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Items: 29

1.

Detecting and quantifying stress granules in tissues of multicellular organisms with the Obj.MPP analysis tool.

De Graeve F, Debreuve E, Rahmoun S, Ecsedi S, Bahri A, Hubstenberger A, Descombes X, Besse F.

Traffic. 2019 Sep;20(9):697-711. doi: 10.1111/tra.12678. Epub 2019 Aug 6.

PMID:
31314165
2.

CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.

Montagne L, Derhourhi M, Piton A, Toussaint B, Durand E, Vaillant E, Thuillier D, Gaget S, De Graeve F, Rabearivelo I, Lansiaux A, Lenne B, Sukno S, Desailloud R, Cnop M, Nicolescu R, Cohen L, Zagury JF, Amouyal M, Weill J, Muller J, Sand O, Delobel B, Froguel P, Bonnefond A.

Mol Metab. 2018 Jul;13:1-9. doi: 10.1016/j.molmet.2018.05.005. Epub 2018 May 16.

3.

Neuronal RNP granules: from physiological to pathological assemblies.

De Graeve F, Besse F.

Biol Chem. 2018 Jun 27;399(7):623-635. doi: 10.1515/hsz-2018-0141. Review.

PMID:
29641413
4.

Sumoylation regulates FMRP-mediated dendritic spine elimination and maturation.

Khayachi A, Gwizdek C, Poupon G, Alcor D, Chafai M, Cassé F, Maurin T, Prieto M, Folci A, De Graeve F, Castagnola S, Gautier R, Schorova L, Loriol C, Pronot M, Besse F, Brau F, Deval E, Bardoni B, Martin S.

Nat Commun. 2018 Feb 22;9(1):757. doi: 10.1038/s41467-018-03222-y.

5.

Loss-of-function mutations in ADCY3 cause monogenic severe obesity.

Saeed S, Bonnefond A, Tamanini F, Mirza MU, Manzoor J, Janjua QM, Din SM, Gaitan J, Milochau A, Durand E, Vaillant E, Haseeb A, De Graeve F, Rabearivelo I, Sand O, Queniat G, Boutry R, Schott DA, Ayesha H, Ali M, Khan WI, Butt TA, Rinne T, Stumpel C, Abderrahmani A, Lang J, Arslan M, Froguel P.

Nat Genet. 2018 Feb;50(2):175-179. doi: 10.1038/s41588-017-0023-6. Epub 2018 Jan 8.

6.

High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children.

Foucan L, Larifla L, Durand E, Rambhojan C, Armand C, Michel CT, Billy R, Dhennin V, De Graeve F, Rabearivelo I, Sand O, Lacorte JM, Froguel P, Bonnefond A.

J Clin Endocrinol Metab. 2018 Feb 1;103(2):539-545. doi: 10.1210/jc.2017-01956.

PMID:
29216354
7.

A novel NEUROG3 mutation in neonatal diabetes associated with a neuro-intestinal syndrome.

Hancili S, Bonnefond A, Philippe J, Vaillant E, De Graeve F, Sand O, Busiah K, Robert JJ, Polak M, Froguel P, Güven A, Vaxillaire M.

Pediatr Diabetes. 2018 May;19(3):381-387. doi: 10.1111/pedi.12576. Epub 2017 Sep 22.

PMID:
28940958
8.

What Is the Best NGS Enrichment Method for the Molecular Diagnosis of Monogenic Diabetes and Obesity?

Philippe J, Derhourhi M, Durand E, Vaillant E, Dechaume A, Rabearivelo I, Dhennin V, Vaxillaire M, De Graeve F, Sand O, Froguel P, Bonnefond A.

PLoS One. 2015 Nov 23;10(11):e0143373. doi: 10.1371/journal.pone.0143373. eCollection 2015.

9.

A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.

Philippe J, Stijnen P, Meyre D, De Graeve F, Thuillier D, Delplanque J, Gyapay G, Sand O, Creemers JW, Froguel P, Bonnefond A.

Int J Obes (Lond). 2015 Feb;39(2):295-302. doi: 10.1038/ijo.2014.96. Epub 2014 Jun 3.

PMID:
24890885
10.

Highly sensitive diagnosis of 43 monogenic forms of diabetes or obesity through one-step PCR-based enrichment in combination with next-generation sequencing.

Bonnefond A, Philippe J, Durand E, Muller J, Saeed S, Arslan M, Martínez R, De Graeve F, Dhennin V, Rabearivelo I, Polak M, Cavé H, Castaño L, Vaxillaire M, Mandel JL, Sand O, Froguel P.

Diabetes Care. 2014 Feb;37(2):460-7. doi: 10.2337/dc13-0698. Epub 2013 Sep 16.

PMID:
24041679
11.

GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetes.

Bonnefond A, Sand O, Guerin B, Durand E, De Graeve F, Huyvaert M, Rachdi L, Kerr-Conte J, Pattou F, Vaxillaire M, Polak M, Scharfmann R, Czernichow P, Froguel P.

Diabetologia. 2012 Oct;55(10):2845-2847. doi: 10.1007/s00125-012-2645-7. Epub 2012 Jul 18. No abstract available.

PMID:
22806356
12.

Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.

Bonnefond A, Philippe J, Durand E, Dechaume A, Huyvaert M, Montagne L, Marre M, Balkau B, Fajardy I, Vambergue A, Vatin V, Delplanque J, Le Guilcher D, De Graeve F, Lecoeur C, Sand O, Vaxillaire M, Froguel P.

PLoS One. 2012;7(6):e37423. doi: 10.1371/journal.pone.0037423. Epub 2012 Jun 11.

13.

Drosophila apc regulates delamination of invasive epithelial clusters.

De Graeve FM, Van de Bor V, Ghiglione C, Cerezo D, Jouandin P, Ueda R, Shashidhara LS, Noselli S.

Dev Biol. 2012 Aug 1;368(1):76-85. doi: 10.1016/j.ydbio.2012.05.017. Epub 2012 May 22.

14.

Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome.

Bonnefond A, Durand E, Sand O, De Graeve F, Gallina S, Busiah K, Lobbens S, Simon A, Bellanné-Chantelot C, Létourneau L, Scharfmann R, Delplanque J, Sladek R, Polak M, Vaxillaire M, Froguel P.

PLoS One. 2010 Oct 26;5(10):e13630. doi: 10.1371/journal.pone.0013630.

15.

Lack of association of CD36 SNPs with early onset obesity: a meta-analysis in 9,973 European subjects.

Choquet H, Labrune Y, De Graeve F, Hinney A, Hebebrand J, Scherag A, Lecoeur C, Tauber M, Balkau B, Elliot P, Jarvelin MR, Walley AJ, Besnard P, Froguel P, Meyre D.

Obesity (Silver Spring). 2011 Apr;19(4):833-9. doi: 10.1038/oby.2010.226. Epub 2010 Oct 21.

16.

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.

Bouatia-Naji N, Bonnefond A, Cavalcanti-Proença C, Sparsø T, Holmkvist J, Marchand M, Delplanque J, Lobbens S, Rocheleau G, Durand E, De Graeve F, Chèvre JC, Borch-Johnsen K, Hartikainen AL, Ruokonen A, Tichet J, Marre M, Weill J, Heude B, Tauber M, Lemaire K, Schuit F, Elliott P, Jørgensen T, Charpentier G, Hadjadj S, Cauchi S, Vaxillaire M, Sladek R, Visvikis-Siest S, Balkau B, Lévy-Marchal C, Pattou F, Meyre D, Blakemore AI, Jarvelin MR, Walley AJ, Hansen T, Dina C, Pedersen O, Froguel P.

Nat Genet. 2009 Jan;41(1):89-94. doi: 10.1038/ng.277. Epub 2008 Dec 7.

PMID:
19060909
17.

Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value.

Cauchi S, Meyre D, Durand E, Proença C, Marre M, Hadjadj S, Choquet H, De Graeve F, Gaget S, Allegaert F, Delplanque J, Permutt MA, Wasson J, Blech I, Charpentier G, Balkau B, Vergnaud AC, Czernichow S, Patsch W, Chikri M, Glaser B, Sladek R, Froguel P.

PLoS One. 2008 May 7;3(5):e2031. doi: 10.1371/journal.pone.0002031.

18.

A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels.

Bouatia-Naji N, Rocheleau G, Van Lommel L, Lemaire K, Schuit F, Cavalcanti-Proença C, Marchand M, Hartikainen AL, Sovio U, De Graeve F, Rung J, Vaxillaire M, Tichet J, Marre M, Balkau B, Weill J, Elliott P, Jarvelin MR, Meyre D, Polychronakos C, Dina C, Sladek R, Froguel P.

Science. 2008 May 23;320(5879):1085-8. doi: 10.1126/science.1156849. Epub 2008 May 1.

19.

INS VNTR is not associated with childhood obesity in 1,023 families: a family-based study.

Bouatia-Naji N, De Graeve F, Brönner G, Lecoeur C, Vatin V, Durand E, Lichtner P, Nguyen TT, Heude B, Weill J, Lévy-Marchal C, Hebebrand J, Froguel P, Meyre D.

Obesity (Silver Spring). 2008 Jun;16(6):1471-5. doi: 10.1038/oby.2008.209. Epub 2008 Apr 3.

20.

Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study.

Cauchi S, Proença C, Choquet H, Gaget S, De Graeve F, Marre M, Balkau B, Tichet J, Meyre D, Vaxillaire M, Froguel P; D.E.S.I.R. Study Group.

J Mol Med (Berl). 2008 Mar;86(3):341-8. doi: 10.1007/s00109-007-0295-x. Epub 2008 Jan 22.

PMID:
18210030
21.

[Amyloid cardiomyopathy: A rare cause of cerebral embolism].

Saux A, Heroum C, Sportouch C, De Graeve F, Lequellec A, Pagès M.

Rev Neurol (Paris). 2006 Nov;162(11):1128-30. French.

PMID:
17086151
22.

Drosophila melanogaster p-glycoprotein: a membrane detoxification system toward polycyclic aromatic hydrocarbon pollutants.

Vaché C, Camares O, De Graeve F, Dastugue B, Meiniel A, Vaury C, Pellier S, Leoz-Garziandia E, Bamdad M.

Environ Toxicol Chem. 2006 Feb;25(2):572-80.

PMID:
16519321
23.

Kruppel-like factor 6 (KLF6) affects the promoter activity of the alpha1-proteinase inhibitor gene.

Chiambaretta F, Nakamura H, De Graeve F, Sakai H, Marceau G, Maruyama Y, Rigal D, Dastugue B, Sugar J, Yue BY, Sapin V.

Invest Ophthalmol Vis Sci. 2006 Feb;47(2):582-90.

PMID:
16431954
24.

Cell and tissue specific expression of human Krüppel-like transcription factors in human ocular surface.

Chiambaretta F, De Graeve F, Turet G, Marceau G, Gain P, Dastugue B, Rigal D, Sapin V.

Mol Vis. 2004 Nov 23;10:901-9.

25.

The ladybird homeobox genes are essential for the specification of a subpopulation of neural cells.

De Graeve F, Jagla T, Daponte JP, Rickert C, Dastugue B, Urban J, Jagla K.

Dev Biol. 2004 Jun 1;270(1):122-34.

26.

Identification of the Drosophila progenitor of mammalian Krüppel-like factors 6 and 7 and a determinant of fly development.

De Graeve F, Smaldone S, Laub F, Mlodzik M, Bhat M, Ramirez F.

Gene. 2003 Sep 18;314:55-62.

PMID:
14527717
27.

A murine ATFa-associated factor with transcriptional repressing activity.

De Graeve F, Bahr A, Chatton B, Kedinger C.

Oncogene. 2000 Mar 30;19(14):1807-19.

28.

Role of the ATFa/JNK2 complex in Jun activation.

De Graeve F, Bahr A, Sabapathy KT, Hauss C, Wagner EF, Kedinger C, Chatton B.

Oncogene. 1999 Jun 10;18(23):3491-500.

29.

Point mutations causing Bloom's syndrome abolish ATPase and DNA helicase activities of the BLM protein.

Bahr A, De Graeve F, Kedinger C, Chatton B.

Oncogene. 1998 Nov 19;17(20):2565-71.

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