(HCHWA-D): clinicopathologicalWattendorffFrangioneLuyendijk
Through a collaboration with Amylon Therapeutics, the platform is also being developed for CNS indications including HCHWA-D. Recently, validation and expansion of the platform included positive results in clinical trials in cystic fibrosis and initiating a clinical trial in Leber's congenital amaurosis...
Described are methods for removing a proteolytic cleavage site, the HCHWA-D mutation or the amino acids encoded by a trinucleotide repeat expansion from a protein comprising providing a cell that expresses pre-mRNA encoding the protein with an anti-sense oligonucleotide that induces skipping of the...
Volume 13, Supplement 1, 1992, Pages S89 The Third International Conference on Alzheimer's Disease and Related Disorders Blood brain barrier and immunological factors Role of microglial cells in early plaque formation: Absence of microglial cells in diffuse plaques in HCHWA-D: J.M. Rozemuller,...
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Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I -- A review of clinical, radiologic and genetic aspects. Brain Pathol Apr 1996;6(2):111-4.Bornebroek M, Haan J, Maat-Schieman ML, Duinen SG van, Roos RA (1996) Hereditary cerebral hemorrhage with amyloidosis-Dutch ...
Hereditary cerebral hemorrhage with amyloidosis- Dutch type (HCHWA-D): II--a review of histopatho- logical aspects. Brain Pathol 1996; 6: 115-120.Maat-Schieman MLC, Duinen SG, van Bornebroek M, Haan J, Roos RAC. (1996) Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-...
Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D): clinicopathological studies - Wattendorff, Frangione, et al. - 1995 () Citation Context ...). Murakami et al. also include Dutch (E22Q) and Italian (E22K) but there is some dispute about whether these are properly to...
T. A. M. (1995) Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D): clinicopathological studies. J. Neurol. Neurosurg. Psychia- try 59, 699 -705Wattendorff AR, Frangione B, Luyendijk W, Bots GT (1995) Hereditary cerebral haemorrhage with amyloidosis, Dutch...
encoding said protein with an anti-sense oligonucleotide that induces skipping of the exonic sequence that comprises said proteolytic cleavage site, HCHWA-D mutation or trinucleotide repeat expansion, respectively, the method further comprising allowing translation of m RNA produced from said pre-m RNA...