Relevant bibliographies by topics / JHDL

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'JHDL'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "JHDL"

1

Fang, Jia, Gregory J. Hogan, Gaoyang Liang, Jason D. Lieb, and Yi Zhang. "The Saccharomyces cerevisiae Histone Demethylase Jhd1 Fine-Tunes the Distribution of H3K36me2." Molecular and Cellular Biology 27, no. 13 (April 30, 2007): 5055–65. http://dx.doi.org/10.1128/mcb.00127-07.

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ABSTRACT Histone methylation plays important roles in the regulation of chromatin dynamics and transcription. Steady-state levels of histone lysine methylation are regulated by a balance between enzymes that catalyze either the addition or removal of methyl groups. Using an activity-based biochemical approach, we recently uncovered the JmjC domain as an evolutionarily conserved signature motif for histone demethylases. Furthermore, we demonstrated that Jhd1, a JmjC domain-containing protein in Saccharomyces cerevisiae, is an H3K36-specific demethylase. Here we report further characterization of Jhd1. Similar to its mammalian homolog, Jhd1-catalyzed histone demethylation requires iron and α-ketoglutarate as cofactors. Mutation and deletion studies indicate that the JmjC domain and adjacent sequences are critical for Jhd1 enzymatic activity, while the N-terminal PHD domain is dispensable. Overexpression of JHD1 results in a global reduction of H3K36 methylation in vivo. Finally, chromatin immunoprecipitation-coupled microarray studies reveal subtle changes in the distribution of H3K36me2 upon overexpression or deletion of JHD1. Our studies establish Jhd1 as a histone demethylase in budding yeast and suggest that Jhd1 functions to maintain the fidelity of histone methylation patterns along transcription units.
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Antoniou, Alexandros‐Stamatios G., Marilyn J. Davidson, and Cary L. Cooper. "Occupational stress, job satisfaction and health state in male and female junior hospital doctors in Greece." Journal of Managerial Psychology 18, no. 6 (September 1, 2003): 592–621. http://dx.doi.org/10.1108/02683940310494403.

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This study investigates the occupational stress amongst 355 male and female Greek junior hospital doctors (JHDs) working in the Greater Athens area. The initial phase of the research involved in‐depth interviews with a random stratified sample of sixty JHDs, both male and female, in a variety of specialties of junior hospital staff. An extended version of the occupational stress indicator (OSI) questionnaire was developed, incorporating additional items based on the results of the qualitative part of the study, and on previous research findings in the same area. The sample consisted of 193 males and 162 females JHDs, who completed the OSI. Analyses of the data demonstrated that, overall, JHDs presented significantly higher levels of sources of pressure than the normative population and other comparative occupational samples. As regards the various sub‐group comparisons, bivariate analyses revealed that there were significant differences between male and female JHDs in certain aspects of pressure (“career and achievement” and “home/work interface”). Multivariate analyses revealed that predictors of physical and mental ill health and job dissatisfaction were type A behaviour and “demands of the profession” respectively. The research implications of the findings are discussed.
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Douglas, Masako O., Hiroko C. Kataoka, and Kiyomi Chinen. "The Development of Japanese as a Heritage Language in the Los Angeles Conurbation." Heritage Language Journal 10, no. 3 (December 30, 2013): 336–56. http://dx.doi.org/10.46538/hlj.10.3.6.

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This paper examines the current status of Japanese as a heritage language (JHL) in the Los Angeles conurbation, applying the Capacity-Opportunity-Desire (COD) framework. After briefly describing the Japanese-American community and the history of JHL education in the United States with a focus on the Los Angeles conurbation, we review research to date on JHL capacity development in JHL schools and the role of the family in JHL development. We then present the results of two studies and analyze factors that contribute to JHL development,reflecting on COD principles. We conclude by presenting suggestions for future research on JHL based on this framework.
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Jurkić, Tomislav, and Dubravka Kotnik-Karuza. "Modeling of Circumstellar Dust by the DUSTY Code." Proceedings of the International Astronomical Union 7, S282 (July 2011): 247–50. http://dx.doi.org/10.1017/s1743921311027451.

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AbstractWe present a circumstellar dust model around the symbiotic Mira RR Tel obtained by modeling the near-infrared JHKL magnitudes and ISO spectra. In order to follow the evolution of infrared colours in time, the published JHKL magnitudes were corrected by removing the Mira pulsations. The RR Tel light curves show three obscuration events in the near-IR. Using the simultaneously available JHKL magnitudes and ISO spectra in three different epochs, we obtained SEDs in the near- and mid-IR spectral region (1-20 μm) in epochs with and without obscuration.The DUSTY numerical code was used to solve the radiative transfer and to determine the circumstellar dust properties of the inner dust regions around the Mira, assuming a spherical dust temperature distribution in its close neighbourhood. The physical properties of the dust, mass loss and optical depth during intervals with and without obscuration have been obtained. Both JHKL and ISO observations during the obscuration period can be reproduced with a spherical dust envelope, while ISO spectra outside obscuration show a different behaviour. The dynamical behaviour of the circumstellar dust was obtained by modeling the JHKL magnitudes observed during the span of more than 30 years.The DUSTY code was also successfully applied in the modeling of circumstellar dust envelopes of young stellar objects, such as Herbig Ae/Be stars.
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Tereshchenko, Alexander, Vincent Magnotta, Eric Epping, Katherine Mathews, Patricia Espe-Pfeifer, Erin Martin, Jeffrey Dawson, Wenzhen Duan, and Peg Nopoulos. "Brain structure in juvenile-onset Huntington disease." Neurology 92, no. 17 (April 10, 2019): e1939-e1947. http://dx.doi.org/10.1212/wnl.0000000000007355.

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ObjectiveTo assess brain morphometry in a sample of patients with juvenile-onset Huntington disease (JOHD) and several mouse models of Huntington disease (HD) that likely represent the human JOHD phenotype.MethodsDespite sharing the mutation in the Huntingtin gene, adult-onset HD characteristically presents as a hyperkinetic motor disorder, while JOHD typically presents as a hypokinetic motor disease. The University of Iowa Kids-JHD program enrolls individuals 5 to 25 years of age who have already received the clinical diagnosis. A total of 19 children with juvenile HD (JHD) (mean CAG = 72) were studied. Patients with JHD were compared to healthy controls (n = 234) using a cross-sectional study design. Volumetric data from structural MRI was compared between groups. In addition, we used the same procedure to evaluate brain morphology of R6/2, zQ175, HdhQ250 HD mice models.ResultsParticipants with JHD had substantially reduced intracranial volumes. After controlling for the small intracranial volume size, the volumes of subcortical regions (caudate, putamen, globus pallidus, and thalamus) and of cortical white matter were significantly decreased in patients with JHD. However, the cerebellum was proportionately enlarged in the JHD sample. The cerebral cortex was largely unaffected. Likewise, HD mice had a lower volume of striatum and a higher volume of cerebellum, mirroring the human MRI results.ConclusionsThe primary pathology of JOHD extends beyond changes in the striatal volume. Brain morphology in both mice and human patients with JHD shows proportional cerebellar enlargement. This pattern of brain changes may explain the unique picture of hypokinetic motor symptoms in JHD, which is not seen in the hyperkinetic chorea-like phenotype of adult-onset HD.
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Gatto, Emilia Mabel, Virginia Parisi, José Luis Etcheverry, Ana Sanguinetti, Lorena Cordi, Adrian Binelli, Gabriel Persi, and Ferdinando Squitieri. "Juvenile Huntington disease in Argentina." Arquivos de Neuro-Psiquiatria 74, no. 1 (November 24, 2015): 50–54. http://dx.doi.org/10.1590/0004-282x20150192.

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ABSTRACT We analyzed demographic, clinical and genetic characteristics of juvenile Huntington disease (JHD) and it frequency in an Argentinean cohort. Age at onset was defined as the age at which behavioral, cognitive, psychiatric or motor abnormalities suggestive of JHD were first reported. Clinical and genetic data were similar to other international series, however, in this context we identified the highest JHD frequency reported so far (19.72%; 14/71). Age at onset of JHD is challenging and still under discussion. Our findings reinforce the hypothesis that clinical manifestations, other than the typical movement disorder, may anticipate age at onset of even many years. Analyses of JHD cohorts are required to explore it frequency in populations with different backgrounds to avoid an underestimation of this rare phenotype. Moreover, data from selected populations may open new pathways in therapeutic approaches and may explain new potential correlations between HD presentations and environmental or biological factors.
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Blair, Lauren P., Zongzhi Liu, Ramon Lorenzo D. Labitigan, Lizhen Wu, Dinghai Zheng, Zheng Xia, Erica L. Pearson, et al. "KDM5 lysine demethylases are involved in maintenance of 3′UTR length." Science Advances 2, no. 11 (November 2016): e1501662. http://dx.doi.org/10.1126/sciadv.1501662.

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The complexity by which cells regulate gene and protein expression is multifaceted and intricate. Regulation of 3′ untranslated region (UTR) processing of mRNA has been shown to play a critical role in development and disease. However, the process by which cells select alternative mRNA forms is not well understood. We discovered that theSaccharomyces cerevisiaelysine demethylase, Jhd2 (also known as KDM5), recruits 3′UTR processing machinery and promotes alteration of 3′UTR length for some genes in a demethylase-dependent manner. Interaction of Jhd2 with both chromatin and RNA suggests that Jhd2 affects selection of polyadenylation sites through a transcription-coupled mechanism. Furthermore, its mammalian homolog KDM5B (also known as JARID1B or PLU1), but not KDM5A (also known as JARID1A or RBP2), promotes shortening ofCCND1transcript in breast cancer cells. Consistent with these results, KDM5B expression correlates with shortenedCCND1in human breast tumor tissues. In contrast, both KDM5A and KDM5B are involved in the lengthening ofDICER1. Our findings suggest both a novel role for this family of demethylases and a novel targetable mechanism for 3′UTR processing.
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Xi, Song-yang, Yu-hao Teng, Yan Chen, Jie-ping Li, Ying-ying Zhang, Shen-lin Liu, Xi Zou, Jin-yong Zhou, Jian Wu, and Rui-ping Wang. "Jianpi Huayu Decoction Inhibits Proliferation in Human Colorectal Cancer Cells (SW480) by Inducing G0/G1-Phase Cell Cycle Arrest and Apoptosis." Evidence-Based Complementary and Alternative Medicine 2015 (2015): 1–8. http://dx.doi.org/10.1155/2015/236506.

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Jianpi Huayu Decoction (JHD), a Chinese medicine formula, is a typical prescription against multiple tumors in the clinical treatment, which can raise quality of life and decrease complications. The aim of this study is to assess the efficacy of JHD against human colorectal carcinoma cells (SW480) and explore its mechanism. MTT assay showed that JHD decreased the cellular viability of SW480 cells in dose-dependent and time-dependent manner. Flow cytometry analysis revealed that JHD induced G0/G1-phase cell cycle arrest in SW480 cells and had a strong apoptosis-inducing effect on SW480 cells. Meanwhile it enhanced the expression of p27, cleaved PARP, cleaved caspase-3, and Bax and decreased the levels of PARP, caspase-3, Bcl-2, CDK2, CDK4, CDK6, cyclin D1, cyclin D2, cyclin D3, and cyclin E1, which was evidenced by RT-qPCR and Western blot analysis. In conclusion, these results indicated that JHD inhibited proliferation in SW480 cells by inducing G0/G1-phase cell cycle arrest and apoptosis, providing a practicaltherapeutic strategy against colorectal cancer.
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Feki, Fatma, Chahnez Triki, and Nesrine Amara. "Drug-Resistant Myoclonic Epilepsy Revealing Juvenile Huntington's Disease: A Case Report." Journal of Pediatric Epilepsy 07, no. 01 (March 2018): 021–23. http://dx.doi.org/10.1055/s-0038-1641727.

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AbstractJuvenile Huntington's disease (JHD) shares many general clinical features with the adult form. One important difference is that JHD patients experience more epileptic manifestations, sometimes difficult to control. We describe an atypical clinical picture of a genetically confirmed JHD patient diagnosed during evaluation for a progressive myoclonic epilepsy. A female patient with a family history of psychiatric disorders developed recurrent drug-resistant myoclonic seizures at the age of 6 years, followed by extrapyramidal symptoms (rigidity and dystonia). Cognitive impairment, akinetic rigidity syndrome, and dystonia were noticed at the age of 10 years. Epileptiform abnormalities were noted in ictal electroencephalography. Magnetic resonance imaging showed brain atrophy. Genetic testing for HD confirmed the diagnosis. JHD can initially manifest as myoclonic epilepsy. A DNA testing should be performed if clinical history is suggestive.
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Pujol, Jose. "An integrated 3D velocity inversion—joint hypocentral determination relocation analysis of events in the Northridge area." Bulletin of the Seismological Society of America 86, no. 1B (February 1, 1996): S138—S155. http://dx.doi.org/10.1785/bssa08601bs138.

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Abstract A subset of 3371 events recorded in the Northridge area by the Southern California Seismic Network during January to April 1994 was relocated with the joint hypocentral determination (JHD) technique. This analysis showed two unexpected results: (a) the JHD locations are shifted about 3.9 km on average in a northwest direction with respect to the locations determined using a single-event location (SEL) program, and (b) the station corrections vary between −0.55 and 1.26 sec, a rather large range. In addition, the JHD locations are less scattered than the SEL locations. For each station, the weighted average of the arrival time residuals obtained when the events are located with the SEL program (which does not apply distance or error weighting) are generally smaller than the corresponding JHD corrections. The locations determined with SEL and using the weighted average residuals as station corrections do not differ much from the SEL locations, but on average the RMS residuals become as small as those corresponding to the JHD locations. As the magnitude of the station corrections indicates the presence of large lateral velocity variations, a 3D velocity model for the area was determined using the arrival times of 1012 events recorded by at least 17 stations. The initial velocity model was that used routinely by the Southern California Earthquake Center. The first two layers (5.5- and 10.5-km thick) were subdivided into 100 blocks each (12 × 12 km). These layers show a pronounced low-velocity anomaly (24% and 16%, respectively) immediately to the northwest of the epicentral area. This low-velocity zone coincides with the west Ventura Basin. Another pronounced low-velocity zone to the southeast of the epicentral area reflects the presence of the Los Angeles Basin. The locations obtained with the 3D velocity model are consistently to the southeast of the JHD locations, 2.4 km on average. To establish the effect of these pronounced lateral velocity variations on the SEL and JHD locations, synthetic travel times were analyzed. The synthetic times were generated for event locations determined by JHD (shifted by various amounts) and the 3D velocity model and were subsequently treated as the actual data. The most important result of this analysis is that the JHD locations are affected by a quasi-systematic shift in a northwest direction (up to about 2.7 km on average, depending on the initial shift) but that the relative locations are well preserved. Therefore, both the velocity inversion of the actual data and the analysis of the synthetic data indicate that the JHD locations determined for the actual data are quasi-systematically mislocated. To account for this mislocation, an overall shift of 2.5 km to the southeast was applied to all the JHD locations. One of the most important implications of the shifted locations is the possibility that the northeasterly dipping Santa Susana fault, to the northwest of the epicentral area, was seismically active during the aftershock sequence. This feature is more diffuse in other published locations.
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Dissertations / Theses on the topic "JHDL"

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Atwell, James W. "A Multiplexed Memory Port for Run Time Reconfigurable Applications." Thesis, Virginia Tech, 1999. http://hdl.handle.net/10919/36219.

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Configurable computing machines (CCMs) are available as plug in cards for standard workstations. CCMs make it possible to achieve computing feats on workstations that were previously only possible with super computers. However, it is difficult to create applications for CCMs. The development environment is fragmented and complex. Compilers for CCMS are emerging but they are in their infancy and are inefficient.

The difficulties of implementing run time reconfiguration (RTR) on CCMs are addressed in this thesis. Tools and techniques are introduced to simplify the development and synthesis of applications and partitions for RTR applications. A multiplexed memory port (MMP) is presented in JHDL and VHDL that simplifies the memory interface, eases the task of writing applications and creating partitions, and makes applications platform independent. The MMP is incorporated into an existing CCM compiler. It is shown that the MMP can increase the compiler's functionality and efficiency.
Master of Science

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Poetter, Alexandra Vanessa. "JHDLBits: An Open-Source Model for FPGA Design Automation." Thesis, Virginia Tech, 2004. http://hdl.handle.net/10919/10121.

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Today's Field Programmable Gate Array (FPGA) research community could use an extensible tool flow enabling designers to examine new algorithms and new methods of interacting with FPGA configurations. One such flow is JHDLBits, which integrates two prominent FPGA design environments: JHDL and JBits. JHDLBits offers the low-level access and control provided by JBits with the high-level structural circuit design of JHDL. Furthermore, the JHDLBits flow provides greater control of resource manipulation, placement, and routing, and gives researchers a sandbox to explore advanced interactions with FPGA configurations. This thesis presents the overall architecture of the open-source JHDLBits project. Details are provided on how the core components -- JHDL, JBits3 for Virtex-II, the ADB connectivity database, and VTsim, a Virtex-II device simulator -- are linked together to provide an integrated design environment. Strategies and philosophies of the open source movement are also examined to successfully establish the support for and involvement of the FPGA research community throughout the JHDLBits open source endeavor.
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Hunter, Jesse Everett III. "A Device-Level FPGA Simulator." Thesis, Virginia Tech, 2000. http://hdl.handle.net/10919/10041.

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In the realm of FPGAs, many tool vendors offer behaviorally-based simulators aimed at easing the complexity of large FPGA designs. At times, a behaviorally-modeled design does not work in hardware as expected or intended. VTsim, a Virtex-II device simulator, was designed to resolve this and many other design problems by providing a window into the FPGA fabric via a virtual device. VTsim is an event-driven device simulator modeled at the CLB level with multiple clock domain support. Utilizing JBits3 and ADB, VTsim enables simulation and examination of all resources within an FPGA via a virtual device. The only input required by VTsim is a bitstream, which can be generated from any tool suite. The simulator is part of the JHDLBits open-source project, and was designed for rapid response, low memory usage, and ease of interaction.
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DASASATHYAN, SRINIVASAN. "SYNTHESIS OF VIRTUAL PIPELINES ON VIRTEX-BASED FPGAs." University of Cincinnati / OhioLINK, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=ucin990618529.

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Slade, Anthony Lynn. "Designing, Debugging, and Deploying Configurable Computing Machine-based Applications Using Reconfigurable Computing Application Frameworks." Diss., CLICK HERE for online access, 2003. http://contentdm.lib.byu.edu/ETD/image/etd186.pdf.

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Tu, Shengjiang. "Identification Of Histone Demthylases In Budding Yeast And DNA Binding Motifs Of Human Demethylase RBP2." The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1211487400.

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Lienhard, Demian [Verfasser], Michael [Gutachter] Heinzelmann, Dietrich [Gutachter] Boschung, and Walter [Gutachter] Ameling. "Römische fora in Italien. Funktionen und Funktionswandel öffentlicher Platzanlagen vom 3. Jhdt. v. Chr. bis ins 5. Jhdt. n. Chr. / Demian Lienhard ; Gutachter: Michael Heinzelmann, Dietrich Boschung, Walter Ameling." Köln : Universitäts- und Stadtbibliothek Köln, 2017. http://d-nb.info/1210642743/34.

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Herrmann, Moritz Sebastian. "Molecular and genomic studies on the histone lysine demethylase JHDM-1 in Caenorhabditis elegans." Thesis, University of Cambridge, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.648716.

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Eich, Paul [Verfasser], Harald [Gutachter] Keller, and Julius [Gutachter] Schwietering. "Die Maria Lactans : eine Studie ihrer Entwicklung bis in das 13. Jhd. und ein Versuch ihrer Deutung aus der mittelalterlichen Frömmigkeit / Paul Eich ; Gutachter: Harald Keller, Julius Schwietering." Frankfurt am Main : Universitätsbibliothek Johann Christian Senckenberg, 2012. http://d-nb.info/113965103X/34.

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Lin, Chun-Liang, and 林俊良. "Synthetic Lethal Analysis of JHD1 from Saccharomyces cerevisiae." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/11325832639824269059.

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碩士
淡江大學
生命科學研究所碩士班
96
The synthetic lethal screen is a powerful genetic screen that relies on finding the secondary molecular targets. In principle, this screen can identify any mutant gene which causes cell death with a nonlethal “primary” mutation. The synthetic lethal screen is a method of isolating novel mutants whose survival is dependent on the gene of interest. Combining the colony-color assay, this method will offer a means to visually detect a mutant that depends on a plasmid for survival. The synthetic lethal screen must be carry out in the following four processes : (i) The gene function of interest should be disrupted in a strain containing ade2 ade3/ade8 mutations, which result in a white phenotype. (ii) Combining the wild-type gene of interest and ADE3/ADE8 in a plasmid which is then transformed into the strain of step (i). The cells will produce red-white sector, and the white colonies have lost the plasmid. (iii) A mutagenesis will be performed to introduce random mutations into the strain genome. The mutant must dependents on the gene of interest from plasmid of step (ii) for survival and produce red solid colonies. (iv) The synthetic lethal(SL) colonies are transformed with a library. Then the mutants containing complementing DNA are no longer dependent on the gene of interest, and the cells with red-white sectoring are identified. Finally,the synthetic lethal gene can be sequencd from the complement plasmid.
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Books on the topic "JHDL"

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Sharma, Madanlal. Ret ki jhil. Jaipur: Sahityagar, 2005.

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Jhīl vālī laṛkī. [S.l: s.n.], 2010.

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Kehar, ʻUbaidullāh. Jhīl men̲ samundar: Safarnāmah. Karachi: True Vision Communications, 2004.

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Warsi, Q. Roshan galian Jhil mil koochay. Karachi: Dabistan-e-Warsia, 2000.

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JHCL HOME CULTURES VOL 10 ISS 1. London: Bloomsbury Publishing PLC, 2013.

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Haas, Hanns. Geschichte der böhmischen Länder vom 16. Jhdt. bis heute. [Aigen-Voglhub, Austria: Eigenverlag A.-H. Schmidt, 1996.

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Fatwas zum Alkohol unter dem Einfluss neuer Medien im 20. Jhdt. Würzburg: Ergon, 2001.

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Berthold, Alban. Familien in Mutterstadt: Von 1650 bis Anfang des 20. Jhd. Mutterstadt: Ahnenpuzzle, 2013.

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Kästner, Christoph. Chronik: Erinnerungen des ersten evangelischen Pfarrers im Salzkammergut aus dem 18. und 19. Jhdt. Bad Goisern: ELV Schreibwerkstaat der HS 1 Bad Goisern, 1996.

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Humā, Iqbāl. Qadam qadam bahār he: Vādī Kāg̲h̲ān, Sarāl pās aur Sarāl jhīl kā safar nāmah. Lāhaur: Sajjād Pablīkeshanz, 2014.

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Book chapters on the topic "JHDL"

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von Devivere, Beate. "Die Renaissance der Philosophie im 21. Jhdt." In Sinn und Arbeit, 163–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-63384-7_12.

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Glass, I. S. "Seyfert Galaxies in the IRAS Survey and JHKL Photometry." In Light on Dark Matter, 487–88. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4672-9_102.

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Janik, Dieter. "Humanistisch inspirierte Quell- und Flußdichtung in Frankreich und Italien (16. Jhdt.)." In Bandusia, 73–96. Wiesbaden: Vieweg+Teubner Verlag, 1993. http://dx.doi.org/10.1007/978-3-663-11971-5_2.

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Pujol, Jose. "Joint Event Location — The JHD Technique and Applications to Data from Local Seismic Networks." In Advances in Seismic Event Location, 163–204. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-015-9536-0_7.

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Nelson, Brent, and Brad Hutchings. "The JHDL Design and Debug System." In Reconfigurable Computing, 255–73. Elsevier, 2008. http://dx.doi.org/10.1016/b978-012370522-8.50017-0.

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"JHD." In Encyclopedia of Clinical Neuropsychology, 1368. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_4794.

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Quarrell, Oliver. "Juvenile Huntington’s disease and paediatric Huntington’s disease." In Huntington's Disease, 36–43. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780198844389.003.0004.

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Juvenile Huntington’s disease (JHD) is rare. It is usually defined as someone having an onset before 21 years. A more accurate description would be juvenile-onset HD. The origins of this definition are obscure but the distinction has been recognized for many years. The proportions of JHD cases may vary in different parts of the world but a figure of approximately five per cent is useful. JHD is not a separate category but rather part of the spectrum. Whilst it is still useful to think about the needs of young people in terms of the different ways they can present to a doctor some of the limitations of the definition will be explored. As part of the process of developing new drugs the European Medicines Agency (EMA) would like information on how the drug affects children. The term JHD does not cover this accurately so new term, paediatric Huntington’s disease (PHD) has been devised so that young people under the age of 18 years and currently affected by HD can be identified.
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"III. Topfständer (JHD)." In Die Keramik aus dem Friedhof S/SA von Aniba (Unternubien), 305–18. De Gruyter, 2019. http://dx.doi.org/10.1515/9783110620177-010.

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"IV. Opferständer (JHD)." In Die Keramik aus dem Friedhof S/SA von Aniba (Unternubien), 319–28. De Gruyter, 2019. http://dx.doi.org/10.1515/9783110620177-011.

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"VI. Miniaturgefäße (JHD)." In Die Keramik aus dem Friedhof S/SA von Aniba (Unternubien), 342–53. De Gruyter, 2019. http://dx.doi.org/10.1515/9783110620177-017.

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Conference papers on the topic "JHDL"

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Wirthlin, M. J., and B. McMurtrey. "IP delivery for FPGAs using applets and JHDL." In Proceedings of 39th Design Automation Conference. IEEE, 2002. http://dx.doi.org/10.1109/dac.2002.1012584.

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Wirthlin, Michael J., and Brian McMurtrey. "IP delivery for FPGAs using Applets and JHDL." In the 39th conference. New York, New York, USA: ACM Press, 2002. http://dx.doi.org/10.1145/513918.513922.

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3

Castells-Rufas, David, and Jordi Carrabina. "Jumble: A Hardware-in-the-Loop Simulation System for JHDL." In 15th Annual IEEE Symposium on Field-Programmable Custom Computing Machines (FCCM 2007). IEEE, 2007. http://dx.doi.org/10.1109/fccm.2007.54.

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4

Niamat, M., S. Santhanam, and J. Kim. "JHDL Implementation of a BIST Scheme for Testing the Look-Up Tables of SRAM Based FPGAs." In 2006 49th IEEE International Midwest Symposium on Circuits and Systems. IEEE, 2006. http://dx.doi.org/10.1109/mwscas.2006.382278.

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Reports on the topic "JHDL"

1

Bellows, Peter, and Brad Hutchings. JHDL - An HDL for Reconfigurable Systems. Fort Belvoir, VA: Defense Technical Information Center, January 1998. http://dx.doi.org/10.21236/ada450477.

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