Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Erik Willems"'
Autor:
Jonas Halver, Kristin Wenzel, Jandirk Sendker, Carmen Carrillo García, Clemens A. J. Erdelmeier, Erik Willems, Mark Mercola, Nico Symma, Stephanie Könemann, Egon Koch, Andreas Hensel, Dennis Schade
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2019)
Extracts from the leaves and flowers of Crataegus spp. (i.e., hawthorn species) have been traditionally used with documented preclinical and clinical activities in cardiovascular medicine. Based on reported positive effects on heart muscle after isch
Externí odkaz:
https://doaj.org/article/0eb15241d18c4abfbc33eef98723e5c2
Autor:
Rachel A Battaglia, Adriana S Beltran, Samed Delic, Raluca Dumitru, Jasmine A Robinson, Parijat Kabiraj, Laura E Herring, Victoria J Madden, Namritha Ravinder, Erik Willems, Rhonda A Newman, Roy A Quinlan, James E Goldman, Ming-Der Perng, Masaki Inagaki, Natasha T Snider
Publikováno v:
eLife, Vol 8 (2019)
Alexander disease (AxD) is a fatal neurodegenerative disorder caused by mutations in glial fibrillary acidic protein (GFAP), which supports the structural integrity of astrocytes. Over 70 GFAP missense mutations cause AxD, but the mechanism linking d
Externí odkaz:
https://doaj.org/article/1a944b07b95f440191c0e5f0e38980a8
Autor:
Joaquim Cabral-Teixeira, Almudena Martinez-Fernandez, Wenqing Cai, Andre Terzic, Mark Mercola, Erik Willems
Publikováno v:
Stem Cell Research, Vol 15, Iss 1, Pp 88-95 (2015)
Aside from its role in cell membrane integrity, cholesterol is a key component in steroid hormone production. The vital functions of steroid hormones such as estrogen, testosterone, glucocorticoids (Gcrts) and mineralocorticoids (Mnrts) in perinatal
Externí odkaz:
https://doaj.org/article/d4849eae2cf74b3698dd6d3b79b1ba79
Autor:
Sofia Forss, Erik Willems
Publikováno v:
Ethology, 128 (8)
Although curiosity has huge implications for human creativity and learning, its evo-lutionary roots and function in animals remain poorly understood. Modern humans, who lack natural predators, thrive with curiosity, but our ancestors faced more haz-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7436dcceb049e93a59f7f8dd6c38e080
https://hdl.handle.net/20.500.11850/554113
https://hdl.handle.net/20.500.11850/554113
Autor:
Adrian Reich, Courtney A. Miller, Vineet Arora, Gavin Rumbaugh, BanuPriya Sridharan, Murat Kilinc, J. Lloyd Holder, Lukasz Bijoch, Nerea Llamosas, David R. Piper, Louis Scampavia, Camilo Rojas, Timothy P. Spicer, Erik Willems, Ridhima Vij
Publikováno v:
J Neurosci
SYNGAP1is a major genetic risk factor for global developmental delay, autism spectrum disorder, and epileptic encephalopathy.De novoloss-of-function variants in this gene cause a neurodevelopmental disorder defined by cognitive impairment, social-com
Autor:
Rojas C, Lukasz Bijoch, Gavin Rumbaugh, Timothy P. Spicer, Louis Scampavia, Jimmy Holder, David R. Piper, Adrian Reich, Vij R, Nerea Llamosas, Erik Willems, Murat Kilinc, Courtney A. Miller, Arora, BanuPriya Sridharan
SYNGAP1 is a major genetic risk factor for global developmental delay, autism spectrum disorder, and epileptic encephalopathy. De novo loss-of-function variants in this gene cause a neurodevelopmental disorder defined by cognitive impairment, social-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d54cafea3d01ed0cf5ddf15864148201
https://doi.org/10.1101/2020.06.01.127613
https://doi.org/10.1101/2020.06.01.127613
Autor:
Samed Delic, Jasmine A. Robinson, Victoria J. Madden, Parijat Kabiraj, Laura E. Herring, James E. Goldman, Namritha Ravinder, Rhonda A. Newman, Roy A. Quinlan, Ming-Der Perng, Masaki Inagaki, Rachel A. Battaglia, Natasha T. Snider, Adriana S. Beltran, Erik Willems, Raluca Dumitru
Publikováno v:
eLife, 2019, Vol.8, pp.e47789 [Peer Reviewed Journal]
eLife
eLife, Vol 8 (2019)
eLife
eLife, Vol 8 (2019)
Alexander disease (AxD) is a fatal neurodegenerative disorder caused by mutations in glial fibrillary acidic protein (GFAP), which supports the structural integrity of astrocytes. Over 70 GFAP missense mutations cause AxD, but the mechanism linking d
Autor:
Murat Kilinc, Christopher Hubbs, Gavin Rumbaugh, Nerea Llamosas, Erik Willems, Timothy P. Spicer, Fakhar Singhera, Louis Scampavia, David R. Piper, BanuPriya Sridharan
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports
Neurons created from human induced pluripotent stem cells (hiPSCs) provide the capability of identifying biological mechanisms that underlie brain disorders. IPSC-derived human neurons, or iNs, hold promise for advancing precision medicine through dr
Autor:
Raphael Weidmann, Erik Willems
Publikováno v:
physiopraxis. 17:40-41
Mit Armbewegungen die Symptome einer pAVK in den Beinen mindern – auf den ersten Blick eine gewagte These. Doch weit gefehlt: Studien belegen, dass sich Gehstrecke und Lebensqualität durch Armergometertraining ebenso verbessern wie mit einem Golds
Publikováno v:
Proceedings of 35th International Cosmic Ray Conference — PoS(ICRC2017).
The spatial signal distribution of the radio frequency radiation from extensive air showers on the ground contains information on crucial cosmic-ray properties, such as energy and mass. A long standing challenge to access this information experimenta