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    Results: 1 to 50 of 81

    1.

    Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy.

    Boutet E, El Mourabit H, Prot M, Nemani M, Khallouf E, Colard O, Maurice M, Durand-Schneider AM, Chrétien Y, Grès S, Wolf C, Saulnier-Blache JS, Capeau J, Magré J.

    Biochimie. 2009 Jun;91(6):796-803. Epub 2009 Feb 6.PMID: 19278620 [PubMed - indexed for MEDLINE]Related articles

    2.

    Congenital generalized lipodystrophy in an Indian patient with a novel mutation in BSCL2 gene.

    Shirwalkar HU, Patel ZM, Magre J, Hilbert P, Van Maldergem L, Mukhopadhyay RR, Maitra A.

    J Inherit Metab Dis. 2008 Aug 12. [Epub ahead of print]PMID: 18690553 [PubMed - as supplied by publisher]Related articles

    3.

    Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.

    Kim CA, Delépine M, Boutet E, El Mourabit H, Le Lay S, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O'Rahilly S, Dugail I, Capeau J, Lathrop M, Magré J.

    J Clin Endocrinol Metab. 2008 Apr;93(4):1129-34. Epub 2008 Jan 22.PMID: 18211975 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Leptin therapy for partial lipodystrophy linked to a PPAR-gamma mutation.

    Guettier JM, Park JY, Cochran EK, Poitou C, Basdevant A, Meier M, Clément K, Magré J, Gorden P.

    Clin Endocrinol (Oxf). 2008 Apr;68(4):547-54. Epub 2007 Dec 10.PMID: 18076675 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    [Primary lipodystrophies]

    Capeau J, Magré J, Lascols O, Caron M, Béréziat V, Vigouroux C.

    Ann Endocrinol (Paris). 2007 Feb;68(1):10-20. Epub 2007 Feb 21. French. PMID: 17320032 [PubMed - indexed for MEDLINE]Related articles

    6.

    [Lipodystrophic syndromes: congenital or acquired diseases of adipose tissue]

    Capeau J, Vigouroux C, Magré J, Lascols O, Caron M, Bastard JP.

    C R Biol. 2006 Aug;329(8):639-52; discussion 653-5. Epub 2006 Apr 27. French. PMID: 16860281 [PubMed - indexed for MEDLINE]Related articles

    7.

    Diseases of adipose tissue: genetic and acquired lipodystrophies.

    Capeau J, Magré J, Lascols O, Caron M, Béréziat V, Vigouroux C, Bastard JP.

    Biochem Soc Trans. 2005 Nov;33(Pt 5):1073-7. Review.PMID: 16246048 [PubMed - indexed for MEDLINE]Related articles

    8.

    Serum leptin level is a regulator of bone mass.

    Elefteriou F, Takeda S, Ebihara K, Magre J, Patano N, Kim CA, Ogawa Y, Liu X, Ware SM, Craigen WJ, Robert JJ, Vinson C, Nakao K, Capeau J, Karsenty G.

    Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):3258-63. Epub 2004 Feb 20.PMID: 14978271 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Mutations in the seipin and AGPAT2 genes clustering in consanguineous families with Berardinelli-Seip congenital lipodystrophy from two separate geographical regions of Brazil.

    Gomes KB, Fernandes AP, Ferreira AC, Pardini H, Garg A, Magré J, Pardini VC.

    J Clin Endocrinol Metab. 2004 Jan;89(1):357-61.PMID: 14715872 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    [Diabetes and genetic and acquired lipodystrophy syndrome]

    Capeau J, Magré J, Vigouroux C, Caron M, Maachi M, Dubosclard E, Lascols O, Bastard JP.

    Journ Annu Diabetol Hotel Dieu. 2003:99-109. Review. French. No abstract available. PMID: 12868305 [PubMed - indexed for MEDLINE]Related articles

    11.

    Prevalence of mutations in AGPAT2 among human lipodystrophies.

    Magré J, Delépine M, Van Maldergem L, Robert JJ, Maassen JA, Meier M, Panz VR, Kim CA, Tubiana-Rufi N, Czernichow P, Seemanova E, Buchanan CR, Lacombe D, Vigouroux C, Lascols O, Kahn CR, Capeau J, Lathrop M.

    Diabetes. 2003 Jun;52(6):1573-8.PMID: 12765973 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Localization, cDNA sequence and genomic organization of the rat seipin gene (Bscl2) and sequence analysis in inbred rat models of Type 2 diabetes mellitus.

    Kaisaki PJ, Sebag-Montefiore LM, Brown JH, Magre J, Lathrop M, Capeau J, Gauguier D.

    Cytogenet Genome Res. 2002;98(1):71-4.PMID: 12584444 [PubMed - indexed for MEDLINE]Related articles

    13.

    Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy.

    Van Maldergem L, Magré J, Khallouf TE, Gedde-Dahl T Jr, Delépine M, Trygstad O, Seemanova E, Stephenson T, Albott CS, Bonnici F, Panz VR, Medina JL, Bogalho P, Huet F, Savasta S, Verloes A, Robert JJ, Loret H, De Kerdanet M, Tubiana-Rufi N, Mégarbané A, Maassen J, Polak M, Lacombe D, Kahn CR, Silveira EL, D'Abronzo FH, Grigorescu F, Lathrop M, Capeau J, O'Rahilly S.

    J Med Genet. 2002 Oct;39(10):722-33. Erratum in: J Med Genet. 2003 Feb;40(2):150.. PMID: 12362029 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci.

    Heathcote K, Rajab A, Magré J, Syrris P, Besti M, Patton M, Délépine M, Lathrop M, Capeau J, Jeffery S.

    Diabetes. 2002 Apr;51(4):1291-3.PMID: 11916958 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    [Major insulin resistance syndromes: clinical and physiopathological aspects]

    Vigouroux C, Magré J, Desbois-Mouthon C, Lascols O, Cherqui G, Caron M, Capeau J.

    J Soc Biol. 2001;195(3):249-57. Review. French. PMID: 11833462 [PubMed - indexed for MEDLINE]Related articles

    16.

    Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

    Magré J, Delépine M, Khallouf E, Gedde-Dahl T Jr, Van Maldergem L, Sobel E, Papp J, Meier M, Mégarbané A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, Bourut C, Czernichow P, Huet F, Grigorescu F, de Kerdanet M, Lacombe D, Labrune P, Lanza M, Loret H, Matsuda F, Navarro J, Nivelon-Chevalier A, Polak M, Robert JJ, Tric P, Tubiana-Rufi N, Vigouroux C, Weissenbach J, Savasta S, Maassen JA, Trygstad O, Bogalho P, Freitas P, Medina JL, Bonnicci F, Joffe BI, Loyson G, Panz VR, Raal FJ, O'Rahilly S, Stephenson T, Kahn CR, Lathrop M, Capeau J; BSCL Working Group.

    Nat Genet. 2001 Aug;28(4):365-70.PMID: 11479539 [PubMed - indexed for MEDLINE]Related articles

    17.

    Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy.

    Vigouroux C, Magré J, Vantyghem MC, Bourut C, Lascols O, Shackleton S, Lloyd DJ, Guerci B, Padova G, Valensi P, Grimaldi A, Piquemal R, Touraine P, Trembath RC, Capeau J.

    Diabetes. 2000 Nov;49(11):1958-62.PMID: 11078466 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    A new missense mutation in the calcium-sensing receptor in familial benign hypercalcaemia associated with partial lipoatrophy and insulin resistant diabetes.

    Vigouroux C, Bourut C, Guerci B, Ziegler O, Magré J, Capeau J, Meyer L.

    Clin Endocrinol (Oxf). 2000 Sep;53(3):393-8.PMID: 10971459 [PubMed - indexed for MEDLINE]Related articles

    19.

    Late-onset lipoatrophic diabetes. Phenotypic and genotypic familial studies and effect of treatment with metformin and lispro insulin analog.

    Vantyghem MC, Vigouroux C, Magré J, Desbois-Mouthon C, Pattou F, Fontaine P, Lefebvre J, Capeau J.

    Diabetes Care. 1999 Aug;22(8):1374-6. No abstract available. PMID: 10480788 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes.

    Vigouroux C, Fajas L, Khallouf E, Meier M, Gyapay G, Lascols O, Auwerx J, Weissenbach J, Capeau J, Magré J.

    Diabetes. 1998 Mar;47(3):490-2. No abstract available. PMID: 9519760 [PubMed - indexed for MEDLINE]Related articlesFree article

    22.

    Human hormone-sensitive lipase: genetic mapping, identification of a new dinucleotide repeat, and association with obesity and NIDDM.

    Magré J, Laurell H, Fizames C, Antoine PJ, Dib C, Vigouroux C, Bourut C, Capeau J, Weissenbach J, Langin D.

    Diabetes. 1998 Feb;47(2):284-6. No abstract available. PMID: 9519728 [PubMed - indexed for MEDLINE]Related articles

    23.

    Dominant transmission of insulin resistance in a type A family resulting from a heterozygous nonsense mutation in the insulin receptor gene and associated with decreased mRNA level and insulin binding sites.

    Magré J, Karayanni C, Hadjiathanasiou CG, Desbois-Mouthon C, Meier M, Vigouroux C, Stavrinadis C, Sinaniotis C, Caron M, Capeau J.

    Diabetes. 1997 Nov;46(11):1901-3. No abstract available. PMID: 9356044 [PubMed - indexed for MEDLINE]Related articles

    24.

    Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous families.

    Vigouroux C, Khallouf E, Bourut C, Robert JJ, de Kerdanet M, Tubiana-Rufi N, Fauré S, Weissenbach J, Capeau J, Magré J.

    J Clin Endocrinol Metab. 1997 Oct;82(10):3438-44.PMID: 9329383 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    Molecular analysis of the insulin receptor gene for prenatal diagnosis of leprechaunism in two families.

    Desbois-Mouthon C, Girodon E, Ghanem N, Caron M, Pennerath A, Conteville P, Magre J, Besmond C, Goossens M, Capeau J, Amselem S.

    Prenat Diagn. 1997 Jul;17(7):657-63.PMID: 9249867 [PubMed - indexed for MEDLINE]Related articles

    26.

    Major circadian variations of glucose homeostasis in a patient with Rabson-Mendenhall syndrome and primary insulin resistance due to a mutation (Cys284-->Tyr) in the insulin receptor alpha-subunit.

    Desbois-Mouthon C, Magré J, Duprey J, Caron M, Blivet-Van Eggelpoel MJ, Daubas C, Gourmelen M, Chevallier B, Rizkalla S, Robert JJ, Capeau J.

    Pediatr Res. 1997 Jul;42(1):72-7.PMID: 9212040 [PubMed - indexed for MEDLINE]Related articles

    27.

    [Invitation to join the international study group on Berardinelli-Seip syndrome/ lipoatrophic diabetes in the clinical and genetic study of lipoatrophic diabetes]

    Capeau J, Magré J.

    Diabetes Metab. 1996 Jul;22(4):279-81. French. No abstract available. PMID: 8767176 [PubMed - indexed for MEDLINE]Related articles

    28.

    Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping. Berardinelli-Seip Study Group.

    Gedde-Dahl T Jr, Trygstad O, Van Maldergem L, Magré J, van der Hagen CB, Olaisen B, Stenersen M, Mevåg B.

    Acta Paediatr Suppl. 1996 Jun;413:52-8.PMID: 8783773 [PubMed - indexed for MEDLINE]Related articles

    29.

    Deletion of Asn281 in the alpha-subunit of the human insulin receptor causes constitutive activation of the receptor and insulin desensitization.

    Desbois-Mouthon C, Sert-Langeron C, Magre J, Oreal E, Blivet MJ, Flori E, Besmond C, Capeau J, Caron M.

    J Clin Endocrinol Metab. 1996 Feb;81(2):719-27.PMID: 8636294 [PubMed - indexed for MEDLINE]Related articles

    30.

    Analysis of the insulin receptor gene in noninsulin-dependent diabetes mellitus by denaturing gradient gel blots: a clinical research center study.

    Magré J, Goldfine AB, Warram JH, Krolewski AS, Kahn CR.

    J Clin Endocrinol Metab. 1995 Jun;80(6):1882-7.PMID: 7775636 [PubMed - indexed for MEDLINE]Related articles

    31.

    Lipoatrophic diabetes: genetic exclusion of the insulin receptor gene.

    Desbois-Mouthon C, Magré J, Amselem S, Reynet C, Blivet MJ, Goossens M, Capeau J, Besmond C.

    J Clin Endocrinol Metab. 1995 Jan;80(1):314-9.PMID: 7829633 [PubMed - indexed for MEDLINE]Related articles

    32.

    Insulin receptor autophosphorylation sites tyrosines 1162 and 1163 control both insulin-dependent and insulin-independent receptor internalization pathways.

    Reynet C, Caron M, Magré J, Picard J, Cherqui G, Capeau J.

    Cell Signal. 1994 Jan;6(1):35-45.PMID: 8011427 [PubMed - indexed for MEDLINE]Related articles

    33.

    The development of hyperglycaemia in patients with insulin-resistant generalized lipoatrophic syndromes.

    Robert JJ, Rakotoambinina B, Cochet I, Foussier V, Magre J, Darmaun D, Chevenne D, Capeau J.

    Diabetologia. 1993 Dec;36(12):1288-92.PMID: 8307257 [PubMed - indexed for MEDLINE]Related articles

    34.

    [Genetic abnormalities in the insulin receptor in non-insulin-dependent diabetes]

    Capeau J, Desbois C, Magré J.

    Journ Annu Diabetol Hotel Dieu. 1993:37-50. Review. French. No abstract available. PMID: 8331874 [PubMed - indexed for MEDLINE]Related articles

    35.

    Detection of sequence variations in the human insulin-receptor gene by parallel denaturing gradient gel electrophoresis.

    Desbois C, Magré J, Blanquet V, Capeau J, Goossens M, Besmond C.

    Hum Mutat. 1993;2(5):395-403.PMID: 8257993 [PubMed - indexed for MEDLINE]Related articles

    36.

    Molecular genetic approaches to the identification of genes involved in the development of nephropathy in insulin-dependent diabetes mellitus.

    Krolewski AS, Doria A, Magre J, Warram JH, Housman D.

    J Am Soc Nephrol. 1992 Oct;3(4 Suppl):S9-17. Review.PMID: 1457765 [PubMed - indexed for MEDLINE]Related articles

    37.

    In vivo and in vitro characterization of insulin resistance in three cases of lipoatrophic diabetes.

    Robert JJ, Magre J, Reynet C, Darmaun D, Picard J, Capeau J.

    Diabete Metab. 1990 May-Jun;16(3):240-7.PMID: 2210020 [PubMed - indexed for MEDLINE]Related articles

    38.

    Mutation of tyrosine residues 1162 and 1163 of the insulin receptor affects hormone and receptor internalization.

    Reynet C, Caron M, Magré J, Cherqui G, Clauser E, Picard J, Capeau J.

    Mol Endocrinol. 1990 Feb;4(2):304-11.PMID: 2184349 [PubMed - indexed for MEDLINE]Related articles

    39.

    [Insulin receptors]

    Capeau J, Magre J, Reynet C, Cherqui G, Caron M, Melin B, Lascols O, Picard J.

    Ann Med Interne (Paris). 1990;141(2):145-55. Review. French. No abstract available. PMID: 2191616 [PubMed - indexed for MEDLINE]Related articles

    40.

    Tyrosine-kinase defect of the insulin receptor in cultured fibroblasts from patients with lipoatropic diabetes.

    Magré J, Grigorescu F, Reynet C, Caron M, Capony JP, White MF, Picard J, Mirouze J, Capeau J.

    J Clin Endocrinol Metab. 1989 Jul;69(1):142-50.PMID: 2543688 [PubMed - indexed for MEDLINE]Related articles

    41.

    In vitro studies of insulin resistance in patients with lipoatrophic diabetes. Evidence for heterogeneous postbinding defects.

    Magré J, Reynet C, Capeau J, Blivet MJ, Picard J.

    Diabetes. 1988 Apr;37(4):421-8.PMID: 3288531 [PubMed - indexed for MEDLINE]Related articles

    42.

    [Examination of the uterine cervix using the scanning electron microscope]

    Lerat MF, Magre J, Connehaye P, Lerat H, Barreau A.

    J Gynecol Obstet Biol Reprod (Paris). 1975;4(7):907-13. French. PMID: 1219050 [PubMed - indexed for MEDLINE]Related articles

    43.

    [Study of the ovary and Fallopian tube by the scanning electron microscope]

    Lerat MF, Connehaye P, Magre J, Lerat H.

    J Gynecol Obstet Biol Reprod (Paris). 1974 Apr-May;3(3):351-4. French. No abstract available. PMID: 4470732 [PubMed - indexed for MEDLINE]Related articles

    44.

    [Sterilization by celioscopy]

    Magre J, Leroux P, Lerat MF, Herve P, Ledanois A.

    Ouest Med. 1973 May 30;26(12):1295-9. French. PMID: 12257596 [PubMed - indexed for MEDLINE]Related articles

    45.

    [Intestinal complications of the IUD]

    Magre J, Leroux P, Le Mouroux M, Lerat MF, Barnaud M.

    Ouest Med. 1973 May 30;26(12):1281-3. French. PMID: 12257595 [PubMed - indexed for MEDLINE]Related articles

    46.

    [Study of the human placenta by scanning electron microscopy]

    Lerat MF, Connehaye P, Richomme J, Magre J, Bonnaille J.

    J Gynecol Obstet Biol Reprod (Paris). 1973 Apr-May;2(3):233-41. French. No abstract available. PMID: 4807240 [PubMed - indexed for MEDLINE]Related articles

    47.

    [Study of the abnormal and pathologic placenta by the scanning electron microscope]

    Lerat MF, Richomme J, Connehaye P, Magre J, Bonnaillie J.

    J Gynecol Obstet Biol Reprod (Paris). 1972;1(5 Suppl 2):460-3. French. No abstract available. PMID: 4681587 [PubMed - indexed for MEDLINE]Related articles

    48.

    [Cancer of the breast and pregnancy]

    Bonnard J, Marionneau J, Lerat MF, Magre J, Raoult P.

    J Gynecol Obstet Biol Reprod (Paris). 1972;1(5 Suppl 2):377-8. French. No abstract available. PMID: 4681552 [PubMed - indexed for MEDLINE]Related articles

    49.

    [Two probable cases of pleuropulmonary endometriosis]

    Magre J, Leroux P, Lerat MF, Coroller J, Geffriaud M.

    Bull Fed Soc Gynecol Obstet Lang Fr. 1971 Nov-Dec;23(5):690. French. No abstract available. PMID: 5161977 [PubMed - indexed for MEDLINE]Related articles

    50.

    [Endometriosis of obstetrical vulvo-vaginal cicatrices]

    Lerat MF, Magre J.

    Bull Fed Soc Gynecol Obstet Lang Fr. 1971 Nov-Dec;23(5):688-9. French. No abstract available. PMID: 5161976 [PubMed - indexed for MEDLINE]Related articles

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