Philippe GORRY
Philippe GORRY
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TitleCited byYear
Function of the retinoic acid receptors (RARs) during development (I). Craniofacial and skeletal abnormalities in RAR double mutants
D Lohnes, M Mark, C Mendelsohn, P Dolle, A Dierich, P Gorry, ...
Development 120 (10), 2723-2748, 1994
High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice
T Lufkin, D Lohnes, M Mark, A Dierich, P Gorry, MP Gaub, M LeMeur, ...
Proceedings of the National Academy of Sciences 90 (15), 7225-7229, 1993
Two rhombomeres are altered in Hoxa-1 mutant mice
M Mark, T Lufkin, JL Vonesch, E Ruberte, JC Olivo, P DollÚ, P Gorry, ...
Development 119 (2), 319-338, 1993
Mice deficient in cellular retinoic acid binding protein II (CRABPII) or in both CRABPI and CRABPII are essentially normal
C Lampron, C Rochette-Egly, P Gorry, P DollÚ, M Mark, T Lufkin, ...
Development 121 (2), 539-548, 1995
Targeting α-synuclein for treatment of Parkinson's disease: mechanistic and therapeutic considerations
B Dehay, M Bourdenx, P Gorry, S Przedborski, M Vila, S Hunot, ...
The Lancet Neurology 14 (8), 855-866, 2015
The cellular retinoic acid binding protein I is dispensable
P Gorry, T Lufkin, A Dierich, C Rochette-Egly, D Decimo, P Dolle, M Mark, ...
Proceedings of the National Academy of Sciences 91 (19), 9032-9036, 1994
Developmental roles of the retinoic acid receptors
D Lohnes, M Mark, C Mendelsohn, P DollÚ, D Decimo, M LeMeur, ...
The Journal of steroid biochemistry and molecular biology 53 (1-6), 475-486, 1995
COL4A1 mutation in Axenfeld–Rieger anomaly with leukoencephalopathy and stroke
I Sibon, I Coupry, P Menegon, JP Bouchet, P Gorry, I Burgelin, P Calvas, ...
Annals of neurology 62 (2), 177-184, 2007
Spectrum of PTCH1 mutations in French patients with Gorlin syndrome
N Boutet, YJ Bignon, V Drouin-Garraud, P Sarda, M Longy, D Lacombe, ...
Journal of investigative dermatology 121 (3), 478-481, 2003
Pharmacogenetics of human carboxylesterase 2, an enzyme involved in the activation of irinotecan into SN‐38
V Charasson, R Bellott, D Meynard, M Longy, P Gorry, J Robert
Clinical Pharmacology & Therapeutics 76 (6), 528-535, 2004
Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi syndrome patients
M Stef, D Simon, B Mardirossian, MA Delrue, I Burgelin, C Hubert, ...
European journal of human genetics 15 (8), 843-847, 2007
MLH1 and MSH2 protein immunohistochemistry is useful for detection of hereditary non‐polyposis colorectal cancer in young patients
F Paraf, M Gilquin, M Longy, B Gilbert, P Gorry, B Petit, F Labrousse
Histopathology 39 (3), 250-258, 2001
MDM2 expression during mouse embryogenesis and the requirement of p53
T LÚveillard, P Gorry, K Niederreither, B Wasylyk
Mechanisms of development 74 (1-2), 189-193, 1998
Expression of p21WAF1/CIP1 during mouse odontogenesis
A Bloch‐Zupan, T Leveillard, P Gorry, JL Fausser, JV Ruch
European journal of oral sciences 106 (S1), 104-111, 1998
Clinical and genetic study in 22 patients with basal cell nevus syndrome
C Pruvost-Balland, P Gorry, N Boutet, T Magnaldo, G Mamelle, A Margulis, ...
Annales de dermatologie et de venereologie 133 (2), 117-123, 2006
Limited specificity and large overlap of the functions of the mouse RARγ1 and RARγ2 isoforms
V Subbarayan, P Kastner, M Mark, A Dierich, P Gorry, P Chambon
Mechanisms of development 66 (1-2), 131-142, 1997
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma
F Lesueur, M de Lichy, M Barrois, G Durand, J Bombled, MF Avril, ...
British journal of cancer 99 (2), 364-370, 2008
“Sleeping beauty” and her restless sleep: Charles Dotter and the birth of interventional radiology
P Gorry, P Ragouet
Scientometrics 107 (2), 773-784, 2016
Heterozygous mutations in the tumor suppressor gene PATCHED provoke basal cell carcinoma-like features in human organotypic skin cultures
F Brellier, V Bergoglio, A Valin, S Barnay, O Chevallier-Lagente, P Vielh, ...
Oncogene 27 (51), 6601-6606, 2008
Mutation in exon 7 of PTCH deregulates SHH/PTCH/SMO signaling: possible linkage to WNT
V Musani, P Gorry, A Basta-Juzbasic, T Stipic, P Miklic, S Levanat
International journal of molecular medicine 17 (5), 755-759, 2006
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