Journal articles on the topic 'Scas15'
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Silva, Iago Castro da, Eveson Oscar Almeida Conceição, Daniel Santiago Pereira, Hervé Rogez, and 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, no. 2 (January 20, 2023): 223. http://dx.doi.org/10.3390/antibiotics12020223.
Full textGardner, R. J. M. ""SCA16" is really SCA15." Journal of Medical Genetics 45, no. 3 (October 22, 2007): 192. http://dx.doi.org/10.1136/jmg.2007.056341.
Full textKaur, 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, no. 3 (October 8, 2020): 283–89. http://dx.doi.org/10.3233/jhd-200398.
Full textSeixas, Ana I., Martin H. Maurer, Mark Lin, Colleen Callahan, Alka Ahuja, Tohru Matsuura, Christopher A. Ross, Fuki M. Hisama, Isabel Silveira, and Russell L. Margolis. "FXTAS, SCA10, and SCA17 in American patients with movement disorders." American Journal of Medical Genetics Part A 136A, no. 1 (2005): 87–89. http://dx.doi.org/10.1002/ajmg.a.30761.
Full textGhanem, Mustafa H., Andrew J. Shih, Himanshu Vashistha, Latanya N. Coke, Wentian Li, Sun Jung Kim, Kim R. Simpfendorfer, and Peter K. Gregersen. "Investigations into SCAMP5, a candidate lupus risk gene expressed in plasmacytoid dendritic cells." Lupus Science & Medicine 8, no. 1 (November 2021): e000567. http://dx.doi.org/10.1136/lupus-2021-000567.
Full textPouw, Juliëtte N., Michel A. M. Olde Nordkamp, Tom G. O'Toole, Timothy R. D. J. Radstake, Emmerik F. A. Leijten, and Marianne Boes. "Activation-induced colocalisation of SCAMP5 with IFNα in human plasmacytoid dendritic cells." Lupus Science & Medicine 9, no. 1 (March 2022): e000680. http://dx.doi.org/10.1136/lupus-2022-000680.
Full textFlockerzi, Fidelis Andrea, Johannes Hohneck, Matthias Saar, Rainer Maria Bohle, and Phillip Rolf Stahl. "SCARA5 Is Overexpressed in Prostate Cancer and Linked to Poor Prognosis." Diagnostics 13, no. 13 (June 29, 2023): 2211. http://dx.doi.org/10.3390/diagnostics13132211.
Full textFlockerzi, Fidelis Andrea, Johannes Hohneck, Frank Langer, Wolfgang Tränkenschuh, and Phillip Rolf Stahl. "The Role of SCARA5 as a Potential Biomarker in Squamous Cell Carcinoma of the Lung." International Journal of Molecular Sciences 25, no. 13 (July 4, 2024): 7355. http://dx.doi.org/10.3390/ijms25137355.
Full textYousaf, Hammad, Ambrin Fatima, Zafar Ali, Shahid M. Baig, Mathias Toft, and Zafar Iqbal. "A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family." Genes 13, no. 9 (September 17, 2022): 1667. http://dx.doi.org/10.3390/genes13091667.
Full textLee, Unghwi, Chunghon Choi, Seung Hyun Ryu, Daehun Park, Sang-Eun Lee, Kitae Kim, Yujin Kim, and 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, no. 2 (December 28, 2020): e2011371118. http://dx.doi.org/10.1073/pnas.2011371118.
Full textGanesamoorthy, Devika, Damien L. Bruno, Jacqueline Schoumans, Elsdon Storey, Martin B. Delatycki, Danqing Zhu, Morgan K. Wei, Garth A. Nicholson, R. J. McKinlay Gardner, and Howard R. Slater. "Development of a Multiplex Ligation-Dependent Probe Amplification Assay for Diagnosis and Estimation of the Frequency of Spinocerebellar Ataxia Type 15." Clinical Chemistry 55, no. 7 (July 1, 2009): 1415–18. http://dx.doi.org/10.1373/clinchem.2009.124958.
Full textYu, Bowen, Chen Cheng, Yichun Wu, Luqiang Guo, Dandan Kong, Ze Zhang, Yuanyuan Wang, Enlin Zheng, Yingbin Liu, and Yongning He. "Interactions of ferritin with scavenger receptor class A members." Journal of Biological Chemistry 295, no. 46 (September 9, 2020): 15727–41. http://dx.doi.org/10.1074/jbc.ra120.014690.
Full textPakdaman, Yasaman, Siren Berland, Helene J. Bustad, Sigrid Erdal, Bryony A. Thompson, Paul A. James, Kjersti N. Power, et al. "Genetic Dominant Variants in STUB1, Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16." International Journal of Molecular Sciences 22, no. 11 (May 30, 2021): 5870. http://dx.doi.org/10.3390/ijms22115870.
Full textSchuster, S., E. Heuten, A. Velic, J. Admard, M. Synofzik, S. Ossowski, B. Macek, S. Hauser, and L. Schöls. "CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons." Disease Models & Mechanisms 13, no. 10 (October 1, 2020): dmm045096. http://dx.doi.org/10.1242/dmm.045096.
Full textYu, Yanqiu, Joyce Hoi-Yuk Ng, Anise M. S. Wu, Juliet Honglei Chen, Deborah Baofeng Wang, Guohua Zhang, Mengni Du, Dajin Du, Mingxuan Du, and Joseph T. F. Lau. "Psychometric Properties of the Abbreviated Version of the Dual School Climate and School Identification Measure–Student (SCASIM-St15) among Adolescents in China." International Journal of Environmental Research and Public Health 19, no. 24 (December 9, 2022): 16535. http://dx.doi.org/10.3390/ijerph192416535.
Full textCagnoli, Claudia, Chiara Michielotto, Tohru Matsuura, Tetsuo Ashizawa, Russell L. Margolis, Susan E. Holmes, Cinzia Gellera, Nicola Migone, and Alfredo Brusco. "Detection of Large Pathogenic Expansions in FRDA1, SCA10, and SCA12 Genes Using a Simple Fluorescent Repeat-Primed PCR Assay." Journal of Molecular Diagnostics 6, no. 2 (May 2004): 96–100. http://dx.doi.org/10.1016/s1525-1578(10)60496-5.
Full textJumai, Kawuli, Tangjuan Zhang, Bingzhang Qiao, Julaiti Ainiwaer, Haiping Zhang, Zhichao Hou, Idris Awut, Madinyat Niyaz, Liwei Zhang, and Ilyar Sheyhidin. "Highly Expressing SCARA5 Promotes Proliferation and Migration of Esophageal Squamous Cell Carcinoma." Journal of Immunology Research 2022 (June 17, 2022): 1–21. http://dx.doi.org/10.1155/2022/2555647.
Full textWaters, M. F., and S. M. Pulst. "SCA13." Cerebellum 7, no. 2 (June 2008): 165–69. http://dx.doi.org/10.1007/s12311-008-0039-7.
Full textAmato, Davide, Fabio Canneva, Huu Phuc Nguyen, Peter Bauer, Olaf Riess, Stephan von Hörsten, and Christian P. Müller. "Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic rat." Journal of Psychopharmacology 31, no. 4 (November 10, 2016): 461–73. http://dx.doi.org/10.1177/0269881116675510.
Full textRomaniello, Romina, Ludovica Pasca, Elena Panzeri, Fulvio D’Abrusco, Lorena Travaglini, Valentina Serpieri, Sabrina Signorini, et al. "Superior Cerebellar Atrophy: An Imaging Clue to Diagnose ITPR1-Related Disorders." International Journal of Molecular Sciences 23, no. 12 (June 16, 2022): 6723. http://dx.doi.org/10.3390/ijms23126723.
Full textPaucar, Martin, Richard Ågren, Tianyi Li, Simon Lissmats, Åsa Bergendal, Jan Weinberg, Daniel Nilsson, et al. "V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia Exacerbations." Neurology Genetics 7, no. 1 (January 6, 2021): e546. http://dx.doi.org/10.1212/nxg.0000000000000546.
Full textMassey, Sean, Yiran Guo, Lisa G. Riley, Nicole J. Van Bergen, Sarah A. Sandaradura, Elizabeth McCusker, Michel Tchan, et al. "Expanding the Allelic Heterogeneity ofANO10-Associated Autosomal Recessive Cerebellar Ataxia." Neurology Genetics 9, no. 1 (January 23, 2023): e200051. http://dx.doi.org/10.1212/nxg.0000000000200051.
Full textBouskila, Michale, Noor Esoof, Laurie Gay, Emily H. Fang, Maria Deak, Michael J. Begley, Lewis C. Cantley, Alan Prescott, Kate G. Storey, and Dario R. Alessi. "TTBK2 kinase substrate specificity and the impact of spinocerebellar-ataxia-causing mutations on expression, activity, localization and development." Biochemical Journal 437, no. 1 (June 14, 2011): 157–67. http://dx.doi.org/10.1042/bj20110276.
Full textZhao, Jian, Jing Zhu, and William B. Thornhill. "Spinocerebellar ataxia-13 Kv3.3 potassium channels: arginine-to-histidine mutations affect both functional and protein expression on the cell surface." Biochemical Journal 454, no. 2 (August 9, 2013): 259–65. http://dx.doi.org/10.1042/bj20130034.
Full textPark, Won Sun, Jin Han, Nari Kim, Jae-Hong Ko, Sung Joon Kim, and Yung E. Earm. "Activation of inward rectifier K+ channels by hypoxia in rabbit coronary arterial smooth muscle cells." American Journal of Physiology-Heart and Circulatory Physiology 289, no. 6 (December 2005): H2461—H2467. http://dx.doi.org/10.1152/ajpheart.00331.2005.
Full textMoro, Adriana, and Hélio Afonso Ghizoni Teive. "Cognitive impairment in Spinocerebellar ataxia type 10." Dementia & Neuropsychologia 10, no. 4 (December 2016): 310–14. http://dx.doi.org/10.1590/s1980-5764-2016dn1004009.
Full textCho, Jin Whan, Sung Yeon Kim, Sung Sup Park, and Beom S. Jeon. "Spinocerebellar Ataxia Type 12 was not Found in Korean Parkinsonian Patients." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 35, no. 4 (September 2008): 488–90. http://dx.doi.org/10.1017/s0317167100009161.
Full textHubert, Laurence, Magda Cannata Serio, Laure Villoing-Gaudé, Nathalie Boddaert, Anna Kaminska, Marlène Rio, Stanislas Lyonnet, et al. "De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures." Journal of Medical Genetics 57, no. 2 (August 22, 2019): 138–44. http://dx.doi.org/10.1136/jmedgenet-2018-105927.
Full textCho, Seongkyung, and Christopher S. Hayter. "Erratum to: Under pressure: A systematic review of stress and its impact among graduate students." Science and Public Policy 47, no. 6 (December 1, 2020): 893. http://dx.doi.org/10.1093/scipol/scab015.
Full textvan Welie, Mara J., Wouter P. C. Boon, and Bernhard Truffer. "Innovation system formation in international development cooperation: The role of intermediaries in urban sanitation." Science and Public Policy 47, no. 3 (February 19, 2020): 333–47. http://dx.doi.org/10.1093/scipol/scaa015.
Full textKnight, Melanie A., Marina L. Kennerson, Richard J. Anney, Tohru Matsuura, Garth A. Nicholson, Peyman Salimi-Tari, R. J. McKinlay Gardner, Elsdon Storey, and Susan M. Forrest. "Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter:." Neurobiology of Disease 13, no. 2 (July 2003): 147–57. http://dx.doi.org/10.1016/s0969-9961(03)00029-9.
Full textBaran, Enrique J., Karolina Schwendtner, and Uwe Kolitsch. "Vibrational spectra of ScAsO4·H2O." Journal of Raman Spectroscopy 37, no. 12 (2006): 1453–55. http://dx.doi.org/10.1002/jrs.1635.
Full textTeive, Hélio Afonso Ghizoni, Adriana Moro, Mariana Moscovich, Walter Oleskho Arruda, Renato Puppi Munhoz, Salmo Raskin, Gladys Mary Ghizoni Teive, Norberto Dallabrida, and Tetsuo Ashizawa. "Spinocerebellar ataxia type 10 in the South of Brazil: the Amerindian-Belgian connection." Arquivos de Neuro-Psiquiatria 73, no. 8 (August 2015): 725–27. http://dx.doi.org/10.1590/0004-282x20150086.
Full textTeive, Hélio A. G., Walter O. Arruda, Salmo Raskin, Tetsuo Ashizawa, and Lineu César Werneck. "The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene." Arquivos de Neuro-Psiquiatria 65, no. 4a (December 2007): 965–68. http://dx.doi.org/10.1590/s0004-282x2007000600008.
Full textNamikawa, Kazuhiko, Alessandro Dorigo, and Reinhard W. Köster. "Neurological Disease Modelling for Spinocerebellar Ataxia Using Zebrafish." Journal of Experimental Neuroscience 13 (January 2019): 117906951988051. http://dx.doi.org/10.1177/1179069519880515.
Full textMezey, Szilvia E., Josef P. Kapfhammer, and Etsuko Shimobayashi. "Transcriptome Profile of a New Mouse Model of Spinocerebellar Ataxia Type 14 Implies Changes in Cerebellar Development." Genes 13, no. 8 (August 9, 2022): 1417. http://dx.doi.org/10.3390/genes13081417.
Full textVan de Leemput, Joyce, Jayanth Chandran, Melanie Knight, Lynne Holtzclaw, Sonja Scholz, Mark R. Cookson, Henry Houlden, et al. "Deletion at ITPR1 underlies ataxia in mice and humans (SCA15)." PLoS Genetics preprint, no. 2007 (2005): e108. http://dx.doi.org/10.1371/journal.pgen.0030108.eor.
Full textBaviera-Muñoz, Raquel, Lidón Carretero-Vilarroig, Juan Francisco Vázquez-Costa, Carlos Morata-Martínez, Marina Campins-Romeu, Nuria Muelas, Isabel Sastre-Bataller, et al. "Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain." Neurology Genetics 8, no. 6 (November 14, 2022): e200038. http://dx.doi.org/10.1212/nxg.0000000000200038.
Full textPark, Hyeyoung, Han-Joon Kim, and Beom S. Jeon. "Parkinsonism in Spinocerebellar Ataxia." BioMed Research International 2015 (2015): 1–11. http://dx.doi.org/10.1155/2015/125273.
Full textMENDES-JORGE, L., A. VALENÇA, D. RAMOS, M. LOPEZ-LUPPO, J. CATITA, VMR PIRES, V. NACHER, et al. "Scara5 involvement in retinal iron metabolism." Acta Ophthalmologica 91 (August 2013): 0. http://dx.doi.org/10.1111/j.1755-3768.2013.2475.x.
Full textGálvez-Nieto, José Luis, Ítalo Trizano-Hermosilla, and Karina Polanco-Levicán. "Psychometric Evaluation of the School Climate and School Identification Measure—Student on Chilean Students: A Bifactor Model Approach." Children 11, no. 1 (January 11, 2024): 87. http://dx.doi.org/10.3390/children11010087.
Full textJain, Dr Rahul, Dr Pankaj Rathi, Dr Hashash Singh Ishar, Dr Kapil Telang, Dr Dinesh Chouksey, and Dr Ajoy Sodani. "Spinocerebellar Ataxia 17: A clinical Rubik’s cube." American Research Journal of Clinical Case Reports 2, no. 1 (November 28, 2020): 1–3. http://dx.doi.org/10.21694/2639-3069.20002.
Full textde Vos, C. M., J. D. Bregman, and U. J. Schwarz. "Pupil Plane Interferometry: Some Conclusions from SCASIS." Symposium - International Astronomical Union 158 (1994): 419–21. http://dx.doi.org/10.1017/s0074180900108101.
Full textDudding, T. E., K. Friend, P. W. Schofield, S. Lee, I. A. Wilkinson, and R. I. Richards. "Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus." Neurology 63, no. 12 (December 28, 2004): 2288–92. http://dx.doi.org/10.1212/01.wnl.0000147299.80872.d1.
Full textMoscovich, Mariana, Renato Puppi Munhoz, Adriana Moro, Salmo Raskin, Karen McFarland, Tetsuo Ashizawa, Helio A. G. Teive, and Laura Silveira-Moriyama. "Olfactory Function in SCA10." Cerebellum 18, no. 1 (June 19, 2018): 85–90. http://dx.doi.org/10.1007/s12311-018-0954-1.
Full textNuzhnyy, E. P., N. Yu Abramycheva, S. A. Klyushnikov, and S. N. Illarioshkin. "The first family case of spinocerebellar ataxia type 14 in Russia." Neuromuscular Diseases 12, no. 3 (September 21, 2022): 45–51. http://dx.doi.org/10.17650/2222-8721-2022-12-3-45-51.
Full textÁngel, Carlos Ariel, Carlos Alberto Rivillas, Nancy Arciniegas, and Juan Manuel López. "Bases para el manejo de la gotera u ojo de gallo del cafeto en Colombia." Avances Técnicos Cenicafé 490 (April 1, 2018): 1–8. http://dx.doi.org/10.38141/10779/0490.
Full textGunawardane, Kosala, Nalin Bandara, Kasun Subasinghage, and Nihal Kularatna. "Extending the Input Voltage Range of Solar PV Inverters with Supercapacitor Energy Circulation." Electronics 10, no. 1 (January 4, 2021): 88. http://dx.doi.org/10.3390/electronics10010088.
Full textSantos, Laudiane Reis, Hélio Afonso Ghizoni Teive, Francisco Diego Negrão Lopes Neto, Ana Carolina Brandt de Macedo, Neliana Maria de Mello, and Marise Bueno Zonta. "Quality of life in individuals with spinocerebellar ataxia type 10: a preliminary study." Arquivos de Neuro-Psiquiatria 76, no. 8 (August 2018): 527–33. http://dx.doi.org/10.1590/0004-282x20180077.
Full textSalih, M., M. Hamad, M. Seidahmed, A. Binbakheet, I. Alorainy, and N. Kaya. "Founder mutation in RUBCN gene in a second family confirms Salih ataxia (scar15)." Journal of the Neurological Sciences 405 (October 2019): 7. http://dx.doi.org/10.1016/j.jns.2019.10.1558.
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