Christopher Porter
Christopher Porter
Ottawa Hospital Research Institute
Email verificata su ohri.ca
TitoloCitata daAnno
A mitochondria-K+ channel axis is suppressed in cancer and its normalization promotes apoptosis and inhibits cancer growth
S Bonnet, SL Archer, J Allalunis-Turner, A Haromy, C Beaulieu, ...
Cancer cell 11 (1), 37-51, 2007
14312007
CLINICAL PERSPECTIVE
S Bonnet, ED Michelakis, CJ Porter, MA Andrade-Navarro, B Thébaud, ...
Circulation 113 (22), 2630-2641, 2006
4802006
Gene function in early mouse embryonic stem cell differentiation
KH Sene, CJ Porter, G Palidwor, C Perez-Iratxeta, EM Muro, PA Campbell, ...
BMC genomics 8 (1), 85, 2007
1432007
GDB: the human genome database
SI Letovsky, RW Cottingham, CJ Porter, PWD Li
Nucleic Acids Research 26 (1), 94-99, 1998
1371998
Transcriptional dominance of Pax7 in adult myogenesis is due to high-affinity recognition of homeodomain motifs
VD Soleimani, VG Punch, Y Kawabe, AE Jones, GA Palidwor, CJ Porter, ...
Developmental cell 22 (6), 1208-1220, 2012
992012
Study of stem cell function using microarray experiments
C Perez-Iratxeta, G Palidwor, CJ Porter, NA Sanche, MR Huska, ...
FEBS letters 579 (8), 1795-1801, 2005
882005
UTX inhibition as selective epigenetic therapy against TAL1-driven T-cell acute lymphoblastic leukemia
A Benyoucef, CG Palii, C Wang, CJ Porter, A Chu, F Dai, V Tremblay, ...
Genes & development 30 (5), 508-521, 2016
582016
Managing all those bytes: the Human Genome Project
AJ Cuticchia, MA Chipperfield, CJ Porter, W Kearns, PL Pearson
SCIENCE-NEW YORK THEN WASHINGTON- 262, 47-47, 1993
321993
Arab genetic disease database (AGDDB): A population‐specific clinical and mutation database
AS Teebi, SA Teebi, CJ Porter, AJ Cuticchia
Human mutation 19 (6), 615-621, 2002
312002
A 19 bp deletion polymorphism adjacent to a dinucleotide repeat polymorphism at the human dopamine β-hydroxylase locus
J Nahmias, MW Burley, S Povey, C Porter, I Craig, J Wolfe
Human molecular genetics 1 (4), 286-286, 1992
281992
MaSC: mappability-sensitive cross-correlation for estimating mean fragment length of single-end short-read sequencing data
P Ramachandran, GA Palidwor, CJ Porter, TJ Perkins
Bioinformatics 29 (4), 444-450, 2013
272013
Central mutation databases—a review
CJ Porter, CC Talbot, Jr, AJ Cuticchia
Human mutation 15 (1), 36-44, 2000
252000
StemBase
CJ Porter, GA Palidwor, R Sandie, PM Krzyzanowski, EM Muro, ...
Stem Cell Assays, 137-148, 2007
232007
Dinucleotide repeat polymorphism at the human dopamine β-hydroxylase (DBH) locus
CJ Porter, J Nahmias, J Wolfe, IW Craig
Nucleic acids research 20 (6), 1429, 1992
211992
Systematic evaluation of map quality: human chromosome 22
TC Matise, CJ Porter, S Buyske, AJ Cuttichia, EP Sulman, PS White
The American Journal of Human Genetics 70 (6), 1398-1410, 2002
192002
An abnormal mitochondrial-HIF-1-Kv channel pathway disrupts oxygen-sensing and triggers pulmonary arterial hypertension (PAH) in fawn-hooded rats: similarities to human PAH
S Bonnet, ED Michelakis, CJ Porter, MA Andrade-Navarro, B Thébaud, ...
Circulation 113, 2630-2641, 2006
182006
Report of the committee on the genetic constitution of chromosome 9
S Povey, C Falk, M Smith, C Porter
Cytogenetic and Genome Research 58 (1-2), 403-427, 1991
181991
Recent developments in StemBase: a tool to study gene expression in human and murine stem cells
R Sandie, GA Palidwor, MR Huska, CJ Porter, PM Krzyzanowski, ...
BMC research notes 2 (1), 39, 2009
172009
ChIP on SNP-chip for genome-wide analysis of human histone H4 hyperacetylation
JA McCann, EM Muro, C Palmer, G Palidwor, CJ Porter, ...
BMC genomics 8 (1), 322, 2007
152007
A comprehensive view of human chromosome 1
PS White, EP Sulman, CJ Porter, TC Matise
Genome research 9 (10), 978-988, 1999
151999
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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