PMC Articles for MedGen (Select 343607) - PMC

Emily K. Armstrong, Julie Mondon, Adam D. Miller, Andrew T. Revill, Sarah A. Stephenson, Mun Hua Tan, Paul Greenfield, Jared J. Tromp, Patricia Corbett, Sharon E. Hook

Environ Toxicol Chem. 2022 Sep; 41(9): 2162–2180. Published online 2022 Aug 3. doi: 10.1002/etc.5413

PMCID:: PMC9545365

Abstract Article PDF–2.4M

Select item 86491426.

In Vivo Human Single‐Chain Fragment Variable Phage Display‐Assisted Identification of Galectin‐3 as a New Biomarker of Atherosclerosis

Audrey Hemadou, Alexandre Fontayne, Jeanny Laroche‐Traineau, Florence Ottones, Philippe Mondon, Stéphane Claverol, Éric Ducasse, Stéphane Sanchez, Sarah Mohamad, Cyril Lorenzato, Martine Duonor‐Cerutti, Gisèle Clofent‐Sanchez, Marie‐Josée Jacobin‐Valat

J Am Heart Assoc. 2021 Oct 5; 10(19): e016287. Published online 2021 Sep 25. doi: 10.1161/JAHA.120.016287

PMCID:: PMC8649142

Abstract Article PDF–2.4M

Select item 84277557.

The Dual Targeting of FcRn and FcγRs via Monomeric Fc Fragments Results in Strong Inhibition of IgG-Dependent Autoimmune Pathologies

Céline Monnet, Emilie Jacque, Christophe de Romeuf, Alexandre Fontayne, Toufik Abache, Nathalie Fournier, Gilles Dupont, Delphine Derache, Anais Engrand, Aurélie Bauduin, Aurélie Terrier, Alexander Seifert, Cécile Beghin, Alain Longue, Nicholas Masiello, Laetitia Danino, Michel Nogre, Anais Raia, Frederic Dhainaut, Louis Fauconnier, Dieudonnée Togbe, Carmen Reitinger, Falk Nimmerjahn, Wil Stevens, Sami Chtourou, Philippe Mondon

Front Immunol. 2021; 12: 728322. Published online 2021 Aug 26. doi: 10.3389/fimmu.2021.728322

PMCID:: PMC8427755

Abstract Article PDF–5.9M

Select item 77620668.

A COL7A1 Variant in a Litter of Neonatal Basset Hounds with Dystrophic Epidermolysis Bullosa

Teresa Maria Garcia, Sarah Kiener, Vidhya Jagannathan, Duncan S. Russell, Tosso Leeb

Genes (Basel) 2020 Dec; 11(12): 1458. Published online 2020 Dec 4. doi: 10.3390/genes11121458

PMCID:: PMC7762066

Abstract Article PDF–1.2M

Select item 68504679.

Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer‐prone genodermatoses

E. Chacón‐Solano, C. León, F. Díaz, F. García‐García, M. García, M.J. Escámez, S. Guerrero‐Aspizua, C.J. Conti, Á. Mencía, L. Martínez‐Santamaría, S. Llames, M. Pévida, J. Carbonell‐Caballero, J.A. Puig‐Butillé, R. Maseda, S. Puig, R. de Lucas, E. Baselga, F. Larcher, J. Dopazo, M. del Río

Br J Dermatol. 2019 Sep; 181(3): 512–522. Published online 2019 Apr 15. doi: 10.1111/bjd.17698

PMCID:: PMC6850467

Abstract Article PDF–5.0M

Select item 541740310.

Research Resource: Genome-Wide Profiling of Methylated Promoters in Endometriosis Reveals a Subtelomeric Location of Hypermethylation

Bruno Borghese, Sandrine Barbaux, Françoise Mondon, Pietro Santulli, Guillaume Pierre, Giovanna Vinci, Charles Chapron, Daniel Vaiman

Mol Endocrinol. September 1, 2010; 24(9): 1872–1885. doi: 10.1210/me.2010-0160

PMCID:: PMC5417403

Abstract Article

Select item 489832011.

ABCA7 rare variants and Alzheimer disease risk

Kilan Le Guennec, Gaël Nicolas, Olivier Quenez, Camille Charbonnier, David Wallon, Céline Bellenguez, Benjamin Grenier-Boley, Stéphane Rousseau, Anne-Claire Richard, Anne Rovelet-Lecrux, Delphine Bacq, Jean-Guillaume Garnier, Robert Olaso, Anne Boland, Vincent Meyer, Jean-François Deleuze, Philippe Amouyel, Hans Markus Munter, Guillaume Bourque, Mark Lathrop, Thierry Frebourg, Richard Redon, Luc Letenneur, Jean-François Dartigues, Florence Pasquier, Adeline Rollin-Sillaire, Emmanuelle Génin, Jean-Charles Lambert, Didier Hannequin, Dominique Campion

Neurology. 2016 Jun 7; 86(23): 2134–2137. doi: 10.1212/WNL.0000000000002627

PMCID:: PMC4898320

Abstract Article PDF–129K

Select item 440304112.

A single epidermal stem cell strategy for safe ex vivo gene therapy

Stéphanie Droz-Georget Lathion, Ariane Rochat, Graham Knott, Alessandra Recchia, Danielle Martinet, Sara Benmohammed, Nicolas Grasset, Andrea Zaffalon, Nathalie Besuchet Schmutz, Emmanuelle Savioz-Dayer, Jacques Samuel Beckmann, Jacques Rougemont, Fulvio Mavilio, Yann Barrandon

EMBO Mol Med. 2015 Apr; 7(4): 380–393. Published online 2015 Feb 27. doi: 10.15252/emmm.201404353

PMCID:: PMC4403041

Abstract Article PDF–3.5M

Select item 433461513.

Identification of Susceptibility Genes for Peritoneal, Ovarian, and Deep Infiltrating Endometriosis Using a Pooled Sample-Based Genome-Wide Association Study

Bruno Borghese, Jörg Tost, Magalie de Surville, Florence Busato, Frank Letourneur, Françoise Mondon, Daniel Vaiman, Charles Chapron

Biomed Res Int. 2015; 2015: 461024. Published online 2015 Feb 4. doi: 10.1155/2015/461024

PMCID:: PMC4334615

Abstract Article PDF–542K

Select item 398433114.

Combined glyco- and protein-Fc engineering simultaneously enhance cytotoxicity and half-life of a therapeutic antibody

Céline Monnet, Sylvie Jorieux, Nathalie Souyris, Ouafa Zaki, Alexandra Jacquet, Nathalie Fournier, Fabien Crozet, Christophe de Romeuf, Khalil Bouayadi, Rémi Urbain, Christian K Behrens, Philippe Mondon, Alexandre Fontayne

MAbs. 2014 Mar 1; 6(2): 422–436. Published online 2014 Jan 15. doi: 10.4161/mabs.27854

PMCID:: PMC3984331

Abstract Article PDF–1.3M

Select item 398414115.

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

Suzanne Lesage, Isabelle Le Ber, Christel Condroyer, Emmanuel Broussolle, Audrey Gabelle, Stéphane Thobois, Florence Pasquier, Karl Mondon, Patrick A. Dion, Daniel Rochefort, Guy A. Rouleau, Alexandra Dürr, Alexis Brice

Brain. Author manuscript; available in PMC 2014 Apr 15.

Published in final edited form as: Brain. 2013 Feb; 136(Pt 2): 385–391. doi: 10.1093/brain/aws357

PMCID:: PMC3984141

Abstract Article

Select item 376596316.

Idiopathic Parkinson’s disease phenotype related to C9ORF72 repeat expansions: contribution of the neuropsychological assessment

Mariam Annan, Émilie Beaufils, Ursule-Catherine Viola, Patrick Vourc’h, Caroline Hommet, Karl Mondon

BMC Res Notes. 2013; 6: 343. Published online 2013 Aug 29. doi: 10.1186/1756-0500-6-343

PMCID:: PMC3765963

Abstract Article PDF–143K

Select item 365827217.

Global remodelling of cellular microenvironment due to loss of collagen VII

Victoria Küttner, Claudia Mack, Kristoffer TG Rigbolt, Johannes S Kern, Oliver Schilling, Hauke Busch, Leena Bruckner-Tuderman, Jörn Dengjel

Mol Syst Biol. 2013; 9: 657. Published online 2013 Apr 16. doi: 10.1038/msb.2013.17

PMCID:: PMC3658272

Abstract Article PDF–4.1M

Select item 346619218.

A genome-wide approach reveals novel imprinted genes expressed in the human placenta

Sandrine Barbaux, Géraldine Gascoin-Lachambre, Christophe Buffat, Paul Monnier, Françoise Mondon, Marie-Béatrice Tonanny, Amélie Pinard, Jana Auer, Bettina Bessières, Anne Barlier, Sébastien Jacques, Umberto Simeoni, Luisa Dandolo, Franck Letourneur, Hélène Jammes, Daniel Vaiman

Epigenetics. 2012 Sep 1; 7(9): 1079–1090. doi: 10.4161/epi.21495

PMCID:: PMC3466192

Abstract Article PDF–2.0M

Select item 342087019.

Refined Mapping of a Quantitative Trait Locus on Chromosome 1 Responsible for Mouse Embryonic Death

Magalie Vatin, Gaetan Burgio, Gilles Renault, Paul Laissue, Virginie Firlej, Françoise Mondon, Xavier Montagutelli, Daniel Vaiman, Catherine Serres, Ahmed Ziyyat

PLoS One. 2012; 7(8): e43356. Published online 2012 Aug 16. doi: 10.1371/journal.pone.0043356

PMCID:: PMC3420870

Abstract Article PDF–391K

Select item 335524720.

A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease

Anne Rovelet-Lecrux, Solenn Legallic, David Wallon, Jean-Michel Flaman, Olivier Martinaud, Stéphanie Bombois, Adeline Rollin-Sillaire, Agnès Michon, Isabelle Le Ber, Jérémie Pariente, Michèle Puel, Claire Paquet, Bernard Croisile, Catherine Thomas-Antérion, Martine Vercelletto, Richard Lévy, Thierry Frébourg, Didier Hannequin, Dominique Campion, Investigators of the GMAJ project

Eur J Hum Genet. 2012 Jun; 20(6): 613–617. Published online 2011 Dec 14. doi: 10.1038/ejhg.2011.225

PMCID:: PMC3355247

Abstract Article PDF–330K

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PMC Articles for MedGen (Select 343607) (34)
PMC
hypothetical protein MJT46_008004 [Ovis ammon polii x Ovis aries]
hypothetical protein MJT46_008004 [Ovis ammon polii x Ovis aries]
gi|2251156223|gb|KAI4568206.1||gnl| ALAIX|cds.evm.model.A-LG08.628

Protein
hypothetical protein JEQ12_018245 [Ovis aries]
hypothetical protein JEQ12_018245 [Ovis aries]
gi|2015234411|gb|KAG5206672.1||gnl| AEMGP|zangyang_Chr7_G00539.t1.cds41

Protein
zinc finger C3HC-type protein 1 isoform X4 [Homo sapiens]
zinc finger C3HC-type protein 1 isoform X4 [Homo sapiens]
gi|2217367351|ref|XP_047276410.1|

Protein
cytochrome oxidase subunit I, partial (mitochondrion) [Etrumeus micropus]
cytochrome oxidase subunit I, partial (mitochondrion) [Etrumeus micropus]
gi|1101488747|gb|APC02641.1|

Protein

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