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Items: 29

1.

Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.

Kim HG, Rosenfeld JA, Scott DA, Bénédicte G, Labonne JD, Brown J, McGuire M, Mahida S, Naidu S, Gutierrez J, Lesca G, des Portes V, Bruel AL, Sorlin A, Xia F, Capri Y, Muller E, McKnight D, Torti E, Rüschendorf F, Hummel O, Islam Z, Kolatkar PR, Layman LC, Ryu D, Kong IK, Madan-Khetarpal S, Kim CH.

Mol Autism. 2019 Oct 22;10:35. doi: 10.1186/s13229-019-0286-0. eCollection 2019.

2.

The long and short of the S-locus in Turnera (Passifloraceae).

Shore JS, Hamam HJ, Chafe PDJ, Labonne JDJ, Henning PM, McCubbin AG.

New Phytol. 2019 Nov;224(3):1316-1329. doi: 10.1111/nph.15970. Epub 2019 Jul 15.

PMID:
31144315
3.

Modeling of autophagy-related gene expression dynamics during long term fasting in European eel (Anguilla anguilla).

Bolliet V, Labonne J, Olazcuaga L, Panserat S, Seiliez I.

Sci Rep. 2017 Dec 20;7(1):17896. doi: 10.1038/s41598-017-18164-6.

4.

A reassessment of the carnivorous status of salmonids: Hepatic glucokinase is expressed in wild fish in Kerguelen Islands.

Marandel L, Gaudin P, Guéraud F, Glise S, Herman A, Plagnes-Juan E, Véron V, Panserat S, Labonne J.

Sci Total Environ. 2018 Jan 15;612:276-285. doi: 10.1016/j.scitotenv.2017.08.247. Epub 2017 Sep 1.

PMID:
28850848
5.

Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort.

Ha K, Anand P, Lee JA, Jones JR, Kim CA, Bertola DR, Labonne JD, Layman LC, Wenzel W, Kim HG.

Genes (Basel). 2016 Nov 9;7(11). pii: E96.

6.

A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies.

Labonne JD, Graves TD, Shen Y, Jones JR, Kong IK, Layman LC, Kim HG.

BMC Neurol. 2016 Aug 9;16:132. doi: 10.1186/s12883-016-0642-z.

7.

The context dependence of assortative mating: a demonstration with conspecific salmonid populations.

Gauthey Z, Hendry AP, Elosegi A, Tentelier C, Labonne J.

J Evol Biol. 2016 Sep;29(9):1827-35. doi: 10.1111/jeb.12914. Epub 2016 Jun 23.

8.

An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.

Labonne JD, Lee KH, Iwase S, Kong IK, Diamond MP, Layman LC, Kim CH, Kim HG.

Hum Genet. 2016 Jul;135(7):757-71. doi: 10.1007/s00439-016-1668-4. Epub 2016 Apr 22.

PMID:
27106595
9.

No early gender effects on energetic status and life history in a salmonid.

Régnier T, Labonne J, Chat J, Yano A, Guiguen Y, Bolliet V.

R Soc Open Sci. 2015 Dec 2;2(12):150441. doi: 10.1098/rsos.150441. eCollection 2015 Dec.

10.

Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disability.

Labonne JD, Shen Y, Kong IK, Diamond MP, Layman LC, Kim HG.

Mol Cytogenet. 2016 Mar 17;9:24. doi: 10.1186/s13039-016-0234-z. eCollection 2016.

11.

Experimental evidence of population differences in reproductive investment conditional on environmental stochasticity.

Gauthey Z, Panserat S, Elosegi A, Herman A, Tentelier C, Labonne J.

Sci Total Environ. 2016 Jan 15;541:143-148. doi: 10.1016/j.scitotenv.2015.09.069. Epub 2015 Sep 24.

PMID:
26406108
12.

A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies.

Labonne JD, Vogt J, Reali L, Kong IK, Layman LC, Kim HG.

Am J Med Genet A. 2015 Dec;167A(12):3011-8. doi: 10.1002/ajmg.a.37344. Epub 2015 Sep 3.

PMID:
26333423
13.

Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndrome.

Labonne JD, Chung MJ, Jones JR, Anand P, Wenzel W, Iacoboni D, Layman LC, Kim HG.

Gene. 2016 Jan 1;575(1):42-7. doi: 10.1016/j.gene.2015.08.032. Epub 2015 Aug 20.

PMID:
26297997
14.

The concentration of plasma metabolites varies throughout reproduction and affects offspring number in wild brown trout (Salmo trutta).

Gauthey Z, Freychet M, Manicki A, Herman A, Lepais O, Panserat S, Elosegi A, Tentelier C, Labonne J.

Comp Biochem Physiol A Mol Integr Physiol. 2015 Jun;184:90-6. doi: 10.1016/j.cbpa.2015.01.025. Epub 2015 Feb 7.

PMID:
25666363
15.

Differential nuclease sensitivity profiling of chromatin reveals biochemical footprints coupled to gene expression and functional DNA elements in maize.

Vera DL, Madzima TF, Labonne JD, Alam MP, Hoffman GG, Girimurugan SB, Zhang J, McGinnis KM, Dennis JH, Bass HW.

Plant Cell. 2014 Oct;26(10):3883-93. doi: 10.1105/tpc.114.130609. Epub 2014 Oct 31.

16.

Invasion dynamics of a fish-free landscape by brown trout (Salmo trutta).

Labonne J, Vignon M, Prévost E, Lecomte F, Dodson JJ, Kaeuffer R, Aymes JC, Jarry M, Gaudin P, Davaine P, Beall E.

PLoS One. 2013 Aug 21;8(8):e71052. doi: 10.1371/journal.pone.0071052. eCollection 2013.

17.

Changes in nucleosome position at transcriptional start sites of specific genes in Zea mays mediator of paramutation1 mutants.

Labonne JD, Dorweiler JE, McGinnis KM.

Epigenetics. 2013 Apr;8(4):398-408. doi: 10.4161/epi.24199. Epub 2013 Mar 28.

18.

Female effects on offspring energetic status and consequences on early development in yolk feeding brown trout (Salmo trutta).

Régnier T, Bolliet V, Gaudin P, Labonne J.

J Exp Zool A Ecol Genet Physiol. 2012 Jul;317(6):347-58. doi: 10.1002/jez.1728.

PMID:
22777730
19.

The role of body size versus growth on the decision to migrate: a case study with Salmo trutta.

Acolas ML, Labonne J, Baglinière JL, Roussel JM.

Naturwissenschaften. 2012 Jan;99(1):11-21. doi: 10.1007/s00114-011-0861-5. Epub 2011 Nov 20.

PMID:
22101839
20.

Influence of energetic status on ontogenetic niche shifts: emergence from the redd is linked to metabolic rate in brown trout.

Régnier T, Labonne J, Gaudin P, Bolliet V.

Oecologia. 2012 Feb;168(2):371-80. doi: 10.1007/s00442-011-2109-7. Epub 2011 Aug 25.

PMID:
21866348
21.

Positional cloning of the s haplotype determining the floral and incompatibility phenotype of the long-styled morph of distylous Turnera subulata.

Labonne JD, Shore JS.

Mol Genet Genomics. 2011 Feb;285(2):101-11. doi: 10.1007/s00438-010-0590-z. Epub 2010 Nov 27.

PMID:
21113621
22.
23.

Characterization of X-ray-generated floral mutants carrying deletions at the S-locus of distylous Turnera subulata.

Labonne JD, Tamari F, Shore JS.

Heredity (Edinb). 2010 Aug;105(2):235-43. doi: 10.1038/hdy.2010.39. Epub 2010 Apr 14. Erratum in: Heredity. 2010 Aug;105(2):244.

24.

Occurrence and variation of egg cannibalism in brown trout Salmo trutta.

Aymes JC, Larrieu M, Tentelier C, Labonne J.

Naturwissenschaften. 2010 Apr;97(4):435-9. doi: 10.1007/s00114-010-0656-0. Epub 2010 Mar 2.

PMID:
20195564
25.

Assessing maternal effects on metabolic rate dynamics along early development in brown trout (Salmo trutta): an individual-based approach.

Régnier T, Bolliet V, Labonne J, Gaudin P.

J Comp Physiol B. 2010 Jan;180(1):25-31. doi: 10.1007/s00360-009-0385-x. Epub 2009 Jul 1.

PMID:
19568756
26.

High-resolution mapping of the S-locus in Turnera leads to the discovery of three genes tightly associated with the S-alleles.

Labonne JJ, Goultiaeva A, Shore JS.

Mol Genet Genomics. 2009 Jun;281(6):673-85. doi: 10.1007/s00438-009-0439-5. Epub 2009 Mar 13.

PMID:
19283410
27.

Construction of a first genetic map of distylous Turnera and a fine-scale map of the S-locus region.

Labonne JD, Vaisman A, Shore JS.

Genome. 2008 Jul;51(7):471-8. doi: 10.1139/G08-031.

PMID:
18545271
29.

Studies on trachoma. 11. Evaluation of laboratory diagnostic methods under field conditions.

Tarizzo ML, Nabli B, Labonne J.

Bull World Health Organ. 1968;38(6):897-905.

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