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Report on the IASO Stock Conference 2006: early and lifelong environmental epigenomic programming of metabolic syndrome, obesity and type II diabetes.
Published in:
Obesity Reviews, 2007, v. 8, n. 6, p. 487, doi. 10.1111/j.1467-789X.2007.00371.x
By:
- Junien, C.;
- Nathanielsz, P.
Publication type:
Article
Letter to the Editor Identification of the first Lebanese mutation in the LPL gene and description of a rapid detection method.
Published in:
2004
By:
- Abifadel, M.;
- Jambart, S.;
- Allard, D.;
- Rabès, J. P.;
- Varret, M.;
- Derré, A.;
- Chouery, E.;
- Salem, N.;
- Junien, C.;
- Aydénian, H.;
- Boileau, C.
Publication type:
Letter
CTG repeat instability and size variation timing in DNA repair-deficient mice.
Published in:
EMBO Journal, 2003, v. 22, n. 9, p. 2264
By:
- G. Gourdon;
- J. Essers;
- R. Kanaar;
- A. Pastink;
- H. te Riele;
- C. Savouret;
- E. Brisson;
- C. Junien
Publication type:
Article
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases.
Published in:
1981
By:
- Junien, C.;
- Leroux, A.;
- Lostanlen, D.;
- Reghis, A.;
- Boue, J.;
- Nicolas, H.;
- Boue, A.;
- Kaplan, J. C.
Publication type:
journal article
Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.
Published in:
Rheumatology, 2007, v. 46, n. 4, p. 622
By:
- J. Wipff;
- A. Kahan;
- E. Hachulla;
- J. Sibilia;
- J. Cabane;
- O. Meyer;
- L. Mouthon;
- L. Guillevin;
- C. Junien;
- C. Boileau;
- Y. Allanore
Publication type:
Article
Variable features of transient neonatal diabetes mellitus with paternal isodisomy of chromosome 6.
Published in:
European Journal of Human Genetics, 2000, v. 8, n. 2, p. 137, doi. 10.1038/sj.ejhg.5200401
By:
- Marquis, E;
- Robert, J J;
- Benezech, C;
- Junien, C;
- Diatloff-Zito, C
Publication type:
Article
Nutritional developmental epigenomics: immediate and long-lasting effects.
Published in:
2010
By:
- Attig L;
- Gabory A;
- Junien C
Publication type:
Journal Article
Symposium 2: Modern approaches to nutritional research challenges Nutritional developmental epigenomics: immediate and long-lasting effects.
Published in:
Proceedings of the Nutrition Society, 2010, v. 69, n. 2, p. 221, doi. 10.1017/S002966511000008X
By:
- Attig, L.;
- Gabory, A.;
- Junien, C.
Publication type:
Article
Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study.
Published in:
1992
By:
- Chamberlain, J S;
- Chamberlain, J R;
- Fenwick, R G;
- Ward, P A;
- Caskey, C T;
- Dimnik, L S;
- Bech-Hansen, N T;
- Hoar, D I;
- Richards, S;
- Covone, A E;
- Govanni, R;
- Abbs, S;
- Bentley, D R;
- Bobrow, M;
- Rysiecki, G;
- Ray, P N;
- Boileau, C;
- Junien, C;
- Boehm, C;
- Venne, V L
Publication type:
journal article
Profiling of differential gene expression in Wilms tumor by cDNA expression array.
Published in:
Pediatric Nephrology, 2001, v. 16, n. 12, p. 1113, doi. 10.1007/s004670100040
By:
- Rigolet, M.;
- Faussillon, M.;
- Baudry, D.;
- Junien, C.;
- Jeanpierre, C.
Publication type:
Article
Congenital Enzymopenic Methaemoglobinaemia.
Published in:
Acta Haematologica, 1976, v. 56, n. 3, p. 174, doi. 10.1159/000207934
By:
- Mast, A.;
- Milo, R.;
- Junien, C.;
- Leroux, A.;
- Krishnamoorthy, R.;
- Wajcman, H.;
- Labie, D.;
- Kaplan, J.C.
Publication type:
Article
Nutritional epigenomics of metabolic syndrome: new perspective against the epidemic.
Published in:
2005
By:
- Gallou-Kabani C;
- Junien C;
- Gallou-Kabani, Catherine;
- Junien, Claudine
Publication type:
journal article
The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma.
Published in:
2003
By:
- Sempoux C;
- Guiot Y;
- Dahan K;
- Moulin P;
- Stevens M;
- Lambot V;
- de Lonlay P;
- Fournet J;
- Junien C;
- Jaubert F;
- Nihoul-Fekete C;
- Saudubray J;
- Rahier J;
- Sempoux, Christine;
- Guiot, Yves;
- Dahan, Karin;
- Moulin, Pierre;
- Stevens, Martine;
- Lambot, Virginie;
- de Lonlay, Pascale
Publication type:
journal article
Defective satellite cells in congenital myotonic dystrophy.
Published in:
Human Molecular Genetics, 2001, v. 10, n. 19, p. 2079, doi. 10.1093/hmg/10.19.2079
By:
- Furling, D.;
- Coiffier, L.;
- Mouly, V.;
- Barbet, J.P.;
- Lacau St Guily, J.;
- Taneja, K.;
- Junien, C.;
- Butler-Browne, G.S.
Publication type:
Article
An oligonucleotide microarray for mouse imprinted genes profiling.
Published in:
Cytogenetic & Genome Research, 2006, v. 113, n. 1-4, p. 253, doi. 10.1159/000090840
By:
- Vigé, A.;
- Gallou-Kabani, C.;
- Gross, M. S.;
- Fabre, A.;
- Junien, C.;
- Jais, J. P.
Publication type:
Article
Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC.
Published in:
Human Mutation, 1999, v. 13, n. 6, p. 464, doi. 10.1002/(SICI)1098-1004(1999)13:6<464::AID-HUMU6>3.0.CO;2-A
By:
- Gallou, C.;
- Joly, D.;
- Méjean, A.;
- Staroz, F.;
- Martin, N.;
- Tarlet, G.;
- Orfanelli, M.T.;
- Bouvier, R.;
- Droz, D.;
- Chrétien, Y.;
- Maréchal, J.M.;
- Richard, S.;
- Junien, C.;
- Béroud, C.
Publication type:
Article
Familial ligand-defective apolipoprotein B-100: Simultaneous detection of the ARG<sub>3500</sub>→GLN and ARG<sub>3531</sub>→CYS mutations in a French population.
Published in:
Human Mutation, 1997, v. 10, n. 2, p. 160, doi. 10.1002/(SICI)1098-1004(1997)10:2<160::AID-HUMU8>3.0.CO;2-O
By:
- Rabès, JP;
- Varret, M;
- Saint-Jore, B;
- Erlich, D;
- Jondeau, G;
- Krempf, M;
- Giraudet, P;
- Junien, C;
- Boileau, C
Publication type:
Article
Identification of the haplotype associated with the APOB-3500 mutation in a French hypercholesterolemic subject: Further support for a unique European ancestral mutation.
Published in:
Human Mutation, 1993, v. 2, n. 2, p. 145, doi. 10.1002/humu.1380020216
By:
- Loux, N.;
- Saint-Jore, B.;
- Collod, G.;
- Benlian, P.;
- Cambou, J. P.;
- Denat, M.;
- Junien, C.;
- Boileau, C.
Publication type:
Article
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism method.
Published in:
Human Mutation, 1992, v. 1, n. 4, p. 325, doi. 10.1002/humu.1380010411
By:
- Loux, N.;
- Saint-Jore, B.;
- Collod, G.;
- Dairou, F.;
- Benlian, P.;
- Truffert, J.;
- Dastugue, B.;
- Douste-Blazy, P.;
- de Gennes, J. L.;
- Junien, C.;
- Boileau, C.
Publication type:
Article
Multiple acral fibromas in a patient with familial retinoblastoma: a cutaneous marker of tumour-suppressor gene germline mutation?
Published in:
British Journal of Dermatology, 2000, v. 143, n. 4, p. 856, doi. 10.1046/j.1365-2133.2000.03790.x
By:
- Dereure, O.;
- Savoy, D.;
- Doz, F.;
- Junien, C.;
- Guilhou, J-J.
Publication type:
Article
Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans.
Published in:
Journal of Developmental Origins of Health & Disease, 2013, v. 4, n. 2, p. 134, doi. 10.1017/S2040174412000748
By:
- Mayeur, S.;
- Cisse, O.;
- Gabory, A.;
- Barbaux, S.;
- Vaiman, D.;
- Vambergue, A.;
- Fajardy, I.;
- Deloof, S.;
- Junien, C.;
- Laborie, C.;
- Vieau, D.;
- Lesage, J.
Publication type:
Article

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