Identification of new Nerve Growth Factor-responsive immediate-early genes

Autor: L.W.A. (Lenneke) van Hooijdonk, Erno Vreugdenhil, Thomas F. Dijkmans, Carlos P. Fitzsimons, Jessica T. Kamphorst, Theo G. Schouten

Publikováno v: Europe PubMed Central

Stimulation of the PC12 pheochromocytoma cell line with the prototypical neurotrophin Nerve Growth Factor (NGF) induces a cellular response of neuronal differentiation and is therefore a widely used model to gain molecular insight into this process.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d1ad2bf82d8952998c8cfdad0837fd4
https://doi.org/10.1016/j.brainres.2008.10.050

PRRT2 and hemiplegic migraine: a complex association

Autor: Boukje de Vries, Joost Haan, Jessica T. Kamphorst, Arn M. J. M. van den Maagdenberg, Gisela M. Terwindt, Michel D. Ferrari, Lisanne S. Vijfhuizen, Nadine Pelzer

Publikováno v: Neurology. 83(3)

Hemiplegic migraine (HM) is a rare migraine subtype characterized by hemiparesis during the attack and is associated with at least 3 genes: CACNA1A , ATP1A2, and SCN1A .1 Recent reports suggested that the proline-rich transmembrane protein PRRT2 gene

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95307cbc13a9062fc39818bf608caf50
https://pubmed.ncbi.nlm.nih.gov/24928122

MicroRNA 18 and 124a down-regulate the glucocorticoid receptor: implications for glucocorticoid responsiveness in the brain

Autor: Carla S Verissimo, Carlos P. Fitzsimons, Thijs Jan Zweers, Erno Vreugdenhil, E. Ron de Kloet, Jessica T. Kamphorst, Rob Mariman, Danielle L. Champagne, Theo G. Schouten, Joana S. Barbosa, Onno C. Meijer

Publikováno v: Endocrinology. 150(5)

Glucocorticoids (GCs) exert profound effects on a variety of physiological processes, including adaptation to stress, metabolism, immunity, and neuronal development. Cellular responsiveness to GCs depends on numerous factors, including the amount of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::278b78470d180053f604f719ab159b00
https://pubmed.ncbi.nlm.nih.gov/19131573

PRRT2 mutation causes benign familial infantile convulsions

Autor: Boukje de Vries, Arn M. J. M. van den Maagdenberg, Petra M.C. Callenbach, Jessica T. Kamphorst, Robert ten Houten, Irenaeus F.M. de Coo, Stephany C. Koelewijn, Claudia M Weller, Oebo F. Brouwer

Publikováno v: Neurology, 79(21), 2154-2155. LIPPINCOTT WILLIAMS & WILKINS
Neurology, 79(21), 2154-2155
Neurology, 79(21), 2154-2155. Lippincott Williams & Wilkins

Benign familial infantile convulsions (BFIC) is an autosomal dominantly inherited epilepsy syndrome with onset between 3 and 12 months of age. It is characterized by brief seizures with motor arrest, cyanosis, hypertonia, and limb jerks. Seizures res

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc26476658a4f6467569547cf8dac4bc
https://doi.org/10.1212/wnl.0b013e3182752c30

The Drosophila Wnt5 protein mediates selective axon fasciculation in the embryonic central nervous system

Autor: Jessica T. Kamphorst, Jasprina N. Noordermeer, Rene R. Wouda, Monique Radjkoemar-Bansraj, Lee G. Fradkin, Martijn van Schie, Anja W. M. de Jong

Publikováno v: Developmental Biology. (2):362-375

The decision of whether and where to cross the midline, an evolutionarily conserved line of bilateral symmetry in the central nervous system, is the first task for many newly extending axons. We show that Wnt5, a member of the conserved Wnt secreted

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed2619a25b85e6fc1ae1e647a05e7a32