Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Johanna Buchstaller"'
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
Publikováno v:
Cancer Cell. 21:240-252
Summary Tumor-initiating cells have been suggested to be rare in many cancers. We tested this in mouse malignant peripheral nerve sheath tumors (MPNSTs) and found that 18% of primary and 49% of passaged MPNST cells from Nf1 +/− ; Ink4a/Arf −/−
Autor:
Sean J. Morrison, Megan S. Lim, Johanna Buchstaller, Jack T. Mosher, Simon J. Conway, Paul E. McKeever, Luis F. Parada, Paige Snider, Yuan Zhu, Nancy M. Joseph
Publikováno v:
Cancer Cell. 13:129-140
Neurofibromatosis is caused by the loss of neurofibromin (Nf1), leading to peripheral nervous system (PNS) tumors, including neurofibromas and malignant peripheral nerve sheath tumors (MPNSTs). A long-standing question has been whether these tumors a
Autor:
Ueli Suter, Johanna Buchstaller, Heiko Wurdak, Douglas J. Epstein, Maurice Kléber, Hye-Youn Lee, Lukas Sommer, Martin M. Riccomagno, Lars M. Ittner
Publikováno v:
The Journal of Cell Biology
The Journal of cell biology, vol 169, iss 2
The Journal of cell biology, vol 169, iss 2
Canonical Wnt signaling instructively promotes sensory neurogenesis in early neural crest stem cells (eNCSCs) (Lee, H.Y., M. Kléber, L. Hari, V. Brault, U. Suter, M.M. Taketo, R. Kemler, and L. Sommer. 2004. Science. 303:1020–1023). However, duri
Autor:
Beat Schweitzer, Verdon Taylor, Robin J.M. Franklin, Johanna Buchstaller, Peter Smith, Ueli Suter, Christian S. Lobsiger
Publikováno v:
Glia. 36:31-47
Dramatic progress has been made over recent years toward the elucidation of the mechanisms regulating lineage determination and cell survival in the developing peripheral nervous system. However, our understanding of Schwann cell development is limit
Autor:
Dafydd G. Thomas, Anna V. Molofsky, Toshihide Iwashita, Sean J. Morrison, Johanna Buchstaller, Shenghui He
The polycomb gene Bmi-1 is required for the self-renewal of stem cells from diverse tissues, including the central nervous system (CNS). Bmi-1 expression is elevated in most human gliomas, irrespective of grade, raising the question of whether Bmi-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::376f4ebef5f38f4d879daebee62dd489
https://europepmc.org/articles/PMC2996717/
https://europepmc.org/articles/PMC2996717/
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aa8405614849e47c545bc7750bed0b0
https://www.zora.uzh.ch/id/eprint/116005/
https://www.zora.uzh.ch/id/eprint/116005/
Autor:
Matthias Bodmer, Lukas Sommer, Ned Mantei, Reinhard Hoffmann, Ueli Suter, Johanna Buchstaller
Schwann cells develop from multipotent neural crest stem cells and are important for neuronal survival, maintenance of axonal integrity, and myelination. We used transgenic mice expressing green fluorescent protein in a tissue-specific manner to isol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::182bb5f3980c0435be8fe459b190a47d
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/78224
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/78224