Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ruth Rea"'
Partición de una Red Eléctrica de Distribución Aplicando Algoritmos de Agrupamiento K-means y DBSCAN
Publikováno v:
Revista Técnica Energía, Vol 20, Iss 1 (2023)
En este artículo se propone la metodología para realizar la partición eléctrica de una red de distribución utilizando algoritmos de agrupamiento de datos como K-means y DBSCAN. Los datos se obtienen generando variaciones en los parámetros de la
Externí odkaz:
https://doaj.org/article/e6bc6a46181346e8b3606d7b080f8c15
Publikováno v:
Informática y Sistemas, Vol 6, Iss 1, Pp 22-34 (2022)
Currently exist a large amount of news in a digital format that need to be classified or labeled automatically according to their content. LDA is an unsupervised technique that automatically creates topics based on words in documents. The present wor
Externí odkaz:
https://doaj.org/article/be24305013674ef9b2f6e48b3c2563f4
Publikováno v:
Neuron. 41:755-766
Cone photoreceptors tonically release neurotransmitter in the dark through a continuous cycle of exocytosis and endocytosis. Here, using the synaptic vesicle marker FM1-43, we elucidate specialized features of the vesicle cycle. Unlike retinal bipola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a0ad39bc38557a10afea4089a8ff46
https://doi.org/10.1016/s0896-6273(04)00088-1
https://doi.org/10.1016/s0896-6273(04)00088-1
Publikováno v:
European Journal of Neuroscience. 16:186-196
The human disease hyperekplexia is characterized by excessive startle reactions to auditory and cutaneous stimuli. In its familial form, hyperekplexia has been associated with both dominant and recessive mutations of the GLRA1 gene encoding the glyci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c463bc9228712319f7a4901b34cffcc3
https://doi.org/10.1046/j.1460-9568.2002.02054.x
https://doi.org/10.1046/j.1460-9568.2002.02054.x
Publikováno v:
The Journal of Physiology. 538:5-23
Mutations of KCNA1, which codes for the K(+) channel subunit hKv1.1, are associated with the human autosomal dominant disease episodic ataxia type 1 (EA1). Five recently described mutations are associated with a broad range of phenotypes: neuromyoton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1a94797617f8352620ce8ac3db4e85
https://doi.org/10.1113/jphysiol.2001.013242
https://doi.org/10.1113/jphysiol.2001.013242
Autor:
Robert McWilliam, S. Youroukos, L. H. Eunson, A Spauschus, Rocco Liguori, John Stephenson, Ruth Rea, Patrizia Avoni, Dimitri M. Kullmann, C. P. Panayiotopoulos, Michael G. Hanna, Sameer M. Zuberi
Publikováno v:
Annals of Neurology. 48:647-656
Episodic ataxia type 1 (EA1) is an autosomal dominant central nervous system potassium channelopathy characterized by brief attacks of cerebellar ataxia and continuous interictal myokymia. Point mutations in the voltage-gated potassium channel gene K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0700cf63c670e7efc0d8c933b043473e
https://doi.org/10.1002/1531-8249(200010)48:4<647::aid-ana12>3.0.co
https://doi.org/10.1002/1531-8249(200010)48:4<647::aid-ana12>3.0.co
Publikováno v:
The Journal of Cell Biology
We have used digital fluorescence imaging techniques to explore the interplay between mitochondrial Ca2+ uptake and physiological Ca2+ signaling in rat cortical astrocytes. A rise in cytosolic Ca2+ ([Ca2+]cyt), resulting from mobilization of ER Ca2+
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed7b07c5ba5fa9ae8f107a45503cb75b
https://doi.org/10.1083/jcb.145.4.795
https://doi.org/10.1083/jcb.145.4.795
Publikováno v:
Journal of Medical Internet Research, Vol 24, Iss 7, p e37233 (2022)
BackgroundDiabetes is a public health problem worldwide. Although diabetes is a chronic and incurable disease, measures and treatments can be taken to control it and keep the patient stable. Diabetes has been the subject of extensive research, rangin
Externí odkaz:
https://doaj.org/article/b7ef173db53d4ed69570aa9324b73b7e
Autor:
Sue-Yeon, Choi, Bart G, Borghuis, Bart, Borghuis, Ruth, Rea, Edwin S, Levitan, Peter, Sterling, Richard H, Kramer
Publikováno v:
Neuron. 48(6)
How cone synapses encode light intensity determines the precision of information transmission at the first synapse on the visual pathway. Although it is known that cone photoreceptors hyperpolarize to light over 4-5 log units of intensity, the relati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296c7b566e3202ca4143632d33622469
Publikováno v:
The European journal of neuroscience. 16(2)
The human disease hyperekplexia is characterized by excessive startle reactions to auditory and cutaneous stimuli. In its familial form, hyperekplexia has been associated with both dominant and recessive mutations of the GLRA1 gene encoding the glyci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e665a59d407d9d0d97af1b6a40a01229
https://pubmed.ncbi.nlm.nih.gov/12169101
https://pubmed.ncbi.nlm.nih.gov/12169101