Christopher Porter
Christopher Porter
Ottawa Hospital Research Institute
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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
An abnormal mitochondrial-hypoxia inducible factor-1a-Kv channel pathway disrupts oxygen sensing and triggers pulmonary arterial hypertension in fawn hooded rats: similarities …
S Bonnet, ED Michelakis, CJ Porter, MA Andrade-Navarro, B Thébaud, ...
Circulation 113 (22), 2630-41, 2006
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
GDB: the human genome database
SI Letovsky, RW Cottingham, CJ Porter, PWD Li
Nucleic Acids Research 26 (1), 94-99, 1998
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
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
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
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
Managing all those bytes: the Human Genome Project
AJ Cuticchia, MA Chipperfield, CJ Porter, W Kearns, PL Pearson
Science 262 (5130), 47-49, 1993
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
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
Central mutation databases—a review
CJ Porter, CC Talbot, Jr, AJ Cuticchia
Human mutation 15 (1), 36-44, 2000
CJ Porter, GA Palidwor, R Sandie, PM Krzyzanowski, EM Muro, ...
Stem Cell Assays, 137-148, 2007
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
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), 1-6, 2009
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
CMOS Custom Implementation of the SPARC Architecture
M Namjoo, F Abu-Nofal, D Carmean, R Chandramouli, Y Chang, ...
The SPARC Technical Papers, 151-157, 1991
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
Mtf2-PRC2 control of canonical Wnt signaling is required for definitive erythropoiesis
JLM Rothberg, HB Maganti, H Jrade, CJ Porter, GA Palidwor, C Cafariello, ...
Cell discovery 4 (1), 1-16, 2018
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
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