Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jan Minde"'
Publikováno v:
Neurobiology of Disease, Vol 33, Iss 2, Pp 221-228 (2009)
We have previously identified a homozygous missense (R221W) mutation in the NGFB gene in patients with loss of deep pain perception. NGF is important not only for the survival of sensory neurons but also for the sympathetic neurons and cholinergic ne
Externí odkaz:
https://doaj.org/article/c6e43b0ae8af49d485477c773dbdcab6
Publikováno v:
Global Journal of Rare Diseases. :022-026
Context: The purpose of this study was to determine whether the expression of sensory neuropeptides, NK1, 5-HT1A receptors, as well as mast cells in the skin of patients with hereditary neuropathy and sensory and autonomic deficits (HSAN type 5) was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b328a9ffe86db3d5085145d58fa467f3
https://doi.org/10.17352/2640-7876.000018
https://doi.org/10.17352/2640-7876.000018
Autor:
Irene Perini, H. van Ettinger-Veenstra, Leonardo Cerliani, India Morrison, Jan Minde, Marta Ceko
Publikováno v:
Cerebral cortex (New York, N.Y., 30(9), 4858-4870. Oxford University Press
Cerebral Cortex (New York, NY)
Cerebral Cortex (New York, NY)
The evidence that action shapes perception has become widely accepted, for example, in the domain of vision. However, the manner in which action-relevant factors might influence the neural dynamics of acute pain processing has remained underexplored,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::790687d6f5e268c248e8c8e05d9c892c
https://pure.amc.nl/en/publications/mutation-carriers-with-reduced-cafferent-density-reveal-cortical-dynamics-of-painaction-relationship-during-acute-pain(63cb46fa-7041-4d6c-bbb3-ffca88f93630).html
https://pure.amc.nl/en/publications/mutation-carriers-with-reduced-cafferent-density-reveal-cortical-dynamics-of-painaction-relationship-during-acute-pain(63cb46fa-7041-4d6c-bbb3-ffca88f93630).html
Publikováno v:
Journal of Neurophysiology. 116:425-430
The rare nerve growth factor-β (NGFB) mutation R221W causes a selective loss of thinly myelinated fibers and especially unmyelinated C-fibers. Carriers of this mutation show altered pain sensation. A subset presents with arthropathic symptoms, with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbedc2d896652d9c3c806048cd1a0d6f
https://doi.org/10.1152/jn.00667.2015
https://doi.org/10.1152/jn.00667.2015
Autor:
Saad S, Nagi, Andrew G, Marshall, Adarsh, Makdani, Ewa, Jarocka, Jaquette, Liljencrantz, Mikael, Ridderström, Sumaiya, Shaikh, Francis, O'Neill, Dimah, Saade, Sandra, Donkervoort, A Reghan, Foley, Jan, Minde, Mats, Trulsson, Jonathan, Cole, Carsten G, Bönnemann, Alexander T, Chesler, M Catherine, Bushnell, Francis, McGlone, Håkan, Olausson
Publikováno v:
Science Advances
Pain can be signaled as fast as touch in human peripheral nerves.
The canonical view is that touch is signaled by fast-conducting, thickly myelinated afferents, whereas pain is signaled by slow-conducting, thinly myelinated (“fast” pain) or
The canonical view is that touch is signaled by fast-conducting, thickly myelinated afferents, whereas pain is signaled by slow-conducting, thinly myelinated (“fast” pain) or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::662f6df82222265e146575a72181f3e2
https://pubmed.ncbi.nlm.nih.gov/31281886
https://pubmed.ncbi.nlm.nih.gov/31281886
Autor:
Ellen Jørum, Roland Schmidt, Martin Schmelz, Dagrun Sagafos, Tormod Helås, Barbara Namer, Jan Minde, Inge Petter Kleggetveit
Publikováno v:
The Clinical journal of pain. 32(7)
Nerve growth factor (NGF) is a protein important for growth and survival, but also for modulation of sensitivity of nociceptors and sympathetic neurons. The purpose of the present study was to investigate the effects of reduced NGF signaling in patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1b2056484a61500306dc7f61b8d7fc5
https://pubmed.ncbi.nlm.nih.gov/27270876
https://pubmed.ncbi.nlm.nih.gov/27270876
Publikováno v:
Neurobiology of Disease, Vol 33, Iss 2, Pp 221-228 (2009)
We have previously identified a homozygous missense (R221W) mutation in the NGFB gene in patients with loss of deep pain perception. NGF is important not only for the survival of sensory neurons but also for the sympathetic neurons and cholinergic ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73dab1ae46b71ea26cf3c4776de71b57
http://www.sciencedirect.com/science/article/pii/S096999610800257X
http://www.sciencedirect.com/science/article/pii/S096999610800257X
Autor:
Jan Minde, Anna Carlsson, Elisabet Einarsdottir, Monica Holmberg, Olle Svensson, Gösta Holmgren, Göran Solders, Göran Toolanen, Dan Holmberg
Publikováno v:
Human Molecular Genetics. 13:799-805
Identification of genes associated with pain insensitivity syndromes can increase the understanding of the pathways involved in pain and contribute to the understanding of how sensory pathways relate to other neurological functions. In this report we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c45d18076f9a2042f65422642549a6a
https://doi.org/10.1093/hmg/ddh096
https://doi.org/10.1093/hmg/ddh096
Autor:
India Morrison, Inger Nennesmo, Johan Wessberg, Håkan Olausson, Line S. Löken, Jan Minde, Irene Perini
Publikováno v:
Brain : a journal of neurology. 134(Pt 4)
We examined patients with a heritable disorder associated with a mutation affecting the nerve growth factor beta gene. Their condition has been classified as hereditary sensory and autonomic neuropathy type V. Carriers of the mutation show a reductio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8e01e33fd7a213c3e91d552f966caf7
https://pubmed.ncbi.nlm.nih.gov/21378097
https://pubmed.ncbi.nlm.nih.gov/21378097
Autor:
Jan Minde, I Nilsson Remahl, M Aguirre, Göran Toolanen, Monica Holmberg, Inger Nennesmo, Olle Svensson, Thomas Andersson, Göran Solders, M Fulford
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 80(2)
A family with neurological findings similar to hereditary sensory and autonomic neuropathy type V having a point mutation in the nerve growth factor beta (NGFB) gene was recently described. The homozygous genotype gives disabling symptoms. The purpos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06d3aa4881697263c70597770dc309c0
https://pubmed.ncbi.nlm.nih.gov/18420729
https://pubmed.ncbi.nlm.nih.gov/18420729