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Christophe Girard
Christophe Girard
Centre Méditerranéen de Médecine Moléculaire, Nice, France
Verified email at unice.fr
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Cited by
Year
The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase
T Gerken, CA Girard, YCL Tung, CJ Webby, V Saudek, KS Hewitson, ...
Science 318 (5855), 1469-1472, 2007
18082007
Overexpression of Fto leads to increased food intake and results in obesity
C Church, L Moir, F McMurray, C Girard, GT Banks, L Teboul, S Wells, ...
Nature genetics 42 (12), 1086-1092, 2010
8532010
Control of pancreatic β cell regeneration by glucose metabolism
S Porat, N Weinberg-Corem, S Tornovsky-Babaey, R Schyr-Ben-Haroush, ...
Cell metabolism 13 (4), 440-449, 2011
3512011
A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes
P Proks, AL Arnold, J Bruining, C Girard, SE Flanagan, B Larkin, ...
Human molecular genetics 15 (11), 1793-1800, 2006
2662006
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects
S Ellard, SE Flanagan, CA Girard, AM Patch, LW Harries, A Parrish, ...
The American Journal of Human Genetics 81 (2), 375-382, 2007
2472007
Mechanisms underlying excitatory effects of group I metabotropic glutamate receptors via inhibition of 2P domain K+ channels
J Chemin, C Girard, F Duprat, F Lesage, G Romey, M Lazdunski
The EMBO journal, 2003
2322003
Relapsing diabetes can result from moderately activating mutations in KCNJ11
AL Gloyn, F Reimann, C Girard, EL Edghill, P Proks, ER Pearson, ...
Human molecular genetics 14 (7), 925-934, 2005
2302005
Genomic and functional characteristics of novel human pancreatic 2P domain K+ channels
C Girard, F Duprat, C Terrenoire, N Tinel, M Fosset, G Romey, ...
Biochemical and biophysical research communications 282 (1), 249-256, 2001
2142001
Epitope spreading of autoantibody response to PLA2R associates with poor prognosis in membranous nephropathy
B Seitz-Polski, G Dolla, C Payré, CA Girard, J Polidori, K Zorzi, ...
Journal of the American Society of Nephrology 27 (5), 1517-1533, 2016
2042016
p11, an annexin II subunit, an auxiliary protein associated with the background K+ channel, TASK-1
C Girard, N Tinel, C Terrenoire, G Romey, M Lazdunski, M Borsotto
The EMBO journal 21 (17), 4439-4448, 2002
1752002
Emerging roles of secreted phospholipase A2 enzymes: Lessons from transgenic and knockout mice
M Murakami, Y Taketomi, C Girard, K Yamamoto, G Lambeau
Biochimie 92 (6), 561-582, 2010
1692010
Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11
W Mlynarski, AI Tarasov, A Gach, CA Girard, I Pietrzak, L Zubcevic, ...
Nature clinical practice Neurology 3 (11), 640-645, 2007
1322007
Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic β cells recapitulates neonatal diabetes
CA Girard, FT Wunderlich, K Shimomura, S Collins, S Kaizik, P Proks, ...
The Journal of clinical investigation 119 (1), 80-90, 2009
1282009
A gating mutation at the internal mouth of the Kir6. 2 pore is associated with DEND syndrome
P Proks, C Girard, S Haider, AL Gloyn, AT Hattersley, MSP Sansom, ...
EMBO reports 6 (5), 470-475, 2005
1272005
Pancreatic two P domain K+ channels TALK‐1 and TALK‐2 are activated by nitric oxide and reactive oxygen species
F Duprat, C Girard, G Jarretou, M Lazdunski
The Journal of physiology 562 (1), 235-244, 2005
992005
Cancer cell-derived long pentraxin 3 (PTX3) promotes melanoma migration through a toll-like receptor 4 (TLR4)/NF-κB signaling pathway
M Rathore, C Girard, M Ohanna, M Tichet, R Ben Jouira, E Garcia, ...
Oncogene 38 (30), 5873-5889, 2019
912019
PLA2R1 mediates tumor suppression by activating JAK2
D Vindrieux, A Augert, CA Girard, D Gitenay, H Lallet-Daher, C Wiel, ...
Cancer research 73 (20), 6334-6345, 2013
832013
Functional effects of KCNJ11 mutations causing neonatal diabetes: enhanced activation by MgATP
P Proks, C Girard, FM Ashcroft
Human molecular genetics 14 (18), 2717-2726, 2005
812005
Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes
CAJ Girard, K Shimomura, P Proks, N Absalom, L Castano, ...
Pflügers Archiv 453, 323-332, 2006
762006
Mutations at the same residue (R50) of Kir6. 2 (KCNJ11) that cause neonatal diabetes produce different functional effects
K Shimomura, CAJ Girard, P Proks, J Nazim, JD Lippiat, F Cerutti, R Lorini, ...
Diabetes 55 (6), 1705-1712, 2006
762006
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