Khashayar Dashtipour

Dr. Khashayar Dashtipour

MD, PhD; Department of Neurology, School of Medicine, Loma Linda University, 11370 Anderson Suite, B-100, Loma Linda, CA 92354 USA

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 July 2013 in Movement Disorders
Verified
Journal Article
Closed access
PDF file
JRJuan Ramirez‐Castaneda
Juan Ramirez‐Castaneda
Joseph JankovicJoseph Jankovic
Joseph Jankovic
CCCynthia Comella
Cynthia Comella
KDKhashayar Dashtipour
Khashayar Dashtipour
HFHubert H. Fernandez
Hubert H. Fernandez
ZMZoltan Mari
Zoltan Mari


1 July 2012 in Clinical Therapeutics
Verified
Journal Article
Closed access
JCJack J. Chen
Jack J. Chen
WOWilliam G. Ondo
William G. Ondo
KDKhashayar Dashtipour
Khashayar Dashtipour
DSDavid M. Swope
David M. Swope

31 January 2001 in Brain Research
Verified
Journal Article
Open access
KDKhashayar Dashtipour
Khashayar Dashtipour
PTPeter H. Tran
Peter H. Tran
MOMaxine M. Okazaki
Maxine M. Okazaki
JNJ.Victor Nadler
J.Victor Nadler
CRCharles E. Ribak
Charles E. Ribak
Several investigators have shown the existence of dentate granule cells in ectopic locations within the hilus and molecular layer using both Golgi and retrograde tracing studies but the ultrastructural features and synaptic connections of ectopic granule cells were not previously examined. In the present study, the biocytin retrograde tracing technique was used to label ectopic granule cells following injections into stratum lucidum of CA3b of hippocampal slices obtained from epileptic rats. Electron microscopy was used to study hilar ectopic granule cells that were located 20–40 μm from the granule cell layer (GCL). They had ultrastructural features similar to those of granule cells in the GCL but showed differences, including nuclei that often displayed infoldings and thicker apical dendrites. At their origin, these dendrites were 6 μm in diameter and they tapered down to 2 μm at the border with the GCL. Both biocytin-labeled and unlabeled axon terminals formed exclusively asymmetric synapses with the somata and proximal dendrites of hilar ectopic granule cells. The mean number of axosomatic synapses for these cells was three times that for granule cells in the GCL. Together, these data indicate that hilar ectopic granule cells are postsynaptic to mossy fibers and have less inhibitory input on their somata and proximal dendrites than granule cells in the GCL. This finding is consistent with recent physiological results showing that hilar ectopic granule cells from epileptic rats are more hyperexcitable than granule cells in the GCL.

20 March 2001 in Journal of Comparative Neurology
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Journal Article
Closed access
PDF file
XYXiao‐Xin Yan
Xiao‐Xin Yan
JNJoseph Najbauer
Joseph Najbauer
CWCynthia C. Woo
Cynthia C. Woo
KDKhashayar Dashtipour
Khashayar Dashtipour
CRCharles E. Ribak
Charles E. Ribak
MLMichael Leon
Michael Leon

1 July 2017 in Parkinsonism & Related Disorders
Verified
Journal Article
Closed access
RWRobert E. Wharen
Robert E. Wharen
MOMichael S. Okun
Michael S. Okun
BGBarton L. Guthrie
Barton L. Guthrie
RURyan J. Uitti
Ryan J. Uitti
PLPaul Larson
Paul Larson
JOJill L. Ostrem
Jill L. Ostrem