M. Robert

发表

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes

J. Nadeau, K. Schappert, E. Ziętkiewicz, 2004, Mammalian Genome.

4-(Heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs as a novel class of histone deacetylase inhibitors.

A. Kalita, M. Robert, O. Moradei, 2008, Bioorganic & medicinal chemistry letters.

MGCD0103, a novel isotype-selective histone deacetylase inhibitor, has broad spectrum antitumor activity in vitro and in vivo

Sylvain Lefebvre, Daniel Delorme, A. Kalita, 2008, Molecular Cancer Therapeutics.

Development of potential antitumor agents. Synthesis and biological evaluation of a new set of sulfonamide derivatives as histone deacetylase inhibitors.

Daniel Delorme, A. Kalita, M. Robert, 2003, Journal of medicinal chemistry.

N-(2-Amino-phenyl)-4-(heteroarylmethyl)-benzamides as new histone deacetylase inhibitors.

M. Robert, A. Macleod, O. Moradei, 2007, Bioorganic & medicinal chemistry letters.

An Essential Role for DNA Methyltransferase DNMT3B in Cancer Cell Survival*

M. Robert, A. Macleod, S. Morin, 2002, The Journal of Biological Chemistry.

The adipose tissue phenotype of hormone-sensitive lipase deficiency in mice.

N. Laurin, M. Robert, G. Mitchell, 2001, Obesity research.

Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution.

D. Labuda, K. Schappert, A. Duncan, 1994, Genomics.

Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.

C. Pérez-Cerdá, M. Ugarte, A. Duncan, 1996, American journal of human genetics.

Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Clinical Course and Description of Causal Mutations in Two Patients

C. Stanley, Shupei Wang, M. Robert, 2001, Pediatric Research.

1,2-Diamines as inhibitors of co-activator associated arginine methyltransferase 1 (CARM1).

Eric Therrien, M. Robert, J. Besterman, 2009, Bioorganic & medicinal chemistry letters.

N-Benzyl-1-heteroaryl-3-(trifluoromethyl)-1H-pyrazole-5-carboxamides as inhibitors of co-activator associated arginine methyltransferase 1 (CARM1).

Eric Therrien, M. Robert, J. Besterman, 2009, Bioorganic & medicinal chemistry letters.

Discovery of a novel and potent series of thieno[3,2-b]pyridine-based inhibitors of c-Met and VEGFR2 tyrosine kinases.

M. Robert, A. Macleod, A. Vaisburg, 2008, Bioorganic & medicinal chemistry letters.

In vitro cytotoxicity activity of diosquinone, a naphthoquinone epoxide

M. Robert, H. Fong, B. Adeniyi, 2003, Phytotherapy research : PTR.

Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.

C. Obie, D. Valle, M. Kaiser-Kupfer, 1992, The Journal of biological chemistry.

DNMT1 is required to maintain CpG methylation and aberrant gene silencing in human cancer cells

M. Robert, A. Macleod, I. Chute, 2003, Nature Genetics.

Medical aspects of ketone body metabolism.

Shupei Wang, M. Robert, G. Mitchell, 1995, Clinical and investigative medicine. Medecine clinique et experimentale.

3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient mice.

J. Marth, M. Robert, G. Mitchell, 1998, Human molecular genetics.

Hormone-sensitive lipase (Lipe): Sequence analysis of the 129Sv mouse Lipe gene

M. Robert, G. Mitchell, P. Lapierre, 1997, Mammalian Genome.

Hormone-sensitive lipase maps to proximal chromosome 7 in mice and is genetically distinct from the Ad and Tub loci.

J. Nadeau, M. Robert, G. Mitchell, 1994, Genomics.

Molecular prenatal diagnosis of 3‐hydroxy−3‐methylglutaryl coa lyase deficiency

M. Robert, G. Mitchell, A. Burlina, 1995, Prenatal diagnosis.

HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q.

R. Wanders, K. Gibson, M. Robert, 1998, American journal of human genetics.

3-Hydroxy-3-methylglutaryl CoA lyase (HL): mouse and human HL gene (HMGCL) cloning and detection of large gene deletions in two unrelated HL-deficient patients.

R. Wanders, K. Gibson, M. Robert, 1996, Genomics.

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency.

K. Schappert, K. Gibson, M. Robert, 1993, The Journal of biological chemistry.

Studies of 1-C16-2-C6-PC and 1-C6-2-C16-PC rodlike micelles by small-angle neutron scattering

S. H. A. Chen, M. Robert, K. Mortensen, 1994 .

Characterization of the hydroxymethylglutaryl-CoA lyase precursor, a protein targeted to peroxisomes and mitochondria.

M. Robert, G. Mitchell, M. Elsliger, 1996, The Biochemical journal.

Design and synthesis of 4-[(s-triazin-2-ylamino)methyl]-N-(2-aminophenyl)-benzamides and their analogues as a novel class of histone deacetylase inhibitors.

A. Kalita, M. Robert, A. Macleod, 2008, Bioorganic & medicinal chemistry letters.

N-(3-fluoro-4-(2-arylthieno[3,2-b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors.

M. Robert, Nancy Z. Zhou, S. Raeppel, 2009, Bioorganic & medicinal chemistry letters.

N-(4-(6,7-Disubstituted-quinolin-4-yloxy)-3-fluorophenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors.

Sylvain Lefebvre, M. Robert, Nancy Z. Zhou, 2009, Bioorganic & medicinal chemistry letters.

Effect of Probiotics on Incident Ventilator-Associated Pneumonia in Critically Ill Patients: A Randomized Clinical Trial.

Paul W. Dul, John Man-shun Ma, M. Surette, 2021, JAMA.

MGCD0103, a novel isotype-selective histone deacetylase inhibitor, has broad spectrum antitumor activity in vitro and in vivo

A. Kalita, M. Robert, A. Macleod, 2008, Molecular Cancer Therapeutics.