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Items: 1 to 50 of 295

1.
2.

Deficient LRRC8A-dependent volume-regulated anion channel activity is associated with male infertility in mice.

Bao J, Perez CJ, Kim J, Zhang H, Murphy CJ, Hamidi T, Jaubert J, Platt CD, Chou J, Deng M, Zhou MH, Huang Y, Gaitán-Peñas H, Guénet JL, Lin K, Lu Y, Chen T, Bedford MT, Dent SY, Richburg JH, Estévez R, Pan HL, Geha RS, Shi Q, Benavides F.

JCI Insight. 2018 Aug 23;3(16). pii: 99767. doi: 10.1172/jci.insight.99767. eCollection 2018 Aug 23.

3.

Hybrid Fibrillar Xerogels with Unusual Magnetic Properties.

Boulaoued A, Bantignies JL, Le Parc R, Goze-Bac C, Mésini P, Nguyen TT, Al Ouahabi A, Lutz P, Guenet JM.

Langmuir. 2016 Dec 13;32(49):13193-13199. Epub 2016 Nov 29.

PMID:
27951692
4.

The HERC2 ubiquitin ligase is essential for embryonic development and regulates motor coordination.

Cubillos-Rojas M, Schneider T, Hadjebi O, Pedrazza L, de Oliveira JR, Langa F, Guénet JL, Duran J, de Anta JM, Alcántara S, Ruiz R, Pérez-Villegas EM, Aguilar-Montilla FJ, Carrión ÁM, Armengol JA, Baple E, Crosby AH, Bartrons R, Ventura F, Rosa JL.

Oncotarget. 2016 Aug 30;7(35):56083-56106. doi: 10.18632/oncotarget.11270.

5.

Origin of Invariant Gel Melting Temperatures in the c-T Phase Diagram of an Organogel.

Christ E, Blanc C, Al Ouahabi A, Maurin D, Le Parc R, Bantignies JL, Guenet JM, Collin D, Mésini PJ.

Langmuir. 2016 May 17;32(19):4975-82. doi: 10.1021/acs.langmuir.6b00995. Epub 2016 May 5.

PMID:
27088451
6.

Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene.

Perez CJ, Mecklenburg L, Jaubert J, Martinez-Santamaria L, Iritani BM, Espejo A, Napoli E, Song G, Del Río M, DiGiovanni J, Giulivi C, Bedford MT, Dent SYR, Wood RD, Kusewitt DF, Guénet JL, Conti CJ, Benavides F.

J Invest Dermatol. 2015 Dec;135(12):3133-3143. doi: 10.1038/jid.2015.314. Epub 2015 Aug 19.

7.

[The legacy of Mary F. Lyon (1925-2014)].

Guénet JL, Panthier JJ, Avner P, Heard E, Montagutelli X.

Med Sci (Paris). 2015 Jun-Jul;31(6-7):687-9. doi: 10.1051/medsci/20153106024. Epub 2015 Jul 7. French. No abstract available.

8.

Design of Nanohybrid Systems from a Partially Fluorinated Organogelator and Syndiotactic Polystyrene Thermoreversible Gel.

Khan AN, Schmutz M, Lacava J, Al Ouahabi A, Nguyen TT, Mesini PJ, Guenet JM.

Langmuir. 2015 Jul 14;31(27):7666-72. doi: 10.1021/acs.langmuir.5b01339. Epub 2015 Jul 1.

PMID:
26094978
9.

François Jacob, …. an outstanding mentor!

Guénet JL.

Res Microbiol. 2014 Jun;165(5):377-9. doi: 10.1016/j.resmic.2014.05.002. Epub 2014 May 20. No abstract available.

PMID:
24853969
10.

Investigation of the interactions involved in the formation of nanotubes from organogelators.

Khan AN, Nguyen TT, Dobircau L, Schmutz M, Mesini PJ, Guenet JM.

Langmuir. 2013 Dec 31;29(52):16127-34. doi: 10.1021/la404002k. Epub 2013 Dec 18.

PMID:
24321040
11.

The circling mutant Pcdh15roda is a new mouse model for hearing loss.

Torres AA, Rzadzinska AK, Ribeiro AF, Silva DA, Guénet JL, Massironi SM, Godard AL.

Mutat Res. 2013 Nov-Dec;751-752:29-35. doi: 10.1016/j.mrfmmm.2013.09.002. Epub 2013 Sep 14.

PMID:
24044941
12.

Several classical mouse inbred strains, including DBA/2, NOD/Lt, FVB/N, and SJL/J, carry a putative loss-of-function allele of Gpr84.

Perez CJ, Dumas A, Vallières L, Guénet JL, Benavides F.

J Hered. 2013 Jul-Aug;104(4):565-71. doi: 10.1093/jhered/est023. Epub 2013 Apr 24.

13.

Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects.

Steffes G, Lorente-Cánovas B, Pearson S, Brooker RH, Spiden S, Kiernan AE, Guénet JL, Steel KP.

PLoS One. 2012;7(11):e51065. doi: 10.1371/journal.pone.0051065. Epub 2012 Nov 30.

14.

Alopecia in a viable phospholipase C delta 1 and phospholipase C delta 3 double mutant.

Runkel F, Hintze M, Griesing S, Michels M, Blanck B, Fukami K, Guénet JL, Franz T.

PLoS One. 2012;7(6):e39203. doi: 10.1371/journal.pone.0039203. Epub 2012 Jun 19.

15.

Transgenic expression of full-length 2',5'-oligoadenylate synthetase 1b confers to BALB/c mice resistance against West Nile virus-induced encephalitis.

Simon-Chazottes D, Frenkiel MP, Montagutelli X, Guénet JL, Desprès P, Panthier JJ.

Virology. 2011 Aug 15;417(1):147-53. doi: 10.1016/j.virol.2011.05.018. Epub 2011 Jun 17.

16.

Animal models of human genetic diseases: do they need to be faithful to be useful?

Guénet JL.

Mol Genet Genomics. 2011 Jul;286(1):1-20. doi: 10.1007/s00438-011-0627-y. Epub 2011 May 6. Review.

PMID:
21547562
17.

[A new era in rat genetics].

Cohen-Tannoudji M, Guénet JL.

Med Sci (Paris). 2011 Apr;27(4):387-90. doi: 10.1051/medsci/2011274014. Epub 2011 Apr 28. Review. French.

18.

A mutation in the gene encoding mitochondrial Mg²+ channel MRS2 results in demyelination in the rat.

Kuramoto T, Kuwamura M, Tokuda S, Izawa T, Nakane Y, Kitada K, Akao M, Guénet JL, Serikawa T.

PLoS Genet. 2011 Jan 6;7(1):e1001262. doi: 10.1371/journal.pgen.1001262.

19.

Mouse Strains and Genetic Nomenclature.

Guénet JL, Benavides FJ.

Curr Protoc Mouse Biol. 2011 Mar 1;1(1):213-38. doi: 10.1002/9780470942390.mo100181.

PMID:
26068994
20.

Fine-tuning the morphology of self-assembled nanostructures of propargyl ammonium-based amphiphiles.

Morin E, Guenet JM, Díaz DD, Remy JS, Wagner A.

J Phys Chem B. 2010 Oct 7;114(39):12495-500. doi: 10.1021/jp104911e.

PMID:
20839865
21.

Two hypomorphic alleles of mouse Ass1 as a new animal model of citrullinemia type I and other hyperammonemic syndromes.

Perez CJ, Jaubert J, Guénet JL, Barnhart KF, Ross-Inta CM, Quintanilla VC, Aubin I, Brandon JL, Otto NW, DiGiovanni J, Gimenez-Conti I, Giulivi C, Kusewitt DF, Conti CJ, Benavides F.

Am J Pathol. 2010 Oct;177(4):1958-68. doi: 10.2353/ajpath.2010.100118. Epub 2010 Aug 19.

22.

The stromal gene encoding the CD274 antigen as a genetic modifier controlling survival of mice with γ-radiation-induced T-cell lymphoblastic lymphomas.

Santos J, González-Sánchez L, Villa-Morales M, Ors I, López-Nieva P, Vaquero C, González-Gugel E, Fernández-Navarro P, Roncero AM, Guenet JL, Montagutelli X, Fernández-Piqueras J.

Oncogene. 2010 Sep 23;29(38):5265-73. doi: 10.1038/onc.2010.280. Epub 2010 Jul 19.

PMID:
20639904
23.

Stress-induced sphingolipid signaling: role of type-2 neutral sphingomyelinase in murine cell apoptosis and proliferation.

Devillard R, Galvani S, Thiers JC, Guenet JL, Hannun Y, Bielawski J, Nègre-Salvayre A, Salvayre R, Augé N.

PLoS One. 2010 Mar 23;5(3):e9826. doi: 10.1371/journal.pone.0009826.

24.

Progressive Purkinje cell degeneration in tambaleante mutant mice is a consequence of a missense mutation in HERC1 E3 ubiquitin ligase.

Mashimo T, Hadjebi O, Amair-Pinedo F, Tsurumi T, Langa F, Serikawa T, Sotelo C, Guénet JL, Rosa JL.

PLoS Genet. 2009 Dec;5(12):e1000784. doi: 10.1371/journal.pgen.1000784. Epub 2009 Dec 24.

25.

Hybrid thermoreversible gels from covalent polymers and organogels.

Dasgupta D, Srinivasan S, Rochas C, Ajayaghosh A, Guenet JM.

Langmuir. 2009 Aug 4;25(15):8593-8. doi: 10.1021/la804185q.

PMID:
19292503
26.

A role for stroma-derived annexin A1 as mediator in the control of genetic susceptibility to T-cell lymphoblastic malignancies through prostaglandin E2 secretion.

Santos J, González-Sánchez L, Matabuena-Deyzaguirre M, Villa-Morales M, Cozar P, López-Nieva P, Fernández-Navarro P, Fresno M, Díaz-Muñoz MD, Guenet JL, Montagutelli X, Fernández-Piqueras J.

Cancer Res. 2009 Mar 15;69(6):2577-87. doi: 10.1158/0008-5472.CAN-08-1821. Epub 2009 Feb 24.

27.

Alopecia and male infertility in oligotriche mutant mice are caused by a deletion on distal chromosome 9.

Runkel F, Aubin I, Simon-Chazottes D, Büssow H, Stingl R, Miething A, Fukami K, Nakamura Y, Guénet JL, Franz T.

Mamm Genome. 2008 Oct-Dec;19(10-12):691-702. doi: 10.1007/s00335-008-9150-9. Epub 2008 Nov 11.

PMID:
19002527
28.

Innate resistance to flavivirus infections and the functions of 2'-5' oligoadenylate synthetases.

Mashimo T, Simon-Chazottes D, Guénet JL.

Curr Top Microbiol Immunol. 2008;321:85-100. Review.

PMID:
18727488
29.

Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels.

Szatanik M, Vibert N, Vassias I, Guénet JL, Eugène D, de Waele C, Jaubert J.

Neurogenetics. 2008 Oct;9(4):237-48. doi: 10.1007/s10048-008-0136-2. Epub 2008 Jul 5.

PMID:
18604572
30.

The mitochondrial protease AFG3L2 is essential for axonal development.

Maltecca F, Aghaie A, Schroeder DG, Cassina L, Taylor BA, Phillips SJ, Malaguti M, Previtali S, Guénet JL, Quattrini A, Cox GA, Casari G.

J Neurosci. 2008 Mar 12;28(11):2827-36. doi: 10.1523/JNEUROSCI.4677-07.2008.

31.

Mx1 causes resistance against influenza A viruses in the Mus spretus-derived inbred mouse strain SPRET/Ei.

Vanlaere I, Vanderrijst A, Guénet JL, De Filette M, Libert C.

Cytokine. 2008 Apr;42(1):62-70. doi: 10.1016/j.cyto.2008.01.013. Epub 2008 Mar 10.

PMID:
18334301
32.

Sphingomyelin degradation is a key factor in dentin and bone mineralization: lessons from the fro/fro mouse. The chemistry and histochemistry of dentin lipids.

Goldberg M, Opsahl S, Aubin I, Septier D, Chaussain-Miller C, Boskey A, Guenet JL.

J Dent Res. 2008 Jan;87(1):9-13. No abstract available.

33.

Interspecific recombinant congenic strains between C57BL/6 and mice of the Mus spretus species: a powerful tool to dissect genetic control of complex traits.

Burgio G, Szatanik M, Guénet JL, Arnau MR, Panthier JJ, Montagutelli X.

Genetics. 2007 Dec;177(4):2321-33. Epub 2007 Oct 18.

34.

Progressive motor neuronopathy: a critical role of the tubulin chaperone TBCE in axonal tubulin routing from the Golgi apparatus.

Schaefer MK, Schmalbruch H, Buhler E, Lopez C, Martin N, Guénet JL, Haase G.

J Neurosci. 2007 Aug 15;27(33):8779-89.

35.

Ursodesoxycholic acid and heme-arginate are unable to improve hematopoiesis and liver injury in an erythropoietic protoporphyria mouse model.

Abitbol M, Puy H, Sabaté JM, Guénet JL, Deybach JC, Montagutelli X.

Physiol Res. 2006;55 Suppl 2:S93-101.

36.

Inducing mutations in the mouse genome with the chemical mutagen ethylnitrosourea.

Massironi SM, Reis BL, Carneiro JG, Barbosa LB, Ariza CB, Santos GC, Guénet JL, Godard AL.

Braz J Med Biol Res. 2006 Sep;39(9):1217-26.

37.

crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1).

Conti V, Aghaie A, Cilli M, Martin N, Caridi G, Musante L, Candiano G, Castagna M, Fairen A, Ravazzolo R, Guenet JL, Puliti A.

Int J Mol Med. 2006 Oct;18(4):593-600.

PMID:
16964410
38.

Two quantitative trait loci affecting progressive hearing loss in 101/H mice.

Mashimo T, Erven AE, Spiden SL, Guénet JL, Steel KP.

Mamm Genome. 2006 Aug;17(8):841-50. Epub 2006 Aug 4.

PMID:
16897347
39.
40.

Cmv4, a new locus linked to the NK cell gene complex, controls innate resistance to cytomegalovirus in wild-derived mice.

Adam SG, Caraux A, Fodil-Cornu N, Loredo-Osti JC, Lesjean-Pottier S, Jaubert J, Bubic I, Jonjic S, Guénet JL, Vidal SM, Colucci F.

J Immunol. 2006 May 1;176(9):5478-85.

41.

Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse.

Simon-Chazottes D, Tutois S, Kuehn M, Evans M, Bourgade F, Cook S, Davisson MT, Guénet JL.

Genomics. 2006 May;87(5):673-7. Epub 2006 Mar 6.

42.

Assessing the genetic component of the susceptibility of mice to viral infections.

Guénet JL.

Brief Funct Genomic Proteomic. 2005 Nov;4(3):225-40. Review.

PMID:
16420748
43.

The radiation-induced nackt (nkt) allele is a loss-of-function mutation of the mouse cathepsin L gene.

Benavides F, Perez C, Blando J, Guénet JL, Conti CJ.

J Immunol. 2006 Jan 15;176(2):702-3. No abstract available.

44.

The 2',5'-oligoadenylate synthetase 1b is a potent inhibitor of West Nile virus replication inside infected cells.

Kajaste-Rudnitski A, Mashimo T, Frenkiel MP, Guénet JL, Lucas M, Desprès P.

J Biol Chem. 2006 Feb 24;281(8):4624-37. Epub 2005 Dec 21.

45.

The mouse genome.

Guénet JL.

Genome Res. 2005 Dec;15(12):1729-40. Review.

46.

[Sphingomyelinases and osteogenesis imperfecta].

Aubin I, Guénet JL.

Med Sci (Paris). 2005 Dec;21(12):1034-5. French. No abstract available.

47.

A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.

Aubin I, Adams CP, Opsahl S, Septier D, Bishop CE, Auge N, Salvayre R, Negre-Salvayre A, Goldberg M, Guénet JL, Poirier C.

Nat Genet. 2005 Aug;37(8):803-5. Epub 2005 Jul 17.

PMID:
16025116
48.

Mutation at the Lmx1a locus provokes aberrant brain development in the rat.

Kuwamura M, Muraguchi T, Matsui T, Ueno M, Takenaka S, Yamate J, Kotani T, Kuramoto T, Guénet JL, Kitada K, Serikawa T.

Brain Res Dev Brain Res. 2005 Mar 31;155(2):99-106.

PMID:
15804398
49.

Is the lingual forming part of the incisor a structural entity? Evidences from the fragilitas ossium (fro/fro) mouse mutation and the TGFbeta1 overexpressing transgenic strain.

Opsahl S, Septier D, Aubin I, Guenet JL, Sreenath T, Kulkarni A, Vermelin L, Goldberg M.

Arch Oral Biol. 2005 Feb;50(2):279-86. Epub 2004 Nov 11.

PMID:
15721162
50.

A mouse model provides evidence that genetic background modulates anemia and liver injury in erythropoietic protoporphyria.

Abitbol M, Bernex F, Puy H, Jouault H, Deybach JC, Guénet JL, Montagutelli X.

Am J Physiol Gastrointest Liver Physiol. 2005 Jun;288(6):G1208-16. Epub 2005 Jan 27.

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