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    Results: 1 to 20 of 177

    1.

    p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.

    Kassem SA, Ariel I, Thornton PS, Hussain K, Smith V, Lindley KJ, Aynsley-Green A, Glaser B.

    Diabetes. 2001 Dec;50(12):2763-9.PMID: 11723059 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism.

    Suchi M, MacMullen CM, Thornton PS, Adzick NS, Ganguly A, Ruchelli ED, Stanley CA.

    Mod Pathol. 2006 Jan;19(1):122-9.PMID: 16357843 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.

    Verkarre V, Fournet JC, de Lonlay P, Gross-Morand MS, Devillers M, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.

    J Clin Invest. 1998 Oct 1;102(7):1286-91.PMID: 9769320 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma.

    Sempoux C, Guiot Y, Dahan K, Moulin P, Stevens M, Lambot V, de Lonlay P, Fournet JC, Junien C, Jaubert F, Nihoul-Fekete C, Saudubray JM, Rahier J.

    Diabetes. 2003 Mar;52(3):784-94.PMID: 12606521 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.

    Fournet JC, Mayaud C, de Lonlay P, Gross-Morand MS, Verkarre V, Castanet M, Devillers M, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.

    Am J Pathol. 2001 Jun;158(6):2177-84.PMID: 11395395 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome.

    Grandjean V, Smith J, Schofield PN, Ferguson-Smith AC.

    Proc Natl Acad Sci U S A. 2000 May 9;97(10):5279-84.PMID: 10779549 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    p57(KIP2) is not mutated in hepatoblastoma but shows increased transcriptional activity in a comparative analysis of the three imprinted genes p57(KIP2), IGF2, and H19.

    Hartmann W, Waha A, Koch A, Goodyer CG, Albrecht S, von Schweinitz D, Pietsch T.

    Am J Pathol. 2000 Oct;157(4):1393-403.PMID: 11021841 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.

    Fournet JC, Verkarre V, De Lonlay P, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.

    Ann Endocrinol (Paris). 1998;59(6):485-91.PMID: 10189991 [PubMed - indexed for MEDLINE]Related articles

    9.

    Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy.

    Kassem SA, Ariel I, Thornton PS, Scheimberg I, Glaser B.

    Diabetes. 2000 Aug;49(8):1325-33.PMID: 10923633 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

    Glaser B, Ryan F, Donath M, Landau H, Stanley CA, Baker L, Barton DE, Thornton PS.

    Diabetes. 1999 Aug;48(8):1652-7.PMID: 10426386 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome.

    Gaston V, Le Bouc Y, Soupre V, Vazquez MP, Gicquel C.

    Horm Res. 2000;54(1):1-5.PMID: 11182628 [PubMed - indexed for MEDLINE]Related articles

    12.

    Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism.

    Fournet JC, Mayaud C, de Lonlay P, Verkarre V, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.

    Horm Res. 2000;53 Suppl 1:2-6.PMID: 10895035 [PubMed - indexed for MEDLINE]Related articles

    13.

    Human p57(KIP2) defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour.

    Taniguchi T, Okamoto K, Reeve AE.

    Oncogene. 1997 Mar 13;14(10):1201-6.PMID: 9121769 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Congenital hyperinsulinism: molecular basis of a heterogeneous disease.

    Meissner T, Beinbrech B, Mayatepek E.

    Hum Mutat. 1999;13(5):351-61. Review.PMID: 10338089 [PubMed - indexed for MEDLINE]Related articles

    15.

    A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism.

    Nestorowicz A, Inagaki N, Gonoi T, Schoor KP, Wilson BA, Glaser B, Landau H, Stanley CA, Thornton PS, Seino S, Permutt MA.

    Diabetes. 1997 Nov;46(11):1743-8.PMID: 9356020 [PubMed - indexed for MEDLINE]Related articles

    16.

    Dominantly inherited hyperinsulinaemic hypoglycaemia.

    de Lonlay P, Giurgea I, Sempoux C, Touati G, Jaubert F, Rahier J, Ribeiro M, Brunelle F, Nihoul-Fékété C, Robert JJ, Saudubray JM, Stanley C, Bellanné-Chantelot C.

    J Inherit Metab Dis. 2005;28(3):267-76. Review.PMID: 15868462 [PubMed - indexed for MEDLINE]Related articles

    17.

    Diabetes and hypoglycaemia in young children and mutations in the Kir6.2 subunit of the potassium channel: therapeutic consequences.

    Flechtner I, de Lonlay P, Polak M.

    Diabetes Metab. 2006 Dec;32(6):569-80. Review.PMID: 17296510 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Comparative reverse transcription-polymerase chain reaction and in situ hybridization analyses of human imprinted p57KIP2 and insulin-like growth factor 2 gene transcripts in fetal kidney and Wilms' tumors using archival tissue.

    Soejima H, McLay J, Hatada I, Mukai T, Jinno Y, Niikawa N, Yun K.

    Lab Invest. 1998 Jan;78(1):19-28.PMID: 9461119 [PubMed - indexed for MEDLINE]Related articles

    19.

    [Congenital hyperinsulinism in newborn and infant]

    Giurgea I, Ribeiro MJ, Boddaert N, Touati G, Robert JJ, Saudubray JM, Jaubert F, Bellanné-Chantelot C, Brunelle F, Nihoul-Fékété C, de Lonlay P.

    Arch Pediatr. 2005 Nov;12(11):1628-35. Epub 2005 Sep 28. Review. French. PMID: 16198094 [PubMed - indexed for MEDLINE]Related articles

    20.

    Disruption of imprinted genes at chromosome region 11p15.5 in paediatric rhabdomyosarcoma.

    Anderson J, Gordon A, McManus A, Shipley J, Pritchard-Jones K.

    Neoplasia. 1999 Oct;1(4):340-8.PMID: 10935489 [PubMed - indexed for MEDLINE]Related articlesFree article

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