BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 11340066)

  • 1. Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder.
    Spodsberg N; Jacob R; Alfalah M; Zimmer KP; Naim HY
    J Biol Chem; 2001 Jun; 276(26):23506-10. PubMed ID: 11340066
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characteristics and structural requirements of apical sorting of the rat growth hormone through the O-glycosylated stalk region of intestinal sucrase-isomaltase.
    Spodsberg N; Alfalah M; Naim HY
    J Biol Chem; 2001 Dec; 276(49):46597-604. PubMed ID: 11577111
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency.
    Keiser M; Alfalah M; Pröpsting MJ; Castelletti D; Naim HY
    J Biol Chem; 2006 May; 281(20):14393-9. PubMed ID: 16543230
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structural determinants required for apical sorting of an intestinal brush-border membrane protein.
    Jacob R; Alfalah M; Grünberg J; Obendorf M; Naim HY
    J Biol Chem; 2000 Mar; 275(9):6566-72. PubMed ID: 10692463
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
    Jacob R; Zimmer KP; Schmitz J; Naim HY
    J Clin Invest; 2000 Jul; 106(2):281-7. PubMed ID: 10903344
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
    Gericke B; Amiri M; Scott CR; Naim HY
    Biochim Biophys Acta Mol Basis Dis; 2017 Mar; 1863(3):817-826. PubMed ID: 28062276
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.
    Alfalah M; Keiser M; Leeb T; Zimmer KP; Naim HY
    Gastroenterology; 2009 Mar; 136(3):883-92. PubMed ID: 19121318
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Naturally occurring mutations in intestinal sucrase-isomaltase provide evidence for the existence of an intracellular sorting signal in the isomaltase subunit.
    Fransen JA; Hauri HP; Ginsel LA; Naim HY
    J Cell Biol; 1991 Oct; 115(1):45-57. PubMed ID: 1717481
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The glucose-regulated protein GRP94 interacts avidly in the endoplasmic reticulum with sucrase-isomaltase isoforms that are associated with congenital sucrase-isomaltase deficiency.
    Hoter A; Naim HY
    Int J Biol Macromol; 2021 Sep; 186():237-243. PubMed ID: 34242650
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
    Husein DM; Rizk S; Naim HY
    Nutrients; 2020 Dec; 13(1):. PubMed ID: 33375084
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
    Ouwendijk J; Moolenaar CE; Peters WJ; Hollenberg CP; Ginsel LA; Fransen JA; Naim HY
    J Clin Invest; 1996 Feb; 97(3):633-41. PubMed ID: 8609217
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.
    Sander P; Alfalah M; Keiser M; Korponay-Szabo I; Kovács JB; Leeb T; Naim HY
    Hum Mutat; 2006 Jan; 27(1):119. PubMed ID: 16329100
    [TBL] [Abstract][Full Text] [Related]  

  • 13. O-linked glycans mediate apical sorting of human intestinal sucrase-isomaltase through association with lipid rafts.
    Alfalah M; Jacob R; Preuss U; Zimmer KP; Naim H; Naim HY
    Curr Biol; 1999 Jun; 9(11):593-6. PubMed ID: 10359703
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.
    Ritz V; Alfalah M; Zimmer KP; Schmitz J; Jacob R; Naim HY
    Gastroenterology; 2003 Dec; 125(6):1678-85. PubMed ID: 14724820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital sucrase-isomaltase deficiency: summary of an evaluation in one family.
    Chumpitazi BP; Robayo-Torres CC; Opekun AR; Nichols BL; Naim HY
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2(0 2):S36. PubMed ID: 23103651
    [No Abstract]   [Full Text] [Related]  

  • 16. Congenital sucrase-isomaltase deficiency.
    Treem WR
    J Pediatr Gastroenterol Nutr; 1995 Jul; 21(1):1-14. PubMed ID: 8576798
    [No Abstract]   [Full Text] [Related]  

  • 17. Molecular cloning of sucrase-isomaltase cDNA in the house musk shrew Suncus murinus and identification of a mutation responsible for isolated sucrase deficiency.
    Ito T; Hayashi Y; Ohmori S; Oda S; Seo H
    J Biol Chem; 1998 Jun; 273(26):16464-9. PubMed ID: 9632713
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.
    Marcadier JL; Boland M; Scott CR; Issa K; Wu Z; McIntyre AD; Hegele RA; Geraghty MT; Lines MA
    CMAJ; 2015 Feb; 187(2):102-107. PubMed ID: 25452324
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.
    Henström M; Diekmann L; Bonfiglio F; Hadizadeh F; Kuech EM; von Köckritz-Blickwede M; Thingholm LB; Zheng T; Assadi G; Dierks C; Heine M; Philipp U; Distl O; Money ME; Belheouane M; Heinsen FA; Rafter J; Nardone G; Cuomo R; Usai-Satta P; Galeazzi F; Neri M; Walter S; Simrén M; Karling P; Ohlsson B; Schmidt PT; Lindberg G; Dlugosz A; Agreus L; Andreasson A; Mayer E; Baines JF; Engstrand L; Portincasa P; Bellini M; Stanghellini V; Barbara G; Chang L; Camilleri M; Franke A; Naim HY; D'Amato M
    Gut; 2018 Feb; 67(2):263-270. PubMed ID: 27872184
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Four mutations in the SI gene are responsible for the majority of clinical symptoms of CSID.
    Uhrich S; Wu Z; Huang JY; Scott CR
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S34-5. PubMed ID: 23103650
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.