Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Anna Rożen"'
Autor:
Agata Suleja, Katarzyna Milska-Musa, Łukasz Przysło, Marzena Bednarczyk, Marcin Kostecki, Dominik Cysewski, Paweł Matryba, Anna Rozensztrauch, Michał Dwornik, Marcin Opacki, Robert Śmigiel, Kacper Łukasiewicz
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background Angelman syndrome (AS) is a rare neurodevelopmental disease caused by imprinting disorders that impede the production of the ubiquitin E3A ligase protein (UBE3A). AS affects multiple systems, with the main symptoms including epile
Externí odkaz:
https://doaj.org/article/8a78ed5c3bf449f580b3452a7074d394
Publikováno v:
Frontiers in Psychiatry, Vol 14 (2023)
BackgroundDown Syndrome (DS; OMIM #190685), known as trisomy 21, is one of the most common genetic disorders in the human population and the commonest known cause of intellectual disability. The study was conducted to investigate the quality of life
Externí odkaz:
https://doaj.org/article/6a0da6974cac4b95a646be0d6c9dd2ed
Autor:
Magdalena Kłaniewska, Malgorzata Rydzanicz, Joanna Kosińska, Mateusz Biela, Anna Walczak, Elżbieta Szmida, Anna Rozensztrauch, Rafał Płoski, Robert Śmigiel
Publikováno v:
Pediatria Polska, Vol 96, Iss 2, Pp 148-152 (2021)
CLOVES syndrome is a rare dysmorphic syndrome with multiple defects caused by somatic activating mutations in the PIK3CA gene on chromosome 3q26.32. There are currently less than 200 individuals worldwide living with CLOVES syndrome (OMIM: 612918, OR
Externí odkaz:
https://doaj.org/article/8cbc9b869ca44d05a73d2111c9516a41
Autor:
Helen R. P. Phillips, Elizabeth M. Bach, Marie L. C. Bartz, Joanne M. Bennett, Rémy Beugnon, Maria J. I. Briones, George G. Brown, Olga Ferlian, Konstantin B. Gongalsky, Carlos A. Guerra, Birgitta König-Ries, Julia J. Krebs, Alberto Orgiazzi, Kelly S. Ramirez, David J. Russell, Benjamin Schwarz, Diana H. Wall, Ulrich Brose, Thibaud Decaëns, Patrick Lavelle, Michel Loreau, Jérôme Mathieu, Christian Mulder, Wim H. van der Putten, Matthias C. Rillig, Madhav P. Thakur, Franciska T. de Vries, David A. Wardle, Christian Ammer, Sabine Ammer, Miwa Arai, Fredrick O. Ayuke, Geoff H. Baker, Dilmar Baretta, Dietmar Barkusky, Robin Beauséjour, Jose C. Bedano, Klaus Birkhofer, Eric Blanchart, Bernd Blossey, Thomas Bolger, Robert L. Bradley, Michel Brossard, James C. Burtis, Yvan Capowiez, Timothy R. Cavagnaro, Amy Choi, Julia Clause, Daniel Cluzeau, Anja Coors, Felicity V. Crotty, Jasmine M. Crumsey, Andrea Dávalos, Darío J. Díaz Cosín, Annise M. Dobson, Anahí Domínguez, Andrés Esteban Duhour, Nick van Eekeren, Christoph Emmerling, Liliana B. Falco, Rosa Fernández, Steven J. Fonte, Carlos Fragoso, André L. C. Franco, Abegail Fusilero, Anna P. Geraskina, Shaieste Gholami, Grizelle González, Michael J. Gundale, Mónica Gutiérrez López, Branimir K. Hackenberger, Davorka K. Hackenberger, Luis M. Hernández, Jeff R. Hirth, Takuo Hishi, Andrew R. Holdsworth, Martin Holmstrup, Kristine N. Hopfensperger, Esperanza Huerta Lwanga, Veikko Huhta, Tunsisa T. Hurisso, Basil V. Iannone, Madalina Iordache, Ulrich Irmler, Mari Ivask, Juan B. Jesús, Jodi L. Johnson-Maynard, Monika Joschko, Nobuhiro Kaneko, Radoslava Kanianska, Aidan M. Keith, Maria L. Kernecker, Armand W. Koné, Yahya Kooch, Sanna T. Kukkonen, H. Lalthanzara, Daniel R. Lammel, Iurii M. Lebedev, Edith Le Cadre, Noa K. Lincoln, Danilo López-Hernández, Scott R. Loss, Raphael Marichal, Radim Matula, Yukio Minamiya, Jan Hendrik Moos, Gerardo Moreno, Alejandro Morón-Ríos, Hasegawa Motohiro, Bart Muys, Johan Neirynck, Lindsey Norgrove, Marta Novo, Visa Nuutinen, Victoria Nuzzo, P. Mujeeb Rahman, Johan Pansu, Shishir Paudel, Guénola Pérès, Lorenzo Pérez-Camacho, Jean-François Ponge, Jörg Prietzel, Irina B. Rapoport, Muhammad Imtiaz Rashid, Salvador Rebollo, Miguel Á. Rodríguez, Alexander M. Roth, Guillaume X. Rousseau, Anna Rozen, Ehsan Sayad, Loes van Schaik, Bryant Scharenbroch, Michael Schirrmann, Olaf Schmidt, Boris Schröder, Julia Seeber, Maxim P. Shashkov, Jaswinder Singh, Sandy M. Smith, Michael Steinwandter, Katalin Szlavecz, José Antonio Talavera, Dolores Trigo, Jiro Tsukamoto, Sheila Uribe-López, Anne W. de Valença, Iñigo Virto, Adrian A. Wackett, Matthew W. Warren, Emily R. Webster, Nathaniel H. Wehr, Joann K. Whalen, Michael B. Wironen, Volkmar Wolters, Pengfei Wu, Irina V. Zenkova, Weixin Zhang, Erin K. Cameron, Nico Eisenhauer
Publikováno v:
Scientific Data, Vol 8, Iss 1, Pp 1-12 (2021)
Measurement(s) earthworm communities • Abundance • organic material • Diversity • environmental properties Technology Type(s) digital curation Factor Type(s) location Sample Characteristic - Organism Lumbricina Sample Characteristic - Environ
Externí odkaz:
https://doaj.org/article/1ab16444dcef45e8978f9f8bcd392b98
Publikováno v:
BMC Microbiology, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Tolerance to antibiotics and persistence are associated with antibiotic treatment failures, chronic-relapsing infections, and emerging antibiotic resistance in various bacteria, including Staphylococcus aureus. Mechanisms of persi
Externí odkaz:
https://doaj.org/article/baf6e7fc961f4f639db71f7099baffd8
Autor:
Joseph Thachil Francis, Anna Rozenboym, Lee von Kraus, Shaohua Xu, Pratik Chhatbar, Mulugeta Semework, Emerson Hawley, John Chapin
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Lost sensations, such as touch, could be restored by microstimulation (MiSt) along the sensory neural substrate. Such neuroprosthetic sensory information can be used as feedback from an invasive brain-machine interface (BMI) to control a robotic arm/
Externí odkaz:
https://doaj.org/article/be09eb10f3ef44429cab7eb982ebe622
Autor:
Magdalena Klaniewska, Krystian Toczewski, Anna Rozensztrauch, Michal Bloch, Agata Dzielendziak, Piotr Gasperowicz, Ryszard Slezak, Rafał Ploski, Małgorzata Rydzanicz, Robert Smigiel, Dariusz Patkowski
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
The MYCN oncogene encodes a transcription factor belonging to the MYC family. It is primarily expressed in normal developing embryos and is thought to be critical in brain and other neural development. Loss-of-function variants resulting in haploinsu
Externí odkaz:
https://doaj.org/article/5c17636ad65c4694a5c87f7f90539229
Publikováno v:
Journal of Education, Health and Sport, Vol 8, Iss 7, Pp 67-77 (2018)
Fetal Alcohol Syndrome (FAS) is the group of conditions observed in children who happened to be exposed to the effects of alcohol in their prenatal development. Some very characteristic symptoms, belonging to three groups, such as: craniofacial abnor
Externí odkaz:
https://doaj.org/article/f64b6716d3bd414c9a6bf9076d70f299
Publikováno v:
Journal of Education, Health and Sport, Vol 7, Iss 9, Pp 575-584 (2017)
Gestational diabetes mellitus involves about 10% of women in Poland. The consequences of untreated gestational diabetes mellitus are seen in the prenatal development. The nursing care for the diabetes mother's newborns should be started in the moment
Externí odkaz:
https://doaj.org/article/e36c3ac375364d28b98f882e91680686
Publikováno v:
Journal of Education, Health and Sport, Vol 7, Iss 5, Pp 410-418 (2017)
The newborn's pain is often recognized incompetently and what worse even ignored. Pain is part of the body's defense system and alert the organism to possible danger. Human fetuses are capable of feeling pain since 20 weeks of gestation age. The cons
Externí odkaz:
https://doaj.org/article/6642d15a93364924ae1d40b6fe082826