| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sonto Silindile Mkhabela, Hussein Shimelis, Abe Shegro Gerrano, Jacob Mashil. Drought Tolerance Assessment of Okra ( Life (Basel, Switzerland). vol 13. issue 3. 2023-03-29. PMID:36983840. |
twenty-six genetically diverse okra accessions were screened under non-stressed (ns) and drought-stressed (ds) conditions under a controlled glasshouse environment using a 13 × 2 alpha lattice design in three replicates, in two growing seasons. |
2023-03-29 |
2023-08-14 |
Not clear |
| Susanna Pagni, Helena Martins Custodio, Adam Frankish, Jonathan M Mudge, James D Mills, Sanjay M Sisodiy. SCN1A: bioinformatically-informed revised boundaries for promoter and enhancer regions. Human molecular genetics. 2023-01-30. PMID:36715146. |
pathogenic variations in the sodium voltage-gated channel alpha subunit 1 (scn1a) gene are responsible for multiple epilepsy phenotypes, including dravet syndrome (ds), febrile seizures (fs), and genetic epilepsy with febrile seizures plus (gefs+). |
2023-01-30 |
2023-08-14 |
human |
| Lisa M Clayton, Edwina Williams, Simona Balestrini, Sanjay M Sisodiy. Case report: Dravet syndrome, feeding difficulties and gastrostomy. Frontiers in neurology. vol 13. 2022-09-30. PMID:36176564. |
dravet syndrome (ds) is a developmental and epileptic encephalopathy associated with variants in the voltage-gated sodium channel alpha 1 subunit ( |
2022-09-30 |
2023-08-14 |
Not clear |
| Damián Sánchez-Ramírez, Rafael Medrano-Guzmán, Fernando Candanedo-González, Jazmín De Anda-González, Luis Enrique García-Rios, Vadim Pérez-Koldenkova, Marcos Gutiérrez-de la Barrera, Sara Rodríguez-Enríquez, Marco Velasco-Velázquez, Silvia Cecilia Pacheco-Velázquez, Patricia Piña-Sánchez, Héctor Mayani, Alejandro Gómez-Delgado, Alberto Monroy-García, Ana Karen Martínez-Lara, Juan José Montesino. High expression of both desmoplastic stroma and epithelial to mesenchymal transition markers associate with shorter survival in pancreatic ductal adenocarcinoma. European journal of histochemistry : EJH. vol 66. issue 1. 2022-02-17. PMID:35174683. |
the purpose of this study was to investigate the association between expression of ds and emt markers and survival variability in patients diagnosed with pdac. we examined the expression levels of ds markers alpha smooth muscle actin (α-sma), fibronectin, and vimentin, and the emt markers epithelial cell adhesion molecule (epcam), pan-cytokeratin, and vimentin, by immunohistochemistry using a tissue microarray of a retrospective cohort of 25 patients with pdac. |
2022-02-17 |
2023-08-13 |
Not clear |
| Masahiro Kanatani, Tadashi Adachi, Ryoichi Sakata, Yoko Nishimura, Yoshiaki Saito, Yoshihiro Maegaki, Yasuhiro Watanabe, Ritsuko Hanajim. Dravet syndrome with parkinsonian symptoms and intact dopaminergic neurons: A case report. Brain & development. vol 43. issue 3. 2021-10-04. PMID:33199159. |
dravet syndrome (ds) is severe myoclonic epilepsy in infancy and associated with a heterozygous mutation of the gene for the sodium channel alpha 1 subunit (scn1a). |
2021-10-04 |
2023-08-13 |
Not clear |
| Maggi Janelly Barrientos-Roldán, Carlos Antonio Abella-Medrano, Sergio Ibáñez-Bernal, César Antonio Sandoval-Rui. Landscape Anthropization Affects Mosquito Diversity in a Deciduous Forest in Southeastern Mexico. Journal of medical entomology. 2021-09-03. PMID:34477878. |
we measured alpha diversity using the shannon index (h'), shannon exponential (eh) and simpson dominance (ds), and beta diversity using jaccard's coefficient of similarity (ij). |
2021-09-03 |
2023-08-13 |
human |
| Ágnes Till, Judith Zima, Anett Fekete, Judit Bene, Márta Czakó, András Szabó, Béla Melegh, Kinga Hadzsie. Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy. Seizure. vol 74. 2020-11-16. PMID:31765958. |
the vast majority of mutations responsible for epilepsy syndromes such as genetic epilepsy with febrile seizures plus (gefs+) and dravet syndrome (ds) occur in the gene encoding the type 1 alpha subunit of neuronal voltage-gated sodium channel (scn1a). |
2020-11-16 |
2023-08-13 |
Not clear |
| Berhanu T Ertiro, Yoseph Beyene, Biswanath Das, Stephen Mugo, Michael Olsen, Sylvester Oikeh, Collins Juma, Maryke Labuschagne, Boddupalli M Prasann. Combining ability and testcross performance of drought-tolerant maize inbred lines under stress and non-stress environments in Kenya. Plant breeding = Zeitschrift fur Pflanzenzuchtung. vol 136. issue 2. 2020-10-01. PMID:28781399. |
forty-nine experimental three-way cross hybrids, generated from a 7 × 7 line by tester crosses, and six commercial checks were evaluated across 11 optimum, ds and ln sites in kenya in 2014 using an alpha lattice design with two replicates per entry at each site. |
2020-10-01 |
2023-08-13 |
Not clear |
| Marcel Ruiz-Mejia. Outer Brain Oscillations in Down Syndrome. Frontiers in systems neuroscience. vol 13. 2020-10-01. PMID:31139056. |
the first sections focus specially on the alpha phenotype consistently observed in ds subjects, as well as its description in ds childhood and aging. |
2020-10-01 |
2023-08-13 |
mouse |
| Marcel Ruiz-Mejia. Outer Brain Oscillations in Down Syndrome. Frontiers in systems neuroscience. vol 13. 2020-10-01. PMID:31139056. |
in this direction, a view of alpha and gamma rhythms generated by the cerebral cortex as a tool for evaluating an unbalance between excitation and inhibition in ds is claimed, which points out toward an over-inhibited network. |
2020-10-01 |
2023-08-13 |
mouse |
| Sarah Hamburg, Richard Rosch, Carla Marie Startin, Karl John Friston, André Strydo. Dynamic Causal Modeling of the Relationship between Cognition and Theta-alpha Oscillations in Adults with Down Syndrome. Cerebral cortex (New York, N.Y. : 1991). vol 29. issue 5. 2020-06-17. PMID:30877793. |
results suggest intrinsic self-inhibition within the alpha network is associated with individual differences in cognitive ability in adults with ds, and may provide a potential therapeutic target for cognitive enhancement. |
2020-06-17 |
2023-08-13 |
Not clear |
| Xiaoguang Shi, Wenxin He, Shanshan Guo, Bingying Zhang, Shuanglai Ren, Kunmei Liu, Tao Sun, Jianqi Cu. RNA-seq Analysis of the SCN1A-KO Model based on CRISPR/Cas9 Genome Editing Technology. Neuroscience. vol 398. 2019-03-18. PMID:30529264. |
dravet syndrome (ds) is a disease that is primarily caused by the inactivation of the scn1a-encoded voltage-gated sodium channel alpha subunit (nav1.1). |
2019-03-18 |
2023-08-13 |
Not clear |
| Antonella Izzo, Rosanna Manco, Ferdinando Bonfiglio, Gaetano Calì, Tiziana De Cristofaro, Simone Patergnani, Rita Cicatiello, Rosella Scrima, Mariastella Zannini, Paolo Pinton, Anna Conti, Lucio Nitsc. NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome. Human molecular genetics. vol 23. issue 16. 2016-03-22. PMID:24698981. |
our recent studies on ds fetal hearts and fibroblasts have suggested that one of the possible causes of mitochondrial dysfunction is the downregulation of peroxisome proliferator-activated receptor gamma, coactivator 1 alpha (pgc-1α or ppargc1a)--a key modulator of mitochondrial function--and of several nuclear-encoded mitochondrial genes (nemgs). |
2016-03-22 |
2023-08-13 |
human |
| Joana Acha, Alejandro Pérez, Doug J Davidson, Manuel Carreira. Cognitive characterization of children with Dravet syndrome: A neurodevelopmental perspective. Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence. vol 21. issue 5. 2016-02-23. PMID:25270117. |
dravet syndrome (ds) is an epilepsy of infantile onset, usually related to a mutation in gene sodium channel alpha 1 subunit, that leads to different typological seizures before the first year of life. |
2016-02-23 |
2023-08-13 |
Not clear |
| Carlos M Tejero-Gonzalez, David Martinez-Gomez, Jorge Bayon-Serna, Rocio Izquierdo-Gomez, Jose Castro-Piñero, Oscar L Veig. Reliability of the ALPHA health-related fitness test battery in adolescents with Down syndrome. Journal of strength and conditioning research. vol 27. issue 11. 2014-11-10. PMID:23442277. |
the extended alpha health-related fitness test battery was performed twice within 1 month in 17 apparently healthy adolescents, aged 12-18 years, with ds who had an intelligence quotient ≥ 35. |
2014-11-10 |
2023-08-12 |
Not clear |
| Carlos M Tejero-Gonzalez, David Martinez-Gomez, Jorge Bayon-Serna, Rocio Izquierdo-Gomez, Jose Castro-Piñero, Oscar L Veig. Reliability of the ALPHA health-related fitness test battery in adolescents with Down syndrome. Journal of strength and conditioning research. vol 27. issue 11. 2014-11-10. PMID:23442277. |
the alpha health-related fitness battery is reliable for measuring health-related components of fitness in adolescents with ds. |
2014-11-10 |
2023-08-12 |
Not clear |
| Gea Guerrier. Putative chitin synthases from Branchiostoma floridae show extracellular matrix-related domains and mosaic structures. Genomics, proteomics & bioinformatics. vol 10. issue 4. 2013-06-21. PMID:23084775. |
in particular, the presence of a discoidin (ds) and a sterile alpha motif (sam) domain was found in nine identified proteins. |
2013-06-21 |
2023-08-12 |
Not clear |
| Gregory L Holmes, Alex C Bender, Edie X Wu, Rod C Scott, Pierre Pascal Lenck-Santini, Richard P Mors. Maturation of EEG oscillations in children with sodium channel mutations. Brain & development. vol 34. issue 6. 2012-10-12. PMID:21940124. |
the majority of children with ds carry mutations of the gene scn1a, which codes for the alpha subunit of the type 1 voltage-gated sodium channel and is important for the function of interneurons. |
2012-10-12 |
2023-08-12 |
Not clear |
| Gregory L Holmes, Alex C Bender, Edie X Wu, Rod C Scott, Pierre Pascal Lenck-Santini, Richard P Mors. Maturation of EEG oscillations in children with sodium channel mutations. Brain & development. vol 34. issue 6. 2012-10-12. PMID:21940124. |
in ds children between 3 and 5years there were significant decreases in percentage of alpha power compared to controls and in ds children over age 6years there was a marked increase of theta and decrease of alpha compared to controls. |
2012-10-12 |
2023-08-12 |
Not clear |
| Jung Sub Lee, Kuen Tak Suh, Jeung Il Kim, Jong Min Lim, Tae Sik Go. Association of estrogen receptor gene polymorphism in patients with degenerative lumbar spondylolisthesise. Journal of Korean Neurosurgical Society. vol 50. issue 5. 2012-08-23. PMID:22259687. |
the purpose of this study was to investigate the possible association of estrogen receptor alpha (erα) gene polymorphisms in a cohort of degenerative spondylolisthesis (ds) patients. |
2012-08-23 |
2023-08-12 |
Not clear |