Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tyrosine 3-Monooxygenase/genetics"'
Autor:
Joop Van Heerikhuize, Maria T. Panayotacopoulou, Dick F. Swaab, Unga A. Unmehopa, Yiannis I. Malidelis
Publikováno v:
Neuroendocrinology, 81(5), 329-338. S. Karger AG
Neuroendocrinology, 81(5), 329-38. S. Karger AG
Neuroendocrinology, 81(5), 329-38. S. Karger AG
Previous studies indicated that in the human paraventricular nucleus (PVN) and in the supraoptic nucleus (SON) tyrosine hydroxylase (TH) – the first and rate-limiting enzyme in catecholamine synthesis – is localized mainly in magnocellular neuros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5de6ac9d1f4a7a9c37acb9eaa409c9a
https://hdl.handle.net/20.500.11755/f40997c3-b309-4689-9fc5-941cfa4ae6a1
https://hdl.handle.net/20.500.11755/f40997c3-b309-4689-9fc5-941cfa4ae6a1
Autor:
Zsuzsanna Callaerts-Vegh, Patrick Callaerts, Michiel Van Boxelaere, Jason Clements, Rudi D'Hooge
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0188537 (2017)
PLoS ONE
PLoS ONE
Alterations in the social and cognitive domain are considered important indicators for increased disability in many stress-related disorders. Similar impairments have been observed in rodents chronically exposed to stress, mimicking potential endophe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dacca5aac8b5b09c81f4aa30e28aff34
https://doi.org/10.1371/journal.pone.0188537
https://doi.org/10.1371/journal.pone.0188537
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia
Autor:
Stéphane Thobois, Alexandra Durr, Agnès Camuzat, Diane Doummar, Cécile Cazeneuve, Emmanuel Roze, Chankannira Sân, Alexis Brice, Delphine Bouteiller, Brigitte Chabrol, Myriem Abada, Pierre Castelnau, David Grabli, Fabienne Clot, Estelle Fedirko, Karine Nguyen, G. Ponsot, Alana Ward, Michael Hutchinson, Marie Vidailhet, Roger Gil, Pierre Landrieu, Fabienne Picard, Annick Toutain, Philippe Damier, Eric LeGuern
Publikováno v:
Brain, Vol. 132, No Pt 7 (2009) pp. 1753-1763
Dopa-responsive dystonia is a childhood-onset dystonic disorder, characterized by a dramatic response to low dose of L-Dopa. Dopa-responsive dystonia is mostly caused by autosomal dominant mutations in the GCH1 gene (GTP cyclohydrolase1) and more rar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::547340db28c5d294148743735356ab65
https://archive-ouverte.unige.ch/unige:19747
https://archive-ouverte.unige.ch/unige:19747
Autor:
Sarah Sigrist, Oliver Tschopp, Maurice Matter, Michael Brändle, Karim Abid, Stefan Fischli, Frédéric Triponez, Christoph Henzen, Eric Grouzmann, Tilman Drechser, Henryk Zulewski, Stefan Bilz
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0125426 (2015)
PLoS ONE
Plos One, vol. 10, no. 5, pp. e0125426
PLOS ONE, Vol. 10, No 5 (2015) P. e0125426
PLoS ONE
Plos One, vol. 10, no. 5, pp. e0125426
PLOS ONE, Vol. 10, No 5 (2015) P. e0125426
Pheochromocytoma (PHEO) and paraganglioma (PGL) are catecholamine-producing neuroendocrine tumors that arise respectively inside or outside the adrenal medulla. Several reports have shown that adrenal glucocorticoids (GC) play an important regulatory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::714d9c9ef068d2d605021de6ca13939a
https://doi.org/10.1371/journal.pone.0125426
https://doi.org/10.1371/journal.pone.0125426