Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laura Tikker"'
Autor:
Linas Mazutis, Marjo Salminen, Francesca Morello, Juha Partanen, Daniel Borshagovski, Kaia Achim, Nuri Estartús, Laura Tikker, Laura Lahti, Mantas Survila, Alessio Delogu, Petri Törönen, Samir Sadik-Ogli, Laura Knaapi, Anna Kirjavainen
Publikováno v:
Morello, F, Borshagovski, D, Survila, M, Tikker, L, Sadik-Ogli, S, Kirjavainen, A, Estartús, N, Knaapi, L, Lathi, L, Törönen, P, Mazutis, L, Delogu, A, Salminen, M, Achim, K & Partanen, J 2020, ' Molecular fingerprint and developmental regulation of the tegmental GABAergic and glutamatergic neurons derived from the anterior hindbrain ', Cell Reports, vol. 33, no. 2, pp. 108268 . https://doi.org/10.1016/j.celrep.2020.108268
Cell reports, Cambridge, MA : Cell Press, 2020, vol. 33, iss. 2, art. no. 108268, p. [1-26]
Cell reports, Cambridge, MA : Cell Press, 2020, vol. 33, iss. 2, art. no. 108268, p. [1-26]
Tegmental nuclei in the ventral midbrain and anterior hindbrain control motivated behavior, mood, memory and movement. These nuclei contain inhibitory GABAergic and excitatory glutamatergic neurons, whose molecular diversity and development remain la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e758657ee5c73ac27649791103e61a0
https://kclpure.kcl.ac.uk/en/publications/07927685-ec1a-40df-a61b-e347e515f6bd
https://kclpure.kcl.ac.uk/en/publications/07927685-ec1a-40df-a61b-e347e515f6bd
Autor:
Laura Tikker, Eva-Maria Oja, Katrin Ruisu, Keiu Kask, Tambet Tõnissoo, Margus Pooga, Raivo Raid, Sirje Lulla, Riho Meier, Teet Velling
Publikováno v:
Developmental Neurobiology. 78:374-390
Autosomal recessive disorders such as Fukuyama congenital muscular dystrophy, Walker-Warburg syndrome, and the muscle-eye-brain disease are characterized by defects in the development of patient's brain, eyes, and skeletal muscles. These syndromes ar
Autor:
Merly Saare, Kirstin Karis, Margus Pooga, Laura Tikker, Tambet Tõnissoo, Riho Meier, Alar Karis, Keiu Kask, Katrin Ruisu
Publikováno v:
Developmental Neurobiology. 75:984-1002
RIC8A is a noncanonical guanine nucleotide exchange factor for a subset of Gα subunits. RIC8A has been reported in different model organisms to participate in the control of mitotic cell division, cell signalling, development and cell migration. Sti
Autor:
Keiu, Kask, Laura, Tikker, Katrin, Ruisu, Sirje, Lulla, Eva-Maria, Oja, Riho, Meier, Raivo, Raid, Teet, Velling, Tambet, Tõnissoo, Margus, Pooga
Publikováno v:
Developmental neurobiology. 78(4)
Autosomal recessive disorders such as Fukuyama congenital muscular dystrophy, Walker-Warburg syndrome, and the muscle-eye-brain disease are characterized by defects in the development of patient's brain, eyes, and skeletal muscles. These syndromes ar
Autor:
Juha Partanen, Suman Kumar, Jenni E. Anttila, Caisa Inkinen, Maarja Haugas, Marjo Salminen, Mikko Airavaara, Merja H. Voutilainen, Laura Tikker, Laura Lahti
Publikováno v:
Development.
Local inhibitory GABAergic and excitatory glutamatergic neurons are important for midbrain dopaminergic and hindbrain serotonergic pathways controlling motivation, mood, and voluntary movements. Such neurons reside both within the dopaminergic nuclei
Publikováno v:
Mechanisms of Development. 145:S94
Autor:
Keiu, Kask, Katrin, Ruisu, Laura, Tikker, Kirstin, Karis, Merly, Saare, Riho, Meier, Alar, Karis, Tambet, Tõnissoo, Margus, Pooga
Publikováno v:
Developmental neurobiology. 75(9)
RIC8A is a noncanonical guanine nucleotide exchange factor for a subset of Gα subunits. RIC8A has been reported in different model organisms to participate in the control of mitotic cell division, cell signalling, development and cell migration. Sti