract: The Open Science Prize was established with the following objectives: first, to encourage the crowdsourcing of open data to make breakthroughs that are of biomedical significance; second, to illustrate that funders can indeed work together when ... ...

    Abstract The Open Science Prize was established with the following objectives: first, to encourage the crowdsourcing of open data to make breakthroughs that are of biomedical significance; second, to illustrate that funders can indeed work together when scientific interests are aligned; and finally, to encourage international collaboration between investigators with the intent of achieving important innovations that would not be possible otherwise. The process for running the competition and the successes and challenges that arose are presented.
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2017-08-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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