Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Asami OGURO"'
Autor:
Rosemary A. Bamford, Amila Zuko, Madeline Eve, Jan J. Sprengers, Harm Post, Renske L. R. E. Taggenbrock, Dominique Fäβler, Annika Mehr, Owen J. R. Jones, Aurimas Kudzinskas, Josan Gandawijaya, Ulrike C. Müller, Martien J. H. Kas, J. Peter H. Burbach, Asami Oguro-Ando
Publikováno v:
Open Biology, Vol 14, Iss 5 (2024)
The neuronal cell adhesion molecule contactin-4 (CNTN4) is genetically associated with autism spectrum disorder (ASD) and other psychiatric disorders. Cntn4-deficient mouse models have previously shown that CNTN4 plays important roles in axon guidanc
Externí odkaz:
https://doaj.org/article/ba72db2116e74e9ea015ee3338ab6914
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
The human SH-SY5Y neuroblastoma cell line is widely used in neuroscience research as a neuronal cell model. Following differentiation to a neuron-like state, SH-SY5Y cells become more morphologically similar to neurons and form functional synapses. P
Externí odkaz:
https://doaj.org/article/4f4beaa55d2d4303ac60a3508c4db0e3
Autor:
Asami Oguro-Ando, Rosemary A. Bamford, Wiedjai Sital, Jan J. Sprengers, Amila Zuko, Jolien M. Matser, Hugo Oppelaar, Angela Sarabdjitsingh, Marian Joëls, J. Peter. H. Burbach, Martien J. Kas
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Neurodevelopmental and neuropsychiatric disorders, such as autism spectrum disorders (ASD), anorexia nervosa (AN), Alzheimer’s disease (AD), and schizophrenia (SZ), are heterogeneous brain disorders with unknown etiology. Genome wide studi
Externí odkaz:
https://doaj.org/article/53f044de4fd74bb99a68f5ff4e2e7313
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
Autism spectrum disorder (ASD) is a complex neurodevelopmental condition characterized by restrictive and repetitive behaviors, alongside deficits in social interaction and communication. The etiology of ASD is largely unknown but is strongly linked
Externí odkaz:
https://doaj.org/article/631df88b998745afb289c698daf7f0ca
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2021)
Autism spectrum disorder (ASD) is characterized by impaired social interaction, language delay and repetitive or restrictive behaviors. With increasing prevalence, ASD is currently estimated to affect 0.5–2.0% of the global population. However, its
Externí odkaz:
https://doaj.org/article/2e7b143b18a74772a295f80a9f0011e5
Autor:
Amila Zuko, Asami Oguro-Ando, Harm Post, Renske L.R.E. Taggenbrock, Roland E. van Dijk, Maarten Altelaar, Albert J R Heck, Alexander G Petrenko, Bert van der Zwaag, Yasushi Shimoda, R. Jeroen Pasterkamp, J. Peter H. Burbach
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 9 (2016)
In view of important neurobiological functions of the cell adhesion molecule contactin-6 (Cntn6) that have emerged from studies on null-mutant mice and autism spectrum disorders (ASD) patients, we set out to examine pathways underlying functions of C
Externí odkaz:
https://doaj.org/article/c6bf140738f3416cb64bb637ae7ca4b6
Autor:
Charli E. Harlow, Josan Gandawijaya, Rosemary A. Bamford, Emily-Rose Martin, Andrew R. Wood, Peter J. van der Most, Toshiko Tanaka, Hampton L. Leonard, Amy S. Etheridge, Federico Innocenti, Robin N. Beaumont, Jessica Tyrrell, Mike A. Nalls, Eleanor M. Simonsick, Pranav S. Garimella, Eric J. Shiroma, Niek Verweij, Peter van der Meer, Ron T. Gansevoort, Harold Snieder, Paul J. Gallins, Dereje D. Jima, Fred Wright, Yi-hui Zhou, Luigi Ferrucci, Stefania Bandinelli, Dena G. Hernandez, Pim van der Harst, Vickas V. Patel, Dawn M. Waterworth, Audrey Y. Chu, Asami Oguro-Ando, Timothy M. Frayling
Publikováno v:
American Journal of Human Genetics, 109(9), 1638-1652. CELL PRESS
Hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHIs) are currently under clinical development for treating anemia in chronic kidney disease (CKD), but it is important to monitor their cardiovascular safety. Genetic variants can be used a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5af52c8198d180333920474519e29d
https://research.rug.nl/en/publications/dbc76815-e070-4ba9-801d-e653aebb2f58
https://research.rug.nl/en/publications/dbc76815-e070-4ba9-801d-e653aebb2f58
Autor:
Atsushi KOBAYASHI, Satoko GOMIKAWA, Asami OGURO, Akira YAMAZAKI, Shinji SATO, Hirofumi MAEKAWA
Publikováno v:
Japan Journal of Food Engineering. 22:87-101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70c2a3f37aae75960a4777a7e5d7c5ec
https://doi.org/10.11301/jsfe.21593
https://doi.org/10.11301/jsfe.21593
Publikováno v:
Journal of Visualized Experiments.
Potassium chloride cotransporters 2 (KCC2) is a member of the solute carrier family 12 (SLC12) of cation-chloride-cotransporters (CCCs), found exclusively in the neuron and is essential for the proper functioning of Cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72fe421023b2d9fb2ba3df83c8016cda
https://doi.org/10.3791/64179
https://doi.org/10.3791/64179
Autor:
Charli E Harlow, Vickas V Patel, Dawn M Waterworth, Andrew R Wood, Robin N Beaumont, Katherine S Ruth, Jessica Tyrrell, Asami Oguro-Ando, Audrey Y Chu, Timothy M Frayling
Publikováno v:
Human molecular genetics.
Prolyl hydroxylase (PHD) inhibitors are in clinical development for anaemia in chronic kidney disease. Epidemiological studies have reported conflicting results regarding safety of long-term therapeutic haemoglobin (Hgb) rises through PHD inhibition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12672b8b214116fea85a4dc0e62003e1
https://pubmed.ncbi.nlm.nih.gov/36048866
https://pubmed.ncbi.nlm.nih.gov/36048866