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  • 1
    In: Journal for ImmunoTherapy of Cancer, BMJ, Vol. 4, No. S1 ( 2016-11)
    Type of Medium: Online Resource
    ISSN: 2051-1426
    Language: English
    Publisher: BMJ
    Publication Date: 2016
    detail.hit.zdb_id: 2719863-7
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  • 2
    In: Neuro-Oncology, Oxford University Press (OUP), Vol. 22, No. Supplement_2 ( 2020-11-09), p. ii174-ii174
    Abstract: H3K27M-mutant midline lesions were recently reclassified by the WHO as “Diffuse Midline Glioma” (DMG) based on their molecular signature. DMG is one of the most common and most lethal pediatric brain tumors; terminal progression is typically caused by local progression or secondary leptomeningeal dissemination. H3K27M mutations have also been infrequently associated with a histologically diverse set of lesions, particularly spinal masses with early leptomeningeal spread, but the role of H3K27M in these atypical lesions remains poorly understood. CASE PRESENTATION A 15-year-old girl was found to have a T2/FLAIR-hyperintense and heterogeneously contrast-enhancing thalamic mass accompanied by severe leptomeningeal enhancement along the entire neuraxis. Initial infectious workup was negative, and open intracranial biopsy was inconclusive. Follow-up spinal arachnoid biopsy was diagnostic for H3K27M neuroepithelial tumor, thereafter classified as DMG. Biopsy also showed focal p53 immunopositivity, variable immunoreactivity for GFAP and synaptophysin, and an increased proliferation index, altogether suggestive of a glioneuronal origin. She received craniospinal irradiation (CSI) to 41.4Gy with a boost to the thalamic lesion to 54Gy. Imaging 1-month post-radiation demonstrated significant treatment response only with residual enhancement at the conus. CONCLUSIONS This case report describes the unique presentation of an H3K27M-mutant midline lesion with significant craniospinal leptomeningeal spread on admission and atypical glioneuronal histopathological markers. Given her avid leptomeningeal disease, spinal dural biopsy could have been considered earlier given its diagnostic yield in classifying the lesion as DMG. This lesion, however, additionally demonstrated synaptophysin positivity. Per extensive literature review, this histopathology is also potentially consistent with diffuse leptomeningeal glioneuronal tumor (DLGNT). This patient’s uniquely marked treatment response to CSI is also not typically observed in DMG, further supporting the possibility of an alternative molecular identity. In atypical DMG cases, particularly with early leptomeningeal spread, additional consideration of clinical and histopathological context is warranted for accurate diagnosis and prognostication.
    Type of Medium: Online Resource
    ISSN: 1522-8517 , 1523-5866
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2020
    detail.hit.zdb_id: 2094060-9
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  • 3
    In: Journal of Vascular Surgery, Elsevier BV, Vol. 72, No. 3 ( 2020-09), p. e300-
    Type of Medium: Online Resource
    ISSN: 0741-5214
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2020
    detail.hit.zdb_id: 1492043-8
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  • 4
    In: Developmental Biology, Elsevier BV, Vol. 319, No. 2 ( 2008-07), p. 336-345
    Type of Medium: Online Resource
    ISSN: 0012-1606
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2008
    detail.hit.zdb_id: 1463203-2
    SSG: 12
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  • 5
    In: Child's Nervous System, Springer Science and Business Media LLC, Vol. 37, No. 7 ( 2021-07), p. 2347-2356
    Type of Medium: Online Resource
    ISSN: 0256-7040 , 1433-0350
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 1463024-2
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  • 6
    Online Resource
    Online Resource
    The American Association of Immunologists ; 2016
    In:  The Journal of Immunology Vol. 196, No. 1_Supplement ( 2016-05-01), p. 211.12-211.12
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 196, No. 1_Supplement ( 2016-05-01), p. 211.12-211.12
    Abstract: One hallmark of pancreatic ductal adenocarcinoma (PDAC) is the dense stroma that includes activated myofibroblast-like cells termed ‘pancreatic stellate cells’ (PSC). We hypothesized that antitumor immunity is restrained by PSC, and that key pathways can be identified to augment efficacy of immunotherapy. To gain insight into the most relevant soluble factors and pathways, primary PSC (n=10) were isolated from PDAC patients. A normal human pancreatic fibroblast (HPF) cell line was used as a control. RNA obtained from PSC or HPF underwent nanostring analysis using the nCounter PanCancer Immune Profiling panel. Cytokine and chemokine expression in supernatants was measured via bioplex analysis or ELISA. Unsupervised clustering analysis revealed the greatest fold change in IL-6 transcript between PSC and HPF, versus other cytokines in the panel. Abundant IL-6 expression was validated in supernatants by bioplex analysis, and was accompanied by other cytokines, most notably, MCP-1, VEGF and SDF-1. Supernatants from human PSC also expanded suppressive myeloid cells from bulk, human peripheral blood mononuclear cells. Analysis of a separate cohort of human pancreatic tumors (n=12) via immunohistochemistry further revealed abundant IL-6 protein in stromal regions of tumors. This prominent stromal localization of IL-6, and STAT3 phosphorylation STAT3 was also evident in pancreata from mice with mutant Kras-driven, PDAC. These data point to stromal IL-6 as a target in PDAC, and complement our data confirming plasma IL‑6 as a poor prognostic factor in a large cohort (n=73) of treatment naïve PDAC patients. Ongoing studies are exploring the role of IL-6 in PSC and the effect of targeting this cytokine in combination with immunotherapy.
    Type of Medium: Online Resource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Language: English
    Publisher: The American Association of Immunologists
    Publication Date: 2016
    detail.hit.zdb_id: 1475085-5
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  • 7
    In: Molecular Cancer Research, American Association for Cancer Research (AACR), Vol. 16, No. 8_Supplement ( 2018-08-01), p. A20-A20
    Abstract: Introduction: The effect of chemotherapy on the presence of tumor-infiltrating lymphocytes (TILs) and expression of PD1 and PD-L1 is unclear. We sought to describe the differences in the percentage (%) of TILs, cytotoxic T lymphocytes (CTL), and expression of PD1/PD-L1 in tumors of patients (pts) with operable breast cancer (BC) treated with neoadjuvant chemotherapy (NAC) who were enrolled in a biomarker study at our institution (IRB protocol# 2010C0036). Methods: A multicolor immune-histochemical multiplex assay simultaneously detecting PD1, PD-L1, and CD8 expressing cells was performed on formalin-fixed, paraffin-embedded diagnostic pretreatment biopsy or resected tumor specimen following NAC in 18 of 26 pts participating in the study. A cut-off of ≥1% was considered positive for PD1 and PD-L1 expression. We evaluated stromal and intratumoral CTLs by estimating % of stroma and tumor that contained CD8+ cells. In addition, stromal TILs (sTILs) were identified on full-face hematoxylin and eosin stained sections and defined as the % of tumor stroma containing infiltrating lymphocytes. Pathologic complete or near-complete response (pCR) was analyzed based on residual cancer burden (RCB) score and defined as RCB class 0 or I. Analysis of all slides was performed by an expert breast pathologist. Since the number of pts was limited, we only provide descriptive statistics (mean, range). In addition, because most pts had only a biopsy or only residual tumor available for the analysis, we divided pts into 2 separate cohorts based on what tissue was available. Results: Of 18 pts, biopsy was analyzed in 7 (Bx cohort) and residual tumor was analyzed in 11 pts (RT cohort). The median age of study pts was 48 (range 32-70); 11 (61%), 6 (33%), and 1 (6%) of pts were Caucasian, African American, and Hispanic, respectively. Ten pts (5 in Bx and RT cohorts each) had triple-negative BC (TNBC), 4 had HER2+ BC (1 and 3 in Bx and RT cohorts, respectively), and 4 had hormone receptor-positive, HER2- BC (1 and 3 in Bx and RT cohorts, respectively). Eight pts (44%) had pCR. In the bx cohort, 85% of pts had pCR while 18% of pts in the RT cohort had minimal residual disease (RCB class I). In the Bx cohort, average % of sTILs was 30% (range 2-70%), including 1 pt (14%) with lymphocyte predominant tumor (≥50% of sTILs). The % of sTILs was similar in the 11 residual tumors (mean 22, range 2-60) with 2 pts having lymphocyte predominant tumors. Average % of CTLs was 19 (range 1-50) in the Bx cohort and 14 (range 1-50) in the RT cohort. An average % of intratumoral CTLs was 8 (range 1-30) and 7.5 (range 0-40) while the average % of stromal CTLs was 25 (range 1-60) and 19 (range 1-60) in the Bx and RT cohorts, respectively. Similar % and trends were seen in 10 TNBC pts. PD-L1 expression was seen in 86% and 36% of tumors in the Bx and RT cohorts, respectively, with majority of expression present in the stroma. All cases of intratumoral PD-L1 expression were also positive for stromal PD-L1 expression. This difference was also seen in the TNBC pts (80% vs. 40% of tumors were PD-L1+ in Bx and RT cohorts, respectively). An average PD-L1 intensity was approximately 3% in both cohorts (range 1-20%). Expression of PD1 was very low (1% intensity in 3 pts in Bx cohort and in 1 pt in RT cohort) and it was seen on CD8+ CTLs. Conclusion: Our study preliminarily shows that percent of sTILs and stromal and intratumoral CTLs does not differ between pretreatment biopsy and residual tumors following NAC. Lower proportion of residual tumors were PD-L1+ compared to pretreatment biopsy specimen. The study limitations include small number of subjects and lack of comparison in the same pts. Future studies are needed to confirm these findings. Citation Format: Robert Wesolowski, Zaibo Li, Christopher McQuinn, Maryam Lustberg, Bhuvaneswari Ramaswamy, Anne Noonan, Raquel Reinbolt, Sagar Sardesai, Jeffrey B. VanDeusen, Nicole Williams, William E. Carson, III. Analysis of tumor infiltrating lymphocytes and expression of PD1 and PD-L1 in breast tumors prior to and after neoadjuvant chemotherapy [abstract]. In: Proceedings of the AACR Special Conference: Advances in Breast Cancer Research; 2017 Oct 7-10; Hollywood, CA. Philadelphia (PA): AACR; Mol Cancer Res 2018;16(8_Suppl):Abstract nr A20.
    Type of Medium: Online Resource
    ISSN: 1541-7786 , 1557-3125
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2018
    detail.hit.zdb_id: 2097884-4
    SSG: 12
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  • 8
    Online Resource
    Online Resource
    American Institute of Aeronautics and Astronautics (AIAA) ; 2023
    In:  Journal of Aircraft Vol. 60, No. 5 ( 2023-09), p. 1437-1460
    In: Journal of Aircraft, American Institute of Aeronautics and Astronautics (AIAA), Vol. 60, No. 5 ( 2023-09), p. 1437-1460
    Abstract: This paper presents a summary of system identification flight testing and results for a variety of large and small fixed-wing and multirotor unmanned air systems at Texas A & M University from 1999 to 2023. The six different types of vehicles range from a large powered parafoil, to a fixed-wing vehicle with synthetic jet-actuated roll control effectors, to a radially asymmetric multirotor, to large and small fixed-wing vehicles, and to a Steppe eagle. The observer/Kalman filter identification algorithm is used to generate linear time-invariant state-space models, and the results for both near-real-time online model generation and postflight offline model generation are presented. The use and efficacy of a variety of test input types and their sensitivity to exogenous inputs such as turbulence, in addition to identified model evaluation and selection criteria, are discussed. Several generations of low size, weight, power, and cost flight-test instrumentation including the Developmental Flight-Test Instrumentation data acquisition package are also presented. Challenges that arose from the flight-testing campaigns along with solutions are highlighted in the paper.
    Type of Medium: Online Resource
    ISSN: 0021-8669 , 1533-3868
    Language: English
    Publisher: American Institute of Aeronautics and Astronautics (AIAA)
    Publication Date: 2023
    detail.hit.zdb_id: 160481-8
    detail.hit.zdb_id: 2025892-6
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  • 9
    Online Resource
    Online Resource
    Elsevier BV ; 2011
    In:  Postharvest Biology and Technology Vol. 61, No. 1 ( 2011-7), p. 1-14
    In: Postharvest Biology and Technology, Elsevier BV, Vol. 61, No. 1 ( 2011-7), p. 1-14
    Type of Medium: Online Resource
    ISSN: 0925-5214
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2011
    detail.hit.zdb_id: 1498582-2
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2023
    In:  Monthly Notices of the Royal Astronomical Society Vol. 522, No. 2 ( 2023-04-21), p. 2047-2064
    In: Monthly Notices of the Royal Astronomical Society, Oxford University Press (OUP), Vol. 522, No. 2 ( 2023-04-21), p. 2047-2064
    Abstract: A recent measurement of the Lyman-limit mean free path at z = 6 suggests it may have been very short, motivating a better understanding of the role that ionizing photon sinks played in reionization. Accurately modelling the sinks in reionization simulations is challenging because of the large dynamic range required if ∼104−108M⊙ gas structures contributed significant opacity. Thus, there is no consensus on how important the sinks were in shaping reionization’s morphology. We address this question with a recently developed radiative transfer code that includes a dynamical sub-grid model for the sinks based on radiative hydrodynamics simulations. Compared to assuming a fully pressure-smoothed intergalactic medium, our dynamical treatment reduces ionized bubble sizes by $10-20~{{\ \rm per\ cent}}$ under typical assumptions about reionization’s sources. Near reionization’s midpoint, the 21 cm power at k ∼ 0.1 hMpc−1 is similarly reduced. These effects are more modest than the $30-60~{{\ \rm per\ cent}}$ suppression resulting from the higher recombination rate if pressure smoothing is neglected entirely. Whether the sinks played a significant role in reionization’s morphology depends on the nature of its sources. For example, if reionization was driven by bright (MUV & lt; −17) galaxies, the sinks reduce the large-scale 21 cm power by at most 20  per cent, even if pressure smoothing is neglected. Conveniently, when bright sources contribute significantly, the morphology in our dynamical treatment can be reproduced accurately with a uniform sub-grid clumping factor that yields the same ionizing photon budget. By contrast, if MUV ∼ −13 galaxies drove reionization, the uniform clumping model can err by up to 40  per cent.
    Type of Medium: Online Resource
    ISSN: 0035-8711 , 1365-2966
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2023
    detail.hit.zdb_id: 2016084-7
    SSG: 16,12
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