Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Journal of Biological Chemistry|January 27, 1998
The axonally secreted serine proteinase inhibitor, neuroserpin, inhibits plasminogen activators and plasmin but not thrombinT Osterwalder, P Cinelli, A Baici, et al.
Human Mutation|March 27, 1999
Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneityA R Janecke, M Meins, M Sadeghi, et al.
Cytogenetic and Genome Research|November 20, 2002
Identification and characterization of murine Brunol4, a new member of the elav/bruno familyM Meins, S Schlickum, C Wilhelm, et al.
Cytogenetic and Genome Research|February 14, 2003
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosisR Trappe, D Böhm, J Kohlhase, et al.
Neuropediatrics|November 7, 2007
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander diseaseH Hartmann, J Herchenbach, U Stephani, et al.
American Journal of Medical Genetics. Part A|April 23, 2004
First non-mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter --> q22.1::q22.1 --> pter) is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q- syndromeM Meins, D Böhm, A Großmann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 8, 2001
Progressive neuronal and motor dysfunction in mice overexpressing the serine protease inhibitor protease nexin-1 in postmitotic neuronsM Meins, P Piosik, N Schaeren-Wiemers, et al.
Cytogenetic and Genome Research|March 2, 2012
Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown originE Klein, M Rocchi, A Ovens-Raeder, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 1997
Endogenous serine protease inhibitor modulates epileptic activity and hippocampal long-term potentiationA Lüthi, H Van der Putten, F M Botteri, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
Pageof 3