Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Ned Mantei"'
Publikováno v:
Neurobiology of Disease, Vol 18, Iss 3, Pp 656-668 (2005)
Point mutations affecting PMP22 can cause hereditary demyelinating and dysmyelinating peripheral neuropathies. In addition, duplication and deletion of PMP22 are associated with Charcot–Marie–Tooth disease Type 1A (CMT1A) and Hereditary Neuropath
Externí odkaz:
https://doaj.org/article/597398d24f864d579360615941f8f320
Autor:
Peter Young, Ned Mantei, Ueli Suter, Klaus V. Toyka, Philipp Berger, Suzana Atanasoski, Sonja Bonneick, Matthias Boentert, Carsten Wessig
Publikováno v:
Human Molecular Genetics, 14 (23)
Human molecular genetics
Human molecular genetics
Human Molecular Genetics, 14 (23)
ISSN:0964-6906
ISSN:1460-2083
ISSN:0964-6906
ISSN:1460-2083
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::487b835ad8688666b72adac3e882bac5
http://doc.rero.ch/record/295231/files/ddi400.pdf
http://doc.rero.ch/record/295231/files/ddi400.pdf
Jagged1 Ablation Results in Cerebellar Granule Cell Migration Defects and Depletion of Bergmann Glia
Publikováno v:
Developmental Neuroscience. 28:70-80
Jagged1 is a ligand for members of the Notch family of receptors. Mutations in the human JAG1 gene are the major cause of Alagille syndrome, an autosomal dominant disorder affecting the liver, heart, eye, skeleton, kidneys, and craniofacial structure
Autor:
Annick Bonnet, Udo Bartsch, Nicole Schaeren-Wiemers, Diane L. Sherman, Ned Mantei, Frances Kern, Beat Erne, Michael Erb, Ueli Suter
Publikováno v:
The Journal of Cell Biology
The myelin and lymphocyte protein (MAL) is a tetraspan raft-associated proteolipid predominantly expressed by oligodendrocytes and Schwann cells. We show that genetic ablation of mal resulted in cytoplasmic inclusions within compact myelin, paranodal
Autor:
Ned Mantei
Publikováno v:
FEBS Letters. 590:2049-2050
Publikováno v:
Journal of Neurochemistry. 83:1380-1388
The L2/HNK-1 carbohydrate is carried by many neural recognition molecules and is involved in neural cell interactions during development, regeneration in the peripheral nervous system, synaptic plasticity, and autoimmune-based neuropathies. Its key s
Autor:
Lukas Sommer, Patrick Matthias, Arianna Baggiolini, Valérie Brügger, Stine Büchmann-Møller, Stefanie Engler, Ueli Suter, Paige Snider, Pirmin Lötscher, Ned Mantei, Sandra Varum Tavares, Teppei Yamaguchi, Simon J. Conway, Nessy John, Claire Jacob
Publikováno v:
Journal of Neuroscience
The Journal of neuroscience : the official journal of the Society for Neuroscience
The Journal of Neuroscience
The Journal of neuroscience : the official journal of the Society for Neuroscience
The Journal of Neuroscience
Schwann cells, the myelinating glia of the peripheral nervous system (PNS), originate from multipotent neural crest cells that also give rise to other cells, including neurons, melanocytes, chondrocytes, and smooth muscle cells. The transcription fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12ca7fc0d2b4cdcd45590d01fa39a956
https://www.zora.uzh.ch/id/eprint/105610/
https://www.zora.uzh.ch/id/eprint/105610/
Publikováno v:
Journal of Neurobiology. 38:428-439
The effects of L1-Fc and CHL1-Fc fusion proteins on neuronal survival were investigated. Cerebellar granule neurons of mouse and hippocampal neurons of rat embryo undergo apoptosis when cultured in serum-free medium. Treatment with chimeric proteins
Autor:
Jennifer K. Taylor, Peter G. Traber, Tao Levy, Ned Mantei, Sanyin Siang, Werner Boll, EunRan Suh
Publikováno v:
DNA and Cell Biology. 16:1419-1428
Intestinal phospholipase A/lysophospholipase (IPAL) is an intestine-specific brush-border enzyme expressed during development and along the intestinal crypt-villus axis in a pattern similar to another well characterized brush-border enzyme, sucrase-i
Publikováno v:
Nature Genetics. 17:346-349
The adhesion molecule L1 is a member of the immunoglobulin super-family1. L1 is involved in various recognition processes in the CMS and PNS2–3, and binding to L1 can activate signal transduction pathways4,5. Mutations in the human L1 gene are asso