Artigos de revistas sobre o tema "Scas15"
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Silva, Iago Castro da, Eveson Oscar Almeida Conceição, Daniel Santiago Pereira, Hervé Rogez e 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, n.º 2 (20 de janeiro de 2023): 223. http://dx.doi.org/10.3390/antibiotics12020223.
Texto completo da fonteGardner, R. J. M. ""SCA16" is really SCA15". Journal of Medical Genetics 45, n.º 3 (22 de outubro de 2007): 192. http://dx.doi.org/10.1136/jmg.2007.056341.
Texto completo da fonteKaur, 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, n.º 3 (8 de outubro de 2020): 283–89. http://dx.doi.org/10.3233/jhd-200398.
Texto completo da fonteSeixas, Ana I., Martin H. Maurer, Mark Lin, Colleen Callahan, Alka Ahuja, Tohru Matsuura, Christopher A. Ross, Fuki M. Hisama, Isabel Silveira e Russell L. Margolis. "FXTAS, SCA10, and SCA17 in American patients with movement disorders". American Journal of Medical Genetics Part A 136A, n.º 1 (2005): 87–89. http://dx.doi.org/10.1002/ajmg.a.30761.
Texto completo da fonteGhanem, Mustafa H., Andrew J. Shih, Himanshu Vashistha, Latanya N. Coke, Wentian Li, Sun Jung Kim, Kim R. Simpfendorfer e Peter K. Gregersen. "Investigations into SCAMP5, a candidate lupus risk gene expressed in plasmacytoid dendritic cells". Lupus Science & Medicine 8, n.º 1 (novembro de 2021): e000567. http://dx.doi.org/10.1136/lupus-2021-000567.
Texto completo da fontePouw, Juliëtte N., Michel A. M. Olde Nordkamp, Tom G. O'Toole, Timothy R. D. J. Radstake, Emmerik F. A. Leijten e Marianne Boes. "Activation-induced colocalisation of SCAMP5 with IFNα in human plasmacytoid dendritic cells". Lupus Science & Medicine 9, n.º 1 (março de 2022): e000680. http://dx.doi.org/10.1136/lupus-2022-000680.
Texto completo da fonteFlockerzi, Fidelis Andrea, Johannes Hohneck, Matthias Saar, Rainer Maria Bohle e Phillip Rolf Stahl. "SCARA5 Is Overexpressed in Prostate Cancer and Linked to Poor Prognosis". Diagnostics 13, n.º 13 (29 de junho de 2023): 2211. http://dx.doi.org/10.3390/diagnostics13132211.
Texto completo da fonteFlockerzi, Fidelis Andrea, Johannes Hohneck, Frank Langer, Wolfgang Tränkenschuh e Phillip Rolf Stahl. "The Role of SCARA5 as a Potential Biomarker in Squamous Cell Carcinoma of the Lung". International Journal of Molecular Sciences 25, n.º 13 (4 de julho de 2024): 7355. http://dx.doi.org/10.3390/ijms25137355.
Texto completo da fonteYousaf, Hammad, Ambrin Fatima, Zafar Ali, Shahid M. Baig, Mathias Toft e Zafar Iqbal. "A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family". Genes 13, n.º 9 (17 de setembro de 2022): 1667. http://dx.doi.org/10.3390/genes13091667.
Texto completo da fonteLee, Unghwi, Chunghon Choi, Seung Hyun Ryu, Daehun Park, Sang-Eun Lee, Kitae Kim, Yujin Kim e 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, n.º 2 (28 de dezembro de 2020): e2011371118. http://dx.doi.org/10.1073/pnas.2011371118.
Texto completo da fonteGanesamoorthy, Devika, Damien L. Bruno, Jacqueline Schoumans, Elsdon Storey, Martin B. Delatycki, Danqing Zhu, Morgan K. Wei, Garth A. Nicholson, R. J. McKinlay Gardner e 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, n.º 7 (1 de julho de 2009): 1415–18. http://dx.doi.org/10.1373/clinchem.2009.124958.
Texto completo da fonteYu, Bowen, Chen Cheng, Yichun Wu, Luqiang Guo, Dandan Kong, Ze Zhang, Yuanyuan Wang, Enlin Zheng, Yingbin Liu e Yongning He. "Interactions of ferritin with scavenger receptor class A members". Journal of Biological Chemistry 295, n.º 46 (9 de setembro de 2020): 15727–41. http://dx.doi.org/10.1074/jbc.ra120.014690.
Texto completo da fontePakdaman, 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, n.º 11 (30 de maio de 2021): 5870. http://dx.doi.org/10.3390/ijms22115870.
Texto completo da fonteSchuster, S., E. Heuten, A. Velic, J. Admard, M. Synofzik, S. Ossowski, B. Macek, S. Hauser e L. Schöls. "CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons". Disease Models & Mechanisms 13, n.º 10 (1 de outubro de 2020): dmm045096. http://dx.doi.org/10.1242/dmm.045096.
Texto completo da fonteYu, Yanqiu, Joyce Hoi-Yuk Ng, Anise M. S. Wu, Juliet Honglei Chen, Deborah Baofeng Wang, Guohua Zhang, Mengni Du, Dajin Du, Mingxuan Du e 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, n.º 24 (9 de dezembro de 2022): 16535. http://dx.doi.org/10.3390/ijerph192416535.
Texto completo da fonteCagnoli, Claudia, Chiara Michielotto, Tohru Matsuura, Tetsuo Ashizawa, Russell L. Margolis, Susan E. Holmes, Cinzia Gellera, Nicola Migone e 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, n.º 2 (maio de 2004): 96–100. http://dx.doi.org/10.1016/s1525-1578(10)60496-5.
Texto completo da fonteJumai, Kawuli, Tangjuan Zhang, Bingzhang Qiao, Julaiti Ainiwaer, Haiping Zhang, Zhichao Hou, Idris Awut, Madinyat Niyaz, Liwei Zhang e Ilyar Sheyhidin. "Highly Expressing SCARA5 Promotes Proliferation and Migration of Esophageal Squamous Cell Carcinoma". Journal of Immunology Research 2022 (17 de junho de 2022): 1–21. http://dx.doi.org/10.1155/2022/2555647.
Texto completo da fonteWaters, M. F., e S. M. Pulst. "SCA13". Cerebellum 7, n.º 2 (junho de 2008): 165–69. http://dx.doi.org/10.1007/s12311-008-0039-7.
Texto completo da fonteAmato, Davide, Fabio Canneva, Huu Phuc Nguyen, Peter Bauer, Olaf Riess, Stephan von Hörsten e Christian P. Müller. "Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic rat". Journal of Psychopharmacology 31, n.º 4 (10 de novembro de 2016): 461–73. http://dx.doi.org/10.1177/0269881116675510.
Texto completo da fonteRomaniello, 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, n.º 12 (16 de junho de 2022): 6723. http://dx.doi.org/10.3390/ijms23126723.
Texto completo da fontePaucar, 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, n.º 1 (6 de janeiro de 2021): e546. http://dx.doi.org/10.1212/nxg.0000000000000546.
Texto completo da fonteMassey, 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, n.º 1 (23 de janeiro de 2023): e200051. http://dx.doi.org/10.1212/nxg.0000000000200051.
Texto completo da fonteBouskila, Michale, Noor Esoof, Laurie Gay, Emily H. Fang, Maria Deak, Michael J. Begley, Lewis C. Cantley, Alan Prescott, Kate G. Storey e Dario R. Alessi. "TTBK2 kinase substrate specificity and the impact of spinocerebellar-ataxia-causing mutations on expression, activity, localization and development". Biochemical Journal 437, n.º 1 (14 de junho de 2011): 157–67. http://dx.doi.org/10.1042/bj20110276.
Texto completo da fonteZhao, Jian, Jing Zhu e 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, n.º 2 (9 de agosto de 2013): 259–65. http://dx.doi.org/10.1042/bj20130034.
Texto completo da fontePark, Won Sun, Jin Han, Nari Kim, Jae-Hong Ko, Sung Joon Kim e 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, n.º 6 (dezembro de 2005): H2461—H2467. http://dx.doi.org/10.1152/ajpheart.00331.2005.
Texto completo da fonteMoro, Adriana, e Hélio Afonso Ghizoni Teive. "Cognitive impairment in Spinocerebellar ataxia type 10". Dementia & Neuropsychologia 10, n.º 4 (dezembro de 2016): 310–14. http://dx.doi.org/10.1590/s1980-5764-2016dn1004009.
Texto completo da fonteCho, Jin Whan, Sung Yeon Kim, Sung Sup Park e 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, n.º 4 (setembro de 2008): 488–90. http://dx.doi.org/10.1017/s0317167100009161.
Texto completo da fonteHubert, 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, n.º 2 (22 de agosto de 2019): 138–44. http://dx.doi.org/10.1136/jmedgenet-2018-105927.
Texto completo da fonteCho, Seongkyung, e Christopher S. Hayter. "Erratum to: Under pressure: A systematic review of stress and its impact among graduate students". Science and Public Policy 47, n.º 6 (1 de dezembro de 2020): 893. http://dx.doi.org/10.1093/scipol/scab015.
Texto completo da fontevan Welie, Mara J., Wouter P. C. Boon e Bernhard Truffer. "Innovation system formation in international development cooperation: The role of intermediaries in urban sanitation". Science and Public Policy 47, n.º 3 (19 de fevereiro de 2020): 333–47. http://dx.doi.org/10.1093/scipol/scaa015.
Texto completo da fonteKnight, Melanie A., Marina L. Kennerson, Richard J. Anney, Tohru Matsuura, Garth A. Nicholson, Peyman Salimi-Tari, R. J. McKinlay Gardner, Elsdon Storey e Susan M. Forrest. "Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter:". Neurobiology of Disease 13, n.º 2 (julho de 2003): 147–57. http://dx.doi.org/10.1016/s0969-9961(03)00029-9.
Texto completo da fonteBaran, Enrique J., Karolina Schwendtner e Uwe Kolitsch. "Vibrational spectra of ScAsO4·H2O". Journal of Raman Spectroscopy 37, n.º 12 (2006): 1453–55. http://dx.doi.org/10.1002/jrs.1635.
Texto completo da fonteTeive, Hélio Afonso Ghizoni, Adriana Moro, Mariana Moscovich, Walter Oleskho Arruda, Renato Puppi Munhoz, Salmo Raskin, Gladys Mary Ghizoni Teive, Norberto Dallabrida e Tetsuo Ashizawa. "Spinocerebellar ataxia type 10 in the South of Brazil: the Amerindian-Belgian connection". Arquivos de Neuro-Psiquiatria 73, n.º 8 (agosto de 2015): 725–27. http://dx.doi.org/10.1590/0004-282x20150086.
Texto completo da fonteTeive, Hélio A. G., Walter O. Arruda, Salmo Raskin, Tetsuo Ashizawa e Lineu César Werneck. "The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene". Arquivos de Neuro-Psiquiatria 65, n.º 4a (dezembro de 2007): 965–68. http://dx.doi.org/10.1590/s0004-282x2007000600008.
Texto completo da fonteNamikawa, Kazuhiko, Alessandro Dorigo e Reinhard W. Köster. "Neurological Disease Modelling for Spinocerebellar Ataxia Using Zebrafish". Journal of Experimental Neuroscience 13 (janeiro de 2019): 117906951988051. http://dx.doi.org/10.1177/1179069519880515.
Texto completo da fonteMezey, Szilvia E., Josef P. Kapfhammer e Etsuko Shimobayashi. "Transcriptome Profile of a New Mouse Model of Spinocerebellar Ataxia Type 14 Implies Changes in Cerebellar Development". Genes 13, n.º 8 (9 de agosto de 2022): 1417. http://dx.doi.org/10.3390/genes13081417.
Texto completo da fonteVan 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, n.º 2007 (2005): e108. http://dx.doi.org/10.1371/journal.pgen.0030108.eor.
Texto completo da fonteBaviera-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, n.º 6 (14 de novembro de 2022): e200038. http://dx.doi.org/10.1212/nxg.0000000000200038.
Texto completo da fontePark, Hyeyoung, Han-Joon Kim e Beom S. Jeon. "Parkinsonism in Spinocerebellar Ataxia". BioMed Research International 2015 (2015): 1–11. http://dx.doi.org/10.1155/2015/125273.
Texto completo da fonteMENDES-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 (agosto de 2013): 0. http://dx.doi.org/10.1111/j.1755-3768.2013.2475.x.
Texto completo da fonteGálvez-Nieto, José Luis, Ítalo Trizano-Hermosilla e Karina Polanco-Levicán. "Psychometric Evaluation of the School Climate and School Identification Measure—Student on Chilean Students: A Bifactor Model Approach". Children 11, n.º 1 (11 de janeiro de 2024): 87. http://dx.doi.org/10.3390/children11010087.
Texto completo da fonteJain, Dr Rahul, Dr Pankaj Rathi, Dr Hashash Singh Ishar, Dr Kapil Telang, Dr Dinesh Chouksey e Dr Ajoy Sodani. "Spinocerebellar Ataxia 17: A clinical Rubik’s cube". American Research Journal of Clinical Case Reports 2, n.º 1 (28 de novembro de 2020): 1–3. http://dx.doi.org/10.21694/2639-3069.20002.
Texto completo da fontede Vos, C. M., J. D. Bregman e 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.
Texto completo da fonteDudding, T. E., K. Friend, P. W. Schofield, S. Lee, I. A. Wilkinson e R. I. Richards. "Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus". Neurology 63, n.º 12 (28 de dezembro de 2004): 2288–92. http://dx.doi.org/10.1212/01.wnl.0000147299.80872.d1.
Texto completo da fonteMoscovich, Mariana, Renato Puppi Munhoz, Adriana Moro, Salmo Raskin, Karen McFarland, Tetsuo Ashizawa, Helio A. G. Teive e Laura Silveira-Moriyama. "Olfactory Function in SCA10". Cerebellum 18, n.º 1 (19 de junho de 2018): 85–90. http://dx.doi.org/10.1007/s12311-018-0954-1.
Texto completo da fonteNuzhnyy, E. P., N. Yu Abramycheva, S. A. Klyushnikov e S. N. Illarioshkin. "The first family case of spinocerebellar ataxia type 14 in Russia". Neuromuscular Diseases 12, n.º 3 (21 de setembro de 2022): 45–51. http://dx.doi.org/10.17650/2222-8721-2022-12-3-45-51.
Texto completo da fonteÁngel, Carlos Ariel, Carlos Alberto Rivillas, Nancy Arciniegas e Juan Manuel López. "Bases para el manejo de la gotera u ojo de gallo del cafeto en Colombia". Avances Técnicos Cenicafé 490 (1 de abril de 2018): 1–8. http://dx.doi.org/10.38141/10779/0490.
Texto completo da fonteGunawardane, Kosala, Nalin Bandara, Kasun Subasinghage e Nihal Kularatna. "Extending the Input Voltage Range of Solar PV Inverters with Supercapacitor Energy Circulation". Electronics 10, n.º 1 (4 de janeiro de 2021): 88. http://dx.doi.org/10.3390/electronics10010088.
Texto completo da fonteSantos, Laudiane Reis, Hélio Afonso Ghizoni Teive, Francisco Diego Negrão Lopes Neto, Ana Carolina Brandt de Macedo, Neliana Maria de Mello e Marise Bueno Zonta. "Quality of life in individuals with spinocerebellar ataxia type 10: a preliminary study". Arquivos de Neuro-Psiquiatria 76, n.º 8 (agosto de 2018): 527–33. http://dx.doi.org/10.1590/0004-282x20180077.
Texto completo da fonteSalih, M., M. Hamad, M. Seidahmed, A. Binbakheet, I. Alorainy e N. Kaya. "Founder mutation in RUBCN gene in a second family confirms Salih ataxia (scar15)". Journal of the Neurological Sciences 405 (outubro de 2019): 7. http://dx.doi.org/10.1016/j.jns.2019.10.1558.
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