Auswahl der wissenschaftlichen Literatur zum Thema „Scas15“
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Zeitschriftenartikel zum Thema "Scas15"
Silva, Iago Castro da, Eveson Oscar Almeida Conceição, Daniel Santiago Pereira, Hervé Rogez und Nilton Akio Muto. „Evaluation of the Antimicrobial Capacity of Bacteria Isolated from Stingless Bee (Scaptotrigona aff. postica) Honey Cultivated in Açai (Euterpe oleracea) Monoculture“. Antibiotics 12, Nr. 2 (20.01.2023): 223. http://dx.doi.org/10.3390/antibiotics12020223.
Der volle Inhalt der QuelleGardner, R. J. M. „"SCA16" is really SCA15“. Journal of Medical Genetics 45, Nr. 3 (22.10.2007): 192. http://dx.doi.org/10.1136/jmg.2007.056341.
Der volle Inhalt der QuelleKaur, Jaslovleen, Shaista Parveen, Uzma Shamim, Pooja Sharma, Varun Suroliya, Akhilesh Kumar Sonkar, Istaq Ahmad et al. „Investigations of Huntington’s Disease and Huntington’s Disease-Like Syndromes in Indian Choreatic Patients“. Journal of Huntington's Disease 9, Nr. 3 (08.10.2020): 283–89. http://dx.doi.org/10.3233/jhd-200398.
Der volle Inhalt der QuelleSeixas, Ana I., Martin H. Maurer, Mark Lin, Colleen Callahan, Alka Ahuja, Tohru Matsuura, Christopher A. Ross, Fuki M. Hisama, Isabel Silveira und Russell L. Margolis. „FXTAS, SCA10, and SCA17 in American patients with movement disorders“. American Journal of Medical Genetics Part A 136A, Nr. 1 (2005): 87–89. http://dx.doi.org/10.1002/ajmg.a.30761.
Der volle Inhalt der QuelleGhanem, Mustafa H., Andrew J. Shih, Himanshu Vashistha, Latanya N. Coke, Wentian Li, Sun Jung Kim, Kim R. Simpfendorfer und Peter K. Gregersen. „Investigations into SCAMP5, a candidate lupus risk gene expressed in plasmacytoid dendritic cells“. Lupus Science & Medicine 8, Nr. 1 (November 2021): e000567. http://dx.doi.org/10.1136/lupus-2021-000567.
Der volle Inhalt der QuellePouw, Juliëtte N., Michel A. M. Olde Nordkamp, Tom G. O'Toole, Timothy R. D. J. Radstake, Emmerik F. A. Leijten und Marianne Boes. „Activation-induced colocalisation of SCAMP5 with IFNα in human plasmacytoid dendritic cells“. Lupus Science & Medicine 9, Nr. 1 (März 2022): e000680. http://dx.doi.org/10.1136/lupus-2022-000680.
Der volle Inhalt der QuelleFlockerzi, Fidelis Andrea, Johannes Hohneck, Matthias Saar, Rainer Maria Bohle und Phillip Rolf Stahl. „SCARA5 Is Overexpressed in Prostate Cancer and Linked to Poor Prognosis“. Diagnostics 13, Nr. 13 (29.06.2023): 2211. http://dx.doi.org/10.3390/diagnostics13132211.
Der volle Inhalt der QuelleFlockerzi, Fidelis Andrea, Johannes Hohneck, Frank Langer, Wolfgang Tränkenschuh und Phillip Rolf Stahl. „The Role of SCARA5 as a Potential Biomarker in Squamous Cell Carcinoma of the Lung“. International Journal of Molecular Sciences 25, Nr. 13 (04.07.2024): 7355. http://dx.doi.org/10.3390/ijms25137355.
Der volle Inhalt der QuelleYousaf, Hammad, Ambrin Fatima, Zafar Ali, Shahid M. Baig, Mathias Toft und Zafar Iqbal. „A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family“. Genes 13, Nr. 9 (17.09.2022): 1667. http://dx.doi.org/10.3390/genes13091667.
Der volle Inhalt der QuelleLee, Unghwi, Chunghon Choi, Seung Hyun Ryu, Daehun Park, Sang-Eun Lee, Kitae Kim, Yujin Kim und Sunghoe Chang. „SCAMP5 plays a critical role in axonal trafficking and synaptic localization of NHE6 to adjust quantal size at glutamatergic synapses“. Proceedings of the National Academy of Sciences 118, Nr. 2 (28.12.2020): e2011371118. http://dx.doi.org/10.1073/pnas.2011371118.
Der volle Inhalt der QuelleDissertationen zum Thema "Scas15"
Salimbeni, Simona. „Déficience en TDP1 et instabilité génomique dans les cellules non-réplicatives“. Thesis, Toulouse 3, 2020. http://www.theses.fr/2020TOU30065.
Der volle Inhalt der QuelleSpinocerebellar ataxia with axonal neuropathy (SCAN1) is a rare recessive neurodegenerative syndrome associated with cerebellar atrophy and peripheral neuropathy. It is caused by a homozygous missense mutation in the tyrosyl-DNA phosphodiesterase-1 (TDP1) gene (A1478G). This results in a substitution of histidine for arginine-493 (H493R) in the TDP1 catalytic site, leading to a reduced TDP1 activity. TDP1 hydrolyses the bond between a DNA 3’-end and a tyrosyl moiety within a trapped topoisomerase I cleavage complex (TOP1cc). TDP1 not only excises trapped TOP1ccs but also processes other 3’-end-blocking lesions, including 3’-phosphoglycolates that result from oxidation. Even so, how TDP1 H493R mutation promotes the SCAN1 phenotype, which is associated with the death of post-mitotic neurons, is unclear. DNA double-strand breaks (DSBs) are infrequent but among the most harmful genomic lesions. Their defective repair can induce cell death, and they have been implicated in the pathogenesis of several human diseases, including neurodegenerative syndromes. Hence, my Ph.D. objective was to investigate whether the SCAN1 phenotype could be related to an accumulation of DSBs in non-replicating cells harboring the H493R mutation of TDP1. The only available models to study the impact of TDP1 H493R mutation were lymphoblastoid cell lines derived from SCAN1 patients compared to those of healthy individuals. Hence, we have generated models of osteosarcoma U2OS cells homozygous for TDP1 H493R or TDP1 KO employing the CRISPR-Cas9 technique. We have also generated primary lung WI38 hTERT fibroblasts TDP1 KO. We found that both TDP1 H493R and TDP1 KO cells accumulate endogenous DSBs, primarily in the G1 phase of the cell cycle compared to S phase. A similar increase of DSBs was observed in quiescent WI38 hTERT cells following depletion of TDP1 with siRNA, suggesting the replication-independent nature of DSBs. Treatment of TDP1 H493R and TDP1 KO cells with camptothecin to induced trapped TOP1ccs, further suggests that accumulation of DSBs could be related to the defective removal of TOP1ccs. Next, we asked whether DSB accumulation in those cells could be related to an increase in DSB production and/or a defect in their repair. Notably, R-loop structures that form co-transcriptionally can induce DSBs in non-replicating cells. We found that TDP1 deficiency modulated R-loop levels at some gene loci, raising the possibility of their implication in DSB formation. Analysis of DSB repair following camptothecin treatment revealed that both TDP1 H493R and TDP1 KO cells were defective in the repair of DSBs in G1 but not in S, with TDP1 H493R having the most pronounced effect. These results suggest that DSBs would accumulate specifically in TDP1-deficient cells that do not undergo replication, due to a defective repair of those breaks. Together, our results provide insights on the etiology of the SCAN1 neurodegenerative syndrome. This work was supported by a PhD fellowship under the French-Italian University VINCI Program 2016
Vuillaume, Isabelle. „Identification d'un nouveau locus responsable d'une ataxie spinocérébelleuse héréditaire (SCA21) : approche gène-candidat“. Lille 2, 2003. http://www.theses.fr/2003LIL2MT27.
Der volle Inhalt der QuelleKelp, Alexandra [Verfasser]. „Generierung und Charakterisierung eines transgenen Rattenmodells der Spinozerebellären Ataxie Typ 17 (SCA17) / Alexandra Kelp“. München : Verlag Dr. Hut, 2015. http://d-nb.info/1075409616/34.
Der volle Inhalt der QuelleSchuster, Stefanie [Verfasser]. „Deciphering the effect of mutant STUB1 on the heat shock response in SCAR16 patient-derived cells / Stefanie Schuster“. Tübingen : Universitätsbibliothek Tübingen, 2020. http://d-nb.info/1216501882/34.
Der volle Inhalt der QuelleÖhlund, Rebecca. „Könsskillnader i välbefinnande utifrån val av fysisk aktivitet“. Thesis, Örebro universitet, Institutionen för juridik, psykologi och socialt arbete, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-43343.
Der volle Inhalt der QuelleThe society encourages individuals to promote their health habits in order to improve their well-being. The aim was to investigate the effect of different types of physical activity on experience of general health in well-being in men and woman. Sixty men and women in ages 25-50 years old were randomly chosen from training facilities to answer the 12-item General Health Questionnaire (GHQ-12) and Swedish Core Affect Scale (SCAS). The results showed a significant increase in positive well-being due to the practice of physical activity, but there were no gender difference. However, it was found a significant interaction effect of age and physical activity on health, the men who walked and women who conditioning trained showed highest well-being and general health. The conclusion was that the well-being increase regardless of sex after physical activity, however, different activities gave varying increases between the sexes.
Bampi, Giovana Bavia. „Estudo de haplótipos em famílias com ataxia espinocerebelar tipo 10(SCA10) : evidências de um efeito fundador da mutação“. reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2015. http://hdl.handle.net/10183/119618.
Der volle Inhalt der QuelleSpinocerebellar ataxia type 10 is a rare autosomal dominant neurodegenerative disorder characterized by progressive cerebellar ataxia and epilepsy in some cases. The disease is caused by a pentanucleotide ATTCT expansion in intron 9 of the ATXN10 gene, which is located at locus 22q13.3. Normal alleles range from 10 to 29 repeats while mutant allele range from 800 to 4,500 repeats. SCA10 has only been described so far in admixed patients from American countries such as Mexico, Brazil, Argentina, Venezuela, Colombia, United States and more recently Peru. The self-declared Amerindian ancestry by patients and the absence of SCA10 in European and Asian countries leads to the hypothesis of a mutation founder effect in the Native American populations. The aim of this study was to investigate the hypothesis of a common ancestral origin of ATXN10 mutation. Samples analyzed were from 16 Brazilian families, 21 Peruvian families with SCA10. In addition to patient samples, 48 healthy individuals of Indigenous Quechua from Peru were also included in the laboratorial analyses along with 51 Brazilian controls from a previous study. Our data has shown that 19CGGC14-shared haplotype was found in 46.8% of Brazilian and in 62.8% of Peruvian families. Frequencies from both groups are not statistically different from Quechua controls (57.3%), but they are statistically different from Brazilian controls (11.8%) (p<0.001). However, the mutation ethno-geographical origin remains unclear. The minimal common haplotype was expanded by including two additional polymorphic markers that are found at high prevalence in two haplotypes in Native American populations aiming to shed light on the chromosome region ancestry where the mutation arose. Two frequent haplotypes, 19-13-CGGC-14-10 and 19-15- CGGC-14-10 were identified in Indigenous Quechua controls, with relative frequencies of 14.3% and 13.3% respectively. The second most frequent haplotype in Quechuas, 19-15- CGGC-14-10, is found in 50.0% of Brazilian and in 64.7% of Peruvian families with SCA10. These findings corroborate the hypothesis of a Native American ancestry of the mutation.
Tang, Matthew Y. „Gene reprogramming by K48R mutant ubiquitin in a mouse model of SCA1“. Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/27054.
Der volle Inhalt der QuelleKeiser, Megan Kathryn. „Gene therapies for spinocerebellar ataxia type 1“. Diss., University of Iowa, 2013. https://ir.uiowa.edu/etd/2540.
Der volle Inhalt der QuelleZhou, Tong. „ROLE OF TYROSYL-DNA PHOSPHODIESTERASE (TDP 1) ON REPAIR OF 3′-PHOSPHOGLYCOLATE (3′- PG) TERMINATED DNA DOUBLE-STRAND BREAKS (DSBS) AND IN RESPONSE TO OXIDATIVE STRESS“. VCU Scholars Compass, 2012. http://scholarscompass.vcu.edu/etd/2933.
Der volle Inhalt der QuellePatterson, Erika K. „The social class attitudes scale (SCAS) : instrument development and estimates for reliability and validity /“. free to MU campus, to others for purchase, 2003. http://wwwlib.umi.com/cr/mo/fullcit?p3099621.
Der volle Inhalt der QuelleBücher zum Thema "Scas15"
Gatti, Paula. Juan Antonio Scasso. Montevideo]: IHA, 2009.
Den vollen Inhalt der Quelle findenMuseo degli arazzi Scassa (Asti, Italy), Hrsg. Museo degli arazzi Scassa. Milano: Skira, 2010.
Den vollen Inhalt der Quelle findenScassa, Arazzeria, und Rocca di Umbertide, centro per l'arte contemporanea, Hrsg. Scassa arazziere: L'arazzeria di Asti. Città di Castello: Petruzzi, 2010.
Den vollen Inhalt der Quelle findenAvanzo, Donatella. Da Kandinsky a Botero: Tutti in un filo : l'Arazzeria Scassa e l'arte del '900. Milano: Skira, 2018.
Den vollen Inhalt der Quelle findenState Collaborative of Assessment and Student Standards. Health Education Assessment Project., Council of Chief State School Officers. und ToucanEd Publications (Firm), Hrsg. Assessing health literacy: CCSSO-SCASS Health Education Project. Soquel, CA: ToucanEd Publications, 1999.
Den vollen Inhalt der Quelle finden(Firm), SWAT, und Institute of Chartered Accountants in England and Wales., Hrsg. SCAS & VSCAS companies' accounts disclosure checklist. (s.l.): Accountancy Books, 1992.
Den vollen Inhalt der Quelle findenAssumpção, Paschoalino. O teatro amador em Santo André: A Sociedade de Cultura Artística (SCASA) e o Teatro de Alumínio. Santo André, SP: Alpharrabio Edições, 2000.
Den vollen Inhalt der Quelle findenA palazzo e in villa: Busti antichi e all'antica di Gio. Vincenzo Imperiale patrizio genovese. Genova: Sagep editori, 2017.
Den vollen Inhalt der Quelle findenFerraris, Massimo. Banda Di Scassi. Lulu Press, Inc., 2014.
Den vollen Inhalt der Quelle findenWhitehill and SWAT Ltd Clark. The Scas & Vscas Model Audit File. Accountancy Books, 1993.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Scas15"
Toyoshima, Yasuko, und Hitoshi Takahashi. „Spinocerebellar Ataxia Type 17 (SCA17)“. In Polyglutamine Disorders, 219–31. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-71779-1_10.
Der volle Inhalt der Quellede Vos, C. M., J. D. Bregman und U. J. Schwarz. „Pupil Plane Interferometry: Some Conclusions from SCASIS“. In Very High Angular Resolution Imaging, 419–21. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0880-5_85.
Der volle Inhalt der QuelleManto, Mario, und Christophe Habas. „Ataxies autosomales dominantes (SCAs)“. In Le cervelet, 205–13. Paris: Springer Paris, 2013. http://dx.doi.org/10.1007/978-2-8178-0447-7_23.
Der volle Inhalt der QuelleIshikawa, Kinya. „Molecular Pathogenesis in Spinocerebellar Ataxia Type 31 (SCA31)“. In Contemporary Clinical Neuroscience, 507–16. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-75817-2_26.
Der volle Inhalt der QuelleKlir, George J. „Soft Computer-Aided System Theory and Technology (SCAST)“. In Computer Aided Systems Theory — CAST '94, 13–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/3-540-61478-8_64.
Der volle Inhalt der QuelleVos, C. M., J. D. Bregman und U. J. Schwarz. „SCASIS, Diffraction Limited Imaging using a Redundant Pupil Plane Interferometer“. In Diffraction-Limited Imaging with Very Large Telescopes, 379–88. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2340-9_24.
Der volle Inhalt der QuelleHernández-Ferrándiz, Daniel, Juan J. Pantrigo und Raul Cabido. „SCASA: From Synthetic to Real Computer-Aided Sperm Analysis“. In Bio-inspired Systems and Applications: from Robotics to Ambient Intelligence, 233–42. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-06527-9_23.
Der volle Inhalt der QuelleMariotti, Caterina, Mario Fichera und Lorenzo Nanetti. „How to Design a Therapeutic Trial in SCAs“. In Contemporary Clinical Neuroscience, 265–89. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-24345-5_8.
Der volle Inhalt der QuelleZijlstra, Timo, Karim Bigou und Arnaud Tisserand. „FPGA Implementation and Comparison of Protections Against SCAs for RLWE“. In Lecture Notes in Computer Science, 535–55. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-35423-7_27.
Der volle Inhalt der QuelleOkazawa, Hitoshi, und Hikari Tanaka. „Molecular Dissection and Therapeutic Application of SCA1 Pathologies Revealed by Comprehensive Approaches“. In Contemporary Clinical Neuroscience, 479–86. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-75817-2_24.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Scas15"
Wu, Jiejian, Linghe Kong, Haifeng Tang und Tom Z. J. Fu. „SCASys“. In SIGCOMM '21: ACM SIGCOMM 2021 Conference. New York, NY, USA: ACM, 2021. http://dx.doi.org/10.1145/3472716.3472857.
Der volle Inhalt der QuelleSteadman, Matt, und Steve Adler. „SCAsat Audio Distribution “Best of Satellite, Best of WAN”“. In SMPTE Australia Conference. IEEE, 2015. http://dx.doi.org/10.5594/m001603.
Der volle Inhalt der QuelleKbar, Ghassan, Shady Aly und Bhaa Alhanafi. „Smart and Context Aware Search for University Campus (SCASUC)“. In 2012 International Conference on Multimedia Computing and Systems (ICMCS). IEEE, 2012. http://dx.doi.org/10.1109/icmcs.2012.6320141.
Der volle Inhalt der QuelleBandara, Nalin, Kosala Gunawardane und Nihal Kularatna. „Exprimental verification of Supercapacitor Assisted Sub Module Inverter (SCASMI) Technique“. In 2020 2nd IEEE International Conference on Industrial Electronics for Sustainable Energy Systems (IESES). IEEE, 2020. http://dx.doi.org/10.1109/ieses45645.2020.9210666.
Der volle Inhalt der QuelleLeino, Marina S., Jane A. Warner, Nick Platt und Donna E. Davies. „The Scavenger Receptor SCARA5 Is Expressed In Human Alveolar Epithelial Cells“. In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a4975.
Der volle Inhalt der QuelleKelshaw, Patricia, Cook Nathan, Iverson Grant, Terry Douglas, Cortes Nelson, Hacherl Samantha, Erdman Nicholas und Caswell Shane. „12.12 The test-retest reliability of the child SCAT5“. In 6th International Conference on Concussion in Sport. BMJ Publishing Group Ltd and British Association of Sport and Exercise Medicine, 2024. http://dx.doi.org/10.1136/bjsports-2023-concussion.181.
Der volle Inhalt der QuelleYeshwanth, V., Ankur Deshwal, Sundeep Krishnadasan, Seungwon Lee und Joonho Song. „Sparse CNN Architecture Search (Scas)“. In 2020 IEEE International Conference on Multimedia and Expo (ICME). IEEE, 2020. http://dx.doi.org/10.1109/icme46284.2020.9102879.
Der volle Inhalt der QuelleLi, Yuanyuan, Zhexin Li, Yu Liu und Yumei Wang. „SCAST: Wireless Video Multicast Scheme Based on Segmentation and Softcast“. In 2017 IEEE Wireless Communications and Networking Conference (WCNC). IEEE, 2017. http://dx.doi.org/10.1109/wcnc.2017.7925618.
Der volle Inhalt der QuellePrato, Thomas, Julianne Schmidt und Robert Lynall. „2.17 The relationship between symptom severity and child SCAT5 performance“. In 6th International Conference on Concussion in Sport. BMJ Publishing Group Ltd and British Association of Sport and Exercise Medicine, 2024. http://dx.doi.org/10.1136/bjsports-2023-concussion.208.
Der volle Inhalt der QuelleBruce, Jared, Willem Meeuwisse, Paul Comper, Michael Hutchison, John Rizos, Joanie Thelen, Stephanie Ruppen und Ruben Echemendia. „3.2 Development of SCAT5 reliable change metrics in professional hockey“. In 6th International Conference on Concussion in Sport. BMJ Publishing Group Ltd and British Association of Sport and Exercise Medicine, 2024. http://dx.doi.org/10.1136/bjsports-2023-concussion.42.
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