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Items: 1 to 50 of 520

1.

Updating the classification of inherited neuropathies: Results of an international survey.

Magy L, Mathis S, Le Masson G, Goizet C, Tazir M, Vallat JM.

Neurology. 2018 Feb 2. pii: 10.1212/WNL.0000000000005074. doi: 10.1212/WNL.0000000000005074. [Epub ahead of print]

PMID:
29429969
2.

The nature of nurture: Effects of parental genotypes.

Kong A, Thorleifsson G, Frigge ML, Vilhjalmsson BJ, Young AI, Thorgeirsson TE, Benonisdottir S, Oddsson A, Halldorsson BV, Masson G, Gudbjartsson DF, Helgason A, Bjornsdottir G, Thorsteinsdottir U, Stefansson K.

Science. 2018 Jan 26;359(6374):424-428. doi: 10.1126/science.aan6877.

PMID:
29371463
3.

RNA-Targeted Therapies and Amyotrophic Lateral Sclerosis.

Mathis S, Le Masson G.

Biomedicines. 2018 Jan 15;6(1). pii: E9. doi: 10.3390/biomedicines6010009. Review.

4.

Reconstructing an African haploid genome from the 18th century.

Jagadeesan A, Gunnarsdóttir ED, Ebenesersdóttir SS, Guðmundsdóttir VB, Thordardottir EL, Einarsdóttir MS, Jónsson H, Dugoujon JM, Fortes-Lima C, Migot-Nabias F, Massougbodji A, Bellis G, Pereira L, Másson G, Kong A, Stefánsson K, Helgason A.

Nat Genet. 2018 Feb;50(2):199-205. doi: 10.1038/s41588-017-0031-6. Epub 2018 Jan 15.

PMID:
29335549
5.

Acute Brachial Radiculoplexopathy and Giant Cell Arteritis.

Duval F, Lacoste I, Galli G, Chaumont H, Solé G, Léger F, Damon-Perrière N, Rouanet M, Le Masson G, Mathis S.

Neurologist. 2018 Jan;23(1):23-28. doi: 10.1097/NRL.0000000000000162.

PMID:
29266041
6.

Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations.

Olafsson S, Stridh P, Bos SD, Ingason A, Euesden J, Sulem P, Thorleifsson G, Gustafsson O, Johannesson A, Geirsson AJ, Thorsson AV, Sigurgeirsson B, Ludviksson BR, Olafsson E, Kristjansdottir H, Jonasson JG, Olafsson JH, Orvar KB, Benediktsson R, Bjarnason R, Kristjansdottir S, Gislason T, Valdimarsson T, Mikaelsdottir E, Sigurdsson S, Jonsson S, Rafnar T, Aarsland D, Djurovic S, Fladby T, Knudsen GP, Celius EG, Myhr KM, Grondal G, Steinsson K, Valdimarsson H, Bjornsson S, Bjornsdottir US, Bjornsson ES, Nilsson B, Andreassen OA, Alfredsson L, Hillert J, Kockum IS, Masson G, Thorsteinsdottir U, Gudbjartsson DF, Stefansson H, Hjaltason H, Harbo HF, Olsson T, Jonsdottir I, Stefansson K.

NPJ Genom Med. 2017 Aug 8;2:24. doi: 10.1038/s41525-017-0027-2. eCollection 2017.

7.

Study of the Construction of the Tiacumicin B Aglycone.

Jeanne-Julien L, Masson G, Astier E, Genta-Jouve G, Servajean V, Beau JM, Norsikian S, Roulland E.

J Org Chem. 2018 Jan 19;83(2):921-929. doi: 10.1021/acs.joc.7b02909. Epub 2018 Jan 2.

PMID:
29260550
8.

History and current difficulties in classifying inherited myopathies and muscular dystrophies.

Mathis S, Tazir M, Magy L, Duval F, Le Masson G, Duchesne M, Couratier P, Ghorab K, Solé G, Lacoste I, Goizet C, Vallat JM.

J Neurol Sci. 2018 Jan 15;384:50-54. doi: 10.1016/j.jns.2017.10.051. Epub 2017 Nov 2.

PMID:
29249377
9.

Single-Molecule Study Reveals How Receptor and Ras Synergistically Activate PI3Kα and PIP3 Signaling.

Buckles TC, Ziemba BP, Masson GR, Williams RL, Falke JJ.

Biophys J. 2017 Dec 5;113(11):2396-2405. doi: 10.1016/j.bpj.2017.09.018.

10.

COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA.

Jensson BO, Hansdottir S, Arnadottir GA, Sulem G, Kristjansson RP, Oddsson A, Benonisdottir S, Jonsson H, Helgason A, Saemundsdottir J, Magnusson OT, Masson G, Thorisson GA, Jonasdottir A, Jonasdottir A, Sigurdsson A, Jonsdottir I, Petursdottir V, Kristinsson JR, Gudbjartsson DF, Thorsteinsdottir U, Arngrimsson R, Sulem P, Gudmundsson G, Stefansson K.

BMC Med Genet. 2017 Nov 14;18(1):129. doi: 10.1186/s12881-017-0490-8.

11.

Did Jules Dejerine describe AMAN at the end of the 19th century?

Mathis S, Magy L, Le Masson G, Vallat JM.

Neurology. 2017 Oct 17;89(16):1749-1753. doi: 10.1212/WNL.0000000000004527.

PMID:
29038133
12.

SmartPilot® view-guided anaesthesia improves postoperative outcomes in hip fracture surgery: a randomized blinded controlled study.

Leblanc D, Conté M, Masson G, Richard F, Jeanneteau A, Bouhours G, Chrétien JM, Rony L, Rineau E, Lasocki S.

Br J Anaesth. 2017 Nov 1;119(5):1022-1029. doi: 10.1093/bja/aex317.

PMID:
29028921
13.

Experimental Evidences Supporting Training-Induced Benefits in Spontaneously Hypertensive Rats.

Masson GS, Michelini LC.

Adv Exp Med Biol. 2017;999:287-306. doi: 10.1007/978-981-10-4307-9_16.

PMID:
29022269
14.

Integron Digestive Carriage in Human and Cattle: A "One Health" Cultivation-Independent Approach.

Chainier D, Barraud O, Masson G, Couve-Deacon E, François B, Couquet CY, Ploy MC.

Front Microbiol. 2017 Sep 27;8:1891. doi: 10.3389/fmicb.2017.01891. eCollection 2017.

15.

Enantioselective Brønsted Acid Catalysis as a Tool for the Synthesis of Natural Products and Pharmaceuticals.

Merad J, Lalli C, Bernadat G, Maury J, Masson G.

Chemistry. 2017 Oct 5. doi: 10.1002/chem.201703556. [Epub ahead of print] Review.

PMID:
28981209
16.

Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.

Arnadottir GA, Jensson BO, Marelsson SE, Sulem G, Oddsson A, Kristjansson RP, Benonisdottir S, Gudjonsson SA, Masson G, Thorisson GA, Saemundsdottir J, Magnusson OT, Jonasdottir A, Jonasdottir A, Sigurdsson A, Gudbjartsson DF, Thorsteinsdottir U, Arngrimsson R, Sulem P, Stefansson K.

BMC Med Genet. 2017 Oct 2;18(1):103. doi: 10.1186/s12881-017-0466-8.

17.

Parental influence on human germline de novo mutations in 1,548 trios from Iceland.

Jónsson H, Sulem P, Kehr B, Kristmundsdottir S, Zink F, Hjartarson E, Hardarson MT, Hjorleifsson KE, Eggertsson HP, Gudjonsson SA, Ward LD, Arnadottir GA, Helgason EA, Helgason H, Gylfason A, Jonasdottir A, Jonasdottir A, Rafnar T, Frigge M, Stacey SN, Th Magnusson O, Thorsteinsdottir U, Masson G, Kong A, Halldorsson BV, Helgason A, Gudbjartsson DF, Stefansson K.

Nature. 2017 Sep 28;549(7673):519-522. doi: 10.1038/nature24018. Epub 2017 Sep 20.

PMID:
28959963
18.

Graphtyper enables population-scale genotyping using pangenome graphs.

Eggertsson HP, Jonsson H, Kristmundsdottir S, Hjartarson E, Kehr B, Masson G, Zink F, Hjorleifsson KE, Jonasdottir A, Jonasdottir A, Jonsdottir I, Gudbjartsson DF, Melsted P, Stefansson K, Halldorsson BV.

Nat Genet. 2017 Nov;49(11):1654-1660. doi: 10.1038/ng.3964. Epub 2017 Sep 25.

PMID:
28945251
19.

Whole genome characterization of sequence diversity of 15,220 Icelanders.

Jónsson H, Sulem P, Kehr B, Kristmundsdottir S, Zink F, Hjartarson E, Hardarson MT, Hjorleifsson KE, Eggertsson HP, Gudjonsson SA, Ward LD, Arnadottir GA, Helgason EA, Helgason H, Gylfason A, Jonasdottir A, Jonasdottir A, Rafnar T, Besenbacher S, Frigge ML, Stacey SN, Magnusson OT, Thorsteinsdottir U, Masson G, Kong A, Halldorsson BV, Helgason A, Gudbjartsson DF, Stefansson K.

Sci Data. 2017 Sep 21;4:170115. doi: 10.1038/sdata.2017.115.

20.

Recurrent network dynamics reconciles visual motion segmentation and integration.

Medathati NVK, Rankin J, Meso AI, Kornprobst P, Masson GS.

Sci Rep. 2017 Sep 12;7(1):11270. doi: 10.1038/s41598-017-11373-z.

21.

Chronic inflammatory demyelinating polyradiculoneuropathy-causing myelopathy.

Mathis S, Duval F, Solé G, Tourdias T, Le Masson G.

Muscle Nerve. 2018 Feb;57(2):E102-E103. doi: 10.1002/mus.25756. Epub 2017 Aug 17. No abstract available.

PMID:
28786217
22.

An overview of hydrogen deuterium exchange mass spectrometry (HDX-MS) in drug discovery.

Masson GR, Jenkins ML, Burke JE.

Expert Opin Drug Discov. 2017 Oct;12(10):981-994. doi: 10.1080/17460441.2017.1363734. Epub 2017 Aug 17. Review.

PMID:
28770632
23.

Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

Styrkarsdottir U, Helgason H, Sigurdsson A, Norddahl GL, Agustsdottir AB, Reynard LN, Villalvilla A, Halldorsson GH, Jonasdottir A, Magnusdottir A, Oddson A, Sulem G, Zink F, Sveinbjornsson G, Helgason A, Johannsdottir HS, Helgadottir A, Stefansson H, Gretarsdottir S, Rafnar T, Almdahl IS, Brækhus A, Fladby T, Selbæk G, Hosseinpanah F, Azizi F, Koh JM, Tang NLS, Danesphour M, Mayordomo JI, Welt C, Braund PS, Samani NJ, Kiemeney LA, Lohmander LS, Christiansen C, Andreassen OA, Consortium A, Magnusson O, Masson G, Kong A, Jonsdottir I, Gudbjartsson D, Sulem P, Jonsson H, Loughlin J, Ingvarsson T, Thorsteinsdottir U, Stefansson K.

Nat Genet. 2017 Jul 27;49(8):1286. doi: 10.1038/ng0817-1286b. No abstract available.

PMID:
28747754
24.

Asymmetric α-Sulfonyl- and α-Phosphoryl-Oxylation of Ketones by a Chiral Hypervalent Iodine(III).

Levitre G, Dumoulin A, Retailleau P, Panossian A, Leroux FR, Masson G.

J Org Chem. 2017 Nov 17;82(22):11877-11883. doi: 10.1021/acs.joc.7b01597. Epub 2017 Jul 31.

PMID:
28731345
25.

Synthesis of a Tiacumicin B Protected Aglycone.

Jeanne-Julien L, Masson G, Astier E, Genta-Jouve G, Servajean V, Beau JM, Norsikian S, Roulland E.

Org Lett. 2017 Aug 4;19(15):4006-4009. doi: 10.1021/acs.orglett.7b01744. Epub 2017 Jul 19.

PMID:
28723103
26.

Visual stimulation quenches global alpha range activity in awake primate V4: a case study.

Deneux T, Masquelier T, Bermudez MA, Masson GS, Deco G, Vanzetta I.

Neurophotonics. 2017 Jul;4(3):031222. doi: 10.1117/1.NPh.4.3.031222. Epub 2017 Jun 28.

PMID:
28680907
27.

Enantioselective Organocatalytic Intramolecular Aza-Diels-Alder Reaction.

Jarrige L, Blanchard F, Masson G.

Angew Chem Int Ed Engl. 2017 Aug 21;56(35):10573-10576. doi: 10.1002/anie.201705746. Epub 2017 Jul 24.

PMID:
28661020
28.

Identification of sequence variants influencing immunoglobulin levels.

Jonsson S, Sveinbjornsson G, de Lapuente Portilla AL, Swaminathan B, Plomp R, Dekkers G, Ajore R, Ali M, Bentlage AEH, Elmér E, Eyjolfsson GI, Gudjonsson SA, Gullberg U, Gylfason A, Halldorsson BV, Hansson M, Holm H, Johansson Å, Johnsson E, Jonasdottir A, Ludviksson BR, Oddsson A, Olafsson I, Olafsson S, Sigurdardottir O, Sigurdsson A, Stefansdottir L, Masson G, Sulem P, Wuhrer M, Wihlborg AK, Thorleifsson G, Gudbjartsson DF, Thorsteinsdottir U, Vidarsson G, Jonsdottir I, Nilsson B, Stefansson K.

Nat Genet. 2017 Aug;49(8):1182-1191. doi: 10.1038/ng.3897. Epub 2017 Jun 19.

PMID:
28628107
29.

Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.

Sigurdsson S, Alexandersson KF, Sulem P, Feenstra B, Gudmundsdottir S, Halldorsson GH, Olafsson S, Sigurdsson A, Rafnar T, Thorgeirsson T, Sørensen E, Nordholm-Carstensen A, Burcharth J, Andersen J, Jørgensen HS, Possfelt-Møller E, Ullum H, Thorleifsson G, Masson G, Thorsteinsdottir U, Melbye M, Gudbjartsson DF, Stefansson T, Jonsdottir I, Stefansson K.

Nat Commun. 2017 Jun 6;8:15789. doi: 10.1038/ncomms15789.

30.

Cardiovascular Risk Stratification in Patients with Metabolic Syndrome Without Diabetes or Cardiovascular Disease: Usefulness of Metabolic Syndrome Severity Score.

Masson W, Epstein T, Huerín M, Lobo LM, Molinero G, Angel A, Masson G, Millán D, De Francesca S, Vitagliano L, Cafferata A, Losada P.

High Blood Press Cardiovasc Prev. 2017 Sep;24(3):297-303. doi: 10.1007/s40292-017-0209-0. Epub 2017 May 13.

PMID:
28502055
31.

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.

Zink F, Stacey SN, Norddahl GL, Frigge ML, Magnusson OT, Jonsdottir I, Thorgeirsson TE, Sigurdsson A, Gudjonsson SA, Gudmundsson J, Jonasson JG, Tryggvadottir L, Jonsson T, Helgason A, Gylfason A, Sulem P, Rafnar T, Thorsteinsdottir U, Gudbjartsson DF, Masson G, Kong A, Stefansson K.

Blood. 2017 Aug 10;130(6):742-752. doi: 10.1182/blood-2017-02-769869. Epub 2017 May 8.

32.

A Normalization Mechanism for Estimating Visual Motion across Speeds and Scales.

Gekas N, Meso AI, Masson GS, Mamassian P.

Curr Biol. 2017 May 22;27(10):1514-1520.e3. doi: 10.1016/j.cub.2017.04.022. Epub 2017 May 4.

PMID:
28479319
33.

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.

Haraldsdottir S, Rafnar T, Frankel WL, Einarsdottir S, Sigurdsson A, Hampel H, Snaebjornsson P, Masson G, Weng D, Arngrimsson R, Kehr B, Yilmaz A, Haraldsson S, Sulem P, Stefansson T, Shields PG, Sigurdsson F, Bekaii-Saab T, Moller PH, Steinarsdottir M, Alexiusdottir K, Hitchins M, Pritchard CC, de la Chapelle A, Jonasson JG, Goldberg RM, Stefansson K.

Nat Commun. 2017 May 3;8:14755. doi: 10.1038/ncomms14755.

34.

Flow Perturbation Mediates Neutrophil Recruitment and Potentiates Endothelial Injury via TLR2 in Mice: Implications for Superficial Erosion.

Franck G, Mawson T, Sausen G, Salinas M, Masson GS, Cole A, Beltrami-Moreira M, Chatzizisis Y, Quillard T, Tesmenitsky Y, Shvartz E, Sukhova GK, Swirski FK, Nahrendorf M, Aikawa E, Croce KJ, Libby P.

Circ Res. 2017 Jun 23;121(1):31-42. doi: 10.1161/CIRCRESAHA.117.310694. Epub 2017 Apr 20.

PMID:
28428204
35.

Current view and perspectives in amyotrophic lateral sclerosis.

Mathis S, Couratier P, Julian A, Corcia P, Le Masson G.

Neural Regen Res. 2017 Feb;12(2):181-184. doi: 10.4103/1673-5374.200794. Review.

36.

A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.

Bjornsson E, Helgason H, Halldorsson G, Helgadottir A, Gylfason A, Kehr B, Jonasdottir A, Jonasdottir A, Sigurdsson A, Oddsson A, Thorleifsson G, Magnusson OT, Gretarsdottir S, Zink F, Kristjansson RP, Asgeirsdottir M, Swinkels DW, Kiemeney LA, Eyjolfsson GI, Sigurdardottir O, Masson G, Olafsson I, Thorgeirsson G, Holm H, Thorsteinsdottir U, Gudbjartsson DF, Sulem P, Stefansson K.

Hum Mol Genet. 2017 Jun 15;26(12):2364-2376. doi: 10.1093/hmg/ddx123.

PMID:
28398513
37.

Description of the EuroTARGET cohort: A European collaborative project on TArgeted therapy in renal cell cancer-GEnetic- and tumor-related biomarkers for response and toxicity.

van der Zanden LFM, Vermeulen SH, Oskarsdottir A, Maurits JSF, Diekstra MHM, Ambert V, Cambon-Thomsen A, Castellano D, Fritsch A, Garcia Donas J, Guarch Troyas R, Guchelaar HJ, Hartmann A, Hulsbergen-van de Kaa C, Jaehde U, Junker K, Martinez-Cardus A, Masson G, Oosterwijk-Wakka J, Radu MT, Rafnar T, Rodriguez-Antona C, Roessler M, Ruijtenbeek R, Stefansson K, Warren A, Wessels L, Eisen T, Kiemeney LALM, Oosterwijk E.

Urol Oncol. 2017 Aug;35(8):529.e9-529.e16. doi: 10.1016/j.urolonc.2017.03.009. Epub 2017 Apr 3.

38.

Analysis of phosphoinositide 3-kinase inhibitors by bottom-up electron-transfer dissociation hydrogen/deuterium exchange mass spectrometry.

Masson GR, Maslen SL, Williams RL.

Biochem J. 2017 May 16;474(11):1867-1877. doi: 10.1042/BCJ20170127.

39.

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

Styrkarsdottir U, Helgason H, Sigurdsson A, Norddahl GL, Agustsdottir AB, Reynard LN, Villalvilla A, Halldorsson GH, Jonasdottir A, Magnusdottir A, Oddson A, Sulem G, Zink F, Sveinbjornsson G, Helgason A, Johannsdottir HS, Helgadottir A, Stefansson H, Gretarsdottir S, Rafnar T, Almdahl IS, Brækhus A, Fladby T, Selbæk G, Hosseinpanah F, Azizi F, Koh JM, Tang NLS, Daneshpour MS, Mayordomo JI, Welt C, Braund PS, Samani NJ, Kiemeney LA, Lohmander LS, Christiansen C, Andreassen OA; arcOGEN consortium, Magnusson O, Masson G, Kong A, Jonsdottir I, Gudbjartsson D, Sulem P, Jonsson H, Loughlin J, Ingvarsson T, Thorsteinsdottir U, Stefansson K.

Nat Genet. 2017 May;49(5):801-805. doi: 10.1038/ng.3816. Epub 2017 Mar 20. Erratum in: Nat Genet. 2017 Jul 27;49(8):1286.

PMID:
28319091
40.

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.

Smith D, Helgason H, Sulem P, Bjornsdottir US, Lim AC, Sveinbjornsson G, Hasegawa H, Brown M, Ketchem RR, Gavala M, Garrett L, Jonasdottir A, Jonasdottir A, Sigurdsson A, Magnusson OT, Eyjolfsson GI, Olafsson I, Onundarson PT, Sigurdardottir O, Gislason D, Gislason T, Ludviksson BR, Ludviksdottir D, Boezen HM, Heinzmann A, Krueger M, Porsbjerg C, Ahluwalia TS, Waage J, Backer V, Deichmann KA, Koppelman GH, Bønnelykke K, Bisgaard H, Masson G, Thorsteinsdottir U, Gudbjartsson DF, Johnston JA, Jonsdottir I, Stefansson K.

PLoS Genet. 2017 Mar 8;13(3):e1006659. doi: 10.1371/journal.pgen.1006659. eCollection 2017 Mar.

41.

Fluorinated Sulfilimino Iminiums: Efficient and Versatile Sources of Perfluoroalkyl Radicals under Photoredox Catalysis.

Daniel M, Dagousset G, Diter P, Klein PA, Tuccio B, Goncalves AM, Masson G, Magnier E.

Angew Chem Int Ed Engl. 2017 Mar 27;56(14):3997-4001. doi: 10.1002/anie.201700290. Epub 2017 Mar 2.

PMID:
28252241
42.

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation.

Bjornsdottir G, Benonisdottir S, Sveinbjornsson G, Styrkarsdottir U, Thorleifsson G, Walters GB, Bjornsson A, Olafsson IH, Ulfarsson E, Vikingsson A, Hansdottir R, Karlsson KO, Rafnar T, Jonsdottir I, Frigge ML, Kong A, Oddsson A, Masson G, Magnusson OT, Gudbjartsson T, Stefansson H, Sulem P, Gudbjartsson D, Thorsteinsdottir U, Thorgeirsson TE, Stefansson K.

Nat Commun. 2017 Feb 22;8:14265. doi: 10.1038/ncomms14265.

43.

A genome-wide association study yields five novel thyroid cancer risk loci.

Gudmundsson J, Thorleifsson G, Sigurdsson JK, Stefansdottir L, Jonasson JG, Gudjonsson SA, Gudbjartsson DF, Masson G, Johannsdottir H, Halldorsson GH, Stacey SN, Helgason H, Sulem P, Senter L, He H, Liyanarachchi S, Ringel MD, Aguillo E, Panadero A, Prats E, Garcia-Castaño A, De Juan A, Rivera F, Xu L, Kiemeney LA, Eyjolfsson GI, Sigurdardottir O, Olafsson I, Kristvinsson H, Netea-Maier RT, Jonsson T, Mayordomo JI, Plantinga TS, Hjartarson H, Hrafnkelsson J, Sturgis EM, Thorsteinsdottir U, Rafnar T, de la Chapelle A, Stefansson K.

Nat Commun. 2017 Feb 14;8:14517. doi: 10.1038/ncomms14517.

44.

The Flash-Lag Effect as a Motion-Based Predictive Shift.

Khoei MA, Masson GS, Perrinet LU.

PLoS Comput Biol. 2017 Jan 26;13(1):e1005068. doi: 10.1371/journal.pcbi.1005068. eCollection 2017 Jan.

45.

Selection against variants in the genome associated with educational attainment.

Kong A, Frigge ML, Thorleifsson G, Stefansson H, Young AI, Zink F, Jonsdottir GA, Okbay A, Sulem P, Masson G, Gudbjartsson DF, Helgason A, Bjornsdottir G, Thorsteinsdottir U, Stefansson K.

Proc Natl Acad Sci U S A. 2017 Jan 31;114(5):E727-E732. doi: 10.1073/pnas.1612113114. Epub 2017 Jan 17.

46.

Enantioselective Three-Component Amination of Enecarbamates Enables the Synthesis of Structurally Complex Small Molecules.

Dumoulin A, Bernadat G, Masson G.

J Org Chem. 2017 Feb 3;82(3):1775-1789. doi: 10.1021/acs.joc.6b03093. Epub 2017 Jan 25.

PMID:
28092703
47.

Cardiomyocyte-specific ablation of CD36 accelerates the progression from compensated cardiac hypertrophy to heart failure.

Sung MM, Byrne NJ, Kim TT, Levasseur J, Masson G, Boisvenue JJ, Febbraio M, Dyck JR.

Am J Physiol Heart Circ Physiol. 2017 Mar 1;312(3):H552-H560. doi: 10.1152/ajpheart.00626.2016. Epub 2017 Jan 6.

PMID:
28062415
48.

A novel complex I inhibitor protects against hypertension-induced left ventricular hypertrophy.

Matsumura N, Robertson IM, Hamza SM, Soltys CM, Sung MM, Masson G, Beker DL, Dyck JR.

Am J Physiol Heart Circ Physiol. 2017 Mar 1;312(3):H561-H570. doi: 10.1152/ajpheart.00604.2016. Epub 2017 Jan 6.

PMID:
28062414
49.

Chiral Hypervalent Iodine(III) Catalyst Promotes Highly Enantioselective Sulfonyl- and Phosphoryl-oxylactonizations.

Gelis C, Dumoulin A, Bekkaye M, Neuville L, Masson G.

Org Lett. 2017 Jan 6;19(1):278-281. doi: 10.1021/acs.orglett.6b03631. Epub 2016 Dec 23.

PMID:
28009522
50.

The relative contribution of noise and adaptation to competition during tri-stable motion perception.

Meso AI, Rankin J, Faugeras O, Kornprobst P, Masson GS.

J Vis. 2016 Dec 1;16(15):6. doi: 10.1167/16.15.6.

PMID:
27936270

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